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Marine and Freshwater Research Marine and Freshwater Research Society
Advances in the aquatic sciences
RESEARCH ARTICLE

Contrasting patterns of genetic structure and disequilibrium in populations of a stone-cased caddisfly (Tasimiidae) from northern and southern Australia

Alicia Slater Schultheis A D , Richard Marchant B and Jane Margaret Hughes C
+ Author Affiliations
- Author Affiliations

A Biology Department, Stetson University, 421 N. Woodland Blvd. Unit 8264, DeLand, FL 32723, USA.

B Museum of Victoria, GPO Box 666, Melbourne, Victoria 3001, Australia.

C Griffith School of Environment, Griffith University, Nathan, Queensland 4111, Australia.

D Corresponding author. Email: aschulth@stetson.edu

Marine and Freshwater Research 59(3) 235-245 https://doi.org/10.1071/MF07104
Submitted: 22 May 2007  Accepted: 26 February 2008   Published: 30 April 2008

Abstract

In marine and freshwater invertebrate populations, microscale genetic differentiation or ‘genetic patchiness’ is thought to result from variation in the abundance and genetic composition of new recruits at a particular location. In the present study, the role of the adult emergence patterns in genetic patchiness was examined using mtDNA and two microsatellite loci to compare patterns of genetic differentiation in asynchronously (subtropical) and synchronously emerging (temperate) populations of the stone-cased caddisfly Tasimia palpata. A 550 base pair region of the mitochondrial cytochrome c oxidase subunit I gene (COI) was sequenced in at least 14 individuals from each population. Genetic structure was detected only at the reach scale in the subtropical populations and no genetic differentiation was detected in temperate populations. There were more deviations from Hardy–Weinberg equilibrium (HWE) in subtropical populations than in temperate populations where 44% and 12.5%, respectively, of tests for deviations from HWE were significant. Although distinct patterns of genetic structure and deviations from HWE were observed in the subtropical and temperate populations of T. palpata, no conclusive evidence was found to suggest that the differences are caused by differences in emergence patterns. We hypothesise that genetic patchiness must be caused by post-recruitment processes, most likely the preservation of oviposition ‘hotspots’ in subtropical streams.

Additional keywords: dispersal, microsatellites, mtDNA, recruitment, Trichoptera.


Acknowledgements

We thank Mia Hillyer and David Hurwood for their assistance in collecting samples and Melissa Gibbs for assistance with the illustrations. This work was supported by NSF grant INT-0076202 to A. Schultheis and a grant from the Australian Research Council to J. Hughes, S. Bunn, and R. Marchant.


References

Baker, A. M. , Williams, S. A. , and Hughes, J. M. (2003). Patterns of spatial genetic structuring in a hydropsychid caddisfly (Cheumatopsyche sp. AV1) from southeastern Australia. Molecular Ecology 12, 3313–3324.
Crossref | GoogleScholarGoogle Scholar | PubMed | Cartwright D. I. (1997) ‘Preliminary guide to the identification of late instar larvae of Australian Ecnomidae, Philopotamidae and Tasimiidae (Insecta: Trichoptera).’ Identification Guide No. 10. (Cooperative Research Centre for Freshwater Ecology, Albury, NSW.)

Clement, M. , Posada, D. , and Crandall, K. (2000). TCS: a computer program to estimate gene genealogies. Molecular Ecology 9, 1657–1660.
Crossref | GoogleScholarGoogle Scholar | PubMed | Lenfant P., and Planes S. (2002) Temporal genetic changes between cohorts in a natural population of a marine fish, Diplodus sargus. Biological Journal of the Linnaean Society 76, 9–20.

Li, G. , and Hedgecock, D. (1998). Genetic heterogeneity, detected by PCR-SSCP, among samples of larval Pacific oysters (Crassostrea gigas) supports the hypothesis of large variance in reproductive success. Canadian Journal of Fisheries and Aquatic Sciences 55, 1025–1033.
Crossref | GoogleScholarGoogle Scholar | Schneider S., Roessli D., and Excoffier L. (2000). ‘ARLEQUIN ver. 2.000: A software for population genetics analysis.’ (Genetics and Biometry Laboratory, University of Geneva, Switzerland.)

Schultheis, A. S. , and Hughes, J. M. (2005). Spatial patterns of genetic structure among populations of a stone cased caddisfly (Trichoptera: Tasimiidae) in south-east Queensland, Australia. Freshwater Biology 50, 2002–2010.
Crossref | GoogleScholarGoogle Scholar |

Schultheis, A. S. , Weigt, L. A. , and Hendricks, A. C. (2002). Gene flow, dispersal, and nested clade analysis among populations of the stonefly Peltoperla tarteri in the southern Appalachians. Molecular Ecology 11, 317–327.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Slatkin, M. (1985). Gene flow in natural populations. Annual Review of Ecology and Systematics 16, 393–430.
Crossref | GoogleScholarGoogle Scholar |

Svensson, B. W. (1974). Population movements of adult Trichoptera at a South Swedish stream. Oikos 25, 157–175.
Crossref | GoogleScholarGoogle Scholar |

Sweeney, B. W. , Funk, D. H. , and Vannote, R. L. (1987). Genetic variation in stream mayfly (Insecta: Ephemeroptera) populations of eastern North America. Annals of the Entomological Society of America 80, 600–612.


Van Oosterhout, C. , Hutchinson, W. F. , Wills, D. P. M. , and Shipley, P. (2004). MICRO-CHECKER: Software for identifying and correcting genotyping errors in microsatellite data. Molecular Ecology Notes 4, 535–538.
Crossref | GoogleScholarGoogle Scholar |

Watts, R. J. , Johnson, M. S. , and Black, R. (1990). Effects of recruitment on genetic patchiness in the urchin Echinometra mathaei in Western Australia. Marine Biology 105, 145–151.
Crossref | GoogleScholarGoogle Scholar |

Watts, P. C. , Rouquette, J. R. , Saccheri, I. J. , Kemp, S. J. , and Thompson, D. J. (2004). Molecular and ecological evidence for small-scale isolation by distance in an endangered damselfly, Coenagrion mercuriale. Molecular Ecology 13, 2931–2945.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Weir, B. S. , and Cockerham, C. C. (1984). Estimating F-statistics for the analysis of population structure. Evolution 38, 1358–1370.
Crossref | GoogleScholarGoogle Scholar |

Whitlock, M. C. , and McCauley, D. E. (1999). Indirect measures of gene flow and migration: FST ≠ 1/(4Nm + 1). Heredity 82, 117–125.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Wilcock, H. R. , Hildrew, A. G. , and Nichols, R. A. (2001). Genetic differentiation of a European caddisfly: past and present gene flow among fragmented larval habitats. Molecular Ecology 10, 1821–1834.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Wilcock, H. R. , Bruford, M. W. , Hildrew, A. G. , and Nichols, R. A. (2005). Recruitment, kin and the spatial genetic structure of a caddisfly Plectrocnemia conspersa in a southern English stream. Freshwater Biology 50, 1499–1514.
Crossref | GoogleScholarGoogle Scholar |

Wilcock, H. R. , Bruford, M. W. , Nichols, R. A. , and Hildrew, A. G. (2007). Landscape, habitat characteristics and the genetic population structure of two caddisflies. Freshwater Biology 52, 1907–1929.
Crossref | GoogleScholarGoogle Scholar |

Zera, A. J. (1981). Genetic structure of two species of waterstriders (Gerridae: Hemiptera) with differing degrees of winglessness. Evolution 35, 218–225.
Crossref | GoogleScholarGoogle Scholar |

Zickovich, J. M. , and Bohonak, A. J. (2007). Dispersal ability and genetic structure in aquatic invertebrates: a comparative study in southern California streams and reservoirs. Freshwater Biology 52, 1982–1996.
Crossref | GoogleScholarGoogle Scholar |