MotivationThe BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community‐led open‐source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene.Main types of variables includedThe database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record.Spatial location and grainBioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km2 (158 cm2) to 100 km2 (1,000,000,000,000 cm2).Time period and grainBioTIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year.Major taxa and level of measurementBioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates.Software format.csv and .SQL.
ABSTRACT. The National Biodiversity Strategy developed in Chile aims to protect 10% of the surface area of the most relevant marine ecosystems. The waters around the Juan Fernández Archipelago were not protected until 2014, when a Multiple Use Marine Protected Area was created in the 12 nautical miles around the archipelago, which includes five marine parks in sites of high conservation value. Three of these parks are located around Robinson Crusoe Island. This study aims to define a baseline for monitoring the impact of the marine protected area and provides ecological information to improve the understanding of coastal marine ecosystems around Robinson Crusoe Island. In addition to a characterization of bathymetry and habitats, intertidal and subtidal communities were sampled using transects and quadrats within the marine parks. We quantified species richness and abundances, which were later organized into functional groups for algae and trophic groups for mobile organisms. Although species richness did not vary between sites nor among the habitats sampled, we observed important differences in species abundance and composition as well as in functional and trophic groups both between sites and habitats. Among our results, we highlight: a) the dominance of endemic algae in intertidal and subtidal (mainly corticated and corticated foliose) habitats, b) high abundances of macroinvertebrate herbivores in intertidal habitats and detrivores in subtidal habitats, c) dominance of invertivorous fish in the subtidal, which are the primary predators of mobile benthic organisms. This characterization includes both the inter and subtidal coastal communities of the Juan Fernández Archipelago.
As quantitative tools, drill holes have been used to calculate predation frequencies in time and space. These traces can also inform predator preference and some strategies predators use to drill on prey (e.g., edge drilling, site stereotypy, or alternative modes of predation when there is no drill hole). In this study, our goal was to leverage the informative power of drill holes to characterize the predatory habits of muricid gastropods from the central coast of Chile. We integrated information from experiments and death assemblages (DAs) to unveil the predatory strategy of Ancathina monodon, Crassilabrum crasilabrum, and Concholepas concholepas on the mobile gastropod Tegula tridentata and the sessile bivalve Perumytilus purpuratus. Experiments supported previous findings for predatory strategies (basal spine for Ancathina and alternative modes of predation for Concholepas), and showed the stereotypic predation of Crassilabrum on Tegula—a herbivore that is devastating subtidal kelp forests. Based on drill holes from DAs, at least 11 molluscan families are consumed by muricids in these communities. DAs also helped validate the stereotypic predation of Crassilabrum on Tegula, as drill holes were found in the same position both in experiments and DAs. Despite their thinner shells, mytilids were well represented in DAs and were found with drill holes in the five locations sampled. We describe for the first time the predatory strategy of Crassilabrum in Chile and confirm that muricids other than Concholepas are active predators on subtidal rocky habitats from the southeastern Pacific Ocean, a region that is still understudied.
The spawning sites, embryonic development, and initial larval stages were described for the Chilean kelpfish, Myxodes viridis. Six different egg clutches were found attached by an elastic filament to the fronds of the subtidal kelp, Lessonia trabeculata, at shallow depths (0-7 m). All egg clutches were cared by one large (>15 cm TL) male, and egg color varied depending on the developmental stage. Embryonic development until hatching was categorized into 7 stages, which were completed within about 18 days in the laboratory. Recently hatched larvae presented fully pigmented eyes, a well-developed mouth with major shape changes in the head during the first week suggesting their ability to feed on plankton early in their larval development.
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