378 Genus Junonia Huebner

Total Page:16

File Type:pdf, Size:1020Kb

378 Genus Junonia Huebner AFROTROPICAL BUTTERFLIES. MARK C. WILLIAMS. http://www.lepsocafrica.org/?p=publications&s=atb Updated 10 March 2021 Genus Junonia Hübner, [1819] Pansies In: Hübner, [1816-[1826]. Verzeichniss bekannter Schmettlinge 34 (432 + 72 pp.). Augsburg. Type-species: Papilio lavinia Cramer, by subsequent designation (Scudder, 1872. Report of the Peabody Academy of Science 1871: 43 (24-82).) [extralimital]. Junonia takes precedence over Precis and Alcyoneis, Doubleday, 1847 in Doubleday & Westwood, [1846-52]. The genera of diurnal Lepidoptera, London: 206 [1849] (1: 1-250 pp.; 2: 251-534 pp.). London.; see also Cowan, 1970. Annotationes Rhopalocerologicae 1970 41, 49, 54 (70 pp.). Berkhamsted. = Coryphaeola Butler, 1878. Annals and Magazine of Natural History (5) 2: 284 (283-297). Type-species: Kallima eurodoce Westwood, by original designation. = Kallimula Holland, 1920. Bulletin of the American Museum of Natural History 43: 149 (109- 369). Type-species: Kallimula osborni Holland, by original designation. = Kamilla Collins & Larsen, 1991c. In: Larsen, 1991c. The butterflies of Kenya and their natural history 352, 444 (490 pp.). Oxford. Type-species: Papilio cymodoce Cramer, by original designation. Synonymized by Wahlberg et al., 2005. Synonyms based on extralimital type-species: Alcyoneis Hübner; Aresta Billberg. Little Pansy, Junonia sophia. Image courtesy of Jeremy Dobson. The genus Junonia belongs to the Family Nymphalidae Rafinesque, 1815; Subfamily Nymphalinae Rafinesque, 1815; Tribe Junoniini Reuter, 1896. The other genera in the Tribe Junoniini in the Afrotropical Region are Salamis, Protogoniomorpha, Precis and Hypolimnas. Junonia (Pansies) is a cosmopolitan genus of about 36 species, 20 of which are Afrotropical. Two of the Afrotropical species have extralimital extensions. Ten species are Oriental (eight endemic), three are Australasian, four are Neotropical and one is Nearctic. Notwithstanding the arguments of De Lesse (1952) and Fontaine (1985), who clearly showed that they are distinct genera, Junonia and Precis have often been treated as congeneric. However, recent molecular work has conclusively shown that they are not only distinct genera, but that they are not even sister genera 1 (Wahlberg et al., 2005, Williams 2007a). Relevant literature: Kodandaramaiah & Wahlberg, 2007 [Historical biogeography]. Williams, 2007a [Differentiation from Precis]. *Junonia africana (Richelmann, 1913) Cameroon Pansy Precis africana Richelmann, 1913. Internationale Entomologische Zeitschrift 7: 106 (105-106). Type locality: Cameroon: “Jaunde, im Innern Kameruns”. Distribution: Cameroon. Specific localities: Cameroon – Yaounde (TL). Early stages: Nothing published. Larval food: Nothing published. *Junonia artaxia Hewitson, [1864] African Pansy Junonia artaxia Hewitson, [1864] in Hewitson, [1862-6]. Illustrations of new species of exotic butterflies 3: 26 (124 pp.). London. Precis artaxia Hewitson, 1864. Dickson & Kroon, 1978. Precis (Junonia) artaxia (Hewitson, 1864). Pringle et al., 1994: 122. Junonia artaxia Hewitson, 1864. Williams, 2007. Junonia artaxia. Male. Left – upperside; right – underside. Chakankulu, 20 km n.e. of Lusaka, Zambia. 7 March 1999. Images M.C. Williams ex J. Greyling Collection. 2 Junonia artaxia. Female. Left – upperside; right – underside. Roan Farm, 20 km n.e. of Lusaka, Zambia. 7 March 1999. Images M.C. Williams ex J. Greyling Collection. Alternative common name: Commodore. Type locality: “Zambesi”. Distribution: Angola (east), Democratic Republic of Congo (Lomami, Kabinda, Lualaba, Shaba, Tanganika), Burundi, Kenya (south-west), Tanzania (south and west), Malawi, Zambia, Mozambique, Zimbabwe. Specific localities: Kenya – Kisumu (Neave, 1904); Kisii, South Kavirondo (Stoneham, 1951-1965). Tanzania – Konde-Unyika (Thurau, 1903); Uhehe, Iringa (Thurau, 1903); Ngara District to Ufipa (Kielland, 1990d); Mbeya (Kielland, 1990d); Tabora (Kielland, 1990d); Nguru Mountains (Kielland, 1990d); Rubeho Mountains (Kielland, 1990d); Mikumi (Kielland, 1990d); Uzungwa Range (Kielland, 1990d); Katavi National Park (Fitzherbert et al., 2006). Malawi – Mt Mulanje (Congdon et al., 2010); Nyika N.P. Zambia – Ikelenge (Heath et al., 2002); Mwinilunga (Heath et al., 2002); Chingola (Heath et al., 2002); Mufulira (Heath et al., 2002); Kitwe (Heath et al., 2002); Kapiri Mposhi (Heath et al., 2002); Victoria Falls (Heath et al., 2002); Nyika (Heath et al., 2002). Mozambique – Mount Chiperone (Timberlake et al., 2007); Mt Yao [-12.4432 36.5114] (Congdon & Bayliss, 2013). Zimbabwe – Harare (Mullin); Zambezi Valley escarpment (Pringle et al., 1994); Burma Valley (Pringle et al., 1994); Chipinga (Pringle et al., 1994); Laurenceville, Vumba (male illustrated above). Habitat: Brachystegia woodland (Heath et al., 2002). In Tanzania it occurs at altitudes from near sea-level to 2 300 m (Kielland, 1990d). Habits: A fairly sluggish butterfly that flies away quickly if approached but soon resettles on rocks or the ground in the shade of trees. When resting near dead leaves the underside affords good camouflage (Pringle et al., 1994). Flight period: August to March (Pinhey, vide Van Son, 1979). There are fairly distinct seasonal forms and both fly together from December to February (the Cooksons, vide Pringle et al., 1994). Early stages: Congdon et al., 2017 [final instar larva]. Larval food: Hygrophila sp. (Acanthaceae) [Larsen, 1991c: 346]. Phaulopsis sp. (Acanthaceae) [Congdon et al., 2017; Igawa, Tanzania]. nachtigali Dewitz, 1879 (as sp. of Precis). Nova Acta Academiae Caesarea Leopoldino-Carolinae Germanicum Naturae Curiosorum 4 (2): 194 (173-212). Angola: “aus dem 10° S.B. und zwischen dem 17- 22° O.L. von Greenw.”. 3 nobilitata Thurau, 1903 (as sp. of Precis). Berliner Entomologische Zeitschrift 48: 137 (117-143). [Tanzania]: “Konde-Unyika; Uhehe, Iringa”. *Junonia chorimene (Guérin-Méneville, 1844) Golden Pansy Vanessa chorimene Guérin-Méneville, 1844. Iconographie du règne animal de G. Cuvier. Insectes 476 (576 pp.). Paris. Junonia chorimene. Male. Left – upperside; right – underside. Fort Portal, Uganda. 7 June 2017. J. Dobson. Images M.C. Williams ex Dobson Collection. Junonia chorimene. Female. Left – upperside; right – underside. Semuliki National Park, Uganda. 4 June 2017. J. Dobson. Images M.C. Williams ex Dobson Collection. Type locality: Senegal: “les bords de la riviere Casamance, Sénégal”. Diagnosis: Similar to Junonia stygia but differs in the paler ground colour and clear orange-brown markings. Also similar to Junonia natalica but lacks the three postdiscal white spots (Kielland, 1990d). Distribution: Senegal, Gambia, Guinea-Bissau (Aurivillius, 1910), Guinea, Mali, Sierra Leone, Liberia, Ivory Coast, Burkina Faso, Ghana, Togo, Benin (throughout), Nigeria, Democratic Republic of Congo (Uele, Ituri, Kivu, Lualaba), Sudan, Ethiopia, Uganda, Kenya (north, west), Tanzania (north), Arabia (south-west), Yemen. Specific localities: Senegal – Basse Casamance (TL). Gambia – Abuko, Bijilo, Pirang, Brufut, Finto Minareg, Bulok, Penjem, Brufut, Sanyang, Farasutu, 4 Keneba, Farafenni, Janjanbureh Island, Basse (Jon Baker, pers. comm, May 2020). Liberia – Wologizi (Safian et al., 2020); Wonegizi (Safian et al., 2020). Ghana – Cape Coast (Larsen, 2005a); Bobiri Butterfly Sanctuary (Larsen et al., 2007); Boabeng-Fiema Monkey Sanctuary (Larsen et al., 2009). Benin – Noyau Central, Lama Forest (Fermon et al., 2001); Houeyogbe Forest (Coache & Rainon, 2016); see Coache et al., 2017. Nigeria – Oban Hills (Larsen, 2005a). Democratic Republic of Congo – Ituri Forest (Ducarme, 2018); Semuliki Valley (Ducarme, 2018). Uganda – Semuliki N.P. (Davenport & Howard, 1996). Kenya – South Kavirondo (Larsen, 1991c); Tiriki (Larsen, 1991c); Malakisi (Larsen, 1991c); Kitale (Larsen, 1991c); Ol Jogi Ranch, near Nanuki (Williams, unpublished). Tanzania – Near Seronera in the Serengeti (single record) (Kielland, 1990d). Habitat: Riverine vegetation (Kielland, 1990d). Guinea and Sudan savanna in West Africa but found on the coast in the dry season and also in cleared areas in the forest zone (Larsen, 2005a). Dry river beds are often frequented (Larsen, 1991c). Habits: A reasonably common butterfly, that is very fond of flowers (Larsen, 2005a). In the Sudan savanna on hot days small numbers of specimens take advantage of the dense shade under mango and Boscia trees (Larsen, 1991c; 2005a). Early stages: Nothing published. Larval food: Asystasia mysurensis (Roth) T.Anderson (Acanthaceae) [Van Someren, 1974: 319; as Asystasia schimperi T. Anderson]. Barleria species (Acanthaceae) [Larsen, 1991c: 347]. Hypoestes species (Acanthaceae) [Larsen, 2005a]. Justicia leikipiensis S.Moore (Acanthaceae) [Van Someren, 1974: 319]. Paulowilhelmia species (Acanthaceae) [Larsen, 1991c: 347]. Ruellia species (Acanthaceae) [Larsen, 1991c: 347]. orthosia Klug, 1845 in Klug, 1829-45 (as sp. of Vanessa). In: Ehrenburg, C.G., Symbolae Physicae, seu icones et descriptiones corporum naturalium novarum aut minus cognitorum pl. 48 ([183] pp.). “Arabia deserta”. ethyra Feisthamel, 1850 (as sp. of Salamis). Annales de la Société Entomologique de France (2) 8: 250 (247-262). Senegal: “Cazamance”. angulata Aurivillius, 1913 in Seitz, 1908-25 (as d.s.f. of Precis chorimene). Die Gross-Schmetterlinge der Erde, Stuttgart (2) 13 Die Afrikanischen Tagfalter: 220 (614 pp.). Ethiopia: “Abyssinia”. *Junonia goudotii (Boisduval, 1833) Island Brown Pansy 5 Island Brown Pansy, Junonia goudotii male. Perinet, Madagascar. Image courtesy Raimund Schutte. Vanessa goudotii Boisduval, 1833. Nouvelles Annales
Recommended publications
  • Biolphilately Vol-64 No-3
    BIOPHILATELY OFFICIAL JOURNAL OF THE BIOLOGY UNIT OF ATA MARCH 2020 VOLUME 69, NUMBER 1 Great fleas have little fleas upon their backs to bite 'em, And little fleas have lesser fleas, and so ad infinitum. —Augustus De Morgan Dr. Indraneil Das Pangolins on Stamps More Inside >> IN THIS ISSUE NEW ISSUES: ARTICLES & ILLUSTRATIONS: From the Editor’s Desk ......................... 1 Botany – Christopher E. Dahle ............ 17 Pangolins on Stamps of the President’s Message .............................. 2 Fungi – Paul A. Mistretta .................... 28 World – Dr. Indraneil Das ..................7 Secretary -Treasurer’s Corner ................ 3 Mammalia – Michael Prince ................ 31 Squeaky Curtain – Frank Jacobs .......... 15 New Members ....................................... 3 Ornithology – Glenn G. Mertz ............. 35 New Plants in the Philatelic News of Note ......................................... 3 Ichthyology – J. Dale Shively .............. 57 Herbarium – Christopher Dahle ....... 23 Women’s Suffrage – Dawn Hamman .... 4 Entomology – Donald Wright, Jr. ........ 59 Rats! ..................................................... 34 Event Calendar ...................................... 6 Paleontology – Michael Kogan ........... 65 New Birds in the Philatelic Wedding Set ........................................ 16 Aviary – Charles E. Braun ............... 51 Glossary ............................................... 72 Biology Reference Websites ................ 69 ii Biophilately March 2020 Vol. 69 (1) BIOPHILATELY BIOLOGY UNIT
    [Show full text]
  • Phylogenetic Relationships and Historical Biogeography of Tribes and Genera in the Subfamily Nymphalinae (Lepidoptera: Nymphalidae)
    Blackwell Science, LtdOxford, UKBIJBiological Journal of the Linnean Society 0024-4066The Linnean Society of London, 2005? 2005 862 227251 Original Article PHYLOGENY OF NYMPHALINAE N. WAHLBERG ET AL Biological Journal of the Linnean Society, 2005, 86, 227–251. With 5 figures . Phylogenetic relationships and historical biogeography of tribes and genera in the subfamily Nymphalinae (Lepidoptera: Nymphalidae) NIKLAS WAHLBERG1*, ANDREW V. Z. BROWER2 and SÖREN NYLIN1 1Department of Zoology, Stockholm University, S-106 91 Stockholm, Sweden 2Department of Zoology, Oregon State University, Corvallis, Oregon 97331–2907, USA Received 10 January 2004; accepted for publication 12 November 2004 We infer for the first time the phylogenetic relationships of genera and tribes in the ecologically and evolutionarily well-studied subfamily Nymphalinae using DNA sequence data from three genes: 1450 bp of cytochrome oxidase subunit I (COI) (in the mitochondrial genome), 1077 bp of elongation factor 1-alpha (EF1-a) and 400–403 bp of wing- less (both in the nuclear genome). We explore the influence of each gene region on the support given to each node of the most parsimonious tree derived from a combined analysis of all three genes using Partitioned Bremer Support. We also explore the influence of assuming equal weights for all characters in the combined analysis by investigating the stability of clades to different transition/transversion weighting schemes. We find many strongly supported and stable clades in the Nymphalinae. We are also able to identify ‘rogue’
    [Show full text]
  • Lepidoptera Collecting in Kenya and Tanzania
    Vol. 4 No. 1 1993 BROS: Kenya and Tanzania Lepidoptera 17 TROPICAL LEPIDOPTERA, 4(1): 16-25 LEPIDOPTERA COLLECTING IN KENYA AND TANZANIA EMMANUEL BROS DE PUECHREDON1 "La Fleurie," Rebgasse 28, CH-4102 Binningen BL, Switzerland ABSTRACT.- Situated in tropical Africa, on both sides of the Equator, Kenya and Tanzania possess an extraordinary rich Lepidoptera fauna (according to Larsen's latest book on Kenya: 871 species only for the Rhopalocera and Grypocera). The present paper reports on the author's participation in a non-entomological mini-expedition during January 1977 across those two countries, with comments on the areas where collecting was possible and practiced by him as a serious amateur lepidopterist. In addition there are photos of some interesting landscapes and, last but not least, a complete list of all the species captured and noted. RESUME.- En pleine Afrique equatoriale, a cheval sur 1'Equateur, le Kenya et la Tanzanie possedent une faune de Lepidopteres extraordinairement riche (871 especes seulement pour les Rhopaloceres et Hesperiides du Kenya, selon le tout recent ouvrage de Larsen). La presente note relate une mini-expedition non specifiquement entomologique en Janvier 1977 a travers ces deux pays, avec commmentaires de 1'auteur, lepidopteriste amateur eclaire, sur les lieux ou il a eu la possibilite de collectionner, recit agremente de quelques photos de biotopes interessants et surtout avec la liste complete des especes capturees et notees. KEY WORDS: Acraeinae, Africa, Arctiidae, Cossidae, Danainae, distribution, Ethiopian, Eupterotidae, Hesperiidae, Limacodidae, Lymantriidae, Noctuidae, Notodontidae, Nymphalidae, Papilionidae, Pieridae, Psychidae, Pyralidae, Saturniidae, Satyrinae, Thaumetopoeinae. In January 1977, I had the opportunity of participating in a Mt.
    [Show full text]
  • African Butterfly News!
    LATE WINTER EDITION: JULY / AUGUST AFRICAN 2017-4 THE BUTTERFLY LEPIDOPTERISTS’ SOCIETY OF AFRICA NEWS LATEST NEWS Welcome to the Late Winter edition of African Butterfly News! African Butterfly News celebrates its first year of existence; the first edition, 2016-5, was circulated in September last year. The photographic competition commenced in August 2016, so the annual award will be made in the next, Spring Edition – for purposes of the photographic competition, the season starts in August and ends in July. A reminder that the newsletter is circulated every two months: Late Summer (January and February) – circulated in January Autumn (March and April) – circulated in March Early Winter (May and June) – circulated in May Late Winter (July and August) – circulated in July Spring (September and October) – circulated in September Early Summer (November and December) – circulated in November You will all be aware of the devastating fires that the southern Cape experienced in June. Dave and Hanna Edge, LepSoc Africa’s Treasurer and Membership Secretary respectively, were caught up in this drama, and had to evacuate their house (refer to Dave’s eyewitness account below). Fortunately, the building survived the fire, although the nearby Brenton Blue Reserve was incinerated. All fences, sign boards and marker-posts were destroyed – it is hoped that some larvae or pupae of the Brenton Blue (Orachrysops niobe) are still alive, safely underground. See a report under COREL under the “Projects” section. Some of you may have seen an article in the Sunday Times, by Aaron Hyman, a friend of Christopher Dobson. This magazine relies on material from you, the members of LepSoc Africa.
    [Show full text]
  • Check-List of the Butterflies of the Kakamega Forest Nature Reserve in Western Kenya (Lepidoptera: Hesperioidea, Papilionoidea)
    Nachr. entomol. Ver. Apollo, N. F. 25 (4): 161–174 (2004) 161 Check-list of the butterflies of the Kakamega Forest Nature Reserve in western Kenya (Lepidoptera: Hesperioidea, Papilionoidea) Lars Kühne, Steve C. Collins and Wanja Kinuthia1 Lars Kühne, Museum für Naturkunde der Humboldt-Universität zu Berlin, Invalidenstraße 43, D-10115 Berlin, Germany; email: [email protected] Steve C. Collins, African Butterfly Research Institute, P.O. Box 14308, Nairobi, Kenya Dr. Wanja Kinuthia, Department of Invertebrate Zoology, National Museums of Kenya, P.O. Box 40658, Nairobi, Kenya Abstract: All species of butterflies recorded from the Kaka- list it was clear that thorough investigation of scientific mega Forest N.R. in western Kenya are listed for the first collections can produce a very sound list of the occur- time. The check-list is based mainly on the collection of ring species in a relatively short time. The information A.B.R.I. (African Butterfly Research Institute, Nairobi). Furthermore records from the collection of the National density is frequently underestimated and collection data Museum of Kenya (Nairobi), the BIOTA-project and from offers a description of species diversity within a local literature were included in this list. In total 491 species or area, in particular with reference to rapid measurement 55 % of approximately 900 Kenyan species could be veri- of biodiversity (Trueman & Cranston 1997, Danks 1998, fied for the area. 31 species were not recorded before from Trojan 2000). Kenyan territory, 9 of them were described as new since the appearance of the book by Larsen (1996). The kind of list being produced here represents an information source for the total species diversity of the Checkliste der Tagfalter des Kakamega-Waldschutzge- Kakamega forest.
    [Show full text]
  • Download Full-Text
    Research in Zoology 2015, 5(2): 32-37 DOI: 10.5923/j.zoology.20150502.02 First Records of Butterfly Diversity on Two Remote Islands on the Volta Lake of Ghana, the Largest Reservoir by Total Surface Area in the World Daniel Opoku Agyemang1, Daniel Acquah-Lamptey1,*, Roger Sigismond Anderson2, Rosina Kyerematen1,2 1Department of Animal Biology and Conservation Science, University of Ghana, Legon, Ghana 2African Regional Postgraduate Programme in Insect Science, University of Ghana, Legon, Ghana Abstract The construction of the Akosombo Dam in Ghana for hydroelectric energy led to the creation of many islands on the Volta Lake. The biological diversity on these islands is unknown and so a rapid assessment was conducted in January 2014 as part as a region wide assessment to determine the butterfly diversity on two of these islands, Biobio and Agbasiagba. Diversity indices were computed for both islands using the Shannon-Weiner index, Margalef’s index for richness and Whittaker’s index for comparison of diversity between the two islands. A total of eight hundred and eighty-one (881) individual butterflies representing forty-five (45) species belonging to eight (8) families were recorded during the study. Thirty-nine (39) species of butterflies were recorded on Biobio island whiles twenty-eight (28) species were recorded on Agbasiagba. This was expected as the larger islands are expected to support more species than smaller ones, with Biobio island being relatively bigger than Agbasiagba. The shared species of butterflies on both islands were twenty-two (22) representing 48.9% of the total species accumulated. Indicator species like Junonia oenone, Danaus chrysippus and Papilio demodocus were also recorded indicating the degraded floral quality of the Islands.
    [Show full text]
  • Fasanbi SHOWCASE
    Threatened Species Monitoring PROGRAMME Threatened Species in South Africa: A review of the South African National Biodiversity Institutes’ Threatened Species Programme: 2004–2009 Acronyms ADU – Animal Demography Unit ARC – Agricultural Research Council BASH – Big Atlassing Summer Holiday BIRP – Birds in Reserves Project BMP – Biodiversity Management Plan BMP-S – Biodiversity Management Plans for Species CFR – Cape Floristic Region CITES – Convention on International Trade in Endangered Species CoCT – City of Cape Town CREW – Custodians of Rare and Endangered Wildflowers CWAC – Co-ordinated Waterbird Counts DEA – Department of Environmental Affairs DeJaVU – December January Atlassing Vacation Unlimited EIA – Environmental Impact Assessment EMI – Environmental Management Inspector GBIF – Global Biodiversity Information Facility GIS – Geographic Information Systems IAIA – International Association for Impact Assessment IAIAsa – International Association for Impact Assessment South Africa IUCN – International Union for Conservation of Nature LAMP – Long Autumn Migration Project LepSoc – Lepidopterists’ Society of Africa MCM – Marine and Coastal Management MOA – memorandum of agreement MOU – memorandum of understanding NBI – National Botanical Institute NEMA – National Environmental Management Act NEMBA – National Environmental Management Biodiversity Act NGO – non-governmental organization NORAD – Norwegian Agency for Development Co–operation QDGS – quarter-degree grid square SABAP – Southern African Bird Atlas Project SABCA – Southern African
    [Show full text]
  • Howdy, Bugfans, the Buckeye (Precis Coenia) Belongs to The
    Howdy, BugFans, The Buckeye (Precis coenia) belongs to the Order Lepidoptera (“scaled wings”) which includes the butterflies and the moths. Of the 12,000 species of Lepidoptera in North America north of Mexico, only about 700 are butterflies. In common, along with the usual six-legs-three-body-parts insect stuff, moths and butterflies have four wings that are covered with easily-rubbed-off scales (the upper surface of a butterfly’s wing often has a different pattern then the lower surface does), and mouthparts in the form of a coiled tube called a proboscis that is used for feeding on liquids like nectar and sap. They do Complete Metamorphosis, moving from egg to larva (caterpillar) to pupa (in a chrysalis or cocoon) to adult. Caterpillars chew; butterflies and moths sip. General rules for telling them apart are that butterflies sit with their wings held out to the side or folded vertically above their bodies, and moths hold their wings flat over or wrapped around their body. Butterflies have a thickened tip/knob on the end of their antennae; moths’ antennae may be bare or feathery, but are never knobbed. Butterflies are active by day (the BugLady has some night-feeding Northern Pearly-eyes who haven’t read that part of the rulebook); moths are generally active in late afternoon and through the night. Some day-flying moths have bright colors, but as a group, moths tend to be drab. Because of their pigmented and/or prismatic scales, many butterflies are the definition of the word “dazzling.” Buckeyes belong in the “Brush-footed butterfly” family, a large group of strong fliers whose front legs are noticeably hairy and are reduced in size (leading to a nickname – “four-footed butterflies”).
    [Show full text]
  • Duke University Dissertation Template
    Evolutionary trends in phenotypic elements of seasonal forms of the tribe Junoniini (Lepidoptera: Nymphalidae) by Jameson Wells Clarke Department of Biology Duke University Date:_______________________ Approved: ___________________________ H. Fred Nijhout, Ph.D., Supervisor ___________________________ V. Louise Roth, Ph.D. ___________________________ Sonke Johnsen, Ph.D. Thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in the Department of Biology in the Graduate School of Duke University 2017 i v ABSTRACT Evolutionary trends in phenotypic elements of seasonal forms of the tribe Junoniini (Lepidoptera: Nymphalidae) by Jameson Wells Clarke Department of Biology Duke University Date:_______________________ Approved: ___________________________ H. Fred Nijhout, Ph.D., Supervisor ___________________________ V. Louise Roth, Ph.D. ___________________________ Sonke Johnsen, Ph.D. An abstract of a thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in the Department of Biology in the Graduate School of Duke University 2017 Copyright by Jameson Wells Clarke 2017 Abstract Seasonal polyphenism in insects is the phenomenon whereby multiple phenotypes can arise from a single genotype depending on environmental conditions during development. Many butterflies have multiple generations per year, and environmentally induced variation in wing color pattern phenotype allows them to develop adaptations to the specific season in which the adults live. Elements of butterfly
    [Show full text]
  • Mt Mabu, Mozambique: Biodiversity and Conservation
    Darwin Initiative Award 15/036: Monitoring and Managing Biodiversity Loss in South-East Africa's Montane Ecosystems MT MABU, MOZAMBIQUE: BIODIVERSITY AND CONSERVATION November 2012 Jonathan Timberlake, Julian Bayliss, Françoise Dowsett-Lemaire, Colin Congdon, Bill Branch, Steve Collins, Michael Curran, Robert J. Dowsett, Lincoln Fishpool, Jorge Francisco, Tim Harris, Mirjam Kopp & Camila de Sousa ABRI african butterfly research in Forestry Research Institute of Malawi Biodiversity of Mt Mabu, Mozambique, page 2 Front cover: Main camp in lower forest area on Mt Mabu (JB). Frontispiece: View over Mabu forest to north (TT, top); Hermenegildo Matimele plant collecting (TT, middle L); view of Mt Mabu from abandoned tea estate (JT, middle R); butterflies (Lachnoptera ayresii) mating (JB, bottom L); Atheris mabuensis (JB, bottom R). Photo credits: JB – Julian Bayliss CS ‒ Camila de Sousa JT – Jonathan Timberlake TT – Tom Timberlake TH – Tim Harris Suggested citation: Timberlake, J.R., Bayliss, J., Dowsett-Lemaire, F., Congdon, C., Branch, W.R., Collins, S., Curran, M., Dowsett, R.J., Fishpool, L., Francisco, J., Harris, T., Kopp, M. & de Sousa, C. (2012). Mt Mabu, Mozambique: Biodiversity and Conservation. Report produced under the Darwin Initiative Award 15/036. Royal Botanic Gardens, Kew, London. 94 pp. Biodiversity of Mt Mabu, Mozambique, page 3 LIST OF CONTENTS List of Contents .......................................................................................................................... 3 List of Tables .............................................................................................................................
    [Show full text]
  • Origin of the Mechanism of Phenotypic Plasticity in Satyrid Butterfly Eyespots
    SHORT REPORT Origin of the mechanism of phenotypic plasticity in satyrid butterfly eyespots Shivam Bhardwaj1†*, Lim Si-Hui Jolander2, Markus R Wenk1,2, Jeffrey C Oliver3, H Frederik Nijhout4, Antonia Monteiro1,5* 1Department of Biological Sciences, National University of Singapore, Singapore, Singapore; 2Department of Biochemistry, National University of Singapore, Singapore, Singapore; 3Office of Digital Innovation & Stewardship, University of Arizona, Tucson, United States; 4Department of Biology, Duke University, Durham, United States; 5Yale-NUS College, Singapore, Singapore Abstract Plasticity is often regarded as a derived adaptation to help organisms survive in variable but predictable environments, however, we currently lack a rigorous, mechanistic examination of how plasticity evolves in a large comparative framework. Here, we show that phenotypic plasticity in eyespot size in response to environmental temperature observed in Bicyclus anynana satyrid butterflies is a complex derived adaptation of this lineage. By reconstructing the evolution of known physiological and molecular components of eyespot size plasticity in a comparative framework, we showed that 20E titer plasticity in response to temperature is a pre-adaptation shared by all butterfly species examined, whereas expression of EcR in eyespot centers, and eyespot sensitivity to 20E, are both derived traits found only in a *For correspondence: subset of species with eyespots. [email protected] (SB); [email protected] (AM) Introduction Present address: †Department
    [Show full text]
  • The Butterflies of Taita Hills
    FLUTTERING BEAUTY WITH BENEFITS THE BUTTERFLIES OF TAITA HILLS A FIELD GUIDE Esther N. Kioko, Alex M. Musyoki, Augustine E. Luanga, Oliver C. Genga & Duncan K. Mwinzi FLUTTERING BEAUTY WITH BENEFITS: THE BUTTERFLIES OF TAITA HILLS A FIELD GUIDE TO THE BUTTERFLIES OF TAITA HILLS Esther N. Kioko, Alex M. Musyoki, Augustine E. Luanga, Oliver C. Genga & Duncan K. Mwinzi Supported by the National Museums of Kenya and the JRS Biodiversity Foundation ii FLUTTERING BEAUTY WITH BENEFITS: THE BUTTERFLIES OF TAITA HILLS Dedication In fond memory of Prof. Thomas R. Odhiambo and Torben B. Larsen Prof. T. R. Odhiambo’s contribution to insect studies in Africa laid a concrete footing for many of today’s and future entomologists. Torben Larsen’s contribution to the study of butterflies in Kenya and their natural history laid a firm foundation for the current and future butterfly researchers, enthusiasts and rearers. National Museums of Kenya’s mission is to collect, preserve, study, document and present Kenya’s past and present cultural and natural heritage. This is for the purposes of enhancing knowledge, appreciation, respect and sustainable utilization of these resources for the benefit of Kenya and the world, for now and posterity. Copyright © 2021 National Museums of Kenya. Citation Kioko, E. N., Musyoki, A. M., Luanga, A. E., Genga, O. C. & Mwinzi, D. K. (2021). Fluttering beauty with benefits: The butterflies of Taita Hills. A field guide. National Museums of Kenya, Nairobi, Kenya. ISBN 9966-955-38-0 iii FLUTTERING BEAUTY WITH BENEFITS: THE BUTTERFLIES OF TAITA HILLS FOREWORD The Taita Hills are particularly diverse but equally endangered.
    [Show full text]