Phylogeny of Utetheisa s. str. (Lepidoptera : Noctuidae : Arctinae) with comments on the evolution of colour, hind wing scales and origin of New World species
M. A. DaCostaUniversity of Minnesota, Department of Entomology, 219 Hodson Hall, 1980 Folwell Avenue, St. Paul, MN 55108, USA. Present address: Wake Forest University, Department of Biology, PO Box 7325, Winston-Salem, NC 27109, USA. Email: dacostma@wfu.edu
Invertebrate Systematics 24(2) 113-130 https://doi.org/10.1071/IS08006
Submitted: 8 February 2008 Accepted: 12 March 2010 Published: 29 June 2010
Abstract
Species of Utetheisa Hübner incorporate pyrrolizidine alkaloids into their defence strategy where they are protective against both invertebrate and vertebrate predators, and courtship behaviours by males incorporate the alkaloids into their pheromones. Although Utetheisa’s chemical ecology is well understood, the systematics is less clear. A phylogeny of Utetheisa was constructed based on adult morphology. The final data matrix consisted of 29 species and 105 characters (268 states) from adults scored from both nongenitalic and genitalic characters as follows: 3 head (8 states), 4 leg (8 states), 21 wing (49 states), 44 male abdominal and genitalic characters (124 states), and 33 female abdominal and genitalic characters (79 states). The resulting parsimony and Bayesian analyses demonstrated that Utetheisa s. str. is monophyletic and sister to U. Pitasila (Moore). UtetheisaAtasca (Swinhoe) is more closely related to outgroup taxa than it is to other Utetheisa species. Monophyly of Utetheisa s. str. is strongly supported by a posterior probability of 0.98. Colour was lost once and male wing androconia evolved independently in several species, all of which feed on hosts in Boraginaceae. Forbes’ hypothesis of an Old World origin for the genus is corroborated and two origins for New World species are supported.
Acknowledgements
I thank the following people for their suggestions on the project: G. Heimpel, R. Holzenthal, G.Weiblen, S. Weller and A. Roe. F. Keith Barker and J. Egge provided assistance with analyses in MrBayes. M. Conner, R. Simmons, J. Zaspel and two anonymous reviewers improved earlier drafts of the manuscript with comments. The following curators generously provided specimens and gave permission to perform whole body dissections. Acronyms of the institution providing specimens follow Heppner and Lamas (1982) and are followed by the name of the individual(s) who prepared the loan: American Museum of Natural History, New York (AMNH) (R. Schuh, S. Rab-Green), Bishop Museum, Honolulu (BPBM) (A. Samuelson), California Academy of Sciences, San Francisco (CAS) (B. Fisher), Carnegie Museum of Natural History, Pittsburgh (CM) (J. Rawlins, R. Davidson), Cornell University Insect Collection, Ithaca (CU) (J. Liebherr, E.R. Hoebeke), Field Museum of Natural History, Chicago (FMNH) (J. Boone), The Albert J. Cook Arthropod Research Collection, Michigan State University (ARC) (G. Parsons), National Museum of Natural History, Smithsonian Institution, Washington D.C. (NMNH) (M. Pogue, R. Simmons, D. Harvey), Natural History Museum, London (BMNH) (M. Honey, D. Goodger), Natural History Museum of Los Angeles County (LACM) (J. Donahue), Zoologisches Forschungsinstitut und Museum Alexander Koenig, Bonn (MAK) (D. Stüning, G. Brehm), and University of Minnesota, St. Paul, Insect Museum (UMSP) (R. Holzenthal, P. Clausen). This study was supported in part by NSF/DEB-9981416 (SJW), Minnesota Experiment Station MN17-022 (SJW), MD received funding from the Ernst Mayer travel grant for animal systematics (Museum of Comparative Zoology at Harvard) and Dayton-Wilkie Fund (Bell Museum of Natural History, University of Minnesota).
Bremer K.
(1988) The limits of amino acid sequence data in angiosperm phylogenetic reconstruction. Evolution 42, 795–803.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Bremer K.
(1994) Branch support and tree stability. Cladistics 10, 295–304.
| Crossref | GoogleScholarGoogle Scholar |
Conner W. E.,
Eisner T.,
Vander Meer R. K.,
Guerrero A., Meinwald J.
(1981) Precopulatory sexual interactions in an arctiid moth (Utetheisa ornatrix): role of a pheromone derived from alkaloids. Behavioral Ecology and Sociobiology 9, 227–235.
| Crossref | GoogleScholarGoogle Scholar |
DaCosta M. A., Weller S. J.
(2005) Phylogeny and classification of Callimorphini (Lepidoptera: Arctiidae: Arctiinae). Zootaxa 1025, 1–94.
DaCosta M. A.,
Larson P.,
Donahue J., Weller S. J.
(2006) Phylogeny of the Milkweed tussocks (Arctiidae: Arctiinae: Phaegopterini) and its implications for the evolution of ultrasound communication. Annals of the Entomological Society of America 99, 723–742.
| Crossref | GoogleScholarGoogle Scholar |
de Vos R.
(2007) The Utetheisa species of the subgenera Pitasila, Atasca, and Raanya subg. n. (Insecta, Lepidoptera: Arctiidae). Aldrovandia 3, 31–120.
Efron B.
(1979) Bootstrap methods: another look at the jackknife. Annals of Statistics 7, 1–26.
| Crossref | GoogleScholarGoogle Scholar |
Forbes W. T. M.
(1916) On the tympanum of certain Lepidoptera. Psyche 23, 183–192.
| Crossref | GoogleScholarGoogle Scholar |
Forbes W. T. M.
(1917) Notes on the West Indian Syntomidae and Arctiidae (Lepidoptera). Bulletin of the American Museum of Natural History XXXVII, 339–345.
Forbes W. T. M.
(1941) The position of Utetheisa galapagensis (Lepidoptera, Arctiidae). Journal of the New York Entomological Society XLIX, 101–110.
Forbes W. T. M.
(1960) The Lepidoptera of New York and neighboring states. Part 4: Agaristidae through Nymphalidae including butterflies. Cornell University Agriculture Experiment Station Memoir 371, 12–41.
Garrett S. E.,
Conner W. E., Roque-Albelo L.
(2008) Alkaloidal protection of Utetheisa galapagensis (Lepidoptera: Arctiidae) against an invertebrate and a vertebrate predator in the Galapagos Islands. Galapagos Research 65, 2–6.
Huelsenbeck J. P., Ronquist F.
(2001) MRBAYES: Bayesian inference of phylogeny. Bioinformatics 17, 754–755.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Jordan K.
(1939) On the constancy and variability of the differences between the Old World species of Utetheisa (Lepid.; Arctiidae). Novitates Zoologicae 41, 251–291.
Kass R. E., Raftery A. E.
(1995) Bayes factors. American Statistical Association 90, 773–795.
| Crossref | GoogleScholarGoogle Scholar |
Kishino H., Hasegawa M.
(1989) Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in Hominoidea. Journal of Molecular Evolution 29, 170–179.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Lewis P. O.
(2001) A likelihood approach to estimating phylogeny from discrete morphological character data. Systematic Biology 50, 913–925.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Luh C. J.
(1937) The skeletal structures of the tympanum of the Arctiidae (Order Lepidoptera). Peking Natural History Bulletin 2, 315–328.
Mappes J.,
Marples N., Endler J. A.
(2005) The complex business of survival by aposematism. Trends in Ecology & Evolution 20, 598–603.
| Crossref | GoogleScholarGoogle Scholar |
Miller J. S.
(1991) Cladistics and classification of the Notodontidae (Lepidoptera: Noctuoidea) based on larval and adult morphology. Bulletin of the American Museum of Natural History 204, 35–112.
Pease R. W.
(1968) Evolution and hybridization in the Utetheisa ornatrix complex (Lepidoptera: Arctiidae). I. Inter- and Intrapopulation variation and its relation to hybridization. Evolution 22, 719–735.
| Crossref | GoogleScholarGoogle Scholar |
Richards A. G.
(1932) Comparative skeletal morphology of the noctuid tympanum. Entomological Society of America 13, 1–43.
Ronquist F., Huelsenbeck J. P.
(2003) MRBAYES 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 19, 1572–1574.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Roque-Albelo L.,
Schroeder F. C.,
Conner W. E.,
Bezzerides A.,
Hoebeke E. R.,
Meinwald J., Eisner T.
(2002) Chemical defense and aposematism: the case for Utetheisa galapagensis. Chemoecology 12, 153–157.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Rowe C., Guilford T.
(2000) Aposematism: to be red or dead. Trends in Ecology & Evolution 15, 261–262.
| Crossref | GoogleScholarGoogle Scholar |