Click here for the original journal page (in Acrobat pdf format).

The text below is grayed out because it is not intended to be read. It is a necessarily imperfect OCR of the original and is only used by a search engine.


Journal of the Lepidopterists' Society 34(2), 1980, 127-132

DIANESIA, A NEW GENUS OF RIODINIDAE FROM THE WEST INDIES

Donald J. Harvey

Division of Biological Sciences, University of Texas, Austin, Texas 78712

AND

Harry K. Clench1

Section of Insects and Spiders, Carnegie Museum of Natural History, Pittsburgh, Pennsylvania 15213

ABSTRACT. Dianesia, gen. n., is proposed for the riodinid butterfly originally described as Charis carteri Holland. This species, endemic to Cuba and the Bahamas, has long been considered a member of the genus Apodemia, from which, however, it is quite distinct. A morphological description and notes on the biology of D. carteri are presented.

Holland (1902) described the metalmark Charis carteri from specimens collected on New Providence Island, Bahamas. Ten years later, Skinner (1912) described Mesosemia ramsdeni from La Yberia, Cuba. Stichel (1911: 290) provisionally transfered carteri to the genus Apodemia Felder & Felder, an action accepted by subsequent authors (e.g. Bates, 1935; Rindge, 1952; West, 1966; Riley, 1975). We agree with Riley (loc. cit.) in considering ramsdeni to be a subspecies of carteri. These two taxa represent the only members of the Riodinidae known from the West Indies, and both remained rare in collections. No additional information was gleaned about carteri until our field-work in the Bahamas during the 1970's. Differences in wing pattern and adult behavior suggested that carteri was not congeneric with North and Central American Apodemia, and this suspicion was confirmed by comparisons of their appendages and genitalia. We therefore propose the following new genus.

Dianesia Harvey and Clench, new genus

Type species: Charis carteri Holland (nominate subspecies).

Description. Eyes naked, yellow-green in life. Palpi (Fig. 1) slender, appressed to head, not extending beyond frontal vestiture; third segment stubby, one-seventh (male) to one-fifth (female) length of second (in Apodemia2 ratio one-third to almost one-half). Antennae slender, seven-tenths length of forewing costa; comprised of 38-39 segments, the terminal 13 forming a weak club. Forewing (Fig. 2) and hindwing (Fig. 3) not differing consistently in any one character from the range of variation present in Apodemia2. Male foreleg (Fig. 4) very slender; tibia with a single spine (absent in Apodemia2); tarsus apparently dimerous, equal in length to tibia. Female

1  Deceased, 1 April 1979.

2  Species examined: male and female m. mormo Felder & Felder, palmeri Edwards, walkeri Godman & Salvin, multiplaga Schaus, and hypoglauca Godman & Salvin.

128                                                Journal of the Lepidopterists' Society

Figs. 1-6. Dianesia carteri. 1, 6 palpus; 2, 6 forewing venation; 3, 6 hindwing venation; 4, 6 foreleg; 5, 9 foreleg; 6, 9 hindleg. Scale lines = 1 mm (upper line for Figs. 2, 3; lower line for Figs. 1, 4-6).

foreleg (Fig. 5) slender, tarsal subsegments with short spines. Male and female mid-and hindlegs lack tibial spurs, although spines are present. Male and female hindleg (Fig. 6) with dorsal spines on tibia (absent in Apodemia2).

Male genitalia (Figs. 7-9). Uncus weakly lobed, each lobe with a bluntly pointed tooth (absent in Apodemia3); vinculum in lateral view with an abrupt angle above middle and therefore anteriorly concave (nearly straight or anteriorly convex in Apodemia3); valvae simple (bifurcate in Apodemia3), posterior edge lightly sclerotized, becoming membranous towards attachment to vinculum, free ventrally, joined dorsally over the aedeagus by a lightly sclerotized band; saccus reduced, shallowly rounded; aedeagus elongate and slender, slightly curved (bent 45 to 90 degrees in Apodemia3).

3 Species examined include those listed in Footnote 2, in addition to male and female nais Edwards, chisosensis Freeman and hepburni Godman & Salvin (male only).

Volume 34, Number 2

129

Figs. 7-12. Genitalia of Dianesia carteri. 7, 6 lateral view; 8, 6 ventral view, setae on right side omitted; 9, 6 dorsal view of uncus, tegumen and vinculum; left falx and setae on right side omitted; 10, 9 dorsal view—posterior end; 11, 9 right lateral view—posterior end; 12, 9 corpus bursae. Scale line = 1 mm.

Female genitalia (Figs. 10-12). Eighth sternite punctate, lacking ridges and not sclerotized near ostium bursae (weak ridges present, sclerotized in Apodemia3 except multiplaga); ostium bursae dorsoventrally compressed, narrowing towards sclerotized antrum; lamella antevaginalis spatulate and heavily sclerotized, barely covering ostium bursae; lamella postvaginalis weakly sclerotized; ductus seminalis enters dorsally; due-

130

Journal of the Lepidopterists' Society

Figs. 13-16. Dianesia carteri. 13, 6 dorsal view; 14, 6 ventral view; 15, 9 dorsal view; 16, 9 ventral view.

tus bursae very narrow, very lightly sclerotized, straight (usually heavily sclerotized, with a sharp to slight bend in Apodemia3), surface punctate, with irregular folds, opening widely into corpus bursae; corpus bursae dorso-ventrally flattened, surface uniformly punctate, with surface folds around junction with ductus bursae.

Relationships. Morphologically, Dianesia can be readily separated from Nearctic Apodemia3 (type species: m. mormo Felder & Felder) by the characters noted in the description. Without a complete reanalysis of the New World Riodinidae it is impossible to determine the closest affinities of Dianesia. Its wing pattern (Figs. 13-16), particularly the tornal eyespot on each wing (above and below), is unusual and resembles that of no other riodinid known to us except, perhaps, for a few vague similarities in some mainland Neotropical species (Lemonias zygia Hubner, Calospila luciana (Fabricius), Elaphrotis thelephus (Cramer)). Genitalic comparisons, however, reveal no close relation to these species. Two South American species attributed to Apodemia, stalachtioides Butler and castanea Prittwitz, were also examined. Differences in genitalia and appendages indicate that they are not congeneric with North and Central American Apodemia. Their correct generic assignment is under study.

Natural History. Biological observations on Dianesia carteri in the Bahamas have been published elsewhere (Clench, 1967, 1977a, b). During May-June 1978, Harvey made additional observations at two N. Andros localities, which, together with the above references, form the basis for the following account.

Volume 34, Number 2

131

We have found Dianesia carteri in several types of habitat. At West Bay, Little San Salvador, Clench (1977b) found a single female in sparse, open scrub averaging 2 m high. The area had open, sandy ground between the shrubs, which included both fan and Sargent palms, Seagrape (Coccoloba uvifera), and a small leafed shrub on which the specimen was found. On both N. and S. Andros, Clench (1976, 1977a) found it flying in stunted, virgin pineland with few scattered shrubs near the coast. On N. Andros, Harvey found D. carteri relatively common at Stafford Creek. Most adults seen were perched along a path that ran through a small "coppice," an area of hardwoods with a diverse flora. At Red Bay, a small colony was discovered at a short row of shrubs that bordered the road from the settlement to the public dock. In all instances, D. carteri appeared to be very localized, and was usually rare.

Adults perched on the underside of leaves, assuming a characteristic posture: wings almost flat against the leaf, antennae held close together and extended dorsad at a slight angle from the axis of the thorax. This posture resembles that of most Neotropical riodinids, but differs from Nearctic Apodemia, which perch on the upperside of leaves or on stems. The perch sites chosen varied from less than 20 cm, to more than 2 m above the ground. At Stafford Creek, certain perch sites appeared to be especially favored by males. When removed from these sites, they were usually replaced by other males in less than 30 min, and certain sites were almost invariably occupied during almost three weeks of intermittent observation.

When visiting flowers, the wings were held outspread. Flowers utilized near Stafford Creek included Lantana involucrata (Clench, 1977a), Bursera simarouba, and Coccoloba uvifera. The latter two also attracted other butterflies, particularly lycaenids. At Red Bay, the flowers of Cordia bahamensis were visited, and one female was seen shortly after having been caught at the flowers by a species of Phymata (Hemiptera: Phymatidae).

Flight activity of D. carteri extended throughout the daylight hours, beginning and ending when most butterflies were inactive. The female from Little San Salvador was taken at 0730 h. At Stafford Creek, males were observed perching as early as 0830 h, and on several occasions were seen visiting Bursera flowers around sunset (1930 h).

Despite many hours of field observation, we observed neither courtship nor oviposi-tion, and the larval hostplant and immatures remain unknown. The restriction of D. carteri to coastal areas (we have not seen any at distances greater than several hundred meters from open salt water) suggests that the larval hostplant may be similarly restricted.

ACKNOWLEDGMENTS

One of us (DJH) would like to extend thanks to the following people: Rose Blanchard (director) and the staff of the Forfar Field Station, International Field Studies, Stafford Creek, for their hospitality and for providing transportation during my visit on N. Andros; Mr. Colin Higgs, Ministry of Fisheries and Agriculture, for providing permits to work in the Bahamas; Lee D. and Jacqueline Miller, Allyn Museum of Entomology, for providing facilities, access to the collections under their care, and in addition, much useful advice and technical assistance; Jacqueline Miller also prepared the drawings of wing venation (all other drawings by DJH); and to Arthur C. Allyn for the photographs of the adults. Partial support from a NSF Graduate Fellowship is acknowledged. Field work by HKC was supported by the M. Graham Netting Research Fund and the Holland Fund (Carnegie Museum of Natural History) and by the World Wildlife Fund.

132

Journal of the Lepidopterists' Society

Literature Cited

Bates, M. 1935. The butterflies of Cuba. Bull. Mus. Comp. Zool. (Harvard) 78: 63-

258. Clench, H. K. 1976. In search of rare butterflies. Bahamas Naturalist 2(1): 2-8.

--------- 1977a. A list of the butterflies of Andros, Bahamas. Ann. Carnegie Mus. 46:

173-194.

--------- 1977b. Butterflies of the Carnegie Museum Bahamas Expedition, 1976. Ann.

Carnegie Mus. 46: 265-283.

Holland, W. J. 1902. Two new species of Bahama Lepidoptera. Ann. Carnegie Mus.

1: 486-489. Riley, N. D. 1975. A field guide to the butterflies of the West Indies. Demeter Press,

New York. 224 p. RlNDGE, F. H. 1952. The butterflies of the Bahama Islands, British West Indies. Amer.

Mus. Novit. 1563, 18 p. STICHEL, H. 1911. Fam. Riodinidae. In Wytsman, P., Genera Insectorum. P. Wytsman,

Brussels. 452 p. West, B. K. 1966. Butterflies of New Providence Island, Bahamas. Ent. Rec. 78: 174-

179, 206-210.

Journal of the Lepidopterists' Society 34(2), 1980, 132

A RECORD OF ITAME ABRUPTATA(GEOMETRIDAE) FROM NEW YORK

During a preliminary survey of the insects associated with ninebark, Physocarpus opulifolius (L.) Maxim (Rosaceae), I reared a small lepidopterous larva, collected in a state park in the Finger Lakes Region of New York, to the adult stage. It proved to be the ennomine geometrid Itame abruptata (Walker). This is apparently the first record of this species from New York. The identification was made by John G. Franclemont, Cornell University, Ithaca, N.Y. This reared specimen is in the personal collection of Dr. Franclemont, and bears these labels: "N.Y.: Taughannock Falls State Park, US 89 at bridge, 8 mi. N. of Ithaca, Tompkins County, E. R. Hoebeke & M. E. Carter/ EX: Physocarpus opulifolius/ larva coll. May 16, 1979; pupated by May 27; adult emergence June 7."

Itame abruptata is known to occur from northern Ontario south to western Pennsylvania and west to eastern Minnesota and Missouri (McGuffin 1977, J. Lepid. Soc. 31: 269-274), but appears to be only locally abundant in certain areas of its range. Additional collections of larvae of J. abruptata have been made from ninebark in the south-central region of Pennsylvania (Harrisburg and environs) by A. G. Wheeler, Jr. (Pa. Dept. Agric, Harrisburg, Pa.). These reared specimens are in the collections of Cornell University and the Pennsylvania Department of Agriculture. This species is not well represented in North American collections.

E. Richard Hoebeke, Department of Entomology, Cornell University, Ithaca, New York 14853.