Skip to main content Skip to main navigation menu Skip to site footer
Type: Article
Published: 2016-02-09
Page range: 84–120
Abstract views: 127
PDF downloaded: 2

Geometric morphometrics and molecular systematics of Xanthocnemis sobrina (McLachlan, 1873) (Odonata: Coenagrionidae) and comparison to its congeners

Plant Health & Environment Laboratory, Investigation and Diagnostic Centres and Response, Ministry for Primary Industries, 231 Morrin Rd, Auckland 1072, New Zealand.
Partnership Ranger, Tongariro District Office, Department of Conservation, 33 Turanga Place, Turangi 3334, New Zealand.
School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.
School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand Department of Plant Pathology and Emerging Pathogens Institute, University of Florida, Gainesville, FL 32611, U.S.A. Electron Microscope Unit, Division of Medical Biochemistry, Department of Clinical Laboratory Sciences, University of Cape Town, Observatory 7700, South Africa.
School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand
School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand
School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand
School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand
Department of Ecology, Lincoln University, PO Box 85084, Christchurch 7647, New Zealand.
Department of Ecology, Lincoln University, PO Box 85084, Christchurch 7647, New Zealand.
Department of Ecology, Lincoln University, PO Box 85084, Christchurch 7647, New Zealand.
Odonata Chatham Island damselflies dragonflies New Zealand North Island South Island Zygoptera

Abstract

The taxonomy of the damselfly genus Xanthocnemis is revised, with particular focus on populations inhabiting the North Island of New Zealand. Earlier studies revealed two species: X. sobrina, restricted to cool, shaded streams in kauri forests and other forested areas, and X. zealandica, a common species throughout New Zealand except the Chatham and subantarctic islands. A field study encompassing aquatic habitats throughout the whole North Island was carried out to establish the relationship between morphological variation (body size and various morphological traits over the entire body) observed by previous researchers with ecological conditions and/or geographical location. The main aim was to propose reliable diagnostic features that could be used in future studies. Morphological and molecular variation was assessed. Morphological examination included assigning landmarks for all body parts corresponding to the external morphological features that are usually used in Odonata taxonomy. Molecular analysis targeted fragments of the 28S and 16S rRNA genes. Congruence was sought between both types of data, statistical support for two morphological types previously described as different species and a maximum likelihood phylogenetic tree in conjunction with a pairwise genetic distance matrix constructed from the DNA sequences obtained from the sampled specimens. Geometric morphometrics revealed statistically significant differentiation between specimens identified as X. zealandica and X. sobrina for four traits: (1) dorsal view of the head for both sexes as well as male appendages from (2) dorsal, (3) ventral and (4) lateral views. Wings appeared different when analysed for males only. Molecular analysis, however, grouped all specimens into a single undifferentiated cluster with very low mean pairwise distance (<0.01) between them showing almost no variation at the molecular level among the sampled populations on the North Island. Therefore, an additional analysis of the mitochondrial cytochrome c-oxidase I gene was carried out comparing randomly selected North Island specimens to Xanthocnemis specimens targeted in other molecular studies (Nolan et al. 2007, Amaya-Perilla et al. 2014). The analysis of the COI gene confirmed that all North and South Island isolates of Xanthocnemis cluster together in a well-supported clade with pairwise identity >96% and ~93% pairwise identity with X. tuanuii sequences obtained from the Chatham Island specimens. A careful investigation of the thin plate spline deformations generated for the geometric morphometric landmarks showed that the significant variations in the appendages of the Xanthocnemis specimens appeared to be the result of size, rather than shape, differences. Therefore, X. sobrina is proposed as a synonym of X. zealandica. Recently Amaya-Perilla et al. (2014) synonymised X. sinclairi with X. zealandica and confirmed the status of the Chatham Island X. tuanuii as a distinct species. It is therefore proposed that the genus Xanthocnemis consists of two species only: zealandica occurring all over the North, South and Stewart Islands, and tuanuii, endemic to Chatham and Pitt islands. Considering several statistical tests involving body measurements and ecological variables recorded during the field study, as well as various discussion points from similar studies of other species of Odonata, two alternative hypotheses are proposed for future testing. The first hypothesis synonymises X. sobrina with X. zealandica and suggests a possible explanation for the evolution of the two morphological traits that have previously been considered diagnostic for these species. The second hypothesis suggests that as typical X. sobrina were not sampled during this study this could represent a species that is now extinct, unless future studies prove it otherwise.

 

References

  1. Adams, D.C., Rohlf, F.J. & Slice, D.E. (2004) Geometric morphometrics: ten years of progress following the ‘revolution’. Italian Journal of Zoology, 71 (1), 5–16.

    http://dx.doi.org/10.1080/11250000409356545

    Alfken, J. (1903) Beitrag zur Insectenfauna der hawaiischen und neuseeländisch Inseln (Ergebnisse einer Reise nach dem Pacific) Schauinsland 1896–97. Zoologische Jahrbücher, Abteilung für Systematic, Ökologie and Geographie der Tiere, 19, 561–628.

    Allendorf, W., Leary, R., Spruell, P. & Wenburg, J. (2001) The problem with hybrids: setting conservation guidelines. Trends in Ecology & Evolution, 16 (11), 613-622.

    Amaya-Perilla, C., Marinov, M., Holwell, G., Varsani, A., Stainton, D., Kraberger, S., Dayaram, A., Curtis, N., Cruickshank, R. & Paterson, A. (2014) Comparative study of the Chatham Islands Odonata, II: Morphometric and molecular comparison between Xanthocnemis tuanuii Rowe, 1981 and X. zealandica (McLachlan, 1873) with notes on the taxonomic position of Xanthocnemis sinclairi Rowe, 1987 (Zygoptera: Coenagrionidae). International Dragonfly Fund—Report, 75, 1–27.

    Armstrong, J.S. & Corbet, P.S. (1980) Conversations about New Zealand dragonflies. Societas Internationalis Odonatologica, Rapid Communications, 2, 1–73.

    Asahina, S. (1974) Interspecific hybrids among the Odonata. Japanese Journal of Zoology, 17 (2), 67–75.

    Asahina, S. (1981) Further records of interspecific hybrid among Odonata. Tombo, 24 (1/4), 17–22.

    Atropos (2013) UK journal for butterfly, moth and dragonfly enthusiasts. Autumn, 2013, 50, 83–86.

    Boyes, J.W., van Brink, J.M. & Kiauta, B. (1980) Sixteen dragonflies karyotypes from the Republic of South Africa and Swaziland, with evidence of the possible hybrid nature of Orthetrum julia falsum Longfield (Anisoptera: Libellulidae). Odonatologica, 9 (2), 131–145.

    Calvert, P.P. (1893) Pairing of different species. Entomological News, 4, 1–268.

    Dijkstra, K.-D., Kalkman, V., Dow, R., Stokvis, F. & van Tol, J. (2014) Redefining the damselfly families: a comprehensive molecular phylogeny of Zygoptera (Odonata). Systematic Entomology, 39, 68–96.

    http://dx.doi.org/10.1111/syen.12035

    Deacon, K.J.G. (1979) The seasonality of four Odonata species from mid Canterbury, South Island, New Zealand. PhD-thesis, University of Canterbury, Christchurch, New Zealand, 209 pp.

    Edgar, R. (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Research, 32, 1792–1797.

    http://dx.doi.org/10.1093/nar/gkh340

    Freeland, J.R. & Conrad, K.F. (2002) Genetic similarity within and among populations of the Variable and Azure damelflies (Coenagrion pulchellum and C. puella). Hydrobiologia, 479 (1–3), 69–73.

    http://dx.doi.org/10.1023/A:1021058231151

    Guindon, S., Dufayard, J., Lefort, V., Anisimova, M., Hordijk, W. & Gascuel, O. (2010) New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Systematic Biology, 59, 307–321.

    http://dx.doi.org/10.1093/sysbio/syq010

    Hassal, C., Keat, S., Thompson, D. & Watts, P. (2014) Bergmann’s rule is maintained during a rapid range expansion of a damselfly. Global Change Biology, 20, 475–482.

    http://dx.doi.org/ 10.1111/gcb.12340

    Hayashi, F., Dobata, S. & Futahashi, R. (2005) Disturbed population genetics: Suspected introgressive hybridization between two Mnais damselfly species (Odonata). Zoological Science, 22, 869–881.

    http://dx.doi.org/10.2108/zsj.22.869

    Heads, M. (1998) Biogeographical disjunction along the Alpine fault, New Zealand. Botanical Journal of the Linnean Society, 63, 161–176.

    http://dx.doi.org/10.1111/j.1095-8312.1998.tb01512.x

    Heads, M. & Craw, R. (2004) The Alpine fault biogeographic hypothesis revisited. Cladistics, 20, 184–190.

    http://dx.doi.org/10.1111/j.1096-0031.2004.00009.x

    Holwell, G. (2008) Geographic variation in genital morphology of Ciulfina praying mantids. Journal of Zoology, 276, 108–114.

    http://dx.doi.org/10.1111/j.1469-7998.2008.00475.x

    Holwell, G. & Herberstein, M. (2010) Chirally dimorphic male genitalia in praying mantids (Ciulfina: Liturgusidae. Journal of Morphology, 271, 1176–1184.

    http://dx.doi.org/10.1002/jmor.10861

    Holwell, G., Winnick, C., Tregenza, T. & Herberstein, M. (2010) Genital shape correlates with sperm transfer success in the praying mantis Ciulfina klassi (Insecta: Mantodea). Behavioral Ecology and Sociobiology, 64 (4), 617–625.

    http://dx.doi.org/10.1007/s00265-009-0879-2

    Hutton, F. (1898) On a collection of insects from the Chatham Islands with descriptions of three new species. Transactions and Proceedings New Zealand Institute, 30, 155–60.

    Hutton, F. (1899) The Neuroptera of New Zealand. Transactions and Proceedings of New Zealand Institute, 31, 208–249.

    Hudson, G. (1904) New Zealand Neuroptera. A popular introduction to the life-histories and habits of may-flies, dragon-flies, caddis-flies and allied insects inhabiting New Zealand. Including notes on their relation to angling. West, Newman and Co., London, 102 pp.

    Ishizawa, N. (2008) Three events in oviposition behaviour of Sympetrum frequens Selys. Digest of Japanese Odonatological Short Communications, 21, 1–10.

    Jordan, S., Simon, C. & Polhemus, D. (2003) Molecular systematics and adaptive radiation of Hawaii's endemic damselfly genus Megalagrion (Odonata: Coenagrionidae). Systematic Biology, 52 (1), 89–109.

    http://dx.doi.org/10.1080/10635150390132803

    Kamigaki, K. (2001) Intergeneric tandem of Sympetrum frequens male and Pantala flavescens female. Sympetrum Hyogo, 7/8, 1–9.

    Kiauta, B. (1971) An unusual case of precocious segregation and chromosome fragmentation in the primary spermatocytes of the damselfly, Calopteryx virgo meridionalis Selys, 1873, as evidence for a possible hybrid character of some populations of the Calopteryx virgo-complex (Odonata, Zygoptera: Calopterygidae). Genen Phaenen, 14 (2), 32–40.

    Kimmins, D.E. (1970) A list of the type-specimens of Odonata in the British Museum (Natural History). Part III. Bulletin of the British Museum (Natural History) Entomology, 24 (6), 171–205.

    Kosterin, O.E. (2000) Observation on an intergeneric copulation between a male Cordulia aenea (L.) and a female Epitheca bimaculata (Charp.) (Anisoptera: Corduliidae). Notulae Odonatologicae, 5 (5), 55–56.

    Macfarlane, R. (1979) Notes on insects of the Chatham Islands. New Zealand Entomologist, 7 (1), 64–70.

    http://dx.doi.org/10.1080/00779962.1979.9722334

    Marinov, M. & McHugh, P. (2010) Comparative study of the Chatham Islands Odonata: Morphological variability, behaviour and demography of the endemic Xanthocnemis tuanuii Rowe, 1987. International Dragonfly Fund—Report, 30, 1–44.

    May, M. (2002) Phylogeny and taxonomy of the damselfly genus Enallagma and related taxa (Odonata: Zygoptera: Coenagrionidae). Systematic Entomology, 27, 387–408.

    http://dx.doi.org/10.1046/j.1365-3113.2002.00188.x

    McPeek, M., Shen, L., Torrey, J. & Farid, H. (2008) The tempo and mode of three-dimensional morphological evolution in male reproductive structures. The American Naturalist, 171 (5), 158–178.

    http://dx.doi.org/10.1086/587076

    McPeek, M., Symes, L., Zong, D. & McPeek, C. (2011) Species recognition and patterns of population variation in the reproductive structures of a damselfly genus. Evolution, 65 (2), 419–428.

    http://dx.doi.org/10.1111/j.1558-5646.2010.01138.x

    Moore, N. (1989) A visitor’s observations on the dragonflies of New Zealand and their conservation. New Zealand Entomologist, 12, 5–13.

    http://dx.doi.org/10.1080/00779962.1989.9722555

    Muhire, B., Varsani, A. & Martin, D. (2014) SDT: A virus classification tool based on pairwise sequence alignment and identity calculation. PLoS One, 9 (9), e108277.

    http://dx.doi.org/10.1371/journal.pone.0108277

    Mutanen, M. & Pretorius, E. (2007) Subjective visual evaluation vs traditional and geometric morphometrics in species delimitation: a comparison of moth genitalia. Systematic Entomology, 32 (2), 371–386.

    http://dx.doi.org/10.1111/j.1365-3113.2006.00372.x

    Nolan, L., Hogg, I., Sutherland, D., Stevens, M. & Schnabel, K. (2007) Allozyme and mitochondrial DNA variability within the New Zealand damselfly genera Xanthocnemis, Austrolestes, and Ischnura (Odonata). New Zealand Journal of Zoology, 34, 371–380.

    http://dx.doi.org/10.1080/03014220709510097

    Otto, J. & Wilson, K. (2001) Assessment of the usefulness of ribosomal 18S and mitochondrial COI sequences in Prostigmata phylogeny. In: Halliday, R., Walter, D., Proctor, H., Norton, R. & Colloff, M. (Eds.), Acarology: Proceedings of the 10th International Congress. Melbourne, CSIRO, pp. 100–109.

    Posada, D. (2009) Selection of models of DNA evolution with jModelTest. Methods in Molecular Biology, 537, 93–112.

    http://dx.doi.org/10.1007/978-1-59745-251-9_5

    Piersani, S., Frati, F., Conti, E., Gaino, E., Rebora, M. & Salerno, G. (2014) First evidence of the use of olfaction in Odonata behaviour. Journal of Insect Physiology, 62, 26–31.

    Rowe, R. (1981) A new species of Xanthocnemis Tillyard (Odonata: Coenagrionidae) from the Chatham Islands, New Zealand. Records of the Auckland Institute and Museum, 18, 205–209.

    Rowe, R. (1985) A taxonomic revision of the genus Xanthocnemis (Odonata: Coenagrionidae) and an investigation of the larval behaviour of Xanthocnemis zealandica. PhD-thesis, University of Canterbury, Christchurch, New Zealand, 296 pp.

    Rowe, R. (1987) The dragonflies of New Zealand. Auckland University Press, Auckland, 260 pp.

    Rowe, R., Moore, S. & Marinov, M. (2013) Xanthocnemis sobrina. The IUCN Red List of Threatened Species. Version 2014.2. Available from: www.iucnredlist.org (accessed 15 August 2014)

    Sánches-Guillén, R.A., Cordoba-Aguilar, A., Cordero-Rivera, A. & Wellenreuther, M. (2014) Genetic divergence predicts reproductive isolation in damselflies. Journal of Evolutionary Biology, 27 (1), 76–87.

    http://dx.doi.org/10.1111/jeb.12274

    Schorr, M. & Paulson, D. (2014) World list of Odonata. Available from: http://www.pugetsound.edu/academics/academic-resources/slater-museum/biodiversity-resources/dragonflies/world-odonata-list/ (accessed 13 August 2014)

    Tamura, K., Peterson, D., Peterson, N., Stecher, G., Nei, M. & Kumar, S. (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Molecular Biology and Evolution, 28, 2731–2739.

    http://dx.doi.org/10.1093/molbev/msr121

    Tillyard, R. (1913) On some new and rare Australian Agrionidae. Proceedings of the Linnean Society New South Wales, 37, 403–479.

    Turgeon, J. & McPeek, M. (2002) Phylogenetic analysis of a recent radiation of Enallagma damselflies (Odonata: Coenagrionidae). Molecular Ecology, 11, 1989–2001.

    http://dx.doi.org/10.1046/j.1365-294X.2002.01580.x

    Turgeon, J., Stoks, R., Thum, R., Brown, J. & McPeek, M. (2005) Simultaneous quaternary radiation of three damselfly clades across the Holarctic. The American Naturalist, 165 (4), 78–107.

    http://dx.doi.org/10.1086/428682

    Ugai, S. (2000) Hybrid records of dragonflies in Japan. Nature & Insects, 35 (11), 18–22.

    Verberk, W. & Atkinson, D. (2013) Why polar gigantism and Palaeozoic gigantism are not equivalent: effects of oxygen and temperature on the body size of ectotherms. Functional Ecology, 27 (6), 1275–1285.

    http://dx.doi.org/10.1111/1365-2435.12152

    Wallis, G. & Trewick, S. (2001) Finding fault with vicariance: A critique of Heads (1998). Systematic Biology, 50 (4), 602–609.

    http://dx.doi.org/10.1080/10635150119078

    Westfall, M. & May, M. (2006) Damselflies of North America. 2nd edition. Scientific, Gainesville, FL, 502 pp.

    Wise, K.A.J. (1965) An annotated list of the aquatic and semi-aquatic insects of New Zealand. Pacific Insects, 7 (2), 191–216.

    Wise, K.A.J. (1973) A list of bibliography of the aquatic and water-associated insects of New Zealand. Records of the Auckland Institute and Museum, 10, 143–187.

    Wise, K.A.J. (1977) A synonymic checklist of the Hexapoda of the New Zealand sub-region: The smaller orders. Bulletin of the Auckland Institute and Museum, 11, 1–176.