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The spider fauna active on the bark of trees in forests on eight sites in different regions in Germany was investigated. Trunk eclectors at about 2-4 meters height on living trees were used in different regions of Germany (SW Bavaria, Hesse, Brandenburg) between 1990 and 2003. In Hesse eclectors were also used on dead beech trees (standing and lying). In this study data, mainly from beech (Fagus sylvatica) and spruce (Picea abies), from May to October are compared – whole year samples (including winter) are only available from Hesse. A total of 334 spider species were recorded with these bark traps, i.e. about one third of the spider species known from Germany. On average, each of the eight regions yielded 140.5 (± 26.2) species, each single tree 40.5 (± 12.2) species and 502 (±452) adult spiders per season (i.e. May to Oct.). The 20 most abundant species are listed and characterised in detail. Six of the 20 species were not known to be abundant on bark, three prefer conifers and three beech/broadleaf. Even in winter (December-March) there was a remarkably high activity on the trunks. However, only a few species occur exclusively or mainly in winter. Finally, the rarity of some bark spider species is discussed and details (all known records in Germany, phenology) of four of them are presented (Clubiona leucaspis, Gongylidiellum edentatum, Kratochviliella bicapitata, Oreonetides quadridentatus). The diversity and importance of the spider fauna on bark in Central Europe is still underestimated.
Three different male and female super-specific types are distinguished according to variations in the morphology of the bulb and spermathecae within the genus Nemesia Audouin, 1826. Plotting the distributions of these sexual types on a map of the Mediterranean indicates the existence of geography-related sub-generic diversity in which the Nemesia fauna of the eastern Mediterranean differs markedly from that of the western Mediterranean. While the eastern Mediterranean Nemesia fauna is highly homogeneous, the fauna of the western Mediterranean is very diverse. The eastern and western Nemesia faunae appear to overlap in the central Mediterranean. Efforts to relate the specific bulb types to the particular types of spermathecae described here were only partly successful.
New data on the distribution were the reported: Buksendya river (153º15’E, 59º12’N), Yama valley (152º59’E, 60º00’N) and Nayakhan river (158º15’E, 62º33’N), mostly single birds in late summer, autumn or early winter. Resident breeding pairs regularly occur only in the Chelomdzha and further to the west – in Inya and Ulbeya valleys, and upper heads of the Kava valley (Fig. 1). New observations in the Inya valley (July-August 1999) and in the Chelomdzha valley (July 2003) have proved that the Blakiston’s Fish Owl dwells in lush flood-plain woods along the middle and lower streams of both of these valleys. Currently, the Blakiston’s Fish Owl steadily occurs within the limits of Kava-Chelomdza forestry of the Magadansky State Reserve (Tarkhov & Potapov 1986), and, most likely, the Chelomdzha valley forms currently the north-eastern limit of the species range. In the Chelomdzha valley the regular duet singing of the Blakiston’s Fish Owl begins from early February. Usually the birds display in the evenings, 20-40 min after sunset. The longevity of evening vocalizations increases from 3-5 min in first week of February to 30-50 min in mid-March. The intervals between strophes vary from 14-55 s, 27 s on average (n = 48). The chicks hatched between 2nd and 5th of May. Daytime hours the parents spend nearby the nest in the crowns of larches. During intense chick’s growth the parents visit the nest 4-5 times in a night. Search for food and hunting takes from 40-60 min. According to photo documents, the parents feed the chicks with sculpins and graylings (18–30 cm in length). The parents spend midnight hours nearby the nest. Becoming 50 days old the chicks leave the nest and roams around supervised by the parents.
This review lists Agama smithii Boulenger 1896 as a synonym of Agama agama (Linnaeus 1758), Agama trachypleura Peters 1982 as a synonym of Acanthocercus phillipsii (Boulenger 1895) and describes for the first time Acanthocercus guentherpetersi n. sp. Without more convincing evidence, Chamaeleon ruspolii Boettger 1893 cannot be accepted as specifically distinct from Chamaeleo dilepis Leach 1819, nor Chamaeleo calcaricarens Böhme 1985 from C. africanus Laurenti 1768. Consequently, 101 species of lizard are currently recognised in Ethiopia, of which some 40% appear to be denizens of the Somali-arid zone. This significant proportion is attributable in part to the importance of the Horn of Africa as a centre for reptilian diversification and endemicity, in part to the fact that this lowland fauna was rather extensively sampled during the 1930s, but also to the conspicuous neglect of lizards in other regions of the country. Mountain and forested habitats are widespread in Ethiopia, so it seems extraordinary to record only five saurian species which are believed to be endemic in such environments. The inference that there are many more still to be discovered has important implications for conservation, because montane forest is known to be among the most threatened of Ethiopian biomes and there is clearly an urgent need for its herpetofauna to be more thoroughly researched and documented.
The taxonomy, diversity, and distribution of the aquatic insect order Trichoptera, caddisflies, are reviewed. The order is among the most important and diverse of all aquatic taxa. Larvae are vital participants in aquatic food webs and their presence and relative abundance are used in the biological assessment and monitoring of water quality. The species described by Linnaeus are listed. The morphology of all life history stages (adults, larvae, and pupae) is diagnosed and major features of the anatomy are illustrated. Major components of life history and biology are summarized. A discussion of phylogenetic studies within the order is presented, including higher classification of the suborders and superfamilies, based on recent literature. Synopses of each of 45 families are presented, including the taxonomic history of the family, a list of all known genera in each family, their general distribution and relative species diversity, and a short overview of family-level biological features. The order contains 600 genera, and approximately 13,000 species.
The former and current distribution of the quokka, Setortix brachyurus, was mapped from published and all available unpublished records. At the time of European settlement the quokka was widespread and abundant and its distribution encompassed an area of approximatelyThe former and current distribution of the quokka, Setortix brachyurus, was mapped from published and all available unpublished records. At the time of European settlement the quokka was widespread and abundant and its distribution encompassed an area of approximately 41 200 km2 of south-west Western Australia inclusive of two offshore islands, Bald Island and Rottnest Island. Historical reports indicated an extensive population decline occurred in the 1930s. The decline continued, with a previously undocumented decline apparent in the period from 1980 to 1992. However, this decline may be an artefact of the time scales used for mapping and may well equate with a previously reported decline lor a suite of south -west mammals in the 1970s. By 1992 the quokka´s distribution had been reduced to an area of approximately 17800 km2. An increased awareness of the presence of the quokka on the mainland has resulted in numerous reportings of quokka presence since 1992, has confimled the existence of several populations at the northern extent of the quokka´´s known geographic range and indicated the cmrent, 2005, distribution to be similar to that in 1992. However, survey and population estimates at six of these mainland locations from the northem jarrah forest indicated low abundance. There have been no population estimates elsewhere on the mainland. Two populations have been reported tiom the Swan Coastal Plain, but neither has been confirmed extant. Predation by the introduced fox, Vulpes vulpes, is implicated as a major cause of the quokka´s initial decline, while ongoing predation, habitat destruction and modification through altered tire regimes have contributed to the continued decline. Specific conservation management actions are recommended, namely: (i) Implementing an active adaptive management program in the northern jarrah forest to determine quokka population response to habitat manipulation through the use of fIre, fox baiting and pig control; (ii) Surveying the Stirling fumge and Green Range populations with emphasis placed on determining population size and population genetic structure; (iii) Surveying the reported occurrences from the Swan Coastal Plain, with emphasis on unambiguously determining presence. If confirmed, priority should he directed to assessing population size and determining the management requirements to ensure persistence of the population; (iv) Surveying southem forest and south coast populations to assess quokka population size, the extent of movement between sllbpopulations and assessment of the range of habitat types used by quokkas. The latter should be combined with spatial analyses of known extant populations and suitable and potentially suitable habitat; (v) Determining the role of tire in establishing and maintaining preferred habitat of southern forest and south coast populations; and (vi) Establishing a program to assess the potential effects from management operations.