NOTES ON LIFE HISTORIES OF SATYRINAE IN THE SOLOMON ISLANDS (LEPIDOPTERA: NYMPHALIDAE)

Similar documents
THE LIFE HISTORY AND ECOLOGY OF HESPERIA NABOKOVI IN THE DOMINICAN REPUBLIC (LEPIDOPTERA: HESPERIIDAE)

Entomology Research Laboratory The University of Vermont South Burlington, Vermont USA

M. C. WILLIAMS AND J. BOOMKER

Chapter 26 Phylogeny and the Tree of Life

Red Admiral (Early Stages)

Lecture 11 Friday, October 21, 2011

DNA Sequencing as a Method for Larval Identification in Odonates

Brown Hairstreak (Early Stages)

The Current Status of Mosquito Systematics. Lewis T. Nielsen Department of Biology University of Utah Salt Lake City, Utah 84112

Modern Evolutionary Classification. Section 18-2 pgs

FINAL INSTAR CATERPILLAR AND METAMORPHOSIS OF AMBLYCHIA HYMENARIA (GUENÉE) IN SINGAPORE (LEPIDOPTERA: GEOMETRIDAE: ENNOMINAE)

Title. Author(s)Lewvanich, Angoon. Issue Date Doc URL. Type. File Information SCHOENOBIINAE)

Mosquito Systematics Vol. 6(Z) June 1974

Figure 1. Consider this cladogram. Let s examine it with all three species concepts:

The practice of naming and classifying organisms is called taxonomy.

14. GROWTH STUDIES ON GLOBOROTALIA EXILIS BLOW AND GLOBOROTALIA PERTENIUS BEARD IN THE HOLE 154A SECTION, LEG 15, DEEP SEA DRILLING PROJECT

Global biodiversity: how many species of arthropods are there? George Weiblen Plant Biology

Two new species of Nymphalidae (Satyrinae) from Vietnam (Lepidoptera, Rhopalocera) by A. L. M onastyrskii received

ESTIMATION OF CONSERVATISM OF CHARACTERS BY CONSTANCY WITHIN BIOLOGICAL POPULATIONS

JOHN B. HEPPNER" Depaltment of Entomology and Nematology, University of Florida, Gainesville, Florida 32611

CLASSIFICATION AND EVOLUTION OF CAMINALCULES:

Host Relations and Distribution of New Guinea

Need for systematics. Applications of systematics. Linnaeus plus Darwin. Approaches in systematics. Principles of cladistics

Chapter 19: Taxonomy, Systematics, and Phylogeny

MEXICAN BROMELIAD WEEVIL REPORT 12 JANUARY 2013

Mite Genotype vs. Fern Genotype

S. W. FROST. Frost Entomological Museum, The Pennsylvania State University, Department of E ntomology, University Park, Penn.

LECTURE 08. Today: 3/3/2014

Reconstructing the history of lineages

Title. Author(s)SHIMADA, Kimio. CitationLow temperature science. Ser. B, Biological sciences. Issue Date Doc URL. Type.

Historical Biogeography. Historical Biogeography. Systematics

Kansas State University Department of Entomology Newsletter

Biology of sweet potato weevil, Cylas formicarius F. on sweet potato

Introduction. Ludwigia alternifolia, Peter Hoch

Chapter 17A. Table of Contents. Section 1 Categories of Biological Classification. Section 2 How Biologists Classify Organisms

ESS 345 Ichthyology. Systematic Ichthyology Part II Not in Book

FINAL INSTAR CATERPILLAR AND METAMORPHOSIS OF EUMELEA LUDOVICATA GUENÉE, 1857, IN SINGAPORE (LEPIDOPTERA: GEOMETRIDAE: DESMOBATHRINAE)

Musk thistle and Canada thistle

Plant Systematics. What is Systematics? or Why Study Systematics? Botany 400. What is Systematics or Why Study Systematics?

Text and photos by Caitlin LaBar. Prepared for USFWS in June 2009 Revised February 2014

No. 9] Hormonal Control of Butterfly Seasonal Forms 1083

ROGH Docent Program Week 4: Orchid Biology.

Biology 2. Lecture Material. For. Macroevolution. Systematics

On the Validity of the Name teyahalee as Applied to a Member of the Plethodon glutinosus Complex (Caudata: Plethodontidae): A New Name

SPECIATION. REPRODUCTIVE BARRIERS PREZYGOTIC: Barriers that prevent fertilization. Habitat isolation Populations can t get together

Chapter 26. Phylogeny and the Tree of Life. Lecture Presentations by Nicole Tunbridge and Kathleen Fitzpatrick Pearson Education, Inc.

A new species of Hypolycaena (C. & R. Felder, 1862) from Papua, Indonesia (Lepidoptera: Lycaenidae)

PHYLOGENY AND SYSTEMATICS

STUDENT PROJECT FINAL REPORT TO THE UNIVERSITY OF HAWAI I MARINE OPTION PROGRAM

Biogeography expands:

CHAPTER 26 PHYLOGENY AND THE TREE OF LIFE Connecting Classification to Phylogeny

1/17/2012. Class Aves. Avian Systematics. Avian Systematics. Subclass Sauriurae

Screening Aid. Pine Sawyer Beetles Monochamus sutor (Linnaeus) and M. alternatus Hope. Joseph Benzel

Evolution Problem Drill 10: Human Evolution

CHAPTER 10 Taxonomy and Phylogeny of Animals

Screening Aid. Asiatic Rice Borer Chilo suppressalis (Walker) Todd M. Gilligan 1 and Steven C. Passoa 2

Introduction to Lepidoptera

Integrative Biology 200A "PRINCIPLES OF PHYLOGENETICS" Spring 2012 University of California, Berkeley

LAGOWSKA, B. Department of Entomology, University of Agriculture ul. K. Leszczyñskiego 7, Lublin, Poland ABSTRACT

Welcome to the 4H Entomology Project!

Dectes Stem Borer: A Summertime Pest of Soybeans

Applications of Genetics to Conservation Biology

Evolutionary Morphology of Land Plants

Biology 211 (2) Week 1 KEY!

Cover Page. The handle holds various files of this Leiden University dissertation.

Part 1: Naming the cultivar

AP Environmental Science I. Unit 1-2: Biodiversity & Evolution

General Patterns in Evolution

BULLETIN OF THE ALLYN MUSEUM

8/23/2014. Phylogeny and the Tree of Life

Outline. Classification of Living Things

Patterns in Evolution - Novelty

Patterns in Evolution - Novelty. Uses of Phylogenetic Analysis. Allows mapping order of character state changes

SEASONAL VARIATION IN THE LITTLE SULPHUR BUTTERFLY, EUREMA LISA LISA, IN CENTRAL FLORIDA: HOW IT COMPARES TO OTHER SYMPATRIC EUREMA SPECIES

Biology 1B Evolution Lecture 9 (March 15, 2010), Speciation Processes

This work is licensed under the Creative Commons Attribution-Noncommercial-Share Alike 3.0 United States License. To view a copy of this license,

Lecture V Phylogeny and Systematics Dr. Kopeny

Ontario Western Bean Cutworm Trap Network

Soybean stem fly outbreak in soybean crops

AToL: Collaborative research on ant phylogeny: a comprehensive evolutionary tree for the world s premier social organisms

Biological Control of the Banana Skipper,

7. M2/1 Subfamily Caesalpinoideae. A flower of Bauhinia sp. shows floral morphology typical of the species in the subfamily Caesalpinoideae.

Bamboo. Rosa Isela Perez, Master Gardener Trainee 2016

JOURNAL OF THE LEPIDOPTERISTS' SOCIETY

Boise Parks & Recreation 2016 Monarch Report

Early theories: Joseph Hooker (1853) vs. Charles Darwin (1859)

Genetic Lab 3. Drosophila Fly

Lepcey. Studies on some aspects of the biology and ecology of Citrus butterfly Papilio demoleus (Papilionidae: Lepidoptera) on citrus in Vietnam

Identifying Thrips & Their Damage in New England Greenhouses

Name: Class: Date: ID: A

Conceptually, we define species as evolutionary units :

Bee common name. Search

The Life System and Environmental & Evolutionary Biology II

Pest Species of Copitarsia Hampson in the Neotropics: Identification and Hosts

Taxonomy and Biodiversity

How Biological Diversity Evolves

The process by which the genetic structure of populations changes over time.

Creating an e-flora for South Africa

Postgraduate teaching for the next generation of taxonomists

Evidences Supporting Darwin s Theory of Evolution Through Natural Selection

Transcription:

Vol. 12 Suppl. 1 2001 SOURAKOV and EMMEL: Life Histories of Solomons Satyrinae TROPICAL LEPIDOPTERA, 12 (Suppl. 1): 7-12 NOTES ON LIFE HISTORIES OF SATYRINAE IN THE SOLOMON ISLANDS (LEPIDOPTERA: NYMPHALIDAE) ANDREI SOURAKOV1 AND THOMAS C. EMMEL Dept. of Entomology & Nematology, Univ. of Florida, Gainesville, Florida 32611 Dept. of Zoology, University of Florida, Gainesville, Florida 32611, USA ABSTRACT.- Immature stages of Mycalesis splendent, M. interrupta, M. perseus, Orsotriaena medus, and Argyronympha pulchra from the Solomon Islands are described, and the taxonomic implications of these data are discussed. Mycalesis and Orsotriaena exhibit similarities to other Mycalesini, such as the African genus Bicyclus, but also show strong intrageneric differences and affinity of Orsotriaena to other primitive satyrine tribes. Argyronympha shares some characters with other advanced Satyrinae (e.g., Erebiini of the Holarctic region). Divergence of immature stages found in different members of M. splendens group supports splitting taxonomic decisions made by the previous authors based on adult morphology. KEY WORDS: Argyronympha, biogeography, eggs, Erebiini, Hypocystini, immatures, larvae, life histories, Mycalesini, Mycalesis, Orsotriaena, pupae, Solomon Islands. taxonomy. Accumulating data on the morphology of Satyrinae immature stage has been a principal ongoing project of the first author. During this work, divergence of eggs, larvae, and pupae at different taxonomic levels has been assessed for various satyrine genera (e.g., Sourakov, 1995, 1996; Sourakov and Emmel, 1997a,b). The ultimate goal of the project is to reconstruct the phylogeny of the Satyrinae using the morphology of immatures, characters of which were largely unavailable for earlier studies (e.g., Miller, 1968). However, reaching this goal requires collecting of a wealth of new data through rearing and morphological analysis. Meanwhile, the published fragmented descriptions will, we believe, provide students of a particular genus or tribe with valuable information for smaller-scale evolutionary studies. During our July-August 1998 expedition to the Solomon Islands, we had the opportunity to obtain eggs from five species of Satyrinae, representing three genera and two tribes: Mycalesis splendens Mathew (Fig. II), M. interrupta Grose-Smith (Fig. II), M. perseus (Fabricius) (Fig. 3G), and Orsotriaena medus (Fabricius) (Fig. 2G) of the Mycalesini, and Argyronympha pulchra Mathew of the Hypocystini. Though the last instar larvae and pupae have been previously illustrated for M. perseus and for O. medus (Parsons, 1998; Igarashi and Haruo, 1998), we are providing more complete descriptions of the biology of these wide-spread taxa and compare them to other Mycalesis species of the Solomons and to the con-specific populations from other regions, whose immature stages differ slightly from the presented here. M. splendens and M. interrupta, which by some authors (e.g., D'Abrera, 1977) were considered con-specific, were recently shown to be separate species, which also form distinct subspecies on different islands (Tennent, 2001). Only seeing the latter work prior to its publication in this supplement allowed us to identify our material correctly. Our data on immature stages support nicely Tennent's taxonomic conclusions of M. interrupta being a distinct species, those conclusions based entirely on adult morphology. MATERIALS AND METHODS Adult females were kept in inflated zip-lock bags, and were ex- 1 - This study was completed during the first author's employment at the California Academy of Sciences, San Francisco, CA 94118, posed to ambient light at the room temperature. In the case of M. interrupta, oviposition on unidentified palm sprouts was observed in the wild of Ronongga island. The egg was glued on the underside of the leaf of a 3-inch-tall plant. Therefore, palm leaves were provided for females of this species and to the similar species from Guadalcanal (M. splendens) and from Malaita (unidentified). Palm leaves were also given to females of Argyronympha pulchra species group: all females of Argyronympha were kept together on the assumption that they represent a single species, and it was found only later that some authors (e. g., D'Abrera, 1977) consider every major island to have a separate subspecies or even species of the A. pulchra group). We also obtained several eggs from a single Mycalesis female from Malaita, where, according to Tennent, two species occur: M. splendens malaitensis Uemura and M. biliki Tennent. These are cryptic species, differing in male genitalic structures, while a female for the latter of them is unknown. Therefore, correct identification of the female specimen, from which we acquired the eggs, is impossible at the moment. In contrast to the M. splendens group, M. perseus and 0. medus are common and widespread species of open habitats and, without doubt, feed on a wide variety of native and exotic grasses. Females of these two species collected on Guadalcanal were provided only with dry grass stems, on which they readily laid eggs. All females were fed daily with 25% sugar solution. Larvae of all instars were photographed, using extension tubes and ring flash. Scanning Electron Microscopy was performed on a Hitachi S-520 instrument, after eggs and larvae had been prepared by a critical point drying procedure. Larvae of Mycalesis Hubner and Orsotriaena Wallengren were reared to the pupal stage on a variety of lawn grasses. Larvae of Argyronympha Mathew refused substitute hosts and, therefore, only eggs and first instar larvae are available for description. MORPHOLOGY OF IMMATURE STAGES Eggs: In Mycalesini (Mycalesis and Orsotriaena), the eggs arc round and white, with thin shell; at closer magnification, they are covered with shallow concave hexagonal cells. This structure is similar to that observed in African Mycalesini previously illustrated for genus Bicyclus Kirby and the genus Hallelesis Condamin (Sourakov and Emmel, 1997a, p. 20).

2A 2B

Vol. 12 Suppl. I 2001 SOURAKOV and EMMEL: Life Histories of Solomons Satyrinae In Argyronympha, the egg is much more nymphaloid, with vertical ribs and hemispherical shape (Fig. 5A), supporting the notion (Miller, 1968) of the Hypocystini being a primitive tribe (Miller's conclusion was based on the adult character of long front legs, atypical of other Satyrinae). The differences in egg size shown in Fig. 5A could be an individual variation, but might also be traced to populations from different islands, populations that are considered by some to be separate species. First instar larvae: This stage in the past proved to be most conservative among closely related Satyrinae. Such seems to be the case with the Mycalesini considered here. There are practically no structural differences between larvae (Fig. 5B, E, F), and in fact, they are similar to the previously studied African members of the tribe (Sourakov and Emmel, 1997a). Coloration of the head, however, is a different matter: white with some brown markings on the front in O. medus (Fig. 2A), it is glossy black in M. perseus (Fig. 3A), light brown in M. interrupta and in Malaita unidentified population (Fig. 1A), and glossy black in M, splendens (Fig. IB). In Argyronympha (Fig. 5C-D), the head is covered with loose reticulation and the stemmata are strongly enlarged, especially the stcmma 3, which is the feature of the most advanced members of Satyrinae (Sourakov, 1997). The head lacks horns and the setae of both head and body are short and bulbous terminally, with long setae only on the anal segment. With these features, the larvae resemble those of the northern temperate genus Erebia Dalman (Sourakov, unpublished). Later instars: Divergence of larvae increases with instars. In O. medus, the head horns become very long, the ground coloration of the head and body remains green, and only head horns and anal projections are pink (Fig. 2C-D). In M. perseus, the head horns are short throughout the larval stage, while body coloration changes. The larva is green in the second instar (Fig. 3B-C), but wide reddish-brown mid-dorsal and spiracular stripes appear in the later instars (Fig. 3D-E). In the second instar of M. splendens, the head horns are equal in length to those of the second instar of 0. medus (Fig. 6), but do not increase in length in further instars as much as the length increases in larvae of the latter species (Fig. 1E-H). M. splendens and M. interrupta still have noticeable differences in the second and third instars. The second instar larvae of M. splendens have a green body with head and anal projections colored dark brown (Fig. 1C), while M. interrupta has light brown mid-dorsal and spiracular stripes and light brown head (Fig. ID). In the last instar (Fig. 1G-H), these two species become similar. Head setae, which are long in O. medus and M. perseus (Fig. 6A, C), are short in M. splendens/interrupta (Fig. 6B). The head surface of the latter two species is practically smooth, and only slightly reticulate. It is coated with rougher reticulation in M. perseus, and is covered with the numerous tubercle-like projections in O. medus (Fig. 6). Pupae: In Mycalesis, pupae are similar, with slight differences in shape and coloration (Fig. U and 3F), resembling those of African Mycalesini, as illustrated in Sourakov and Emme! (1997a), for example. However, the Orsotriaena pupa is strikingly different (Fig. 2E, F), with narrow and long body shape and with very long pilifers, resembling Zethera Felder of Zetherini and Lethe and Neorina Westwood of Lethini (Wolfe, 1996; Igarashi and Haruo, 1998). DISCUSSION As is the case with many groups of organisms, the biogeography of Satyrinae is a puzzle. Due to the lack of fossils, we can only guess the age of the modern genera and tribes. It is clear, though, that the dispersal of the Satyrinae (if the present distribution could be explained by it) has happened after the evolution of the major modern lineages. This conclusion is supported by similarities between butterfly populations of lands as far apart as Africa and the Solomon Islands: for instance, the immature stages of Mycalesis described here are similar in many respects to those of Bicyclus in Africa. Argyronympha, a member of the Hypocystini, the tribe endemic to the Australian region, shows similarities to, for example, Erebia of Erebiini or Cercyonis of Maniolini in the Holarctic Region. Miller (1968) states that Mycalesini or Hypocystini are the most likely links between Elyminiinae and Satyrinae, which are the primitive and the advanced subfamilies, respectively, of the old family Satyridae in Miller's classification (Fig. 7). Data presented in this paper suggest that Mycalesini show similarities to Ypthimini and Pronophilini (e. g., round shape and faceted structure of round thin-shelled eggs, larval head horns), while Argyronympha of Hypocystini is closer in its egg and first instar larval morphology to Maniolini, Satyrini, and Erebiini. Proper cladistic analysis of the subfamily is needed to determine inter-tribal relationships in satyrines. Genus Orsotriaena exhibits plesiomorphic characters found in other tribes (Zetherini and Lethini), and therefore, might be the more ancestral of the two Mycalesini genera examined here. Of interest is the observation of larval divergence in the M. splendens group, The adults of this species and M. interrupta are extremely similar, with slight differences in wing pattern and male genitalia (see Tennent, 2001 for complete account). We, for example, did not notice these differences until the difference in head color was noted in the larvae. The divergence in immature stages, caused by different selective pressures on different islands, might be the cause of the ongoing adaptive radiation. The above case where larvae are more divergent than adults is not unique on the intrageneric level: the first author's study of the West Indian genus Calisto (Satyrinae) showed often higher morphological divergence among immatures of this genus than was found in its adults (e.g., Sourakov, 1996, 2000). Finally, when comparing the immatures illustrated here with the illustrations found in Igarashi and Haruo (1998), we can see that the last instar larva and the pupa of M. perseus from the Philippines are different from the population described here. Larvae lack the pink stripes, while pupae have a row of white paradorsal spots, respectively. We also can note that the immatures of M. splendens group are the closest in appearance to the ones of M. ita C. & R. Felder, the species to which it is also the closest in wing pattern characters (other species illustrated in the above work are M. ingoleta C. & R. Felder; M. sangaica Butler; M. tagala C. & R. Felder; M. anaxoides Marshal; and M. maianeas Hewitson). ACKNOWLEDGMENTS We would like to acknowledge with deep appreciation the invaluable assistance of the following persons and agencies in ably handling the logistics, collecting permits, and export permits associated with our field work in the Solomon Islands: Mr. Tobais Labaseni and Mr. Abraham Baenanisia (Director, Solomon Islands Development Trust); Mr. Moses Biliki (Director, Environment and Conservation); Mr. Moffet Behulu (Chairman of Fig. 1. Mycalesis splendens group: (1A) 1st instar larva, Malaita population; phenotype of this larva is also characteristic of M. interrupta; (IB) 1st instar larva, M. splendens guadalcanalensis; (1C) the same, 2d instar larva; (ID) 2d instar larva of M. i. Interrupta, Ronongga island; (IE-IF) the same, 4th instar larva; (IG-1H) the same, 5th instar larva; ( II) adult females, M. i. interrupta Ronongga island (top) and M. splendens guadalcanalensis, Guadalcanal island (bottom); (1J) pupa, M. splendens guadalcanalensis. Fig. 2. Orsotriaena medus; (2A) 1st instar larva; (2B) 3d instar larva; (2C-2D) 4th instar larva; (2E-2F) Pupa; (20) Adult male. Fig. 3. Mycalesis perseus; (3A) 1st instar larvae; (3B-3C) 2d instar larva; (3D-3E) 5th instar larva; (3F) Pupa; (3G) Adult male. Fig. 4. Argyronympha pulchra.

10 SOURAKOV and EMMEL: Life Histories of Solomons Satyrinae TROPICAL LEPIDOPTERA Fig. 5. (A) Eggs of Argyronympha pulchra (X50); (B) Head of the 1st instar larva of Orsotriaena medus; (C-D) 1st instar larva of Argyronympha pulchra, front (C), and back (D); (E) Front end of the 1st instar larva of O. medus; (F) Back end of the 1st instar larva of M. perseus.

Vol. 12 Suppl. 1 2001 SOURAKOV and EMMEL: Life Histories of Solomons Satyrinae 11 Fig- 6. Entire head (top) and a close-up of the head surface (bottom) of the second instar larvae of (A) Mycalesis perseus', (B) Mycalesis sp leadens; (C) Orsoiriaena rnedus. the Research Committee and Under-Secretary); Mr. Robert Pongi (Chief Administrative Officer); and Hon. S. Aumanu (Minister, Ministry of Education and Human Resources Development); Mr. Narcily Pule (Provincial Secretary, Western Province, S. I.); Mr. Pratt L. Loe (Provincial Secretary, Gadalcanal Province, S. I.); Mr. Musu I. Kevu for the Provincial Secretary, Malaita Province, S. I.); the Hon. Bartholemew Uluf'alu (Prime Minister, Republic of Solomon Islands); Mr. Richard Anning (Go West Tours, Munda, New Georgia Island, S. I.); Mr. Peter Hundleby (Solomon Sights and Sounds, Honiara, S. I.); and Steven D. Schlachta (Expedition Travel, Inc.). Many local people and butterfly farmers also generously granted their permission to collect on their lands and shared their knowledge of both host plants and butterflies with us. Mr. Phil Ackery and Mr. W. John Tennent of the British Museum, London, reviewed the manuscript and we are grateful for their many useful suggestions. Mr. Darel Ubick (Assistant Curator, California Academy of Sciences) helped with the SEM work. This work was made possible by Expedition Travel, Inc., of Florida, and by the California Academy of Sciences, San Francisco. LITERATURE CITED D'Abrera, B. 1977. Butterflies of the Australian Region. Melbourne: Landsdowne Pr. 415pp. Igarashi, S., and F. Haruo 1998. The Life Histories of Asian Butterflies. Vol. 1. Tokyo: Tokai Univ. Pr. 549pp, 317pl. Miller, L. D. 1968. The higher classification, phylogeny and zoogeography of the Satyridae (Lepidoptera). Mem. Amer. Em. Soc. (Lanham), 24:1-174 Parsons, M. J. [1998]. The Butter/lies of Papua New Guinea: their Systematic^ and Biology. London: Academic Pr. 736pp, 26+136 pi. (1999) Sourakov, A. 1995. Systematics, evolutionary biology and population genetics of the Cercyonis pegala group (Nymphalidae: Satyrinae). Holarctic Lepid. (Gainesville), 2:1-21. 1996. Notes on the genus Calisto, with descriptions of the immature stages (Part 1) (Lepidoptera: Nymphalidae: Satyrinae). Trap. Lepid. (Gainesville), 7:9 Ml 2. 1997. Do "facets" and size variation in larval stemmata of satyrines indicate better vision? News Lepid. Soc. (Los Angeles), 39(1):10-11. 2000. Notes on the genus Calisto, with descriptions of the immature stages (Part 2) (Lepidoptera: Nymphalidae: Satyrinae). Trop. Lepid. (Gainesville), 10:73-79. Sourakov A., and T. C. Emmel 1997a. Bicyclus and Hallelesis: their immature stages and taxonomic relationships (Nymphalidae: Satyrinae). Trop. Lepid. (Gainesville). 8 (Suppl.

12 SOURAKOV and EMMEL: Life Histories of Solomons Satyrinae TROPICAL LEPIDOPTERA -Melanargiini -Satyrini -Pronophilini -Dirini Hypocystini -Erebiini -Maniolini -Coenonymphini -Ypthimini -Euptychini -Ragadiini -Eritini 'Mycalesini "Elymiiiini -Zetherini Lethini Fig. 7. Position of the tribes mentioned in text on the current phylogenetic tree of Satyrinae (after Miller, 1968). 3): 14-22. 1997b. Ypthima and Ypthimomorpha: their immature stages and taxonomic relationships (Nymphalidae: Satyrinae). Trap. Lepid. (Gainesville), 8 (Suppl. 3):23-28. Tennent, W. J. 2001. A review of the genus Mycalesis in the Solomons Archipelago, with descriptions of eight new taxa (Lepidoptera: Nymphalidae: Satyrinae). Trop. Lepid. (Gainesville), 12 (Suppl. l):13-24. Wolfe V. K. 1996. Notes on the early stages ofzethera musides (Lepidoptera: Nymphalidae: Satyrinae). Trop. Lepid. (Gainesville), 7:147-150.