«a.» a; g :1? J” ... . . & a.“ ".33“, . 6 : ’ nun“ . fhmvfi x . (.3 E i» g: . .9 . . ‘ .3: :31. . i .. Jndflt‘lfiau. ,rT. .) : 4. L x : 3.1!... v. ‘ 1.. ’szukflpiphahfi‘.’ It. .rLXIXot; (r '31.}: 1 3A, . . ”:4? .1 L33. :1! .mpmhf \ .. . | 5 JR“ $3.2m I'll" I! l' ‘I’ '7 HR??? 3.3303 LIBPARY WM” Michigar. State University This is to certify that the thesis entitled USING SCOUTING AND DISEASE FORECASTERS TO MANAGE FOLIAR BLIGHTS 0F CARROTS presented by Ryan Scott Bounds has been accepted towards fulfillment of the requirements for M.S. _ Plant Pathology fiegree 1n Major professor Date 6/1! 1/03 0.7639 MS U is an Affirmative Action/Equal Opportunity Institution PLACE IN RETURN Box to remove this checkout from your record. TO AVOID FINES return on or before date due. MAY BE RECALLED with earlier due date if requested. DATE DUE DATE DUE DATE DUE 6/01 c-JCIFICIDatoDuopes-pJ 5 USING SCOUTING AND DISEASE FORECASTERS TO MANAGE FOLIAR BLIGHTS OF CARROTS By Ryan Scott Bounds A THESIS Submitted to Michigan State University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Department of Plant Pathology 2003 ABSTRACT USING SCOUTING AND DISEASE FORECASTERS TO MANAGE FOLIAR BLIGHTS OF CARROTS By Ryan Scott Bounds Fungal foliar blights of carrots, caused by Alternaria dauci and Cercospora carotae, result in necrotic lesions on leaves and petioles that may cause defoliation, decreasing the efficiency of mechanical harvest. Fungicides are applied every 7 to 10 days, regardless of weather conditions or disease pressure. The objectives of these studies were to evaluate Tom-Cast and other disease forecasters for timing sprays and to determine when to apply the first spray based on field scouting and disease incidence thresholds. The Tom-Cast system was the most effective and reliable disease forecaster tested, resulting in a fungicide savings of $47.25 and $54.88 per acre in 2001 and 2002, respectively, compared with the 7-day schedule, while providing similar blight control. Chlorothalonil alternated with azoxystrobin was applied every 10 days or according to Tom-Cast with a threshold of 15, 20, or 25 disease severity values (DSVs). Sprays for these programs were initiated prior to symptom development, or when foliage was infected at a trace, 5%, or 10% level. Up to four sprays were omitted saving $46.05 and $41.85 per acre in 2001 and 2002, respectively, and comparable disease control was achieved by initiating applications when a trace amount of the foliage was blighted and applying subsequent sprays according to Tom-Cast 15 DSV, compared with the 10-day spray schedule initiated prior to disease development. DEDICATION In memory of Louis Willard Harper (1936-2001), former Crops Club advisor and professor of Crop Science at California Polytechnic State University, San Luis Obispo. Thank you for all your inspiration. iii ACKNOWLEDGEMENTS I would like to thank the people who contributed to the success and completion of these studies. Dr. Mary Hausbeck, my major professor, provided guidance and numerous opportunities for me to sink my teeth into applied plant pathology. Brian Cortright and Sheila Linderman offered technical assistance. To my family and loved ones — I wouldn’t be where I am today without your love and support. You have been the most supportive people during my graduate education and every day of my life. iv TABLE OF CONTENTS LIST OF TABLES .................................................................................. LIST OF FIGURES ................................................................................. LITERATURE REVIEW Introduction Alternaria dauci Cercospora carotae Disease Control Strategies Disease Scouting Disease Forecasting Literature Cited CHAPTER I. COMPARING DISEASE FORECASTING SYSTEMS FOR TIMING FUNGICIDE APPLICATIONS TO CONTROL ALTERN ARIA AND CERCOSPORA BLIGHTS OF CARROTS. . Abstract Introduction Materials and Methods Results Discussion Literature Cited CHAPTER II. TIMING FUNGICIDE APPLICATIONS ACCORDING TO FIELD SCOUTING AND TOM-CAST TO CONTROL ALTERNARIA AND CERCOSPORA BLIGHTS OF CARROTS ......................... Abstract Introduction Materials and Methods Results Discussion Literature Cited APPENDIX A. SUMMARY OF WEATHER DATA, FUNGICIDE APPLICATION DATES, AND FINAL DISEASE ASSESSMENTS FOR FIELD STUDIES IN 2001 AND 2002 .......... APPENDIX B. PESTICIDE APPLICATION EQUIPMENT STUDIES IN 2001 ...... 1 .vi xii OWNF‘ 00 11 16 20 21 22 24 30 35 38 39 40 41 43 5 1 92 96 98 13 LIST OF TABLES Table Page CHAPTER I. COMPARING DISEASE FORECASTING SYSTEMS FOR TIMING FUNGICIDE APPLICATIONS TO CONTROL ALTERNARIA AND CERCOSPORA BLIGHTS OF CARROTS 1. Effect of disease caused by A. dauci and C. carotae on yield of ‘Cellobunch’ carrots left untreated or sprayed with the fungicide Chlorothalonil (1.29 kg a.i./ha) applied every seven days or according to disease forecasters and number of fungicide applications and cost of fungicide programs in 2001 and 2002 ............... 28 2. Effect of disease caused by A. dauci and C. carotae on the area under the disease progress curve for petiole and leaf blight on ‘Cellobunch’ carrots left untreated or sprayed with the fungicide Chlorothalonil (1.29 kg a.i.lha) applied every seven days or according to disease forecasters in 2001 and 2002 ................................ 31 3. Effect of disease caused by A. dauci and C. carotae on petiole health of ‘Cellobunch’ carrots left untreated or sprayed with the fungicide Chlorothalonil (1.29 kg a.i./ha) applied every seven days or according to disease forecasters in 2001 and 2002 ................................................................................... 34 CHAPTER II. TIMING FUNGICIDE APPLICATIONS ACCORDING TO FIELD SCOUTING AND TOM-CAST TO CONTROL ALTERNARIA AND CERCOSPORA BLIGHTS OF CARROTS 4. Summary of disease assessment variables that were not normally distributed and accompanying transformations used to normalize variables ......................... 50 5. Number of fungicide applications and cost of fungicide programs per acre for ‘Early Gold’, ‘Cellobunch’, and ‘Prime Cut’ carrots left untreated or sprayed with Chlorothalonil (1.29 kg a.i.fha) alternated with azoxystrobin (0.11 kg a.i./ha) initially applied based on disease incidence thresholds and reapplied every 7 or 10 days or according to Tom—Cast in 2001 and 2002 ................................... 52 6. Effects of spray initiation timings and application intervals on yield of ‘Prime Cut’ carrots treated with the fungicides Chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) used to control foliar blights caused by A. dauci and C. carotae in 2002 ............... 53 vi LIST OF TABLES (cont’d) Table Page 7. 10. 11. 12. Effect of the fungicides Chlorothalonil (1 .29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.lha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) on yield of ‘Early Gold’ carrots infected with A. dauci and C. carotae in 2001 and 2002. . 54 Effect of the fungicides Chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) on yield of ‘Cellobunch’ carrots infected with A. dauci and C. carotae in 2001 and 2002. . ....55 Effect of the fungicides Chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.lha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) on yield of ‘Prime Cut’ carrots infected with A. dauci and C. carotae in 2001 ................... 56 Effects of spray initiation timings and application intervals on the area under the disease progress curve for petiole and leaf blights caused by A. dauci and C. carotae on ‘Early Gold’ carrots treated with the fungicides Chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.lha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 and 2002 ............................................................... 60 Effect of spray initiation timings for each application interval on the area under the disease progress curve of petiole blight caused by A. dauci and C. carotae on ‘Early Gold’ carrots treated with the fungicides Chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 ........................................................................... 63 Effects of spray initiation timings and application intervals on the area under the disease progress curve and final ratings for petiole health of ‘Early Gold’ carrots treated with the fungicides Chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) for control of A. dauci and C. carotae in 2001 and 2002 ...................................... 64 vii LIST OF TABLES (cont’d) Table 13. Effect of spray initiation timings for each application interval on the final petiole health evaluation assessing disease caused by A. dauci and C. carotae on ‘Early Gold’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 ...................................................... 67 14. Effects of spray initiation timings and application intervals on the area under the disease progress curve for petiole and leaf blights caused by A. dauci and C. carotae on ‘Cellobunch’ carrots treated with the fungicides chlorothalonil (1 .29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.fha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 and 2002 ........................................... 71 15. Effects of spray initiation timings and application intervals on the area under the disease progress curve and final ratings for petiole health of ‘Cellobunch’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) for control of A. dauci and C. carotae in 2001 and 2002 ...................................... 73 16. Effects of spray initiation timings and application intervals on the area under the disease progress curve for petiole and leaf blights caused by A. dauci and C. carotae on ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 ....................................................... 79 17. Effect of spray initiation timings for each application interval on the area under the disease progress curve of petiole blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 ........................................................................... 81 viii LIST OF TABLES (cont’d) Table 18. 19. 20. 21. Effects of spray initiation timings and application intervals on the area under the disease progress curve for petiole and leaf blights caused by A. dauci and C. carotae on ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2002 ................................................ 83 Effect of spray initiation timings for each application interval on the area under the disease progress curve of petiole blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.lha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2002 ........................................................................... 85 Effect of spray initiation timings for each application interval on the area under the disease progress curve of leaf blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.1 1 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2002 ........................................................................... 88 Effects of spray initiation timings and application intervals on the area under the disease progress curve and final ratings for petiole health of ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) for control of A. dauci and C. carotae in 2002 .................................... 90 APPENDIX A. SUMMARY OF WEATHER DATA, FUNGICIDE 22. 23. APPLICATION DATES, AND FINAL DISEASE ASSESSMENTS FOR FIELD STUDIES IN 2001 AND 2002 Weather data and Disease Severity Values (DSV) from the Michigan State University Muck Soils Experimental Farm during the 2001 and 2002 growing seasons ........................................................................................... 99 Dates of chlorothalonil (1 .29 kg a.i.lha) applications on ‘Cellobunch’ carrots in 2001 ........................................................................................... 100 ix Table 24. 25. 26. 27. 28. 29. 30. 31. 32. LIST OF TABLES (cont’d) 13 Dates of chlorothalonil (1.29 kg a.i.lha) applications on ‘Cellobunch’ carrots in 2002 .......................................................................................... 101 Summary of the effects of disease caused by A. dauci and C. carotae on petiole blight, leaf blight, and yield of ‘Cellobunch’ carrots left untreated or sprayed with the fimgicide chlorothalonil (1 .29 kg a.i.lha) applied every seven days or according to disease forecasters in 2001 and 2002 ...................... 102 Weather data and Disease Severity Values (DSV) from the trial site near Fremont, MI during the 2001 and 2002 growing seasons ............................... 103 Dates of fungicide applications on ‘Early Gold’ and ‘Cellobunch’ carrots using chlorothalonil (1 .29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) in 2001 .................................................................................. 104 Dates of fungicide applications on ‘Early Gold’ and ‘Cellobunch’ carrots using chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.lha) in 2002 ................................................................................. 105 Dates of fungicide applications on ‘Prime Cut’ carrots using chlorothalonil (1 .29 kg a.i.fha) alternated with azoxystrobin (0.11 kg a.i./ha) in 2001 ............... 106 Dates of fungicide applications on ‘Prime Cut’ carrots using chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) in 2002 ............... 107 Summary of the effects of disease caused by A. dauci and C. carotae on petiole blight, leaf blight, and yield of ‘Early Gold’ carrots left untreated or sprayed with the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% leaf blight and reapplied at 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 and 2002 ........................................................................................ 109 Summary of the effects of disease caused by A. dauci and C. carotae on petiole blight, leaf blight, and yield of ‘Cellobunch’ carrots left untreated or sprayed with the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.fha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% leaf blight and reapplied at 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 and 2002 ........................................................................................ 1 10 LIST OF TABLES (cont’d) Table Page 33. Summary of the effects of disease caused by A. dauci and C. carotae on petiole blight, leaf blight, and yield of ‘Prime Cut’ carrots left untreated or sprayed with the fungicides chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% leaf blight and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001 and 2002 ........................................................................................ 11 1 APPENDIX B. PESTICIDE APPLICATION EQUIPMENT STUDIES IN 2001 34. Effect of nozzle type on foliar blights caused by Alternaria dauci and Cercospora carotae on ‘Goliath’ carrots in 2001 ......................................... 116 35. Effect of fungicides on foliar blights caused by Alternaria dauci and Cercospora carotae on ‘Goliath’ carrots in 2001 ......................................... 117 36. Effect of nozzle type on foliar blights caused by Altemaria dauci and Cercospora carotae on ‘Goliath’ carrots in 2001 ......................................... 120 37. Effect of fungicides on foliar blights caused by Alternaria dauci and Cercospora carotae on ‘Goliath’ carrots in 2001 ......................................... 121 xi LIST OF FIGURES Figure Page CHAPTER I. COMPARING DISEASE FORECASTING SYSTEMS FOR TIMING FUNGICIDE APPLICATIONS TO CONTROL ALTERNARIA AND CERCOSPORA BLIGHTS OF CARROTS 1. Disease progress curves for petiole and leaf blight caused by A. dauci and C. carotae on ‘Cellobunch’ carrots left untreated or treated with the fungicide chlorothalonil (1.29 kg a.i.lha) applied every 7 days or according to disease forecasters in 2001 and 2002 .................................................................. 33 CHAPTER II. TIMING FUNGICIDE APPLICATIONS ACCORDING TO FIELD SCOUTING AND TOM-CAST TO CONTROL ALTERNARIA AND CERCOSPORA BLIGHTS OF CARROTS 2. Disease progress curves for leaf blight caused by A. dauci and C. carotae on ‘Early Gold’ carrots left untreated or treated with chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002 .......................................................................................... 58 3. Disease progress curves for petiole blight caused by A. dauci and C. carotae on ‘Early Gold’ carrots left untreated or treated with chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002 .......................................................................................... 59 4. Disease progress curves for petiole blight caused by A. dauci and C. carotae on ‘Cellobunch’ carrots left untreated or treated with chlorothalonil (1.29 kg a.i.fha) alternated with azoxystrobin (0.11 kg a.i./ha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002 .......................................................................................... 68 5. Disease progress curves for leaf blight caused by A. dauci and C. carotae on ‘Cellobunch’ carrots left untreated or treated with chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.lha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002 .......................................................................................... 69 xii LIST OF FIGURES (cont’d) '6 Figure age 6. Disease progress curves for leaf blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots left untreated or treated with chlorothalonil (1 .29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002 .......................................................................................... 76 7. Disease progress curves for petiole blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots lefi untreated or treated with chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002 .......................................................................................... 77 8. Disease progress curves for petiole and leaf blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots lefi untreated or treated with chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.lha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 7 days in 2002 ............................................................... 78 xiii LITERATURE REVIEW Introduction In 2001, Michigan harvested 6,300 acres of carrots (Daucus carota L. var. sativa DC.) that yielded 115,500 tons for use in fresh market and processing (NASS, 2003). Carrots grown for the fresh market were grown on 4,800 acres and valued at $23.2 million. Carrots for processing were grown on 1,500 acres and valued at $2.2 million. Michigan ranks third and fifth for production of fresh market and processing carrots, respectively, and the state ranks third in total carrot production. California, Washington, Colorado, Texas, and Wisconsin rank first, second, fourth, fifih, and sixth, respectively, in total carrot production (NASS, 2003). Michigan carrots are grown in deep, well-drained mineral and muck soils. Carrots are planted during mid-April to mid-June and are harvested from the beginning of August through November. Carrots are harvested by a machine that loosens the soil and simultaneously grips the foliage, pulling the roots from the soil (Zandstra et al., 1986). In Michigan, Alternaria leaf blight and Cercospora leaf blight are the most common pathogens affecting carrot foliage. Alternaria dauci (Kuhn) Groves & Skolko (Groves and Skolko, 1944) is favored by periods of warm, wet environmental conditions (Doran and Guba, 1928). Similarly, Cercospora carotae (Passerini) Solheim is favored by warm periods and high relative humidity. Environmental conditions that enhance the grth of these pathogens frequently occur during the carrot-growing season in Michigan. Both pathogens cause foliar blight resulting in a reduction of photosynthetic capacity and weakening the petioles and foliage needed for mechanical harvest. Carrot tops weakened by blight are easily detached from the root when gripped by mechanical harvesters, resulting in unharvested carrots (Gillespie and Sutton, 1979; Strider, 1963). Traditionally, blights are controlled through the use of protectant fungicides applied every 7 to 10 days, from July through September (Gillespie and Sutton, 1979). Calendar-based spray schedules typically require 5 to 9 applications and may result in unneeded sprays, increasing production costs (Gillespie and Sutton, 1979), and the likelihood of pathogens developing chemical insensitivity (Bolkan and Reinert, 1994). Alternaria dauci Alternaria dauci is distributed worldwide (Rotem, 1994) and is considered a preeminent foliar pathogen in most carrot-growing regions (Hooker, 1944; Maude, 1966; Netzer and Kenneth, 1969; Scott and Wenham, 1973). The fungus was first reported in the United States as Macrosporium carotae Ellis & Langlois (Ellis and Langlois, 1890). The pathogen has a limited host range, infecting only wild carrot (Daucus carota L.) and cultivated carrot (Daucus carota L. var. sativa DC.), both in the family Apiaceae (Doran and Guba, 1928). The fungus is classified in the phylum Deuteromycota, order Hyphomycetes, and family Dematiaceae (Rotem, 1994). Conidiophores of A. dauci are olive-brown, septate, simple or branched, variable in length, and 6-10u in diameter. Conidia are dark olive-brown, obclavate, with long beaks, having 7-10 transverse septa and few longitudinal septa, born singly or in short chains, and 150-25011 long by 15-25u in diameter (Groves and Skolko, 1944). In general, A. dauci is capable of producing spores at all temperatures that occur during the growing season (Strandberg, 1977). C onidia germinate over a wide temperature range from 16° to 28° C, but germinate best at 22° to 24° C (Doran and Guba, 1928). Hooker (1944) concluded that maximum mycelial growth occurs at 28° C, and most conidia germinate between 20° and 37° C. Sporulation is favored by darkness, a minimum leaf wetness duration of 10 h, and temperatures from 11 to 23° C (Langenberg, 1975). Though often confused with C. carotae, A. dauci generally infects older foliage (Doran and Guba, 1928; Hooker, 1944; Maude, 1966), producing dark brown to black irregularly shaped lesions along leaf margins. Under favorable conditions, blight symptoms develop four to six days after inoculation and Sporulation occurs within eight to ten days (Strandberg, 1977). Chlorosis surrounding the Alternaria lesion is more pronounced than that caused by C. carotae (Hooker, 1944). The lesions expand and join together, producing a blighted or burned appearance on the foliage. Severely infected petioles may become girdled and disengage from the root. A. dauci can infect all parts of the carrot inflorescence (Strandberg, 1983), resulting in contaminated seed. Mycelium may penetrate the inner layer of the pericarp tissue, and conidiophores protrude through the pericarp (N etzer and Kenneth, 1969). Conidia adhering to the surface of seeds can germinate after 9 months (Strandberg, 1983) or up to 30 months (Netzer and Kenneth, 1969) when stored at ambient conditions; thus, infected seeds serve as a source of long-tenn primary inoculum (Strandberg, 1983). When seeds are infected with A. dauci, pre or post-emergence damping-off may occur (Maude, 1966; Neergaard, 1945; Netzer and Kenneth, 1969). Infected seedlings may increase inoculum levels and contribute to early season leaf blight epidemics (Strandberg, 1984). Concentrations of airborne A. dauci conidia and weather variables were recorded in an area of intensive carrot production in Ontario (Langenberg et al., 1977). Peak numbers of conidia were trapped between 1300 hours and 1500 hours. The declining number of trapped conidia after 1500 hours were not correlated with weather variables, but were assumed to be an indication of the number of mature conidia available for dispersal. Release of A. dauci conidia was correlated with increasing temperatures, increasing wind, decreasing RH, and drying of the foliage. Rain removed airborne conidia from the air and contributed to prolonged periods of leaf wetness, which reduced the number of airborne conidia by restricting spore liberation. Although wind temporarily increased spore liberation and numbers of airborne conidia, extensive high winds damaged conidiophores and resulted in few trapped conidia following the wind period (Langenberg et al., 1977). Other field studies indicate that plentiful amounts of conidia are produced following nights of 95—1 00% RH or leaf wetness for 8-12 hours (Strandberg, 1977). Spore abundance is not well correlated with hours of RH above 95%, but hours of leaf wetness are correlated with number of conidia trapped. Following daybreak, and when the RH fell below 80%, conidia are liberated and disseminated by wind. Wind speeds 2- 3 m/sec are needed to dislodge large numbers of conidia (Strandberg, 1977). Seasonal differences in the onset and development of Alternaria blight epidemics have been observed. Doran and Guba (1928) found that young carrot plants (up to eight weeks) were moderately resistant to infection, but susceptibility increased with plant age. Hooker (1944) observed that older leaves were more susceptible to infection, causing the disease to progress more rapidly at the end of the season. Zimmer and McKeen (1969) suggested that the interaction of photoperiod and temperature was the cause of seasonal differences. Strandberg (1977) attributed late season epidemics to the increased duration of leaf wetness, typical during the cool, longer nights of late summer and early fall. Cercospora carotae Cercospora carotae occurs in temperate regions and is considered an important foliar pathogen in most carrot-producing areas (Arcelin and Kushalappa, 1991; Thomas, 1943). C. carotae has a wide host range in the genus Daucus, infecting wild and cultivated carrots (Daucus carota L. and Daucus carota L. var. sativa DC.), D. hispanicus Gouan, D. maritimus Lam., D. pulcherrimus Koch ex DC., D. maximus Desf., D. gingidium L., and D. pusillus Mich. (Thomas, 1943). The fungus is classified in the phylum Deuteromycota, order Hyphomycetes, and family Dematiaceae (Solheim, 1929). Conidiophores of C. carotae are light yellow-brown, amphigenous, simple, straight to subflexous, non-stromatic, with minute conidial scars near the tip, and 15-45p. long by 3-5u in diameter. Conidia are at first cylindrical then become narrowly obclavate, bacilliforrn, hyaline to subhyline, continuous or obscurely 1-8 septate, and 30- 115111 long by 2-3u in diameter (Solheim, 1929). The life cycle of C. carotae is similar to that of A. dauci. C. carotae grows rapidly between 19° and 28° C, and maximum germination is observed at 16° to 28° C. Sporulation occurs between 13° and 28° C but requires free moisture (Thomas, 1943). Hooker (1944) made similar findings; the majority of conidia germinated at 20° to 32° C, and the optimum temperature for mycelial development was 28° C. Wind is assumed as the primary disseminating agent of C. carotae. Thomas (1943) collected conidia on agar plates, exposed for 3 min, located 3, 30, and 92 m downwind from severely blighted carrot fields. Infection occurs only through stomata via a germ tube (Thomas, 1943). Lesions may occur on the foliage and first appear as pinpoint chlorotic spots that expand and generate necrotic centers. Generally, lesions located away from the edge of the leaf are circular, and lesions along leaf margins and petioles are elongate. A light gray or silvery mass of conidia may be observed macroscopically on lower surfaces of the lesion during periods of high humidity. Lesion expansion and Sporulation continues until spots coalesce and the leaflet is killed (Thomas, 1943). The relationship of temperature and leaf wetness duration on infection of C. carotae was examined using a quantitative model developed under controlled experimental conditions (Carisse and Kushalappa, 1990). In general, infection occurs following 12 h of leaf wetness at temperatures 16, 20, 24, 28, and 32° C, and increases with wetness duration, except at 32° C where infection decreases with increasing periods of leaf wetness. Leaf wetness duration of 24 h and temperatures between 20 and 28° C are required to promote extensive infection of C. carotae. Maximum numbers of lesions were produced in growth chambers held at 16, 20, 24, and 28° C with 96 h of leaf wetness (Carisse and Kushalappa, 1990). Carisse and Kushalappa (1992) examined the influence of interrupted wet periods and relative humidity on infection by C. carotae. An interrupted wet period consisted of 24 h of initial leaf wetness and 12 h of final leaf wetness, separated by a dry period of 3, 6, 12, 18, 24, 30, or 36 h. Continuous leaf wetness durations were 36, 39, 42, 48, 54, 60, 66, and 72 h. In general, fewer lesions per plant were produced during interrupted wet periods than continuous wet periods. However, plants subjected to the 3 to 24 h dry periods, except for the 12 h dry period, produced more lesions than plants held at continuous leaf wetness for 36 h. Therefore, germinated spores can survive dry periods and resume infection when subjected to an additional wetness period. The number of lesions per plant increased with temperatures of 16 to 28° and with an increase in humidity level (Carisse and Kushalappa, 1992). Carisse et a1. (1993) investigated the effect of temperature and duration of different moisture conditions on sporulation of C. carotae. No sporulation occurred at a relative humidity g 92%, but abundant conidia were produced under leaf wetness, 96% RH, and 96% RH preceded by 12 h of leaf wetness. Sporulation increased with increasing duration of moisture period or leaf wetness and increasing temperature from 16 to 28° C. Maximum sporulation was observed at 28° C after 96 h of leaf wetness, although all temperature-moist conditions sporulated after 48 h. In general, numerous conidia were produced after 48 h of leaf wetness at 20 to 28° C. The temperature range for conidial infection is similar to that for sporulation, therefore, temperatures between 16 and 32° C accompanied by leaf wetness or RH 196% for 24 h are considered favorable periods for sporulation of C. carotae (Carisse et al., 1993). Disease Control Strategies Alternaria and Cercospora leaf blights are managed through crop rotation, disease-free seed, tolerant cultivars, and fungicide applications. Crop rotation was recommended by Doran & Guba (1928) to obtain partial control of A. dauci and C. carotae because these fungi overwinter in the soil and on infected carrot debris and may infect subsequent carrot plantings. Deep plowing or the destruction of infected carrot tops and planting of non-host crops following carrot production is encouraged to prevent high levels of inoculum deposition in the soil. However, C. carotae was recovered ten months after infected carrot leaves were placed in wire containers and buried 10 and 15 cm below the soil surface (Thomas, 1943). A. dauci survived longer on petioles on the surface of the soil than on petioles buried at depths of 10 and 20 cm, although the experiment duration was only five months (N etzer and Kenneth, 1969). Survival of A. dauci is negatively correlated with increasing soil moisture (Pryor et al., 2002). Fallow carrot fields in a warm, dry carrot production area in California allowed A. dauci to survive on infected foliage on and below the soil surface for up to one year; reduced survival was observed in irrigated alfalfa and rose fields and in a warm, moist carrot field in Florida. Plowing under of infected carrot residue hastens decomposition thereby reducing survival, and may be more beneficial for cooler carrot production areas where decomposition rates are slower (Pryor et al., 2002). Volunteer carrot plants (Pryor et al., 2002) and alternate hosts provide a source of inoculum for present and future carrot plantings and should be removed from carrot-growing areas (Doran and Guba, 1928). Seed treatments reduce damping-off of carrot plants, but these measures may not entirely eradicate A. dauci from carrot seed. Maude (1966) claimed complete eradication of A. dauci from carrot seeds by a 24-hour soak at 30° C in a 0.2% thirarn suspension, without compromising seed germination. Strandberg (1984) repeated Maude’s experiment with a larger number of seeds and a more sensitive assay method and observed Alternaria blight symptoms, indicating that the seed treatment did not entirely eradicate the pathogen. The use of 0.5% iprodione seed-soak for 24 hours at 30° C apparently eradicated A. dauci from medium sized seed samples, but 0.01% infected seedlings were detected in a larger seed sample using a similar assay method (Strandberg, 1984). Although hot water seed treatments have been tested (Strandberg, 1988), this application alone is incapable of eliminating A. dauci without banning the seed (Strandberg and White, 1989). In commercial carrot production, planting large quantities of treated carrot seeds may result in several hundred infected plants per hectare, sufficient to cause an Alternaria blight epidemic (Strandberg, 1984). Cultivar resistance to A. dauci and C. carotae was examined for 50 unsprayed carrot varieties and breeding selections in 1999 (James et al., 1999). Forty percent of the cultivars examined produced AUDPC (Area Under the Disease Progress Curve) values that were significantly less than the susceptible standard varieties. All 50 cultivars showed symptoms of blight, and no cultivars displayed complete resistance to both A. dauci and C. carotae. In another study, Strandberg et a1. (1972) evaluated 331 carrot varieties from 31 countries for resistance to A. dauci and found nine varieties capable of containing blight symptoms for the entire growing season without any fungicidal application. Cercospora-tolerant plants exhibit fewer and smaller lesions than susceptible cultivars (Angell and Gabelman, 1968). Cultivars with complete resistance to A. dauci or C. carotae have not been identified, but blight tolerant cultivars are available. Santos et a1. (2000) examined the use of gibberellic acid (GA) applications to control Alternaria blight. Applications of (GA) or iprodione decreased the severity of blight and increased the top and root weights compared to the untreated control. Disease severity decreased linearly with an increase in GA concentration, although the high GA concentration (250 mg/L) increased the amount of foliage at the expense of root mass. The reduction in disease severity of the GA treated plants may be a result of the increase in leaf length and more upright appearance of plants, allowing greater air circulation through the crop canopy (Santos et al., 2000). Fungicides are relied on as disease control tools. Traditionally, blights are controlled through the use of protectant fungicides applied every 7 to 10 days, from July 10 through September (Gillespie and Sutton, 1979). Currently, two protectant active ingredients (chlorothalonil and copper-based fungicides) and two systemic active ingredients (iprodione and azoxystrobin) are registered to control Alternaria and Cercospora (iprodione not registered) leaf blights in Michigan (Bird et al., 2002). F ungicide resistance of A. dauci to iprodione has been reported (Fancelli and Kimati, 1991). In addition, iprodione and chlorothalonil are pesticides classified as B2 carcinogens and are scheduled for review by the EPA under the Food Quality Protection Act (FQPA). The future availability of these products is uncertain. One Michigan food processor does not allow the use of iprodione on carrots because it is a B2 carcinogen and residues are a concern. Azoxystrobin (Quadris, Syngenta Crop Protection, Greensboro, NC), a recently registered reduced risk systemic fungicide, is an effective tool to control Alternaria and Cercospora blights in rotation with protectant fungicides (Hausbeck et al., 2000; James and Stevenson, 1999). Use of this product in rotation with protectant fungicides already used by Michigan growers may reduce the number of B2 carcinogenic fungicide applications. Most growers employ disease management practices to reduce the occurrence and development of Alternaria and Cercospora blights, otherwise, harvesting losses are often incurred. For example, a Wisconsin study reported the standard weekly fungicide program yielded 15.7 tons/A while the untreated plot yielded 11.7 tons/A and resulted in 23.8% unmarketable carrots (James and Stevenson, 1999). Disease Scouting Growers and agricultural consultants utilize field scouting to monitor pests, soil moisture, projected yield, and other various aspect of a field or the crop grown in the 11 field. Such observations often contribute to the decision making process for implementing management strategies. One disease forecasting system used to time sprays for controlling A. dauci on carrots incorporates the use of field scouting to determine when the first fungicide application should be made (Gillespie and Sutton, 1979). Fields are scouted and the first fimgicide spray is applied when blight symptoms developed on 1 to 2% of the foliage. This level of disease was selected because it was the first observable stage of Alternaria blight. In each of four years, one to three spays were saved by delaying the initial fungicide application until blight symptoms were detected by scouting compared with the standard fungicide schedule (Gillespie and Suuon,l979) A tomato Integrated Pest Management (IPM) program advised that fields should be scouted one or two times per week for diseases and insects (Keinath et al., 1996). Fungicide sprays to control early blight (Alternaria solani) were initiated when 3 to 6% of the leaf area showed symptoms of disease. The IPM scouted plots were initially sprayed 42 days after the standard weekly fungicide schedule commenced. The delay in initiating the IPM treatment resulted in higher disease severity and a reduction in yield of extra large fruit compared to the weekly fungicide schedule. Management of early blight using scouting in the tomato IPM program was unsuccessfirl, but may be improved by lowering the spray initiation threshold to 1 to 3% leaf area blighted (Keinath et al., 1996). Disease Forecasting European studies in the early to mid-19005 on infection periods for Plasmopara viticola and Phytophthora infestans represented the beginning of disease forecasting. Other terms describing the concept of disease forecasting include disease predictive l2 schemes and disease warning systems, but the term “disease forecasting” will be used here. Most disease forecasting systems rely on weather variables (Zadoks, 1984), in conjunction with the biology and epidemiology of the pathogen, to predict infection or developmental periods of the disease on a particular host (Krause and Massie, 1975). Forecasting systems are appropriate for diseases that are economically significant, somewhat variable between seasons, controlled by available and economical methods, and known to depend on specific weather factors, as investigated by laboratory or other experiments (Bourke, 1970). Furthermore, disease-forecasting systems are suited for IPM systems. The potential benefits from using disease-forecasting systems include cost effective disease control, increased attention of farmers to the biology of the cropping system, and reduced environmental contamination (Johnson, 1987). A disease forecasting model was created to 1) identify environmental conditions that favor the development of early blight on tomato, and 2) enhance the efficiency of fungicide use (Madden et al., 1978). FAST (Forecaster of Alternaria solani on Tomato) uses daily values for maximum and minimum air temperature, hours of leaf wetness, maximum and minimum air temperatures during the leaf wetness period, hours of relative humidity greater than 90%, and rainfall (Madden et al., 1978). Field studies proved the weather-prompted FAST system to be as effective as standard spray regimes for controlling early blight (Madden et al., 1978). FAST was subsequently evaluated for predicting infection periods and timing fungicide applications for control of Stemphylium vesicarium on pear (Montesinos, 1992). Commercial orchard studies showed that FAST resulted in 28-3 8% fewer fungicide applications, compared with the standard 7-day l3 commercial schedule, while maintaining the same level of disease control (Montesinos, 1992). The FAST system was modified by RE. Pitblado to meet the needs of Ontario tomato growers for controlling early blight (Alternaria solani Sorauer), septoria leaf spot (Septoria lycopersici), and fruit anthracnose (Collectotricum coccodes) (Pitblado, 1988, 1992). The refined system, Tom-Cast (TOMato disease foreCASTer), calculates daily disease severity values (DSVs) based on hours of leaf wetness and the average air temperature during the wetness period. Sprays are initiated when the DSV reaches a threshold value, and, after spraying, the DSV is reset to zero (Pitblado, 1992). Tom-Cast was evaluated as a disease management tool for timing fungicide applications to control purple spot (Stemphylium vesicarium) on asparagus (Meyer et al., 2000). The Tom-Cast spray program prompted an equal or fewer number of sprays and provided better disease control than the 14-day standard program. Additionally, some newly established asparagus plots managed according to Tom-Cast resulted in increased fern stands (Meyer et al., 2000). Gillespie and Sutton (1979) developed a predictive system for timing fungicide applications for the control of Alternaria leaf blight on carrots. The criteria of the system were to: 1) apply the initial fungicide application after 1 to 2% of the foliage showed symptoms of blight; 2) apply subsequent fungicide applications only when the 36 hour predicted weather favored the development of blight; and 3) apply fimgicide at no more than a minimum of 7 or 10 days (Gillespie and Sutton, 1979). Commercial field experiments showed that two to four weather-timed sprays proved the predictive system controlled blight as effectively as six or seven weekly applications. In addition, this 14 program eliminated the need for one to three sprays before the blight symptoms reached 1 to 2% (Gillespie and Sutton, 1979). A disease forecasting system has been developed for timing sprays to control Cercospora apii (Fres.) on celery (Berger, 1969a, 1969b). A hygrothennograph and spore trap were used to identify sporulation periods. Sporulation increased following nights when temperatures ranged from 15 to 30° C and the relative humidity was near 100% for 8 or more hours. Fewer spores were caught following nights when the temperature dropped below 15° C regardless of the duration of high humidity. If temperatures fell below 12° C, two consecutive nights with humidity levels near 100% and temperatures ranging from 15 to 30° C were required for C. apii to resume significant sporulation. Five to fifteen sprays were saved during the 1968 winter growing season by utilizing the disease forecaster to time fungicide applications (Berger, 1969b). There is substantial evidence that disease forecasting systems can reduce the number of fungicide applications per season or increase the efficacy of sprays by prompting sprays only when the environment is conducive for disease development. Disease forecasting systems may be appropriate for managing Alternaria and Cercospora blights in Michigan. 15 LITERATURE CITED Angell, F .F., and Gabelman, W.H. 1968. Inheritance of resistance in carrot, Daucus carota var. sativa, to the leaf spot fungus, Cercospora carotae. Proceedings of the American Society for Horticultural Science 93:434-437. Arcelin, R., and Kushalappa, AC. 1991. A survey of carrot diseases on muck soils in the southwestern part of Quebec. Canadian Plant Disease Survey 71:147-153. Berger, R.D. 1969a. A celery Early Blight spray program based on disease forecasting. Proceeding from Florida State Horticultural Society Meeting 82:107-111. . 1969b. Forecasting Cercospora blight of celery in Florida. (Abstr.) Phytopathology 5921018. Bird. G., Bishop, B., Grafius, E.J., Hausbeck, M.K., Jess, L.J., Kirk, W., and Pett, W. 2002. Insect, disease and nematode control for commercial vegetables. East Lansing, Michigan State University. E - 312, 44-47. Bolkan, HA, and Reinert, W.R. 1994. Developing and implementing IPM strategies to assist farmers: an industry approach. Plant Disease 78:545-550. Bourke, P.M.A. 1970. Use of weather information in the prediction of plant disease epiphytotics. Annual Review of Phytopathology 12:345-370. Carisse, 0., and Kushalappa, AC. 1990. Development of an infection model for Cercospora carotae on carrot based on temperature and leaf wetness duration. Phytopathology 80: 1233-1238. . 1992. Influence of interrupted wet periods, relative humidity, and temperature on infection of carrots by Cercospora carotae. Phytopathology 82:602-606. Carisse, 0., Kushalappa, A.C., and Cloutier, DC. 1993. Influence of temperature, leaf wetness, and high relative humidity duration on sporulation of Cercospora carotae on carrot leaves. Phytopathology 83:338-343. Doran, W.L., and Guba, ER 1928. Blight and leaf-spot of carrot in Massachusetts. Amherst, Massachusetts Agricultural Experiment Station. Bulletin # 245, 270-278. Ellis, J .B., and Langlois, AB. 1890. New species of Louisiana fungi. Journal of Mycology 6:35-37. Fancelli, M.I., and Kimati, H. 1991. Occurence of iprodione resistant strains of Alternaria dauci. Summa Phytopathologica 17:135-146. 16 Gillespie, T.J., and Sutton, J .C. 1979. A predictive scheme for timing fungicide applications to control Alternaria leaf blight in carrots. Canadian Journal of Plant Pathology 1:95-99. Groves, J .W., and Skolko, A.J. 1944. Notes on seed-bome fungi. ll. Alternaria. Canadian Journal of Research 22:217-234. Hausbeck, M.K., Cortright, RD, and Lindennan, SD. 2000. Chemical control of Alternaria blight in carrot, 1999. Fungicide and Nematicide Tests 55:153-154. Hooker, J.W. 1944. Comparative studies of two carrot leaf diseases. Phytopathology 34:606-612. James, R.V., and Stevenson, W.R. 1999. Evaluation of selected fungicides to control carrot foliar blights, 1998. Fungicide and Nematicide Tests 54:131. James, R.V., Stevenson, W.R., and Rand, RE. 1999. Evaluation of carrot cultivars and breeding selections to identify resistance to foliar blights, 1999. Madison, University of Wisconsin. Wisconsin vegetable disease control trials, 1999, 73-75. Johnson, KB. 1987. The role of predictive systems in disease management. Edited by P. S. Teng., Crop loss assessment and pest management. APS Press, St. Paul, MN, pp. 1 76-190. Keinath, A.P., DuBose, V.B., and Rathwell, PI. 1996. Efficacy and economics of three fungicide application schedules for early blight control and yield of fresh-market tomato. Plant Disease 80: 1277-1282. Krause, RA, and Massie, LB. 1975. Predictive systems: modern approaches to disease control. Annual Review of Phytopathology 13:31-47. Langenberg, W.J. 1975. Carrot leaf blight (Alternaria dauci) development in relation to enviromental factors and fungicide applications. M.Sc. Thesis, University of Guelph, Ontario. pp.119. Langenberg, W.J., Sutton, J .C ., and Gillespie, T.J. 1977. Relation of weather variables and periodicities of airborne spores of Alternaria dauci. Phytopathology 67:879-883. Madden, L., Pennypacker, SP, and MacNab, AA. 1978. FAST, a forecast system for Alternaria solam' on tomato. Phytopathology 68: 1354-1358. Maude, RB. 1966. Studies on the etiology of black rot, Stemphylium radicinum (Meier, Drechsl. & Eddy) Neerg, and leaf blight, Alternaria dauci (Kuhn) Groves & Skolko, on carrot crops; and on fungicide control of their seed-bome infection phases. The Annals of Applied Biology 57:83-93. 17 Meyer, M.P., Hausbeck, M.K., and Podolsky, R. 2000. Optimal fungicide management of purple spot of asparagus and impact on yield. Plant Disease 84:525-530. Montesinos, E. 1992. Evaluation of FAST as a forecasting system for scheduling fungicide sprays for control of Stemphylium vesicarium on pear. Plant Disease 76:1221-1226. NASS. 2003. Vegetables 2002 summary. Agricultural Statistics Board, USDA. Neergaard, P. 1945. Danish species of Alternaria and Stemphylium. Humphrey Millford, Oxford University Press, London, pp.560. Netzer, D., and Kenneth, RC. 1969. Persistence and transmission of Alternaria dauci (Kuhn) Groves & Skolko in the semi-arid conditions of Israel. The Annals of Applied Biology 63:289-294. Pitblado, RE. 1988. Development of a weather-timed fungicide spray program for field tomatoes. (Abstr.) Canadian Journal of Plant Pathology 10:371. . 1992. Development and implementation of Tom-Cast. Ontario Ministry of Agriculture and Food. Pryor, B.M., Strandberg, J.O., Davis, R.M., Nunez, J.J., and Gilbertson, R.L. 2002. Survival and persistence of A lternaria dauci in carrot cropping systems. Plant Disease 86:1115-1122. Rotem, J. 1994. The genus Altemaria: biology, epidemiology, and pathogenicity. APS, St. Paul, MN, pp.326. Santos, P., Nunez, J .J ., and Davis, RM. 2000. Influence of gibberellic acid on carrot growth and severity of Alternaria leaf blight. Plant Disease 84:555-558. Scott, DJ, and Wenham, HT. 1973. Occurrence of two seed-home pathogens, Alternaria radicina and Alternaria dauci, on imported carrot seed in New Zealand. New Zealand Journal of Agricultural Research 16:247-250. Solheim, W.G. 1929. Morphological studies on the genus Cercospora. Illinois Biological Monographs 12:43-44. Strandberg, J .O. 1977. Spore production and dispersal of Alternaria dauci. Phytopathology 67: 1262-1266. . 1983. Infection and colonization of inflorescences and mericarps of carrot by Alternaria dauci. Plant Disease 67:1351-1353. 18 . 1984. Efficacy of fungicides against persistence of Alternaria dauci on carrot seed. Plant Disease 68:39-42. . 1988. Detection of Alternaria dauci on carrot seed. Plant Disease 72:531-534. Strandberg, J .O., and White, J .M. 1989. Response of carrot seeds to heat treatments. Journal of the American Society for Horticultural Science 114:766-769. Strandberg, J .O., Bassett, M.J., Peterson, CE, and Berger, RD. 1972. Sources of resistance to A lternaria dauci. (Abstr.) Hort Science 7:345. Strider, D.L. 1963. Control of Alternaria blight of carrot. Plant Disease Reporter 47:66- 69. Thomas, H.R. 1943. Cercospora blight of carrot. Phytopathology 33:114-125. Zadoks, J .C. 1984. A quarter century of disease warning, 1958-1983. Plant Disease 68:352-355. Zandstra, B.H., Grafius, E.J., Wamcke, DD, and Lacy, ML. 1986. Commercial vegetable recommendations: carrots. East Lansing, MI, Michigan State University, Cooperative Extension Services. E-1437, 1-6. Zimmer, RC, and McKeen, W.E. 1969. Interaction of light and temperature on sporulation of the carrot foliage pathogen Alternaria dauci. Phytopathology 59:743- 749. 19 CHAPTER I. COMPARING DISEASE FORECASTING SYSTEMS FOR TIMING FUNGICIDE APPLICATIONS TO CONTROL ALTERNARIA AND CERCOSPORA BLIGHTS OF CARROTS 20 ABSTRACT Alternaria dauci and Cercospora carotae cause foliar blight of carrots and can reduce the harvestable yield in severely blighted fields. Traditionally, fungicides are applied every 7 to 10 days, regardless of weather conditions or disease pressure. The objective of this study was to evaluate available disease forecasting systems for timing fungicide sprays to limit foliar blights, including 1) a modified disease forecaster previously tested for timing sprays to control Cercospora apii on celery, 2) an Alternaria disease forecaster designed to time sprays for controlling A. dauci on carrots but not yet tested in Michigan, and 3) Tom-Cast, originally developed to predict the occurrence of diseases on tomatoes. Chlorothalonil was applied every seven days or according to the forecasting systems in 2001 and 2002. Sprays applied according to Tom-Cast 15 DSV resulted in a fungicide savings of $47.25 and $54.88 per acre in 2001 and 2002, respectively, compared with the 7-day schedule, while providing similar blight control. The number of sprays was reduced when fungicides were applied according to modified predictive systems for Alternaria and Cercospora compared with the 7-day schedule, but acceptable blight control was not always achieved. The Tom-Cast disease forecaster was easy to use and reliable for determining the appropriate timing of fungicide applications on CEII'TOIS. 21 INTRODUCTION Alternaria dauci (Kiihn) Groves & Skolko and Cercospora carotae (Passerini) Solheim infect the leaves and petioles of carrots (Daucus carota L. var. sativa DC.) causing a foliar blight that contributes to harvesting losses. Alternaria blight symptoms initially appear as irregularly shaped necrotic lesions along leaf margins (Hooker, 1944). Symptoms of Cercospora blight are more distinct and appear as small, pinpoint necrotic lesions surrounded by a chlorotic halo (Thomas, 1943). Both fungi are capable of infecting carrot petioles and cause tan to black colored lesions surrounded by a light tan or gray halo. Petiole infection occurs when favorable conditions are maintained for long durations inside the dense crop canopy. If favorable conditions persist, entire leaflets and petioles become blighted and will not withstand the pull of mechanical harvesters. An increase in harvesting difficulty and yield reduction occurs when severely blighted foliage detaches from the root during mechanical harvest or when plants are defoliated by blights (Gillespie and Sutton, 1979; Strider, 1963). Carrot growers in Michigan are advised to apply registered fungicides at 7 to 14 day intervals following crop emergence (Bird et al., 2002). However, calendar based spray schedule do not take into account when environmental conditions are unfavorable for blight development and needless sprays can be applied. Numerous disease forecasting systems exist that alert growers when a fungicide spray is needed based on environmental conditions. One such system has been developed for timing sprays to control Cercospora apii (Fres.) on celery (Berger, 1969a, 1969b). A hygrothennograph and spore trap were used to identify sporulation periods. Sporulation increased following nights when temperatures ranged from 15 to 30° C and the relative 22 humidity (RH) was near 100% for eight or more hours. Fewer spores were caught following nights when the temperature dropped below 15° C regardless of the duration of high humidity. If temperatures fell below 12° C, two consecutive nights with humidity levels near 100% and temperatures ranging from 15 to 30° C were required for C. apii to resume significant sporulation. Five to fifteen sprays were saved during the 1968 winter growing season by utilizing the disease forecaster to time fungicide applications (Berger, 1969b) Gillespie and Sutton (1979) developed a disease forecasting system to time fungicide applications for controlling Alternaria blight of carrots. The criteria of the system included the following: 1) apply the initial fungicide application after 1 to 2% of the foliage showed symptoms of blight; 2) apply subsequent fungicide applications only when the 36 hour predicted weather favored the development of blight; and 3) apply fungicide at no more than a minimum of 7 or 10 days. To determine if the upcoming 36 hours were favorable for blight development, the system used forecasted weather information to produce an infection index that was calculated by comparing forecasted temperatures and estimated leaf wetness durations. Regional forecasts of rain, cloud cover, and wind speeds were used to derive the leaf wetness duration. Commercial field experiments showed that two to four weather-timed sprays controlled blight as effectively as six or seven weekly applications. In addition, this program eliminated the need for one to three sprays before the blight symptoms reached 1 to 2% compared with the standard fimgicide schedule (Gillespie and Sutton, 1979). The Tom-Cast disease forecasting system is a modified version of F .A.S.T. (Forecaster for Alternaria solam’ Sorauer on Tomato). Tom-Cast was designed to include 23 control for anthracnose fruit rot (Collectotrichum coccodes (Wallr.) Hughes) and Septoria leaf spot (Septoria lycopersici (Speg)) in addition to early blight (Alternaria solam' Sorauer) (Pitblado, 1988). For each 24-hour period (11:00 AM to 11:00 AM), Tom-Cast uses the hours of leaf wetness and the average temperature during the wetness periods to calculate a Disease Severity Value (DSV) ranging from O to 4, corresponding to environmental conditions unfavorable to highly favorable for disease development. Daily DSV values are summed and accumulate until a threshold value is reached, a fungicide spray is applied, and the DSV total is reset to zero (Pitblado, 1988, 1992). With increases in production costs and public concerns regarding pesticide use, it is desirable to evaluate Integrated Pest Management (IPM) methods for managing Alternaria and Cercospora blights of carrots. Improved methods for determining the appropriate timing of fungicide applications are needed to make blight control more cost effective without compromising quality and yield. The objective of this study was to evaluate available disease forecasting systems for timing sprays to limit foliar blights, including 1) a modified disease forecaster previously tested for timing sprays to control Cercospora apii on celery, 2) an Alternaria disease forecaster designed to time sprays for controlling A. dauci on carrots but not yet tested in Michigan, and 3) Tom-Cast, originally developed to time sprays for controlling diseases on tomatoes. MATERIALS AND METHODS Plot establishment. Plots were established at the Michigan State University Muck Soils Experimental Farm in Bath, Michigan in 2001 and 2002. Beds were formed and ‘Cellobunch’ carrot seeds were planted on 14 May 2001 and 21 May 2002 in I-Ioughton Muck soil, previously planted with potato. Seeds were spaced 1.43 cm apart in 24 rows spaced 45.7 cm apart on three-row raised beds measuring 162.6 cm from center to center. Plant populations were 631,583/ha (2001) and 484,97l/ha (2002). All treatment plots were 6.1 m long. One and a half meter sections of unsprayed carrots separated treatment plots within beds, and one bed of carrots was left untreated between treatment beds. Natural inoculum was relied on for infecting plants. Weeds, insects, and fertilization requirements were managed according to standard production practices (Bird et al., 2002; Wamcke et al., 1992; Zandstra, 2002). Plots were sprinkler irrigated as needed. Weather monitoring. Hourly measurements of temperature, relative humidity, and leaf wetness duration were obtained using a digital data recorder (WatchDog Temperature and Relative Humidity Logger 3684; Spectrum Technologies, Inc., Plainfield, Illinois) placed in the field prior to row closure in mid-June. The external leaf wetness sensor (WatchDog Leaf Wetness Sensor 3666; Spectrum Technologies, Inc., Plainfield, Illinois) was located in the upper 75% of the crop canopy in the center of an unsprayed bed at a 45° angle facing north. Data were downloaded every other day to a laptop computer using a computer program (Specware 6.01; Spectrum Technologies, Inc., Plainfield, Illinois) equipped to calculate DSVs for the Tom-Cast system. The program was set to record temperatures from 0 to 100° C and to detect leaf wetness whenever moisture was present on the leaf wetness grid. A summary of weather data and DSV accumulation from the trial site in 2001 and 2002 is listed in Appendix A (Table 22). Disease forecasting programs and fungicide treatments. A modified version of the C. apii disease forecasting system was tested in this study. The modified system 25 omitted the spore trap and relied solely on hourly measurements of temperature and relative humidity. A fungicide spray was applied if all of the following criteria were met: 1) no fungicide was applied during the past seven days; 2) 3 12 hours of R.H. 2 90% were recorded the previous day (0700 yesterday to 0600 today); 3) temperatures ranged 15-27° C during previous day; 4) temperatures during the past three days were 3 12° C or, if the temperature was below 12° C, the night temperatures (2200 to 0700) on the two succeeding nights (yesterday and the day before yesterday; yesterday being 2200 last night until 0700 this morning) were 2 15° C and had R.H. 3 95%. Modifications to the original forecasting system were made according to recommendations (M.L. Lacy, unpublished data). Sprays were applied according to a modified disease forecaster designed to time sprays for controlling A. dauci on carrots (Gillespie and Sutton, 1979). In the present study, fungicides were applied only after 1 to 2% of the foliage displayed disease symptoms, with a minimum reapplication interval of seven days. Subsequent sprays were applied the day before forecasted rain or before nights when the forecasted minimum temperature was 2 16° C. The Tom-Cast disease forecasting systems was tested for timing sprays to control Alternaria and Cercospora blights. For each 24-hour period (1 1 :00 AM to 11:00 AM), Tom-Cast used the hours of leaf wetness and the average temperature during the wetness periods to calculate a DSV ranging from 0 to 4, corresponding to environmental conditions unfavorable to highly favorable for disease development (Pitblado, 1992). Daily DSVs were summed and accumulated until a threshold value of 15 DSV was reached, a fungicide spray was applied, and the DSV total was reset to zero. 26 Chlorothalonil (Bravo Ultrex 82.5WDG at 1.29 kg a.i./ha, Zeneca Ag Products, Wilmington, DE) was applied to all treatment plots, excluding the control. Fungicides were applied with a C02 backpack sprayer (R & D Sprayers, Opelousas, LA) equipped with three Teejet XR11002VS flat-fan nozzles (Spraying Systems Co., Wheaton, IL) spaced 45.7 cm apart, operating at 344.8 kPa, and delivering 467.6 liters/ha. Sprays were applied every seven days or according to the modified Cercospora predictor, the modified Alternaria predictor, or Tom-Cast using a threshold of 15 DSVs. Treatment plots were arranged in a randomized complete block design and replicated four times. Initial sprays for the weekly schedule and Tom-Cast were applied prior to blight symptom development on 2 July 2001 and 8 July 2002. The modified Cercospora predictor prompted the first application on 24 July 2001 and 11 July 2002. Initial sprays for the Alternaria predictor occurred when the 1 to 2% blight threshold was reached on 14 August 2001 and 4 August 2002. In 2001, the 7-day schedule, modified Cercospora predictor, modified Alternaria predictor, and Tom-Cast treatments received 13, 4, 5, and 8 chlorothalonil applications, respectively. In 2002, the 7-day schedule, modified Cercospora predictor, modified Alternaria predictor, and Tom-Cast treatments received 13, 7, 6, and 6 chlorothalonil applications, respectively. The total cost of each fungicide program was calculated by multiplying the number of applications by the cost of chlorothalonil used (Table 1). Dates of fungicide applications are listed in Appendix A (Tables 23 and 24). Disease assessment. All disease assessments were made from the center 3.05 m of the middle row of each plot. Leaf blight severity was determined biweekly (2001) or weekly (2002) using an expanded Alternaria leaf blight assessment key (Strandberg 27 .33 u a M35 32 owcmm coutcocam want—3. 8 9:288 :58th bEmocEwB Ho: 08 3:2 2:3 05 3 330:8 5:38 a 5:23 £802 » .mumoo Define—WE .8 .33 docs ova—2: Ho: meow «$80 .325 £593 2a zoos £53 a 695% 5:5 See Esaseozfio 38 Space as was 85:53 was <38 N .88 new Sow 69900 N :o 22» 055.8% 8 3:92.» 20>» Soon 98 .5580 05 3 8.682 was» owE—om 05 .cBmoEmnéca; 053 83 come we 38 226:: 2: me E mo.m .350 05 Eofi 80th N £85 ”3. Esau; See; m mafia; m 8.50m. 3.5. a 8.? w a 5.2 53:30-51; 3:. a 3:. m as :5 BEBE “5822 .82 3.3 A 8.2 v a 2.: 29285 28888 .82 3:: 2 32$ 2 as a}: a: 23 o cod 9 .a wig: 832:: a a a a $.80 a 2 ma 3.80 a 2 m a .A 5 22> 3258; ~c¢~ .eca .88 can SON E 9:253: oEommze Co 7.8 was mcosmozmmm oEEch mo .8263: EB E28088 033% 9 @6803 no mafia 296m Ego cozama Annie wv— am. 3 :cofifiEoEU eEBwSa 05 £5 Bxfiam no BEBE: c2 80th .nocznozou. Co 22» co 6898.6 .9 new .8353 .V .3 @858 0.83% we Hoobm .— flash. 28 1988). Plots were visually assessed as having 0, 1, 5, 10, 20, or 40% leaf blight, and the key was expanded to estimate 60, 80, and 100% leaf blight. Petiole disease incidence was determined biweekly (2001) or weekly (2002) by counting the number of plants with one or more lesions. Petiole disease severity was evaluated concurrently with petiole disease incidence using the following scale: 1 = average of 0 to 5 lesions per plant; 2 = 6 to 20 lesions; 3 = 21 to 50 lesions; 4 = more than 50 lesions; 5 = dead. An additional petiole rating was conducted to estimate the overall health, amount of dead and living petioles, and condition of petioles for harvest. Petiole health was determined on the day before harvest in 2001 and weekly in 2002 starting 2 September and continuing with other disease evaluations until harvest. The following scale (l-lO) was used to assess petiole health: where l = petioles healthy and vigorous to 10 = petioles unhealthy, weak, or dead. The area under the disease progress curve (AUDPC) was calculated to express the cumulative disease incidence on petioles, severity of disease on petioles, leaf blight, and petiole health (2002 only) by the calculation described by Shaner and Finney (1977): n A UDPC -: §1[(Yi+m+ Yr )/2][xi+1- xi ] where Y,- = percent foliar blight, percent petiole blight, or petiole health rating at the ith observation, X,- = time (days) at the ith observation, and n = total number of observations. Carrots in the center 3.05 m of the middle row of each plot were hand-harvested, the foliage was removed at the crown. and roots were weighed to determine yield on 2 October 2001 and 2002. Leaves showing blight symptoms were periodically removed from untreated buffer rows and examined under magnification (ZOOX) in the laboratory to confirm the presence of A. dauci and/or C. carotae. 29 Statistical analysis. Data for all disease assessments and yield were analyzed with analysis of variance (ANOVA) using the Proc GLM procedure of the Statistical Analysis System (SAS Institute, Cory, NC) in which a linear model including treatment, year, year by treatment, and replicate nested within year were factors. The assumptions of normality and equal variances were examined using the residuals from the ANOVA. Normality was examined using the Proc Univariate procedure of SAS, and the equal variance assumption was assessed by plotting the residuals. The AUDPC data for petiole blight incidence were not normally distributed and were transformed to normality using: square root (AUDPC). There were significant year by treatment interactions for the AUDPC data for petiole blight severity and the petiole health data from the final rating, so analyses were done separately for each year using an analysis of a randomized complete block experiment. Data were analyzed using a linear model that included treatment and replicate as factors using the Proc GLM procedure of SAS. Treatment effects were examined using Tukey’s Studentized Range (HSD) test. RESULTS The 7-day schedule was the most costly fungicide program (Table 1), since it required 13 applications. In 2001, the modified Cercospora predictor, modified Alternaria predictor, and Tom-Cast disease forecaster eliminated nine, eight, and five applications, respectively, saving $85.05, $75.60, and $47.25 per acre compared with the 7-day schedule. In 2002, the modified Cercospora predictor, modified Alternaria predictor, and Tom-Cast disease forecaster eliminated six, seven, and seven applications, respectively, saving $47.04, $54.88, and $54.88 per acre compared with the 7-day schedule. 30 82 owcmm 888....me 98x2... 2 mpg—8.888 888:8 3:82.“in 8: 2a .832 2:8 2: 3 326:8 2828 a 22:3 mgoE > £28828 EoEEob...80> Emociwfi a 8 26 12888 BSA—£8 203 So» some 80¢ Sam 3 .88 cog—£388-83 $65 038 of. .8553 2: 08:83 9 AUmQD» 8mm x 850885 Ens—82:80» of 5:3 “yo—con 803 Noom Ea Sow Soc 88 8mm 62:0 mmohwoa 0386 2: Bus: 88 u Umn5< » .88 n 8 H88 .God A A: :8anme 8: 83 83882 .88 8m 8m 5 8 8... w u >8 2 80.5.; 53888. .88 as 88 a o 8... m u 8885 «.8522 8882 52888. .88 8.. 58 E 5 8“ v n 88:82; 888800 3:602 ”NOON was Sow E 2 n >38 no .I. 88825 888% m0 598:: wEBo=£ 2: 3382 35880:. 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A summary of final disease assessments is listed in Appendix A (Table 25). According to the AUDPC data, all fungicide treatments were equally effective in significantly reducing petiole blight severity and leaf blight compared with the untreated (Table 2). The AUDPC data of petiole blight incidence indicated that the Tom-Cast system was comparable to the 7-day schedule and the modified Cercospora predictor. The 7-day schedule significantly reduced the incidence of petiole blight compared with the modified Cercospora predictor. Disease in the untreated plots and the modified Alternaria predictor plots did not differ (Table 2). Untreated plots reached final petiole health ratings of 8.25 and 8.50 in 2001 and 2002, respectively and were significantly different from all of the fungicide treatments (Table 3). The petiole health data suggest that all fungicide treatments were similar, and according to the AUDPC data reduced disease compared with the untreated plots. In 2001, the 7-day schedule and Tom-Cast improved petiole health compared with the modified Alternaria predictor. Tom-Cast was also similar to the modified Cercospora predictor, which had a significantly higher petiole health rating compared to the 7-day schedule. In 2002, the modified Cercospora predictor and Tom-Cast application schedules were not significantly different from the 7-day schedule. Although the modified Cercospora predictor and Tom-Cast treatments were comparable to the 32 2001 2002 100 4 1 >330 J E = .2 ‘3 60 l l h. .5 4o 4 .33 :8 20 a 9 1 9- l 0 '1 7” ‘__._ Untreated 60 fl 0- 7-day Q __._— Modified Cercospora Predictonr 1,50 l- 9— . Modified Alternaria Predictor ~ 2 40 J —._ Tom-Cast 15 DSV an E 3 '18 2 ° 1 '4 1 ~ 3 PMEB=$E¥=$=1 ¢o°o°oquQ QQ" as éégcago we“ vvvv 99° recs/o "'°° M" Figure 1. Disease progress curves for petiole and leaf blight caused by A. dauci and C. carotae on ‘Cellobunch’ carrots left untreated or treated with the fungicide chlorothalonil (1.29 kg a.i.fha) applied every 7 days or according to disease forecasters in 2001 and 2002. 33 .53 u A. H55 58 owned comccovam mane—3r 8 wEEooom Ensure 3:82.:ch 8: 08 8:2 2:3 2: E 326:8 5:28 a 5:23 232 > docofiflfi EoEEobtmox EmoEcwfi m 2 26 32838 vowing 203 So» :03 Bob «:5 3 .033 $8on 0386 05 $25 3.8 u UmDD< x 69% co £83 iguana: two—oxen H 2 8 £88m? 28 3:8: 8.033 n ~ 223, UB3. 2 9 _ a mafia 83256 33 5.8: 223m » 5038038 doom Ea Sow E o 98 w u >mQ m. ~95-th 53:00am“: .88 28 Son 5 o 28 m n 58605 «5E2? woo—.282 ”begooamoh .83 98 Sam E N. 98 v n 88:55 288800 3:634 ”meow use 58 E 2 H 36$ 6 H 388:5 ”£83m mo “3:5: wage—.8 05 3382 $5.53; N 58v 2:: 58v 2.6. 58v 8.2 60535 3:9 m «53> ”— mfig m 25% m ~33: m 2:? m 8.30% a mi as 23 a 2.2. $328953 a com 0 26 a 3.3 BEBE «5622.82 as 8.». a 86 m 2.? BEBE 83828.82 a am a 2: a 83 a: 0 com c m2 b 3.92 832:5 83 83 83 swag: 35m “28%,,“er 0.53 ”255.8; 228.. 223.. .88 93 Sam E E29828 038% o. @6808 do what :38 Dog “xx—mam Amp—2.x 3 mm. 3 €23,825 oEBwSc 2: 5;» 835m 8 BEBE: t2 $2.80 boa—50:00. mo :23: 2033 no 2388 U 98 85% .V 3 @828 0386 go 80am .m 03:. 34 modified Alternaria predictor, the Alternaria predictor resulted in significantly more disease than the 7-day schedule (Table 3). The analysis of yield indicated a significant treatment effect (Table 1). All fungicide-treated plots were similar to one another, but the untreated had significantly lower yields than the modified Cercospora predictor and Tom-Cast treatments. All disease forecasters provided similar disease control compared with the 7-day schedule by limiting the AUDPC for petiole blight severity, petiole health, and leaf blight. However, the modified Cercospora and Alternaria predictors were not always as effective as Tom-Cast in limiting the AUDPC for petiole blight incidence and improving the final petiole health rating. DISCUSSION Carrot growers in Michigan have been concerned that they may be applying fungicides more frequently than needed and when environmental conditions do not favor blight development. An alternative method of scheduling fungicide applications was needed. The goal of this study was to determine if disease forecasting systems could be used to effectively time fungicide applications to control Alternaria and Cercospora blights without compromising yield. Although the Tom-Cast disease forecaster generally eliminated the least number of sprays compared with the other forecasting systems tested, it was the most effective in consistently limiting disease when compared to the 7-day schedule. In addition, Tom- Cast was the most reliable and simple disease forecaster tested in this study. The hourly measurements of leaf wetness and temperature during the wetness periods were downloaded to a laptop computer equipped with the Specware program that calculated 35 the DSV accumulation each day. The automated system eliminated the tedious calculations required to time sprays according to the modified Cercospora predictor. The use of in-field environmental measurements was a benefit of Tom-Cast disease forecaster when compared with the modified Alternaria predictor. For example, the leaf wetness sensor detected the moisture generated by irrigation events, thereby extending the hours of leaf wetness used in the DSV calculation. The modified Cercospora predictor required daily monitoring once the 7-day spray interval expired. If at least 12 hours with RH. 390% had occurred and temperature requirements were met, several other measurements from the previous two and three days had to be considered before a spray was prompted. The calculation process was not automated using a computer program and required a considerable amount of time that growers would likely avoid. The modified Alternaria predictor required a spray the day before forecasted rain assuming seven days had passed since the last fungicide application. Plots at the muck farm were irrigated, but irrigation was not considered as a rain event in this study. If irrigation was considered as a rain event, the modified Alternaria predictor would have prompted several more sprays because plots were irrigated once and sometime twice a week during July and August. The projected number of sprays applied according to the modified Alternaria predictor would have been similar to that of the 7-day schedule if overhead irrigations were considered as rain events. The yield measurements recorded in this study does not reflect yields that may be recorded in a commercial production situation where carrots are mechanically harvested. All carrots in 3.05 m of the center row were hand harvested, whereas yield losses may 36 have become increasingly evident if plots were harvested mechanically. Based on observations from mechanically harvested commercial carrot fields, yield reduction occurs frequently when the final petiole health is a rating of five or above. Disease forecasting is a viable and economical alternative to the calendar-based fungicide schedule currently used in Michigan. The disease forecasters tested in this study prompted fewer sprays than the 7-day treatment, but did not always provide disease control similar to the 7-day schedule. The Tom-Cast disease forecasting system controlled disease as effectively as the 7-day schedule while reducing the number of sprays by 38 and 54% in 2001 and 2002, respectively. The adoption of disease forecasting systems will likely depend on the reliability and simplicity of the particular system. Tom—Cast was a dependable and economical system for timing fungicide sprays to control Alternaria and Cercospora blights of carrots. 37 LITERATURE CITED Berger, R.D. 1969a. A celery Early Blight spray program based on disease forecasting. Proceeding from Florida State Horticultural Society Meeting 82:107-111. . 1969b. Forecasting Cercospora blight of celery in Florida. (Abstr.) Phytopathology 5921018. Bird, 6., Bishop, B., Grafius, E.J., Hausbeck, M.K., Jess, L.J., Kirk, W., and Pett, W. 2002. Insect, disease and nematode control for commercial vegetables. East Lansing, Michigan State University. E - 312, 44-47. Gillespie, T.J., and Sutton, J .C. 1979. A predictive scheme for timing fungicide applications to control Alternaria leaf blight in carrots. Canadian Journal of Plant Pathology 1295-99. Hooker, J .W. 1944. Comparative studies of two carrot leaf diseases. Phytopathology 34:606-612. Pitblado, RE. 1988. Development of a weather-timed fungicide spray program for field tomatoes. (Abstr.) Canadian Journal of Plant Pathology 10:371. . 1992. Development and implementation of Tom-Cast. Ontario Ministry of Agriculture and Food. Shaner, G., and Finney, RR. 1977. The effect of nitrogen fertilization on the expression of slow-mildewing resistance in Knox wheat. Phytopathology 67:1051-1056. Strandberg, J.O. 1988. Establishment of Alternaria leaf blight on carrots in controlled environments. Plant Disease 72:522-526. Strider, D.L. 1963. Control of Alternaria blight of carrot. Plant Disease Reporter 47:66- 69. Thomas, HR. 1943. Cercospora blight of carrot. Phytopathology 33:114-125. Wamcke, D.D., Christenson, D.R., Jacobs, L.W., Vitosh, M.L., and Zandstra, EH. 1992. Fertilizer recommendations for vegetable crops in Michigan. East Lansing, MI, Michigan State University. E - SSOB, 20-24. Zandstra, EH. 2002. Weed control guide for vegetable crops. East Lansing, MI, Michigan State University. E - 433, 16. 38 CHAPTER II. TIMING FUNGICIDE APPLICATIONS ACCORDING TO FIELD SCOUTING AND TOM-CAST TO CONTROL ALTERNARIA AND CERCOSPORA BLIGHTS OF CARROTS 39 ABSTRACT Fungal foliar blights of carrots, caused by Alternaria dauci and Cercospora carotae, result in necrotic lesions on leaves and petioles that may cause defoliation, decreasing the efficiency of mechanical harvest. Traditionally, fungicides are applied every 7 to 10 days, regardless of weather conditions or disease pressure. The primary objectives of this study were to evaluate the Tom-Cast disease forecasting system for timing fimgicide sprays to control foliar blights, and to determine when to apply the first spray based on field scouting and disease incidence. Chlorothalonil alternated with azoxystrobin was applied every 10 days or according to Tom-Cast with a threshold of 15, 20, or 25 disease severity values (DSVs). Sprays for these programs were initiated prior to symptom development, or when foliage was infected at a trace, 5%, or 10% level. Up to four sprays were omitted saving $46.05 and $41.85 per acre in 2001 and 2002, respectively, and comparable disease control was achieved by initiating applications when a trace amount of the foliage was blighted and applying subsequent sprays according to Tom-Cast 15 DSV, compared with calendar-based sprays initiated prior to blight symptom development. Field scouting and the Tom-Cast disease forecaster appear to be valuable tools for determining the appropriate timing of fungicide applications on carrots while making blight control more cost effective. 40 INTRODUCTION Alternaria dauci (Kuhn) Groves & Skolko and Cercospora carotae (Passerini) Solheim, the fungi causing Alternaria blight and Cercospora blight, are the two prominent foliar pathogens that affect carrots (Daucus carota L. var. sativa DC.) in Michigan (Hausbeck and Harlan, 2003) and other areas (Arcelin and Kushalappa, 1991; James and Stevenson, 1999). Symptoms of A. dauci normally develop along leaf margins but can also affect the petioles and are characterized by irregularly shaped necrotic lesions. Small, pinpoint necrotic lesions caused by C. carotae are initially surrounded by a chlorotic halo and develop on the leaves or petioles. A dense crop canopy provides conditions favorable for disease development prompting Alternaria and Cercospora lesions to coalesce. If entire leaflets and petioles become blighted, they may not be able to withstand the pull of mechanical harvesters, and unharvested carrots will remain in the soil. Carrots in Michigan are grown for fresh market, processing, and the cut and peel market. The three production systems use specific cultivars, plant spacing, and plant populations for their respective uses (Zandstra et al., 1986). Although no disease resistant cultivars are available, there are cultivars that exhibit levels of genetic tolerance to foliar blights (James et al., 1999; Strandberg etal., 1972). Recommendations for controlling Alternaria and Cercospora blights in Michigan are to apply registered fungicides at 7 to 14 day intervals after carrot seedlings have emerged (Bird et al., 2002). Typically, growers will follow the recommended spray interval, but they will rarely apply their first fungicide spray before the plants are large enough to touch within the rows. Michigan carrot growers rely on two B2 carcinogenic 41 fungicides, chlorothalonil and iprodione, to control Alternaria and Cercospora blights. Pesticides classified as B2 carcinogens are scheduled for review by the EPA under the Food Quality Protection Act (FQPA), and the future availability of these products is uncertain. One Michigan food processor does not allow the use of iprodione on carrots because it is a B2 carcinogen and residues are a concern. In addition, fungicide resistance of A. dauci to iprodione has been reported (Fancelli and Kimati, 1991 ). Azoxystrobin (Quadris, Syngenta Crop Protection, Greensboro, NC), a recently registered reduced risk systemic fungicide, is an effective tool to control Alternaria and Cercospora blights in rotation with protectant fungicides (Hausbeck et al., 2000; James and Stevenson, 1999). Use of this product in rotation with protectant fungicides already used by Michigan growers may reduce the number of B2 carcinogenic fungicide applications. A disease forecasting system (FAST) was developed for timing fungicide applications to control early blight on tomato caused by Alternaria solani (Ellis & G. Martin) Sorauer (Madden et al., 1978). The forecaster uses a series of environmental inputs to alert growers as to when these conditions favor early blight development, and to subsequently prompt fungicide applications. Tom-Cast, a modification of FAST, warns growers when to control anthracnose fruit rot (Collectotrichum coccodes (Wallr.) Hughes) and Septoria leaf spot (Septoria lycopersici (Speg)) as well as A. solani. For each 24-hour period (11:00 AM to 11:00 AM), Tom-Cast uses the hours of leaf wetness and the average temperature during the wetness periods to calculate a Disease Severity Value (DSV) ranging from 0 to 4, corresponding to environmental conditions unfavorable to highly favorable for disease development. Daily DSV values are summed 42 and accumulated until a threshold value is reached, a fungicide spray is applied, and the DSV total is reset to zero (Pitblado, 1992). The objectives of this study were to 1) determine whether the Tom-Cast disease forecasting system can be used to time fungicide applications to control Alternaria and Cercospora blights of carrots, 2) set the critical DSV threshold for timing fungicide applications according to Tom-Cast, and 3) determine whether field scouting and disease incidence thresholds can be used to initiate spray programs. MATERIALS AND METHODS Plot establishment. Plots were established at the Michigan State University Muck Soils Experimental Farm in Bath, Michigan and at a commercial carrot field in Fremont, Michigan in 2001 and 2002. Beds at the Muck Soils Experimental Farm (hereafter referred to as the research farm) were formed and carrot seeds of the fresh market cultivar ‘Cellobunch’ and the processing cultivar ‘Early Gold’ were planted on 14 May 2001 and 21 May 2002 in Houghton Muck soil, previously planted with potato. Seeds were spaced 2.54 cm (‘Early Gold’) and 1.43 cm (‘Cellobunch’) apart in rows spaced 45.7 cm apart on three-row raised beds measuring 162.6 cm from center to center. Plant populations of ‘Early Gold’ were 431,657/ha (2001) and 418,775/ha (2002), and populations of ‘Cellobunch’ were 609,047/ha (2001) and 510,043/ha (2002). The study located in Fremont (hereafter referred to as the commercial field) was established with carrot seeds of the cut and peel cultivar ‘Prime Cut’ planted on 28 May 2001 and 6 June 2002 in Granby Mucky Sand, previously planted with corn. Seeds were placed 3.25 cm apart in four seed lines per row with rows spanning 15.2 cm and centered 43.2 cm apart in three-row raised beds measuring 172.7 cm from center to center. Plant populations 43 were 1,444,156/ha (2001) and 1,328,887/ha (2002). All treatment plots were 6.1 m long. One and a half meter sections of unsprayed carrots separated treatment plots within beds, and one bed of carrots was left untreated between treatment beds. Natural inoculum was relied on for infecting plants. Weeds, insects, and fertilization requirements were managed according to standard production practices (Bird et al., 2002; Wamcke et al., 1992; Zandstra, 2002). Plots were sprinkler irrigated as needed. Weather monitoring and disease forecasting. Hourly measurements of temperature and leaf wetness duration were obtained using a digital data recorder (WatchDog Leaf Wetness and Temperature Logger 3610TWD; Spectrum Technologies, Inc., Plainfield, Illinois) located in the upper 75% of the crop canopy in the center of an unsprayed bed at a 45° angle facing north. Data recorders were place in the plots prior to row closure in mid-June. Data were downloaded every other day to a laptop computer using a computer program (Specware 6.01; Spectrum Technologies, Inc., Plainfield, Illinois) equipped to calculate DSVs for the Tom-Cast system. The program was set to record temperatures from 0 to 100° C and to detect leaf wetness whenever moisture was present on the leaf wetness grid. Summaries of weather data and DSV accumulation from the trial sites are listed in Appendix A (Tables 22 and 26). Chlorothalonil (Bravo Ultrex 82.5WDG at 1.29 kg a.i.lha, Zeneca Ag Products, Wihnington, DE) alternated with azoxystrobin (Quadris 2.08F at 0.11 kg a.i.lha, Syngenta Crop Protection, Greensboro, NC) were applied to all treatment plots, excluding the control. Fungicides were applied with a CO; backpack sprayer (R & D Sprayers, Opelousas, LA) equipped with three Teejet XRl 1002VS flat-fan nozzles (Spraying Systems Co., Wheaton, IL) spaced 45.7 cm apart, operating at 344.8 kPa, 44 and delivering 467.6 liters/ha. Fields were scouted for disease symptoms using a disease damage index key (Strandberg, 1988), and spray programs were initiated prior to symptom development (0%), or when disease was evident on a trace amount, 5%, or 10% of the foliage. Initial sprays at the research farm occurred on 2 July (0%), 30 July (trace), 15 August (5%), and 25 August (10%) in 2001 and 8 July (0%), 19 July (trace), 1 August (5%), and 13 August (10%) in 2002. Initial sprays were applied at the commercial field on 8 July (0%), 20 July (trace), 25 July (5%), and 1 August (10%) in 2001 and 15 July (0%), 22 July (trace), 5 August (5%), and 19 August (10%) in 2002. Subsequent sprays were applied every 10 days or according to Tom-Cast at intervals of 15, 20, or 25 DSVs. In 2002, a 7-day fungicide schedule was included in the commercial field study to reflect the typical application schedule followed by commercial (cut and peel) carrot growers in the area. Treatment plots were assigned to each variety and replicated four times in a randomized complete block design. At the research farm, Tom-Cast prompted eight, six, and five sprays in 2001 and six, five, and four sprays in 2002 for the 15 DSV, 20 DSV, and 25 DSV thresholds, respectively, for spray programs initiated prior to disease symptom development. Five, four, and three sprays (2001 and 2002) were applied for the Tom-Cast 15, 20, and 25 DSV thresholds, respectively, for sprays programs initiated when a trace amount of blight symptoms developed. Fungicide sprays initiated when 5% of the foliage was blighted resulted in three, two, and two sprays in 2001 and four, three, and two sprays in 2002 for the Tom-Cast 15, 20, and 25 DSV thresholds, respectively. Two, one, and one spray(s) in 2001 and three, two, and two sprays in 2002 were applied for the Tom-Cast 15, 20, and 45 25 DSV thresholds, respectively, for treatments initiated when 10% blight symptoms developed. Ten-day spray interval treatments initiated prior to disease symptom development scheduled nine applications in 2001 and 2002. Ten-day spray interval treatments initiated when a trace amount of blight symptoms developed resulted in six and eight applications in 2001 and 2002, respectively. Ten-day spray interval treatments initiated when 5% of the foliage was blighted prompted four and seven applications in 2001 and 2002, respectively. Ten-day spray interval treatments initiated when 10% blight symptoms developed scheduled three and five applications in 2001 and 2002, respectively. Dates of fungicide applications are listed in Appendix A (Tables 27 and 28). At the commercial field, Tom-Cast prompted nine, seven, and five sprays in 2001 and eight, six, and five sprays in 2002 for the 15 DSV, 20 DSV, and 25 DSV thresholds, respectively, for spray programs initiated prior to disease symptom development. Eight, six, and five sprays in 2001 and seven, six, and four sprays in 2002 were applied for the Tom-Cast 15, 20, and 25 DSV thresholds, respectively, for sprays programs initiated when a trace amount of blight symptoms developed. F ungicide sprays initiated when 5% of the foliage was blighted resulted in seven, five, and four sprays in 2001 and five, four, and three sprays in 2002 for the Tom-Cast 15, 20, and 25 DSV thresholds, respectively. Six, five, and four sprays in 2001 and four, three, and three sprays in 2002 were applied when sprays were initiated when 10% blight symptoms developed for the Tom-Cast 15, 20, and 25 DSV thresholds, respectively, for treatments initiated when 10% blight symptoms developed. Ten-day spray interval treatments initiated prior to disease development scheduled nine and eight applications in 2001 and 2002. Ten-day spray 46 interval treatments initiated when a trace amount of blight symptoms developed resulted in seven and eight applications in 2001 and 2002, respectively. Ten-day spray interval treatments initiated when 5% of the foliage was blighted prompted seven and six applications in 2001 and 2002. Ten-day spray interval treatments initiated when 10% of the foliage was blighted scheduled six and five applications in 2001 and 2002, respectively. Sprays were applied on a 7-day schedule at the commercial field in 2002 only. Twelve, eleven, nine, and seven sprays were applied on a 7-day schedule for treatments that started prior to blight occurrence or when a trace amount, 5%, or 10% of the foliage was diseased, respectively. Dates of fungicide applications are listed in Appendix A (Tables 29 and 30). Disease assessment. All disease assessments were made from the center 3.05 m of the middle row of each plot at the research farm and from carrots in the four seed lines of the middle 1.52 m of the center row in the commercial field. Leaf blight severity was assessed biweekly (research farm only, 2001) or weekly using an expanded Alternaria leaf blight assessment key (Strandberg, 1988). Plots were visually assessed as having 0, l, 5, 10, 20, or 40% leaf blight, and the key was expanded to estimate 60, 80, and 100% leaf blight. Petiole disease incidence was determined biweekly (research farm only, 2001) or weekly by counting the number of plants with one or more lesions. Petiole disease severity was evaluated concurrently with petiole disease incidence using the following scale: 1 = average of 0 to 5 lesions per plant; 2 = 6 to 20 lesions; 3 = 21 to 50 lesions; 4 = more than 50 lesions; 5 = dead. An additional petiole rating was conducted to estimate the overall health, amount of dead and living petioles, and condition of petioles for harvest; petiole health was not recorded in 2001 at the commercial field. 47 Petiole health was determined on the day before harvest at the muck farm in 2001 and weekly at the research farm and commercial field in 2002 starting on 27 August and 26 August, respectively and continuing with the other disease evaluations until harvest. The following scale (1-10) was used to assess petiole health: from 1 = petioles healthy and vigorous to 10 = petioles unhealthy, weak, or dead. The area under the disease progress curve (AUDPC) was calculated to express the cumulative disease incidence on petioles, severity of disease on petioles, leaf blight, and petiole health (2002 only) by the calculation described by Shaner and Finney (1977): n AUDPC = Z [(Y + v )/2][x - x ] i=1 i+nl i i+l i where Y, = percent foliar blight, percent petiole blight, or petiole health rating at the ith observation, X,- = time (days) at the ith observation, and n = total number of observations. Carrots in the center 3.05 m of the middle row of each plot were hand-harvested, the foliage was removed at the crown. and roots were weighed to determine yield on 2 October 2001 and 3 October 2002 at the research farm and 27 September 2001 and 8 October 2002 in the commercial field. Leaves showing blight symptoms were periodically removed from untreated buffer rows and examined under magnification (200X) in the laboratory to confirm the presence of A. dauci and/or C. carotae. Statistical and economic analysis. ‘Early Gold’ and ‘Cellobunch’ varieties were individually analyzed as single experiments with replicates across years, and the experiment was designed as a split-plot in time, with each year’s data representing a randomized complete block design. Data for all variables were initially analyzed using analysis of variance (ANOVA) in which a linear model including treatment, year, year by treatment, and replicate nested within year as factors was analyzed using the Proc GLM 48 procedure of the Statistical Analysis System (SAS Institute, Cory, NC). The assumptions of normality and equal variances were examined using the residuals from the ANOVA. Normality was examined using the Proc Univariate procedure of SAS, and the equal variance assumption was assessed by plotting the residuals. Data that did not pass normality tests were transformed (Table 4). When the year by treatment interaction was significant for a variable, analyses were done separately for each year using an analysis of a randomized complete block experiment. Data were analyzed using a linear model that included treatment and replicate as factors using the Proc GLM procedure of SAS (SAS Institute, Cory, NC). The 17 treatments examined in the ‘Early Gold’, ‘Cellobunch’, and ‘Prime Cut’ (2001 only) experiments represent a four (initiation timings) by four (application intervals) factorial with an untreated control as the 17th treatment. Twenty-one treatments were tested on ‘Prime Cut’ in 2002, due to the addition of a 7-day application interval, representing a four (initiation timings) by five (application intervals) factorial with an untreated control as the 21St treatment. The ‘Prime Cut’ experiments during 2001 and 2002 were analyzed separately using a linear model that included treatment and replicate as factors using the Proc GLM procedure of SAS. When the ANOVA indicated a significant difference among the treatments, the differences among the treatments were examined by decomposing the treatment sum of squares into four component sum of squares: (1) the difference between the average of the spray treatments and the untreated control; (2) differences between initiation timings; (3) differences between application intervals; (4) an interaction between initiation timings and application intervals. When the analyses did not detect a significant interaction 49 .300 00808053505 40:50:50: E00050; 0038 5 00.90306 5005 0:0 800 00808050550: 4055920: wEms 00003500 003 005053 0005 5a 000398 505305 5285.888. .0 a? Buses: 3 8.. 2:8 0.53. 58 555... 20% 228 .30 2:5. Ea 0.53. 558. 50% 228 283200. N 2 2.5. -- 0.5:... 581555. 205 223.5 .30 25.5. 2 2.3 2 + 053$ 02 0.5:.... 502.. :3 E 035. -- 0.53. 5:28 20% 2.50.5 22:50:00. : as 2 8:3 6.53: 82 223 0.5:... 58 8:02.05 20% 2.50.5 2 2.3. 6.523 8.: 223 0.53. 20% .33 S 2.5 2 + 053$ 02 0.53. 5:83 20% 2.50.5 .28 :30. 00.3.9.2. 0.50:. nezafiueumuaeh .0333.» RES—TE. Z u0Euemuabioam 233:0 0033.5? 05.085: 9 000: 52550850: mamas—0950000 0:0 0053506 3.0800: 5: 0503 :2: 0055.5.» 50850000 000006 mo Efifism .v 0:38 50 between initiation timings and application intervals, the main effects of initiation timing and application interval were examined using the Waller-Duncan Bayesian k-ratio t-test (Steel et al., 1997) to determine which initiation timing or application interval had the best mean. When a significant initiation timing by application interval interaction occurred, the effect of initiation timings for each application interval were determined using the Waller-Duncan Bayesian k-ratio t-test. The total cost of each fungicide program was calculated by multiplying the number of applications by the cost of the fungicide used (Table 5). Fungicide costs for one application of chlorothalonil were $9.45 and $7.84 per acre in 2001 and 2002, respectively; one application of azoxystrobin cost $13.58 and $13.08 per acre in 2001 and 2002, respectively. RESULTS The effect of treatment was highly significant for all disease assessments on the three cultivars examined. Treatments significantly affected yield of ‘Prime Cut’ carrots in 2002 (Table 6), but did not affect yield of ‘Early Gold’ (Table 7), ‘Cellobunch’ (Table 8), or ‘Prime Cut’ carrots in 2001 (Table 9). For each cultivar, all fungicide-treated plots had significantly less disease on leaves and petioles compared with the untreated plots. Timing the initial fungicide application based on scouting for leaf blight thresholds of 0%, trace, 5%, and 10% had a highly significant effect on all disease assessments for the three cultivars examined. Application interval significantly affected most disease assessments, but did not affect: ‘Early Gold’ AUDPC data for petiole blight incidence in 2002; ‘Cellobunch’ AUDPC data for petiole blight incidence; ‘Cellobunch’ AUDPC data for petiole blight severity; ‘Prime Cut’ AUDPC data for petiole blight severity in 2002. 51 .0800 3:008 8 58288 .3: .8: 8205 .8 80 $080 :80 0000.020 05 :83 0000.050 0 £80 Egg 5803.5 £003 £008 Ea A 803 £58 a 6:330 505 288 00228820 00 88 022050 0:0: 005.528 33 $0.80 N 52 EON m 8.00 v NOON N 3.0 _ $3 OEON m OOO»V v NOON N mONN N ..\..m 0w. 2» v _m.mm m OEON m vam m 000:. 8.00 m _m.mm m 5.; 0 36m m .xeo >mQ mN .000-th Oth m _m.mm m NOON N 3.0 L XO— 0w. 3 v 3.2 m Oth m mONN N .xcm :NO 0 mode O vw. S» v 8.00 v. 000; RNO O mm.wn .\. 8.00 m deO O .xeo >mD ON 800-th $.20 .0 mode O OEwN m mO.mN N $9 $9. m mmwn N. vwév v vam m .xem SOB 0 :NO w mode m 36m m 000:. 00.3 m Om._O_ O RNO O :.NO w .xeo >mQ 2 809509 mod... m mode 0 mode m vam m ..\..O_ PNO O mmdn n SOn N. no.3. v ..\..n 09mm w 0.2:. 0 09mm w mode 0 008:. 09mm w 005: O 3.8 a 3.5— a e\..O >003 8.2 N. -- -- -- -- -- -- *3 mm. .0 0 -- -- -- -- -- -- o\..m 3N: _ _ -- -- -- -- -- -- 000:. mm.mN~ N_ -- -- -- -- -- -- .c\..O >00 \. O0.0 O O0.0 O O0.0 O O0.0 O BEBE: aunm t 50:33.: NOON SON NOON SON 0:0 0.0.02.8 00:00:97. .000 0.5.5. BEE—0:00. 0:0 .200 2.5a. .NOON 0:0 SON 5 800-50... 0: 3205000 5 0.30 O_ :0 N. fi0>0 033:8: 0:0 02080:: 00:02.05 808% :0 083 02an .3025 $5.00 wx :Ov :Eobmxxowa £3 0000:0005 $52.0 wx ON. 5 .52050520 :23 @0558 5 00:00:50 c0. 38.80 .000 08th. 0:0 35:30:00. ..200 300m. :0.“ 0:00 :0: 8:05:00: 020%:3 O0 800 0:0 8:230:30 020%:3 O0 000802 .m 035. Table 6. Effects of spray initiation timings and application intervals on yield of ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) used to control foliar blights caused by A. dauci and C. carotae in 2002. Treatment Yield (kg)z Initiation timing 0% 5.50 ay Trace 5.75 a 5% 5.10 b 10% 4.77 b Application interval y. 7 day 5.38 a 10 day 5.32 a Tom-Cast 15 DSV 5.19 a Tom-Cast 20 DSV 5.39 a Tom-Cast 25 DSV 5.14 a Source F value P value Treatment 2.70 0.0016 Initiation timing 10.47 <.0001 Application interval 0.58 0.6803 Timing*interval interaction 1.44 0.1738 Untreated vs. treated 3.00 0.0886 z Carrots from the center 3.05 m of the middle row of each plot were hand-harvested, the foliage was removed at the crown, and roots were weighed to determine yield on 8 October 2002. y Initiation timing means followed by the same letter are not significantly different according to Waller-Duncan Bayesian k-ratio t-test (k-ratio = 100). " Application interval means followed by the same letter are not significantly different according to Waller-Duncan Bayesian k-ratio t-test (k-ratio = 100). 53 Table 7. Effect of the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) on yield of ‘Early Gold’ carrots infected with A. dauci and C. carotae in 2001 and 2002. Treatment Yield (kg)z Untreated 1 3 .34 10 day 0% 14.62 Trace 15.51 5% 14.90 10% 13.39 Tom-Cast 15 DSV 0% 14.57 Trace 14.26 5% 13.90 10% 13.40 Tom-Cast 20 DSV 0% 15.04 Trace 15.86 5% 13.91 10% 13.56 Tom-Cast 25 DSV 0% 14.82 Trace 14.29 5% 13.78 10% 13.81 Source P value P value Treatment 1 .33 0. 1968 Z Carrots from the center 3.05 m of the middle row of each plot were hand-harvested, the foliage was removed at the crown, and roots were weighed to determine yield on 2 October 2001 and 3 October 2002. 54 Table 8. Effect of the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i.lha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 10-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) on yield of ‘Cellobunch’ carrots infected with A. dauci and C. carotae in 2001 and 2002. Treatment Yield (kgf Untreated 9.70 10 day 0% 12.03 Trace 11.17 5% 12.06 10% 11.23 Tom-Cast 15 DSV 0% 11.83 Trace 11.63 5% 10.90 10% 10.59 Tom-Cast 20 DSV 0% 12.39 Trace 11.15 5% 11.45 10% 12.15 Tom-Cast 25 DSV 0% 12.23 Trace 10.81 5% 10.25 10% 10.28 Source F value P value Treatment 1 .62 0.0775 z Carrots from the center 3.05 m of the middle row of each plot were hand-harvested, the foliage was removed at the crown, and roots were weighed to determine yield on 2 October 2001 and 3 October 2002. 55 Table 9. Effect of the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) on yield of ‘Prime Cut’ carrots infected with A. dauci and C. carotae in 2001. Treatment Yield (kg)z Untreated 7.53 10 day 0% 9.03 Trace 9.67 5% . 9.77 10% 10.23 Tom-Cast 15 DSV 0% 9.07 Trace 9.46 5% 9.76 10% 9.05 Tom-Cast 20 DSV 0% 9.22 Trace 9.67 5% 9.27 10% 9.99 Tom-Cast 25 DSV 0% 9.33 Trace 8.58 5% 8.61 10% 8.32 Source F value P value Treatment 1.38 0.1897 z Carrots from the center 3.05 m of the middle row of each plot were hand-harvested, the foliage was removed at the crown, and roots were weighed to determine yield on 27 September 2001. 56 The interaction of initial spray timings and application intervals was significant (P < 0.05) for the following variables: ‘Early Gold’ AUDPC data for petiole blight incidence in 2001; ‘Early Gold’ data for the final petiole health rating in 2001; ‘Prime Cut’ AUDPC data for petiole blight incidence in 2001; ‘Prime Cut’ AUDPC data for petiole blight incidence in 2002; ‘Prime Cut’ AUDPC data for leaf blight in 2002. The significant interaction of initiation timing and application interval indicated that the disease control provided by the application intervals was dependent on the time of the initial fungicide application. Assessment of initial spray timing on ‘Early Gold’ carrots. The time of initial disease occurrence and progression of disease in untreated plots were different for the two years this study was conducted. Leaf blight was detected on 30 July and 18 July in 2001 and 2002, respectively (Figure 2). Levels of disease increased, where 100% petiole infection was observed on 4 September 2002 (Figure 3). In 2001, untreated plots reached 89.5% petiole infection on 28 September. A summary of final disease assessments is listed in Appendix A (Table 31). The AUDPC data suggest that spray programs that were initiated prior to blight occurrence or when the first sign of disease was detected significantly reduced the incidence of petiole blight in 2002 and percentage of leaf blight throughout the growing season compared with spray programs that were initiated when 5 or 10% disease symptoms occurred (Table 10). Petiole blight severity was significantly higher for spray programs that were initiated when 5 or 10% leaf blight was detected compared with spray programs that were initiated prior to disease or at the first disease detection. Petiole blight severities of spray programs initiated when a trace amount of leaf blight developed 57 2001 2002 70 . lO—day A60. —.— Untreated \° .0 0% 50 8: l _.,__ Trace €540 l ——v~—< 50/0 3: 3o . —._ 10% “a 20 . 0 '3 10 . 0 . . 70 ' lTom—Cast #:60J 15 DSV €50 . 31040 . E 30 1 ’5 20 . l '4 10 . o . 70. T ‘ ' ' * r 01 Tom-Cast I Tom-Cast ; A60 « 20 DSV . 20 DSV l 6:50 . l, l E i i g H | no “I 1 s 1‘ J .‘3 p i n l +1 . . . T - 0O - C1 0 . . . Tom-Cast l A60 25 DSV 25 DSV * °\° 0 E0 o a o '51 o O '4 o 0 Figure 2. Disease progress curves for leaf blight caused by A. dauci and C. carotae on ‘Early Gold’ carrots lefi untreated or treated with chlorothalonil (1 .29 kg a.i.fha) alternated with azoxystrobin (0.11 kg a.i./ha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002. 58 2001 2002 100 * a; 10—day i 80 , —°—- Untreated 3 ° 0% .. ---- Trace * 60 ‘ é — v- - 5% 5 40 ‘ —'_ loo/0 .2 '3 20 - 0 0.. 0 - 100 ? lTom-Cast e, 30 15 st : .2 *5 60 . .2 .5 40 + £ '5 20 « 0 a. . 0 . , . C C , - . , ma . 100 4 .. *7 »; Tom-Cast Tom-Cast g at so 20 st .1 20 DSV ~ 4; t: 02/ ‘29: 60 J ‘1 "XV I .2 i /.° 1 E 40 4 ‘i ' i 0 . '3 20 4 f i u 1 a. 0 g! i ‘ f f _ IL r Y j V l 100 ‘ Tom-Cast ] Tom-Cast i 80 25 DSV 60 & O Petiole Infection (%) N G Figure 3. Disease progress curves for petiole blight caused by A. dauci and C. carotae on ‘Early Gold’ carrots left untreated or treated with chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002. 59 .0000 008800500300 030:0 030: 2:. .00:0_:0> 05 0025000 0: A 0 + 00530.0 wB w:_00 0088,0050: 0:03 0:09 0 00:00:25 3080000100» 0:025:30 0 00 0:0 0.0000050 0003050 0:03 :00» 0000 80:0 0:0D 0 000.000 0:800:00 :00 003 5:00:85 0580005100.» 000 :003 0200: 0:03 NOON 0:0 :OON 80:0 000 0:09 .0>::0 000:w0:: 000000 05 :00:: 00:0 H UmQD< 0 :000.v 00.00: :000.v 00.00 0000.0 00.: :000.v 00.00 0280.2 02000:: 00000 00.0 0000.0 00.0 0000.0 00.: :0000 00.0 800225030000058: :000.v 00.0: 0000.0 00.0 0:000 02 0000.0 00.0 050500080000. :000.v 00.00 :000.v :000 :000.v 00.00 :000.v 00.00 0580000000: :000.v 00.00 :000.v 00.0: :000.v 00.0 :000.v 00.0: 00050020 0333 m m3-0> m 0563 m 0590 mm 0500: L 03000: L .039» m 3&9.» n— mukaom. 0 00.000 0 00.00 0 02000 0.000: >00 00 0000-800 0 00.000 00 0:.00 0 0.00:0 000:0: 000008-88. 0 00.00: 0 0:00 0 00.00:. :0000 000280-500 0 00.00: 0 00.00 .0 00.0000 :0000 0.00: _0>:0::m 5000:0090. 0 00.5. 0 00.00: 0 00.000 00.0000 .00: 0 :0000 0 00.00 0 00.0000 0.000: .00 0 00.00: 0 00.00 0 00.0000 00.000 88.0 0 :000: 0 00.00 .0 00.020 00.00: .00 wEE: :00025 0000 .800 320:0 :03 .0030 08520:: 20:... 0.000.: 085.00.; 0000000003 00000 .NOON 0:0 SON :m A>mQV 0020> 50050 000000 0N :0 .ON .2 :0 0000-800. 0: w:_0:0000 :0 0.03005 .000 O_ 00 000—90000: 0:0 $3 :0 .000 .0000 .00 0_0>0_ 000000 :0 :0 308 ::0:::0.0>00 000000 0: St: 00:0EE :20.» 006.00 wx 2.8 50000080 505 00:00:00.0 005.00 wx ON. C 28.058020 000_0_m:& 0:: £05 00000:: 000::00 .200 0.8m. :0 0000000 U 0:0 00:00 .00 .3 000000 00:33 .000— 0:0 20:00 :00 0>::0 000:w0:: 000000 05 :00:: 00:0 0:: :0 0_0>:0:E 5000:0000 0:0 0w:_::0 :00025 00:00 .00 0:00am .3 030,—. 60 .80. n 000:0: :00:-: 000:.:. :0.00>0m. :00::D-:0..0>> 0: 0050:0000 30:00.00 >.::000.:w.0 :0: 0:0 :0::0. 00:00 00: :3 0030..0.: 5:200 0 55.3 0:008 .0>:0::. :0000..0.0.< . .So. u 000:0: :00:-: 000:.:. :0.00>0m. 50:00:23,? 0: w:.0:0000 E05000 00:85:30 :0: 0:0 :0::0. 0800 0:: .3 0032.00 5:200 0 500.3 0:008 w:.::0 :0000.:. 0 0:00 0008008000300. 03000 0.00: 00.... .00:0.:0> 2.: 000.080 0: 60.933 :00: 0:00.00 w:.0: 0000:0005: 0:03 0:00 .:0000:0::. .0>:0::.*w:0:0 ::000.:w.0 0 0: 0:0 0050:0000 :0: 0:03 .0>:0::. 500000.00 0:0 w:.::0 :0000.:. :0 0:00....0 00.... > 0:00 005800502000. 03000 0.0.0: 00% .00:0.:0> 0;: 000.080 0: 00.0500. :00: 0:00.00 00:00 00050080: 0:03 0:00. ; A0.::00: c. 030,—. 61 were not significantly different than the spray programs initiated prior to disease development (Table 10). The analysis of AUDPC means for petiole blight incidence in 2001 indicated significant spray initiation timing by application interval interaction (Table 10). This suggested that the differences observed in the application intervals were dependent on the spray initiation timing. Initiation timings for the 10-day application interval were all significantly different from one another with spray programs initiated at lower blight incidence thresholds providing better disease control (Table 11). For the Tom-Cast 15 and 25 DSV application intervals, respectively, initiation timings were similar for sprays initiated prior to blight occurrence and when a trace of disease symptoms were detected, and were significantly lower than initiation timings of 5 and 10%, which also differed from one another. Tom-Cast 20 DSV spray programs that started when 5 or 10% blight occurred were similar but the AUDPC of these were significantly higher compared with programs that were initiated when blight was first detected. Also, the AUDPC of the Tom-Cast 20 DSV interval that started when disease was detected was higher than the AUDPC of the program that was initially sprayed prior to blight symptom development (Table 11). The AUDPC data suggest that petiole health was significantly improved by applying the initial fungicide prior to disease detection or when disease symptoms were first detected compared with spray programs initiated at 5 or 10% leaf blight threshold (Table 12). In 2002, final petiole health ratings indicated no significant difference between spray programs initiated prior to blight symptom development and spray programs initiated when the first sign of disease symptoms were detected. Both the 5 and 62 Table 11. Effect of spray initiation timings for'each application interval on the area under the disease progress curve of petiole blight caused by A. dauci and C. carotae on ‘Early Gold’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 10-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001. Application interval Petiole blight incidence Initiation timing AUDPC (disease*day)z 10 day 0% 23.54 ay Trace 531.59 b 5% 1309.56 c 10% 1980.04 d Tom-Cast 15 DSV 0% 113.28 a Trace 165.99 a 5% 811.42 b 10% 2550.12 c Tom-Cast 20 DSV 0% 134.76 a Trace 513.11 b 5% 2354.31 c 10% 1985.52 c Tom-Cast 25 DSV 0% 725.61 a Trace 966.79 a 5% 1523.94 b 10% 2418.96 c Z AUDPC = area under the disease progress curve. Data were transformed using square root (AUDPC) to stabilize the variance. The table shows back-transformed data. y Means within each application interval followed by the same letter are not significantly different according to the Waller-Duncan Bayesian k-ratio t-test (k-ratio = 100). 63 £28885 .mEoEerE: “:8:in a 2 26 85:36 8: 803 EEBE cocwozqnm new wEE: 533:5 mo “acute of. x d2882£ EoEfiobiav» 282.:ch a 2 26 32838 BEA—£8 803 30% some Eob Sam A A864: 285,? so: mag 5:862: Eon—32:30» 2: 8:82. “co—com 203 Noom can SON Soc «ED .958 mmocwoa 033% 05 cows: 38 u UmQD< s 58v 2% 53v 8.2. 58v 3.: Bag .9 BEBE: 88¢ a; $85 e3 $93 woo ceases 3306255? 58v woe 58v 3.: 58¢ 2.8 ates 823233 58v 8.5 88v 8.8 58v 3% was: SE25 58v 2.: 88v 8.8 58v and $08.8: min.» A— msmi m mass m m5?» m m3~a> m MRNS» n.— 99.30% a Re Se 9 N3: >8 2 3.8.53 a one a a wow: >8 omsauéfi a 3m w? a 2.9; >8 2 eaoéoh a :3 2.4 .a 3:; .33: BEBE cosmo=am< 0 3e 8: a 422 :2 a 88 :3 a mg: :m a w? ohm a 8.9: 83. a 86 ad an 3.3 :o was: 83:5 88 .83 was: .2: héasafi 0.53 .5530; 5.8.. 228.. .moom can SON E 686.56 .0 can Base «do 15:8 Sm A>mQV mos—g 355m 0336 mm 5 .om .2 an “£0-th 8 @6308 8 23.82: b8 3 8 tom—name 98 $2 8 xxx». .08.: mo £32 0386 8 co $.88 “cacao—gov 038% 2 Sta BREE 5:3 Enid we. _ <8 :50?»on :23 BEES—a 35.: me. am. 3 ace—9:825 moEommcé of 5:3 @285 $0th .200 beam. mo :58: 22qu .5.“ mw—Efi Rec use 958 $2on 0386 2: .595 38 2: co mEEBE 5:8:QO “Em meEu :osaEE 3ch do maoofim .2 03:. 64 .82 n 28.3: no: 2.8-8. §_8.€m caucsadofi? 9 9:?on “cognate bucmoficwfi no: 8a 8:2 2:3 2: 3 BBB—ow 5:28 a :32? 2:88 BEBE ceasing > .82 u 283: 68-. 2.8-x 553m gangs—33 8 mEEooom EobbG 32:85ch 8: 2w 5:2 08mm 2: 3 BBB—om 5:28 a £53, £32: wEEc :2855 a .2583 2 2...; 65 10% spray initiation thresholds differed from one another and differed from the lower spray initiation thresholds (Table 12). The analysis of the final petiole health rating in 2001 indicated a significant interaction between spray initiation and application interval (Table 12). This suggested that the differences observed in the application intervals were dependent on the spray initiation timing. Initiation timings of 5 or 10% leaf blight were similar for the 10-day spray schedule and Tom-Cast 20 DSV treatment, but were significantly higher than the program started at a trace of blight symptoms (Table 13). Programs that were initiated prior to disease development significantly improved petiole health compared with the program started at a trace amount of blight. Tom-Cast 15 DSV programs initiated prior to disease development or when a trace amount developed were similar and were significantly lower than programs initiated when 5% blight appeared. The program started when 10% blight developed was significantly higher compared with the program initiated when 5% blight developed. All of the spray initiation timings for the Tom-Cast 25 DSV treatment were different, and final ratings increased as the spray initiation threshold increased (Table 13). Assessment of initial spray timing on ‘Cellobunch’ carrots. Disease progressed rapidly on ‘Cellobunch’ carrots during both years of this study. The incidence of petiole blight was observed on 5% and 36% of the untreated plants on 8 August 2001 and 7 August 2002, respectively (Figure 4). Untreated plots reached 84% and 100% petiole blight incidence on 28 September 2001 and 4 September 2002, respectively. Leaf blight in 2001 progressed from 4% on 17 August to 50% on 22 September (Figure 5). In 2002, severe leaf blight developed during the period of 11 September through 2 October 66 Table 13. Effect of spray initiation timings for each application interval on the final petiole health evaluation assessing disease caused by A. dauci and C. carotae on ‘Early Gold’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 10-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001. Application interval Final Initiation timing Petiole health2 10 day 0% 1.50 ay Trace 3.00 b 5% 6.00 c 10% 6.00 c Tom-Cast 15 DSV 0% 2.25 a Trace 1.50 a 5% 4.25 b 10% 7.50 c Tom-Cast 20 DSV 0% 2.00 a Trace 4.50 b 5% 6.75 c 10% 7.50 c Tom-Cast 25 DSV 0% 4.25 a Trace 5.25 b 5% 6.75 c 10% 7.75 d z Petiole health was evaluated using the following scale; where 1 = petioles healthy and vigorous to 10 = petioles unhealthy, weak, or dead. y Means within each application interval followed by the same letter are not significantly different according to the Waller-Duncan Bayesian k-ratio t-test (k-ratio = 100). 67 2001 100 < ‘ A lO-day Flo-day °\° --°— Untreated ”\H ' v 80 < 0 / l g o 0/0 ,1 /'~‘“—"‘; P "v" Trace // 4 5 60 * __ Q __ 50/ , / r 53 —» - 103A. .45 - _ / / .5. 4M // ‘6 /./ 2 //¢ / e r" / '5 20« // ,4» ,,,,,, 44 l m 4”’/’ / 0* f” 9 'i’ (,3 4 W , , , 1 100 w; Tom-Cast Tom-Cast 2‘. so. 15 nsv A g /’r"’,/ 0- /V *5 60 ‘ // / 4 / a /. / V 4 5 40 « .4 / ’ .. .2 / a ________ a e 20‘ 4_,/ —————— ._ 1‘ a: gif’ O 0‘ ‘3 :3 o r f - g 1 g 100 t I »; Tom-Cast I Tom-Cast / N g 80* 20 st / .. 20 DSV s 4 »~ '4: 60 4 / .-—-—-—4"'“' .L i a: / / / .. / [4 v E 40 4 ////V"7 «1 I :2 / /// /’/’ / i Q / //’ /’/ / '5 20 * ///"A//' r// +1 //' /o l a /,// ._49””” o // ( 0< (' ””””””” ‘” , / , . fie . , ~ ‘ 100 l _ . z; Tom-Cast _ Tom-Cast ; r ,4; 3 a) so. 25 st W4; .. 25nsv 2‘ 4” . r / . g l/// / / {Fr/l/ ‘/'/ o o l E 60 4 // // / / +1 ,/ //’I /V’/ o i :2 / / , v” ,x' . t n" f l r: ‘ / ,2 / //‘ 1 fl / ° l u— 40 // /j’ /, o 71 /// I/ o .2 // ////" 1’ / i' I/ I ’/ t ‘1 G /‘,/” // ' / / l '5 20 i 4/ ’4'” i‘ (, I/xf a: ,f/ l”,44' ‘ v/ 0 ///,I’ O O / O 41 D 4 . - . . x \ 05' my, 90 96 Q § (\va-‘VAV SN % '0 N N ’V " '5 ~ w w '5 ’5 A: Figure 4. Disease progress curves for petiole blight caused by A. dauci and C. carotae on ‘Cellobunch’ carrots left untreated or treated with chlorothalonil (1 .29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002 68 Leaf Blight (%) Leaf Blight (%) Leaf Blight (%) Leaf Blight (%) 2001 2002 u—SNUACIIOQ QOCGGGO bUIG GOO 10~ ‘ 10-day ‘ + Untreated i “V— 50/0 J Tom-Cast r | l 0% -~—‘ Trace :tfi'j —'— 10% :i‘:_-t;::f’_—::i::;:t -- L' Y Y Y— Ti: -k—i—T_i"'—i"—_’_'}:TI‘ZI:T:L 15 DSV Tom-Cast -J_. -HJ.._ _.L .__J__ J .-..L_‘ -_4L__ _ 15 DSV Tom-Cast 20 DSV ::l;:::l:*:::i:‘ O5 G M O i Tom-Cast fill! CC o? I-‘N OGO 25 DSV Tom-Cast i 20 DSV Tom-Cast 25 DSV \ s°v ’\ Figure 5. Disease progress curves for leaf blight caused by A. dauci and C. carotae on ‘Cellobunch’ carrots left untreated or treated with chlorothalonil (1 .29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i./ha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002. 69 when disease in untreated plots progressed from 25 to 70% (Figure 5). A summary of final disease assessments is listed in Appendix A (Table 32). According to the AUDPC data, spray programs initiated prior to blight occurrence were most effective in limiting the incidence of petiole blight and leaf blight, and no similarities were observed among the initiation timings (Table 14). Spray programs initiated when a trace amount of blight developed were effective in limiting petiole blight severity and did not differ from programs that started prior to blight occurrence. The 5% initiation timing was significantly different from both the lower thresholds, and it provided significantly better disease control compared with the 10% initiation timing (Table 14). The petiole health data suggest that programs initiated prior to disease or when a trace amount of blight developed significantly lowered the AUDPC compared to the 5 and 10% initiation timings, which did not differ (Table 15). In 2001, spray programs initiated prior to blight occurrence improved final petiole health compared with later initiation timings, which differed fi'om one another. In 2002, spray programs initiated when a trace amount of blight developed were effective in improving petiole health and did not differ from programs that started prior to blight occurrence. The 5% initiation timing was significantly different from both the lower thresholds. The 5% initiation timing provided significantly better disease control than the 10% initiation timing (Table 15). Assessment of initial spray timing on ‘Prime Cut’ carrots. Disease was detected on 20 July 2001 and 22 July 2002 in the commercial field studies. Leaf blight in untreated plots reached 60% by 27 September in 2001 and 45% by 30 September in 2002 70 .0000 008000000: 0.000 03000 0300 2:. 00:200.» 05 0025000 2 2 + UAQD 00000.55 RwOO NEO m _ 0N.O 0N; SwoO NnO 000000002 EEBEEEEC. 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C :00—050.850 0022203 05 505 000002 000200 £25020? :0 020.50 .0 0:0 .8000 .0. an 08:00 0223 .00. 0:0 20:00 00.“ 03:0 000200: 000020 05 000:: 000 05 :0 0.03005 00:02:50 0:0 0wEE: 0000201000000 0800mm .3 030,—. 71 .80. u 0003: 002-0 0003. 000003 000000-028? 8 $008000 E000Ofi0 >_0:00c_:w_0 8: 000 0000— 0E00 05 03 0032.8 0.0200 0 5505 0:008 330:: 00000200? > .82 n 00030 008-0 008-0. 000003 0000000233 2 $008000 8000*“? 30:00E0wm0 8: 000 .0002 0800 0.0 3 00328.0 08200 0 0023 0:008 @080 000000: a A0283 3 030,—. 72 .83 u 038$: “m3-“ 038$— 2885mm gangs—33 9 9:888 880.89% bay—momiwmm 8: 8a 5:2 088 05 .3 326:8 5:28 a £53, 388 9:8: conga: x 8826825 “5:388:33 BEEF—ma a 8 26 5.888% 35:88 803 So» :08 Eat Sam A .023 mmogwoa 0886 05 528 88 u DADD< N 58V mw.5_ Soov cogmm _ooo.v chm @835 .m> 338:5 memd 56 886 a5.o 5306 956 530885 RES—HerErw _ooo.v mg: 386 5‘5 o _ mod on. m BEBE cocmoznaaw 58V N ~ .2 58V owdm Soov 55.3 mafia: :ocmEE Soov 500 _ooo.v mm. 2 Soov 5 _ .m 80838.5 888 m 249» m 88E m min; m 33; m 85»; m 858%. a 2.5 a cod 9 368 >mD mm “mags—5... n m5.© . a mod a made— >mD om “.30-th a $6 a mmé as $.52 >mQ m _ ~30-th a w? a m2. 3.. 8.2. 5 2 12:35 .5585.an o 3.5 w 3.5 5 Emma— $2 a $6 0 3.0 n 362 fan a $6 a 09m m co._~_ 88H. m mmd a OWN gm N5.w: go @883 .8585: 83 33 M52: .25— .??8833 0.33. .5535. 5.3.. 2.59.— .88 can Sow E 88989 O was 82% .Vgo 35:8 .88 A>mav 82m.» 5833 0386 mm Ho 65. .2 a “$0-th 8 $6.83 8 mEEBE b6 2 8 3:858 28 $3 Ho .fcm .08: .3 £26— 83va E S €58 8083—33 0336 9 SE @0325 5:3 Enid my. 2.8 25835on FEB 8382? QED.“ wx am: 2:22.825 moflawca 2: 5:5 6285 99:8 .aocsnozou. be 5:82 20:3 ho.“ $58 3:: can 023 $8on ommoflo 2: 6.8: was 05 co mEEBE Samoa—mam 88 meE: cougar: 58% go 9855 .2 03:. 73 F-.. HE... «I‘m-h .82 u 233: .82 233. 56on CMUCflQJB—Eg OH wcmfihOoum “:95.ch ~A=¢mofimfiwmm “O: 0.5 .530— OEMw on: %D $030=0m fiED—Oo a G133? mcmoe Banzai fiOSflOSQQ< 3 .5253 2 as: 74 (Figure 6). In 2001, the incidence of petiole blight in untreated plots was 19% on 2 August and increased to 92% by 28 August (Figure 7). In 2002, the incidence of petiole blight in untreated plots was 24% on 5 August and progressed to 85% by 19 August (Figure 7). A 7-day application schedule was included in the 2002 commercial field trial, and it controlled disease effectively when applications were initiated at low disease thresholds (Figure 8). A summary of final disease assessments is listed in Appendix A (Table 33). The 2001 leaf blight AUDPC data indicated that programs started when 5% blight symptoms developed provided significantly less disease control than programs initiated at earlier disease thresholds but significantly limited leaf blight compared with programs started when 10% blight developed (Table 16). Spray programs initiated when 10% blight developed resulted in a higher AUDPC for petiole blight severity compared with the programs that started at lower disease incidence thresholds. Treatments that were initiated prior to disease, when a trace amount of disease was detected, or when 5% leaf blight occurred did not differ in limiting petiole blight severity (Table 16). The analysis of AUDPC for petiole blight incidence in 2001 indicated a significant interaction between the initiation timing and the application intervals, suggesting that the differences observed in the application intervals was dependent on the spray initiation timing (Table 16). The initiation timing for the lO-day and Tom-Cast 2O DSV intervals, respectively, differed from one another, with the programs started prior to blight occurrence providing the highest disease control (Table 17). When following the Tom-Cast 15 DSV application interval, the spray thresholds of 5 and 10% blight did not differ and provided significantly less disease control compared with the program that was 75 2001 2002 {lo-day ilO-day l A; 50 ‘ * —°— Untreated 1 £50 + <>~ 0% + *' ---- Trace ! 4: g“ l —-«~—- 5% l E 30 «'4 _._ 10%, ll 3 20 J T, J ___L_ __ _ l H}..-- _L._ T Y Y 7 T 1 V V Y Y T Tom-Cast 15 DSV _.._.1____.L_. Leaf Blight (%) b O H-—t—-—+—L—t—:f——l— r f Tom-Cast 20 DSV Tom-Cast 20 DSV L I 4 _‘L._—L_.l L Leaf Blight (%) 3 G Tom-Cast {Tom-Cast 1 25 st l 25 st l 41 Leaf Blight (%) A O 101 Figure 6. Disease progress curves for leaf blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots left untreated or treated with chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002. 76 2001 2002 7; ‘ lO-day l E, « —°— Untreated l g 0 0°/o i .5 ,_ —-v-- Trace . 2 _._ 5% .. E 1 1,“ —._ 10‘70/ 4 o .. 3 R J // «- 20 . / /:-—-_1’~ . o , r_K ’\ E rfiflM/ O l O / V’/ \~-1L\' 0 ‘ 9" ‘ i - . . . . 5 100 fi Tom-Cast Tom-Cast i 30 15 DSV 15 DSV , S b O Petiole Infection (%) :l:::l‘.m—‘*t——+—-‘ ‘ 20 /J—"“—k\\ 0, (‘V/ O o 7' .1 0 3’ i"- 5 . 5 . ..- - , . - .J 100 « A i Tom-Cast Tom-Cast 1 \° 1, 30 l 20 DSV <4 20 DSV . = r“~l ‘. i I '3 60 . / .4 A ' . u // fix; a —'—r // 0 £ 40 / 27’ / \ j// o o ,/ "' / ,,/( O 9.. F” o 0 ‘3 . - - l . . . . - 100 F ,9. lTom-Cast T Tom-Cast i 30 25 st l = 1 .2 l ‘93 60 i "" l E. 40 < 1:. 2 z '5 20 + , 9’ // l7 0 / ; G- i A/ l! 6 +2 (1:: v % W N‘ A? g? N N N W N Figure 7. Disease progress curves for petiole blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots left untreated or treated with chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 10 days or according to Tom-Cast using intervals of 15, 20, or 25 DSVs in 2001 and 2002. 77 2002 100* \° iaso< 1 a: .2 g 60 l a .5. 40 l 2 :3 20' i Q) a. o .i 70 1 ? 6° ‘ —°— Untreated ‘ E504 0 0% *- —+-Trace -= 4 E40 _v__5% a: i h- e l 0 A T l xxx :55 QQ QNSQSVVVVQQ‘OQD‘OQ x~~h¢3§59$Q§ Figure 8. Disease progress curves for petiole and leaf blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots left untreated or treated with chlorothalonil (1.29 kg a.i.lha) alternated with azoxystrobin (0.11 kg a.i.lha) applied prior to blight symptom development (0%) or at disease levels of trace, 5%, 10% and reapplied every 7 days in 2002. 78 .82 n 008-00 603 008-0— 006050m 000558233 00 80000000 8000506 500000880 00: 000 00:0— 0800 0.0 3 0032—8 08200 0 00.005 0:008 @080 00000:: 3 05:08.8: 2 008000880 00 000 0300 80D x 00008005 003005358: 0:005:90 0 00 0:0 0058006 00: 0803 .0302: 000000000 0:0 wEE: 00000:: .00 0000.000 05. a .0200 mmeoa 0000000 05 800:: 0000 u UAQD< N 52V 8.0% 58v 3.80 88v 2.05 0280 .2 0280:: :20 8.0 850.0 05.0 055.0 30 8008350235...??? 809v 2.8 558.0 3m 88v 02: 050258088392. 58v 8.x 58v 05.5 58v 2.3 056080305 82? 8.8 58v 8.8 38v 8.: 05.58; 039.» m msgp & 3:6: am $39» m @533 am 0333 m 90.30%. a 8.0% n 2.8 5.58 >m0 08.30.80... 0 3.03 00 :30 8.3.8 >m0 8000-th a $.08 0 50.50 0358 502000-055 a $08. .0 05.8 6.28 .03: 02:85 :0000:00< o 3.80 a 00.00 SEEN $2 a 8.0:. 0 55.00 05.8% gm a 3.5.8 0 50.50 8.32 80F 0 00.0mm 30 $3 03:: $0 MES: 000000: Ewa— ..00A .b_..0>0w A00:020.: SEE 2000.— 055.02... Nan—533.3 000:0 .Som 5 9mm: 32? 090050 000020 mm 80 .om .2 00 0000-80... 2 90000000 80 £902: 500 o_ 00 033000. 0:0 $2 00 5\% .000: 00 m_0>0_ 000080 00 80 005.8 80800—300 000080 00 000.0 0200:: 0003 $5.00 mo— :.8 0505050800 505 0808200 05.00 wx mm. 3 0:0—0500020 m00_0_w:& 05 £05 00000: $0800 .50 08:9 :0 080000 0 0:0 .8000 .V 50 000000 0.3me 000— 000 20000 800 03:0 000E000 000080 05 800:: 0000 05 :0 E0302: 00002—000 0:0 358: 000000: 58% 00 $00tm .0— 030% 79 .80: n 0:00-00 0003 0:00-0— 00:00x0m 0000090233 00 9:000000 000000.00 300005030 00: 000 0000— 0800 0:0 3 00323.: 55:00 0 0:005 0:008 030:: 00:00:090~ > .5283 0. 030.0 80 Table 17. Effect of spray initiation timings for each application interval on the area under the disease progress curve of petiole blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1 .29 kg a.i.lha) alternated with azoxystrobin (0.1 1 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at lO-day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2001. Application interval Petiole blight incidence Initiation timing AUDPC (disease*day)z 10 day 0% 1049.92 ay Trace 1434.77 b 5% 2276.12 c 10% 3281.62 d Tom-Cast 15 DSV 0% 742.57 a Trace 1090.16 b 5% 2294.45 0 10% 2563.06 c Tom-Cast 20 DSV 0% 1377.56 a Trace 1 810.05 b 5% 2175.69 c 10% 2924.79 (1 Tom-Cast 25 DSV 0% 2723.46 b Trace 1823.63 a 5% 2876.55 bc 10% 3060.42 c z AUDPC = area under the disease progress curve. y Means within each application interval followed by the same letter are not significantly different according to the Waller-Duncan Bayesian k-ratio t-test (k-ratio = 100). 81 initiated when a trace amount of disease was detected. The highest disease control was achieved when the initial application was made prior to blight symptom development and subsequent applications were made according to Tom-Cast 15 DSV. This program differed from the initiation timing where sprays were applied following blight detection. Tom-Cast 25 DSV spray programs initiated when a trace amount of disease was detected resulted in higher disease control compared to programs that were initiated prior to blight symptom development or when disease was evident on 5% of the foliage. Programs that started when 5% of the foliage was blighted did not differ from programs that were initiated when 10% leaf blight occurred (Table 17). The 2002 AUDPC data suggest that spray programs initiated when a trace amount of blight symptoms were detected effectively limited petiole blight severity and were comparable with the programs that were initiated prior to blight development (Table 18). Programs that started when 5 or 10% blight developed did not differ and were significantly different than programs that were initiated at lower blight incidence thresholds (Table 18). There was a significant interaction between initiation timing and application interval for AUDPC of petiole blight incidence in 2002, indicating that the differences observed in the application intervals depended on the spray initiation timing (Table 18). Seven-day spray programs that were initiated prior to disease occurrence did not differ from programs that were started afier a trace amount of disease was present (Table 19). Programs that were started when 5% blight developed were significantly less effective in controlling blight compared with programs that were initiated at lower initiation timings, and the 5% blight initiation timing provided significantly better disease control compared 82 00:000000: _03000_*w0:0: 0000::0w0 0 00 000 00000000 :00 0003 .0320: 00:00:30 000 wEE: 00:0:0: .00 0000000 0:0. x 020000000: 030053000: 0000:0030 0 0: 000 00500000 :00 0003 330.5 00:00:30 000 @005 00:02:: .«0 0000.000 0:0. 0 .0300 00050000 000000 0.: 00000 0000 n 0093.00 ~ 500V 009: 0000.v 2.00 800v 30m 0280.9 0280:: 080.0 20 003.0 :0 800.0 00.0 80202508.000580. 080.0 00.0 0000.0 ~00 0000.0 :0 0505808003 _000.v 0000 500v 00.2 500v 8.00 0580800000 .000.v 03: _000.v 02. 500v 00.: 05:08; 053» m 059» um NSC; m 3303 m 059» n— 05?» m 90.50% 00.000 0 00.02 00.080 >00 0280-050 00.000 0 0000 00.008 >00 0280-500. 0200 0 0000 00002 >00 0:80-80 000: 0 00.02 00.000 0002 00000 .0 00.8 00.00: E: 7035:: comumozmmxx 00.00. 0 00.02 00.0000 .02 00.000 0 00.0: 00.0000 .3 00.000 0 00.00 00.002 80: 0:00 30 020 2.05 :0 wEE: 00:0::: .2000 03.. 00050 08522: BE... 0.0000 .5232... 0000008000 0003V .moom 01>qu 000_0> @3000 000000 mm 00 .om .m: :0 000-th 0: w0_0._0000 00 0.03000: 00 c: 00 0 .0 00:00:02 000 0\0o_ 00 .000 .000: 00 0_0>0_ 000000 .0 00 0008 000000.000 000000 0: 0000 020:0: 00:3 0500 w: 2.8 05000580 :03 000000000 0500 m: cm. 3 :00—0503030 0006000.: 0.: :03 00:00: 000000 .000 00:00. 00 0000.30 .9 000 .8000 .V 03 000000 00:00:: 000— 000 20:00 00.: 0300 0000w000 000000 05 00000 000 0.: 00 203005 00:00:90 000 0wEE: 00:0EE 00000 .00 0:00am .2 030,—. 83 .80: H 0:00.00 :00:-: 0000- 00.0000 000005-0203 0: w0000000 :00-:0::0 >::000.-::0m_0 :00 000 00:0: 0000 00 >0 00320.: 000000 0 00:05 00000 _0>.:0.:0_ :00—000.0000” .80: H 0:00.05 :00: 000.0- .00_0.0>0 > 000005-0235 0: w0000000 0000:: 0 300000-2030 :00 00 00:0: 0000 00: >0: 00320: 0.0200 0 00:05 0000.0 WEE“ 00.00050” .0308: M: 030,—. 84 Table 19. Effect of spray initiation timings for each application interval on the area under the disease progress curve of petiole blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1 .29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2002. Application interval Petiole blight incidence Initiation timinL AUDPC (disease*day)z 7 day 0% 167.20 ay Trace 403.85 a 5% 2953.36 b 10% 3506.80 c 10 day 0% 3207.73 b Trace 935.06 a 5% 3414.87 bc 10% 3745.63 c Tom-Cast 15 DSV 0% 203.17 a Trace 1206.41 b 5% 3573.35 c 10% 4064.68 (1 Tom-Cast 20 DSV 0% 616.44 a Trace 1933.81 b 5% 3670.45 c 10% 3281.77 c Tom-Cast 2S DSV 0% 2156.40 a Trace 2015.16 3 5% 4131.24 c 10% 3427.55 b Z AUDPC = area under the disease progress curve. 3’ Means within each application interval followed by the same letter are not significantly different according to the Waller-Duncan Bayesian k-ratio t-test (k-ratio = 100). 85 with programs that were initiated when 10% blight developed. Ten-day spray programs that were initiated when a trace amount of disease developed provided better disease control than programs initiated prior to blight development or when sprays were applied at the 5% blight threshold. Programs that were initiated when 10% blight developed provided the least disease control, and were not significantly different from the programs that were started when 5% blight symptoms developed. Tom-Cast 15 DSV spray programs that were initiated prior to disease symptom development were most effective in controlling disease. Programs that were initiated when a trace amount of disease was detected, when 5% blight developed, and when 10% blight developed were all significantly different from one another, with the least control provided by the 10% initiation timing. Tom-Cast 20 DSV program significantly reduced petiole blight incidence more effectively compared with programs that were initiated at a trace amount of disease. Programs that were initiated when 5 or 10% blight developed did not differ, however, both programs did not control disease as effectively as the programs that were initiated when a trace amount of disease was detected. Tom-Cast 25 DSV programs that were initiated prior to blight symptoms or when disease was evident on a trace amount of the foliage did not differ, and provided better disease control than programs started when 10% blight developed. Programs that were started when 5% blight symptoms occurred were the least effective in controlling disease, and were significantly different than programs initiated when 10% blight developed (Table 19). There was a significant interaction between the initiation timing and the application interval for AUDPC of leaf blight in 2002, indicating that the differences observed in the application intervals depended on the spray initiation timing (Table 18). 86 Using the 7-day and Tom—Cast 20 DSV applications intervals, respectively, programs that were initiated prior to disease development were most effective in controlled leaf blight (Table 20). Programs that were started when a trace amount of blight developed, when 5% blight developed, or when 10% blight developed were all significantly different fiom one another, with the 10% initiation timing resulting in the highest AUDPC. Ten-day spray programs that were started after a trace amount of blight developed were the most effective in controlling leaf blight compared with programs that were initiated prior to disease development or when 5% blight occurred. Programs that were started when 10% blight developed provided the least disease control and were significantly different from programs that were initiated prior to blight symptoms or when disease was evident on 5% of the foliage. Tom-Cast 15 DSV spray programs that were initiated when disease was apparent on a trace amount of the foliage were not significantly different than programs that were initiated prior to disease development. Programs that were started when 5% leaf blight occurred controlled leaf blight less effectively than programs started at earlier thresholds but were more effective than the programs that started when 10% blight occurred. Tom-Cast 25 DSV spray programs that were initiated prior to disease development provided the best disease control and were significantly different from programs that were started when a trace amount of the foliage was blighted. Programs that were initiated when 5 or 10% blight developed did not differ from one another, but were significantly less effective in controlling leaf blight than the programs initiated when a trace amount of blight developed (Table 20). The 2002 AUDPC data of petiole health and final petiole health indicated that programs that were initiated prior to disease development were similar to programs that 87 Table 20. Effect of spray initiation timings for each application interval on the area under the disease progress curve of leaf blight caused by A. dauci and C. carotae on ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1 .29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) in 2002. Application interval Leaf blight Initiation timing AUDPC (disease"‘day)z 7 day 0% 159.00 ay Trace 213.00 b 5% 310.38 c 10% 350.88 (1 10 day 0% 274.63 b Trace 176.00 a 5% 284.50 b 10% 527.88 c Tom-Cast 15 DSV 0% 138.50 a Trace 174.88 a 5% 286.50 b 10% 413.63 c Tom-Cast 20 DSV 0% 173.50 a Trace 229.13 b 5% 388.50 c 10% 432.25 (1 Tom-Cast 25 DSV 0% 199.88 a Trace 238.00 b 5% 404.88 c 10% 395.50 c z AUDPC = area under the disease progress curve. y Means within each application interval followed by the same letter are not significantly different according to the Waller-Duncan Bayesian k-ratio t-test (k-ratio = 100). 88 .l.“ were sprayed when a trace amount of disease developed (Table 21). Sprays that were applied when 5% blight occurred provided less disease control compared with spray programs that were initiated at lower disease thresholds, but were more effective in improving petiole health than programs that were initiated when 10% blight symptoms occurred (Table 21). Assessment of fungicide application interval on ‘Early Gold’ carrots. The main effect of application interval had a significant effect on all ‘Early Gold’ disease assessments except the AUDPC data for petiole blight incidence in 2002 (Table 10). Disease progressed rapidly in 2002 (Figure 3), and an increase in petiole blight resulted compared with the 2001 growing season. The AUDPC data suggest that the lO-day interval and Tom—Cast 15 DSV intervals limited petiole blight severity when compared with the Tom-Cast 25 DSV interval (Table 10). The Tom-Cast 20 DSV interval was similar to both the 10-day, Tom-Cast 15 DSV, and Tom-Cast 25 DSV intervals. Leaf blight AUDPC was controlled most effectively by the 10-day or Tom-Cast 15 DSV application intervals when compared to the Tom-Cast 20 or 25 DSV intervals, which differed from one another (Table 10). The AUDPC and 2002 final rating data for petiole health suggest that the lO-day and Tom-Cast 15 DSV application intervals improved petiole health compared with the Tom-Cast 20 and 25 DSV intervals (Table 12). Spray programs using the Tom-Cast 20 or 25 DSV intervals did not differ and were the least effective in controlling disease (Table 12). Assessment of fungicide application interval on ‘Cellobunch’ carrots. Application interval had no effect on the AUDPC values of petiole blight incidence or 89 Table 21. Effects of spray initiation timings and application intervals on the area under the disease progress curve and final ratings for petiole health of ‘Prime Cut’ carrots treated with the fungicides chlorothalonil (1.29 kg a.i./ha) alternated with azoxystrobin (0.11 kg a.i./ha) when initiated prior to disease development (0%) or at disease levels of trace, 5%, or 10% and reapplied at 7 or 10 day intervals or according to Tom-Cast at 15, 20, or 25 disease severity values (DSV) for control of A. dauci and C. carotae in 2002. Petiole health Treatment AUDPC (disease*day)’ Final ratingy Initiation timing 0% 125.93 a" 4.90 a Trace 131.08 a 5.00 a 5% 157.30 b 6.10 b 10% 190.80 c 6.75 c Application interval 7 day 137.69 abW 4.94 a 10 day 163.88 cd 6.06 bc Tom-Cast 15 DSV 131.34 a 5.38 ab Tom-Cast 20 DSV 151.69 be 5.81 bc Tom-Cast 25 DSV 171.78 (1 6.25 c Source F value P value F value P value Treatment 5.90 <.0001 4.05 <.0001 Initiation timing 22.90 <.0001 14.26 <.0001 Application interval 6.02 0.0004 4.05 0.0056 Timing*interval interaction 0.70 0.7480 0.63 0.8068 Untreated vs. treated 16.89 <.0001 14.50 0.0003 z AUDPC = area under the disease progress curve. y Petiole health was evaluated using the following scale; where l = petioles healthy and vigorous to 10 = petioles unhealthy, weak, or dead. " Initiation timing means within a column followed by the same letter are not significantly different according to Waller-Duncan Bayesian k-ratio t-test (k-ratio = 100). w Application interval means within a column followed by the same letter are not significantly different according to Waller-Duncan Bayesian k-ratio t-test (k—ratio = 100). 90 severity (Table 14). According to the AUDPC data, the lO-day and Tom-Cast 15 DSV intervals were similar and most effective in controlling leaf blight when compared with the Tom-Cast 20 and 25 DSV intervals, which did not differ (Table 14). Similarly, the 10-day and Tom-Cast 15 DSV intervals reduced the petiole health AUDPC compared with the Tom-Cast 20 and 25 DSV intervals, but the later intervals did not differ from the Tom-Cast 15 DSV schedule (Table 15). The final petiole health data suggest that the 10- day and Tom-Cast 15 DSV intervals were similar in 2001 and 2002 and improved petiole health compared with the Tom-Cast 20 and 25 DSV intervals, which did not differ (Table 15). Assessment of fungicide application interval on ‘Prime Cut’ carrots. According to the 2001 AUDPC data, the 10-day, Tom-Cast 15 DSV, and Tom-Cast 20 DSV were equally effective in controlling petiole blight severity and leaf blight (Table 16). Tom-Cast 25 DSV was the least effective in controlling petiole blight severity and it did not differ from the Tom-Cast 20 DSV application interval. Additionally, Tom-Cast 25 DSV was not effective in controlling leaf blight and was significantly different from all other application intervals (Table 16). In 2002, application interval did not have a significant effect on the AUDPC of petiole blight severity in 2002 (Table 18). The AUDPC of petiole health and final petiole health data suggest that Tom-Cast 15 DSV and the 7-day interval were most effective in limiting disease (Table 21). The AUDPC data indicate that the 7-day schedule was not significantly different than Tom-Cast 20 DSV. The 10-day schedule was similar to Tom- Cast 20 DSV and Tom-Cast 25 DSV, which provided the least disease control. The 2002 final petiole data suggest that the Tom-Cast 15 DSV interval did not differ from the 10- 91 day schedule or Tom-Cast 20 DSV. Tom-Cast 25 DSV, which was the least effective in improving petiole health, was not significantly different than the 10-day schedule or Tom-Cast 20 DSV application interval (Table 21). DISCUSSION Carrot growers in Michigan have been concerned about applying fungicides when environmental conditions do not favor blight development. The cost of these unneeded sprays became paramount as production costs continued to increase. It was desirable to develop methods for reducing fungicide input to economically produce carrots. The goals of this study were to investigate disease incidence thresholds determined by field scouting for timing the initial fungicide application and to examine the use of the Tom- Cast disease forecasting system for timing fungicide application intervals to control Alternaria and Cercospora blights on carrots. The economic benefits of using field scouting to time initial sprays and using Tom-Cast to time subsequent sprays are exemplified in situations where growers do not use either disease management strategy. In 2001, standard lO-day fungicide schedules required nine sprays for each cultivar tested, whereas the number of applications was reduced to eight (‘Early Gold’ and ‘Cellobunch’) or remained the same with nine sprays (‘Prime Cut’) by using Tom-Cast 15 DSV to determine spray intervals. Applying the initial application when blight was first detected in the field saved an additional three sprays (‘Early Gold’ and ‘Cellobunch’) and one spray (‘Prime Cut’). In 2002, standard fungicide schedules required nine sprays (‘Early Gold’ and ‘Cellobunch’) and eight sprays (‘Prime Cut’), whereas the number of fungicide applications was reduced to six applications (‘Early Gold’ and ‘Cellobunch’) and or remained the same with nine 92 applications (‘Prime Cut’) by using Tom-Cast 15 DSV to determine spray intervals. Applying the initial fungicide application when blight was first detected in the field saved one additional spray (‘Early Gold’, ‘Cellobunch’, and ‘Prime Cut’). In seasons with conditions highly favorable for blight development, the Tom-Cast program may not reduce the number of sprays or production costs, but it may be beneficial in improving the timing of fungicide applications to prevent severe blight epidemics and crop loss. Ben-Noon et a1. (2001) examined timings of spray initiation for controlling A. dauci on carrots and attempted to create a disease threshold model describing when the first spray should be applied. Initial sprays were delayed until 14 and 28 days afier the common management practice in the growing area. Higher fungicide efficacy was observed with spray schedules that were initiated earlier in the season relative to the first occurrence of disease. The model was not validated, and recommendations were made to apply fungicides in a prophylactic manner to achieve leaf blight control. The scouting studies conducted in this research indicated different results. The time of spray initiation was successfully delayed until the first detection of disease symptoms, without compromising disease control. In many cases, the scouting and Tom-Cast program resulted in disease control that was similar to standard fungicide schedules that were initiated prior to disease occurrence while eliminating up to four sprays per season. The results of the present study agree with the findings of Gillespie and Sutton (1979). One to three sprays were omitted by delaying the initial fungicide application until blight symptoms developed on 1 to 2% of the foliage. Conversely, delaying the initial fungicide application is not recommended for other cr0ps. Keinath et a1. (1996) tested a scouting-based spray program for scheduling fimgicide applications for 93 controlling early blight of tomato. According to this spray program, fields were scouted twice per week until disease symptoms appeared on 3 to 6% of the foliage when a weekly fungicide program commenced. The scouting program delayed the initial fungicide application for 42 days and saved six sprays compared with the standard 7-day fungicide program. The scouting program resulted in lower yields of extra-large fruit and increased disease severity compared with the standard 7-day program. The negative impact of the scouting program presented a risk to growers, and it was recommended that growers continue to apply fungicides prior to disease occurrence (Keinath et al., 1996). Tom-Cast has been used to successfully time fungicide applications for managing other pathogens of vegetable crops. Tom-Cast was evaluated as a disease management tool for timing fungicide applications to control purple spot (Stemphylium vesicarium (Wallr.) E. Simmons) on asparagus (Meyer et al., 2000). The Tom-Cast spray program prompted an equal or fewer number of sprays and provided better disease control than the l4-day standard program. Additionally, some newly established asparagus plots managed according to Tom-Cast resulted in increased fern stands (Meyer et al., 2000). The yield measurements recorded in these studies do not reflect yields that may be recorded in a commercial production situation where carrots are mechanically harvested. All carrots in 3.05 m of the center row were hand harvested, whereas yield losses may have become evident if plots were harvested mechanically. Therefore, differences in yield (where applicable) are attributed to leaf blight’s ability to reduce the photosynthetic capacity of plants. A large-scale field trial, where carrots are mechanically harvested, is needed to determine the effect of treatments on yield reduction attributed to the condition of foliage. 94 Tom-Cast should be used in conjunction with other effective IPM methods. Cultural controls, such as crop rotation and the plowing under of carrot residue following harvest, should continue to prevent A. dauci and/or C. carotae inoculum from accumulating in infected carrot foliar residues (Pryor et al., 2002). New fungicides, as they become available, should be tested for disease control efficacy when used in a scouting and Tom-Cast spray program. The results of these studies may prompt others to examine the effect of using systemic fungicides for the initial application when disease symptoms are present in the field. In addition, the use of disease scouting and Tom-Cast may be explored for use in other cropping systems. 95 ‘ m'cuxhr‘. A . n i I. LITERATURE CITED Arcelin, R., and Kushalappa, AC. 1991. A survey of carrot diseases on muck soils in the southwestern part of Quebec. Canadian Plant Disease Survey 71 :147-153. Ben-Noon, E., Shtienberg, D., Shlevin, E., Vintal, H., and Dinoor, A. 2001. Optimization of chemical suppression of Alternaria dauci, the causal agent of Alternaria leaf blight in carrots. Plant Disease 85: 1 149-1 156. Bird, G., Bishop, B., Grafius, E.J., Hausbeck, M.K., Jess, L.J., Kirk, W., and Pett, W. 2002. Insect, disease and nematode control for commercial vegetables. East Lansing, Michigan State University. E - 312, 44-47. F ancelli, M.I., and Kimati, H. 1991. Occurence of iprodione resistant strains of Alternaria dauci. Summa Phytopathologica 17:135-146. Gillespie, T.J., and Sutton, J .C. 1979. A predictive scheme for timing fungicide applications to control Alternaria leaf blight in carrots. Canadian Journal of Plant Pathology 1:95-99. Hausbeck, M.K., and Harlan, BR. 2003. Chemical control of Alternaria and Cercospora leaf blights in carrot, 2002. Fungicide and Nematicide Tests 58 (in press). Hausbeck, M.K., Cortright, B.D., and Lindennan, SD. 2000. Chemical control of Alternaria blight in carrot, 1999. Fungicide and Nematicide Tests 55:153-154. James, R.V., and Stevenson, W.R. 1999. Evaluation of selected fungicides to control carrot foliar blights, 1998. Fungicide and Nematicide Tests 54:131. James, R.V., Stevenson, W.R., and Rand, RE. 1999. Evaluation of carrot cultivars and breeding selections to identify resistance to foliar blights, 1999. Madison, University of Wisconsin. Wisconsin vegetable disease control trials, 1999, 73-75. Keinath, A.P., DuBose, V.B., and Rathwell, PI. 1996. Efficacy and economics of three fungicide application schedules for early blight control and yield of fresh-market tomato. Plant Disease 80: 1277-1282. Madden, L., Pennypacker, SP, and MacNab, A.A. 1978. FAST, a forecast system for Alternaria solam' on tomato. Phytopathology 68:1354-1358. Meyer, M.P., Hausbeck, M.K., and Podolsky, R. 2000. Optimal fungicide management of purple spot of asparagus and impact on yield. Plant Disease 84:525-530. Pitblado, RE 1992. Development and implementation of Tom-Cast. Ontario Ministry of Agriculture and Food. 96 Pryor, B.M., Strandberg, J .O., Davis, R.M., Nunez, J .J ., and Gilbertson, R.L. 2002. Survival and persistence of Alternaria dauci in carrot cropping systems. Plant Disease 86:1115-1122. Shaner, G., and Finney, RE. 1977. The effect of nitrogen fertilization on the expression of slow-mildewing resistance in Knox wheat. Phytopathology 67:1051-1056. Steel, R.G.D., Torrie, J.H., and Dickey, D. 1997. Principals and procedures of statistics: a biometrical approach. 3rd ed. McGraw-Hill, New York, pp.197-198. Strandberg, J .O. 1988. Establishment of Alternaria leaf blight on carrots in controlled environments. Plant Disease 72:522-526. Strandberg, J .O., Bassett, M.J., Peterson, CE, and Berger, RD. 1972. Sources of resistance to Alternaria dauci. (Abstr.) Hort Science 7:345. Wamcke, D.D., Christenson, D.R., Jacobs, L.W., Vitosh, M.L., and Zandstra, EH. 1992. Fertilizer recommendations for vegetable crops in Michigan. East Lansing, MI, Michigan State University. E - 5503, 20-24. Zandstra, EH. 2002. Weed control guide for vegetable crops. East Lansing, MI, Michigan State University. E - 433, 16. Zandstra, B.H., Grafius, E.J., Wamcke, DD, and Lacy, ML. 1986. Commercial vegetable recommendations: carrots. 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Hausbeck Alternaria Blight; Alternaria dauci Michigan State University Cercospora Blight; Cercospora carotae Department of Plant Pathology East Lansing, MI 48824 Evaluation of spray application equipment to manage foliar blights of carrot, 2001. This study was conducted at a cooperator’s farm in Oceana County, M1 on a Freesoil sand field previously planted to corn. Carrot ‘Goliath’ seeds were planted on 27 Apr at a spacing of 1.75 in. to rows spaced 18 in. apart on three-row beds centered 64 in. apart. Treatment plots were seven beds wide and 40 ft long with 10 it of unsprayed buffer between plots and one bed of unsprayed carrots on either side of the plot. The center bed of the plot was used as an untreated drive row, and the three beds to the left and right were sprayed with different spray nozzle systems. Fungicides were applied with a trailer spray rig equipped with two independent spray nozzle systems pulled by a 40 hp high clearance tractor traveling at 3 mph. The three treated beds on the left of the drive row were sprayed with a conventional boom elevated 12 to 16 in. above the crop canopy and equipped with eleven XR11003VS flat fan nozzles spaced 20 in. apart. Spray solutions were mixed in S-gal tanks pressurized by C02 and calibrated to deliver 20 gal/A at a nozzle pressure of 20 psi. The three treated beds on the right of the drive row were sprayed with a boom located 4 to 5 fi above the crop canopy that was mounted with three air-assisted nozzles spaced 64 in. apart. The motor used to generate power for the air- assisted system was operated at a hydraulic pressure of 1600 psi that propelled the fans to spin at 5000 rpm. Spray solutions were mixed in a 30-gal tank and the boom was pressurized by a hydraulic roller pump calibrated to deliver 10 gal/A. Weeds, insects, fertilization, and irrigation were managed according to standard production practices. Five treatments were randomly assigned within each of four blocks. Nozzle type was not randomized for treatment plots because the tractor only traveled in one direction down the drive rows. As a result, nozzle type is confounded with direction of travel and consequently the side of the plot. The analyses assume that no systematic differences exist between the two sides of the plot. As a whole, the experiment represents a split plot design in which fungicide treatments are the whole plots and nozzle types are the sub- plots. Seven applications were made at lO-day intervals on 12 and 23 Jul; 2, 14, and 23 Aug; and 4 and 13 Sep. Disease assessments were recorded on 8 and 28 Aug; 15 and 29 Sep; and 9 Oct from the middle bed in the center 10 ft of the middle row from both sides of each plot. Carrots in the center 10 ii of the middle row of each plot were hand- harvested, the foliage removed at the crown, and roots weighed to determine yield on 9 Oct. Disease pressure was light until 1 Sep, when a severe epidemic of Alternaria and Cercospora blights developed. The interaction between nozzle type and treatment was not significant for any of the data analyzed, so the best treatment did not depend on nozzle type. The air-assisted nozzles significantly reduced the percentage of plants with petiole lesions throughout the season based on the AUDPC and at the time of final evaluation compared with the conventional nozzles (Table 34). Disease severity on the petioles did not differ between nozzle types nor did petiole health. All fungicide regimes 114 significantly reduced disease severity on petioles and improved petiole health compared with the untreated but did not significantly affect yield (Table 35). Quadris alternated with Bravo, regardless of nozzle type, significantly reduced the percentage of plants with petiole lesions compared with Quadris alternated with Kocide and the untreated control. 115 Angus: .8... 8:2 82:85 33x3. 9 mam—:88 “=80ch 368$sz 8: 8a .832 o: 8 3:2 2:3 05 3 325:8 5:28 a £53, $862 > .336 go £83 $53655 why—osonne 9 map—ow? S530: may—oral 80:3 6.QO o_ 8 _ a no 38 2:8: 226; 3 8338.5: 8 38.8?ch on go: 2:8 oBmtm> 63va 98 .OmAuv .omAmHm .om-oum Jana Com £562 20on Tel 80:? 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Base: 3: 22> 2:8; 382% .33 85205 6.53. @555 32.2 Ba .558: 228A 223 222 .Som 5 30:8 .5230. :0 836.56 568889 98 .835» 6.2328; .3 888 8:33 .828 :o moflflwca mo Hootm .mm 033—. 117 CARROT (Daucus carota ‘Goliath’) R.S. Bounds and MK. Hausbeck Alternaria Blight; Alternaria dauci Michigan State University Cercospora Blight; Cercospora carotae Department of Plant Pathology East Lansing, MI 48824 Evaluation of spray application equipment and reduced fungicide rates to manage foliar blights of carrot, 2001. This study was conducted at a cooperator’s farm in Oceana County, M1 on a Freesoil sand field previously planted to corn. Carrot ‘Goliath’ seeds were planted on 27 Apr at a spacing of 1.75 in. to rows spaced 18 in. apart on three-row beds centered 64 in. apart. Treatment plots were seven beds wide and 40 it long with 10 ft of unsprayed buffer between plots and one bed of unsprayed carrots on either side of the plot. The center bed of the plot was used as an untreated drive row, and the three beds to the left and right were sprayed with different spray nozzle systems. Fungicides were applied with a trailer spray rig equipped with two independent spray nozzle systems pulled by a 40 hp high clearance tractor traveling at 3.0 mph. The three treated beds on the left of the drive row were sprayed with a conventional boom elevated 12 to 16 in. above the crop canopy and equipped with eleven XR11003VS flat fan nozzles spaced 20 in. apart. Spray solutions were mixed in S-gal tanks pressurized by C02 and calibrated to deliver 20 gal/A at a nozzle pressure of 20 psi. The three treated beds on the right of the drive row were sprayed with a boom located 4 to 5 it above the crop canopy that was mounted with three air-assisted nozzles spaced 64 in. apart. The motor used to generate power for the air- assisted system was operated at a hydraulic pressure of 1600 psi that propelled the fans to spin at 5000 rpm. Spray solutions were mixed in a 30-ga1 tank and the boom was pressurized by a hydraulic roller pump calibrated to deliver 10 gal/A. Weeds, insects, fertilization, and irrigation were managed according to standard production practices. Fungicides were applied at 75% of the labeled rate and at the labeled rate. Seven treatments were included in this study: an untreated control, Bravo 82.5WDG applied at 1.1 and 1.4 lb/A; Kocide 53.8DF applied at 1.1 and 1.5 lb/A; and Quadris 2.08F applied at 4.7 and 6.2 fl oz/A. Treatments were randomly assigned within each of four blocks. Nozzle type was not randomized for treatment plots because the tractor only traveled in one direction down the drive rows. As a result, nozzle type is confounded with direction of travel and consequently the side of the plot. The analyses assume that no systematic differences exist between the two sides of the plot. As a whole, the experiment represents a split plot design in which fungicide treatments are the whole plots and nozzle types are the sub-plots. Treatments were compared by decomposing the treatment SS into four components to address the following questions: (1) Do the untreated plots differ from the average treated plot; (2) Is there a fungicide main effect that explains overall differences in the three fungicides used; (3) Is there a rate main effect that explains overall differences in the two rates used; and (4) Is there an interaction between fungicide and rate to explain if differences in the fungicides depend on rate at which the fungicide was applied? Seven applications were made at lO-day intervals on 12 and 23 Jul; 2, 14, and 23 Aug; and 4 and 13 Sep. Disease assessments were recorded on 8 and 28 Aug; 15 and 29 Sep; and 9 Oct from the middle bed in the center 10 ft of the middle row from both sides of each plot. Carrots in the center 10 ft of the middle row of each plot were 118 hand-harvested, the foliage removed at the crown, and roots weighed to determine yield on 9 Oct. Disease pressure was light until 1 Sep, when a severe epidemic of Alternaria and Cercospora blights developed. The interaction between nozzle type and treatment was not significant for any of the data analyzed, so the best treatment did not depend on nozzle type. Furthermore, since the previous interaction was not significant, the best nozzle type did not depend on the fungicide used or the rate applied. The air-assisted nozzles, irrespective of the fungicide or rate used, significantly reduced petiole blight and improved petiole health compared with the conventional nozzles (Table 36). The interaction between fungicide and rate was not significant for either petiole blight or petiole health, so the best fungicide did not depend on the rate applied. In addition, the main effect of rate was not significant. The significant main effect of fungicide indicates that Bravo and Quadris significantly reduced the AUDPC, petiole blight incidence, petiole blight severity, and improved petiole health compared with Kocide (Table 37). Bravo significantly reduced petiole blight incidence compared with Quadris. Yield was not significantly affected by nozzle type or treatment, but yield losses may have become evident if plots were harvested mechanically. 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