Each year at the height of the flowering period, each tree in the experiment was rated on the catkins it carried. So far, there has been no effect of the differential fertilizer treatments on the production of catkins. However, there have been very highly significant differences between the Potomac and the Reed. In 1950, only four of the 36 Reed trees produced catkins, whereas 32 of the 36 Potomac trees flowered, and approximately half of them were heavily loaded. In 1951, the number of Reed trees producing catkins was 12 of the 36, whereas 35 Potomac trees flowered. The amount of pistillate flowering during the two years was small on both varieties and not greatly different; this indicates that their nut-bearing potentialities may be about the same. The amount of pollen produced by the Reed variety has always been considered ample for cross-pollinating the Potomac, even though the former has been a light producer of catkins.
Records of dates of flowering of the two original trees over a 10-year period, and of these young orchard trees over a 3-year period, show that there is great variability in time of flowering, depending upon the sequence of weather events each season. Fertilizer treatments have had no measureable effect. The trees have shed pollen as early as January and as late as April, and stigma receptivity sometimes has continued intermittently for two months. The average period of flowering at Beltsville is the last week of February to the first week in March. Both varieties have flowered at the same time under all seasonal conditions observed. This means that additional pollinators will not be necessary when the varieties are planted together in an orchard.
Symptoms of Scorch
The visible symptoms of scorch do not begin to appear under conditions at Beltsville until about the middle of July or later. The first symptom is fading of the green color, especially around the margins of the leaf blade. Sometimes this chlorosis results in blotches, which may extend for a considerable distance from the margin towards the mid-rib. This stage is of short duration, as the tissues of marginal chlorotic areas or those of the blotches soon die, roll up, and turn brown. Some leaves show yellow blotchiness over most, if not all, of the surface and this may develop into brown patches of dead tissue or the yellow leaves may fall before the tissues die. The older leaves, those at the base of a shoot, are generally the first to show chlorosis and scorch, and the terminal leaves are the last to show such symptoms. On severely affected trees all the leaves on a shoot may be scorched at the time scorching is observed. Severely affected trees drop part or all of their leaves prematurely. The leaves dropped are those that are scorched or that show yellow blotches. Such trees do not make satisfactory growth, they set few nuts, and the nuts are usually poorly filled at harvest. The symptoms of scorch on filbert leaves are similar in many respects to magnesium-deficiency symptoms on apple (1, 5, 6)[11] and tung leaves (3).
Leaf Analyses[12]
No differences in appearance of the trees as regards leaf scorch were noticed the first year after the differential fertilizer treatments were applied. However, in late July and early August of the second season, severe leaf scorch developed on the trees that had received potassium alone or nitrogen plus potassium, and scorch developed to some extent on the check trees. On August 15, 1950, leaf samples for chemical analyses were taken from each tree in all replications and composited by treatments into six samples. The data on the chemical composition of the leaves as affected by the differential fertilizer treatments are given in table 1.
These data show that the fertilizers applied to the trees were taken up by them and that the composition of the leaves was significantly affected. The trees in treatments 2, 3, and 6, which did not receive nitrogen in the fertilizer, had lower percentages of nitrogen in the leaves than those from the other plots. Their light green color indicated that in the middle of August they were deficient in nitrogen when its concentration was 2.3 percent or less.
Table 1. Chemical composition (oven-dry basis) of filbert leaves collected August 15, 1950, from fertilizer experiment, Beltsville, Md.
| Treatment | Composition of leaves | Ratio | Mg (percent) | |||||
| Ash | N | P | K | Ca | Mg | K (percent) | ||
| % | % | % | % | % | % | |||
| 1. Nitrogen | 6.68 | 2.52 | .129 | .945 | 1.30 | .143 | .151 | |
| 2. Phosphorus | 8.56 | 2.29 | .160 | .885 | 1.60 | .186 | .210 | |
| 3. Potassium | 9.39 | 2.31 | .150 | 1.650 | 1.93 | .155 | .094 | |
| 4. Complete | 7.18 | 2.43 | .133 | 1.175 | 1.63 | .132 | .112 | |
| 5. Nitrogen and potassium | 7.62 | 2.49 | .119 | 1.480 | 1.33 | .110 | .073 | |
| 6. Check | 7.38 | 2.32 | .188 | .890 | 1.70 | .149 | .167 | |
Potassium applications produced the greatest effect on leaf composition, as they increased the concentration of that element in the leaves by 0.285 to 0.760 percentage unit over that in the leaves from the check trees. In addition, it seems likely that this great increase in the potassium content of the leaves was accompanied by a decrease in their magnesium content, since this usually has been found to result. When the ratios of the percentage of magnesium to the percentage of potassium in the leaves were calculated, it was found that they were rather low for the trees that had been fertilized with potassium. The magnesium-potassium ratio was highest in the leaves from the trees fertilized with phosphorus only, followed in order by the check and nitrogen treatments.