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Phenotypic plasticity acts to increase the performance of plants under stress. Leaf morphological plasticity and its causes in different environments are incompletely understood. We measured the leaf morphological parameters of Quercus acutissima Carr. seedlings, including leaf size, leaf shape and venation pattern, assessing the effects of different habitat conditions on leaf morphological plasticity. A field study in forest edge and understory was combined with experiments simulating different light and water conditions. Leaf morphology variations occurred over most of the parameters, and the causes were consistent between the field study and lab experiment. Leaf size decreased with low supply of light and water. Leaf length and width were only affected by leaf area. The leaf petiole did not lengthen under shade stress, suggesting a trade-off relationship between functional tissues and support structures. Leaf shape became narrower in drought and broader in the shade, as reflected in changes in three leaf fractions. Higher vein density played a part in enhancement of mechanical support and water supply. Leaves with more teeth show more active photosynthesis, but are disadvantageous in xeric environments because of higher transpiration. Light was the main factor inducing leaf morphological plasticity. The variations caused by drought were due mainly to the allometry. Our results showed that the leaves of Q. acutissima seedlings respond to different habitats with phenotypic plasticity of morphology, suggesting that this is an important mechanism for seedlings to adapt to broader ecological amplitudes.
We studied the variation of linear measurements and skull capacity in Lowland European bisonBison bonasus bonasus (Linnaeus, 1758) during postnatal development, and the dependencies of the parameters in relation to sex, age, and body mass of the animals. Material consisted of 599 bison skulls (310 males and 289 females), within the age range of 1 month to 21 years (males) and to 27 years (females). In the group of calves to 1 year old, no sex connected differences in skull measurements were observed, whereas the skull capacity in older calves was significantly larger (0.01>p>0.001) in males than in females. From the third year of life, most skull measurements display characteristics of sexual dimorphism. Skull development in both sexes is most intensive during the first three years of life, and slows from the age of 5. In older individuals of both sexes (≥ 6 years), orbital breadth continues growing and, in females, breadth of splanchnocranium continues increasing. Growth in a bison’s skull capacity is most intensive up to the third year of life and slows from the age of 5. During postnatal development, a bison skull grows proportionally except the neurocranium, which grows slightly slower in comparison with basal length and its development finishes earlier than that of splanchnocranium. In ontogenesis, a bison skull grows much slower compared to body mass. In relation to body mass, skull capacity and the height of neurocranium grow most slowly while orbital breadth grows most intensively. The results obtained were compared with data on skull sizes of bison born in 1930–1950 and bred in captivity and with skulls of the American bisonBison bison. Inbreeding is probably responsible for some types of phenotypic abnormalities in the skull which appear in modern European bison.
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