44 research outputs found

    Retrospective stock assessment of the Emperor red snapper (Lutjanus sebae) on the Seychelles Bank between 1977 and 2006

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    The Emperor red snapper, Lutjanus sebae, known as “Bourzwa” in the Seychelles, is distributed throughout the Indo-West Pacific from the southern Red Sea and East Africa to New Caledonia, north to Japan and south to Australia. It occurs near coral or rocky reefs and also over adjacent sand flats and gravel patches between 5 and 180 m deep (Allen, 1985; Anderson, 1986). Juveniles are frequently commensal with sea urchins (Kuiter and Tonozuka, 2001), and are found in nearshore, turbid waters (Williams and Russ, 1992), mangrove areas (Allen, 1985), and around coastal and offshore reefs (Williams and Russ, 1992). Larger L. sebae are generally found deeper, although they are also known to move into shallower water during winter (McPherson et al., 1988; Williams and Russ, 1992). Prey items include fish, crabs, other benthic crustaceans, and cephalopods. Lutjanus sebae is a large, long-lived species, attaining a maximum size of 116 cm fork length (McPherson and Squire, 1992) and maximum age of 34 years (Newman and Dunk, 2002). Despite an absence of data on its population structure, mixing, and identity, the population on the Seychelles Bank has been considered to be a unit stock for assessment purposes because of its remote location (e.g. Lablache and Carrara, 1988; Mees, 1992)

    Author Correction: The FLUXNET2015 dataset and the ONEFlux processing pipeline for eddy covariance data

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    The following authors were omitted from the original version of this Data Descriptor: Markus Reichstein and Nicolas Vuichard. Both contributed to the code development and N. Vuichard contributed to the processing of the ERA-Interim data downscaling. Furthermore, the contribution of the co-author Frank Tiedemann was re-evaluated relative to the colleague Corinna Rebmann, both working at the same sites, and based on this re-evaluation a substitution in the co-author list is implemented (with Rebmann replacing Tiedemann). Finally, two affiliations were listed incorrectly and are corrected here (entries 190 and 193). The author list and affiliations have been amended to address these omissions in both the HTML and PDF versions

    The FLUXNET2015 dataset and the ONEFlux processing pipeline for eddy covariance data.

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    The FLUXNET2015 dataset provides ecosystem-scale data on CO2, water, and energy exchange between the biosphere and the atmosphere, and other meteorological and biological measurements, from 212 sites around the globe (over 1500 site-years, up to and including year 2014). These sites, independently managed and operated, voluntarily contributed their data to create global datasets. Data were quality controlled and processed using uniform methods, to improve consistency and intercomparability across sites. The dataset is already being used in a number of applications, including ecophysiology studies, remote sensing studies, and development of ecosystem and Earth system models. FLUXNET2015 includes derived-data products, such as gap-filled time series, ecosystem respiration and photosynthetic uptake estimates, estimation of uncertainties, and metadata about the measurements, presented for the first time in this paper. In addition, 206 of these sites are for the first time distributed under a Creative Commons (CC-BY 4.0) license. This paper details this enhanced dataset and the processing methods, now made available as open-source codes, making the dataset more accessible, transparent, and reproducible

    Author Correction: The FLUXNET2015 dataset and the ONEFlux processing pipeline for eddy covariance data

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    The FLUXNET2015 dataset and the ONEFlux processing pipeline for eddy covariance data

    Get PDF
    The FLUXNET2015 dataset provides ecosystem-scale data on CO2, water, and energy exchange between the biosphere and the atmosphere, and other meteorological and biological measurements, from 212 sites around the globe (over 1500 site-years, up to and including year 2014). These sites, independently managed and operated, voluntarily contributed their data to create global datasets. Data were quality controlled and processed using uniform methods, to improve consistency and intercomparability across sites. The dataset is already being used in a number of applications, including ecophysiology studies, remote sensing studies, and development of ecosystem and Earth system models. FLUXNET2015 includes derived-data products, such as gap-filled time series, ecosystem respiration and photosynthetic uptake estimates, estimation of uncertainties, and metadata about the measurements, presented for the first time in this paper. In addition, 206 of these sites are for the first time distributed under a Creative Commons (CC-BY 4.0) license. This paper details this enhanced dataset and the processing methods, now made available as open-source codes, making the dataset more accessible, transparent, and reproducible.Peer reviewe

    Arbuscular mycorrhizal community structure on co-existing tropical legume trees in French Guiana

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    Aims We aimed to characterise the arbuscular mycorrhizal fungal (AMF) community structure and potential edaphic determinants in the dominating, but poorly described, root-colonizing Paris-type AMF community on co-occurring Amazonian leguminous trees. Methods Three highly productive leguminous trees (Dicorynia guianensis, Eperua falcata and Tachigali melinonii were targeted) in species-rich forests on contrasting soil types at the Nouragues Research Station in central French Guiana. Abundant AMF SSU rRNA amplicons (NS31-AM1 & AML1-AML2 primers) from roots identified via trnL profiling were subjected to denaturing gradient gel electrophoresis (DGGE), clone library sequencing and phylogenetic analysis. Results Classical approaches targeting abundant SSU amplicons highlighted a diverse root-colonizing symbiotic AMF community dominated by members of the Glomeraceae. DGGE profiling indicated that, of the edaphic factors investigated, soil nitrogen was most important in influencing the AMF community and this was more important than any host tree species effect. Conclusions Dominating Paris-type mycorrhizal leguminous trees in Amazonian soils host diverse and novel taxa within the Glomeraceae that appear under edaphic selection in the investigated tropical forests. Linking symbiotic diversity of identified AMF taxa to ecological processes is the next challenge ahead

    The production and turnover of extramatrical mycelium of ectomycorrhizal fungi in forest soils: role in carbon cycling

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    Variability of stem and branch maintenance respiration in a Pinus pinaster tree

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    CO2, CH4 and N2O fluxes from soil of a burned grassland in Central Africa

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    The impact of fire on soil fluxes of CO2, CH4 and N2O was investigated in a tropical grassland in Congo Brazzaville during two field campaigns in 2007–2008. The first campaign was conducted in the middle of the dry season and the second at the end of the growing season, respectively one and eight months after burning. Gas fluxes and several soil parameters were measured in each campaign from burned plots and from a close-by control area preserved from fire. Rain events were simulated at each campaign to evaluate the magnitude and duration of the generated gas flux pulses. In laboratory experiments, soil samples from field plots were analysed for microbial biomass, net N mineralization, net nitrification, N2O, NO and CO2 emissions under different water and temperature soil regimes. One month after burning, field CO2 emissions were significantly lower in burned plots than in the control plots, the average daily CH4 flux shifted from net emission in the unburned area to net consumption in burned plots, no significant effect of fire was observed on soil N2O fluxes. Eight months after burning, the average daily fluxes of CO2, CH4 and N2O measured in control and burned plots were not significantly different. In laboratory, N2O fluxes from soil of burned plots were significantly higher than fluxes from soil of unburned plots only above 70% of maximum soil water holding capacity; this was never attained in the field even after rain simulation. Higher NO emissions were measured in the lab in soil from burned plots at both 10% and 50% of maximum soil water holding capacity. Increasing the incubation temperature from 25 °C to 37 °C negatively affected microbial growth, mineralization and nitrification activities but enhanced N2O and CO2 production. Results indicate that fire did not increase post-burning soil GHG emissions in this tropical grasslands characterized by acidic, well drained and nutrient-poor soi
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