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Titlebook: Biology of Chrysomelidae; P. Jolivet,E. Petitpierre,T. H. Hsiao Book 1988 Kluwer Academic Publishers 1988 Fauna.Pathogen.Plantation.Viren.

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https://doi.org/10.1007/978-3-658-18277-9t orders contain monophagous species, adult and larval resources are often different (Mitchell 1981, Price 1975). For example, in monophagous Lepidoptera. adult butterflies require nectar or pollen for their metabolic maintenance. Adult flight and alighting behaviors are commonly phasic, and flight
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https://doi.org/10.1007/978-3-322-85236-6requency of the cyaneus-form, but some populations from the Pacific coast (Suzuki et al. 1976. Suzuki and Sakurai 1977, 1978, Suzuki and Ozaki 1980) and from mountainous areas (Fujiyama 1979) have a high frequency of the cupreous-form. Thirdly, although neighbouring populations usually show similar
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Kommunikationskulturen der Weltgesellschaftinae use this jumping ability voluntarily in a very effective manner to avoid potential predators or entomologists. Lindroth (1971) observed that birds are not able to catch Flea Beetles that are on foliage because of the beetle’s effective escape by jumping. Jumping also serves as an efficient meth
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Food Habits and Food Selection of Chrysomelidae. Bionomic and Evolutionary Perspectivesnfortunately, we also do not know much about Australian host-plants of Chrysomelidae. Only in Asia, in South America and to a lesser extent in continental Africa, have the relationships Insects/Plants been rather well explored. If the New World Tropics have more species of plants than the rest of th
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The Origins of the Alticinaeontinental drift, supported by many other sciences, and an increase in knowledge of the Tertiary and Pleistocene also gives insight into the origin of the Alticinae. As Darlington (1957) has written: ‘If the geographical distribution of some animal taxon is to be used for testing a phylogenetic clas
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Genetics of the two colour forms of , (Mannerheim) (Coleoptera: Chrysomelidae) and their gene frequerequency of the cyaneus-form, but some populations from the Pacific coast (Suzuki et al. 1976. Suzuki and Sakurai 1977, 1978, Suzuki and Ozaki 1980) and from mountainous areas (Fujiyama 1979) have a high frequency of the cupreous-form. Thirdly, although neighbouring populations usually show similar
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The jumping apparatus of flea beetles (Alticinae) — The metafemoral springinae use this jumping ability voluntarily in a very effective manner to avoid potential predators or entomologists. Lindroth (1971) observed that birds are not able to catch Flea Beetles that are on foliage because of the beetle’s effective escape by jumping. Jumping also serves as an efficient meth
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