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    A new species of Trichosalpinx (Orchidaceae: Pleurothallidinae) from Costa Rica
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    Abstract 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).
    Endemism
    Sobralia abadorum (Orchidaceae) - a new orchid species from Peru Sobralia Ruiz & Pav. is one of the largest genus in Orchidaceae. It comprises about 150 species distributed from Mexico to Bolivia. In this paper, a new species of Sobralia from Peru, S. abadorum , is described and illustrated. Its taxonomic affinity is briefly discussed. An analysis of ITS sequences indicates an isolate position of this new species.
    Orchidaceae
    Citations (2)
    Studies on endemism are always of high interest in biogeography and contribute to better understanding of the evolution of species and making conservation plans. The present study aimed to investigate the endemism patterns of planthoppers in China by delimiting centers of endemism and areas of endemism. We collected 6,907 spatial distribution records for 860 endemic planthopper species from various resources. Centers of endemism were identified using weighted endemism values at 1° grid size. Parsimony analysis of endemicity and endemicity analysis were employed to detect areas of endemism at 1°, 1.5°, and 2° grid sizes. Six centers of endemism located in mountainous areas were identified: Taiwan Island, Hainan Island, eastern Yungui Plateau, Wuyi Mountains, western Qinling Mountains, and western Yunnan. We also delimited six areas of endemism, which were generally consistent with centers of endemism. Our findings demonstrated that mountainous areas have an essential role in facilitating the high level of endemism and formation of areas of endemism in planthoppers through the combined effects of complex topography, a long-term stable environment, and geological events. Dispersal ability and distribution of host plants also have important effects on the patterns of planthoppers’ endemism.
    Endemism
    Endemic goitre
    Endemic diseases
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    Abstract Endemic species are important for biodiversity conservation. Yet, quantifying endemism remains challenging because endemism concepts can be too strict (i.e., pure endemism) or too subjective (i.e., near endemism). We propose a data-driven approach to objectively estimate the proportion of records inside a given the target area (i.e., endemism level) that optimizes the separation of near-endemics from non-endemic species. We apply this approach to the Atlantic Forest tree flora using millions of herbarium records retrieved from multiple sources. We first report an updated checklist of 5044 species for the Atlantic Forest tree flora and then we compare how species-specific endemism levels obtained from herbarium data match species-specific endemism accepted by taxonomists. We show that an endemism level of 90% separates well pure and near-endemic from non-endemic species, which in the Atlantic Forest revealed an overall endemism ratio of 45% for its tree flora. We also found that the diversity of pure and near endemics and of endemics and overall species was congruent in space. Our results for the Atlantic Forest reinforce that pure and near endemic species can be combined to quantify regional endemism and therefore to set conservation priorities taking into account endemic species distribution. We provided general guidelines on how the proposed approach can be used to assess endemism levels of regional biotas in other parts of the world.
    Endemism
    Herbarium
    Global biodiversity
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    Abstract Levels of endemism are usually expressed as percentage of endemics among all species recorded in a given area. Endemism levels also vary among taxa, yet inter‐taxon variation in endemism levels has received much less attention. We used the Italian tenebrionids to investigate how endemism levels vary among different but related lineages. We evaluated endemism variations among taxonomic levels both as a percentage of endemics to the number of species included in a given taxon (i.e. the tendency of a taxon to produce endemics) and as a percentage to the total number of species (i.e. the importance of that taxon to the overall endemic component). We also considered the residuals of regression lines of endemics against non‐endemics. We tested the influence of phylogenetic position, lifestyle, and body size on the percentage of endemics within genera. Use of percentages and residuals gave similar outcomes. Pimeliinae were the subfamily with the highest level of endemism. Erodiini, Pimeliini, Tentyriini, Asidini, Opatrini, and Pedinini were among the tribes with the highest endemism levels. Asida , Pimelia , Tentyria, and Opatrum were the genera with the highest levels of endemism. Phylogenetic position and body size affected significantly endemism levels, with genera including larger species being also those with higher endemism, whereas lifestyle was not significant. This suggests that endemism in the Italian tenebrionid beetles is phylogenetically constrained and that lines including larger species (which are possibly less subject to passive dispersal) tend to be richer in endemics, independently from their lifestyle.
    Endemism
    Citations (4)