L'expertise devant la juridiction administrative de première instance: quelques réflexions sur le statut de l'instruction
In: La revue administrative: histoire, droit, société, Band 62, Heft 370, S. 378-382
ISSN: 0035-0672
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In: La revue administrative: histoire, droit, société, Band 62, Heft 370, S. 378-382
ISSN: 0035-0672
In: The Howard Journal of Criminal Justice, Band 19, Heft 1-3, S. 85-101
ISSN: 1468-2311
In: Sociology: the journal of the British Sociological Association, Band 9, Heft 2, S. 367-368
ISSN: 1469-8684
In: Sociology: the journal of the British Sociological Association, Band 6, Heft 1, S. 159-160
ISSN: 1469-8684
In: Sociology: the journal of the British Sociological Association, Band 5, Heft 2, S. 265-266
ISSN: 1469-8684
In: Sociology: the journal of the British Sociological Association, Band 4, Heft 2, S. 283-284
ISSN: 1469-8684
In: Economica, Band 25, Heft 100, S. 369
In: The Howard Journal of Criminal Justice, Band 10, Heft 1, S. 44-50
ISSN: 1468-2311
In: The Economic Journal, Band 68, Heft 269, S. 128
Summary Modelling species distribution and abundance is important for many conservation applications, but it is typically performed using relatively coarse‐scale environmental variables such as the area of broad land‐cover types. Fine‐scale environmental data capturing the most biologically relevant variables have the potential to improve these models. For example, field studies have demonstrated the importance of linear features, such as hedgerows, for multiple taxa, but the absence of large‐scale datasets of their extent prevents their inclusion in large‐scale modelling studies.We assessed whether a novel spatial dataset mapping linear and woody‐linear features across the UK improves the performance of abundance models of 18 bird and 24 butterfly species across 3723 and 1547 UK monitoring sites, respectively.Although improvements in explanatory power were small, the inclusion of linear features data significantly improved model predictive performance for many species. For some species, the importance of linear features depended on landscape context, with greater importance in agricultural areas. Synthesis and applications. This study demonstrates that a national‐scale model of the extent and distribution of linear features improves predictions of farmland biodiversity. The ability to model spatial variability in the role of linear features such as hedgerows will be important in targeting agri‐environment schemes to maximally deliver biodiversity benefits. Although this study focuses on farmland, data on the extent of different linear features are likely to improve species distribution and abundance models in a wide range of systems and also can potentially be used to assess habitat connectivity. This study demonstrates that a national‐scale model of the extent and distribution of linear features improves predictions of farmland biodiversity. The ability to model spatial variability in the role of linear features such as hedgerows will be important in targeting agri‐environment schemes to maximally deliver ...
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As countries advance in greenhouse gas (GHG) accounting for climate change mitigation, consistent estimates of aboveground net biomass change (∆AGB) are needed. Countries with limited forest monitoring capabilities in the tropics and subtropics rely on IPCC 2006 default ∆AGB rates, which are values per ecological zone, per continent. Similarly, research into forest biomass change at a large scale also makes use of these rates. IPCC 2006 default rates come from a handful of studies, provide no uncertainty indications and do not distinguish between older secondary forests and old‐growth forests. As part of the 2019 Refinement to the 2006 IPCC Guidelines for National Greenhouse Gas Inventories, we incorporate ∆AGB data available from 2006 onwards, comprising 176 chronosequences in secondary forests and 536 permanent plots in old‐growth and managed/logged forests located in 42 countries in Africa, North and South America and Asia. We generated ∆AGB rate estimates for younger secondary forests (≤20 years), older secondary forests (>20 years and up to 100 years) and old‐growth forests, and accounted for uncertainties in our estimates. In tropical rainforests, for which data availability was the highest, our ∆AGB rate estimates ranged from 3.4 (Asia) to 7.6 (Africa) Mg ha−1 year−1 in younger secondary forests, from 2.3 (North and South America) to 3.5 (Africa) Mg ha−1 year−1 in older secondary forests, and 0.7 (Asia) to 1.3 (Africa) Mg ha−1 year−1 in old‐growth forests. We provide a rigorous and traceable refinement of the IPCC 2006 default rates in tropical and subtropical ecological zones, and identify which areas require more research on ∆AGB. In this respect, this study should be considered as an important step towards quantifying the role of tropical and subtropical forests as carbon sinks with higher accuracy; our new rates can be used for large‐scale GHG accounting by governmental bodies, nongovernmental organizations and in scientific research ; CIFOR sobre REDD +, Agencia Noruega para la Cooperación al Desarrollo (Norad) , Iniciativa Internacional sobre el Clima (IKI) , entre otros. ; Revisión por pares.
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As countries advance in greenhouse gas (GHG) accounting for climate change mitigation, consistent estimates of aboveground net biomass change (∆AGB) are needed. Countries with limited forest monitoring capabilities in the tropics and subtropics rely on IPCC 2006 default ∆AGB rates, which are values per ecological zone, per continent. Similarly, research into forest biomass change at a large scale also makes use of these rates. IPCC 2006 default rates come from a handful of studies, provide no uncertainty indications and do not distinguish between older secondary forests and old-growth forests. As part of the 2019 Refinement to the 2006 IPCC Guidelines for National Greenhouse Gas Inventories, we incorporate ∆AGB data available from 2006 onwards, comprising 176 chronosequences in secondary forests and 536 permanent plots in old-growth and managed/logged forests located in 42 countries in Africa, North and South America and Asia. We generated ∆AGB rate estimates for younger secondary forests (≤20 years), older secondary forests (>20 years and up to 100 years) and old-growth forests, and accounted for uncertainties in our estimates. In tropical rainforests, for which data availability was the highest, our ∆AGB rate estimates ranged from 3.4 (Asia) to 7.6 (Africa) Mg ha−1 year−1 in younger secondary forests, from 2.3 (North and South America) to 3.5 (Africa) Mg ha−1 year−1 in older secondary forests, and 0.7 (Asia) to 1.3 (Africa) Mg ha−1 year−1 in old-growth forests. We provide a rigorous and traceable refinement of the IPCC 2006 default rates in tropical and subtropical ecological zones, and identify which areas require more research on ∆AGB. In this respect, this study should be considered as an important step towards quantifying the role of tropical and subtropical forests as carbon sinks with higher accuracy; our new rates can be used for large-scale GHG accounting by governmental bodies, nongovernmental organizations and in scientific research.
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As countries advance in greenhouse gas (GHG) accounting for climate change mitigation, consistent estimates of aboveground net biomass change (∆AGB) are needed. Countries with limited forest monitoring capabilities in the tropics and subtropics rely on IPCC 2006 default ∆AGB rates, which are values per ecological zone, per continent. Similarly, research into forest biomass change at a large scale also makes use of these rates. IPCC 2006 default rates come from a handful of studies, provide no uncertainty indications and do not distinguish between older secondary forests and old‐growth forests. As part of the 2019 Refinement to the 2006 IPCC Guidelines for National Greenhouse Gas Inventories, we incorporate ∆AGB data available from 2006 onwards, comprising 176 chronosequences in secondary forests and 536 permanent plots in old‐growth and managed/logged forests located in 42 countries in Africa, North and South America and Asia. We generated ∆AGB rate estimates for younger secondary forests (≤20 years), older secondary forests (>20 years and up to 100 years) and old‐growth forests, and accounted for uncertainties in our estimates. In tropical rainforests, for which data availability was the highest, our ∆AGB rate estimates ranged from 3.4 (Asia) to 7.6 (Africa) Mg ha(−1) year(−1) in younger secondary forests, from 2.3 (North and South America) to 3.5 (Africa) Mg ha(−1) year(−1) in older secondary forests, and 0.7 (Asia) to 1.3 (Africa) Mg ha(−1) year(−1) in old‐growth forests. We provide a rigorous and traceable refinement of the IPCC 2006 default rates in tropical and subtropical ecological zones, and identify which areas require more research on ∆AGB. In this respect, this study should be considered as an important step towards quantifying the role of tropical and subtropical forests as carbon sinks with higher accuracy; our new rates can be used for large‐scale GHG accounting by governmental bodies, nongovernmental organizations and in scientific research.
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Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. The sensitivity of tropical forest carbon to climate is a key uncertainty in predicting global climate change. Although short-term drying and warming are known to affect forests, it is unknown if such effects translate into long-term responses. Here, we analyze 590 permanent plots measured across the tropics to derive the equilibrium climate controls on forest carbon. Maximum temperature is the most important predictor of aboveground biomass (-9.1 megagrams of carbon per hectare per degree Celsius), primarily by reducing woody productivity, and has a greater impact per °C in the hottest forests (>32.2°C). Our results nevertheless reveal greater thermal resilience than observations of short-term variation imply. To realize the long-term climate adaptation potential of tropical forests requires both protecting them and stabilizing Earth's climate.
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This paper is a product of the T-FORCES forest monitoring network (Tropical Forests in the Changing Earth System), supported by an ERC Advanced Grant to O.L.P. and by many institutions, NGOs, government agencies and local communities in Malaysia, Brunei, and Indonesia. We are grateful for historical plot data contributed by the Center for Tropical Forest Science (CTFS; two LAM plots and one BEL plot), the Global Ecosystem Monitoring network (GEM; two LAM plots), Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam (Brunei plots), Kagoshima University (KIS and KIU plots), Forest Department Sarawak (BKO, LAM, MER and GMU plots), Forest Research Centre, Sabah Forestry Department (SEP plots), the Tropenbos Kalimantan project (ITCI plots), Project Barito Ulu, supported by Indonesian Institute of Sciences (LIPI) (BUL plots), and the STREK project, supported by CIRAD, The Ministry of Forestry of Indonesia, and INHUTANI I (STR plots). We are indebted to a great many individuals who contributed to historical data collection. Contemporary fieldwork was supported by a grant from the ERC (T-FORCES) and from NERC (grants NER/A/S/2000/00532, NE/B503384/1, NE/N012542/1). L.Q. was supported by T-FORCES, CIFOR and NERC NE/P00363X/1. S.L.L. was supported by a Royal Society University Research Fellowship, T-FORCES and a Phillip Leverhulme Prize. O.L.P. is supported by T-FORCES and a Royal Society Wolfson Research Merit Award. M.J.P.S. is supported by T-FORCES and NERC NE/N012542/1. L.F.B. was supported by a NERC studentship to the University of Leeds and a RGS-IBG Henrietta Hutton grant. R.H. was supported by a University of Brunei Darussalam Research Fellowship (2011) and a long-term research project RVO 67985939 from the Czech Academy of Sciences. S.L. received additional support from Primate Conservation Inc. M.S. was supported by a Ministry of Education, Youth and Sports grant of the Czech Republic INGO II LG15051. R.R.E.V. was supported by the Netherlands Foundation for the Advancement of Tropical Research (WOTRO, grant No. W76-217). We thank Forest Department Sarawak, Sabah Biodiversity Centre, Sabah Forestry Department, Forest Department Brunei, Institute for Biodiversity and Environmental Research, University of Brunei Darussalam and Indonesia Ministry of Research, Technology, and Higher Education for research permissions. We thank Bako National Park, Lambir Hills National Park, Gunung Mulu National Park, Kuala Belalong Field Study Centre (KBFSC), Glen Reynolds (SEARRP), Danum Valley Conservation Area, Rainforest Discovery Centre Sepilok, Sepilok Laut Reception Centre, Borneo Orangutan Survival Foundation (BOSF), Sungai Wain Protection Forest Management Unit, WWF East Kalimantan and PT. ITCIKU East Kalimantan for logistical support for fieldwork. We thank Timothy Baker, Roel Brienen, Emanuel Gloor, Adriane Esquivel Muelbert and Nicolas Labrière for comments on the manuscript. We thank our deceased colleagues, John Proctor and Suriantata, for their invaluable contributions to both historical work and our wider understanding of tropical forest ecology. ; Peer reviewed ; Publisher PDF
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