In the Serengeti ecosystem of East Africa, grazing ungulates prefer areas with elevated grass Na, suggesting that some grasses tolerate both high soil Na and defoliation. We performed a factorial Na-by-defoliation greenhouse study with five abundant Sporobolus congeners to explore whether Serengeti grasses possess traits which: (i) confer tolerance to both Na and defoliation (cross-tolerance); ...

We compared growth rates among mature interior Douglas-fir (Pseudotsuga menziesii var. glauca (Beissn.) Franco) trees showing resistance or susceptibility to defoliation caused by western spruce budworm (Choristoneura occidentalis Freeman), and among clones and half-sib seedling progeny of these trees in a greenhouse. We also investigated bud burst phenology and photosynthetic responses of clon...

We examined the effects of fertilization and gypsy moth defoliation on condensed tannin concentration (%CT) of hybrid poplar (Populus x canadensis cv 'Eugeneii') fine roots in the summers of 1997 and 1998. This factorial experiment included two defoliation treatments (defoliated and a foliated control) and fertilization treatments (100 kg nitrogen (N) ha(-1) and an unfertilized control). Gypsy ...

After defoliation by herbivores, some plants exhibit enhanced rates of photosynthesis and growth that enable them to compensate for lost tissue, thus maintaining their fitness relative to competing, undefoliated plants. Our aim was to determine whether compensatory photosynthesis and growth would be altered by increasing concentrations of atmospheric CO2 , Defoliation of developing leaflets on ...

Widespread and prolonged defoliation by the European winter moth, Operophtera brumata L., has occurred in forests of eastern Massachusetts for more than a decade and populations of winter moth continue to invade new areas of New England. This study characterized the forests of eastern Massachusetts invaded by winter moth and related the duration of winter moth defoliation estimated using dendro...

Gypsy moth defoliation of oak trees has been shown to lead to increased tannin levels, which, in turn, lead to reduced gypsy moth growth and fecundity. In laboratory experiments, increased tannin levels can interfere with the transmission of a virus that is consumed by larvae on oak foliage, and high mortality rates of larvae in the field are sometimes associated with low levels of defoliation....

Induced changes in root carbohydrate pools are commonly assumed to determine plant defoliation tolerance to herbivores. However, the regulation and species specificity of these two traits are not well understood. We determined herbivory-induced changes in root carbohydrates and defoliation tolerance in seven different solanaceous plant species and correlated the induced changes in root carbohyd...

Leaf blight and defoliation caused by Cylindrocladium pteridis is one of the main leaf diseases found in Brazilian eucalypt plantations in warm and high rainfall regions. The inter and intraspecific variability in the intensity of defoliation indicate that your control can be achieved by planting resistant genotypes. In order to guide breeding programs and to predict the stability of resistance...

We examined the effects of fertilization and gypsy moth defoliation of hybrid poplar (Populus ×canadensis Moench ‘Eugenei’) on ectomycorrhizal (ECM) and arbuscular mycorrhizal (AM) fungal colonization, ECM richness, and ECM composition in the summers of 1997 and 1998. The factorial experiment included two levels of defoliation (defoliated and control) and fertilization (100 kg N·ha–1 and contro...

We present results from a terrestrial laser scanner (TLS) and mobile mapping system (MMS) based investigation on forest defoliation caused by the European pine sawfly (Neodiprion sertifer) in a Scots pine dominated forest. The TLS and MMS results are compared with simultaneous visual estimation of the defoliation intensity as percentage of needle loss in the living crown. The capability of TLS ...