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CONTENT - International Society of Zoological Sciences

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S2 ICZ2008 - Abstracts<br />

Closing the ring: biogeography <strong>of</strong> the salamander ring species<br />

Ensatina eschscholtzii<br />

Shawn R. Kuchta 1 , Duncan Parks 2 , Rachel Lockridge Mueller 3 and<br />

David B. Wake 4<br />

1<br />

Lund University, Department <strong>of</strong> Animal Ecology, Ecology Building,<br />

Sölvegatan 37, SE-223 62, Lund, Sweden<br />

2<br />

Mt. Angel Seminary, St. Benedict, OR 97373, USA<br />

3<br />

Department <strong>of</strong> Biology, Colorado State University, Fort Collins, CO<br />

80523-1878, USA<br />

4<br />

Museum <strong>of</strong> Vertebrate Zoology, Department <strong>of</strong> Integrative Biology,<br />

University <strong>of</strong> California Berkeley, Berkeley, CA 94720-3160, USA<br />

Ring species exhibit a circular arrangement <strong>of</strong> populations around a<br />

central barrier, with reproductively isolated parts overlapping at one<br />

point in the ring, yet morphological and genetic intergradation<br />

elsewhere. They evolve when two or more lineages descend from a<br />

common ancestor and become reproductively isolated while<br />

maintaining their connectivity through a chain <strong>of</strong> interbreeding<br />

populations. The salamander Ensatina eschscholtzii is a classic<br />

example <strong>of</strong> a ring species. In the original biogeographical scenario,<br />

the point <strong>of</strong> ring closure was situation in southern California, USA.<br />

Here we develop an alternative biogeographic scenario that is<br />

informed by the geomorphological development <strong>of</strong> California, and<br />

situates the point <strong>of</strong> ring closure in central coastal California. To<br />

distinguish between these two biogeographical alternatives, mtDNA<br />

sequence data was collected from 385 individuals from 224<br />

populations, and a Bayesian phylogeny was inferred. The two<br />

biogeographical scenarios were tested against our Bayesian<br />

topology, including the associated Bayesian 95% credible set <strong>of</strong><br />

trees. Our Bayesian topology contradicts the new biogeographic<br />

hypothesis.<br />

Evolution <strong>of</strong> the chromosomal organization in the Sophophora<br />

subgenus <strong>of</strong> Drosophilidae : the nucleolus organizer region<br />

Laurence Monti 1,2 , Nicole Chaminade 2 , Jean-Luc Da Lage 2 , Marie-Louise<br />

Cariou 2 , Françoise Lemeunier 2 and Sylvie Aulard 2<br />

1 present address: Laboratoire Stress, Défenses et Reproduction des<br />

Plantes, Université de Reims, Champagne, Ardenne. Campus Moulin de<br />

la Housse Bat 8 – BP 1039 51687 Reims cedex 2, France<br />

2 Laboratoire Evolution, Génomes et Spéciation, CNRS, Avenue de la<br />

Terrasse, 91198 Gif-sur-Yvette cedex, France<br />

In Drosophila, the heterochromatic sequences are found into specific<br />

chromosomal regions and submitted to rapid evolution. Due to its<br />

heterochromatic localisation, and its highly conserved structure in Insects,<br />

the nucleolus organizer region (NOR) is a useful tool to study the<br />

rearrangements <strong>of</strong> the chromosomal architecture.<br />

Using fluorescent in situ hybridization, we have analysed 54 species<br />

belonging to different groups <strong>of</strong> the Sophophora subgenus.<br />

The presence <strong>of</strong> one NOR on each sexual chromosome (X and Y), already<br />

known in Drosophila melanogaster, has been detected for the 16 other<br />

species studied in the melanogaster group. However, NORs on the Y<br />

chromosome <strong>of</strong> D. simulans and D. sechellia have lost the 28s rDNA<br />

genes.<br />

In the 26 species <strong>of</strong> the montium group, the NORs are also localised on the<br />

sex chromosomes but their number can vary between 1 and 3, which<br />

implies the loss or the gain <strong>of</strong> a NOR in some species. In conclusion, the<br />

presence <strong>of</strong> NORs on sexual chromosomes is an ancestral feature for<br />

these two groups.<br />

On the contrary, the 12 species <strong>of</strong> the ananassae group show quite<br />

different pattern, most <strong>of</strong> them showing only one NOR, on chromosome 4.<br />

This could be related to data on chromosomal evolution that point<br />

out the hypothesis <strong>of</strong> a translocation between the X or the Y<br />

chromosome (depending on authors) and chromosome 4 in D.<br />

ananassae. Such an event could explain the presence <strong>of</strong> the NOR<br />

on this autosome without rejecting that NORs on sexual<br />

chromosomes are ancestral for the Sophophora subgenus.<br />

- 12 -<br />

The Crassostrea oyster species in China<br />

Haiyan Wang 1,2 , Gu<strong>of</strong>an Zhang 1 , Xiao Liu 1 and Ximing Guo 2<br />

1Institute<br />

<strong>of</strong> Oceanology, Chinese Academy <strong>of</strong> <strong>Sciences</strong>, Qingdao,<br />

Shandong, PRC<br />

2<br />

Haskin Shellfish Research Laboratory, Institute <strong>of</strong> Marine and<br />

Coastal <strong>Sciences</strong>, Rutgers University, Port Norris, New Jersey, USA<br />

China is the home to many oyster species. Crassostrea species are<br />

most common and commercially important in China. There is<br />

considerable confusion about the classification <strong>of</strong> Crassostrea<br />

species in China. In the past five years, we collected and analyzed<br />

thousands <strong>of</strong> oysters at typical sites along the coast <strong>of</strong> China. By<br />

comparing the morphology and sequences <strong>of</strong> 16S, COI and 28S<br />

gene, we found seven Crassostrea species occurring along the coast<br />

<strong>of</strong> China. One <strong>of</strong> our studies is on the taxonomic status <strong>of</strong> the red<br />

and white forms <strong>of</strong> C. rivularis (Gould, 1861), which shows that the<br />

red oyster is the same species as C. ariakensis; the white oyster is<br />

the same species as a newly described species, C. hongkongensis<br />

(Wang et al., 2004). Another study is on the classification <strong>of</strong> small<br />

cupped oysters along the coast <strong>of</strong> China, which includes three<br />

species, C. gigas, C. angulata and C. sikamea. Recently we found<br />

that C. nippona and C. iredalei were also presented in China. Our<br />

studies clarified the classification <strong>of</strong> Crassostrea species in China,<br />

providing basic information for oyster classification, aquaculture and<br />

the protection <strong>of</strong> oyster resources in China.<br />

Guo X., S. Ford and F. Zhang. 1999. J. Shellfish Res., 18:19-31.<br />

Wang H. and X Guo, 2008. J. Shellfish Res., 27(3):481-487.<br />

Wang H., X. Guo, G. Zhang and F. Zhang. 2004. Aquaculture (242):<br />

137-155.<br />

Wang H., G. Zhang, X. Liu and X. Guo. 2008. J. Shellfish Res.,<br />

27(3):495-503.<br />

The unexpected ecology <strong>of</strong> allopatric speciation<br />

John Wiens<br />

New York, 11794-5245, Stony Brook, U.S.A.<br />

Allopatric speciation is widely considered to be the most common <strong>of</strong><br />

the thre geographic modes. Yet, there has been suprisingly little<br />

focus on the evolutionary and ecological processes that cause<br />

species to become allopatric. In this talk, I will discuss recent<br />

research from my lab looking at this neglected aspect <strong>of</strong> speciation.<br />

Consideration <strong>of</strong> how a species becomes split into allopatric populat!<br />

ions leads to an unexpected view: that the key to geographic<br />

isolation is not necessarily the adaptive divergence <strong>of</strong> different<br />

populations, but rather the failure <strong>of</strong> an ancestral species to adapt to<br />

environmental change in part <strong>of</strong> its geographic range. Thus, the<br />

ecological similarity <strong>of</strong> species over time (niche conservatism) may<br />

<strong>of</strong>ten be essential to their geographic isolation; if all species could<br />

quickly adapt to any environmental conditions, there would be few<br />

geographic barriers to gene flow and little allopatric speciation. I will<br />

describe how we have tested and supported this model <strong>of</strong> allopatric<br />

speciation through niche conservatism in North American<br />

salamanders. However, the situation is more complicated in tropical<br />

salamanders, where closely related species tend to occur in<br />

dissimilar environments. Explanations for these divergent patterns<br />

will be addressed, along with their implications for the causes <strong>of</strong> the<br />

latitudinal diversity gradient. Research on the evol! utionary ecology<br />

<strong>of</strong> allopatry will be placed within the larger conceptual framework <strong>of</strong><br />

speciation research. Finally, the relationships between speciation,<br />

niche conservatism, and other topics in ecology and evolution will be<br />

discussed (e.g., responses to climate change, spread <strong>of</strong> invasive<br />

species, community assembly, historical biogeography).

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