GROWTH, LEAF COMPOSITION AND NUTRIENT-ELEMENT BALANCE OF MONTMORENCY C H E E R Y (Frunus c e r a s u s , L.)— Effect of Varying Concentrat ions of Ten Nutrient-Elements py Roy Kenneth Simons A THESIS Submitted to the School of Graduate Studies of Michigan State College of Agriculture and Apolied Science in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Department of Horticulture 1951 Table of Contents Page Acknowledgments Introduction --- 1 Review of Literature ---------------------------- 3 Materials and M e t h o d s --------------------- 9 Results — ----------------------------------- - - - — Growth ---------------------------------Leaf Composition and NutrientElement Balance ---------------------Di s c ussion Summary --------------------------------- ------------------------------------- Literature Cited ---- Aooendix Table 1-10, Inclusive--Growth 13 13 21 33 24I4. I4.7 Acknowledgments The author expresses anrjreciatlon to Dr. A. L. K e n worthy who spent m uch time and assisted in P l a n n i n g the experiment, and in the preparation of the manuscrint; G. E. Steinbauer, to Dr. K. B. Tukey, Dr. and to Dr. L. M. Turk for their consultation and editorial assistance in the p r e p a r a t i o n of the manuscript. assistance of Mr. Also the E. L. Froebsting, Jr. in m a i n ­ taining the nutrient solution applications when it was necessary for the author to be absent was appreciated. The auth o r is grateful to the Institute of Nutrition, M i c h i g a n State College, for its financial assistance during the course of this study. GROWTH, LEAF COMPOSITION AND NUTRIFNT-ELEMENT BALANCE OF MONTMOR E N C Y CHERRY (Prunus c e r a a u s , L . )— Effect of V a r y i n g Concentrations oi* Ten Nutrient-Elements R oy Kenneth Simons Introduction Several workers have investigated critical levels of certain nutrient-elements in relation to the appearance of deficiency s y m p t o m s . Goodall and Gregory ( H 4.) brought together the various leaf composition values reported to be associated w ith the occurrence of deficiency symptoms for certain nutrient-elements in various crops. 'They also summarized leaf composition values reported to be associat­ ed with plants not showing symptoms. The range In leaf composition for plants showing deficiency symptoms frequent­ ly Included a p o r t i o n of the range In leaf composition for olants not showing symptoms. Field surveys in commercial cherry orchards show con­ siderable variation In leaf composition. Many of the values correspond to those found for plants showing defi­ ciency symptoms (17)- Recent concepts and Interpretations of nutrient-element balance (1 5 # 16# 2 5 # 26) point out that a nutrient-element can be considered to be deficient only in relation to the other n u t r i e n t - e l e m e n t s . element balance intensities vary, for normal plants likewise vary. Thus, as nutrient- leaf composition values 2 Concentrations of nutrient-elements have been found to influence plant growth significantly without causing visible symptoms of shortages or excesses. This influence may be considered to be associated w ith the balance or relationships of nutrient-elements or intensity of nutrient elements, w h ich m a y be called h i d d e n deficiency or excess. According to these concepts, growth, leaf composition, and nutrient-element balance should be affected by varying con­ centrations of essential nutrient-elements. Most of the investigations of this nature have been conducted on crops other than Montmorency cherry (Frunus cerasus, L . ) and have dealt with only a few of the essen­ tial nutrient-elements. show very low vigor. ciated, M any commercial cherry orchards This low vigor is believed to be asso in part, with h i d d e n deficiencies, or with excesses of one or more nutrient-elements. This study was initiated to determine the extent to which growth, leaf composition and nutrient-element balance might be affected by variations of individual nutrientelements in nutrient solutions supplied Montmorency cherry trees. 3 Literature Review The influence on growth of various concentrations of certain nutrient-elements has been reported by several workers. Brown (5), C u llinan and Batjer (9) and Waltman (2 8 ), w o r k i n g w ith peaches reported that nitrogen had a greater Influence on growth than phosphorus. Brown (9) considered phosphorus to have less effect on growth than nitrogen, potassium, calcium or magnesium, while potassium and calcium were second to nitrogen. Waltman (28) found the peach to be more sensitive to phosphorus defi­ ciency than was the atrple • Apple tree growth was increased as the nitrogen con­ centration Increased to 168 npm by Batjer and D e g m a n (1)* and Cullinan and Eatjer (9)» There was no significant d if­ ference in growth between 60 and 168 p p m (1). Cullinan, Scott and Waugh (10) obtained best peach tree growth at 60 oom of nitrogen. Erown (E>) found that a concentration of 1000 nom of nitrogen produced less peach tree growth than did 100 o nm of nitrogen. The effect of this high concentra­ tion of nitrogen was reduced by increasing the concentration of phosphorus, potassium, or calcium. Chapman and Liebig (7) found 6-7 P p m of nitrogen would maintain vigorous citrus tree growth. However, I4.2 O ppm of nitrogen was not harmful to terminal growth, but reduced top/root ratio. W i l l c o x (29) stated that application of phosphorus and p o t assium to agronomic crops relieved nitrogen toxicity. k Phosphorus concentrations from Ij. to 1+0 p p m did not affect apple tree growth a c c ording to Batjer and Degm an (1 ), while concentrations of 0 and 2 n p m reduced growth. Cullinan, Scott and Wau^h (10) found neach growth not to be affected by phosphorus concentrations above 1+ ppm. Cullinan and Batjer (9) stated that terminal growth of peaches was not reduced at 2 ppm if the levels of nitrogen and p h o s ­ phorus were maintained. Brown (£) found with peaches that increasing phosphorus f rom 2 to 20 p p m resulted in increased growth, but further increase of phosphorus to 200 ppm did not increase growth. Increasing the concentration of nitro­ gen or potassium increased bhe growth produced by the higher concentrations of phosphorus. Edgerton (12) found that growth of McIntosh apples in­ creased as the p o t a s s i u m concentration Increased to 200 ppm, while Delicious apple tree growth Increased as potassium was increased to 100 ppm. Batjer and D e g m a n (1) reported apple tree growth to decrease as the potassium concentrations were reduced below 117 ppm. A p o t assium concentration of 10 ppm resulted in the greatest growth of p e a c h trees In a study by Cullinan, Scott a n d Waugh (10). Brown (5) found that a concentration of 800 p p m of p o t a s s i u m did not reduce growth except w hen calcium was high, or phosphorus or nitrogen was low. Cullinan a n d Batjer (9) found that terminal growth of peach trees was not reduced by using 2 ppm of p o t a s s i um if 5 a oroper level of nitrogen and phosphorus was maintained, itfhen p o t a s s i u m was high, D a v i d s o n and Blake (11) found that increased calcium concentrations would increase growth, but would not prevent calcium deficiency symptoms. Boynton and Burrell (3), and Cain (6 ) found a reciprocal relation­ ship between the concentration of p o t assium and ma g n e sium in that h i g h concentrations of one would result in defi­ ciency symptoms of the other. were reported by Nightingale Balanced multiple deficiencies (23) to result in a normal a p ­ pearing pineapple plant of reduced size. Ma n y relationships have been reported to exist be­ tween nutrient-elements contained in the leaves. stated that fundamentally, each nutrient-element is antag­ onistic, at least potentially, of the other elements. Brown ($) to the accumulation of each This would imply that as one ele­ ment increased in the leaves there is a corresponding in­ crease or decrease in the other nutrient elements. Boynton and Com p t o n (1+), Cain (6 ) and Kenworthy and Penne (1 8 ) found that applications of nitrogen fertilizers Increased leaf nitrogen, cal c i u m and magnesium, but de­ creased leaf phosphorus and potassium. Beeson (2) found that concentrations of nitrogen would reduce the concentra­ tions of other e l e m e n t s • Brown (5) found that increasing the nitrogen content of the nutrient solution resulted in decreased absorption of phosphorus, potassium, and calcium, but increased 6 magnesium absorption* Leaf analysis for potassium, however, was reported by Batjer and Degm a n (1 ) not to be influenced by nitrogen concentration of the nutrient solution* Cha p ­ man and Liebig (7) found that Increased nitrogen concentra­ tions did not denress phosphorus absorption, but that de­ creased nit r o g e n concentrations resulted in increased phosphorus absorption. Cullinan, Scott and Waugh (10) also found that Phosphorus absorption was highest with low nitro­ gen c o n c e n t r a t i o n s • Nightingale (23) reported that low nitrate absorp t i o n resulted in free absorption of phosphorus by pineapple plants in soils low in phosphorus. Lilleland and Brown (22) found poor growth (which m a y be due to low nitrogen) was frequently associated with low p h o s p h o r u s ,and many good orchards were low in phosphorus. Kenworthy and Gilligan (19) found a positive relationship between leaf nitrogen and leaf Phosphorus w h e n the a v a i l a b i l i t y of p hos­ phorus was very low, but w ith high phosphorus availability this relationship was negative. Increasing the phosphorus concentration in the nutrient solution ac c ording to Brown (£), had little affect upon nitrogen absorption, but decreased the absorption of potas­ sium, calcium, and magnesium. The decreased absorption of potassium caused by increased phosphorus was eliminated by increasing n itrogen and p o t assium concentrations. Evans, Lathwell, and Nederski (13) in w ork with soybeans found that phosphorus deficiency Increased potassium and calcium 7 absorption, but h a d little effect upon the absorption of the m i nor elements. Kenworthy and Benne Phosphorus applications were found by (18) to increase nitrogen, potassium, and manganese absorption, while calcium and m a g nesium ab­ sorption decreased. Increasing the notassium concentration did not influence the leaf analysis for potassium In the work reported by ^atjer and D e g m a n (1) and Cullinan, Scott and Waugh (10), Brown (£) found that Increasing potassium concentrations had little effect u n o n nitrogen absorption, but decreased the absorption of calcium and magnesium. Increasing the calcium concentration did not relieve the reduced calcium absorp­ tion associated w i t h h i£h potassium. Chapman and Liebig (7 ) found that Increasing calcium and potassium simultaneous­ ly resulted In decreased calcium and increased potassium absorption. W h e n D a vidson and Blake (11) increased p o t a s ­ sium concentrations from U+O to £90 p p m there resulted in only a slight increase in p o t assium absorption, but decreased absorption of calcium a n d magnesium. Nightingale (23) found that additional potassium was needed for nitrate absorp­ tion if both carbohydrates and nitrates were high* Reeve end Shive (2lf.) reported that as p o t assium supply was In­ creased boron accumulation increased, A deficiency of potas­ sium resulted in Increased absorption of calcium and p h o s ­ phorus, and decreased absorption of manganese, copper, and boron, according.to Evans, iron? Lathwell and Mederski (13)* e K enworthy and Eenne (18) found that p o t a s s i u m applications to reach trees, w h e n p o t a s s i u m was deficient, resulted In increased a b s o r p t i o n of potassium, calcium, and manganese, and decreased a b s o r p t i o n of nitrogen, phosphorus, and magnesium. Increased c a l c i u m concentration, end Blake (11), ac c o r d i n g to D a v i d s o n caused a slight decrease in p o t a s s i u m and Increased phosphorus absorption. Reeve and Shive (2J+) found that cal c i u m tended to check b o r o n Injury o n tomatoes, and that hi g h a b s o r p t i o n of c a l c i u m a n d requirement for each other. Evans, boron increased the Lathwell, and Mederski (1 3 ) reported that w i t h soybeans a cal c i u m deficiency r e ­ sulted in increased analysis for magnesium, phosphorus, potassium, and boron, ganese, copper, but decreased the analysis for m a n ­ iron, a n d calcium. T h e i r w o r k also showed that a de f i c i e n c y of m a g n e s i u m increased potassium, and de ­ creased phosph o r u s a n d boron absorption; while m a g n e sium excess resulted in decreased a b s o r p t i o n of potassium, and calcium. Boron d e f i c i e n c y Increased cal c i u m and magnesium. Manganese defici e n c y increased phosphorus, potassium, and boron, but h a d no effect on m i n o r element absorption. Materials and Methods This experiment was conducted at the Horticultural farm at M i c h i g a n State College during the summer of 191*9. The trees were grown from M a y 26 to September l£. The experi­ mental lay-out is shown in Figure 1* One-year-old Montmorency cherry trees were used. The trees were selected in the nursery for uniformity in size and growth, and small sizes were taken in order to reduce the carry-over of nutrients. The containers were £0-oound berry cans, h a v i n g a dia­ meter of 12 3/8 inches, and a height of 13 inches, with a capacity of approximately one cubic foot. They were enamel coated on the inside, and before use were painted with a water-proof asphalt emulsion. A drainage outlet was made on the side of the container near the bottom to facilitate drainage of any excess water or nutrient solution. Each tree was washed free of soil before planting. The shoots were pruned to approximately 12 Inches or higher if necessary so as to leave a m i n i m u m of three leaf buds. broken roots were removed. All Each tree was then weighed and planted in an Oshtemo sand--a soil of low fertility. The trees were planted w i t h the bud union at, or Just below, the soil level, and immediately watered. Deionized water (20, 21) obtained by the use of synthetic resins (Amberlite I-R U E and I-R 120*) was u sed throughout the ^Manufactured by R o h m and Maas bompany, Philadelphia 5# M a • 9 Figure 1 Experimental Layout at the Horticultural Farm. Trees used in this study are located in the back portion of the foreground. Figure To accompany Pago 9 10 e x p e riment. A set of de-ionizing towers, using ij.-inch olexiglas tubes was constructed, and the water passed through I-H 120 to absorb all cations, and on through 1-R !(. B to absorb all anions. The anion exchange resin was r e ­ generated with 1+ ner cent sodium carbonate, and the cation exchange resin regenerated w i t h 1*. ner cent hydrocloric acid when the de-ionized water contained more than 6 p p m soluble salts. All leaf buds were left on the tree after nlanting until arnrcximately I4. cm of growth was made. At this stage all but three shoots were removed. Five replicate trees were planted for each treatment. Also, twenty-one additional trees were used to calculate the dry weight of the trees planted. This was accomplished by determining the p e r cent moisture of the twenty-one additional trees, and using this as a n index of the m oi s ­ ture content of the planted trees. Ten nutrient-elements were used with five different levels for each. A m e d i a n level, or so-called "optimum" concentration was u sed as a basis for comparison. This median level was determined f r o m published work concerning nutrient solutions for fruit trees (5) (28). Each nutrient- element was varied f r o m this "optimum" concentration by in­ creasing or decreasing the amount used. The optimum con­ centration contained twice the amount of the 1/2X optimum level, and the 2X optimum level contained four times the 11 amount of the 1/2X optimum; while the fourth level, ipt optimum, contained eight times that of the 1/2X optimum. A zero level was used in which the nutrient-element was omit ted. This arrangement provided for nutrient-element levels corresponding to the ratios 0 , 1 , 2 , I4., and 8 . This olan for each of the ten nutrient-elements made a total of 1+1 treatments, using one m e d i a n level, or ootimum treatment, for all nutrient-elements. A n additional treat­ ment was nlanted which received only de-ionizea water. Stock solutions of chemically cure NH^NO^, KC1, CaCl2 , MgSC^, H 3 FO3 , KnSO^, CuSC^, ZnSO^, and F e S 0|j were prepared Individually for each of the nutrient-elements Prom these stock solutions a dilute solution for each treat­ ment was prepared In which the elements were combined in definite rroportions. The dilute solutions were kept in 5-gallon bottles, and the solutions were replaced w hen algae growth became evident. The initial pH of the solutions was approximately 1^..5- 5 -0 , but no attempt was made to adjust this value. The concentration of the nutrient-elements at the different levels is shown in Table 1. One quart of nutrient solution was apolied each day throughout the growing season. Late in the season when the weather was cooler, nutrient solutions were not aoolied as frequently as earlier in the season. Since the rain was not kept out of the cans, an application of nutrient solu­ tions was made after each rain in order to maintain the desired concentration. Table 1. Concentration of the Various Mutrient-Llevents T’sed in the Nutrient Solutions for t^e Different Treatments nh4no3 Nitrogen 0 112.0 22k.0 448.0 696.0 p 3f °^ Phosphorus c 34-0 68.0 136.0 272.0 PCI Potassium 0 43.0 66.0 172.0 31A.0 CaCl2 Calcium 0 88.0 176.0 352.0 70l|..0 mci± Magnesium 0 29.0 58.0 116.0 232.0 MnSOl^ Manganese 0 2.5 5.0 10.0 20.0 H3EO3 Boron 0 1.5 3.0 6.0 12.0 accompany FeSO^ Iron 0 1.0 2.0 k.o 8.0 ZnSO^ Zinc 0 1.0 2.0 4 .0 8.0 CuS0|^ Cooper 0 1.0 2.0 I4.O 8.0 Page NutrientElement To Nutrient-Element Concentration or Level Omitted 2X optimum I4.X optimum 1/2X optimum Optimum ppm ppm nnm ppm ppm Compound used 11 12 The experiment was September 15* l9i|-9 * terminated during the week of The three most uniform trees were selected to obtain growth records and leaf analysis. Two trees from each treatment were carried throughout the winter for additional observations. Each of the three selected trees was harvested as follows: shoots; leaves removed from the shoots severed from the m a i n trunk, and the trunk separated from the roots; roots then washed carefully; shoots, trunk and roots cut into smaller nieces to facili­ tate drying; various parts of each tree placed separately in a paper bag, and put immediately in the forced draft dehydrator regulated to 60 degrees centigrade. After the samples had been in the dehydrator for several days, each sample was weighed. The leaves were ground w i t h a Viley mill, using a lj.0mesh screen. The various replications were composited, mixed thoroughly, and then divided into duplicate samples. One sample was sent to the chemical laboratory for nitrogen analysis, u s ing the Kjeldahl method, and bhe other sample sent to the National Spectrographic Laboratories, Cleveland, Ohio, for spectrographic analysis for P, K, Ca, Mg, Pe, Cu, B, and Mn. 13 Presentation or results G-rowth Altering the concentration or any one nutrientelement and keening all other nutrient-elements at the op­ timum concentration resulted in a considerable variation in growth. The results of growth measurements are presented in Tables 2 to 11, inclusive* Dry weight increase and shoot growth in relation to varying concentrations of nutrientelements are presented in Figures 2 and 3* Maximum growth was obtained w hen the nutrient-solution contained the m e d i a n or optimum concentration of all nu ­ trient elements. Significantly less tree growth, as measured by dry weight increase of the entire tree various dry weight of the tree parts, and length of terminal growth, was ob­ tained when the concentration of a nutrient-element was reduced £0 p e r cent (1/2X optimum), cent from optimum (2X optimum). or increased 100 per Omitting the nutrient- element, or increasing the concentration to !j.X optimum usually resulted in less tree growth than reducing the con­ centration of the nutrient-element to 1/2X optimum, or in­ creasing the concentration to 2X optimum. This reduction in growth, however, was not significant. Wet increase in dry weight of shoots and length of terminal growth was influenced significantly by varying the concentration of any one of the ten nutrient - e l e m e n t s • Table 2. Influence of Varying Nitrogen Concentration in Nutrient Solution upon Net Increase in Dry Weight, Dry Weight of Various Tree Parts, and Length of Terminal Growth entire tree Dry we ight of < Nitrogen When” After -- Ref ” concentration planted growth increase gm gm m Dry weight of various tree parts after growth Boots "trunk Shoots leaves gm gm gm gm Omitted 35.3* 71.6 36.3#* 44.7 12.3#* 5.2*# 1/2X optimum 45-4 95.5 49.8# 52.1 18.1 9.6*# Optimum 48.5 119.5 71.0 60.7 20.7 2X optimum 48.2 84.0 35*7## 42.1 17.8 8.2*# 15.8 ipC optimum 46.9 77.2 30.3*# 38.1 14.9* 10.6## 13.4 124.1# 20.0 26.5 30.0 39.9 5.4 7.2 4.5 6.0 11.2 14.8 46.7 62.0 15.6 21.6 66.3** 79.6** 179.7 92.6## To accompany Page Least significant difference * 13•2 --## — it 17.5 16.5 9.4* Terminal growth cm 13 1 Table 3* Influence of Varying Thosphorus Concentration in Nutrient Solution upon Net Increase in Dry Weight, Dry Weight of Various Tree Farts, and Length of Terminal Growth Dry weiriit of entire tree Phosphorus When After fret concentration planted growth increase gm gm gm Dry weight of various tree parts after growth ftoots Trunk Shoots Leaves gm gm gm gm Terminal growth cm Omitted U0.2 68.3 28.1*# 39.2 12.9## £.2** 11.0 61.£## 1/2 optimum £0 .1 91.8 1*1.7#* 1(8.7 20.0 7.9## 15.2 86•6** Optimum 1*8.5 119.5 71.0 60.7 20.7 2X optimum 1(1*.6 88.1 1(3•£## 1(6.6 16.1 8 .9** 16.£ 9 £•1** I4.X optimum 1(1.0 87.3 1*6.2* 1*1**3 16.6 9.1*#* 16.8 9 8.6** 20.0 26.£ 30.0 39.9 5-1* 7.2 1*.5 6.0 11.2 11*.8 1(6.7 62.0 21.6 179.7 To accompany Page Least significant difference * — 5i 13-2 *# — 1< 17.5 16.£ 13 Table 1. Influence of Varying Fofcassium Concentration in Nutrient Solution upon Net Increase in Dry Weight, Dry Weight of Various Tree Parts, and Length of Terminal Growth Dry weight of entire tree Potassium When After Het increase growth concentration planted gm gm gm Dry weight of various tree parts after growth_____ Hoots leaves Trunk Shoots gm gm gm gm Omitted 1*5.0 71.0 26.0## 38.9 15.5 9.9## 10.6 81.3** 1/2 optimum 1*6.2 83.1 36.9*# id*.7 16.5 7.6## 11.2 110.8** Ootimum 1*8.5 119.5 71.0 60.7 20.7 16.5 21.6 179.7 2X optimum 1*6.1* 96.9 50.5* 50.1* 18 4 10.2** 17.9 118.5** IX optimum 1*1.2 81.0 39.8#* 1*1**7 14.7* 7.i|.** 11.2 111.0*# 20.0 26..9 30.0 39.9 7.2 54 1*5 6.0 11.2 11.8 16.7 62.0 Terminal growth cm To accompany Page 13 Least significant difference » — $i 13.2 ** — it 17.5 Table Influence of Varying Calcium Concentration in Nutrient Solution upon Net Increase in Dry Weight, Dry Weight of Various Tree Farts, and Length of Terminal Growth Dry weight of entire tree UKen After $et Calcium growth increase concentration Dianted gm gm m Dry weight of various tree parts after growth Roots' Trunk Snoots EeJ gm gm gm gm Omitted Ul.2 79.0 37.8** 1*1.1* 15.0 7.3** 15.2 97•1#* 1/2 optimum 44*7 67.7 43*0** 1*9.2 15.8 8.2** 14.4 81.8** Optimum W.5 119.5 71.0 60.7 20.7 2X optimum 33.5» 79.7 46 •2* 43.1 12.6-::-* ipC optimum 38.1 81.0 1*2.9*# 1*4.8 13.3** 20.0 26.5 30.0 39.9 5.4 7.2 cm 8 .9** 14.8 113.8** 6 .3** 14.6 111.6** 4.5 6.0 11.2 14.8 46.7 62.0 Page 179.7 accompany 21.6 16.5 To Least significant difference ---13.2 * --5% ttS— 1% 17.5 Terminal 13 Table 6. Influence of Varying Magnesium Concentration in Nutrient Solution upon Net Increase in Dry Weight, Dry height of Various Tree Parts, and Length of Terminal Growth Dry we ight of entire tree After ?fet When Magnesium concentration planted growth increase gm gm gm Dry weight of various tree parts after growth Roots Trunk Snoots Leaves gm gm gm gm Terminal growth cm 36.9 87.0 50.0* 49.5 14.0* 8 .3*# 15.1 1/2 optimum U3-3 89.7 46.4* 48.9 16.3 10.2-:;-* 1^.3 123.0* Optimum 48.5 119.? 71.0 60.7 20.7 16.5 21.6 179.7 2X optimum 41.6 116.3 74.7 58.3 39.5 15.8 22.7 141.3 IpC optimum 464 101.3 54-9 56.6 18.3 9.9** 16.5 116.3* 20.0 26.? 30.0 39.9 5-4 7.2 4-5 6.0 23 88•3** accompany Page 46.7 62.0 To Least significant difference * --$% 13.2 ** — 1i 17.5 CM CO • • Omitted 13 Table 7* Influence of Varying Manganese Concentration in Nutrient Solution upon Net Increase in Dry height, Dry Weight of Various Tree Parts, and Length of Terminal Growth Dry weight of entire tree Manganese 4ien After Jfet increase concentration nlanted growth gm gm gm Dry weight of various tree parts after growth______ Roots Shoots Leaves Trunk gm gm gm gm Omitted 55.0 18.4 42.6 17.6 71.0 60.7 20.7 1034 $9.0 Optimum 48.5 119.5 2X optimum U3.6 90.6 47 .0* 49.8 16.4 4X optimum 51.? 104.5 53.0 59.4 17.1 20.0 26.5 30.0 39.9 5.4 7.2 Least significant difference * — 13.2 — ** — 1i 17.5 — 8 .7*-# 13.7 73.1*# 21.6 179.7 15.1 111.3** 10.5* 17.4 100.1** 4*5 6.0 11.2 14.6 46,7 62.0 16.5 9.3** Page 82.7 129.7# accompany 37.8 18.6 To 1/2 optimum 11.4* Terminal growth cm 13 Table 8. Influence of Varying Boron Concentration in Nutrient Solution uoon Net Increase in Dry height, Dry Weight of Various Tree Parts, and Length of Terminal Growth Dry weight of entire tree Dry weight of various tree Boron When concentration planted gm After growth gm Net increase gm Omitted 52.9 111*-3 61.3 63.6 20.6 1/2 ootimum ipO.U 90.0 1*9.6# 1*7.7 16.3 Optimum 1*8.5 119.5 71.0 60.7 20.7 16.5 21.6 179.7 2X optimum 42.1 105.8 63.6 50.5 23.1 13.0 19.0 150.0 1*X optimum 1*6.1 81.1* 35.2## 1*24 17.6 7.9## 13.1* 106.6#* 20.0 26.5 30.0 39.9 1*.5 6.0 11.2 11*.8 1*6.7 62.0 parts after growth Hoots Trunk Shoots Leaves gm gm gm m 11.3* 9 .9*# Terminal growth cm 18.5 102.1## 16.0 96.0*# To Page 5.1* 7.2 accompany Least significant difference * — 5% 13.2 *# — 1^ 17,5 13 Table 9. Influence of Varying Iron Concentration in Nutrient Solution uoon Net Increase in Dry Weight, Dry Weight of Various Tree Parts, and Length of Terminal Growth Dry weight of entire tree Dry weight of various tree Iron When After Set"" parts after growth Terminal concentration planted growth Increase____ Roots flruhk Shoots Leaves growth gm gm gm gm cm gm gm m 43*3 65.1 1/2 optimum 36.2 88.9 119.5 Optimum 14-9.1 lh.6 7.3** 4.0 83.3** 52.7 14-7.0 16.3 9 .t o 16.0 101. t o 71.0 60.7 20.7 21.6 179.7 16.5 To Omitted 77.5 l|.2.to 39.8 154 8. 0*# 4*2 91.t o i|.X optimum 35*9 72.6 36.7*# 14-0.3 13.0 7.1#* 12.2 97.t o 20.0 26.5 30.0 39.9 54 7.2 I4-. 5 11.2 4 4 fc6.7 62.0 6.0 13 Least slgnifleant difference # — 5? 13*2 ■JHt --l1 ^ 17*5 — Page 35.5 Accompany 2X optimum Table 10. Influence of Varying Copper Concentration In Nutrient Solution upon Net Increase in Dry Weight, Dry Weight of Various Tree Parts, and Length of Terminal Growth Dry weight of entire tree Cooper When After Net growth Increase concentration planted gm gm gm Roots gm Omitted 35.lt 79.6 l|it.lt*« 1/2 optimum 32.3* 75.9 Optimum ite.5 119.5 2X optimum 39.1; 1|X optimum ia .9 Dry weight of various tree Terminal growth cm 154 7.3*# 12.8 07.3** lt3.6ftft 36.1 15.1 7 .8## 4-9 104.3** 71.0 60.7 20.7 21.6 179.7 69.lt 50.0* 49.2 16.1 4.9 112.5** 91t>2 52.3 44-5 20.7 10.7* 18.2 46.6 20.0 26.S 30.0 39.9 54 7.2 4.5 6.0 11.2 4.8 46.7 62.0 Least significant difference £ 13*2 ** — ii 17.5 16.5 9.1** Page 4*3 Leaves gm accompany Shoots gm To Trunk gm 13 i Table 11. Influence of Varying Zinc Concentration in Nutrient Solution upon Net Increase in Dry Weight, Dry veight of Various Tree Parts, and Length of Terminal Growth Dry we ipjit of entire tree When Zinc After Net concentration planted growth increase gm gm gm Dry weight of various tree parts after growth Hoots Trunk Shoots Leaves gm gm gm gm Terminal growth cm 39.8 94.7 a -6 45.2 20.4 11.3* 17.6 121.3* l/2 optimum 32.8. 92.8 60.0 43.1 17.7 12.3 19.6 132.5* Optimum 48.5 119.5 71.0 60.7 20.7 16.5 21.6 179.7 2X optimum 35.7 69.7 54.0* 45.2 16.8 10.6* 17.0 117.0** lj.X optimum 43.6 63.3 39.7*# 42.3 19.3 8 .0** 13.6 84 •3-“* 20.0 26.5 30.0 39.9 5.4 7.2 4.5 6 .0 11.2 14.8 46.7 62.0 To Omitted accompany Page Least significant difference * --st 13.2 ** ~r£ 17.5 13 Figure 2. Length of Shoot Growth and Dry Weight Increase for Varying Concentrations of Nitrogen, Phosphorus, Potassium, Calcium, and Kagnesium. To accompany Pag© 3-3 *t * 1 Figure 3. Length of Shoot Growth and Dry Weight Increase for Varying Concentrations of Manganese, Eoron, Iron, Zinc, and Cooper. •wet m w w-i wtm w t i — £l O^Bd XUBUUIOOOB OJ, m v « m n t m m w a M 'i m m Poot or trunk growth, or dry weight of leaves produced, was not affected significantly by altering the concentration of any one of the various n u t r i e n t - e l e m e n t s . A number of excentions were found from the above gen­ eralizations. Net increase in dry weight was not signifi­ cantly below m a x i m u m when iron and zinc were 1/2 optimum or when manganese, trient solution. boron, or zinc were omitted x'rom the n u ­ Pet increase in dry weight produced by a concentration 2X ontimum for magnesium or boron was not significantly below maximum. for magnesium, manganese, Concentrations ipC optimum or Conner did not reduce the net 1 increase in dry weight significantly below maximum. D r y weight of shoots was significantly below maximum when all of the nutrient-elements except zinc were used in concentrations 1/2X ootimum. A significant reduction in dry weight of shoots resulted with the omission of any one of the nutrient-elements. Concentrations 2X ontimum of m a gnesium or boron did not nroduce shoot growth signifi­ cantly less than maximum. Concentrations ipC optimum for each nutrient-element produced shoot growth significantly below m a x i m u m . Terminal growth signif icantly below m a x i m u m was p r o ­ duced when any one of the nutrient-elements was 1/2X optimum or omitted. Concentrations 2X optimum produced terminal growth significantly below m a x im um except for magnesium and boron* Concentrations I4X optimum produced terminal growth significantly below m a x i m u m in all cases, except for cooper* None of* the variations in nutrient-element concentration resulted in a significant variation in dry weight of roots or leaves, except where nitrogen was omitted. Trunk growth, however, was significantly below maximum in the following cases: nitrogen omitted or lj.X optimum, phosphorus omitted, potassium ipt optimum, calcium 2X, or ij_X optimum, magnes.ium omitted, and iron IpC optimum. Dry height I n c r e a s e : Table 12 shows the relative effects of the ten nutrient-elements upon dry weight increase, shoot crrowth and the other measurements of growth. Potassium, when omitted, resulted in less dry weight increase than obtained w hen any one of the other nine n u ­ trient-elements were omitted. The other nine, when omitted, produced dry weight increases in the following increasing order: sium, phosphorus, nitrogen, calcium, zinc, manganese, and boron. iron, Conner, ma gne­ This order of nutrient- elements was rearranged as follows when the concentration was 1/2X optimum: potassium, phosphorus, calcium, manganese, magnesium, boron, nitrogen, cooper, iron, and zinc. Nutrient-element concentrations above optimum showed that the effect of the different elements was dependent upon con­ centration. Nitrogen resulted in less dry weight increase at both 2X optimum and other elements. optimum than produced by the The other nutrient elements, w he n used at concentrations 2X of optimum, produced dry weight in the following increasing order: iron, phosphorus, calcium* Table 12. Relative Effect of Various Concentrations of Several NutrientElements Dnon Increase in Dry height Nutrient-element Omitted Dry wt. increase Rank gm 1/2X optimum Dry wt. increase Rank gm 2X optimum Dry wt. increase Rank gm 1*X optimum Dry wt. increase Rank gm 36.3 3 1*9.8 8 35-7 1 30.3 1 Phosnborus 26.1 2 1*1.7 2 43-5 3 1*6.2 7 Potassium 26.0 1 36.9 1 50.5 7 39.6 5 Calcium 37.8 i* 1*3.0 3 46.2 1* 1*2.9 6 Magnesium 50.0 7 lj6.lt 6 74-7 10 51*.9 10 Manganese 59.0 9 44-8 5 47.0 5 53.0 9 Boron 61.3 10 49.6 7 63*6 9 35.2 2 Iron 1*1.8 5 52.7 9 1*2.0 2 36.7 3 Conner 10*4 6 1)3.6 k 50.0 6 52.3 8 Page Zinc 51*.8 8 60.0 10 51*.0 8 3^.7 1* 1£ To Nitrogen accoirmany Dry weight increase at optimum concentration— 71.0 grams 16 manganese, corner, potassium, Concentrations I4X zinc, boron, and. magnesium* oobimum resulted in the f ol lowing order in regard to increasing dry weight production: boron, iron, manganese, zinc, potassium, nitrogen, calcium, phosphorus, copper, and magnesium. Shoot G r o w t h : Table 13 shows the relative effects of various concentrations of several nutrient-elements upon shoot growth. The amount of shoot growth nroduced when each element was omitted fell into a very narr ow range. The same amount of shoot growth was nroduced when either nitro­ gen or phosphorus was omitted; however, when no ta s si um was omitted, slightly more shoot growth was nroduced. Calcium, iron, and corner ranked third in shoot growth production. M a g n e s i u m ranked fourth, while boron, and zinc ranked fifth in the p r o d u c t i o n of shoot growth. As the concen tr at io n of the nutrient-elements was re ­ duced to 1/2X optimum, cooper h a d the greatest effect in s unpressing shoot growth. The other nutrient-elements may be arranged in the following order with regard to their suopressing shoot growth: manganese, nitrogen, potassium, phosphorus, iron, boron, magnesium, calcium, and zinc. W hen u sed at concentrations of 1/2X optimum, n itrogen and iron resulted in the same amount of shoot growth. When the concentration was 2X optimum, nitrogen pro­ duced less shoot growth than pr oduced w h e n the other nutrient- Table 13. Relative Effect of Various Concentrations of Several Nutrient Elements unon Shoot Growth Nutrient-element Omitted Shoot Rank growth gm 1/2X optimum Shoot Rank growth gm 2X optimum Shoot growth Rank gm 1*X optimum Shoot growth Rank gm 5.2 1 9.6 6 8.2 1 10.6 9 Phosphorus 5.2 1 7.9 3 8.9 3 94 6 Potassium 5.9 2 7.6 2 10.2 7 74 2 Calcium 7.3 3 £.2 k 8.9 3 8.3 5 Magnesium 8.3 h 10.2 8 15.8 9 9.9 7 Manganese 11.1*. 6 8.7 5 9.3 5 10.5 8 Eoron 11.3 5 9.9 7 13.0 8 7.9 3 Iron 7.3 3 9.6 6 8.0 2 7.1 1 Cooper 7.3 3 7.8 1 9.1 k 10.7 10 Page 11.3 5 12.3 9 10.6 6 8.0 k 16 Shoot growth at optimum— 16.5 grams accompany Zinc To Nitrogen nts were u sed et the 2X opti mu m concentration. The lng nutri e nt -e le me nt s m ay be arranged in the following 1 of sunore ss in g effects: manganese, iron, p h o s p h o r u s , calcium, zinc, potassium, and boron, h e greatest d ep ressing effect u n o n shoot growth, reg f r o m in cr ea si ng the concentration of the nutrientits to ontimum, was associated with iron and the e ffec t was associa t ed with corner. The depressing ef- of the r e m a in in g elements m a y be arranged in the fol; order: potassium, slum, manganese, T er mi n a l Growth: I*- by the var io us boron, zinc, calcium, phosphorus, nitrogen, and corner. Terminal growth was affected differconcentrations of the nutrient-ele- studied (Table 11+ and Figures Ij. to 8, inclusive), p h o s p h o r u s n roduced less terminal growth than the nut ri e nt -e le me nt s w h e n the various nutrient-elements 1omitted. The other nutrient-elements nroduced ter- growth w h e n omitted in the f o l l ow i ng increasing nitrogen, ootasslum, p- boron, iron, corner, magnesium, zinc, and manganese. cal- W h e n the concentration of 'i n u tr i e n t - e l e m e n t was reduced to 1/2X optimum, the ftsest re duction in terminal growth was associated with pr panese, nitrogen, and calcium. The remaining nutrient- g§: a©nts had the following order of decreasing effects: phorus, boron, calcium, iron, conper, potassium, zinc, magnesium. 17 elements were used et the 2X opt im um concentration. The remaining nutrient-e le me nt s m a y be arra ng ed in the fo llowing order of s un or essing effects: Conner, manganese, iron, phosphorus, calcium, zinc, potassium, and boron. The greatest depressing effect unon shoot growth, re­ sulting from increasing the concentration of the nutrientelements to I4X optimum, was associated with iron and the least effect was associated with Conner. The depressing ef­ fects of the remaining elements may be arranged in the fol­ lowing order: potassium, boron, zinc, calcium, phosphorus, magnesium, manganese, nitrogen, and copper. Term in al G r o w t h : Terminal growth was affected differ­ ently by the various concentrations of the n u t r i e nt -e le ­ ments studied (Table 11+ and Figures I4. to 8 , inclusive). Fhosphorus p ro du c e d less terminal growth than the other nutrient- el em en t s w h e n the various nutrient-elements were omitted. The other nutrient-elements pr od uc ed ter­ minal growth w h e n omitted in the f o l l ow in g increasing order: nitrogen, potassium, cium, boron, iron, copper, magnesium, zinc, and manganese. cal­ W h e n the concentration of each n u t r i e n t- el em en t was reduced to 1/2X optimum, the greatest reduction in terminal growth was associated w it h manganese, nitrogen, and calcium. The re ma in in g nutrient- elements h a d the f o l l ow in g order of d e c r e as in g effects: phosphorus, boron, and magnesium. calcium, iron, copper, potassium, zinc, Table 14. Relative Effect of Various Concentrations of Several NutrientElements unon Terminal Growth Nutrient-element Nitrogen Omitted Terminal Rank growth cm 2 68.3 1/2X optimum Terminal Bank growth cm 2 79.6 2X optimum Terminal growth Rank cm 2 92.8 4X ontimum Terminal growth Rank cm 124,1 9 61.5 1 86.6 4 95.1 3 98.6 3 Potassium 61.3 3 110.8 8 lie.5 7 114.0 7 Calcium 97.1 7 81.6 3 113.8 6 111.6 6 Magnesium 88.3 6 123.0 10 141.3 9 116.3 6 Manganese 129.7 10 73.1 1 111.3 4 100.1 4 Eoron 102.1 8 96.0 5 150.0 10 108.6 5 Iron 63.3 4 101.0 6 91.0 1 97.0 2 Cooper 87.3 5 101.3 7 112.5 5 11*6.6 10 121.3 9 132.5 9 117.0 8 84-3 1 accomnany Page Zinc To Phosphorus 17 Terminal growth at ootimum--179.7 centimeters Figure lj.. Growth in Relation to Varying Concentrations of Nitrogen (above) and Fhosphorus (below). (Center--Ootimum; Increasing Concentration from Left to Right). Figure To accompany Page 17 Figure 5 Growth in Relation to Varying Concentrations of Potassium (above) and Calcium (below). (Center — Optimum; Increasing Concentration from Left to Right). To aecomoany Page 17 Figure 6 Growth in Relation to Varying Concentrations of Magnesium (above) and Manganese (below). (Center — Optimum: Increasing Concentration from Left to Right). Figure To accompany Page 17 Figure 7 Growth in Relation to Varying Concentrations of Boron (above) and Iron (below). (Center — Optimum; Increasing Concentration from Left to Bight). To accompany Page 17 W Figure \ .f+.u: r Figure P Growth In Relation to Varying Concentration of 7inc (above) and Conner (below). (Center — Ontiinuin; Increasing Concentration from Left to Fdght). To accomoany Page 17 18 Increasing the concentration of Iron to 2X ontimum resulted In less terminal growth than produced for she other nutrient-elements. Other nutrlent-elements produced terminal growth in the increasing following order: nhosnhorus, manganese, magnesium, copper, calcium, potassium, nitrogen, zinc, and boron. ’.-/hen bhe concentration of the nutrient-elements was increased to 2|X optimum, growth. zinc produced the least terminal The other nutrlent-elements produced terminal growth in the following Increasing order: Iron, phosphorus, m a n ­ ganese, boron, calcium, potassium, magnesium, nitrogen, and Conner. Root G r o w t h : Although root growth (Table I?) was not affected significantly by the various concentrations of the different nutrient-elements, there were some differences shat should be noted. As the optimum concentration of each element was re­ duced to 1/2X optimum, sulted f r om conper. the least amount of root growth re­ The other nutrlent-elements produced progressively increased root growth in the following order: manganese, zinc, potassium, sium, calcium, and nitrogen. iron, boron, phosphorus, m a gne­ The amount of root growth pro­ duced with magnesium, manganese, boron, iron, copper, and zinc at 1/2X optimism was less than when these nutrientelements were omitted from the nutrient solution. Table l£. Nutrient-element Relative Effect of Various Concentrations of Several NutrientElements uoon hoot Growth Omitted Root growth Rank m 1/2X optimum Root growth Hank gm 2E optimum Root growth Rank gm 4X ootimum Root Rank growth m 44-7 5 $2 .1 10 42.1 2 36.1 1 Fhosohorus 39.2 2 48-7 7 46.6 5 44.3 6 Potassium 38.9 1 44.7 b 50.4 6 44.7 7 Calcium Ui-U 3 49.2 9 43.1 3 44.8 e Magnesium 49.5 e 48.9 6 58.3 10 56.6 9 To Manganese 55.0 9 42.6 2 49.6 7 59.4 10 Boron 63.6 10 47.7 6 50.5 9 42.4 4 Iron 49.1 7 47.0 5 39.8 1 40.3 2 accompany Copoer 44*3 4 38.1 1 49-2 6 44*5 5 Zinc 45.2 6 43.1 3 45.2 4 42.3 3 Page Nitrogen 18 Root growth at optimum— 60.7 grams As the nutrient-elements were increased to the 2X optimum concentration, iron produced the least root growth. The other nutrient-elements produced root growth in the fol­ lowing increasing order: nitrogen, calcium, zinc, phosphor­ us, corner, manganese, potassium, boron, and magnesium. At IpC optimum level all nutrient-elements decreased root growth in relation to optimum. The nutrient-elements produced root growth in the following ascending order: gen, iron, zinc, boron, corner, phosphorus, potassium, cium, magnesium, and manganese. nitro­ cal­ Increasing the concentra­ tion to IpC optimum, as compared to the rate of 2X optimum, resulted in a reduction of root growth for the following n u t r i e n t- el em en ts : nitrogen, phosphorus, potassium, m a gn e­ sium, boron, copper, and zinc. A slight increase in root growth followed the use of calcium and iron, and there was a marked increase for manganese. Trunk G r o w t h : As the elements were omitted Individual­ ly, trunk growth (Table 16) was produced In the following ascending order: nitrogen, phosphorus, magnesium. Iron, calcium, copper, potassium, manganese, zinc, and boron. W h e n the concentration of each nutrient-element was reduced to 1/2X optimum, trunk growth occurred in the following in­ creasing order: copper, calcium, potassium, manganese, iron, magnesium, boron, zinc, nitrogen, and phosphorus. W h e n the concentration of the nutrient-elements was Increased to 2X optimum, calcium produced the least trunk Table 16. Relative Effect of Various Concentrations of Several Nutrient Elements upon Trunk Growth Nutrient-element Omitted Trunk growth Rank gm 1/2X optimum Trunk growth gm Rank 2X optimum Trunk growth gm Rank [|.X optimum Trunk growth Bank gm 12.3 1 18.1 9 17.B 6 4.9 k Phosphorus 12.9 2 20.0 10 16.1 3 16.6 5 Potassium 15.5 7 16.5 6 lfi.lt 7 4-7 3 Calcium 15.0 5 15.8 2 12.8 1 13.3 2 Magnesium 4.0 3 16.3 k 19.5 8 16.3 8 Manganese 184 8 17.6 6 164 k 17.1 6 Boron 20.8 10 16.3 5 23.1 9 17.6 7 Iron 4.6 k 16.3 3 154 2 13.0 1 Copper 154 6 15.1 l 16.1 3 20.7 10 Fage Zinc 204 9 17.7 8 16.6 5 19.3 9 19 accompany Trunk growth at optimum— 20.7 grams To Nitrogen 20 growth. The other nutrlent-elements produced trunk growth In the following increasing order: manganese, iron, p h o s p h o r u s , copper, zinc, nitrogen, Potassium, magnesium, and boron. As the concentration of the nutrient-elements was In­ creased to IpC optimum, Iron produced less trunk growth than the other nutrient-elements. Trunk growth increased progres­ sively for the other nutrient-elements as follows: potassium, calcium, nitrogen, phosphorus, manganese, boron, m agne­ sium, zinc, and copper. Leaf G r o w t h : For treatments in which the nutrient- elements were omitted Individually, nitrogen resulted In the least pr od uc ti on of leaves, while phosphorus and potassium ranked next (Table 17)• The remaining elements produced in­ creasing amounts of leaf growth as follows: magnesium, calcium, copper, zinc, boron, and manganese. nitrogen, phosphorus, potassium, iron, c o m e r , iron, Omitting and zinc p r o­ duced less leaf growth than w he n used at 1/2X optimum, while calcium, magnesium, manganese, and boron increased leaf growth. W h e n the optimum concentration was reduced to 1/2X optimum, manganese produced the least leaf growth, while zinc showed the greatest amount* The other elements produced increasing amounts of leaves as follows: potassium, ma gne­ sium, calcium, copper, phosphorus, nitrogen, boron, and iron. As the concentrations were increased to 2X optimum, iron pr od uc ed less leaf growth than the other nutrient- Table 17* Relative Effect of Various Concentrations of Several NutrientElements upon Leaf Production Nutrient-element Omitted leaf growth Rank gm 1/2X optimum Leaf growth Rank gm 2X optimum leaf growth Bank gm L.X optimum Leaf growth Rank gm 1 15.6 7 19*8 9 134 2 Phosphorus 11.0 3 15*2 6 16.9 6 16.8 7 Potassium 10.6 2 4 .2 2 17*9 8 4*2 Calcium 19*2 7 k 4.8 2 4.6 9 Magnesium 19*1 6 3 22.7 10 16.9 6 Manganese ie.6 10 1 19*1 h 174 8 Eoron i e .9 6 19.0 9 134 2 Iron 4 .0 9 5 8 4*2 1 12.2 1 Copper 12.8 k 44 4-3 13*7 16.0 16.0 4*9 9 4*9 3 18.2 9 Page Zinc 17*6 e 19*6 9 17.0 7 13.6 3 20 accomoany Leaf growth at optimum— 21.6 To 94 Nitrogen 21 elements, while calcium ranked next In leaf production. The other nutrient-elements resulted in increased leaf pro­ duction in the following order: gen, nhosphorus, Conner, manganese, nitro­ zinc, potassium, boron, and magnesium* \nhen the concentration was Increased to optimum, iron had the same magnitude of effect as when the concentration was increased to 2X ontimum. Nitrogen and boron produced the next lowest amount of leaf growth, while the other elements h a d the f ol lowing increasing order in regard to their leaf production: zinc, potassium, phorus, manganese, calcium, magnesium, p hos­ and copper. Leaf Composition and Nutrlent-Element Halance The analysis of the leaves from those trees making maximum growth was considered to represent ootimum leaf composition and nutrient-element balance. Any deviation of a nutrient-element from the optimum concentration resulted in considerable variation In leaf analysis and a corresponding variation In the nutrientelement balance. Some nutrlent-elements showed a definite relationship between nutrient solution concentration and leaf analysis. Cther nutrient-elements, however, exhibited no definite relationship between nutrient solution concen­ tration and leaf analysis. Also, certain nutrient-elements h a d an influence on nutrient-element balance and interrela­ tionships proportional to concentration. 22 ft^itrogen; The influence of varying the concentration of n i t ro ge n in the nutrient solution is shown in Table 15 and figure 9. Phosphorus and. iron, as well as nitrogen, creased while calcium, magnesium, de ­ and boron increased in the leaves when the n i t r og en content of the nutrient solution was r educed below optimum. Potassium decreased w h e n the nitrogen co nc e n t r a t i o n was 1/2X optimum, nitrogen was omitted. but increased when U s i n g a 1/2X optimum concentration of nitr og en in the nutrient solution resulted in an increase in the analysis of cooper and manganese, creased but Conner d e ­ to the ontimum level w he n nitrogen was omitted, while m a n g a ne se decreased below ontimum. Phosnhorus, potassium, magnesium, iron, and manganese decreased, w h i le boron, and cooper, as well as nitrogen, i ncreased w h e n the n i t r o g e n co nc entration of the nutrientsol ut i on was increased above ontimum. C a l c iu m increased as the n i t r o g e n co nc en tr a ti on was increased to 2X optimum, but decreased w h e n the n itrogen c on ce nt r at io n was IjJt optimum. D e c r e a s i n g the n i tr o g e n concent ra ti on in the nutrient s olution resulted in greater total deviations from optimum balance than increasing nitrogen. There was a general trend f o r the p ositive deviations from optimum balance to decrease w i t h o u t m u c h change in the negative deviations as the n i t r o g e n concen tr at io n was increased. A lj.X optimum c on c e n t r a t i o n of nit ro ge n r e sulted in the negative devia- Table IB. Leaf Composition and Nutrient-Element falance as Influenced by Varying Concentrations of Nitrogen in the Nutrient Solution Nitrogen concentration Omitted 84 100 1.00 81 87 1.73 138 0.93 150 62 0.008 61 100 100 100 100 100 0.011 84 0.0008 0.012 0.016 160 300 123 8l 62 138 91 61 100 0.013 100 100 0.0008 0,007 160 17$ 0.012 92 Chart index 137 So 96 76 120 17S Deviation of chart index from optimum balance Positive Negative Difference Total 259 371 0 189 132 146 87 0 113 199 + 113 ♦ 284 0 + 76 - 67 405 458 0 302 331 76 22 Omitted 1/2 ontimum Ontimum 2X ontimum 4X optimum 72 Page Concentration 31 accompany i Dry weight lj.47 0.05 0.88 0.63 0.60 0.010 0.0006 0.007 0.010 lo 4 Dry weight 3.80 0.13 0.76 1.73 0.57 0.006 Chart Index 116 4X ontimum 120 0.78 0.006 0.0005 0.011 100 61 125 27$ Mn i Dry weight 3.26 0.16 1.22 1.25 0.62 0.013 0.0005 0.004 Chart index 2X ontimum 47 E 1.74 139 i Dry weight 2*76 0.14 Chart index Ontimum Ca K i Dry weight 1.54 0.10 1.47 Chart index 1/2 ontimum F H Leaf Composition Pe Cu Mg igure 9* Nutrient-lilement Faience in delation to Varying the Concentration of nitrogen in the Nutrient Solution. Upper left - omitted, un per right - 1/2X optimum, center - optimum, lower left 2X optimum, lower right - i+X optimum. The various bands on each chart (from the edge toward center) represent excess, a p p r o a c h ­ ing excess, optimum, h i d d e n deficiency and deficiency. To accompany Page 22 i o 23 tlons exce ed in g the positive deviations from optimum balance* Apparently, wh e n the n itrogen co nc entration was 1/2 opt im um the n u tr ie n t- el em en t c om po sition d eviated more f r om o n t im u m balance than w h e n nit r og en was omitted* wit h the 1/2 ontimum nitrogen concentration, Also, the nositive deviations exceed the negative deviations f rom ontimum balance m u c h more t h a n w he n n i t r o g e n was omitted from the nutrient solution* Phosphorus: tion of phosphorus cooper, boron, potassium, The influence of v a r y i n g the concentra­ is shown in Table 19, Figure 10* Iron, and m a g n e s i u m increased in the leaves, while calcium, manganese decreased w he n the phos­ phorus content of the nutrient sol ut io n was reduced below optimum* Phosphorus reduced in leaf compos it io n along with a simultaneous re du c ti on in nitrogen. By om itting p h o s ­ phorus f ro m the n utrient solution, n itrogen Increased to ontimum level, and phosphorus decreased to a v er y low level, but corner encroached the ontimum level, while iron, m a n ­ ganese, cotassium, magnesium, and calcium were decreased below ontimum. Iron a n d p o t a s s i u m decreased while phosphorus, copper, boron, calcium, and m a g n e s i u m increased w h e n the phosphorus concentrations of the nutri e nt -s ol ut io n were increased above optimum* ontimum level* N i t r o g e n a n d man ga ne se remained at the Table 19. Leaf Composition and Nutrient-Bilement H-alance as Influenced by Varying Concentrations of Fhosnhorus in the Nutrient Solution Phosphorus concentration N P K Ca Leaf Composition Cu Fe Kg B Mn 3*35 102 0.06 37 0.92 75 1.11 88 0.1+9 79 0.008 61 0.0006 120 0.007 175 0.008 61 l/2 optimum ^Dry weight Chart index 2.89 88 0.09 % 1.06 86 0.95 76 0.73 117 0.016 123 0.0008 160 0.008 200 0.008 61 Optimum ^Dry weight Chart index 3.26 100 0.16 100 1.22 100 1.25 100 0.62 100 0.013 100 0.000< 100 0.001+ 100 0.013 100 2X ontimum ^Dry weight Chart index 346 106 0.19 1.39 111 0.76 122 0.010 76 0.0009 lie 0.9U 77 180 0.008 200 0.013 100 $Dry weight Chart index 3.61 110 0.22 137 1.07 87 1.87 0.61+ 135 0.011 ft} 0.0007 li+0 0.008 200 0.018 138 I4 .X optimum 97 200 0 237 309 199 133 0 1+7 29 - 102 + 67 0 + 190 + 280 296 333 0 28k 338 23 Omitted 1/2 optimum Ontimum 2X ontimum 1+X ontimum Deviation of Chart Index from Ontimum Balance Positive Negative Difference Total Page Concentration 11+9 accompany ^Dry weight Chart index To Omitted gnjre 10. wutrient-Fle^ent Balance in Relation to Varying the Concentration of Fhosnhorua in the Nutrient Solution. IJnner left - omitted, u n n e r righ t - 1/2X ontimum, c e n t e r - ontimum, l o we r left 2 X ontimum, lower r i g h t ’ - i|X ontimum. The v a r i ou s hands on each chart (from the edcre toward center) r e p r es en ts excess, a p p r o a c h i n g excess, ontimum, h i d d e n de fi ci en c y, and d eficiency. To ac co mp a ny Page 23 2i+ W h e n the phosphorus concen tr at i on was increased to i*X ontimum, phosphorus, Conner, boron, calcium, manganese, and m a g n e s i u m increased, while iron and ootassium decreased. There was a slight increase in nitrogen. D e c r e a s i n g the rhosrhorus c o nc entration in the nutrient solution resulted in deviations from ontimum which are c o m­ parable to the increase of nhosnhorus above the ontimum level. ontimum, As the nhosnhorus concentration was increased to IpC the n u t r i e nt - el em en t balance deviated more from ontirrum than w h e n nhosnhorus was omitted. tive deviations However, p o s i ­ exceeded negative deviations exceot when nhosnhorus was omitted. Potasslum: The influence of varying the concentration of o o t a s s i u m in the nutrient solution is shown in Table 20, figure 1 1 . Fhosphorus and iron, as well as potassium, de­ creased and bo ron and Conner increased w h e n the potassium c o nc e nt ra ti on of the nutrient solution was reduced to 1/2X ontimum. Nitrogen, manganese, a nd calcium remained at the ontimum level, while there was a n Increase in magnesium. As compared to the 1/2X onti mu m concentration, potassium, and phosph or us continued to decrease, manganese decreased, while Conn e r incr ea se d wh e n p o t a s s i u m was omitted from the nutrient solution. Eoron and m a g n e s i u m increased, while iron and ohosnhorus d e creased w he n the p o t a s s i u m concentration of the nutrient sol ut io n was increased above optimum. Nitrogen, calcium, an d m an ganese remained near the optimum level. Table 20. Leaf Composition and Nutrient-element balance as Influenced by Varying Concentrations of Potassium In the Nutrient Solution Potassium concentration F K Omitted itDry 3.29 0.08 0.71 50 100 58 1/2 optimum € Dry 3.53 0.13 0.84 81 68 weight Chart index weight Chart index 108 Ca Leaf Composition ?e Cu Mg t :i. * Mn 0.009 225 0.007 53 1.25 0.84 0.009 100 69 135 0.0006 0.008 120 200 0.013 100 1.14 91 0.76 122 0.010 76 0.0007 140 3.26 100 0.16 100 1.22 100 1.25 0.62 100 100 0.0005 100 0.004 100 0.013 100 2X optimum cl Dry 3.38 0.14 87 103 0.97 79 1.20 0.97 0.008 0.0007 96 156 61 140 0.006 150 0.012 92 4X optimum ^ Dry weight Chart Index 3.80 116 1.69 138 0.98 78 0.006 0.014 150 107 weight Chart index weight Chart index 0.009 69 0.0004 80 Deviation of Chart Index from Optimum Balance Positive Negative Difference ffotal 187 163 0 149 135 172 82 0 85 92 + 10 + 8l 0 + 64 + 43 359 2.1+5 0 234 227 2l+ Omitted 1/2 optimum Optimum 2X optimum 4X optimum 0.77 124 Fag© Concentration 0.13 81 0.013 100 accompany t Dry To Optimum igure 11. Nutrient-element Ealance in helation to Varying- the Concentration of Potassium in the Nutrient Solution. U p per left - omitted, u p pe r right - 1/2X optimum, center - optimum, lower left 2X optimum, lower rig ht - IpC optimum. The various bands on each chart (from the edge toward center) represent excess, a p p r o a c h i n g excess, optimum, h i d d e n d e f i c i e n c y and deficiency. To accompany Page 22j. Figure 11 Fotassium Increased when the concentration was J[X ontimum, but showed a decrease at 2X optimum. Cooper in­ creased when the potassium concentration was 2X optimum, but decreased when the concentration was i+X optimum. M a g ne ­ sium was lower wh e n the potassium concentration was ipC opti­ mum than w hen the concentration was 2X optimum. Decreasing the potassium concentration in the nutrient solution resulted In greater total deviations from ontimum balance than Increasing potassium. Fositive deviations from the ontimum balance were nrevalent for all levels of ootas­ sium. Greater total deviations from the optimum balance were observed with 0 ontimum concentration. Nutrient ele­ ment comoosition deviated less from ontimum when the p otas­ sium concentration was 1/2X optimum than w hen ootassium was omitted. Calcium: The Influence of varying the concentration of calcium in the nutrient-solutlon is shown In Table 21, Figure 12. Copper and boron increased, and all other nutrient- elements decreased except nitrogen and magnesium when the calcium content of the nutrient solution was reduced below ontimum. Nitrogen, phosphorus, potassium, and iron were higher when calcium was omitted than when the calcium con­ centration was 1/2X optimum. However, cooper was lower when calcium was omitted than when at 1/2X optimum. Omitting calcium from the nutrient solution caused the calcium to con­ tinue to decrease. M Table 21. Leaf Composition and Nutrient-? lement Balance as Influenced by Varying Concentrations of Calcium in the Nutrient Solution Calcium concentration Omitted N t Dry weight 3.36 Chart index 103 3.12 1/2 optimum % Dry weight Chart index 95 Leaf Composition Cu Fe n B Mn 0.62 0.60 96 1*9 0.011 0* 0.0006 120 0.006 150 0.009 70 0.11 1.04 0.83 0.59 68 66 85 95 0.009 70 0.0007 1U0 0.010 250 0.009 70 0.62 100 0.013 100 F t 0.12 1.13 92 75 Ca 0.16 1.22 100 100 1.25 100 0.0005 100 0.001* 0.013 100 100 2X optimum t Dry weight 0.15 0.95 93 77 1.25 0.51* 0.010 0.0005 100 100 76 87 0.009 0.010 76 225 l^X optimum % Dry weight 0.17 0.92 106 75 1.78 0.66 11*2 106 0.008 200 3.76 Chart index 115 3.23 Chart index 99 Concentration 0.0006 120 Deviation of Chart Index from Ontimum Balance Positive Negative Difference Total 13U l5l 0 91 65 - 61 + 39 0 + 1*9 +109 207 31*1 0 231 239 25 73 190 0 II4.O 17l* 0.012 92 Fage Omitted 1/2 optimum Ontimum 2X optimum i*X ontimum 0.009 69 accorrroany 3.26 ^ Dry weight Chart index 100 ‘To Optimum Figure 12. Nutrient-Element Balance in Relation to Varying: the Concentration of Calcium in the Vutriont Solution. TJ-oper left - omitted, unoer right - 1/2X optimum, center - optimum, lower left 2X optimum, lower right - hX optimum. The various bands o n e ach chart (from the edge toward center) rep re se nt excess, aTDoroaching excess, optimum, h i d d e n de ­ fic ie n cy and deficiency* To accomnany Page 2 5 26 Fotassium, iron, and manganese decreased and boron in­ creased when the calcium concentration was increased, while nitrogen, nhosnhorus, magnesium, and Conner remained near the ontimum level. Calcium increased in the leaves as the concentration was increased i|X ontimum. and c o m e r Fhosnhorus, maenesium, manganese, increased, while nitrogen, iron and boron de­ creased in the leaves when the IjJC concentration is comrared to the 2X concentration of calcium. D ec reasing the calcium concentration in the nutrient solution nroduced greater total deviations from optimum balance than increasing calcium. There was a general trend Tor the positive deviations from optimum balance to increase and the negative deviations concentration was increased. to decrease as the calcium Negative deviations from ooti- mum balance exceeded the positive deviations only when calcium was omitted. Magnesium: The influence of varying the concentration of magnesium in the nutrient solution is shown in Table 22, Figure 13. Fhosnhorus, ootassium, as well as magnesium decreased, calcium, iron, manganese, corner increased, and nitrogen remained near the ontimum level as the magnesium content of the nutrient solution was reduced below optimum. Conner remained within the limits of the optimum level at Table 22. Leaf Composition and Nutrient-Klement Palance as Influenced by Varying Concentrations of Magnesium in the Nutrient Solution Magnesium concentration Omitted i Dry weight Chart index IjJC optimum i Dry weight Mn 67 0.92 73 0.52 0.010 76 83 0.0008 160 0.006 150 0.008 61 3.25 0,10 62 99 1.01 62 1.22 97 0.61* 0.011 0.0005 81* 100 103 0.008 200 0.011 8i|- 3.26 0.16 100 100 1.22 1.25 0.62 0.013 100 100 100 100 O.OOii 0.013 100 100 3.21 Chart index 98 0.13 61 1.21 99 0.76 122 0.011 0.0006 120 85 0.010 250 0.010 76 3.0^ Chart index 93 o.ih 1.04 1.00 0.81 60 130 65 0.007 0.0007 u*o 53 0.007 175 0.010 76 67 1.16 9U 0.0005 100 Concentration 11^ 103 0 192 lij.5 Negative 139 92 0 67 126 Difference + 25 11 0 + 125 + 19 Total 253 195 0 259 271 26 Omitted 1/2 optimum Optimum 2X optimum hX optimum Positive Page Deviation of Chart Index from Optimum Ealance accompany i Dry weight E To 2X optimum o.lk K Leaf Composition Pe Cu Mg 1.00 81 ^ Dry weight 3.1|2 104 Chart index 1/2 optimum i Dry weight Chart index Optimum $ N 6a Pi g-ure 13* Nutrlent-elerent Balance In Relation to Varyinp the Concentration of Magnesium in the Nutrient Solution. TJorer left - omitted, u o o e r r^dit - 1/2X ootimum, cen te r - ootimum, lower left 2X optimum, lower right - lj_X ontimum. The various bands on each chart (from the edge toward center) represent excess, a n n r o a c h i n g excess, optimum, h i d d e n defici e nc y and deficiency. To accoTrmany Fage 26 Figure 13 27 l/2X optimum, but increased w hen magnesium was omitted. Also boron tended to decrease slightly when none of the element was added as compared to 1/2X optimum. Phosphorus, iron, and manganese were reduced when a con­ centration of 2X optimum level was used. crease of Conner, boron, However, an in­ and m agnesium was noted, although nitrogen, Potassium, and calcium remained near the optimum level. U s i n g m ag nesium concentrations [|.X ootimum, magnesium continued to increase, while there was only a slight reduc­ tion in calcium. Potassium, manganese, iron, and p h o s ­ phorus were likewise reduced, while cooper and boron in­ creased when the ma gnesium concentration of the nutrient solution was increased to the I4.X optimum level. Dec reasing the ma gnesium concentration of the nutrientsolution resulted in less total deviations from optimum balance than increasing magnesium. The greatest total deviations from optimum balance was obtained with the ma gnesium concentration of the nutrientsolution at UX optimum. Total deviations from optimum bal­ ance w h en calcium was omitted were essentially the same as at the i+X optimum concentration. Negative deviations from optimum balance exceeded the positive deviations only when mag nesium was omitted from the nutrient-solution. Manganese: The influence of varying the manganese concentration in the nutrient-solution is shown in Table 23# 26 and Figure lLf. Fhosphoras, potassium, iron, and manganese decreased w hen the manganese concentration was below opti­ mum, while copter, and boron increased. However, nitrogen remained near the optimum level when the manganese con­ tent of the nutrient solution was reduced below optimum. Fhosohorus, calcium, and manganese were higher when mang an ­ ese was omitted than when manganese was 1/2X optimum, but potassium, magnesium, iron, Conner, and boron were lower when manganese was omitted than when used at 1/2X ontimum concentration. Using manganese concentrations 2X optimum, phosnhorus, potassium, iron, calcium, and manganese decreased, while boron, and magnesium increased. Nitrogen and conper continued to remain near the optimum level. Fith amplications of manganese at the ipC optimum level, iron was the only element that was decreased significantly. Uanganese, copper, and boron continued to increase in the leaves at this very high level. Nitrogen, phosphorus, potas sium, calcium, and magnesium were near the optimum level w hen the manganese concentration was IpL optimum. D ec reasing the manganese concentration in the nutrientsolution resulted in less total deviations from optimum balance than increasing manganese to the I4JC optimum concen­ tration which resulted in the greatest positive and total deviations from the optimum. Negative deviations fr o m optimum balance exceeded positive deviations w h e n manganese was omitted from the Table 23. Leaf Composition and Vutrient-Element Falance as Influenced by Varying Concentrations of Manganese in the Mutrient Solution Manganese concentration Omitted N Dry weight 3.50 Chart index 107 it 0.1J+ 0.98 80 67 Leaf Composition Mg Fe <5"a Cu p Mn 1.28 0.1*8 0.007 0.0006 120 102 77 53 0.006 150 0.010 76 0.009 69 i Dry weight 1.01 62 1.13 90 0.72 116 0.010 76 0.0007 0.008 11*0 200 Optimum i> Dry weight 1.22 100 1.2? 0.62 100 100 0.013 100 0.000? 100 0.001* 0.013 10c 100 2X optimum fo Dry weight 3.29 0.0? 100 Chart index 31 1.00 1.12 0.83 81 89 133 0.010 76 0.0005 100 0.005 125 0.011 85 1*X optimum 3.22 0.1? v? Dry weight Chart index 98 93 1.11* 1.32 0.72 10? 116 93 0.010 76 0.0007 0.009 11*0 22? 0.02? 192 3.1*8 0.08 Chart index 106 50 3.26 0.16 Chart index 100 100 79 127 - 1*8 206 162 133 + 39 29? 0 ?8 276 0 136 1*0 0 - 60 + 236 0 196 318 28 Omitted 1/2 ootimum Optimum 2X ontimum i*X ontlmum Page Concentration Deviation of Chart Index from Optimum Balance Positive Negative Difference Total accompany 1/2 optimum Figure lij . Mutrient-tler-ent balance in Relation to Varying the Concentration of Fanganese in the Nutrient Solution. inner left - omitted, uoper right - 1/ 2X orttimum, center - ootimum, lower left 2-X ontimum, lower right - Ij-X ootimum. The various bands on each chart (from the edge toward center) represent excess, aorjroechinp excess, ootimum, h id d e n deficiency and deficiency. To aeconroany P a g e 2 8 Figure H4. 29 nutrient so lution and where applied at the rate of 2X optimum concentration. Positive deviations from optimum balance were very nronounced, and the negative deviations were v ery low for the ipC optimum concentration. Boron: The influence of var yi ng the concentration of boron in the nut ri en t solution is shown in fable 21}, Figure 15>. Phosphorus, iron, potassium, and manganese d e ­ creased while copper and boron increased when the boron c o n ­ tent of the nutrient solution was reduced below ontimum.Nitrogen, however, remained near the optimum level. The in­ crease in corner at 1/2X optimum was decreased w h en boron was omitted from the nutrient solution. W h e n boron was o mi t ­ ted, there was an increase of calcium, manganese, and m a g n e ­ sium as compared to us ing boron at 1/2X optimum. Iron, phosphorus, copper, potassium, calcium, m a n g a n ­ ese and m a g n e s i u m decreased while boron increased when the b oron c on ce nt ra ti on of the nutrient solution was increased above optimum. Nitrogen was decreased slightly, but remained near the optimum level. cium, manganese, Iron, phosphorus, potassium, c a l­ and m a g n e s i u m decreased more at the ijJC optimum than at the 2X optimum concentration of boron. the b o r on co nc entration was increased IpC optimum, W hen boron r e ­ mai ne d at a v e ry h i g h level, and copper increased as the b o r o n concentration increased. Nitrogen decreased slight­ ly, but remained w i t h i n the optimum range. D e c r e a s i n g the b o r o n concentration in the nutrientsolution resulted in less total deviations from optimum Table 21*. Leaf Composition and Nutrient-Element pelance as Influenced by Varying Concentrations of Poron in the Nutrient Solution Boron concentration Omitted % Dry weight 3.03 Chart Index 92 1/2 optimum i Dry weight Chart index Optimum P K i Dry weight Chart index V Ca Leaf Composition Fe Cu M? P T*n 0.12 1.11 90 75 1.67 133 0.66 106 0.010 76 0.0006 120 0.007 175 0.011 85 0.1*5 0.009 72 69 0.0009 160 0.007 175 0.006 1*6 1.07 87 1.09 87 3.26 100 0.16 100 1.22 100 1.25 0.62 ICO 100 0.013 100 0.0005 0.001* 0.013 100 100 100 0.009 69 0.0001* 0.015 80 375 2X optimum % Dry weight 1 .1U 91 i*.X optimum i Dry weight 0.85 0 . 1*1 0.006 68 66 3.10 0.09 0.90 Chart index 56 95 73 3.00 0.06 O.78 Chart index 92 63 37 0.50 80 0,0007 0.019 0.001* 11*0 30 1*75 13b 155 0 275 1*15 Negative ^2 173 0 210 298 Total 52 18 0 216 29 Omitted 1/2 optimum Optimum 2X optimum 1|lX optimum Positive Page Deviation of Chart Index from Optimum Ealance Concentration 0.006 1*6 accompany 0.11 68 To 3.22 98 + 65 + 117 1*85 Difference + - 328 0 713 Figure lN. Nutrient-ile^ent Ealance in elation to Varying the Concentration of Eoron in the Nutrient Solution. TTnper left - omitted, unner right - l/2X optimum, center - optimum, lower left 2X ontimum, lower right - J4X optimum. The various bands on each chart (from the edge toward center) represent excess, anproaching excess, optimum, hi dd e n deficiency and deficiency. To accompany Fage 29 Flgur© i9 30 balance than Increasing boron. exceeded optimum, there appears to be a general Increase in positive, negative, t imum balance. W h e n the concentrations and total deviations f rom the op­ Positive, negative, and total deviations f rom ooti mu m balance decreased as the boron concentration was reduced. Negative deviations only exceeded oositlve deviations from opti m um balance w he n the boron concentra­ tion was l/2X optimum. Iron: The influence of v a r y in g the concentration of iron in the nutrient so lution is shown in Table 25?, Figure 16. I ron and p o t a s s i u m decreased while o h o s p h o r u s , copper, and b o r o n increased in the leaves w h e n the iron content of the nutrient so lution was red uc e d below optimum. and c a l ci um r e mained near the optimum level. Nitrogen W h e n iron was omitted m a g n e s i u m and manganese decreased sharply, but iron Increased slightly as compared to 1/2X optimum. As iron was increased to the 2X optimum level, iron, calcium, and p o t a s s i u m were the only elements that d e ­ creased. Phosphorus, copper, boron, a n d magnesium increased while nitrogen, and m a nganese remained near the optimum level. Iron, potassium, a n d phosphorus were at v e r y low levels, while there was an increase in conper, boron, calcium, and m a g n e s i u m w h e n the iron concent ra ti on was increased to ipC optimum. N itrogen and manganese r emained near the optimum Table 25* Leaf Composition and Nutrient-Element Balance as Influenced by Varying Concentrations of Iron In the Nutrient Solution Iron Leaf Composition E % Dry weight Chart index 307 103 0.10 62 1.03 1/2 optimum % Dry weigjit Chart index 3.33 102 0.20 125 t Dry weight Chart index 3.26 100 2X optimum 1*X optimum Optimum Fe Mn 0.50 0.85 69 1.22 97 0.68 109 0.16 100 1.22 100 1.25 100 0.62 0.013 100 100 100 100 % Dry weight 3.61 Chart index 110 0.20 125 0.86 70 1.15 92 0.80 129 0.009 69 0.0007 0.009 Uj.0 225 0.013 100 $ Dry weight Chart index 0.13 81 0.73 59 1.61 128 0.72 116 0.008 61 0.0006 120 0.009 69 0.008 200 0.004 0.013 0.009 225 Deviation of Chart Index from Optimum Balance Positive Negative Difference Total 1*13 219 0 229 196 131 80 0 69 130 + 282 + 139 0 + 160 + 66 0.016 123 510* 299 0 298 326 30 Omitted 1/2 optimum Optimum 2X optimum i*X optimum 0.007 0.0008 160 51* 0.018 0.009 i*5o 70 Fage Concentration 3.50 10? 0.0008 160 B 1.22 81* 97 80 0.010 76 Cu o • o » • o oo OVA Omitted Mg accompany f> To If concentration Ca. Figure 16. Nutrient-Element Balance in Relation to Varying the Concentration of Iron in the Nutrient Solution. Throe r left - omitted, urmer right 1/2X ootimum, center - ootimum, lower left - 2X ootimum, lower right - Lpt ootimum. The various bands on each chart (from the edge toward center) represent excess, approaching excess, optimum, h i d d e n deficiency and deficiency. To a c c o m p a n y Page 30 F ig u r e 16 31 O m i t t i n g ir o n f r o m the n u t r i e n t - s o l u t i o n resu lt ed in g reater total d e v i a t i o n s fr o m o p t im um balance than increas­ ing iron. Total de vi ations f r o m opt im um balance were h i g he r T o r the ij.X t ha n the 2X c o n c e n t r a t i o n of iron. Negative d e v i at io ns f r o m o o t i m u m did not e x c ee d the po sitive d e ­ viations at any c oncentration. creased w i t h each c on ce nt ra ti on . Negative deviations in­ increment of increased or d e c r e a s e d iron Pos it iv e de vi at io n s from optimum increased at the l o w es t concentration, w h i le the positive deviations were lox^er f or the 1+X o p t i m u m than for the 2X optimum con­ centre tion. Zinc: The influence of v a r y i n g the c on c e n t r a t i o n of zinc in the n u t r i e n t - s o l u t i o n is s h o w n in Table 26, Figure 17. Conner, p o t a s si um , nitrogen, iron, and m a g n e s i u m were reduced, and calcium, a n d m a n g a n e s e rem ai ne d near the o p t i mu m level w h e n zinc c o n c e n t r a t i o n s of the n u t r i e n t - s o l u ­ tion w e re r e d u c e d to 1/2X optimum* ‘ T here was an increase for ph o s p h o r u s an d boron. Iron, pho sp ho ru s, potassium, copper, a nd man ga ne se were r e d u ce d and m a g n e s i u m i nc reased as zinc was omitted f r o m the nutrient-solution. Boron, calcium, and m a g n e s i u m w e re above the o p t i m u m l evel w h e n zinc was omitted. I n c r e a s i n g zinc to the 2X o p t i m u m c o n c e n t r a t i o n r e ­ sulted I n nitrogen, Iron, ph os phorus, copper, manganese, and m a g n e s i u m r e m a i n i n g n e a r the o p t i m um level, w h i l e p o t a s s i u m was decreased* Eo ron and c a l c i u m w er e Increased* Table 26. Leaf Composition and Nutrient-Element Ealance as Influenced by Varying Concentrations of Zinc in the Nutrient Solution Zinc concentration N f> K Leaf Composition Ca Pe Cu ms 0.81 130 6 0.007 O.OOOlj. 0.007 0.008 81 61 175 53 Omitted ^ Dry weight Chart index 3.32 101 0.13 81 0.83 68 1.70 136 1/2 optimum ^ Dry weight Chart index 3-57 109 0.19 118 1.03 1.32 0.51 0.013 100 82 105 O.OOOif 0.008 81 200 Ootimum ^ Dry weight Chart index 3.26 0.16 1.22 100 100 100 1.25 0.62 100 100 0.013 100 0.0005 100 2X optimum ^ Dry weight Chart index 3*76 0.17 1D6 115 0.70 57 0.61 98 0.012 92 0.0005 0.009 100 225 ip( optimum i Dry weight 345 0.72 1.31 0.85 0.009 10J+ 137 59 69 0.013 0.010 76 325 Deviation of Chart Index from Optimum Ealance Positive Negative Difference Total 156 53 0 53 96 4 + 79 0 + 120 + 213 - 298 185 0 226 1+0? 31 42 132 0 173 309 0.013 100 Page Omitted 1/2 optimum Optimum 2X optimum IpC optimum O.OOij. 0.013 100 100 accompany Concentration 105 0.0006 120 0.013 100 To Chart Index 0.19 118 1.59 127 Mn Figure 17 • Nutrient-Element Ealance in Relation to Varying- the Concentration of Zinc in the Nutrient Solution. Tinner left - omitted, unper right 1/2X ontimum, center - optimum, lower left - 2X ontimum, lower right - Ipt ontimum. The various bands on each chart (from the edge toward center) represent excess, anproaching excess, ontimum, h i d d e n deficiency and deficiency. To a c c o m p a n y Page 31 Figure 17 32 Phosphorus, copper, bo ron and m a g n e s i u m were above optimum w h e n zinc was applied at the rate or I4X optimum concentration, but a decrease occurred for calcium, m a n ­ ganese, and iron w h e n compared to 2X concentration* Potas­ sium did not change appreciably when the concen tr at io n of the n utrient sol u ti on was increased f r o m 2X to ipt optimum. Inc re as in g the zinc co nc en tr at io n in the nutrients olution res ul t ed in larger total deviations from optimum balance than d e c r e as in g zinc. ’.ilhen none of the element was added, negative deviations exceeded positive deviations, but were not intense. The 1/2X optimum concentration resulted in positive deviations from optimum balance exceeding the negative deviations. As the concentration of zinc in the nutrient s olution was increased 2X and J+X optimum, positive deviations Conner; the net increased. The influence of varying the concentration of copper in the nutrient so lu ti on is shown in Table 27* Figure 18. W h e n the copper concentration was reduced to 1/2X o p­ timum, nitrogen, iron, phosphorus, manganese, as well as copper, remained near the opt im um level range, but potassium decreased. h i g h levels. Boron, calcium, and m a g n e s i u m were at relatively As coop e r was omitted f r om the nutrie nt - so lu ­ tion nitrogen, phosphorus, boron, manganese, and m a g n es i um were reduced, while calcium increased as compared to 1/2X optimum. W h e n cooper was increased to the 2X ootimum concentra­ tion, all of the nutrient-elements were about the same Table 27* Leaf Composition and Nutrient-Element Balance as Influenced by Varying Concentrations of Copper in the Nutrient Solution Leaf Composition Copper concentration N P ■ Omitted % Dry 2.93 0.11 68 89 1/2 optimum i Dry weight 3.55 weight Chart index Chart index Optimum t Dry weight Chart index K 0.87 2.02 161 71 0.16 0.87 100 71 106 3.26 0.16 100 100 Ca 1.22 1.25 0.62 100 100 100 3.63 111 0.13 81 0.79 1.67 6*1- 133 IpC optimum ^ Dry weight Chart index 3.61 116 0.13 61 0.62 67 0.013 0.0005 0.009 0.012 100 100 92 225 0.013 0.0005 100 100 0.87 0.014 lij.0 107 1.25 0.51* 0,008 100 61 87 O.OOi* 100 0.013 100 0.010 250 0.014 107 0.0008 0.00P 160 225 0.010 76 0.0009 180 Deviation of Chart Index from Optimum Balance Positive Negative Difference Total 111 37 0 55 126 + 69 + 173 0 + 273 + 73 291 2^7 0 363 329 32 180 210 0 326 201 0.006 61 Page Omitted 1/2 optimum Optimum 2X optimum 4X optimum 0.006 150 Mn accompany weight Chart index E Cu To % Dry Fe 0.60 0.013 0.0007 100 140 129 1.58 0.94 126 151 2X optimum Concentration Mg Figure IF. Nutrient-Flement Faience in Felation to Var?ring the Concentration of Conner in the Nutrient Solution. Unner left - omitted, unner right 1/2X ontimum, center - ontimum, lower left - 2X ontimum, lower right - IpC ontimum. The various bands on each chart (f rcn the edge toward center) renresent excess, anoroaching excess, optimum, h i d d e n deficiency and def ic iency . To a c c ompany Page 32 Figure 18 33 as u s i n g concentrations of 1/2X optimum, crease in copper. except for an in­ Increasing the c on centration of Conner to IpC ontimum r e s ul te d in below optimum values for iron, manganese, level. and magnesium, while calcium was near the optimum The r e m a i n i n g nutrient-elements were about the same as found for the 2X ontimum concentration, slight Increase excent for a In nitrogen. Increasing the c on centration of Conner In the nutrients o l u ti on n r o d u c e d greater total deviations from ontimum balance than by de cr e as in g corner. Positive deviations ex­ ceeded negative deviations from optimum balance in all c o n ­ centrations of copper. The greatest nositive deviations o ccurred at 2X optimum concentration. Corresrondingly, the next largest p o sitive deviations f rom optimum balance o c ­ curred at 1/2X optimum c o n c e n t r a t i o n s . Discussion Growth of Mo n t m o r e n c y cherry trees anpears to be signi­ fic an t ly affected by either shortages or excesses of all the nutrient-elements more com mo nl y used as fertilizers b e ­ fore visible symotoms of shortages or excesses appear. Nightingale (23) indicated that a r ed uction in size of otherwise normal olant a nd fruit was brought about by v a r y ­ ing the nutrient-elements. Nightingale believed that this c o n d it io n was the result of bala nc ed m ultiple deficiencies* 34 Also Shear, Crane and Meyers (25) believe that at any level of nutritional intensity, there exists a nutritional balance at wh ich optimum growth for that intensity will r e ­ sult, and that at any given level of nutritional intensity, ■provided all nutrient-elements are in proper balance, it is possible to obtain plants that appear normal in every re­ spect, and in which all metabolic processes are normal. They also state that plants m ay be grown at an apparen tl y high level of intensity of nu trition which, in the absence of more vigorous or h i g h e r yielders for comparison, m a y appear to be m a k i n g m a x i m u m growth and yield, and yet the plants m a y be capable of greater yields if a more favorable balance at a lower intensity is brought about. W h e n the amount of growth, as m easured by dry weight increase, produced by using the various concentrations of a n utri e nt -e le me nt are added together, nitrogen is found to restrict growth more pr of oundly than the other nutrientelements. Potassium, phosphorus, mentioned, restrict growth less than nitrogen. elements, and calcium, iron, copper, and manganese, in the order The minor zinc, and boron re­ strict growth less than nitrogen, phosphorus, potassium, calcium. growth. or M a g n e s i u m appears to have the least effect on This w o u ld indicate that a listing of nutrient-ele­ ments in order of their influence up o n growth resulting from variations follows: in nutrient-solution concentration would be as nitrogen, potassium, phosphorus, copper, manganese, calcium, zinc, boron, and magnesium. iron, 35 The characteristic annearances of deficiency and excess symotoms, however, would indicate that this arrange­ ment of nutrient-elements would be changed if vlsable symntoms were present. The results of this study show (Table 12) that the ef­ fectiveness of a given de viation from optimum concentration depends u o o n the nutrient-element. For example, nitrogen r estri ct ed growth at high concentrations more than any of the other nutrient-elements, while at the lowest concentra­ tions, pot as s iu m and phosphorus produced less growth than the other nutrient-elements. However, growth was not as p ro po r t i o n a t e l y reduced as at hig he r concentrations. F rom these studies no one ranking, that would a r r l y to b ot h shortages and excesses of nutrient-elements may be made in rega r d to their influence on growth when out of balance in the nutrient solution. The order of listing given above w o ul d apply to combined effects of shortages and excesses. The listing, in ascending order for growth, which would a p p l y to the combined shortages sium, phosphorus, nitrogen, sium, manganese, excesses, boron, and zinc. cooper, pot as ­ iron, m a g n e ­ In regard to combined the listing in ascending order for growth would be as follows: zinc, calcium, is as follows: nitrogen, boron, manganese, iron, phosphorus, cooper, calcium, potassium, and magnesium. This would 36 indicate that or the ten nutrient-elements studied, a shortage of p o t a s s i u m w ould more adversely affect growth than a shortage of any of the others, while an excess of nitro­ gen would more a d v e r s e l y affect growth than an excess of any of the other nutrient-elements. F o l l o w i n g T h a t c h e r ’s classification of mineral ele­ ments (2 7 )* those nutrient-elements classified as energy storers, n itrogen and phosphorus, h a d the greatest effect in red uc i ng growth. Those nutrient-elements classified as t ra nslocation regulators, potassium, calcium, and magnesium, had less effect u po n growth than the energy storing ele­ ments. The oxid at io n- re d uc tl on regulators, which are iron, manganese, growth. cesses, zinc, and copper, h a d the least effect upon These generalizations would anoly to shortages, ex­ and combined shortages and excesses. At concentrations below optimum, p h o s p h o r u s , of those nutrient-elements classified as energy storers, was more effective than nitrogen in re duction of growth, but as con­ centrations were increased above optimum, nitrogen reduced growth more than phosphorus. When the overall effect of deviations below a n d above optimum are combined, nitrogen was m ore effective than phosphorus. Of those nutrient-ele­ ments classified as translocation regulators, potassium was more effective than calcium, and calcium m or e effective than magnesium. In general, Iron was m ore effective In restricting growth than the other nutrient-elements classified as oxi­ 37 d a t i o n - r e d u c t i o n regulators. greater than manganese, greater than zinc, m u m where The effect of cooper was and the effect of manganese was except with concentrations above opti­ the order was reversed. A c c o r d i n g to Cooper (6), the influence on growth is directly related to the s t a n d a r d electrode potential. The results of the experiment indicate that for the transloca­ tion regulators, as classified by Th atcher (27)# growth had a p ositive re lationship to standard electrode potential. However, those nutrient-elements classified as oxidation- red uc t io n regulators showed a negative relationship. Since the standard electrode potential for ammonia was not avail­ able, this relationship could not be determined for those nut ri e nt -e le me nt s cl as sified as energy storers* If, however, nitrates, all the nitrogen h a d been supplied as there would be no appreciable difference between n i t r o g e n and phosphorus In r elation to growth, because their standard electrode potential Is essentially equal. The work of Brown (5) indicates that n itrogen h a d a greater effect u p o n growth than the other elements. The results of this study indicate that ni trogen h a d a greater influence upon growth than phosphorus at h i g h concentrations. There is considerable evidence that nit ro g en will a f ­ fect the a b s o r p t i o n of the other elements and indirectly Influence growth. Several factors would br ing about this v a r i a t i o n in growth. Such variations m a y depend u p o n the f or m in which the element would be oresent in the substrate w i t h i n the nlant. Also growth variations would result from cationic or anionic unbalances after the elements have been a b s o r b e d and tr anslocated to various parts of the plant. Con ti nu ed applications of nitrogen increased the nitrogen a cc u m u l a t i o n in the leaves, acco r di ng to Shear, Crane, and I’yers (26), and a functional unbalance exists between n i t r og en and some other element. If a nu tr itional unbalance excesses of an element, is created by shortages or this unbalance will affect growth as the specific relationships of these various elements are disrupted. The effects of n itrogen u po n phosphorus, p ho s­ phorus u p o n nitrogen, cal ci u m upon magnesium, po tassium uoon copper, etc. are examples. element relationships, W ith these various nutrient- the intensity and balance of the nutrients would be af fected w i t h i n the plant. A n y variation f r o m opti mu m balance would b r in g about changes that would a lter the metabolic and Physiological processes with in the plant• Leaf analysis, however, In m a n y instances failed to correlate with n u tr ie nt -s ol ut i on concentration. lysis for nitrogen, phosphorus, potassium, Leaf a na ­ calcium, magnesium, and manganese showed a good relationship to the concentra­ tion of these nutrient-e le me nt s in the nutrient-solutioni w hile the leaf analysis f or iron, boron, and copper failed to s how a n y direct relationship to the concentration in the nutrient solution. App ar en tl y the distortion of the bal- J&j 39 ance of nutrient-elements within the leaves had a greater influence uron the absorption of iron, Conner, and boron than the concentration in the nutrient solution, Nutrient- element balance in the leaves was also seriously altered with various concentrations of nitrogen, phosphorus, potas­ sium, calcium, magnesium, and manganese, tut here the absorotion of one of these nutrient-elements apparently is in­ fluenced more by concentration in the nutrient-solution than by the distortion of nutrient-element balance, N ut rient-element balance was disturbed more at the 1/2X optimum than w he n nitrogen, phosphorus, ganese, or boron was omitted. calcium, m a n ­ This would indicate that for these nutr ie nt elements nutrient-element balance w o u ld be easily d i s tu rb e d by a shortage of a nutrient-element, but w h e n the shortage becomes more acute, the distrubance in nutrient-e le me nt balance is reduced because of the lack of sufficient quantities of the nu tr ient-element to seriously influence the a b s o r p t i o n of the other nutrient-elements. F o r the other nutrient-elements corner, (potassium, magnesium, iron, zinc) there would appear to be a direct relation­ ship between the shortage of the nutrient-element and its disturbance of nutrient-element balance. C o n v ersely , n u trie n t-elem en t b a la n c e was d i s t u r b e d m o r e a t 2X o p t i m u m t h a n a t ijX o p t i m u m c o n c e n t r a t i o n s p o ta ssiu m , siu m , and c o p p e r . and c o p p e r , the A p p a ren tly w ith e x c e s s e s d istru b a n ce o f b a la n ce is for of p otas­ more n e a r l y ko a s s o c i a t e d with n u t r i e n t - e l e m e n t i nt er -r elationships than w i t h a n excess or the n ut rient-element. The disturbance or n u t r i e n t - e l e m e n t balance by excesses or nitrogen, phosphorus, calcium, m a g n es iu m, manganese, iron, boron, a nd zinc wo uld a p p e a r to be m o r e de pe nd en t u o o n the excess quan ti ty or the n u t r i e n t - e l e m e n t than u p o n n u t r i e n t - e l e m e n t i n t e r- re l a­ tionships. M a n y w o r k e r s h a v e r eported c e r t a i n relationships b e­ t w ee n nu t r i e n t - e l e m e n t s . K e n w o r t h y and Gi ll ig an (19) showed a posi ti ve r e l a t i o n s h i p b e t we en lear n i t r o g e n and lear p h o s ­ phorus, w h e n p h o s p h o r u s was low. However, Boynton and C o m o t o n (ij.) r ound a negative r e l a t i o n s h i p between nitrogen a n d ph o sp horus, but this relatio ns h ip existed at h i g h e r levels or phospho ru s . As indi ca te d by the data in Table 18, the r e l a t i o n s h i p b e t w e e n n i t r og e n c o n c e n t r a t i o n a nd p h o s ­ p h o r u s a b s o r p t i o n is pos it iv e w h e n the n i t r o g e n c o n c e n t r a ­ t i on is b e l o w optimum, and negative w h e n n i t r o g e n c o n c e nt ra ­ tions were above optimum. Similarly, Shear, Crane a nd M y er s (26) have r eported that a n e g a t i v e r e l a t i o n s h i p exists b e t w e e n p o t a s s i u m and m a n g a n e s e w h e n m a n g a n e s e is above 200 ppm. K e n w o r t h y (18) h a s r o u n d a posi ti ve relati on sh ip b e t w e e n p o t a s s i u m and m a n g a n e s e w h e n m a n g a n e s e was b elow 200 ppm. The data in T a bl e 23 s h o w this r el a t i o n s h i p b e t w e e n m a n g a ne se and p o t a s s i u m is p o s i t i v e w h e n the m a n g a n e s e c o n c e n t r a t i o n is b e l o w optimum, a n d negative w h e n m a n g a n e s e c o n c e nt ra ti on is above optimum. kl Several workers h a v e reported many such.relationships b e t w e e n nutrient-elements. For the most part, these re ­ lationships h av e be e n reported to be either positive or negative, but not of such a nature as indicated above, is, w here the type of relationship changes that in regard to shortages and excesses of a nutrient-element# As indicated by the data of this study, the r elation­ ships b e t w ee n nu trient-element a b s o rp ti on and concentration m a y be different for concentrations bel o w optimum than for concentrations above optimum# In this respect, there are p ot en ti al ly nine different types of relationships which m a y occur. These nine types of relationships m a y be outlined as f o l l o w s : 1* A po sitive c or re la ti on b e t we en nutrient-element a bs or pt io n and nutrient-element concentration w h e n the c on ce nt ra ti o n is either below or above optimum. 2. A negative co rr el at io n betw ee n nutrient-element a bs o r p t i o n and nutrient-element concentration w h e n the co n ce nt ra ti on is either below or above optimum# 3* A positive co rr el at io n between nutrient-element a b s o rp ti on and n ut rient-element concentration w h en the c on ce nt r at io n is b e l ow optimum, and a negative correl a ti on b etween nutrient element a b­ s orption a n d nutrient-element concentration w h e n the co nc entration is above optimum. A negative correlation between nutrient-element absorption and nutrient-element concentration w hen the concentration is below optimum, and a positive correlation between nutrient-element a b ­ sorption and nutrient-element concentration when the concentration is above optimum. No correlation between nutrient-element absorp­ tion and nutrient-element concentration when the concentration is below optimum, and a negative correlation between nutrient-element absorption and nutrient-element concentration w hen the con­ centration is above optimum. No correlation between nutrient-element absorption and nutrient-element concentration w h e n the con­ centration is below optimum, and a positive cor­ relation between nutrient-element absorption and nutrient-element concentration when the concentra­ tion is above optimum. Positive correlation between nutrient-element a b ­ sorption and nutrient-element concentration when the concentration is below optimum, and no correla­ tion between nutrient-element absorption and nutrient-element concentration when the concentra­ tion is above optimum. Negative correlation between nutrient-element a b ­ sorption and nutrient-element concentration when k3 the concentration is below optimum, and no corre­ lation between nutrient-element absorption and nutrient-element concentration when the concentra­ tion is above ortimum. 9. No correlation between nutrient-element absorption and nutrient-element concentration when the concen­ tration is either below or above optimum. The general trends of the relationships between the c o n ­ centration of a given nutrient-element and the absorption of other nutrient-elements are shown in Tables 18 to 27* inclu­ sive. These relationships m a y be classified in regard to the above types as presented in Table 28. The relationshin between the a bs o rption of a nutrientelement and the concentration of nutrient-elements, cases, appears ment. in many to be a characteristic of the nutrient-ele- Nitrogen absorption does not appear to be influenced by the concentration of other nutrient-elements, high corner. Phosohorus, potassium, excepting iron, and manganese, in general, fall in Class 3, indicating that the absorption of these nutrient-elements is decreased when the concentration of any one of the other nutrient-elements is either above or below optimum. Conner and boron appear to be in Class l\.t indicating that the absorption of these nutrient-elements is increased w h e n the concentration of any one of the other nutrient-elements is either below or above optimum. Calcium To accompany Page 1+3 Table 28. Nutrient element varied in the- solution Relative Tyne of Relationship:- Between Various Concentrations of a NutrientElenent and Nutrient-Blement Absorption as Measured by Leaf Analysis. ___ N f Nitrogen 1 3 2 ip 8 3 Phosohorus 9 1 3 l 1 3 Potassium 9 3 1 5 k 3 Calcium 9 7 3 l 9 Magnesium 9 3 3 3 Iron 9 3 3 Conner 9 3 Boron 9 Manganese Zinc # See Page 1+1 Nutrient-Element Absorbed _____ ~K ' Ca Kg fte Cu £ Mn of Relationship# ip 2 1+ 1 U ip 7 3 ip ip 3 1 3 ip ip 3 6 1 3 ip ip 3 3 ip ip 5 ip ip 3 3 S 2 3 3 ip ip 3 9 3 3 9 1 3 ip ip 1 9 9 3 ip ip 3 1 ip 3 li- UU and m agnesiu m do n o t T i t the sh io a b so rp tio n to of these an y one c l a s s , w h ich in d ica tes th at n u trien t-elem en ts has a r e la tio n - co n cen tra tio n o f o t h e r n u t r i e n t - e l e m e n t s w hich i s d e o en d en t unon t h e n u t r i e n t - e l e m e n t whose c o n c e n t r a t i o n is being- v a r i e d . Summary O n e - y e a r - o l d M ontm orency c h e r r y n u tr ie n t-so lu tio n s, trie n t-e lem en ts. u sin g f iv e trees d iffer en t G r o w th w a s m e a s u r e d i n were le v e ls ^rown i n of t e n nu­ term s o f dry w e ig h t in crea se. L e a f c o m n o s i t i o n was d e t e r m i n e d f o r n i t r o g e n , ■ potassium , c a l c i u m , m agnesiu m , iro n , b oron , m anganese, and corner. Maximum g r o w t h when a l l of the Any d e v i a t i o n s , ance r e s u lt e d o f M ontm orency c h e r r y n u trie n t-ele m e n ts as a sh ortage the annearance o f v isa b le was o b t a i n e d w e r e a t optim um b a l a n c e . or e x c e s s , in a s ig n ific a n t trees r e d u ctio n f r o m optim um b a l ­ in grow th w it h o u t sym ptom s o f a d e f i c i e n c y or to x ic ity . R ed u cin g th e co n cen tra tio n s r e d u c e d g ro w th m ore than th e e le m e n ts o ro d u c e d grow th i n nhosnhorus, m anganese, n itr o g en , boron, In cr ea sin g reduced b e lo w ootim u m , p o t a s s i u m o th e r elem en ts* the fo llo w in g ca lciu m , cooper, The r e m a i n i n g in c r e a sin g order: i r o n , m agnesiu m , and z i n c . the c o n ce n tra tio n s g r o w th more t h a n t h e a b o v e optim um , n i t r o g e n oth er elem en ts. The r e m a i n - 45 ing elements produced growth in the following increasing order: iron, p h o s p h o r u s , calcium, potassium, manganese, zinc, boron, copper, and magnesium. Combining the growth produced at all concentrations (below and above optimum), varying the concentration of ni tro­ gen reduced growth more than the other elements. The re­ m aining elements produced growth in the following increas­ ing order: manganese, potassium, phosphorus, calcium, iron, copper, zinc,, boron, and magnesium. In regard to their influence on growth, the various nutrient-elements group themselves according to Physiologi­ cal function. The energy storing elements, nitrogen, and phosphorus, had the greatest influence on growth. location regulators, potassium, The trans- calcium, and magnesium, had less effect uo o n growth than the energy stor in g elements. The oxidation-reduction regulators, Iron, manganese, zinc, and Conner, had the least effect upon growth. At concentrations below optimum, p h o s p h o r u s , of those elements calssified as energy storers, was more effective than nitrogen In reduction of growth, but as concentrations were Increased above optimum, nitrogen reduced growth more than phosphorus. Of those elements classified as translocation regula­ tors, po tassium was more effective than calcium, and calcium was more effective than magnesium. ke Iron was more effective in restricting growth than the other nutrient-elements classified as oxidation-reduc­ tion regulators. The effect of copper was greater than manganese; manganese was greater than zinc when the concentra­ tion was below optimum. Above optimum, the order was re­ versed for copper, manganese, and zinc. Leaf analyses for nitrogen, phosphorus, potassium, calcium, magnesium, and manganese showed a positive rela­ tionship to the concentration of these nutrient-elements In the nutrient-solution. W ith concentrations below optimum, there was a direc.t relationship between the shortage of a given nutrient-ele­ ment and the disturbance of nutrient-element balance for potassium, magnesium, iron, copper, and zinc. Nutrient-element balance was disturbed more at 1/2X optimum for nitrogen, phosphorus, calcium, manganese, and boron than wh e n omitted. Excesses of nitrogen, Phosphorus, calcium, magnesium, manganese, iron, boron, and zinc disturb nutrient-element balance in propor ti o n to the excess quantities. Nutrient- element balance is disturbed more at 2X optimum than at JpC optimum concentration of potassium, and copper. U7 Literature Cited (1) Bather, L. P., and Degman, E. S. Effects of Various amounts of Nitrogen, Potassium, and Phosphorus on Growth and Assimilation in Young Annie Trees. Jour. Agr. ^ a . 60 (2): 101-116. 19U0. (2) Beeson, Kenneth C. The Effect of Mineral Sunnly on the Mineral Concentration and Nutritional Cualitv of Plants. Eot. Rev. 12 (7): I42I4-I499 . 19U6. (3) Boynton, D., and ^urrell, A. P. Fotassium-induced v agnesium Deficiency in the T'clntosh Annie Tree. Soil Sci. 98 (6): i4lj.l-lj.9i4-. I9 I4-I+* (I4.) Boynton, D., and Compton, 0. C. The Influence of Differential Fertilization with Ammonium- Sulfate on the Chemical Composition of McIntosh Apple Leaves. Proc. Amer. S oc. Port. Sci. ij.9: 9-17I9I4I4 . ( 9) Brown, D. S. The Growth and Composition of the Tops of Peach Trees in Sand Culture in helation to Nutrientelement Balance. W. Va. Agr. Exp. Sta. Eul. 322. 19149* (6) Cain, John C. Some Inter-relationships Between Calcium, Magnesium, and Potassium in One-year-old McIntosh Apple Trees Grown in Sand Culture. Proc. Amer. Soc. Fort. Sci. 91: 1-12. I9 Z46. (7) . C h a p m a n , H. TD. , a n d L i e b i g , G e o r g e P., J r . N i t r a t e C o n c e n t r a t i o n and I o n E a la n c e i n R e l a t i o n C itru s N u tr itio n . F i l g a r d i a 13: llf.1-173* 19140. to (8) C o o p e r , F . P . , E f f e c t s o f E n e r g y P r o p e r t i e s o f Some P l a n t N u t r i e n t s on A v a i l a b i l i t y , o n P a t e o f A b s o r p t i o n , and on I n t e n s i t y o f C e r t a i n O x i d a t i o n - r e d u c t i o n R ea ctio n s. S o i l S c i . 69: 7-39. 1990. (9) Cullinan, F. P., and Batjer, L. P. Nitrogen, Phosphorus, and Potassium Inter-relationships in Young Peach and Apple Trees. Soil Sci. 99: 14-9-60. 19U3* (10) Cullinan, F. P., Scoot, D. PT., and Waugh, J. G. The Effects of Varying Amounts of Nitrogen, Fotassium, and Phosphorus on the Growth of Young Peach Trees. Proc. Amer. Soc. Fort. Sci. 36: 61-68. 1939. 48 (11) Davidson, C. W., and Elake, M. A. Nutrient Deficiency and Nutrient balance with the Peach. Proc. Amer. Soc* Fort. Sci. 35: 339-346. 1937. (12) Edgerton, L. J. The Effect of Varying Amounts of Potassium on the Growth and Potassium Accumulation of Young Apple Trees. Plant Fhys. 23: 112-122. 1948. (13) Evans, C. Z., Lathwell, D. J., and Mederski, E. J. Effect of Deficient or Toxic Levels of Nutrients in Solution on Foliar Symptoms and Mineral Content of Soy­ bean Leaves as Measured by Soectrographic Methods. Agronomy Jour. 42: 25-32. 1950. (14) Goodall, D. V., and Gregory, F. G. Chemical Comoosition of Plants as an Index to Their Nutritional Status. Imn. Eur. Fort, and Flant Crons. Tech. Comm. No. 17. 1947. (15) Kenworthy, A. L. A Nutrient-element Balance Chart. M ich. Agr. Exp. Sta. Quart. Bui. 33 (1): 17-19. 1949. (16) Kenworthy, A. L. Wheels of Nutrition: A. Method of Demonstrating Nutrient-element Balance. Froc. Amer. Soc. Fort. Sci. 54: 47-52. 1949. (17) K e n w o r t h y , A. L . L e a v e s from F r u i t 55: 41-46. N u tr ie n t-e le m e n t C o m o o sitio n o f T rees. Proc. A m e r . S o c . I l o r t . S c i . 1950. (18) K e n w o r t h y , A. L. a n d B e n n e , E. J. F e r t i l i z e r s uron L eaf C o m p o sitio n . Mich. S t a t e A g r . E x p . S t a . 1950. The I n f l u e n c e o f U n p u b lish ed D a ta . (19) Kenworthy, A. L., and Gilligan, G. K. Inter-relationshio between the Nutrient Content of Soil, leaves, and Trunk Circumference of Peach Trees. Proc. Amer. S o c . F o r t . S c i . 51: 209-215* 1948. (20) K e n w o r t h y , A. L. a n d H o w a r d , J. N. P u r ifica tio n of W ater by u s e o f S y n t h e t i c io n - e x c h a n g e R e s i n s , U s in g pH as a C o n tro l. S o i l S c i . 57: 293-297* 1944* (21) Liebig, George F . , Jr., and Vanselow, Albert P., and Chapman, F. D. Resins for the Growing of Plants In Controlled Nutrient Cultures. Soil Sci. 55: 371-376. 1943* h9 (22) Lilleland, G., and Brown, J. C. The Fhosphate Nu­ trition of Fruit Trees. IV. The Fhosnhate Content of Feach Leaves from 130 Orchards in California and Some Factors which may Influence It. Proc. Amer. Soc. Fort. Sci. JLj.1r 1-10. 19U2 . (23) Nightingale, G. P. Fotassium and Fhosnhate Nutrition of Fineannle in helation to Nitrate and Carbohydrate reserves. Hot. Gaz. lOlj (2): 191-223* 19l|2* (2 I4.) Reeve, P. and Shive, John N. Fotassium-boron and Calcium-boron Pelationshins in Plant Nutrition. Soil Sci. 97: 1-lU* 19U4* (29) S h e a r , C. F., C r a n e , F. L., a n d wy e r s , A. T. N u trien telem en t B alan ce: A F undam ental C oncent in P la n t N u tritio n . I r o c . Amer. S o c . ^ o r t . S c i . £;7: 239-21+8. 19U6. (26) Shear, C. F., Crane, F. L. , and *'yers, A. T. Nutrientelement Falance: Amplication of the Concept to the Internretation of Foliar Analysis. Proc. Amer. Soc. u ort. Sci. 91: 319-326. 19^8* (27) Thatcher, R. V/. A Proposed Classification of the Chemical Elements with Respect to their Function in Plant Nutrition. Science 79: 1+63-1^66* 1931+* (28) Valtman, C. S. The Effect of Nitrogen and Phosphorus on the Growth of Apple and Feach Trees in Sand Culture. Ky. Agr. Exp. Sta. Bui. 1+10. I9 I4O. (29) V i l l c o x , 0 . V/. Y ield -d e p r essio n E ffe c t of F e r t iliz e r s and i t s M easurem en t I I I A g r o - r B io lo g ic a l A n a l y s i s o f C e r t a i n M u l t i p l e F a c t o r F i e l d T e s t s S h ow in g D e p r e s s i o n by N i t r o g e n . J o u r . A m e r . S o c . A g r o n . 37 (8): 622- 6314 • 19l| 9• APPENDIX Table 1* Dry Weight of Leaves, Shoots, trunk, hoots, Entire tree, and Increase in Dry /eight as Influenced by Varying Levels of Nitrogen in NutrientSolut ions*— grams Nitrogen free concentration number ppm 0 43 85 169 Total Average — 112.0 221*.0 1*8.0 696.O Leaves When Harvested Shodts Roots frunk Tree When planted Net increase 94 11.0 7.8 28.2 94 It.3 54 5.8 15.6 5.2 10.7 13.0 134 37.1 12.3 28.0 52.1* 61.8 91.3 4.3 71.3 131*.1 215.0 •1*4.7 71.6 26.k a* .8 3k-9 106.1 35-3 26.0 1*6*5 36.1* 108.9 36.3 hk 86 128 Total Average — 16.1 13.6 17.3 47-0 15.6 10.8 8.0 10.1 28.9 9.6 16.6 17.5 20.3 51*4 18.1 95.2 51.7 82.5 1*34 109.0 61.3 156.1* 286.7 52.1 95.5 kk-7 37.1 51)..5 136.3 50.5 1*54 53.5 49 4 1*9.8 3 87 129 Total — Average — 21.1 21.1 22.8 65.0 21.6 18.6 ll*.l 16.8 1*9.5 16.5 17.8 18.3 26.0 62.1 20.7 51*.6 1*7.2 80.3 I82.I 60.7 112.1 100.7 45.9 358.7 119.5 1)0.6 1)2.7 62.3 11)5.6 1)8.5 71.5 58.0 83.6 213.1 71.0 Total Average— 16.8 10.9 19.9 47 *6 15.8 7.3 5.3 12.0 21*.6 8.2 19.8 16.8 16.9 53.5 17.8 1*1.6 85*5 1*5.6 78.6 39.1 87.9 126.3 252.0 1*2.1 81*.0 1)8.9 63.8 32.0 11)1j..7 1)8.2 36.6 li*.8 55-9 107.3 35*7 L7 69 131 Total Average— 12.9 12.8 4.7 1*04 134 6.5 7.8 17.6 31.9 10.6 12.1 15.7 17.1 4.9 4.9 1*3.2 74*7 75.0 38.7 32.1* 81.8 14.3 231.5 38.1 77.2 1)7.2 1)7.1 1)6.1) 11)0.7 1)6.9 27.5 27.9 354 90.8 30.3 88 130 172 * All other nutrient-elements constant in nutrient solution k$-k- Table 2. Dry Weight of Leaves, Shoots, Trunk, Roots, Entire Tree, and Increase in Dry Weight as Influenced by Varying Levels of Potassium in NutrientSolution#— grams Phosphorus Tree concentration number Dom 0 1*8 90 m Total — Average — 3 M 91 133 175 Total Average — 66.0 3 87 129 Total Average -136.0 7.3 13.5 12.3 33.1 11.0 2.3 7.0 6.3 15.6 5.2 B.i ie.6 13.7 16.2 15.7 h5*6 15.2 6.9 .9.2 7.6 23.7 7.9 17.6 22.6 19.8 60.0 21.1 21.1 22.6 65.0 21.6 18.6 17.8 18.3 £0 9.8 92 23.0 176 Total Average — 272.0 Leaves When Harvested Shoots Trunk Roots 9 51 177 Total — Average — 16.8 49.6 16.5 18.3 22.0 H.l 16.8 49.5 16.5 5.0 12.8 8.9 26.7 8.9 12.5 11.5 16.8 20.0 hi.o 23.3 95.0 94.1 39.1* 70.0 117.7 209.1 68.3 39.2 93.6 91.8 1*7-3 99.3 1*5-3 88.4 11*6.2 275-5 1*8.7 91.8 20.3 130.5 88.1 44.6 h3.5 96.5 50.7 103.7 34-4 61.7 133.1 261.9 ...44*3 67.3 37.4 47.7 36.1 123.2 59.1 56.0 63.8 9.4 125.1 h3-5 h6.7 43*7 133.9 36-7 16.6 1504 i|9.7 71.5 58.0 63.6 213.1 71.0 12.3 28.3 hh«h 35.5 h5.6 hh.o 56.3 ho. 6 h2.7 62.3 lh5.6 h8.5 145.9 358.7 119.5 11*-4 1*8.3 16.1 38.6 120.8 i|,0.2 15.9 37.0 31.h eh .3 28.1 hi.7 26.0 62.1 20.7 21.6 25.1 57.1 Set increase 50.1 91*.6 1*7-2 80.3 ie2.1 60.7 17.7 19.5 12.7 1*9.9 10.3 50.6 12.0 38.7 12.9 Tree When danted 112.1 100.7 58.9 116.3 1*4.2 84-3 139.8 264.4 46.6 48.0 * Ail other nuirient-elemenfcs constant fn nutrient solution 41.0 69*6 ho.6 23.6 138.7 h6.2 Table 3* Dry height of Leaves, Shoots, Trunk, Roots, Entire Tree and Increase in Dry Weight as Influenced by Varying Levels of Potassium in NutrientSolutiona— grams Fotassium concentration npm 0 Tree number 94 136 178 Total Average 43*0 53 95 137 Total Average 86.0 3 87 129 Total Average 172.0 12 % 138 Total Average 344*0 13 97 l8l Leaves When Harvested Roots Shoots Trunk Tree When planted Net increase 12.5 9*9 9*5 31*9 10.6 7*0 6.7 4.0 17*7 5*9 16.5 15.0 15*2 46*7 15*5 31.6 54-4 30.9 116.9 38.9 67*6 86.0 59*6 213*2 71.0 38.3 60.7 36.1 135.1 45.0 29.3 25.3 23.5 78.1 26.0 12.1 15*3 15*2 42.6 14*2 5*6 9*3 8.1 23.0 7*6 11.8 16.5 21.2 49.5 16.5 76.0 46.5 36.8 77*9 51.0 95*5 134*3 249.4 83.1 44*7 45.5 39.8 534 138.7 U6.2 30.5 38.1 42.1 110.7 36.9 21.1 21.1 22.8 65*0 21.6 18.6 14*1 16.8 49*5 16.5 17*8 18.3 26.0 62.1 20.7 54*6 112.1 47*2 100.7 80.3 145*9 182.1 358.7 60.7 119*5 1*0.6 1*2-7 62.3 11*5.6 1*8.5 71.5 58.0 83.6 213.1 71.0 15*1 15*0 23.6 53*7 17*9 7*7 7*9 15*1 30.7 10.2 13*1 16.6 25*5 55*2 18.4 Ul.2 77*1 58.5 98.0 51*5 115*7 151*2 290.8 50.4 96.9 1|2.1 1*9.5 1*7.6 139.2 1*6.1* 35.0 1*8.5 66.1 151.6 50.5 11.6 19*0 12 •0 42.6 14*2 4*8 10.7 6.7 22.2 7.4 10.7 22.7 10.8 44.2 14*7 38.0 53*9 42.2 134*1 44-7 31*.7 53.8 35.1 123.6 1*1.2 30.1* 52.5 36.6 119.5 39.6 65.1 106.3 71.7 2k3.1 81.0 Total Average * n r other nutrient-elements constant in nutrient solution Table 4* Dry Weight of Leaves, Shoots, Trunk, Roots, Entire Tree and Increase in Dry Weight as Influenced by Varying Levels of Calcium in NutrientSolution#— grains Tree Calcium Concentration number nom 0 56 98 182 Total Average 88,0 57 99 183 176.0 3 87 129 Total Average 352.0 16 58 184 Total Average 701^.0 17 101 185 Total Average Tree .i/hen olanted Net increase 66.6 48.3 42.6 77.1 71.2 33.3 124.4 237.1 79.e 41.4 47.7 43.0 33.0 123.7 41.2 41.1 34.1 36.2 H3*4 37.8 147.7 49.2 99.6 70.9 92.8 263.3 87.7 43.0 46.8 42.5 134.3 44.7 56.6 22.1 50.3 129.0 43.0 17.8 18;3 26.0 62.1 20.7 54*6 47.2 60.3 162.1 60.7 112.1 100.7 145.9 358.7 119.5 40.6 42.7 62.3 145.6 48.5 71.5 58.0 83.6 213.1 71.0 9.6 7.9 9.4 26.9 8.9 11.3 14.5 12.6 38.k 12.8 48.0 83.O Pi.7 43.7 37.8 74.6 129.5 239.3 79.7 43.1 34.7 33.6 32.3 100.6 33.5 48.3 48,1 42.3 138.7 46.2 9.6 10.3 5.2 25.1 8.3 14.2 14.4 11.3 39.9 13.3 57.3 97.4 46.2 89.3 56.6 26.9 134.4 2k3.3 44.5 81.O 44-5 41.6 28.1 114.4 3?.l 52.9 47.5 28.5 128.9 42.9 17.9 12.6 15.2 45.7 15.2 7.5 5.5 9.0 22.0 7.3 15.1 16.2 13.7 45.0 15.0 19.0 7-3 l?.l 43.4 14.4 10.6 4.8 9.2 24.6 5.2 16.5 16.5 11'..6 47.6 15.8 21.1 21.1 22.8 65.0 21.6 18.6 14'.1 16.8 49.5 16.5 14.1 15.6 14.8 44*5 14.8 16.3 16.4 11.2 43.9 14.6 53.5 42.3 *A11 othernutrient-elements constant In nutrient solution AFFENDIX Total Average Leaves When Harvested Shoots Trunk E00 ■Es Table Dry height of Leaves, Shoots, Trunk, Hoots, Entire Tree and Increase in Dry Weight as Influenced by Varying Levels of Magnesium in Nutrient Solution*— grams Tree Magnesium concentration number pnm 0 18 60 186 Total Average — Leaves When Harvested Trunk Shoots Hoots Tree When planted Wet Increase 16.0 16.2 13.2 US.4 15.1 8.3 10.8 5.8 2k.9 8.3 13.6 14.9 14.0 42.1 14.0 73.6 35.7 64.4 105.9 48.5 61.5 146.6 261.0 87.O 49.5 32.3 43.9 34.6 110.8 36.9 41.3 62.0 46.9 150.2 50.0 29.0 103 1W 187 Total — Average — 10.8 16.2 13.9 42-9 14.3 7-2 16.1} 7*1 30.7 10.2 10.8 24.4 13-7 46.9 16.3 47.1 95.8 43.6 146.7 46.9 75.9 114.6 78.5 269.2 89-7 41.2 49.0 39.8 130.0 43.3 34-7 65.8 38.7 139.2 46.4 se.o 3 87 129 Total — Average — 21.1 21.1 22.8 65.0 21.6 18.6 14.1 16.8 49.5 16.5 17.8 18.3 26.0 62.1 20.7 54-6 47.2 80.3 182.1 60.7 112.1 100.7 145.9 358.7 119.5 40.6 42.7 62.3 145.6 48.5 71.5 58.0 63.6 213.1 71.0 116.0 20 62 11*6 Total — Average — 23.5 21.2 23.5 68.2 22.7 15.1 16.5 15.8 47.4 15.6 17.3 16.6 24.6 58.5 19.5 53.4 49.6 72.0 175.0 58.3 109.3 103.9 135.9 349.1 116.3 27.1 37.4 60.4 124-9 41.6 82.2 66.5 75.5 224.2 74-7 232.0 21 63 147 Total Average — 16.7 17.1 1?.8 49.6 16.5 10.1 11.1 8.6 29.8 9.9 13.3 19.0 22.6 54.9 18.3 54-3 94-4 51.5 98.7 64.0 111.0 169.8 304.1 56.6 101.3 41.2 40.6 57.3 139.3 46.4 53.2 57.9 53.7 164.8 54.9 *All othernutrient-elements constant in nutrient solution Table 6. Dry Weight of Leaves, Shoots, Trunk, Roots, Kntire Tree and Increase in Dry Weight as Influenced by Varying Levels of Manganese in NutrientSolution*— grams Manganese concentration ppm Tree number 0 46 190 Total Average 2.5 3 e? 129 Total Average 10.0 — 2l| 150 192 Total Average 20.0 — — 109 151 193 Total Average — Tree 107.2 109.9 93.2 310.3 1034 20.3 16.2 19.3 55.8 16.6 11.9 10.7 11.6 3h-2 114 18.6 174 19.3 55.3 184 56.1) 65.6 1)3.0 165.0 55.0 10.6 19.2 ll.il hi.2 13.7 7.6 10.3 84 26.3 8.7 4 4 21.2 17-3 52.9 17.6 21.1 21.1 22.6 65.0 21.6 18.6 lil.l 16.8 49.5 16.5 4-7 15.8 4.8 h5.3 15.1 10.7 9.6 7.7 28.0 9.3 19.7 194 13.1 52.2 17-4 44 9.7 7.6 31.7 io,5_ When planted Met increase i|0.i| 57.7 35.2 133.3 144 66.8 52.2 58.0 177.0 59.0 65.0 324 52.7 1034 1)2.7 79.6 127.8 2L8.2 1)2.6 82.7 31.2 £2 .6 39.8 113.6 374 33.8 60.8 1)0.0 13l).6 i4.8 17.8 18.3 26.0 62.1 20.7 51).6 1)7.2 80.3 182.1 60.7 112.1 100.7 45.9 358.7 119.5 1)0.6 1)2.7 62.3 11)5.6 1)8.5 71.5 58.0 83.6 213.1 71.0 174 11).3 17.5 1)9.2 164 52.3 95.1 59.5 99.2 37.6 77.6 11)94 271.9 1)9.8 90.6 1)5.2 1)7-8 37.8 130.8 1)3.6 1)9.9 514 39.6 11)1.1 1)7-0 13.6 21.9 16.0 51-5 17.1 674 115.1 59.2 110.2 88.h 51.7 178.3 313.7 594 10li.5 l)e.l) 59.7 1)6.5 151).6 51.5 66.7 50.5 £1.9 159.1 53.0 APPENDIX 23 65 191 Total Average 5.0 « Leaves When Harvested Shoots Trunk Roots Table 7. Dry Weipbt of Leaves, Shoots, Trunk, Roots, Lntire Tree and Increase in Dry Weight as Influenced by Varying Levels of Boron in hutrientSolution#--grams Boron Tree concentration number pom 0 26 68 152 Total Average — Leaves li/hen harvested Shoots Trunk Roots Tree When planted . -^Tet increase 174 16.2 22.0 5^.6 18.5 12.1* 9.7 11.9 34.0 11.3 19.4 19.9 23.1 624 20.8 57.7 65.0 68.2 190.9 63.6 106.9 110.8 125.2 342.9 114.3 46.6 52.9 59.3 158.8 52.9 60.3 57.9 65.9 184.1 61.3 16.9 4.6 16.6 1*8.1 16.0 11.3 9.3 9.2 29.6 9.9 15.5 144 19.2 49.1 16.3 95.1 51.4 54.6 92.9 82.1 37.1 143.1 270.1 90.0 47.7 35.5 43.9 41.9 121.3 40.4 59.6 49.0 40.2 148.8 49.6 Total Average — 21.1 21.1 22.8 65.0 21.6 16.6 14.1 16.8 49.5 16.5 17.8 16.3 26.0 62.1 20.7 54.6 47.2 80.3 182.1 60.7 112.1 100.7 145.9 358.7 119.5 40.6 42.7 62.3 145.6 48.5 71.5 58.0 83.6 213.1 71.0 6.0 112 15*1 196 Total Average — 16.9 21*.1 11*.2 57.2 19.0 16.1 15.7 7.3 39.1 13.0 25.5 28.0 16.0 69.5 23.1 53.0 113.5 60.1 127.9 38.6 76.1 151.7 317.5 50.5 105.8 40.2 52.3 34*0 126.5 42.1 73.3 75.6 42.1 191.0 63.6 12.0 29 155 197 Total Average — 11.1 164 12.8 40.3 134 5.7 10.9 7.1 23.7 7.9 18.2 23.6 11.2 53.0 17.6 40.7 45.2 41.4 127.3 42.4 49.5 53.7 35.3 138.5 46.1 26.2 42.4 37.2 105.8 35.2 1.5 69 153 195 Total Average 3.0 — 3 87 129 75.7 96.1 72.5 244 .3 81.4 *All other nutrient-elements constant in nutrient solution Dry Height of Leaves, Shoots, Trunk, Roots, Lntire Tree and Increase in Dry Height as Influenced by Varying Levels of Iron in MutrientSolutions*— grains Iron concentration Ppm 0 Tree number 30 156 198 Total Average 1 .0 73 115 199 Total Average 2 .0 3 87 129 Total Average 4.0 74 116 200 Total Average 8.0 75 159 201 Total Average Leaves When Harvested Shoots Trunk Roots Tree When planted Net increase 15.3 13*3 13.5 42.1 14.0 7.6 6.8 7.5 21.9 7.3 13.0 154 154 43.8 14.6 68.2 52.3 97.8 62.3 32.9 69.3 147.5 255.3 85.1 49.1 42.6 5l*.9 324 129.9 1*3-3 45.6 42.9 36.9 125-4 41.8 20.5 111-•2 13.3 46.0 . 16.0 12.1 9.1 7.6 28.8 9.6 18.1 15.3 15.6 49.0 16.3 54.4 51.4 35.3 141.1 47.0 105.1 90.0 71.6 266.9 86.9 3? 4 35.2 35.2 10?.8 36.2 66.7 54.8 36.6 158.1 52.7 21.1 21.1 22.8 65.0 21.6 18.6 U 4..I 16.8 49.5 16.5 17.8 16.3 26.0 62.1 20.7 54*6 47.2 80.3 182.1 60.7 112.1 100.7 145.9 358.7 119.5 1*0.6 1*2.7 62.3 11*5.6 1*8.5 71.5 56.0 83.6 213.1 71.0 11.5 12.1 1911 42*7 14.2 14.3 64 11.5 24.2 6.0 14.1 11.3 20.9 46.3 154 42.0 71.9 64.2 32.4 96.6 45.1 119.5 232.7 39.8 77.5 39.1* 29.9 37.2 106.5 35-5 32.5 34.3 59.4 126.2 42.0 11.9 16.2 8.5 36.6 12.2 6.8 9.7 4-9 21.4 l-i 9.7 14.3 15.1 39.1 13.0 64.8 36.4 61.9 102.1 22.6 51.1 218.0 120.9 72.6 40.3 27.8 52.3 27.8 107.9 35-9 37.0 49.8 23.3 110.1 36.7 *Ail othernutrient-elements constant in nutrient solution xiamiciv Table 8. Table 9. Dry Weight of Leaves, Shoots, L’runk, Roots, hntire Tree and Increase in Dry /eight as Influenced by Varying Levels of Zinc in TJutrientSolutiontf— grams Zinc Tree concentration number ppm 0 lie 160 202 Total Average — Leaves When Harvested Shoots Trunk Roots Tree When planted Net increase 12.5 14. 1 7.5 34.1 11.3 21.2 24.5 15.7 61.4 20.4 4 6 .0 43.5 48.3 135.8 45.2 9714 102.0 84*7 284.1 94.7 370 42.3 39.9 119.5 39.8 60.1 59.7 44*8 164.6 54.8 18.0 21.7 19.2 58.9 19.6 9.6 4 .2 13.2 37.0 12.3 15.7 22,2 15.2 53.1 17.7 44.6 45.5 39.3 129.4 43.1 87.9 103.6 86.9 278.4 92.8 40.4 28.9 29.1 98.4 32.8 47.5 74.7 57.8 180.0 60.0 — 21.1 21.1 22.8 65.0 21.6 18.6 14.1 16.8 49.5 16.5 17.8 18.3 26.0 62.1 20.7 54.6 47.2 80.3 182.1 60.7 112.1 100.7 145.9 358.7 119.5 40.6 42.7 62.3 145.6 48.5 71.5 58.0 83.6 213.1 71.0 4*0 ?8 120 204 Total Average ~ 17.0 13.5 20.6 51.1 17.0 8.9 9.2 13.9 32.0 10,6 16.8 15.5 18.1 5°.4 16.8 83.6 41.1 83.5 45.3 49.4 102.0 135.8 269.3 45.2 89.7 35.4 29.1 42.6 107.1 35.7 48.4 54.4 59.4 162.2 54.0 8.0 37 163 205 Total 154 11.1 14.5 41.0 13.6 8.9 4.9 10.4 24.2 6.0 19.4 21.0 17.6 58.0 19.3 42.7 86.4 86.1 49.1 77.6 35.1 126.9 250.1 63.3 42.3 43.5 53.1 34.3 130.9 43.6 42.9 33.0 43.3 119.2 39.7 1,0 2.0 77 119 203 Total Average — 3 87 129 Total Average Average — *All other nutrient-elements constant in nutrient solution APPENDIX 17.7 19*9 15.2 52.6 17.6 Table 10* Dry Weight of Leaves, Shoots, Trunk, hoots, Entire Tree and Increase in Dry Weight as Influenced by Varying Levels of Conner in NutrientSolutiontf— Grains Conner concentration oom Tree number 0 36 80 122 Total Average 1.0 Total Average 2.0 3 87 129 Total Average 4 .0 -- -- 82 8.0 9.7 2 .1 10.1 21.9 7.3 16.9 7.7 21.8 464 154 95.1 52 4 30.2 44.7 99.6 50.3 132.9 239.6 79.8 44.3 47*1 28.6 30.6 106.3 354 4 8 .0 16.1 69.2 133.3 III-.2 13.3 17.2 44-7 1^.9 7.1 6.7 9.6 234 7.8 111•6 4 4 164 454 15.1 43.6 79.5 70.1 35.7 78.2 35.0 114.3 227.8 36.1 75.9 33.5 31.3 32.2 97.0 32.3 46.0 38.8 46.0 130.8 43.6 21.1 21.1 22.8 65.0 21.6 18.6 4 .1 16.6 49.5 16.5 17.8 18.3 26.0 62.1 20.7 54.6 112.1 47.2 100.7 60.3 45.9 162.1 358.7 60.7 119.5 40.6 42.7 62.3 145.6 48.5 71.5 58.0 83.6 213.1 71.0 13.0 7.5 7.2 12.6 27.3 9.1 12.5 15.0 21.0 48.5 16.1 80.5 47.5 42.2 75.9 58.0 112.0 147.7 268.4 49.2 69.4 34.0 36.5 47.7 116.2 39.4 46.5 394 64.3 150.2 50.0 9.0 13.5 9.7 32.2 10.7 19.6 24.3 18.3 62.2 20.7 42.0 84.6 50.2 112.1 85.9 414 133.6 282.6 . 44-^ 94.2 36.8 49.2 39.7 125.7 41.9 47.8 62.9 46.2 156.9 52.3 3* 166 204 14.9 4.9 41 167 209 Total Average -- Net Increase 16.1 4*7 17.6 38 4 12.8 12k Total Average Tree '/hen nlanted 4 .0 2i[.l 16.5 54.6 18.2 ♦Allotbernutrient-elements constant In nutrient solution 444 APPENDIX 39 123 207 Leaves When Farvested Roots Trunk Shoots QBOWTF, L*AF COMPOSIT10W A HD NUTFIPWT-BLFMEWT PA LAWOK OF MOlfTMCPEWCY CHERRY fPrunua o m i u i . L. )— Effect of Varying Conetntratloni of fan Wutrient»Elementa By Boy Kenneth Simone An Abetreet of A THESIS Submitted to the School of Oreduete Studlee of Michigan State College of Agriculture end Applied Science In partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Department of Horticulture 1951 Appro v e d GROWTH* LEAF COMPOSITION AND JttfTF11‘NT-ELEMENT BALANCE OF MONTMORENCY CHERRY (Frunuc etrtiu»» L*)— Effect of Varying Cone antra tIona of Ton Nutrient-Elements By Roy Kenneth Simona ABSTRACT One-year-old Montmorency cherry traaa (Prunua cerasus L.) ware grown In aand culture for ona aaaaon to atady their response to tan different nutrient-elementa when ona ele­ ment waa varied at a time while the remaining elemente ware kept constant* Stock aolutlona of chemically pure HB4 NO3 # I^FO^* KC1, CaClg* MgSO(|» H 3 BO3 , MnSOjj.* CuSQ^* Z&SQ^i and Pe8 Q^ ware prepared Individually for eaeh of the nutrient*elaaianta* From theae atook aolutlona a dilute aolutlon for eaeh treat­ ment waa prepared in Which the elemente ware combined In definite proportions* the optimum concentration* aa determined from the 1 1 tore• ture* was Ca follows: Ititrogen 224 Ft** Manganese 5*0 ppm Phosphorus 68*0 ppm Boron 3*0 ppai Potass lust 66*0 ppm Iron 2*0 ppm Zinc 2*0 ppm Oonper 2*0 ppm Calcium Magnesium 176*0 ppm 58*0 ppm Baeh nutr lent-element waa varied individually from this optimum concentration co aa to provide# for eedb nutrientelament* levelc corresponding to omitted* 1/2X* 2X* and kX optimum* Roy Kenneth Slmosis Growth R*«iup«nenti were recorded Tor dry v«ight incr«*»t or tree parts and length of terminal grovtii* Lear analysis for nitrogen was determined by the KJeldahl method, and speetrograohlc analysis was used ror the determination or P, K, Ca, Mg, Fe, Cu, E, and Mn, The results show that maximum growth was obtained when all the nutrlent-elements were at optimum concentration. Any deviations, as a shortage or an excess, from optimum con­ centrat ion resulted In a significant reduction in growth without the appearance of visible symptoms of a deficiency or toxicity* Reducing the concentration below optimum, potassium re­ duced growth more than did the other elements which produced growth In the following increasing orders Mg, Mn, B, and Zn* F, H, Ca, Fe, As concentrations were increased above optimum, nitrogen reduced growth more than the other nu­ trient elements whleh produced growth in the following in­ creasing orders Fe, P, Ca, K, Zn, B, Mn, Cu, and Mg* The nitrogen concentration, when varied below and above optimum, resulted in less total growth for the five levels than the other nutrlent-elements• The remaining elements produced growth in the following Increasing orders K, ?, Ca, Fe, Cu, M b , Zn, B, and Mg* Leaf analysis for !f, p, K, Ca, Mg, and Mn showed a positive relationship to the concentration of these nutrlentelements in the nutrlent-solutlon* -3- Poy Kenneth Simons With concentrations below optimum, there is * direct relationship between the extent of the shortage of a given nutrient-clement and the disturbance of nutrlent-element balance for K, ?fgv Fe, Cu, and Zn, However, nutrlent- element balance was disturbed more at 1/2X optimum for If, F , Ca, Mn, and 5, than when these nutrlent-elements were omitted. Excesses of R, F, Ca, Mg, Mn, Fa, B, and Zn disturb nutrlent-element balance in proportion to the extent of the excess• The manuscript Includes a discussion of the factors Involved and the relationship between concentration of the nutrlent-solutlon and absorption of the different nutrlentelements by the plant. t