Large tracts of tropical rainforests are being converted into intensive agricultural lands. Such anthropogenic disturbances are known to reduce species turnover across horizontal distances. But it is not known if they can also reduce species turnover across vertical distances (elevation), which have steeper climatic differences. We measured turnover in birds across horizontal and vertical sampling transects in three land-use types of Sri Lanka: protected forest, reserve buffer and intensive-agriculture, from 90 to 2100 m a.s.l. Bird turnover rates across horizontal distances were similar across all habitats, and much less than vertical turnover rates. Vertical turnover rates were not similar across habitats. Forest had higher turnover rates than the other two habitats for all bird species. Buffer and intensive-agriculture had similar turnover rates, even though buffer habitats were situated at the forest edge. Therefore, our results demonstrate the crucial importance of conserving primary forest across the full elevational range available.
1. The conversion of rainforests into agriculture resulted in massive changes in species diversity and community structure. Although the conservation of the remaining rainforests is of utmost importance, identifying and creating a biodiversity-friendly agriculture landscape is vital for preserving biodiversity and their functions.2. Biodiversity studies in agriculture have often been conducted at low elevations.In this study, we compared the functional diversity (FD), phylogenetic diversity (PD) and community structure of birds along an interacting gradient of land use (protected rainforest, reserve buffer and agriculture) and elevation (low, middle and high) in Sri Lanka. Then, we measured the compositional change by identifying how ecological traits (dietary guild, vertical strata, body mass and dispersal ability) and conservation characteristics (forest dependence and threatened status) responded to land use types.3. Elevation and land use interacted with each other to shape bird FD. Depending on the elevation, FD in agriculture was either higher or similar to forest. However, PD was similar across all elevation and land use types. Bird community structure in forest was functionally and phylogenetically clustered in comparison to agriculture.Insectivorous birds declined from forest to agriculture, and so did understorey and middle-storey birds. But frugivorous and canopy birds did not change across land use types, while nectarivores, granivores and carnivores proliferated in agriculture.Forests were dominated by birds with low dispersal abilities, but birds in agriculture had more evenly distributed dispersal abilities. About half of all the individuals in agriculture were composed of forest species, several of which were threatened. 4. Synthesis and applications. Most farmers in Sri Lanka practice agriculture on small farms (c. 2 ha) and rely on services (e.g. pest control and pollination) provided by | 1739
In this paper we record a likely instance of ovo-viviparity in a chlorocyphid damselfly from south-western China. If confirmed, this will be the first record of live birthing in the Odonata: indeed in any member of the Palaeoptera. The widespread Asian damselfly Heliocypha perforata (Percheron, 1835) is proposed to be, at least facultatively, viviparous. A female was observed and filmed appearing to deposit prolarvae directly onto the exposed surface of a half-submerged branch in a small stream in Xishuangbanna Autonomous Dai Prefecture, Yunnan, China. The species is known to deposit eggs in bark crevices close to water but no previous case of actual live births is known.
A single adverse environment event can threaten the survival of small‐ranged species while random fluctuations in population size increase the extinction risk of less‐abundant species. The abundance–range‐size relationship (ARR) is usually positive, which means that smaller‐ranged species are often of low abundance and might face both problems simultaneously.
The ARR has been reported to be negative on tropical islands, perhaps allowing endemic species in such environments to remain extant. But there is a need to understand how endemism and land‐use interact to shape ARR.
Using 41 highly replicated transects along the full elevational gradient of Sri Lanka, we determined the following: (a) the direction of ARR, (b) if endemism affects ARR and (c) if land‐use (rainforest, buffer and agriculture) changes ARR differently for endemics and non‐endemics. Additionally, (d) we identified endemics that had both lower abundances and smaller range sizes, and ranked them from most threatened (specific to rainforests) to least threatened using a weighted‐interaction nestedness estimator.
(a) We found a positive relationship between species abundances and range size. This positive ARR was maintained among endemic and non‐endemic species, across land‐use types and at local and regional scales. (b) The ARR interacted with endemicity and land‐use. Endemics with smaller range sizes had higher abundances than non‐endemics, and particularly higher in rainforests compared to agriculture. In contrast, species with larger range sizes had similar abundances across endemicity and land‐use categories. Many endemics with smaller range sizes are globally threatened; therefore, higher abundances may buffer them from extinction risks. (c) Nine (29%) endemics had both below average abundance and elevational range size. The nestedness estimator ranked the endemics Sri Lanka Whistling Thrush Myophonus blighi, Red‐faced Malkoha Phaenicophaeus pyrrhocephalus, Sri Lanka Thrush Zoothera imbricata and White‐faced Starling Sturnornis albofrontus as the four most vulnerable species to local extinction risk, which corresponds to their global extinction risk.
We demonstrate that ARR can be positive on tropical islands, but it is influenced by endemism and land‐use. Examining shifts in ARR is not only important to understand community dynamics but can also act as a tool to inform managers about species that require monitoring programmes.
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