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Es wird das isolierte Vorkommen einer Acalles micros-Population in einem Buchenwald des Niederbergischen Landes ("Vogelsangbachtal": Deutschland / Kreis Mettmann, NRW) beschrieben. Die Nordgrenze dieser vor allem aus dem nördlichen Mittelmeeraum bekannten, wärmeliebenden Art lag bisher 300 km weiter südlich (Rheinland-Pfalz, Taben-Rodt). Neben einer Differentialdiagnose der Arten Acalles micros, Acalles lemur und Acalles commutatus werden alle Funddaten und eine westpaläarktische Verbreitungskarte von Acalles micros vorgestellt. [Fig. 1] Das nördlichste, isolierte Reliktvorkommen von Acalles micros, das aufgrund der Nähe zum Rhein "fluvial" und wahrscheinlich "postglazial" (warmzeitlich) entstanden ist, war ursprünglich zweifellos bedeutend größer. Vor allem infolge flächenintensiver Rodungen in historischer Zeit wurde der Lebensraum dieser Buchenwaldart erheblich eingeschränkt.
The family Plectopylidae is divided into two subfamilies: Sinicolinae subfam. nov. (included extant genera: Gudeodiscus Páll-Gergely, 2013, Endothyrella Zilch, 1959, Halongella Páll-Gergely, 2015, Sicradiscus Páll-Gergely, 2013, Sinicola Gude, 1899) and Plectopylinae Möllendorff, 1898 (included genera: Chersaecia Gude, 1899, Hunyadiscus Páll-Gergely, 2016, Naggsia Páll-Gergely & Muratov, 2016, Plectopylis Benson, 1860). The Eocene fossil Plectopyloides Yen, 1969 is classified into the Sinicolinae. The Plectopylinae are revised mainly based on historical type and non-type material, and the material of the Florida Museum of Natural History, collected in Thailand in the 1980s. The following species-group taxa are described as new: Chersaecia auffenbergi sp. nov., Chersaecia densegyrata sp. nov., Chersaecia mogokensis sp. nov., Chersaecia reversalis sp. nov., Chersaecia scabra sp. nov., Chersaecia shiroiensis subnagaensis subsp. nov., Hunyadiscus tigrina sp. nov., Naggsia oligogyra sp. nov., Plectopylis crassilabris sp. nov., Plectopylis malayana sp. nov. and Plectopylis thompsoni sp. nov. The genus Endoplon Gude, 1899 is treated as a synonym of Chersaecia. Consequently, the two species classified in Endoplon are members of Chersaecia: Chersaecia brachyplecta (Benson, 1863) comb. nov. and Chersaecia smithiana (Gude, 1897) comb. nov. The genus Plectopylis is redefined, and includes only species with fused anterior and posterior lamellae. Thus, the following species are moved from Plectopylis to Chersaecia: Chersaecia feddeni (Blanford, 1865) comb. nov., Chersaecia goniobathmos (Ehrmann, 1922) comb. nov., Chersaecia leucochila (Gude, 1897) comb. nov., Chersaecia magna (Gude, 1897) comb. nov. and Chersaecia woodthorpei (Gude, 1899) comb. nov. Altogether thirteen species and varieties are moved to the synonymy of valid species: Helix (Plectopylis) brachydiscus Godwin-Austen, 1879 syn. nov., Helix (Plectopylis) ponsonbyi Godwin-Austen, 1888 syn. nov., Plectopylis (Chersaecia) kengtungensis Gude, 1914 syn. nov., Plectopylis (Chersaecia) degerbolae Solem, 1966 syn. nov., Plectopylis lissochlamys Gude, 1897 syn. nov., Helix repercussa Gould, 1856 syn. nov., Plectopylis achatina var. obesa Gude, 1898 syn. nov., Plectopylis achatina var. infrafasciata Gude, 1898 syn. nov. Plectopylis achatina var. venusta Gude, 1898 syn. nov., Plectopylis achatina var. castanea Gude, 1898 syn. nov., Plectopylis achatina var. breviplica Gude, 1898 syn. nov., Plectopylis achatina var. repercussoides Gude, 1899 syn. nov., Plectopylis linterae var. fusca Gude, 1898 syn. nov. Plectopylis (Chersaecia) simplex Solem, 1966 is a subspecies of Chersaecia perarcta (Blanford, 1865), whereas Plectopylis muspratti Gude, 1897 is a subspecies of Chersaecia nagaensis (Godwin-Austen, 1875).
Systematic, faunistic and ecological aspects of the six families and 34 species and subspecies in the order Ephemeroptera currently recorded from Cuba are reviewed based primarily on a reference collection located at the Universidad de Oriente (Santiago de Cuba), collections at the Institute of Ecology and Systematics (Havana) and historic literature. A key to nymphs is included with photographs of significant features of many species. An annotated list of species is presented with comments on type localities, species ecology and distribution. The morpho- ecological types of the nymphs are updated according to current taxonomic changes, and indicator species of organic contamination are analyzed according to the BMWP-Cub index. Based on present data, mayflies are best collected between January and June although many species are present throughout the year, and almost half of the species are widely distributed. Possible routes of penetration from the continents toward Cuba are from South America through the arc of islands formed by the Lesser Antilles, from Central and South America through the peninsula of Yucatan, and via an ancient landspan or island chain from northern South America (GAARlandia). With one exception, there is no evidence for dispersal of species from North America (through Florida) to Cuba (and then to the Antilles) or vice versa. The pattern of geographical distribution of Ephemeroptera inside Cuba is very similar to that of the orders Trichoptera and Odonata. The greatest number of species is found in the Eastern region and the fewest in the Central and Central-East regions. The high endemism (76.5%) is probably due to geographical isolation and processes that bring about this phenomenon together with the low vagility that characterizes the order.
Twelve new species are assigned to the genus Otitoma Jousseaume, 1898 in the family Pseudomelatomidae Morrison, 1966 and herein described: O. hadra sp. nov., O. neocaledonica sp. nov., O. rubiginostoma sp. nov and O. tropispira sp. nov. from New Caledonia; O. boucheti sp. nov., O. nereidum sp. nov. and O. sororcula sp. nov. from the Fiji Islands; O. xantholineata sp. nov. from the Solomon to the Fiji Islands; O. crassivaricosa sp. nov. from Fiji to Hiva Oa Island (Marquesas Archipelago); O. philpoppei sp. nov. from the Philippines but also reported from the Fiji Islands; O. elegans sp. nov. from the Fiji Islands and O. philippinensis sp. nov. from the Philippines. New data on O. carnicolor (Hervier, 1896) are provided. Otitoma mitra (Kilburn, 1986), from Southern Mozambique, is here considered a synonym of O. cyclophora (Deshayes, 1863). Drillia batjanensis Schepman, 1913, previously assigned to the genus Maoritomella Powell, 1942 in the family Borsoniidae Bellardi, 1875, is here assigned to the genus Otitoma. Photographs of the holotype of Drillia batjanensis are provided for the first time. In addition, color photographs of the type specimens of the following species are provided: Drillia kwandangensis Schepman, 1913, D. timorensis Schepman, 1913 and Mitrellatoma mitra Kilburn, 1986.
The frog Pristimantis marmoratus was originally described als Hylodes marmoratus by George A. Boulenger in 1900 based on a single specimen reported to have been collected at the foot of Mount Roraima in Guyana in 1898. We herein discuss the exact location of the type locality of P. marmoratus and provide a redescription of the species based on new material from Kaieteur National Park and from the slopes of Maringma-tepui in Guyana. We also describe the previously unknown vocalization and breeding ecology of the species, and conducted an exploratory molecular analysis of the phylogenetic relationships within the genus Pristimantis represented by the members of the "unistrigatus species group" in the Guiana Shield. Pristimantis marmoratus is a small-sized species mainly distinguished from its known Guiana Shield congeners by the combination of F I < II, SVL ≤ 20.4 in males, presence of vocal slits in males, granular/pustulate dorsal skin with well-developed scapular ridges, basal webbing between fingers, fringes in fingers and toes, crossed iris, diffuse yellow or pale green wash on groin, and absence of flashy colour on axillary/pre-axillary region. The advertisement call consists of a single note repeated at a rate of ca 11 calls/min with a dominant frequency ranging from 2756 to 3101 Hz. Pristimantis marmoratus is primarily arboreal, exclusively active at dusk, and propably restricted to the pristine rainforests of the Pantepui uplands and highlands, east of the Gran Sabana between ca 600 and 1800 m above sea level. Preliminary molecular analyses recovered Pristimantis marmoratus as sister to an unnamed species from the Eastern Guiana Shield. On grounds of the newly established distributional extent we suggest maintaining the IUCN conservation status as Least Concern.
Freshwater is one of the most fundamental resources for life and is the habitat for a wide diversity of species. One of the most diverse aquatic insect taxa is Trichoptera Kirby, 1813, caddisflies. These semi-aquatic insects have aquatic larvae and terrestrial adults and are found all around the globe in freshwater habitats. Water is also one of the most important natural resources for the human population, but alarmingly, freshwaters are among the most threatened natural habitats. Thus, the monitoring and preservation of the quality of freshwater habitats should have a high priority. In order to track changes in the biota a baseline reference is necessary, but freshwater biodiversity is under-studied in many parts of the Earth such as the biodiversity hotspots of the Himalaya and the Hengduan Mountains. This thesis treats the trichopteran genus Himalopsyche Banks, 1940 (Rhyacophilidae) which has its diversity center in the Himalayas and the Hengduan Mountains. Himalopsyche larvae are large and conspicuous and only occur in clean, unpolluted streams. This makes Himalopsyche potentially suited as indicator organisms for freshwater quality monitoring, but taxonomic knowledge is yet insufficient. Based on samples from a field survey in the Hengduan Mountains targeting both larvae and adults I uncovered three new Himalopsyche species which are described in this thesis (Chapter II), and with the aid of molecular data I associated larvae of Himalopsyche to adult species (Chapter I). The molecular association enabled the first comparative morphological study of Himalopsyche species in the larval stage, and the morphological study in Chapter II revealed that there are four distinct larval types of Himalopsyche. However, no diagnostic characters to identify Himalopsyche larvae to species level were found. To understand Himalopsyche larval morphology from an evolutionary perspective, I reconstructed the first molecular phylogeny of the genus (Chapter III). This demonstrated that each larval type corresponds to a deep phylogenetic split, indicating that larval types evolved early in Himalopsyche evolution and remained constant since. Based on the phylogenetic results as well as larval and adult morphology, I re-defined five species groups of Himalopsyche: H. kuldschensis Group, H. lepcha Group, H. navasi Group, H. phryganea Group, and H. tibetana Group. The species groups differ with respect to their diversity centers. The monotypic H. lepcha Group resides in the Himalayas, and the monotypic H. phryganea Group inhabits Western Nearctic. The H. kuldschensis and H. tibetana Groups are geographically overlapping with distributions in the Himalayas, but the distribution of H. kuldschensis Group stretches more to the west to include the Tian Shan, and the H. tibetana Group is more concentrated around the eastern Himalayas and the Hengduan Mountains. The H. navasi Group has a more eastern distribution than most Himalopsyche including isolated areas such as Japan and Indonesia. The earliest split in Himalopsyche divides the H. navasi Group from remaining Himalopsyche, suggesting a more eastern area of origin of Himalopsyche than its current diversity center, with subsequent radiations in the Himalayas and Hengduan Mountains. In addition to the three chapters, in this thesis I discuss further aspects of Himalopsyche biology including genital evolution, species complexes, and Himalopsyche ecology.
Genera of Cryptognathini (Coleoptera: Coccinellidae) are discussed and a key to all recognized genera is provided. Cryptognatha is revised, and species of this genus are keyed. New species, authored by González and Hanley, are Cryptognatha pam, C. kellie, C. hannah, C. whitney, C. karla, C. celia, C. shelia, C. gayle, C. della and C. vicki. The following new synonymies are proposed: Cryptognatha simillima Sicard = Cryptognatha gemellata Mulsant, Cryptognatha fryii Crotch = Cryptognatha pudibunda Mulsant, Cryptognatha bryanti Brèthes = Cryptognatha pudibunda Mulsant. Lectotypes are here designated for Cryptognatha amicta Gorham, C. weisei Brèthes, C. pudibunda Mulsant and C. fryii Crotch.
The new genus Neotrichaphodioides and the new species N. woytkowskii from Peru are described. Aphodius caracanus Balthasar, A. ecuadoriensis Petrovitz, A. forsterianus Balthasar, and A. volxemi Harold are redescribed and figured, and transferred into Neotrichaphodioides, all becoming new combinations. New synonymies of Aphodius martinsi Petrovitz with N. caracanus (Balthasar) and Aphodius squamifer Petrovitz with N. volxemi (Harold) are presented. The lectotype of A. volxemi is here designated.