Biodiversity continues to decline in the face of increasing anthropogenic pressures such as habitat destruction, exploitation, pollution and introduction of alien species. Existing global databases of species’ threat status or population time series are dominated by charismatic species. The collation of datasets with broad taxonomic and biogeographic extents, and that support computation of a range of biodiversity indicators, is necessary to enable better understanding of historical declines and to project – and avert – future declines. We describe and assess a new database of more than 1.6 million samples from 78 countries representing over 28,000 species, collated from existing spatial comparisons of local-scale biodiversity exposed to different intensities and types of anthropogenic pressures, from terrestrial sites around the world. The database contains measurements taken in 208 (of 814) ecoregions, 13 (of 14) biomes, 25 (of 35) biodiversity hotspots and 16 (of 17) megadiverse countries. The database contains more than 1% of the total number of all species described, and more than 1% of the described species within many taxonomic groups – including flowering plants, gymnosperms, birds, mammals, reptiles, amphibians, beetles, lepidopterans and hymenopterans. The dataset, which is still being added to, is therefore already considerably larger and more representative than those used by previous quantitative models of biodiversity trends and responses. The database is being assembled as part of the PREDICTS project (Projecting Responses of Ecological Diversity In Changing Terrestrial Systems – http://www.predicts.org.uk). We make site-level summary data available alongside this article. The full database will be publicly available in 2015.

The PREDICTS project—Projecting Responses of Ecological Diversity In Changing Terrestrial Systems (www.predicts.org.uk)—has collated from published studies a large, reasonably representative database of comparable samples of biodiversity from multiple sites that differ in the nature or intensity of human impacts relating to land use. We have used this evidence base to develop global and regional statistical models of how local biodiversity responds to these measures. We describe and make freely available this 2016 release of the database, containing more than 3.2 million records sampled at over 26,000 locations and representing over 47,000 species. We outline how the database can help in answering a range of questions in ecology and conservation biology. To our knowledge, this is the largest and most geographically and taxonomically representative database of spatial comparisons of biodiversity that has been collated to date; it will be useful to researchers and international efforts wishing to model and understand the global status of biodiversity.

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SummaryFrugivorous White-ruffed ManakinsCorapipo leucorrhoa(Pipridae) showed pro nounced seasonal emigration from a pre-montane wet forest site (550 m) on the Atlantic slope of Costa Rica. “Resident” breeders left the area between August and October, and returned between February and April, at the onset of the breeding season. Female patterns differed from those of males primarily in later departure (October) and later return (April). I documented 57 fruit species in the diet at this locality and monitored phenology for 43 of those species, many of which were understorey members of the Melastomataceae. The emigration did not coincide with a period of local fruit shortage (relative to abundance at the same locality in other months), but the relative abundance and species composition of fruit resources in the areas to which the manakins migrated remains unknown. However, peak resources did coincide with the period in which recent fledglings would be commonest and the period during which most individuals were moulting prior ot emigration. Resources were lowest from November, when residents were absent, untilJune, well into the breeding season. Tentative evidence suggests considerable annual variation, possibly owing to differences in the timing of the rainy season. Individuals captured during the period when almost all “resident” breeders were absent (November) appeared to be transients, and were rarely recaptured. Weights differed between sexes, with females (χ = 12.5 ± 1.0) significantly heavier than males (χ = 11.1 ± 0.8). Males were lightest during the breeding season, intermediate in weight during the moulting period, and both sexes were heaviest during the migration period, when they accumulated subcutaneous fat. Females were lightest during the moult period, at which time many may also have dependent fledglings. Many other frugivores and nectarivores may engage in similar altitudinal migrations. Even where altitudinal migration is not possible, birds might migrate to other habitats with different fruit resources or phenologies. The design of nature reserves should accommodate the possibility of significant altitudinal (or cross-habitat) migration for many species of frugivores and nectarivores.

We studied the relationship between group and individual display in the courtship and social system of the White-ruffed Manakin (Corapipo leucorrhoa altera) in the Atlantic slope foothills of Costa Rica. Between 20 April and 28 May 1989, we searched for display logs and conducted 358 h of observations focused on four display logs. We found logs owned by a single resident male in which activity was continuous, as well as logs and areas where displays were occasional. Six of the eight logs found in the study area were arranged in two clusters separated by about 300 m, although we also found a solitary log 200 m from the nearest active display site. The resident male was at his display site 40.7-93.7% of the time, mostly alone. Residents were visited by other males mainly before 08:00 and less frequently by females later in the day. Residents continually gave advertisement calls during the day and performed several visual displays, including an elaborate Flap-cheewah in which the male would fly steeply upward from the display log to land explosively at high speed a few seconds later, instantly jumping while turning in the air to land facing the original landing point. Two of these displays culminated in copulations. Other common displays were a slow undulating Butterfly flight and Throatflagging in which males slowly moved their heads, exposing the fully erected, contrasting white throat feathers. Males performed the displays alone, in the company of other males, or in the presence of females. We conclude that C. leucorrhoa displays in dispersed leks as found by other authors for C. gutturalis. Each log is owned by a single individual and the visits by other males may have a social function related to the establishment of a dominance hierarchy. We found important similarities between the two species of Corapipo and also with the genus Masius, which supports the proposed close relation between the two groups.