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All species that have been described of the genera mentioned in the title are listed and their systematic position given. The species of Stilifer (with 11 species, including S. inflatus sp.n. and 5. concavus sp.n.) are parasites of starfishes. Scalenostoma (3 species) are parasites of stone corals. Thyca (with 8 species) is removed from Capulidae, and included in Eulimidae. T. hawaiiensis sp.n. is described. The species of Thyca are parasites of starfishes. The species of Mucronalia (including M. trilineata sp.n.) are probably parasites of ophiuroids and Echineulima (with 4–6 species, including E. ponderi sp.n.) are parasites of echinoids. All species are figured, their characteristics are given and their host species and distributions are listed. Keys are given to the species of each genus, except Mucronalia. The genera Stilimella Laseron and Hyperlia Pilsbry are synonymized with Scalenostoma and the genera Kiramodulus Kuroda, Granulithyca Habe and Bessomia Berry are considered subgenera of Thyca.  相似文献   
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Tree planting in the tropics is conducted for a number of reasons including carbon sequestration, but often competes with increasingly scarce water resources. The basics of forest and water relations are frequently said to be well understood but there is a pressing need to better understand and predict the hydrological effects of land‐use and climate change in the complex and dynamic landscapes of the tropics. This will remain elusive without the empirical data required to feed hydrological process models. It is argued that the current state of knowledge is confused by too broad a use of the terms ‘forest’ and ‘(af)forestation’, as well as by a bias towards using data generated mostly outside the tropics and for nondegraded soil conditions. Definitions of forest, afforestation and reforestation as used in the climate change community and their application by land and water managers need to be reconciled.  相似文献   
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Starting with Volume 7, Lethaia will use its pages better by introducing a two-column type area. The amount of text published without charges will remain the same as in preceding volumes, but any optional publication charges received or profit attained will be invested in more pages. To our- authors the new arrangement implies one simple but important change, namely adjustment of published figure size to the page width (140 mm) or column width (67.5 mm) whenever possible. New elements for bibliographic identification ( biblid ) are added to the cover, article-heads, and individual pages.  相似文献   
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Ecological and evolutionary consequences of host–parasite interactions have attracted considerable attention from evolutionary biologists. Previous studies have suggested that immune responsiveness may be genetically or developmentally linked with colour pattern, such that the evolution of animal colour patterns may be influenced by correlated responses to selection for parasite resistance. We studied interactions between the endoparasitic fly Leiophora innoxia (Meigen) (Diptera: Tachinidae) and its colour polymorphic pygmy grasshopper host Tetrix undulata (Sow.) (Orthoptera: Tetrigidae) to test for morph‐specific differences in parasitization and immune defence, and host‐induced variation in parasite phenotypes. Our results revealed that c. 2 and 30% of adult grasshoppers collected from the same natural population in two subsequent years, respectively were parasitized. Parasite prevalence was independent of host sex and colour morph. Pupae were larger if the parasite had developed in a female than in a male host, possibly reflecting host resource value or a physical constraint on larval growth imposed by host body size. Pupal size was also associated with host colour morph, with individuals that had developed in dark morphs being smaller at pupation compared to those that developed in paler morphs. However, immune defence, measured as the encapsulation response to a novel antigen, did not differ among individuals belonging to alternative colour morphs or sexes. Darker morphs warm up more quickly and prefer higher body temperatures than paler ones. Encapsulation was not influenced by maintenance temperature (15 vs. 30 °C), however, suggesting that indirect effects of coloration on parasite resistance mediated via differential body temperature are unlikely. The dependence of parasite body size on host colour morph may thus reflect plasticity of growth and development of the larvae in response to differential host body temperature, rather than variable host immune defence. © 2005 The Linnean Society of London, Biological Journal of the Linnean Society, 2005, 85 , 373–383.  相似文献   
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