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The reproductive development of tomatillo (husk tomato) was investigated in the conditions of central Poland. The developmental cycle of tomatillo in Poland lasts 20-23 weeks, including 6 weeks in a greenhouse or a tunnel and is longer than in Mexico (15 weeks). The plant grows well in Poland and is fruiting aboundantly.The cv. Rendidora B1 was early fruiting and sensitive to drought so it should be cultivated in a garden. Cvs. Bujna and Antocyjanowa were medium late or late and suitable for open-field cultivation. Fruit development lasts about 6 weeks. Fruiting was concentrated on the apparent lateral branches of the 1st and 2 nd order during the large part of a vegetative season. Among the abscised generative organs predominated flowers and at the end of vegetative season the flower buds. The maximum abscission of flower buds and flowers took place about 2-4 weeks after the most intensive flowering and fruit set. The fruits of many individuals are easily cracking. After being abscised they are attacked frequently by Botrytis sp.
In a commerical orchard of 18-year-old trees, 1250 fruits were chosen for observation. The majority of them abscised during the first weeks after anthesis. Afterwards, the abscission gradually descreased, however, in the meantime three additional waves of more intensive shedding occurred which were best visible when the Relative Abscission Rate (RAR) was calculated. The peaks in the RAR curve were preceded by a decrease in the Relative Growth Rate (RGR) of persistent fruits, which suggests that nutritional or other stresses occurred in the whole branch. In the period from May 15th to July 15th, predominantly the smaller fruits were abscised, later on, however, fruits of the same size as the persistent ones were shed. The formula for calculating RAR and RAR is shortly discussed.
Anatomy and surface ultrastructure of the galls induced on oak leaves by the insects – Neuroterus numismalis (Ol.) and Cynips (Diplolepis) quercusfolii L. – were investigated using a scanning electron microscope (SEM) and a light microscope (LM). The observations in SEM and in LM enabled a detailed description of these galls and comparison of their structure with that of the typical oak leaf. In N. numismalis gall, the external distal tissues were classified as similar to phellem (cork), phellogen, and phelloderm, and a lateral marginal tissue as parenchyma with the likely role of a storage tissue. In the young C. quercusfolii gall, the cells of internal, nutritive tissue, on which the larva is grazing, formed globules rising above the surface of larval chamber. Many of them seemed to be destroyed by the larval action. In the gall which attained half of its final size, the tissues near the larval chamber were already partly lignified. The microorganisms (mainly fungi) which live in the oak phyllosphere, occurred also on the galls. We believe that the deep changes in the morphogenetic program of a leaf, which are caused by the gall-forming insects, are impossible without the transfer and the integration of the insect genetic material with that of the host plant. We also postulate that a larva secrets as yet hypothetical substances, which redirect the nutrients transport from the leaf blade towards the gall and support its vital functions.
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