Melissa Hardy

Biology 862

 

Vicariance Biogeography: Using Phylogeny to Evaluate Biogeographic Hypotheses

Annotated Bibliography

 

Altaba, C.  1998.  Testing vicariance: melanopsid snails and Neogene tectonics in the western Mediterranean.  Journal of Biogeography 25:541-551.  Although the title of the paper begins with ‘Testing vicariance,’  the author never tests his hypothesis.  He instead provides a narrative of Mediterranean geology. A good ‘what not to do’ example!

 

Bermingham, E., Freeman, S., and Wood, C. 1992.  Vicariance biogeography in the Pleistocene and speciation in North American wood warblers: A test of Mengel’s model.  Proceedings of the National Academy of Science 89:6624-6628.   Habitat fragmentation and subsequent speciation caused by Pleistocene glaciation is a classic vicariance scenario.  However, this paper indicates that, at least for wood warblers, this may not have been the case.  Along with other recent papers, it suggests that most avian speciation events were pre-Pleistocene and, therefore, vicariance caused by glaciation is less important than was previously thought.

 

Bowen, B. W. and Grant W. S. 1997.  Phylogeography of the sardines (Sardinops Spp.): assessing biogeographic models and population histories in temperate upwelling zones.  Evolution 51:1601-1610.   Although one does not usually think of marine species as having long-term dispersal barriers, this paper addresses one such possible barrier: tropical waters are lethal to some temperate fish.  However, the authors found that the distribution of sardines is most likely due to dispersal.

 

Bremer, K.  Ancestral areas: A cladistic reinterpretation of the center of origin concept.  Systematic Biology 41:436-445.   Bremer argues that dispersal is a valid process and constructs a method as an alternative to purely narrative explanations.  His method uses Camin-Sokal parsimony to estimate the ancestral range of taxa.  He rejects the ‘null model’ of vicariance biogeography: that ancestral distributions were the same as current distributions.

 

Brooks, D. R. 1990.  Parsimony analysis in historical biogeography and coevolution: methodological and theoretical update.  Systematic Zoology 39:14-30.  Brooks parsimony analysis (BPA) was first proposed to evaluate cospeciation hypotheses.  Brooks also extended his method to area-taxa analysis.  Brooks presents a new, improved BPA in this paper.  I found parts of this paper, particularly the tables, confusing.  I had an easier time following Wiley’s (1988) summary of BPA.

 

Connor, E. F.  1991.  Assessing the method of quantitative vicariance biogeography: a simulation study of phenetic similarity analysis.  In Dudley, E. C., ed.  The Unity of Evolutionary Biology.  Dioscorides Press, Portland, Oregon.   This paper proposes a method for evaluating methods of historical biogeography: simulating an area, subjecting it to a vicariant event, and then testing whether the method in question can recover the true area history.  The paper reveals the surprising (to me) result that the phenetic similarity method actually recovers the correct area relationship over 90% of the time. 

 

Croizat, L., Nelson, G., and Rosen, D. E. 1974.  Centers of origin and related concepts.  Systematic Zoology 23:265-287.  This paper rejects the Darwinian center of origin theory in favor of vicariance.  The authors advocate “generalized track analysis,” which seems to be a way of tracing the history of taxa and comparing patterns of distribution.  This rather odd paper quotes extensively from various sources and cites no less than 10 references by Croizat.

 

Hausdorf, B. 1998.  Weighted ancestral area analysis and a solution of the redundant distribution problem.  Systematic Biology 47:445-456.  Hausdorf attempts to revise Bremer’s ancestral area method of analysis by weighting plesiomorphic branches over apomorphic branches and using reversible parsimony rather than Camin-Sokal parsimony.

 

Heads, M. 1999.  Vicariance biogeography and terrane tectonics in the South Pacific: analysis of the genus Abrotanella (Compositae).  Biological Journal of the Linnean Society 67:391-432.   A very long paper that provides an interesting, if somewhat narrative, overview of Abrotanella biogeography, relying heavily on geology.  Although the extensive geologic information is fascinating, there is little emphasis on phylogeny.

 

Hovenkamp, P. 1997.  Vicariance events, not areas, should be used in biogeographical analysis.  Cladistics 13:67-79.   Not worth reading.  Hovenkamp first insists that using taxa as characters on an area cladogram is inappropriate, but then proposes a method which I was unable to distinguish from the methods he criticized.

 

Macey, J. R., Schulte, J. A., Larson, A., Fang, Z., Wang, Y., Tuniyev, B. S., and Papenfuss, T. J.  1998.  Phylogenetic relationships of toads in the Bufo bufo species group from the eastern escarpment of the Tibetan Plateau: A case of vicariance and dispersal.  Molecular Phylogenetics and Evolution 9:80-87.  This paper distinguishes between vicariance and dispersal hypotheses by evaluating whether populations from similar elevations or the same river basins are monophyletic.  It finds a combination of vicariance and dispersal events. 

 

Mayden, R. L. 1988.  Vicariance biogeography, parsimony, and evolution in North American freshwater fishes.  Systematic Zoology 37:329-355.  This excellent study considers the phylogeny of seven highland fish clades and correlates the relationships with changes in river drainages during the Pleistocene. 

 

Murphy, W. J. and Collier, G. E.  1997.  A molecular phylogeny for aplocheiloid fishes (Atherinomorpha: Cyprinodontiformes): The role of vicariance and the origins of annualism.  Molecular Biology and Evolution 14:790-799.  The authors construct a phylogeny for aplocheiloids in order to evaluate dispersal/vicariance hypotheses.  They conclude that the deep splits in this clade correspond to the breaking up of the supercontinent Gondwanaland.

 

Page, R. D. M. 1988.  Quantitative cladistic biogeography: constructing and comparing area cladograms.  Systematic Zoology 37:254-270.  Page describes methods of constructing area cladograms and urges explicit statistical tests of congruence.  He also advises caution in drawing conclusions based solely on congruence of tree, since congruent trees could indicate congruent dispersal, but incongruent trees do not necessarily rule out a vicariant event. 

 

Repetur, C. P., Van Welzen, P. C., and De Vogel, E. F. 1997.  Phylogeny and historical biogeography of the genus Bromheadia (Orchidaceae).  Systematic Botany 22:465-477.  This paper used Brooks parsimony analysis and Bremer’s ancestral areas method to determine the history of this genus.  The authors concluded that both vicariance and dispersal were important factors and, interestingly, that most speciation in this group is sympatric.

 

Ronquist, F. 1997.  Dispersal-vicariance analysis: a new approach to the quantification of historical biogeography.  Systematic Biology 46:195-203.  Ronquist proposes a method to evaluate biogeography by explicitly considering vicariance, dispersal, and extinction.  He assigns costs to dispersal and extinction and accepts the tree with the lowest score as the most likely to be correct.

 

Rosen, D. E. 1978.  Vicariant patterns and historical explanation in biogeography.  Systematic Zoology 27:159-188.    One of the classic papers in vicariance biogeography.  Rosen proposes using reduced area cladograms to determine whether a vicariance event has taken place, and gives an example of reduced area cladograms using two species of freshwater fish.  A ‘must-read.’

 

Schulte, J. A., Macey, J. R., Espinoza, R. E. and Larson, A.  2000.  Phylogenetic relationships in the iguanid lizard genus Liolaemus: multiple origins of viviparous reproduction and evidence for recurring Andean vicariance and dispersal.  Biological Journal of the Linnean Society 69:75-102.  Interesting but long paper evaluating biogeographic and life history hypotheses.  The authors conclude that the lizards’ distributions are due to recurring vicariance and dispersal.

 

Shields, O. 1998.  Upper Triassic Pacific vicariance as a test of geological theories.  Journal of Biogeography 25:203-211.  This paper attempts to test broad geological theories by examining a wide range of taxa on either side of the Pacific.  However, the evidence is pretty sketchy and, although the author explains the importance of molecular dating, he does not provide molecular evidence to corroborate his hypothesis.

 

Strange, R. M. and Burr, B. M. 1997.  Intraspecific phylogeography of North American highland fishes: a test of the Pleistocene vicariance hypothesis.  Evolution 51:885-897.    Strange and Burr test the hypothesis that the highland fish fauna of N. Amer. were separated into disjunct distributions by Pleistocene glaciation.  They do not find congruence between the 6 fish taxa that they use in their study. 

 

Taylor, D. J., Finston, T. L., and Herbert, P. D. N. 1998.  Biogeography of a widespread freshwater crustacean: pseudocongruence and cryptic endemism in the North American Daphnia laevis complex.  Evolution 52:1648-1670.   This paper emphasizes the importance of dating lineage splits and comparing the relative dates to vicariance events.  A lineage split in Daphnia originally appeared to be the result of Pleistocene glaciation, but molecular data estimates the split at about 12 m.y.a.!  An example of ‘pseudocongruence.’

 

Van Tuinen, M., Sibley, C. G., and Hedges, S. B. 1998.  Phylogeny and biogeography of ratite birds inferred from DNA sequences of the mitochondrial ribosomal genes.  Molecular Biology and Evolution 15:370-376.  This paper deals with a hotly debated question in biogeography – are the ratite birds an example of convergent evolution or are they closely related?  This paper presents molecular evidence to support the hypothesis that ratites are derived from a common ancestor which was fragmented during the breakup of Gondwanaland. 

 

Voelker, G.  1999.  Dispersal, vicariance, and clocks: historical biogeography and speciation in a cosmopolitan passerine genus (Anthus: Motacillidae).  Evolution 53:1536-1552.   Voelker introduces molecular clocks to the study of historical biogeography, insisting that they can help in evaluating vicariance hypotheses by timing splits between taxa.  He uses Ronquist’s DIVA method and Bremer’s ancestral area method to make hypotheses about the ancestral range of pipits.

 

Wiley, E. O. 1988.  Vicariance Biogeography.  Annual Review of Ecology and Systematics 19:513-542.  Review article.  Contains a great list of references for pre-1988 vicariance papers.  Valuable for its overview of vicariance biogeography as well as for its review and evaluation of methods.