The limits to biogeographical distributions: insights from the northward range extension of the marine snail, Kelletia kelletii (Forbes, 1852)

By D. Zacherl, S. Gaines, S. Lonhart. 2003

214 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/f97ff02e0291c4adece6e5a3ba438a4156d9f1fd

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In Global and Planetary Change

In Oceanography

Citations in the corpus

Biogeographical patterns of rocky intertidal communities along the Pacific coast of North America (2008, background): “Short-term pulses of increased temperatures, such as those during ENSO events, can also have an impact on species distributional limits (Pearcy & Schoener, 1987; Tanasichuk & Cooper, 2002; Zacherl et al., 2003; Keister et al., 2005; Lluch-Belda et al., 2005).”
Theoretical models of species' borders: single species approaches (2005, unknown): “We also emphasize the need for more explicit studies of non-equilibrial dynamics (e.g. invasions and retractions) along strong environmental gradients (Zacherl et al. 2003).”
Infection dynamics of an oyster parasite in its newly expanded range (2007, background): “Organisms that have expanded into a new range may show very different population structures compared to those in the historic range, having lower densities and more irregular recruitment (Zacherl et al. 2003; Thieltges et al. 2004).”
Recent changes in the distribution of a marine gastropod, Patella rustica Linnaeus, 1758, and their relationship to unusual climatic events (2006, background): “…trophic levels for both sessile and pelagic assemblages (Southward et al., 1995; Holbrook et al., 1997; Sagarin et al., 1999; Wethey, 2002; Beaugrand & Reid, 2003; Borges et al., 2003; Hawkins et al., 2003; Zacherl et al., 2003; Genner et al., 2004; Hiscock et al., 2004; Paine & Trimble, 2004).”
Climate‐driven range extension of a sea urchin: inferring future trends by analysis of recent population dynamics (2009, background): “Given that redistribution of marine species is already occurring in response to recent climate change, generalized predictive models of marine biological responses are likely best informed by examining the physical and physiological context of marine populations already shifting (e.g. Barry et al., ”
Non-commercial Research and Educational Use including without Limitation Use in Instruction at Your Institution, Sending It to Specific Colleagues That You Know, and Providing a Copy to Your Institution's Administrator. All Other Uses, Reproduction and Distribution, including without Limitation Comm (2005, unknown): “From these couplings accurate relative solute geometries and information about solute conformational change can be obtained.”
The impacts of climate change in coastal marine systems. (2006, background): “Actual documentation of latitudinal range shifts is relatively rare, but recent work has identified warming-associated poleward range shifts for a Californian gastropod ( Zacherl et al. 2003 ), a Caribbean coral (Precht & Aronson 2004), and North Sea fishes (Perry et al. 2005).”
Climate change and Australian marine life (2007, background): “Shifts in species distributions associated with ocean warming are documented from rocky shores in Europe, the United States and South America (Barry et al. 1995, Sagarin et al. 1999, Zacherl et al. 2003, Mieszkowska et al. 2005, Rivadeneira & Fernandez 2005, Simkanin et al. 2005).”
A phylogeographical analysis across three biogeographical provinces of the south‐eastern Pacific: the case of the marine gastropod Concholepas concholepas (2009, background): “Species with a pelagic larval phase are highly represented in the suite of species that have shifted their distribution associated with short-term pulses of increased temperatures, such as those during ENSO events (e.g. the gastropod Kelletia kelletia; Zacherl et al., 2003).”
Rising environmental temperatures and biogeography: poleward range contraction of the blue mussel, Mytilus edulis L., in the western Atlantic (2010, background): “Along the Californian and European coastlines, the distributions and abundances of many marine invertebrates, such as gastropods, polychaetes and crustaceans, have changed over the past decades (Barry et al., 1995; Sagarin et al., 1999; Zacherl et al., 2003; Lima et al., 2006; Mieszkowska et al., 20”
Living on the Edge of Two Changing Worlds: Forecasting the Responses of Rocky Intertidal Ecosystems to Climate Change (2006, background): “Such sharp faunal breakpoints corresponding to changes in thermal provinces occur on the western Range shifts of cold-and warmadapted species have already been documented in many of these regions (Herbert et al. 2003; Lima et al. 2006; Mieszkowska et al. 2005, 2006; Zacherl et al. 2003).”
Stability in temperate reef communities over a decadal time scale despite concurrent ocean warming (2010, background): “…species should r 2009 Blackwell Publishing Ltd, Global Change Biology, 16, 122–134 increase in population abundance whilst some coolerwater species should decrease in abundance (Zacherl et al., 2003; Genner et al., 2004; Helmuth et al., 2006; Hobday et al., 2006; Poloczanska et al., 2008).”
Changes in latitudes, changes in aptitudes: Nucella canaliculata (Mollusca: Gastropoda) is more stressed at its range edge (2004, background): “…timely because of the recent biogeographical focus on understanding the underpinnings of species’ biogeographic ranges and predicting how species’ distributions will be affected by global climate change (McCarty 2001, Warren et al. 2001, Parmesan & Yohe 2003, Root et al. 2003, Zacherl et al. 2003).”