Hostname: page-component-788cddb947-55tpx Total loading time: 0 Render date: 2024-10-20T07:19:55.978Z Has data issue: false hasContentIssue false

BIOSYSTEMATICS OF THE GENUS IPS (COLEOPTERA: SCOLYTIDAE) IN NORTH AMERICA: REVIEW OF THE IPS CALLIGRAPHUS GROUP

Published online by Cambridge University Press:  31 May 2012

Gerald N. Lanier
Affiliation:
Department of Environmental and Forest Biology, College of Environmental Science and Forestry, State University of New York, Syracuse, New York, USA 13210
Stephen A. Teale
Affiliation:
Department of Environmental and Forest Biology, College of Environmental Science and Forestry, State University of New York, Syracuse, New York, USA 13210
Juan A. Pajares
Affiliation:
Department of Environmental and Forest Biology, College of Environmental Science and Forestry, State University of New York, Syracuse, New York, USA 13210

Abstract

The recognition of four taxa within the calligraphus species group of the genus Ips DeGeer is supported by breeding experiments, karyology, morphology, ecology, and distributions. Ips calligraphus calligraphus (Germar) occurs in the eastern United States and adjacent parts of Canada. Ips c. ponderosae (Swaine) occurs in the range of Pinus ponderosa in the Black Hills, eastern Rocky Mountains, and in the northern Sierra Madre Oriental in Mexico. Ips c. interstitialis (Eichhoff) occurs in the Caribbean Archipelago but the homogeneity of populations on the islands of Hispaniola and Jamaica and the true type locality are uncertain. Ips apache Lanier infests various pines (excluding pinyon pines) at lower altitudes from southeastern Arizona through Mexico. Populations south of the Isthmus of Tehuantepec in Caribbean pines on the east coast of Central America are provisionally considered to be I. apache. Pairings of female I. calligraphus subspecies with male I. apache were infertile. Reciprocal pairing produced rare, sterile hybrids. Fertility of I. calligraphus subspecies was normal when I. c. calligraphus was the female but reduced when the female was either I. c. ponderosae or I. c. interstitialis. All members of the group had 15 pairs of autosomes plus a sex bivalent (2n = 32) that assumed a “parachute” configuration to give a male meiotic formula of 15 AA + Xyp. Second meiosis chromosomes of I. apache lack some of the heterochromatic arms present in I. calligraphus. Meiotic divisions of rare interspecific hybrids (I. apache ♀ × I. calligraphus s. lato ♂) had numerous autosomal rearrangements, a possible translocation, and oversized (probably tetraploid) spermatozoa. Meiosis was mostly normal in intersubspecific hybrids, but the presence of occasional anaphase bridges or nonmigrating chromosomes and alignment of pachytene homologs revealed inversions and other possible rearrangements. Univariate and multivariate analyses of pars stridens strial width, pronotal width, and male genitalia revealed significant differences among all four taxa.

Résumé

La validité de quatre taxons au sein du groupe calligraphus chez le genre Ips DeGeer est corroborée par les résultats d’expériences d’élevage et par la caryologie, la morphologie, l’écologie et la biogéographie des taxons. Ips calligraphus calligraphus (Germar) vit dans l’est des États-Unis et dans les régions canadiennes adjacentes. La répartition d’Ips c. pondorosae (Swaine) suit celle de Pinus ponderosa, dans les Black Hills, dans l’est des montagnes Rocheuses et dans le nord de la Sierra Madre Oriental au Mexique. Ips. c. interstitialis (Eichhoff) vit dans les Caraïbes, mais l’homogénéité des populations de l’île Hispaniola et de la Jamaïque de même que la localité type demeurent incertaines. Ips apache Lanier infeste divers pins (à l’exception des pins pignons) aux altitudes faibles, du sud-est de l’Arizona au sud du Mexique. Les populations qui vivent au sud de l’isthme de Tehuantepec dans les pins des Caraïbes sur la côte est de l’Amérique centrale sont considérées comme appartenant à l’espèce I. apache jusqu’à nouvel ordre. Les tentatives de croisements entre des femelles des différentes sous-espèces d’I. calligraphus et des mâles d’I. apache ont échoué. Les croisements réciproques ont produit de rares hybrides stériles. Chez l’espèce I. calligraphus, la fertilité était normale dans les cas où les femelles étaient des I. c. calligraphus, mais réduite lorsque les femelles étaient des I. c. ponderosae ou des I. c. interstitialis. Tous les membres du groupe ont 15 paires d’autosomes plus un bivalent sexuel (2n = 32) qui affecte la forme d’un “parachute”, ce qui donne une formule meiotique mâle de 15AA + Xyp. Les chromosomes de la seconde méiose d’I. apache sont dépourvus de certains bras hétérochromatiques présents chez I. calligraphus. Les divisions meiotiques de quelques rares hybrides interspécifiques (♀ I. apache × ♂ I. calligraphus s. lato) ont donné lieu à de nombreux réarrangements autosomiaux, probablement aussi à une translocation, et ont résulté en des spermatozoïdes géants (probablement tétraploïdes). La méiose était à peu près normale chez tous les hybrides intersubspécifiques, mais la présence de quelques ponts chromatidiens ou de chromosomes non migrateurs et l’alignement d’homologues pachytènes ont mis en lumière l’existence d’inversions et peut-être aussi d’autres formes de réarrangements. Des analyses unidimensionnelles et multidimensionnelles de la largeur des stries de la pars stridens, de la largeur du pronotum et de l’aspect des pièces génitales mâles a révélé l’existence de différences significatives entre les quatre taxons.

[Traduit par la rédaction]

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1991

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

Atkinson, T.H., and Equihua-Martinez, A.. 1985. Lista comentada de los Coleopteros Scolytidae y Platypodidae del Valle de Mexico. Folio Ent. Mex. 65: 63108.Google Scholar
Blandford, W.F.H. 1895. Fam. Scolytidae. In Biologia Centrali-Americana 6: 8198.Google Scholar
Browne, F.G. 1977. Additions to the scolytid fauna (Coleoptera: Scolytidae) of the Philippines. Philippine J. Sci. 106: 8588.Google Scholar
Chamberlin, W.J. 1939. The Bark and Timber Beetles of North America. Ore. St. Coll. Coop. Assoc., Corvallis, OR.Google Scholar
Critchfield, W.B., and Little, E.L. Jr, 1966. Geographic Distribution of the Pines of the World. USDA Misc. Publ. 991.Google Scholar
Eichhoff, W. 1869. Neue Amerikanische Borkenkäfer-Gattung und Arten. Berliner Ent. Zeitschrift 12: 273280.CrossRefGoogle Scholar
Etheridge, B.E. 1968. Preliminary observations on the pathology of Pinus caribaea Morelet in British Honduras. Commonwealth Forest Rev. 47: 7280.Google Scholar
Garraway, E. 1986. The biology of Ips calligraphus and Ips grandicollis (Coleoptera: Scolytidae) in Jamaica. Can. Ent. 118: 113121.CrossRefGoogle Scholar
Haack, R. 1988. Technical review of the Ips bark beetle outbreak in the pine forests of the Dominican Republic. Unpubl. Rep., USDA Forest Service International Forestry Office, Washington, DC.Google Scholar
Hilario, F. 1983. Ips, the pine beetle. Habitat Philippines 1: 4547.Google Scholar
Hopping, G.R. 1965. The North American species in Group X of Ips De Geer (Coleoptera: Scolytidae). Can. Ent. 97: 803809.CrossRefGoogle Scholar
Lanier, G.N. 1966. Interspecific mating and cytological studies of closely related species of Ips DeGeer and Orthotomicus Ferrari (Coleoptera: Scolytidae). Can. Ent. 98: 175–88.CrossRefGoogle Scholar
Lanier, G.N. 1970 a. Biosystematics of North American Ips (Coleoptera: Scolytidae). Hopping's Group IX. Can. Ent. 102: 11391163.CrossRefGoogle Scholar
Lanier, G.N. 1970 b. Biosystematics of Ips (Coleoptera: Scolytidae) in North America. Hopping's Group III. Can. Ent. 102: 1404–1123.CrossRefGoogle Scholar
Lanier, G.N. 1971. Cytoplasmic incompatibility and breeding isolation in bark beetles (Coleoptera: Scolytidae). Can. J. Genet. Cytol. 13: 160163.CrossRefGoogle Scholar
Lanier, G.N. 1972. Biosystematics of the genus Ips (Coleoptera: Scolytidae) in North America. Hopping's Groups IV and X. Can. Ent. 104: 361388.CrossRefGoogle Scholar
Lanier, G.N. 1987 a. Discovery of type material of some of Eichhoff's North American species of Ips and Orthotomicus. Coleopt. Bull. 41: 107110.Google Scholar
Lanier, G.N. 1987 b. The validity of Ips cribricollis (Eich.) as distinct from I. grandicollis (Eich.) and the occurrence of both species in Central America. Can. Ent. 119: 179187.CrossRefGoogle Scholar
Lindquist, E.E. 1969. Review of Holarctic Tarsonemid Mites (Acarina: Prostigmata) Parasitizing Eggs of Ipine Bark Beetles. Mem. ent. Soc. Can. 60.Google Scholar
Mirov, N.T. 1967. The Genus Pinus. Ronald Press, New York, NY.Google Scholar
Nei, M. 1972. Genetic distance between species. Am. Nat. 106: 283291.CrossRefGoogle Scholar
SAS Institute Inc. 1985. User's Guide: Statistics, Version 5. Sas Institute Inc., Cary, NC. 965 pp.Google Scholar
Schedl, K.E. 1939. Scolytidae, Coptonotidae Platypodidae mexicanos. An. Es. Nac. Cienc. Biol. 1: 317379.Google Scholar
Schedl, K.E. 1955. Die Kiefern-Borkenkafer Guatemalas. Z. ang. Ent. 38: 148.CrossRefGoogle Scholar
Schwerdtfeger, F. 1956. Scolytidae (Col.) an Pinus-Arten in Mittelamerika, I. Des Genus Ips DeGeer. Z. ang. Ent. 39: 3457.CrossRefGoogle Scholar
Swaine, J.M. 1925. New species of Ipidae (Coleoptera). Can. Ent. 57: 192197.CrossRefGoogle Scholar
Thomas, J.B. 1966. Some Scolytidae from the Sierra Madre Occidental in Mexico. Can. Ent. 98: 871875.CrossRefGoogle Scholar
Viado, G.B. 1979. Notes on insect pests of forest trees. Sylvatrop. 4: 183189.Google Scholar
Wood, D.L., and Stark, R.W.. 1968 a. The life history of Ips calligraphus (Coleoptera: Scolytidae) with notes on its biology in California. Can. Ent. 100: 145151.CrossRefGoogle Scholar
Wood, D.L., and Stark, R.W. 1968 b. Addendum. Can. Ent. 100: 548.Google Scholar
Wood, S.L. 1982. The bark and ambrosia beetles of North and Central America (Coleoptera: Scolytidae), a taxonomic monograph. Great Basin Nat. Mem. 6: 11359.Google Scholar