Changing times, spaces, and faces: tests and implications of adaptive morphological plasticity in the fishes of northern postglacial lakes
By B. Robinson, K. Parsons. 2002
297 citations recorded by the source corpus.
Subfields: Ecological Modeling, Genetics, Geometry and Topology
View Paper: https://www.semanticscholar.org/paper/4e41b51324a0e6b63ebac0c81bb3ab064e3b237c
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecological Modeling
- N. Mouquet
- O. Ronce
- Wilfried Thuiller
- Jennifer A. Lau
- K. Gjelland
- S. Strauss
- Miguel B. Araújo
- Jane Elith
In Genetics
- C. Jastrebski
- Wilfried Thuiller
- Scott P Carroll
- R. Knudsen
- N. Mouquet
- B. Robinson
- O. Ronce
- J. A. Hutchings
In Geometry and Topology
Citations in the corpus
- Evolutionary responses of natives to introduced species: what do introductions tell us about natural communities? (2006, background): “At least 34 fish species exhibit trophic polymorphisms in behaviour, gill raker and jaw structure, and body shape (Robinson & Parsons 2002).”
- Effect of a change in physical structure and cover on fish and fish habitat in freshwater ecosystems – a review and meta-analysis (2007, background): “There are a number of observational studies that attribute competitive interactions to the spatial structuring of fishes in north temperate lakes (Gascon and Leggett 1977; Werner et al. 1977; Keast 1978; reviews by Ross 1986; Robinson and Wilson 1994; Jackson et al. 2001; Robinson and Parsons 2002).”
- Contribution of phenotypic plasticity and heredity to the trophic polymorphism of lacustrine brook charr (Salvelinus fontinalis M.) (2004, background): “Trophic polymorphism appears to be common in fish inhabiting northern latitude lakes (Skúlason and Smith, 1995; Schluter, 1996; Robinson and Parsons, 2002).”
- Natural selection and the evolution of replicated trophic polymorphisms in pumpkinseed sunfish (Lepomis gibbosus) (2004, background): “Replicated patterns of environmentally related phenotypic divergence among independent populations is strong evidence of selection because a consistent association between particular phenotypes and environments is unlikely to have resulted from other non-ecological mechanisms that can also cause div”
- The role of gill raker number variability in adaptive radiation of coregonid fish (2011, background): “, head and body morphology) are associated to fish feeding niche utilization along traditional pelagic-littoral resource axis in many postglacial fish morphs (Schluter 1996; Robinson and Parsons 2002), but very little is known about profundal adaptations.”
- Sympatric diversification as influenced by ecological opportunity and historical contingency in a young species lineage of whitefish (2010, background): “Sympatric forms have commonly diverged along the limnetic–benthic resource axis and occur as morph-pairs with distinct segregation in habitat and food resource use (Schluter and McPhail, 1993; Robinson and Wilson, 1994; Skúlason and Smith, 1995; Robinson and Parsons, 2002).”
- Genetic and environmental components of phenotypic variation in body shape among populations of Atlantic cod (Gadus morhua L.) (2006, background): “Plasticity in fish body shape has been hypothesized to be adaptive (Robinson & Parsons, 2002).”
- Biodiversity and Climate Change: Integrating Evolutionary and Ecological Responses of Species and Communities (2010, background): “Some native fish or plant species have also successfully adapted against novel competitors (Callaway et al. 2005, Robinson & Parsons 2002).”