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.
We investigated the pathways of N 2 production in the oxygen-deficient water column of the eastern tropical South Pacific off Iquique, Chile, at 20uS, through short anoxic incubations with 15 N-labelled nitrogen compounds. The location was characterized by steep chemical gradients, with oxygen decreasing to below detection at ,50-m depth, while nitrite reached 6 mmol L 21 and ammonium was less than 50 nmol L 21 . Ammonium was oxidized to N 2 with no lag phase during the incubations, and when only NH þ 4 was 15 N-labeled, 15 N appeared in the form of 14 N 15 N, whereas 15 N 15 N was not detected. Likewise, nitrite was reduced to N 2 at rates similar to the rates of ammonium oxidation, and when only NO 2 2 was 15 N-labeled, 15 N appeared mainly as 14 N 15 N, whereas 15 N 15 N appeared in only one incubation. These observations indicate that ammonium was oxidized and nitrite was reduced through the anammox reaction, whereas denitrification was generally not detected and, therefore, was a minor sink for nitrite. Anammox rates were highest, up to 0.7 nmol N 2 L 21 h 21 , just below the oxycline, whereas rates were undetectable, ,0.2 nmol N 2 L 21 h 21 , deeper in the oxygen-deficient zone. Instead of complete denitrification to N 2 , oxidation of organic matter during the incubations may have been coupled to reduction of nitrate to nitrite. This process was evident from strong increases in nitrite concentrations toward the end of the incubations. The results point to anammox as an active process in the major open-ocean oxygen-deficient zones, which are generally recognized as important sites of denitrification. Still, denitrification remains the simplest explanation for most of the nitrogen deficiency in these zones.
We present an analysis of seasonal variations in the trophic pathways of carbon in a highly productive coastal upwelling region in the Humboldt current system off Chile. Seasonal changes in phytoplankton, protozooplankton, and bacteria biomass, along with rates of primary production (PP), bacterial growth, secondary production, vertical particle fluxes, and feeding by protozooplankton, omnivorous mesozooplankton, and carnivorous gelatinous zooplankton were determined from July 2004 to June 2005. Phytoplankton biomass and PP were maximal during spring/summer months, associated with upwelling episodes. Heterotrophic nanoflagellates (HNF) were the principal consumers of bacteria, removing .100% of their biomass daily. During autumn/winter, the protozooplankton grazed down a large fraction of HNF production (56% to 96% d 21 ). The mesozooplankton consumed 1-6% of the PP d 21 ; the different size fractions of copepods were omnivorous mostly during autumn/winter months, and ctenophores preyed most strongly on small copepods (0.5% to 5% d 21 ). A large part of the PP was channeled through the microbial food web, and only a small part AcknowledgmentsWe thank the captains and crew of the RV Kay Kay (Universidad de Concepció n, Chile) and the many undergraduate and graduate students who participated in our cruises (L. Lizá rraga, V. Aguilera, C. Aparicio, E. Menschel, and A. Araneda). We also thank José Luis Acuñ a and Albert Calbet for their valuable suggestions that substantially improved an earlier version of the manuscript and two anonymous reviewers for their critical and helpful comments.
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