Hostname: page-component-586b7cd67f-l7hp2 Total loading time: 0 Render date: 2024-11-24T12:10:10.978Z Has data issue: false hasContentIssue false

Systematics and ecology of Anachipteria geminus sp. nov. (Acari: Oribatida: Achipteriidae) from arboreal lichens in western North America

Published online by Cambridge University Press:  02 April 2012

Zoë Lindo*
Affiliation:
Department of Biology, University of Victoria, P.O. Box 3020, Station CSC, Victoria, British Columbia, Canada V8W 3N5
Marilyn Clayton
Affiliation:
Forest Biodiversity Network, Pacific Forestry Centre, Canadian Forest Service, Natural Resources Canada, Victoria, British Columbia, Canada V8Z 1M5
Valerie M. Behan-Pelletier
Affiliation:
Biodiversity Program, Research Branch, Agriculture and Agri-Food Canada, K.W. Neatby Building, Ottawa, Ontario, Canada K1A 0C6
*
1Corresponding author (e-mail: [email protected]).

Abstract

We present the systematics and ecology of a new species of arboreal oribatid mite in the family Achipteriidae, Anachipteria geminussp. nov., a dominant arthropod in canopy lichens associated with western hemlock (Tsuga heterophylla (Raf.) Sarg. (Pinaceae)) and Pacific silver fir (Abies amabilis (Dougl. ex Loud.) Dougl. ex Forbes (Pinaceae)) in the coniferous temperate and montane forests of the Pacific Northwest of North America. The species is described on the basis of the morphology of all active instars plus molecular sequence data for the D3 region of the 28s rRNA (D3-28s) and mitochondrial cytochrome oxidase 1 (CO1) genes. Anachipteria geminus is the dominant oribatid mite in foliose lichens in the upper canopies of Pacific montane conifer trees. Specimens were found in 100% of canopy lichens sampled, and abundances can reach 1450 individuals / 100 g dry mass of lichen. Analysis of the population structure indicates that A. geminus has seasonally stable populations consistent with overlapping generations. Anachipteria geminus expresses morphological character states that require expanding the diagnoses of the genus Anachipteria and the family Achipteriidae. A revised diagnosis and morphological key to species of Anachipteria in Canada are given.

Résumé

Nous présentons la systématique et l’écologie d’une nouvelle espèce d’oribatide arboricole dans la famille Achipteriidae, Anachipteria geminussp. nov., un arthropode dominant dans les lichens de la canopée associés à la pruche de l’ouest (Tsuga heterophylla (Raf.) Sarg. (Pinaceae)) et au sapin gracieux (Abies amabilis (Dougl. ex Loud.) Dougl. ex Forbes (Pinaceae)) dans les forêts de conifères tempérées de montagne du Pacifique au Nord-ouest de l’Amérique du Nord. L’espèce est décrite sur la base de la morphologie de toutes les stades actifs, plus les données d’ordre moléculaires pour la région D3 de 28 rRNA (D3-28) et mitochondrial cytochrome oxidase 1 (CO1). Anachipteria geminus est l’oribatide dominant dans les lichens foliose des canopées supérieures des conifères de montagne du Pacifique au Nord-ouest. Les exemplaires ont été trouvés dans 100 % des lichens des canopées échantillonnés et la densité peut atteindre 1450 individus / 100 g de masse sec du lichen. L’analyse de la structure démographique indique que A. geminus a des populations saisonnièrement stables en accord avec les générations chevauchantes. Anachipteria geminus exprime des états de caractères morphologiques qui exigent le développement de les diagnostiques du genre Anachipteria et de la famille Achipteriidae. Une diagnostique révisée et une clé morphologique aux espèces d’Anachipteria au Canada sont données.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Altschul, S.F., Madden, T.L., Schaffer, A.A., Zhang, J., Zhang, Z., Miller, W., and Lipman, J. 1997. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Research, 25: 33893402.CrossRefGoogle ScholarPubMed
André, H.M. 1985. Associations between corticolous microarthropod communities and epiphytic cover on bark. Holarctic Ecology, 8: 113119.Google Scholar
Barker, M., and Standridge, N. 2002. Ropes as mechanisms for canopy access. In The global canopy handbook. Edited by Mitchell, A.W., Secoy, K., and Jackson, T.. Global Canopy Programme, Oxford, United Kingdom. pp. 1323.Google Scholar
Behan-Pelletier, V.M. 2001. Phylogenetic relationships of Hypozetes (Acari: Tegoribates). In Acarology: Proceedings of the 10th International Congress, Canberra, Australia, 5–10 July 1998. Edited by Halliday, R.B., Walter, D.E., Proctor, H.C., Norton, R.A., and Colloff, M.J.. CSIRO Publishing, Melbourne, Australia. pp. 5057.Google Scholar
Behan-Pelletier, V.M., and Eamer, B. 2004. Diversity of Oribatida in Canada [online]. Available from http://www.cbif.gc.ca/spp_pages/mites/phps/index_e.php [accessed 30 April 2008].Google Scholar
Behan-Pelletier, V.M., and Walter, D.E. 2000. Biodiversity of oribatid mites (Acari: Oribatida) in tree canopies and litter. In Invertebrates as webmasters in ecosystems. Edited by Coleman, D.C. and Hendrix, P.F.. CAB International, Wallingford, United Kingdom. pp. 187202.CrossRefGoogle Scholar
Behan-Pelletier, V.M., Paoletti, M.G., Bisset, B., and Stinner, B.R. 1993. Oribatid mites of forest habitats in northern Venezuela. Tropical Zoology (special issue), 1: 3954.Google Scholar
Clayton, M., and Humble, L.L. 1999. Microarthropod voucher specimens. Technology Transfer Note No. 19, Forestry Research Applications, Pacific Forestry Centre, Canadian Forest Service, Natural Resources Canada, Victoria, British Columbia.Google Scholar
Domes, K., Althammer, M., Norton, R.A., Scheu, S., and Maraun, M. 2007. The phylogenetic relationship between Astigmata and Oribatida (Acari) as indicated by molecular markers. Experimental and Applied Acarology, 42: 159171.CrossRefGoogle ScholarPubMed
Folmer, O., Black, M., Hoeh, W., Lutz, R., and Vrijenhoek, R. 1994. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Molecular Marine Biology and Biotechnology, 3: 294299.Google ScholarPubMed
Grandjean, F. 1932. Observations sur les Oribates (3esérie). Bulletin du Muséum 2e Série, 4: 292306.Google Scholar
Grandjean, F. 1954. Essai de classification des ori-bates (acariens). Bulletin de la Société Zoologique de France, 78: 421446.Google Scholar
Green, R.M., and Klinka, K. 1994. A field guide to site identification and interpretation for the Vancouver Forest Region. Land Management Handbook 28, British Columbia Ministry of Forests, Victoria, British Columbia.Google Scholar
Heethoff, M., Domes, K., Laumann, M., Maraun, M., Norton, R.A., and Scheu, S. 2007. High genetic divergences indicate ancient separation of parthenogenetic lineages of the oribatid mite Platynothrus peltifer (Acari, Oribatida). European Journal for Evolutionary Biology, 20: 392402.CrossRefGoogle ScholarPubMed
Lindo, Z., and Winchester, N.N. 2006. A comparison of microarthropod assemblages with emphasis on oribatid mites in canopy suspended soils and forest floors associated with ancient western redcedar trees. Pedobiologia, 50: 3141.CrossRefGoogle Scholar
Lindo, Z., and Winchester, N.N. 2007. Local–regional boundary shifts in oribatid mite (Acari: Oribatida) communities: species–area relationship in arboreal habitat islands of a coastal temperate rain forest, Vancouver Island, Canada. Journal of Biogeography, 34: 16111621.Google Scholar
Maraun, M., Heethoff, M., Schneider, K., Scheu, S., Weigmann, G., Cianciolo, J., Thomas, R., and Norton, R.A. 2004. Molecular phylogeny of oribatid mites (Oribatida, Acari): evidence for multiple radiations of parthenogenetic lineages. Experimental and Applied Acarology, 33: 183201.CrossRefGoogle ScholarPubMed
Marshall, V.G., Reeves, R.M., and Norton, R.A. 1987. Catalogue of the Oribatida (Acari) of continental United States and Canada. Memoirs of the Entomological Society of Canada, 139: 1418.Google Scholar
Nicolai, V. 1993. The arthropod fauna on the bark of deciduous and coniferous trees in a mixed forest of the Itasca State Park, MN, United States of America. Spixiana, 16: 6169.Google Scholar
Norton, R.A. 1977. A review of F. Grandjean's system of leg chaetotaxy in the Oribatei and its application to the Damaeidae. In Biology of oribatid mites. Edited by Dindal, D.L.. College of Environmental Science and Forestry, State University of New York, Syracuse, New York. pp. 3362.Google Scholar
Pérez-Iñigo, C. 1993. Acari, Oribatida, Poronota. Fauna Iberica. Vol. 3. Museo Nacional de Ciencias Naturales, Consejo Superior de Investigaciones Científicas, Madrid, Spain.Google Scholar
Root, H.T., Kawahara, A.Y., and Norton, R.A. 2007 a. Anachipteria sacculifera n. sp. (Acari: Oribatida: Achipteriidae) from arboreal lichens in New York State. Acarologia, 157: 187195.Google Scholar
Root, H.T., McGee, G.G., and Norton, R.A. 2007 b. Arboreal mite communities on epiphytic lichens of the Adirondack Mountains of New York, United States of America. Northeastern Naturalist, 14: 425438.CrossRefGoogle Scholar
Seniczak, S. 1977. The systematic position of moss mites of the genus Anachipteria Grandjean 1935 (Acarina, Oribatei) in the light of ontogenetic studies. Acarologia, 18: 740747.Google Scholar
Seniczak, S., and Seniczak, A. 2007. Morphology of juvenile stages of Parachipteria bella (Sellnick, 1928) and P. willmanni Hammen, 1952 (Acari: Oribatida: Achipteriidae). Annales Zoologici (Warszawa), 57: 533540.Google Scholar
Seyd, E.L., and Seaward, M.R.D. 1984. The association of oribatid mites with lichens. Zoological Journal of the Linnean Society, 80: 369420.CrossRefGoogle Scholar
Shaldybina, E.S. 1975. External morphology of oribatid mites. In Opredelitel'Obitayushchikh v Pochve Kleshchey. Sarcoptiformes. Edited by Ghilarov, M.S. and Krivolutskii, D.A.. Nauka, Moscow. pp. 2131.Google Scholar
Subías, L.S. 2007. Listado sistemätico, sinonímico y biogeogräfico de los äcaros oribätidos (Acariformes, Oribatida) de mundo (excepto fósiles) [online]. [Originally published in Graellsia, 60(número extra-ordinario): 3305 (2004), actualized in April 2007.] Available at http://www.ucm.es/info/zoo/Artropodos/Catalogo.pdf [accessed 30 April 2008].CrossRefGoogle Scholar
Thompson, J.D., Higgins, D.G., and Gibson, T.J. 1994. CLUSTAL W: improving the sensitivity of progressive multiple alignment through sequence weighting, position specific gap penalties and weight matrix choice. Nucleic Acids Research, 22: 46734680.Google Scholar
Travé, J. 1960. Contribution a l'étude de la faune de la Massane (3ème note), Oribates (Acariens). 2èmepartie. Vie et Milieu, 11: 209232.Google Scholar
Travé, J., and Vachon, M. 1975. François Grandjean 1882–1975 (Notice biographique et bibliographique). Acarologia, 17: 119.Google Scholar
Walter, D.E., and O'Dowd, D.J. 1995. Beneath biodiversity: factors influencing the diversity and abundance of canopy mites. Selbyana, 16: 1220.Google Scholar
Weigmann, G. 2006. Hornmilben (Oribatida). In Die Tierwelt deutschlands. Bd 76. Edited by Dahl, F.. Verlag Goecke & Evers, Keltern, Germany.Google Scholar
Wunderle, I. 1992. Arboricolous and edaphic oribatids (Acari) in the lowland rainforest of Panguana, Peru. Amazoniana, 12: 119142.Google Scholar