Works matching AU Closset‐Kopp, Déborah
Results: 18
Streams are efficient corridors for plant species in forest metacommunities.
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- Journal of Applied Ecology, 2013, v. 50, n. 5, p. 1152, doi. 10.1111/1365-2664.12132
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Drivers of species and genetic diversity within forest metacommunities across agricultural landscapes of different permeability.
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- Landscape Ecology, 2021, v. 36, n. 11, p. 3269, doi. 10.1007/s10980-021-01296-6
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DEFINING PATCH MOSAIC FUNCTIONAL TYPES TO PREDICT INVASION PATTERNS IN A FOREST LANDSCAPE.
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- Ecological Applications, 2007, v. 17, n. 2, p. 464, doi. 10.1890/06-0614
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Remnant Artificial Habitats as Biodiversity Islets into Forest Oceans.
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- Ecosystems, 2015, v. 18, n. 3, p. 507, doi. 10.1007/s10021-015-9843-3
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Differential growth patterns and fitness may explain contrasted performances of the invasive Prunus serotina in its exotic range.
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- Biological Invasions, 2011, v. 13, n. 6, p. 1341, doi. 10.1007/s10530-010-9893-6
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Neighbourhood-based evidence of tree diversity promotion by beech in an old-growth deciduousconiferous mixed forest (Eastern Carpathians).
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- Annals of Forest Research (1844-8135), 2021, v. 64, n. 1, p. 13, doi. 10.15287/afr.2021.2143
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Evaluating structural and compositional canopy characteristics to predict the light‐demand signature of the forest understorey in mixed, semi‐natural temperate forests.
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- Applied Vegetation Science, 2021, v. 24, n. 1, p. 1, doi. 10.1111/avsc.12532
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Does long-term monitoring of tropical forests using permanent plots provide unbiased results?
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- Applied Vegetation Science, 2014, v. 17, n. 4, p. 737, doi. 10.1111/avsc.12097
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Historical continuity and spatial connectivity ensure hedgerows are effective corridors for forest plants: Evidence from the species–time–area relationship.
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- Journal of Vegetation Science, 2021, v. 32, n. 1, p. 1, doi. 10.1111/jvs.12845
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Observer and relocation errors matter in resurveys of historical vegetation plots.
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- Journal of Vegetation Science, 2018, v. 29, n. 5, p. 812, doi. 10.1111/jvs.12673
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A general hypothesis of forest invasions by woody plants based on whole‐plant carbon economics.
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- Journal of Ecology, 2023, v. 111, n. 1, p. 4, doi. 10.1111/1365-2745.14001
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Light availability and land‐use history drive biodiversity and functional changes in forest herb layer communities.
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- Journal of Ecology, 2020, v. 108, n. 4, p. 1411, doi. 10.1111/1365-2745.13339
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Do drivers of forestry vehicles also drive herb layer changes (1970–2015) in a temperate forest with contrasting habitat and management conditions?
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- Journal of Ecology, 2019, v. 107, n. 3, p. 1439, doi. 10.1111/1365-2745.13118
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Drivers of plant species assemblages in forest patches among contrasted dynamic agricultural landscapes.
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- Journal of Ecology, 2011, v. 99, n. 5, p. 1152, doi. 10.1111/j.1365-2745.2011.01840.x
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Fragmentation alters beta-diversity patterns of habitat specialists within forest metacommunities.
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- Ecography, 2012, v. 35, n. 2, p. 124, doi. 10.1111/j.1600-0587.2011.06900.x
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The contribution of patch-scale conditions is greater than that of macroclimate in explaining local plant diversity in fragmented forests across Europe.
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- Global Ecology & Biogeography, 2015, v. 24, n. 9, p. 1094, doi. 10.1111/geb.12345
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Spatial patterns of water-deposited seeds control plant species richness and composition in riparian forest landscapes.
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- Landscape Ecology, 2015, v. 30, n. 10, p. 2133, doi. 10.1007/s10980-015-0236-y
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Landscape genomics and a common garden trial reveal adaptive differentiation to temperature across Europe in the tree species Alnus glutinosa.
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- Molecular Ecology, 2014, v. 23, n. 19, p. 4709, doi. 10.1111/mec.12813
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