Accumulating evidence for a dispersal biogeography of southern cool temperate freshwater fishes
By R. McDowall. 2002
96 citations recorded by the source corpus.
Subfields: Aquatic Science, Genetics, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/1207957ac1f75ed8f2a1290e250afa562c7251bf
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Aquatic Science
In Genetics
In Nature and Landscape Conservation
- Jane Elith
- J. Leathwick
- Steven L. Chown
- Trevor J. Hastie
- M. Heads
- J. Waters
- Kevin J. Gaston
- Antoine Guisan
Citations in the corpus
- Hawaiian biogeography and the islands’ freshwater fish fauna (2003, background): “…of freshwater fish faunas of remote islands, and has been linked with limiting genetic divergence and structuring in freshwater taxa – both in fishes (Goto & Andoh, 1990; Allibone & Wallis, 1993; Ward et al., 1994; Waters et al., 2000; McDowall, 2001, 2002) and in crustaceans (Fievet & Eppe, 2002).”
- Nestedness of Southern Ocean island biotas: ecological perspectives on a biogeographical conundrum (2004, background): “In conclusion, we note that whilst the importance of dispersal in ecology has never been disputed, its significance in historical biogeography has been the subject of a longstanding debate (see review in Myers & Giller, 1988; McDowall, 2002).”
- Towards a panbiogeography of the seas (2005, background): “They have been the topic of much debate between dispersalists (e.g. McDowall, 1964, 2002) who have argued for an Australian centre of origin followed by dispersal to New Zealand and South America, and panbiogeographers (Croizat et al., 1974; Rosen, 1978) who favour vicariance of a widespread…”
- The resurrection of oceanic dispersal in historical biogeography. (2005, background): “If vicariance biogeography was a revolution, we are now in the midst of a counterrevolution, driven primarily by new evidence in favor of oceanic dispersal [11,15, 16 ,26,28,29,39,40].”
- The distribution of South American galaxiid fishes: the role of biological traits and post‐glacial history (2004, background): “McDowall (2002) observed that there is a very clear divergence in distribution patterns between diadromous and non-diadromous species, being diadromous species found virtually throughout New Zealand latitudinal range whereas nondiadromous species have much more localized/latitudinally restricted…”
- Crying wolf, crying foul, or crying shame: alien salmonids and a biodiversity crisis in the southern cool-temperate galaxioid fishes? (2006, background): “Main (1988; Main et al. 1985) found no habitat overlap between G. postvectis and brown trout in a broad-scale survey of South Island West Coast streams.”
- Directional asymmetry of long‐distance dispersal and colonization could mislead reconstructions of biogeography (2005, background): “Repeated large-scale biogeographical patterns that are ascribable to LDD indicate that LDD can be directional (Wardle, 1978; McDowall, 2002; Les et al., 2003; Muñoz et al., 2004; Sanmartı́n & Ronquist, 2004), despite claims by some authors (e.”
- Dispersal, disturbance and the contrasting biogeographies of New Zealand’s diadromous and non‐diadromous fish species (2008, background): “McDowall (2002) explores the case for and against these conflicting explanations, arguing that the overwhelming weight of evidence from both ecological and genetic studies supports the importance of contemporary dispersal.”
- What biogeography is: a place for process (2004, background): “Emerging evidence indicates the same for the southern cool temperate galaxiid fishes – some groups of which appear to have relatively recent dispersal origins in New Zealand (Waters et al., 2000), whereas others may be more ancient, and are perhaps Gondwanan (McDowall, 2002; McDowall & Waters, in pr”
- Marine dispersal as a pre‐requisite for Gondwanan vicariance among elements of the galaxiid fish fauna (2012, background): “Even in New Zealand, where the history of fluvial connectivity has been particularly dynamic (Craw & Norris, 2003), the ranges of non-diadromous species are much smaller than those of diadromous taxa (McDowall, 2002, 2010).”