Drought mediates the importance of stochastic community assembly

By Jonathan M. Chase. Proceedings of the National Academy of Sciences of the United States of America, 2007

1,014 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/4a39c61789956c3bdcd1b68899704bad47fdabd8

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In Global and Planetary Change

Citations in the corpus

Assessing the relative importance of neutral stochasticity in ecological communities (2014, background): “…context, etc.) may contain different species assemblages , and the observation of high compositional variation (i.e. beta diversity) in the absence of environmental heterogeneity is often interpreted as evidence of stochastic processes (Chase 2003, 2007, 2010, Fukami 2004, 2010, Chase et al. 2009).”
Navigating the multiple meanings of β diversity: a roadmap for the practicing ecologist. (2011, background): “Importantly, differences in the relative sizes of multivariate dispersions for different groups can be visualized on unconstrained ordination plots (e.g. Anderson 2006; Chase 2007, 2010).”
Ecological Opportunity and Adaptive Radiation (2016, background): “The presence of an incumbent clade usually prevents another clade from diversifying (Rosenzweig & McCord 1991), just as an incumbent species often prevents colonization of an ecologically similar species (the priority effect) (MacArthur 1972, Chase 2007).”
Resource availability mediates the importance of priority effects in plant community assembly and ecosystem function (2013, result): “Our results support the presumption that under harsh conditions – in our case, low nutrient supply – strong niche selection decreases the importance of stochastic factors in affecting community composition (Chase 2007).”
Rate-specific responses of prokaryotic diversity and structure to nitrogen deposition in the Leymus chinensis steppe (2014, background): “The diversity and species richness loss likely result from niche-selection filtering out species from the native pool that could not tolerate such environmental changes (Chase, 2007) induced by N deposition.”
Regeneration: an overlooked aspect of trait‐based plant community assembly models (2016, background): “equal dispersal abilities across species; seed arrival influenced by parent abundance and chance events) to predictable directed dispersal according to abiotic filters and plant/disperser characteristics (e.g. Nathan & Muller-Landau 2000; Hubbell 2001; Chase 2007; Shipley, Paine & Baraloto 2012).”
Resilience of fishes and invertebrates to prolonged drought in two California streams (2009, background): “Evidence is growing that climatic change and hydroclimatic extremes (such as prolonged drought) can result in gradual changes or dramatic shifts in freshwater communities and assembly processes (Bady et al. 2004, Bêche and Resh 2007, Chase 2007, Daufresne et al. 2007, Durance and Ormerod 2007).”
Pollinator-friendly management does not increase the diversity of farmland bees and wasps (2015, methodology): “Following Colwell et al. (2012), this sample-based abundance data was converted to sample-based incidence data to calculate incidence-based extrapolation curves using a Bernoulli product model.”
Species sorting in space and time—the impact of disturbance regime on community assembly in a temporary pool metacommunity (2010, background): “Chase (2007) suggested that deterministic niche-based pro- cesses would be more important under harsh conditions.”
Pathways, mechanisms and predictability of vegetation change during tropical dry forest succession (2010, background): “, 1997; Holl, 2007) and a convergence in community assembly is expected (Chase, 2007).”
Invertebrate assemblage responses and the dual roles of resistance and resilience to drying in intermittent rivers (2016, background): “In relation to Q1, we hypothesized that flow intermittence and surface water loss would create a disturbance that (i) filters out taxa unable to cope with drying thus leading to more stable, persistent assemblages (less temporal change) at I sites than at P sites or (ii) leads to greater temporal ch”
Dispersal strength determines meta‐community structure in a dendritic riverine network (2015, background): “aquatic habitats that experience severe, recurrent droughts) show a high degree of niche filtering, allowing only those species adapted to the local conditions to persist (Poff, 1997; Chase, 2007).”
Effects of dispersal mode on the environmental and spatial correlates of nestedness and species turnover in pond communities (2017, background): “Ponds are often characterised by stochastic processes both in terms of flora or fauna and environmental conditions (Jeffries 1988, Chase 2007), which may provide some justification for the relatively large proportion of unexplained variation recorded and lead to a less definitive explanation of…”
Patterns of elevational beta diversity in micro‐ and macroorganisms (2012, background): “Recent studies suggest that harsh ‘ecological filters’, such as those resulting from strong human disturbance, reduce the importance of stochastic processes in structuring biotic communities and, hence, reduce the compositional heterogeneity of biotic assemblages among sites (Chase, 2007; Passy & Bl”
Bringing Elton and Grinnell Together: a quantitative framework to represent the biogeography of ecological interaction networks (2016, neutral): “, Chase, J.M., Vellend, M., Inouye, B.D., Freestone, A.L., 676 Sanders, N.J., Cornell, H.V., Comita, L.S., Davies, K.F., Harrison, S.P., Kraft, N.J.B., 677 Stegen, J.C. & Swenson, N.G. (2011) Navigating the multiple meanings of beta678 diversity: a roadmap for the practicing ecologist.”