Bimodal hybrid zones and speciation.
By Chris D. Jiggins, James Mallet. Trends in Ecology & Evolution, 2000
618 citations recorded by the source corpus.
Subfields: Ecology, Evolution, Behavior and Systematics, Genetics, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/9dd151b739bb0b8db63a6b2c84edcc1449507459
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Citations in the corpus
- Reproductive isolation and reproductive output in two sympatric mussel species (Mytilus edulis, M. trossulus) and their hybrids from Newfoundland (2002, background): “Depending on the survival and fertility of hybrids, selection may reinforce reproductive isolating mechanisms to maintain distinct taxa or break down barriers to hybridization, resulting in the fusion of taxa (Coyne and Orr 1997; Jiggins and Mallet 2000; Schluter 2001; Turelli et al. 2001).”
- Evolution of insect‐plant relationships: chemical constraints, coadaptation, and concordance of insect/plant traits (2002, background): “At species borders and hybrid zones, ecological and genetic analyses of differentiation and reproductive isolation can be studied most effectively (Sperling, 1990; Jiggins & Mallet, 2000).”
- The Role of Hybridization in the Evolution of Reef Corals (2006, background): “F or p er so na l u se o nl y. be difficult to detect because they may be much closer genetically or morphologically to one parental species than the other ( Jiggins & Mallet 2000, Naisbit et al. 2003).”
- Multilocus Genetic Analysis of Host Use, Introgression, and Speciation in Host Strains of Fall Armyworm (Lepidoptera: Noctuidae) (2004, background): “Alternatively, divergence could have occurred parapatrically via an ecological shift from one host to another, a speciation mode that is receiving increasing support (Rolan-Alvarez et al. 1997, Feder 1998, Jiggins and Mallet 2000, Berlocher andFeder 2002,Dres andMallet 2002, Funk et al. 2002).”
- Host races in plant-feeding insects and their importance in sympatric speciation. (2002, background): “By contrast, when members of two host races or species are placed in groups according to multiple criteria, a bimodal distribution of genotypes occurs (Mallet 1995, 2001c; Feder 1998; see also Jiggins & Mallet 2000).”
- The speciation revolution (2001, background): “Today the pace is accelerating: arguments for ecological speciation and sympatric and/or parapatric differentiation are ¯ooding in (Jiggins & Mallet, 2000; Schluter, 2001; Via, 2001).”
- Ecological explanations for (incomplete) speciation. (2009, background): “For example, the degree of phenotypic divergence can vary quantitatively [3,7,10], as can the completeness of reproductive isolation [2,4–6,9,10,13–16], the degree of genotypic clustering [18, 19 ], the sharpness of geographic clines in gene frequencies [21] and the extent of lineage sorting [22,23]”
- The pattern and process of mammoth evolution in Eurasia (2005, background): “…in a hybrid zone, which is expected to produce a proportion of mosaic or intermediate individuals as well as those which correspond to the parent populations in all characters; such character distributions are well-known from studies of hybrid zones in modern organisms (Jiggins and Mallet, 2000).”
- Morphology and coexistence of congeneric ectoparasite species: reinforcement of reproductive isolation? (2002, background): “The central prediction is that reinforcement is favoured by strong selection against hybrids and mating patterns evolve that reduce the frequency of unfit hybrid genotypes (Butlin, 1989, 1995; Jiggins & Mallet, 2000).”
- The genic view of the process of speciation (2001, background): “There are many operational species de®nitions for practical use (Coyne, 1994; Harrison, 1998; and other chapters in Howard & Berlocher, 1998; Jiggins & Mallet, 2000).”