Input data, analytical methods and biogeography of Elegia (Restionaceae)

Aim The aim of this paper is to determine the optimal methods for delimiting areas of endemism for Elegia L. (Restionaceae), an endemic genus of the Cape Floristic Region. We assess two methods of scoring the data (presence–absence in regular grids, or in irregular eco‐geographical regions) and three methods for locating biogeographical centres or areas of endemism, and evaluate one method for locating biotic elements. Location The Cape Floristic Region (CFR), South Africa. Methods The distribution of all 48 species of Elegia was mapped as presence–absence data on a quarter‐degree grid and on broad habitat units (eco‐geographical areas). Three methods to delimit areas of endemism were applied: parsimony analysis of endemism (PAE), phenetic cluster analysis, and NDM (‘end em ism’). In addition, we used presence–absence clustering (‘Prabclus’) to delimit biotic elements. The performances of these methods in elucidating the geographical patterns in Elegia were compared, for both types of input data, by evaluating their efficacy in maximizing the proportion of endemics and the number of areas of endemism. Results Eco‐geographical areas perform better than quarter‐degree grids. The eco‐geographical areas are potentially more likely to track the distribution of species. The phenetic approach performed best in terms of its ability to delimit areas of endemism in the study area. The species richness and the richness of range‐restricted species are each highest in the south‐western part of the CFR, decreasing to the north and east. The phytogeographical centres identified in the present study are the northern mountains, the southern mountains (inclusive of the Riviersonderend Mountains and the Cape Peninsula), the Langeberg range, the south coast, the Cape flats, and the west coast. Main conclusions This study demonstrates that (1) eco‐geographical areas should be preferred over a grid overlay in the study of biogeographical patterns, (2) phenetic clustering is the most suitable analytical method for finding areas of endemism, and (3) delimiting biotic elements does not contribute to an understanding of the biogeographical pattern in Elegia. The areas of endemism in Elegia are largely similar to those described in other studies, but there are many detailed differences.     

The biogeography of the Anura of sub-equatorial Africa and the prioritisation of areas for their conservation

There is an increasing need for protected areas to conserve biodiversity efficiently. The Anura of sub-equatorial Africa have received little attention, but we quantitatively analyse a database containing presence-only data for anurans of sub-equatorial Africa to determine patterns of distribution and species richness, and discuss the roles of present and past environmental conditions in shaping these patterns. We consider the distribution of areas rich in endemic, range-restricted and Red Data Book (RDB) species to identify areas of significance to conservation. The Eastern Highlands of Zimbabwe and adjacent area in Mozambique, southeastern Malawi and the northern coast of KwaZulu/Natal are particularly species rich, whereas the southwestern Cape of South Africa and northwestern Zambia exhibit high degrees of endemism. Four major biogeographical sub-regions are identified, which can be further subdivided into provinces. All statistically significant, current environmental factors together account for 52.6% of species richness. Annual maximum rainfall, soil type variation, minimum temperature and range of elevation were all positively correlated with species richness. Thus, both habitat influences and history appear to have influenced patterns of anuran richness in the region. Generally, areas of high species richness coincide with those high in range-restricted, endemic and RDB species. In South Africa, the northeastern coast and southwestern Cape are hypothesised to have been both refugia and centres of speciation. Results suggest that the current reserve system in sub-equatorial Africa is inadequate for the conservation of the full complement of anuran species in the region.     

Diversity, endemism and species turnover of millipedes within the south-western Australian global biodiversity hotspot

Aim To examine how current and historical environmental gradients affect patterns of millipede (Diplopoda) endemism and species turnover in a global hotspot of floristic diversity, and to identify regions of high endemism and taxonomic distinctness for conservation management. Location South‐western Australia. Methods Museum database records of millipedes (subclasses Pentazonia and Helminthomorpha), supplemented with extensive fieldwork, were used to map species richness, species turnover (β‐diversity), weighted endemism, average taxonomic distinctness and variation in taxonomic distinctness in half‐degree grid squares (c. 2500 km²). Generalized linear models were used to examine relationships between these parameters with rainfall (present day and historical), topography and human disturbance (clearing for agriculture and urbanization). Results Millipede species richness, particularly within the order Spirostreptida, and millipede endemism were positively associated with large within‐cell differences in elevation (mountainous regions). Large variation in taxonomic distinctness (unevenness in the taxonomic tree) in higher‐rainfall areas was mainly due to speciation within the Spirostreptida genus Atelomastix. Hotspots of millipede endemism and taxonomic distinctness were identified within three categories of importance: primary (Stirling Range East, Cape Le Grand, Cape Arid, Walpole, Porongurups), secondary (Mount Manypeaks, Bremer Bay, Stirling Range West, Duke of Orleans Bay, Ravensthorpe, Albany, Busselton) and tertiary (Nornalup). A species turnover boundary was positively associated with rainfall, broadly located in the transition zone of 300–600 mm year^?1. Main conclusions The current lack of knowledge on the endemism of invertebrates hampers their incorporation into conservation planning. With this knowledge we can identify global biodiversity hotspots and, at a smaller scale, significant conservation areas within a region. Here we have shown that weighted endemism and taxonomic distinctness are useful tools in identifying centres of high endemism and speciation for millipedes within the south‐west Australian hotspot. Moreover, it is unlikely that either vertebrates or vascular plants will be useful surrogates for identifying significant areas for invertebrate conservation. While other workers have shown that vascular plants, mammals and frogs have different centres of endemism within south‐west Australia, our results show that centres of endemism for millipedes encompass all of these plus other areas.     

Key environmental determinants of global and regional richness and endemism patterns for a wild bee subfamily

Reports of world-wide decline of pollinators, and of bees in particular, raise increasing concerns about maintenance of pollination interactions. While local factors of bee decline are relatively well known and potential mitigation strategies at the landscape scale have been outlined, the regional and continental-scale threats to bee diversity have only been marginally explored. Here we document large-scale spatial patterns for a representative bee subfamily, the determinants of its species richness, and assess major threats to these pollinators. Using a comprehensive global dataset of Colletinae (genera Colletes, also called “polyester” or “cellophane” bees for their underground nests lined with a polyester secretion, and Mourecotelles), a species-rich subfamily whose organismal and physiological ecology is representative of many bees, we measured species richness and endemism on global to continental scales. We explored the relationships between bee species richness and potential environmental stress factors grouped into three categories: contemporary climate, habitat heterogeneity, and anthropogenic pressure. Bees of the subfamily Colletinae demonstrate the reversed latitudinal gradient in species richness and endemism suggested for bees; the highest species richness of Colletinae was found between 30° and 50° latitude in both the northern and southern hemispheres. Centres of endemism largely overlapped with those of species richness. The importance of the Greater Cape Floristic Region, previously identified as a centre of richness and endemism of bees, was confirmed for Colletinae. On the global scale, present-day climate was a significant predictor of species richness as was flowering plant diversity represented by vascular plant species richness and centres of plant diversity. Our main conclusion is that climate change constitutes a potential threat to bee diversity, as does declining diversity of vascular plants. However, a significant overlap between centres of bee richness and plant diversity might increase chances for developing conservation strategies.     

Exploring the Afromontane centre of endemism: Kniphofia Moench (Asphodelaceae) as a floristic indicator

Aim The genus Kniphofia contains 71 species with an African–Malagasy distribution, including one species from Yemen. The genus has a general Afromontane distribution. Here we explore whether Kniphofia is a floristic indicator of the Afromontane centre of endemism and diversity. The South Africa Centre of diversity and endemism was explored in greater detail to understand biogeographical patterns. Location Africa, Afromontane Region, southern Africa, Madagascar and Yemen. Methods Diversity and endemism for the genus were examined at the continental scale using a chorological approach. Biogeographical patterns and endemism in the South Africa Centre were examined in greater detail using chorology, phenetics, parsimony analysis of endemicity (PAE) and mapping of range‐restricted taxa. Results Six centres of diversity were recovered, five of which are also centres of endemism. Eight subcentres of diversity are proposed, of which only two are considered subcentres of endemism. The South Africa Centre is the most species‐rich region and the largest centre of endemism for Kniphofia. The phenetic analysis of the South Africa Centre at the full degree square scale recovered three biogeographical areas that correspond with the subcentres obtained from the chorological analysis. The PAE (at the full degree square scale) and the mapping of range‐restricted taxa recovered two and six areas of endemism (AOEs), respectively. These latter two approaches produced results of limited value, possibly as a result of inadequate collecting of Kniphofia species. Only two AOEs were identified by PAE and these are embedded within two of the six AOEs recovered by the mapping of range‐restricted taxa. All the above AOEs are within the three subcentres found by chorological and phenetic analysis (at the full degree square scale) for the South Africa Centre. Main conclusions The centres for Kniphofia broadly correspond to the Afromontane regional mountain systems, but with some notable differences. We regard Kniphofia as a floristic indicator of the Afromontane Region sensu lato. In southern Africa, the phenetic approach at the full‐degree scale retrieved areas that correlate well with those obtained by the chorological approach.     

Patterns and processes of global riverine fish endemism

Aim To explore global patterns of riverine fish endemism by applying an island biogeography framework to river drainage basins and highlight evolutionary mechanisms producing two kinds of endemism: neo‐endemism, arising from within‐drainage cladogenetic speciation, and palaeo‐endemism, arising from species range contraction or anagenetic speciation. Location World‐wide. Methods We use a uniquely comprehensive data set of riverine fish species distributions to map global fish endemism patterns. We then use the relationships between (1) total species richness and proportions of endemic species and (2) total species richness and a measure of in situ (i.e. within‐drainage basin) probability of speciation by cladogenesis, to identify the two distinct forms of endemism. After separating drainage basins into two different sets according to dominance of one of these two forms, we apply a model averaging procedure to highlight, for both datasets, the environmental and historical variables that better explain endemism patterns. We finally analyse the effect of biotic components related to dispersal ability on the percentages of both kinds of endemism among lineages. Results Our results indicate that the two types of endemism are distributed differently across space and taxonomic lineages: (1) neo‐endemism, positively related to the overall richness of the drainage basin, is essentially linked to in situ cladogenetic speciation and is positively related to drainage basin area, negatively related to climate variability since glacial periods and negatively related to all proxies of dispersal ability; and (2) palaeo‐endemism, not directly contributing to drainage basin richness, is a pure process of extinction through range contraction and/or isolation through time and is mostly related to geographic isolation, glacial history and positively related to marine‐derived origin of families. Main conclusions The non‐random spatial and taxonomic distribution of neo‐endemism and palaeo‐endemism sharply reflects the role of evolutionary processes and provides a way to identify areas of high conservation interest based on their high present and future diversification potential.     

Spatial distributions of European Tenebrionidae point to multiple postglacial colonization trajectories

Many studies have found that species richness in the Western Palaearctic follows a latitudinal trend, yet the importance of geographical and ecological factors in shaping species ranges remains obscure. In this article, we present geographical patterns of darkling beetles (Tenebrionidae), a species‐rich group of arthropods. We relate the spatial distributions of species, instead of simply species richness, to spatial and climatic gradients, and test the effects of area (by species–area relationships), latitude (by various climatic gradients) and environmental diversity (by elevation) using simultaneous autoregressive models to identify major correlates of species richness. We then use nestedness and co‐occurrence analyses to identify glacial refugial centres and postglacial dispersal trajectories responsible for current species ranges. Our results indicate the presence of two refugial centres (in the Iberian and Balkan peninsulas) that appear to have been particularly important in shaping extant tenebrionid ranges. Northern countries were selectively colonized by more tolerant and, possibly, more mobile species, which survived in southern refugia during the Pleistocene glacial maxima, whereas the low dispersal capabilities of many species that evolved in these southern isolated areas prevented their spread northwards. High levels of endemism recorded in Spain and Sardinia suggest that the faunas of these regions originated during the Tertiary period and have remained substantially isolated. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, 105 , 318–329.     

An assessment of endemism and species richness patterns in the Australian Anura

Aim To assemble a continental‐scale data set of all available anuran records and investigate trends in endemism and species richness for the Anura. Location Continental Australia. Methods 97,338 records were assembled, covering 75% of the continent. A neighbourhood analysis was applied to recorded locations for each species to measure richness and endemism for each half‐degree grid square (c. 50 km) in the continent. This analysis was performed for all anurans, and also for each of the three main anuran families found in Australia. A Monte Carlo simulation was used to test a null hypothesis that observed centres of endemism could result simply from an unstructured overlapping of species ranges of different sizes. Results Eleven main centres of anuran endemism were identified, the most important being the Wet Tropics and the south‐west near Bunbury‐Augusta and near Walpole. With the exception of south‐western Australia, all of the identified significant endemic centres are in the northern half of the continent. The regions identified as significant for endemism differed from those identified for species richness and are more localized. Species richness is greatest in the Wet Tropics and the Border Ranges. High species richness also occurs in several areas not previously identified along the east and northern coasts. Main conclusions Weighted endemism provides a new approach for determining significant areas for anuran conservation in Australia and areas can be identified that could be targeted for beneficial conservation gains. Patterns in endemism were found to vary markedly between the three main anuran families, and south‐eastern Australia was found to be far less significant than indicated by previous studies. The need for further survey work in inland Australia is highlighted and several priority areas suggested. Our results for species richness remain broadly consistent with trends previously observed for the Australian Anura.     

Areas of endemism and patterns of diversity for aphids of the Qinghai-Tibetan Plateau and the Himalayas

Aim  The study aimed to identify areas of endemism for aphids in the Qinghai-Tibetan Plateau and the Himalayas (QTPH), and to test congruence between patterns of endemism and patterns of overall species richness identified in a previous study.
Location  The QTPH.
Methods  A distribution data base of 326 endemic aphids in the QTPH was compiled. The study area was divided into a grid of 2°× 2° operative geographical units. Parsimony analysis of endemicity (PAE) was used to identify areas of endemism, and the diversity patterns of endemic species were then mapped using GIS.
Results  We identified 326 endemic species belonging to 138 genera within Adelgidae and 14 subfamilies of Aphididae. Five areas of endemism were found using PAE analysis: the eastern Himalayas, the western Himalayas, north-western Yunnan, southern Tibet and the eastern QTPH. Maps of patterns of endemism identified four major centres for endemic aphids, namely the western Himalayas, the eastern Himalayas (or Sikkim-Assam Himalayas), north-western Hengduan Mountains and the mountains of southern Gansu Province, and three minor centres, southern Tibet, south-eastern Tibet and the eastern Qinghai Province in the north-eastern QTPH.
Main conclusions  Our study identifies major centres of aphid endemism. Furthermore, there is a noticeable congruence between patterns of endemism and patterns of species richness. The patterns of endemism were most likely influenced by the recent uplift of the QTPH.     

The implications of different species concepts for describing biodiversity patterns and assessing conservation needs for African birds

It has been suggested that switching from the widely used Biological Species Concept to a Phylogenetic Species Concept, would result in the appearance of hitherto neglected patterns of endemism. The problem has mainly been analyzed with respect to endemic taxa and for rather limited geographical regions, but will here be analysed for the entire resident avifauna of sub-Saharan Africa. A database of African bird distributions was re-edited to create two new datasets representing 1572 biological species and 2098 phylogenetic species. Species richness patterns were virtually identical with the two taxonomies, and only subtle changes were found in the geographical variation in range-size rarity sum. However, there were some differences in the most range-restricted species, with increased complexity of long-recognized centres of endemism. Overall, then, the large-scale biogeographic patterns are robust to changes in species concepts. This reflects the aggregated nature of endemism, with certain areas acting as "species pumps" and large intervening areas being characterised by a predominance of widespread species which distribute themselves in accordance with contemporary environmental conditions. The percentages of phylogenetic and threatened species captured in a BSC near-minimum set of 64 grid-cells and a PSC near-maximum set, with the same number of grid-cells, are very similar.     

The partitioning of Africa: statistically defined biogeographical regions in sub‐Saharan Africa

Aim To test whether it is possible to establish a common biogeographical regionalization for plants and vertebrates in sub‐Saharan Africa (the Afrotropical Region), using objective multivariate methods. Location Sub‐Saharan Africa (Afrotropical Region). Methods We used 1° grid cell resolution databases for birds, mammals, amphibians and snakes (4142 vertebrate species) and c. 13% of the plants (5881 species) from the Afrotropical Region. These databases were analysed using cluster analysis techniques to define biogeographical regions. A β(sim) dissimilarity matrix was subjected to a hierarchical classification using the unweighted pair‐group method with arithmetic averages (UPGMA). The five group‐specific biogeographical regionalizations were compared against a regionalization developed from a combined database, and a regionalization that is maximally congruent with the five group‐specific datasets was determined using a consensus classification. The regionalizations were interpreted against measures of spatial turnover in richness and composition for the five datasets as well as the combined dataset. Results We demonstrate the existence of seven well‐defined and consistent biogeographical regions in sub‐Saharan Africa. These regionalizations are statistically defined and robust between groups, with minor taxon‐specific biogeographical variation. The proposed biogeographical regions are: Congolian, Zambezian, Southern African, Sudanian, Somalian, Ethiopian and Saharan. East Africa, the West African coast, and the transitions between the Congolian, Sudanian and Zambezian regions are unassigned. The Cape area in South Africa, Afromontane areas and the coastal region of East Africa do not emerge as distinct regions but are characterized by high neighbourhood heterogeneity, rapid turnover of species and high levels of narrow endemism. Main conclusions Species distribution data and modern cluster analysis techniques can be used to define biogeographical regions in Africa that reflect the patterns found in both vertebrates and plants. The consensus of the regionalizations between different taxonomic groups is high. These regions are broadly similar to those proposed using expert opinion approaches. Some previously proposed transitional zones are not recognized in this classification.     

The influence of sampling intensity on the perception of the spatial distribution of tropical diversity and endemism: a case study of ferns from Bolivia

The distribution of tropical plant and animal diversity is still poorly documented, especially at spatial resolutions of practical use for conservation. In the present study, we evaluated the level to which geographical incomplete data availability of species occurrence affects the perception of biodiversity patterns (species richness and endemism) among pteridophytes in Bolivia. We used a data base of Bolivian pteridophytes (27,501 records), divided it into three time periods (1900–70, up to 1990 and up to 2006), and created grid-files at 15'-resolution for species richness and endemism. For each of these biodiversity properties we estimated the species richness (Chao 2) and the index of sampling completeness (C index) per grid, and then all these variables at both species richness and endemism were correlated. Patterns of richness were fairly consistent along all periods; the richest areas were placed along the humid-montane forest, even though they were strongly influenced by collecting intensity. Endemism had a lower degree of correlation with collecting intensity, but varied much more strongly through time than species richness. According to the C index, which gives the ratio between estimated (by Chao 2) and recorded values of species richness and endemism, both biodiversity properties tended to be undersampled in the richest grid cells. Inter-temporal correlations showed sharper differences of correlations for endemism than species richness. Consequently, already in 1970, botanists had a correct idea of the spatial distribution of pteridophyte richness in Bolivia (even though the magnitude was grossly underestimated). In contrast, patterns of endemism, which are of high conservation importance, may not even today be reliably known.     

The Greater Cape Floristic Region

Aim The Cape Floristic Region (CFR) (Cape Floristic Kingdom) is currently narrowly delimited to include only the relatively mesic Cape fold mountains and adjacent intermontane valleys and coastal plains. We evaluate the floristic support for expanding the delimitation to include the whole winter‐rainfall area (arid and mesic climates) into a Greater CFR. Location Southern Africa, particularly the south‐western tip. Methods The initial divisive hierarchical classification analysis twinspan used the presence/absence of vascular plant genera to obtain major floristic groupings in southern Africa. For the more detailed analyses, we scored the flora as present/absent within a set of centres, among which the floristic relationships were investigated (agglomerative methods, upgma and minimum spanning trees). These analyses were conducted with species, genera and families separately. The centres were grouped into five regions. The species richness and endemism was calculated for the centres, regions and combination of regions. The dominant floristic components of each region were sought by calculating the percentage contribution of each family to the flora. Results The divisive method showed that the winter‐rainfall areas are floristically distinct from the rest of southern Africa. The species‐ and generic‐level analyses revealed five regions: CFR, Karoo Region, Hantam‐Tanqua‐Roggeveld Region, Namaqualand Region and Namib‐Desert Region. The CFR has the highest endemism and richness. However, the combination of the CFR, the Hantam‐Tanqua‐Roggeveld Region and the Namaqualand Region results in a higher total endemism. Combined, these three regions almost match the region delimited by the twinspan analysis, and together constitute the Greater CFR. Main conclusions The CFR constitutes a valid floristic region. This is evident from the endemism and the distinctive composition of the flora. However, the total endemism is higher for the whole winter‐rainfall area, and this supports the recognition of the larger unit. If floristic regions are to be delimited only on endemism, then the Greater CFR is to be preferred. If floristic regions are delimited on the composition of their floras at family level, then the support for such a grouping is weaker.     

Centres of plant endemism in China: places for survival or for speciation?

Aim This study aimed to identify the ‘centres of endemism’ of the Chinese spermatophyte flora in order to indirectly detect the locations of past glacial refugia. The role of these areas as places for plant survival (‘plant museums’) and/or areas for plant evolution and speciation (‘plant cradles’) was also assessed. Location China. Methods Distribution patterns of 555 plant endemic taxa, taken as a representative sample of the Chinese endemic flora, were mapped on a 1° × 1° latitude/longitude grid. For each grid cell, species richness (total count of species) and weighted richness (down‐weighting each species by the inverse of its range) were calculated. Grid cells within the top 5% of highest values of weighted richness were considered centres of endemism. Based on available information, all plant taxa included in this study were classified into palaeoendemics and neoendemics, and their distributional patterns were represented separately. Results Twenty areas of endemism were identified in central and southern China, roughly corresponding to mountain ranges, including the Hengduan and Daxue Mountains, the Yungui Plateau, central China Mountains, the Nanling Mountains, eastern China Mountains, and Hainan and Taiwan. Although almost all centres of endemism contained both palaeoendemic and neoendemic taxa, considerable differences in their respective numbers were recorded, with the majority of neoendemics on the eastern fringe of the Tibetan Plateau (Hengduan Mountains sensu lato) but more palaeoendemics towards the east. Main conclusions Owing to their varied topography, the mountainous regions of central and southern China have provided long‐term stable habitats, which allowed palaeoendemics to persist and facilitated the process of speciation. Contrasting patterns between the palaeoendemics and neoendemics within refugia might be attributable to the geological and tectonic history of specific areas. The eastern fringe of the Tibetan Plateau clearly constitutes the ‘evolutionary front’ of China, probably as a result of the uninterrupted uplift of the plateau since the late Neogene. In contrast, the tectonic stability of central and southern China during the Tertiary may have facilitated the persistence of relict plant lineages.     

Modelling the geographic distributions of endemic genera in the eastern Central Asian desert

This study simulates the distributions of 13 endemic and near‐endemic genera (Ammopiptanthus, Sympegma, Iljinia, Elachanthemum, Potaninia, Tugarinovia, Kaschgaria, Sarcozygium, Timouria, Zollikoferia, Stilpnolepis, Synstemon and Tetraena) to indicate areas of plant diversity and conservation importance within the eastern Central Asian desert, and to identify the determinant environmental variables contributing to the spatial distribution patterns. Using known distribution localities and 14 environmental variables, the Maxent and Domain species distribution models were employed to map the patterns of geographic distribution. The power of predictability of the models was tested using the receiver operating characteristic method and the jackknife validation approach, according to the different number of species localities available. The estimated richness and the superimposed potential distributions of 13 genera were used to indicate endemic patterns of distribution. The comparison of Maxent and Domain further identified previously unknown areas of endemism and described the distribution for each taxon. Both observed species occurrence and the species occurrence predicted from the Maxent indicated that the eastern Alashan of Inner Mongolia is the most noticeable endemic area, and the northwestern and northern Tarim Basin of Xinjiang is the secondary center of plant diversity. These regions were then prioritized for conservation importance. Potential evapotranspiration ratio and precipitation seasonality played important roles in driving the observed patterns of endemic distribution.     

Phytogeography, range size and richness of Australian endemic Sauropus (Euphorbiaceae)

Aim To investigate the distribution of Australian species of Sauropus. The information obtained is used to (1) identify areas of highest richness and centres of endemism, (2) investigate latitudinal gradients of richness and range size, (3) determine the types of rarity shown, and (4) provide hypotheses on historical biogeography of the genus within Australia. Location Australia. Methods Specimens from 17 herbaria and field searches were examined and label and field information collated on distribution, habit and habitat. Distribution information was used to map all species within 784 grid cells of 1° × 1° and within the 97 Australian ‘ecological regions’. Morphometric cluster analysis of species was conducted using Kulczynski association and flexible UPGMA on 23 character states. Simple regression was used to correlate species richness, density and range size to changes in latitude. CLIMEX is used to match the climate of the region of highest richness in Australia with other areas of the world. Results Species richness was highest within the tropical north of Australia, and most species were associated with tropical savanna woodlands. Two areas were identified as centres of endemism and these corresponded closely to areas of high species richness. Four morphological groups were identified. One species (Sauropus trachyspermus) was found to be widespread, however all other species had small geographical ranges. Species richness and range size were significantly correlated with changes in latitude. Ten species were found to be of the rarest type, warranting conservation initiatives. Main conclusions Two regions of high richness and endemism of Sauropus occur, Thailand and Australia. Within Australia, the Kakadu‐Alligator River and the Cairns‐Townsville areas were identified as centres of endemism and high species richness for Sauropus. Australian Sauropus in general occur in similar communities and climates as other members of the genus elsewhere. Ten of the 27 species of Australian endemic Sauropus are extremely rare and warrant conservation initiatives. Correlations of latitude to species richness are potentially due to Sauropus radiating from the climatically stable top end of Australia. Increasing range size in more southern latitudes may also be due to stability of climates in the top end or because there is more available land area at these latitudes. Sauropus micranthus, the only non‐endemic species, is probably a more recent invader from the Tertiary period when tropical rain forests where more extensive and congruent with those of New Guinea.     

Can distribution models help refine inventory‐based estimates of conservation priority? A case study in the Eastern Arc forests of Tanzania and Kenya

Aim Data shortages mean that conservation priorities can be highly sensitive to historical patterns of exploration. Here, we investigate the potential of regionally focussed species distribution models to elucidate fine‐scale patterns of richness, rarity and endemism. Location Eastern Arc Mountains, Tanzania and Kenya. Methods Generalized additive models and land cover data are used to estimate the distributions of 452 forest plant taxa (trees, lianas, shrubs and herbs). Presence records from a newly compiled database are regressed against environmental variables in a stepwise multimodel. Estimates of occurrence in forest patches are collated across target groups and analysed alongside inventory‐based estimates of conservation priority. Results Predicted richness is higher than observed richness, with the biggest disparities in regions that have had the least research. North Pare and Nguu in particular are predicted to be more important than the inventory data suggest. Environmental conditions in parts of Nguru could support as many range‐restricted and endemic taxa as Uluguru, although realized niches are subject to unknown colonization histories. Concentrations of rare plants are especially high in the Usambaras, a pattern mediated in models by moisture indices, whilst overall richness is better explained by temperature gradients. Tree data dominate the botanical inventory; we find that priorities based on other growth forms might favour the mountains in a different order. Main conclusions Distribution models can provide conservation planning with high‐resolution estimates of richness in well‐researched areas, and predictive estimates of conservation importance elsewhere. Spatial and taxonomic biases in the data are essential considerations, as is the spatial scale used for models. We caution that predictive estimates are most uncertain for the species of highest conservation concern, and advocate using models and targeted field assessments iteratively to refine our understanding of which areas should be prioritised for conservation.     

Biogeographical analysis of the flea beetle genus Chaetocnema in the Afrotropical Region: distribution patterns and areas of endemism

Aim The areal distributions of Chaetocnema species in the Afrotropical Region have been analysed with the aims of determining the distribution patterns (chorotypes) and identifying the most important areas of endemism for this flea beetle genus in sub‐Saharan Africa. Location Data were collected in sub‐Saharan Africa, including Madagascar. Methods The Afrotropical Region was divided into 103 5° quadrats (operative geographical units, or OGUs). A presence–absence matrix of the Afrotropical Chaetocnema species in the OGUs was analysed by cluster analysis (Baroni Urbani & Buser index and the WPGMA clustering method) to generate distribution pattern data based on similarity of distribution. The most important areas of endemism were identified by parsimony analysis of endemicity. Results The general distribution of Chaetocnema in the Afrotropical Region was found to be associated with moist environments and montane grasslands. Most species exhibit restricted geographical ranges. Cluster analysis revealed 120 spatial distributions that can be grouped into 13 distinct distribution patterns (chorotypes). The most important areas of endemism for Chaetocnema in sub‐Saharan Africa according to the present parsimony analysis of endemicity are: (1) central and eastern Madagascar [endemicity rate (ER) = 61.1%], (2) Western Cape Province (ER = 36.4%), (3) southern Drakensberg (ER = 26.7%), (4) the Shaba Region (ER = 16.7%), and (5) the North‐Kivu Region (ER = 5.0%). Main conclusions There are 123 known species of Chaetocnema in the Afrotropical Region, more than in any other zoogeographical region. About 91% of the species are endemic and they generally exhibit a restricted and often very localized geographical range. The remaining 9% of the species are represented by seven species that also inhabit northern Africa and/or the Arabian peninsula (C. bilunulata Demaison, C. ganganensis Bechyné, C. ljuba Bechyné, C. pulla Chapuis, C. tarsalis Wollaston, and C. wollastoni Baly), three species that widely inhabit the Palaearctic Region (C. conducta (Motschulsky), C. schlaeflini (Stierlin), and C. tibialis (Illiger)), and two species that were introduced (C. confinis Crotch, and C. picipes Stephens).     

Patterns of endemism in south-eastern Pacific benthic polychaetes of the Chilean coast

Aim In this study we evaluate patterns of endemism for benthic polychaete species along the southeastern Pacific coast of Chile. Our goals were (1) to describe latitudinal gradients of endemism and identify areas of high endemism, (2) to evaluate the effect of biogeographical limits on endemism patterns, and (3) to evaluate indirectly the role played by evolutionary dynamics on patterns of endemism. Location South‐eastern Pacific coast of Chile, ranging from Arica (18° S) to Cape Horn (56° S). Methods We used a list of 178 species of endemic, shallow benthic polychaetes to evaluate patterns of endemism. Parsimony analysis of endemicity (PAE) and the endemism index (EI) were used to evaluate hierarchical relationships of endemism between different latitudinal bands, and to identify areas with high degrees of endemism and differences in endemism. We evaluated the effect of biogeographical limits on endemic polychaete fauna by testing for the existence of geometric constraints (mid‐domain effect). The role of evolutionary dynamics on latitudinal patterns of endemism was evaluated with nestedness analysis (NA) using the temperature index. Results The PAE analysis indicated two large, separate areas of endemism: (1) the northern area between 18° S and 38° S, and (2) the southern area between 39° S and 56° S. The endemism index showed a maximum value (32 species) around 39°–41° S. Species‐richness curves of each 3° band of latitude showed a clear mid‐domain effect (69%), but the two maximum points of species richness at mid‐latitudes (36° S to 38° S and 39° S to 41° S) did not correspond to the mid‐domain peak in species richness, presenting a greater number of species than expected by the mid‐domain effect. The nestedness analysis showed that the number of genera reaches a maximum of 70 at mid‐latitudes (36°–41° S), decreasing towards both the northern and southern areas. The spatial distribution of the entire data set of endemic species showed a nested pattern (T° = 24.5°, P < 0.0001). Main conclusions Our results strongly support the existence of a latitudinal gradient of endemism for benthic polychaete species along the Chilean coast. The shape of this gradient is clearly non‐linear, with a marked peak of endemism occurring at mid‐latitudes (36°–41° S, endemism hotspot), which also corresponds to a peak in species richness. Furthermore, this hotspot is the midpoint separating two distinct areas of endemism to the north and south. We suggest that the observed pattern of endemism for benthic polychaete taxa of the Chilean coast can be explained by a combination of geometric constraints and historical mechanisms, such as the processes that affected the Chilean coast during the Neogene (e.g. ENSO, oxygen minimum zone, glaciations).     

Centers of endemism and diversity patterns for typhlocybine leafhoppers （Hemiptera： Cicadellidae： Typhlocybinae） in China

This study identifies ＇centers of endemism＇ for typhlocybine leafhoppers in China, revealing diversity patterns and congruence of patterns between total species rich- ness and endemism. Distribution patterns of 774 Typhlocybinae （607 described and 167 undescribed species） were mapped on a 1.5° × 1.5° latitude/longitude grid. Total species richness, endemic species richness and weighted endemism richness were calculated for each grid cell. Grid cells within the top 5% highest values of weighted endemism richness were considered as ＇centers of endemism＇. Diversity patterns by latitude and altitude were obtained through calculating the gradient richness. A congruence of diversity patterns between total species richness and endemism was confirmed using correlation analysis. To investigate the bioclimatic factors （19 variables） contributing to the congruence be- tween total species richness and endemism, we compared the factor＇s difference between non-endemic and endemic species using the Kruskal-Wallis test. Eleven centers of en- demism, roughly delineated by mountain ranges, were identified in central and southern China, including the south Yunnan, Hengduan Mountains, Qinling Mountains, Hainan Is- land, Taiwan Island and six mountain areas located in western Sichuan, northwest Fujian, southeast Guizhou, southeast Hunan, central and western Guangdong, and north Zhejiang. Total species richness and endemic species richness decreased with increased latitude and had a consistent unimodal response to altitude. The proportions of endemism decreased with increased latitude and increased with rising altitude. Diversity patterns between total species richness and endemism were highly consistent, and ＇Precipitation of Coldest Pe- riod＇ and ＇Temperature of Coldest Period＇ may contribute to the congruence of pattern. Migration ability may play a role in the relationship of endemism and species richness; climate, environment factors and important geologic isolation events can also play crucial effect