The mosses of sub-Saharan Africa : 2., endemism and biodiversity

Based on a recent moss checklist of sub-Saharan Africa, an analysis is made of moss diversity and endemism in the area. There are over 3000 taxa, 77% of which are endemic. Figures for diversity and endemism for each country are listed, mapped and graphed, and endemism is also considered at the genus level. As the bryophyte flora of Africa is comparatively poorly known, it is important to be prudent when drawing conclusions about biodiversity and endemism

Modelling biodiversity scenarios in madagascar under both the effects of climate change and anthropogenic deforestation

Madagascar is widely known for its exceptional biodiversity which is, for the terrestrial part, mainly concentrated in tropical forests. This biodiversity is severely threatened by both climate change and deforestation. The FRB (Fondation pour la Recherche sur la Biodiversité) project named BioSceneMada (http://bioscenemada.net) aims at modelling the biodiversity scenarios in Madagascar under both the effects of climate change and anthropogenic deforestation. In this study we present the first results of the project. We used presence data for more than 5000 species and bioclimatic envelope models to forecast species distribution under the effects of climate change. Species distribution maps were used to identify potential refugia for biodiversity. Combining these results to the projections of a deforestation model, we also identified the potential biodiversity hotspots under a high risk of deforestation. Project results should help define efficient strategies for conserving Madagascan biodiversity. In particular, we promote the inclusion of top priority areas for biodiversity conservation into the current Madagascar protected areas system

An optimality criterion to determine areas of endemism

A formal method was developed to determine areas of endemism. The study region is divided into cells, and the number of species that can be considered as endemic is counted for a given set of cells (= area). Thus, the areas with the maximum number of species considered endemic are preferred. This is the first method for the identification of areas of endemism that implements an optimality criterion directly based on considering the aspects of species distribution that are relevant to endemism. The methodis implemented in two computer programs, NDM and VNDM, available from the authors. © 2002 Society of Systematic Biologists.Fil: Szumik, Claudia Adriana. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Tucumán. Facultad de Ciencias Naturales e Instituto Miguel Lillo. Instituto Superior de Entomología; ArgentinaFil: Cuezzo, Fabiana del Carmen. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Tucumán. Facultad de Ciencias Naturales e Instituto Miguel Lillo. Instituto Superior de Entomología; ArgentinaFil: Goloboff, Pablo Augusto. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Tucumán. Facultad de Ciencias Naturales e Instituto Miguel Lillo. Instituto Superior de Entomología; ArgentinaFil: Chalup, Adriana Elizabeth. Universidad Nacional de Tucumán. Facultad de Ciencias Naturales e Instituto Miguel Lillo. Instituto Superior de Entomología; Argentin

Madagascar's grasses and grasslands:anthropogenic or natural?

Grasses, by their high productivity even under very low pCO2, their ability to survive repeated burning and to tolerate long dry seasons, have transformed the terrestrial biomes in the Neogene and Quaternary. The expansion of grasslands at the cost of biodiverse forest biomes in Madagascar is often postulated as a consequence of the Holocene settlement of the island by humans. However, we show that the Malagasy grass flora has many indications of being ancient with a long local evolutionary history, much predating the Holocene arrival of humans. First, the level of endemism in the Madagascar grass flora is well above the global average for large islands. Second, a survey of many of the more diverse areas indicates that there is a very high spatial and ecological turnover in the grass flora, indicating a high degree of niche specialization. We also find some evidence that there are both recently disturbed and natural stable grasslands: phylogenetic community assembly indicates that recently severely disturbed grasslands are phylogenetically clustered, whereas more undisturbed grasslands tend to be phylogenetically more evenly distributed. From this evidence, it is likely that grass communities existed in Madagascar long before human arrival and so were determined by climate, natural grazing and other natural factors. Humans introduced zebu cattle farming and increased fire frequency, and may have triggered an expansion of the grasslands. Grasses probably played the same role in the modification of the Malagasy environments as elsewhere in the tropics

Deep-sea coral distribution on seamounts, oceanic islands, and continental slopes in the Northeast Atlantic

A database of deep-water (\u3e 200 m) antipatharians, scleractinians, and gorgonians has been assembled for the NE Atlantic to determine what their distribution and diversity was before coral habitats became heavily impacted by bottom fishing gear. Benthic sampling expeditions from 1868–1985 have provided 2547 records showing the deepwater distribution of 22 species of antipatharians, 68 species of scleractinians, and 83 species of gorgonians with the majority of records found from seamounts, oceanic islands, and the continental slope of the warm temperate region. Too little is known about the coral biota of boreal and tropical seamounts to assess their levels of endemism, but on seamounts in the warm temperate region of the NE Atlantic the level endemism in antipatharian, scleractinian and gorgonian corals is low (\u3c 3%). Many of the species found on seamounts are characteristic of oceanic islands in this region and the oceanic islands have a significantly different coral fauna to that recorded at the same depths on the continental slope. Given the key role that corals can play in structuring deep-sea habitats it is hoped that our database will help inform the development of a network of marine protected areas to provide long-term protection for the differing communities found on continental slopes and isolated offshore habitats

Origins of neotropical leafy Hepaticae

The neotropical hepatic flora, predominantly constituted by members of the Jungermanniales and Metzgeriales, includes a disproportionate number of genera which are endemic (over 38) and a number which evidently originated here but have shown slight and in a geological sense, modern dispersal by solitary species. Endemism is confined almost to the Jungermanniales; it is to a large degree of a unique sort: confined to highly apomorphic derivatives, often extremely reduced, sometimes confervoid or thalloid (aside from 'normal' sexual branches). These endemics are derivatives of basically cool-Gondwanalandic suborders, chiefly Lepidoziineae and Cephaloziineae which, in the Antipodes today include a wide range of plesiomorphic taxa. The highest proportion of endemic genera, often stenotypic (1-3 species each) occurs in the upper montane zone: from upper Andean forest to páramo, to the edge of permanent snow and ice; a smaller number occurs at upper elevations of the Guyana Shield, but more occur in the riverine systems that dissect this shield. The taxa found there (i.a., Zoopsidella, Pteropsiella, Schusterolejeunea, Cephalantholejeunea) are among the most apomorphic of all hepatics. The amount of endemism is shown to be higher than in any comparable region of the globe. It is assumed that this is owing to: (a) isolation, exceeding 40 m.y. and probably exceeding 60 m.y.; (b) continuous tectonic activity, preserving the 'raw' and 'pioneer' habitats which are necessary for the survival of 'fugitive', 'shuttle' and other types of pioneer taxa; (c) the antiquity of the Guyana Shield and its riverine system; (d) creation of striking ecological gradients, many biotic islands; (e) fluctuation in extent and degree of isolation of these 'islands', leading to (f) rapid evolution due to genetic drift and perhaps enhanced selection pressures. It is concluded that part of the complexity of the flora is due to preservation of some elements on the old Guyana Shield but most is due to relatively rapid evolution during Tertiary times. A final contributing element has been the fact that movement of the South American plate has been primarily from east to west, so that the relevant land area has not been rafted into regions with very different climatic parameters: the degree of extinction seen in, e.g., India and Australia is not evident here. It is concluded that the amount of endemism seen, and its extreme kinds, 'need' in excess of the 40-60 m.y. time span which seems available. In particular, the large number of high elevation endemics, some (such as Ruizanthus) very isolated, cannot be satisfactorily explained by assuming their evolution in the few million years available since alpine regions were created by the rise of the Andes. It is almost necessary to conclude that limited 'pre-Andes' must have existed and that the ancestors of the isolated taxa seen today in alpine loci in Colombia and Venezuela originated elsewhere. The other side of the outlined scenario is that with the near-total isolation of tropical America until the Andes were elevated, and until the Pliocene connection to North America arose, one would expect to see few and scattered intruders from cool-Gondwanalandic areas and from Laurasia. The modern flora reflects exactly this

The apterous endemic genus Omphra Dejean (Coleoptera: Carabidae: Helluonini) of the Indian subcontinent : taxonomy with notes on habits and distributional patterns

Among the four oriental genera of the tribe Helluonini, Omphra Dejean (Coleoptera: Carabidae), is unique for its endemism to the Indian subcontinent and aptery. High intraspecies variability in morphological characters and limited diagnostic information makes species differentiation of the genus Omphra a complicated task. The present study provides a description of a new species, Omphra drumonti n. sp. from the Western Ghats, redescriptions and a key to the species of Omphra, details of intraspecies variation, discussion of relationships between taxa and distributional patterns of the genus. Based on the distributional patterns in the Indian subcontinent and flightlessness of the genus, inability to cross the physical barrier of the Ganges–Brahmaputra delta between north and peninsular India is indicated as the reason for its absence in the northeastern Indian subcontinent and endemism to the lower Indian subcontinent

Pole-to-Pole Connections : Similarities between Arctic and Antarctic Microbiomes and Their Vulnerability to Environmental Change

Acknowledgments JK acknowledges the Carl Zeiss foundation for PhD funding, the Marie-Curie COFUND-BEIPD PostDoc fellowship for PostDoc funding, FNRS travel funding and the logistical and financial support by UNIS. JK and FK acknowledge the Natural Environment Research Council (NERC) Antarctic Funding Initiative AFI-CGS-70 (collaborative gearing scheme) and logistic support from the British Antarctic Survey (BAS) for field work in Antarctica. JK and CZ acknowledge the Excellence Initiative at the University of Tübingen funded by the German Federal Ministry of Education and Research and the German Research Foundation (DFG). FH, AV, and PB received funding from MetaHIT (HEALTH-F4-2007-201052), Microbios (ERC-AdG-502 669830) and the European Molecular Biology Laboratory (EMBL). We thank members of the Bork group at EMBL for helpful discussions. We acknowledge the EMBL Genomics Core Facility for sequencing support and Y. P. Yuan and the EMBL Information Technology Core Facility for support with high-performance computing and EMBL for financial support. PC is supported by NERC core funding to the BAS “Biodiversity, Evolution and Adaptation” Team. MB was funded by Helge Ax:son Johnsons Stiftelse and PUT1317. DRD acknowledges the DFG funded project DI698/18-1 Dietrich and the Marie Curie International Research Staff Exchange Scheme Fellowship (PIRSES-GA-2011-295223). Operations in the Canadian High Arctic were supported by the Natural Sciences and Engineering Research Council of Canada (NSERC), ArcticNet and the Polar Continental Shelf Program (PCSP). We are also grateful to the TOTAL Foundation (Paris) and the UK NERC (WP 4.3 of Oceans 2025 core funding to FCK at the Scottish Association for Marine Science) for funding the expedition to Baffin Island and within this context Olivier Dargent and Dr. Pieter van West for sample collection, and the Spanish Ministry of Science and Technology through project LIMNOPOLAR (POL200606635 and CGL2005-06549-C02-01/ANT to AQ as well as CGL2005-06549-C02-02/ANT to AC, the last of these co-financed by European FEDER funds). We are grateful for funding from the MASTS pooling initiative (The Marine Alliance for Science and Technology for Scotland), funded by the Scottish Funding Council (HR09011) and contributing institutions. Supplementary Material The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fevo.2017.00137/full#supplementary-materialPeer reviewedPublisher PD

Endemic harvestmen and spiders of Austria (Arachnida: Opiliones, Araneae)

A comprehensive overview of plant, fungus and animal species of Austria revealed a total of 748 endemic and subendemic species, including, 11 harvestman and 46 spider species. Altogether two endemic harvestmen (Nemastoma bidentatum relictum, Nemastoma schuelleri) and 8 endemic spiders (Abacoproeces molestus, Collinsia (caliginosa) nemenziana, Mughiphantes severus, Mughiphantes styriacus, Pelecopsis alpica, Scotophaeus nanus, Troglohyphantes novicordis, Troglohyphantes tauriscus), beside 9 subendemic harvestman and 38 subendemic spider species have been recorded from Austria. Hot-spots of endemism in the Eastern Alps are the north-eastern (Ennstaler Alps) and southern Calcareous Alps (Karawanken, Karnische Alps) and the Central Alps (Hohe Tauern, Gurktaler Alps, Ötztaler and Stubaier Alps). Most of the endemic arachnid species occur from the nival down to the montane zone. Important habitats are rocky areas, caves and woodlands. High absolute numbers and percentages of endemics can be found within the harvestman families Cladonychiidae, Ischyropsalididae and Nemastomatidae and in the spider genera Lepthyphantes s. l. and Troglohyphantes. The conservation status of these highly endangered taxa – 85 % of the spider species and 100 % of the harvestman taxa are endangered in Austria – is poor