119 Genus Amauris Huebner

Total Page:16

File Type:pdf, Size:1020Kb

119 Genus Amauris Huebner AFROTROPICAL BUTTERFLIES 17th edition (2018). MARK C. WILLIAMS. http://www.lepsocafrica.org/?p=publications&s=atb Genus Amauris Hübner, [1816] In: Hübner, [1816-[1826]. Verzeichniss bekannter Schmettlinge 14 (432 + 72 pp.). Augsburg. Type-species: Papilio niavius Linnaeus, by subsequent designation (Scudder, 1875. Proceedings of the American Academy of Arts and Sciences 10: 108 (91-293).). The genus Amauris belongs to the Family Nymphalidae Rafinesque, 1815; Subfamily Danainae Boisduval, 1833; Tribe Danaini Boisduval, 1833; Subtribe Amaurina Le Cerf, 1922. Amauris is the only Afrotropical genus in the Subtribe Amaurina. Amauris is an exclusively Afrotropical genus containing 16 species. Relevant literature: De Vries, 2002 [Differential wing toughness with other taxa]. Amauris species. Final instar larva. Images courtesy Raimund Schutte Amauris species. Pupa. 1 Image courtesy Raimund Schutte Subgenus Amauris Hübner, [1816] In: Hübner, [1816-26]. Verzeichniss bekannter Schmettlinge 14 (432 + 72 pp.). Augsburg. Type-species: Papilio niavius Linnaeus, by subsequent designation (Scudder, 1875. Proceedings of the American Academy of Arts and Sciences 10: 108 (91-293).). *Amauris (Amauris) niavius (Linnaeus, 1758)# Friar Male of the Friar Butterfly (Amauris niavius) at Lake Sibaya, Zululand. Image courtesy Steve Woodhall. Papilio niavius Linnaeus, 1758. Systema Naturae 1, Regnum Animale, 10th edition: 470 (824 pp.). Holmiae. Amauris (Amauris) niavius (Linnaeus, 1758). Pringle et al., 1994: 48. Amauris niavius niavius. Male (Wingspan 75 mm). Left – upperside; right – underside. Wingspan 75 mm. Biakpa Mountain Paradise, Ghana. 24 November 2011. J. Dobson. Images M.C. Williams ex Dobson Collection. Alternative common name: Common Friar. 2 Type locality: [West Africa]: “Indiis”. [False locality.] Distribution: Guinea-Bissau (Aurivillius, 1910), Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo, Benin (Fermon et al., 2001), Nigeria, Cameroon, Equatorial Guinea, Gabon, Congo, Central African Republic, Angola, Democratic Republic of Congo, Sudan, Ethiopia, Uganda, Kenya, Tanzania, Malawi, Zambia, Mozambique, Zimbabwe, Namibia, South Africa, Swaziland (Duke et al., 1999). There is also a single record for the Seychelles (Legrand, 1965). Habitat: Drier forest and disturbed areas in the rainforest zone, penetrating savanna in riverine vegetation. Occasionally in primary rainforest (Larsen, 2005a). In Tanzania the nominate subspecies occurs at altitudes from 800 to 1 600 m and subspecies dominicanus from sea-level to 2 340 m (Kielland, 1990d). Habits: The flight is slow and gliding. Males are strongly attracted to Heliotropium indicum (Boraginaceae) from which they imbibe pyrrolizidine alkaloids, especially from the roots of plants that have been dug up (Sevastopulo, 1974; Larsen, 2005a). Gynura (Asteraceae) and Gliricidia (Fabaceae) are also used by males as a source of alkaloids (Larsen, 2005a). Larsen (1991; 2005a) notes communal roosting, during dry periods, of a few individuals with larger numbers of Amauri ochlea in the Shimba Hills, Kenya. Both sexes are strongly attracted to flowers and males sometimes come to water, excrement and carrion. Important mimics are females of Papilio dardanus and both sexes of Hypolimnas anthedon. Flight period: All year, with a peak in late summer and autumn (Woodhall, 2005). Early stages: Nothing published. Larval food: Cynanchum species (Apocynaceae) [Larsen, 1991c: 259]. Heliotropium indicum [Lawrence, 2014: 51; in error, as this plant is a source of pyrollizidine alkaloids for adults, not a larval host plant]. Marsdenia sylvestris (Retz.) P.I.Forst. (Apocynaceae) [Van Someren, 1974: 324; as Gymnema sylvestre (Retz.) Bull.]. Secamone species (Apocynaceae) [Larsen, 1991c: 259]. Tylophora species (Apocynaceae) [Larsen, 1991c: 259]. Relevant literature: Stritzke et al., 2003 [Sesquiterpenes secreted]. Amauris (Amauris) niavius niavius (Linnaeus, 1758) Papilio niavius Linnaeus, 1758. Systema Naturae 1, Regnum Animale, 10th edition: 470 (824 pp.). Holmiae. Amauris (Amauris) niavius niavius (Linnaeus, 1758). Pringle et al., 1994: 48. Amauris niavius niavius. Male (Wingspan 75 mm). Left – upperside; right – underside. Wingspan 75 mm. Biakpa Mountain Paradise, Ghana. 24 November 2011. J. Dobson. Images M.C. Williams ex Dobson Collection. Type locality: [West Africa]: “Indiis”. [False locality.] 3 Diagnosis: The subspecies dominicanus is distinguished from the nominate subspecies by the more extensive white markings on the upperside of the hindwing (Pringle et al., 1994). Distribution: Guinea-Bissau (Aurivillius, 1910), Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Togo, Benin (Fermon et al., 2001), Nigeria, Cameroon, Equatorial Guinea (Bioko), Gabon, Congo, Central African Republic, Angola, Democratic Republic of Congo, Uganda, Kenya (west and central), Tanzania (west), Zambia (north), Namibia (north). Specific localities: Ghana – Bobiri Butterfly Sanctuary (Larsen et al., 2007); Boabeng-Fiema Monkey Sanctuary (Larsen et al. 2009). Benin – Noyau Central, Lama Forest (Fermon et al., 2001); Benin – Houeyogbe Forest (Coache & Rainon, 2016). Cameroon – Korup (Larsen, 2005a). Equatorial Guinea – Caldera de Luba, Bioko (Martin, 2015). Gabon – Alen Nkoma (Vande weghe, 2010); Iguela (Vande weghe, 2010); Rabi (Vande weghe, 2010); Mboumie (Vande weghe, 2010); Waka (Vande weghe, 2010); Lope (Vande weghe, 2010); Ipassa (Vande weghe, 2010); Langoue (Vande weghe, 2010); Nouna (Vande weghe, 2010); Franceville (Vande weghe, 2010); Camp PPG, Bateke Plateau (Vande weghe, 2010). Central African Republic – Dzanga (Noss, 1998). Democratic Republic of Congo – Kindu, Katanga (male illustrated above). Uganda – Semuliki N.P. (Davenport & Howard, 1996). Tanzania – Western portions of Mpanda, Kigoma and Bukoba (Kielland, 1990d). Zambia – Ikelenge (Heath et al., 2002); Mufulira (Heath et al., 2002); Luongo River (Heath et al., 2002); Kalungwishi River (Heath et al., 2002); Lake Mweru (Heath et al., 2002); Mbala (Heath et al., 2002). Nambia – Namutoni (Ficq; single record). obliterata Dufrane, 1948 (as ab. of Amauris niavius niavius). Bulletin Mensuel de la Société Linnéenne de Lyon 17: 193 (192-194). [Democratic Republic of Congo]: “Congo belge”. Amauris (Amauris) niavius aethiops Rothschild & Jordan, 1903 Amauris niavius aethiops Rothschild & Jordan, 1903. Novitates Zoologicae 10: 503 (491-542). Type locality: [Ethiopia]: “Anderatscha”. Distribution: Sudan (south), Uganda (north), Ethiopia. Specific localities: Sudan – Nagichot Station, Didinga Mountains (Talbot, 1941). Ethiopia – Anderatscha (TL). partita Talbot, 1941 (as f. of Amauris niavius niavius). Entomologist’s Monthly Magazine 77: 210 (210- 216). Sudan: “Didinga Mtns., Nagichot Sta.”. Amauris (Amauris) niavius dominicanus Trimen, 1879# Amauris dominicanus Trimen, 1879. Transactions of the Entomological Society of London 1879: 323 (323-346). Amauris dominicanus Trimen, 1879. Trimen & Bowker, 1887a. Amauris dominicanus Trimen. Swanepoel, 1953a. Amauris niavius dominicanus Trimen, 1879. Dickson & Kroon, 1978. Amauris (Amauris) niavius dominicanus Trimen, 1879. Pringle et al., 1994: 48. 4 Amauris niavius dominicanus. Male (Wingspan 83 mm). Left – upperside; right – underside. Lekgalameetse Nature Reserve, Limpopo Province, South Africa. 19 December 2006. M. Williams. Images M.C. Williams ex Williams Collection. Amauris niavius dominicanus. Female (Wingspan 80 mm). Left – upperside; right – underside. Malelane, Mpumalanga, South Africa. 20 June 2010. J. Dobson. Images M.C. Williams ex Dobson Collection. Type locality: [South Africa]: “Natal”; Mozambique: “Quilimane”; “Zambesi”. Diagnosis: Subspecies dominicanus is distinguished from the nominate subspecies by the more extensive white markings on the upperside of the hindwing (Pringle et al., 1994). Distribution: Kenya (east of the Rift Valley), Tanzania (east, north, south-west), Malawi, Zambia, Mozambique, Zimbabwe (east), South Africa (Limpopo Province, Mpumalanga, KwaZulu-Natal), Swaziland (Duke et al., 1999). A single record from the Seychelles (Mahé island) (Legrand, 1965). Specific localities: Kenya – Marsabit (Larsen, 1991c); Nairobi (Larsen, 1991c); Shimba Hills (Larsen, 1991c). Tanzania – Moshi (Carcasson, 1963); Eastern, northern and south-western parts (Kielland, 1990d); Semdoe Forest Reserve (Doggart et al., 2001); Mt Kilimanjaro (Liseki & Vane-Wright, 2015). Malawi – Mt Mulanje (Congdon et al., 2010); Zomba Mountain (Congdon et al., 2010). Zambia – Mafinga Mountains (Heath et al., 2002). Mozambique – Quilimane (Trimen, 1879); Mount Chiperone (Timberlake et al., 2007); Mt Namuli (Congdon et al., 2010); Mt Mabu (Congdon et al., 2010). Limpopo Province – Lekgalameetse Nature Reserve (“Malta Forest”) (Swanepoel, 1953); Woodbush (Swanepoel, 1953). Mpumalanga – Barberton (Swanepoel, 1953); Marieps Kop (Swanepoel, 1953); Mariepskop area (Henning, 1994c); Buffelskloof Nature Reserve (Williams). KwaZulu-Natal – Durban (male illustrated above); Umkomaas (Swanepoel, 1953); Eshowe (Swanepoel, 1953); Empangeni (Swanepoel, 1953); St Lucia Bay (Swanepoel, 1953); Sodwana Bay (Williams); 5 Kosi Bay Nature Reserve (Pringle & Kyle, 2002); Tembe Nature Reserve (Pringle & Kyle, 2002); Ndumo Nature Reserve (Pringle & Kyle, 2002). Swaziland – Mlawula N. R. (www.sntc.org.sz). Seychelles – Bel-Air, Mahe island (a single record by M. Mason in 1953 (Legrand, 1965)). Note: Specimens in Trans-Nzoia, Kenya are transitional between subspecies niavius and dominicanus (Larsen, 1991c). *Amauris (Amauris) tartarea Mabille, 1876 Monk Male
Recommended publications
  • 309 Genus Amauris Huebner
    AFROTROPICAL BUTTERFLIES. MARK C. WILLIAMS. http://www.lepsocafrica.org/?p=publications&s=atb Updated 27 February 2021 Genus Amauris Hübner, [1816] Friars In: Hübner, [1816-[1826]. Verzeichniss bekannter Schmettlinge 14 (432 + 72 pp.). Augsburg. Type-species: Papilio niavius Linnaeus, by subsequent designation (Scudder, 1875. Proceedings of the American Academy of Arts and Sciences 10: 108 (91-293).). The genus Amauris belongs to the Family Nymphalidae Rafinesque, 1815; Subfamily Danainae Boisduval, 1833; Tribe Danaini Boisduval, 1833; Subtribe Amaurina Le Cerf, 1922. Amauris is the only Afrotropical genus in the Subtribe Amaurina. Amauris (Friars) is an exclusively Afrotropical genus containing 17 species. Relevant literature: De Vries, 2002 [Differential wing toughness with other taxa]. Amauris species. Final instar larva. Images courtesy Raimund Schutte 1 Amauris species. Pupa. Image courtesy Raimund Schutte Subgenus Amauris Hübner, [1816] In: Hübner, [1816-26]. Verzeichniss bekannter Schmettlinge 14 (432 + 72 pp.). Augsburg. Type-species: Papilio niavius Linnaeus, by subsequent designation (Scudder, 1875. Proceedings of the American Academy of Arts and Sciences 10: 108 (91-293).). *Amauris (Amauris) niavius (Linnaeus, 1758)# Giant Friar Male of the Friar Butterfly (Amauris niavius) at Lake Sibaya, Zululand. Image courtesy Steve Woodhall. Papilio niavius Linnaeus, 1758. Systema Naturae 1, Regnum Animale, 10th edition: 470 (824 pp.). Holmiae. Amauris (Amauris) niavius (Linnaeus, 1758). Pringle et al., 1994: 48. Amauris niavius niavius.
    [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]
  • And Ford, I; Ford, '953) on the Other Hand Have Put Forward a View Intermediate Between the Extreme Ones of Darwin on the One Hand and Goldschmidt on the Other
    THE EVOLUTION OF MIMICRY IN THE BUTTERFLY PAPILIO DARDANUS C. A. CLARKE and P. M. SHEPPARD Departments of Medicine and Zoology, University of Liverpool Received23.V.59 1.INTRODUCTION WHENBatesputforward the mimicry hypothesis which bears his name, Darwin (1872), although accepting it, had some difficulty in explaining the evolution of the mimetic resemblance of several distinct species to one distasteful model by a series of small changes, a require- ment of his general theory of evolution. He said "it is necessary to suppose in some cases that ancient members belonging to several distinct groups, before they had diverged to their present extent, accidentally resembled a member of another and protected group in a sufficient degree to afford some slight protection; this having given the basis for the subsequent acquisition of the most perfect resemb- lance ". Punnett (1915) realised that the difficulty is even more acute when one is dealing with a polymorphic species whose forms mimic very distantly related models. Knowing that, in those butterflies which had been investigated genetically, the forms differed by single allelomorphs he concluded that the mimicry did not evolve gradually and did not confer any advantage or disadvantage to the individual. He argued that an allelomorph arises at a single step by mutation and that therefore the mimicry also arises by chance at a single step. Goldschmidt (x) although not denying that mimicry confers some advantage to its possessors also maintained that the resemblance arises fully perfected by a single mutation of a gene distinct from that producing the colour pattern in the model, but producing a similar effect in the mimic.
    [Show full text]
  • Systematics and the Conservation of Biological
    r- rden R. I. Vane-Wright 2 rd, J. Piesman & M. D. Corwin. SYSTEMATICS AND THE is on Nantucket Island, USA: or, lxodes (Ixodes) dammini, n. CONSERVATION OF J. Med. Entomol. 15: 218-234. BIOLOGICAL DIVERSITY' ather, S. I. Moore, M. L. Wilson Incompetence of deer as reser- ase spirochete. Amer. J. Trop. ABSTRACT mier & J. A. Rawlings. 1991. from arthropods col- •urgdofen This paper concerns the role of systematics in efforts to conserve biological diversity. Biodiversity is seen both as Trop. Med. Hyg. 44:469-474. J. an interdisciplinary science (involving ecology and population biology as well as systematics), and as a socio-political Lain, J. H. Oliver, Jr., J. Piesman activity (because of the strongly anthropocentric focus of the Convention on Biological Diversity). Systematics has a . Investigation of the validity of number of key roles to play, especially with respect to maximizing our limited and fragmentary knowledge of biology us- s dammini (Acari: Ixodidae) through the predictive power of natural classification, and in helping to set priorities for conservation when, as is . Acad. Sci. U.S.A. 90: 10221— inevitably the case, resources are limited. After examining ways in which systematists must support the growing needs of society to know more about the Earth's biota, it is concluded that, because of their unique insights into the subject, rsic, U. B. Gobel, B. Graf, S. Jaur- systematists have an equally strong responsibility to take an active lead in many of the issues relating to the study, hwab & G. Zumstein. 1992. An use, and conservation of biological diversity. em for Borrelia burgdmfen based noclonal antibodies and OspA se- lin.
    [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]
  • Archiv Für Naturgeschichte
    © Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zobodat.at Lepidoptera für 1903. Bearbeitet von Dr. Robert Lucas in Rixdorf bei Berlin. A. Publikationen (Autoren alphabetisch) mit Referaten. Adkin, Robert. Pyrameis cardui, Plusia gamma and Nemophila noc- tuella. The Entomologist, vol. 36. p. 274—276. Agassiz, G. Etüde sur la coloration des ailes des papillons. Lausanne, H. Vallotton u. Toso. 8 °. 31 p. von Aigner-Abafi, A. (1). Variabilität zweier Lepidopterenarten. Verhandlgn. zool.-bot. Ges. Wien, 53. Bd. p. 162—165. I. Argynnis Paphia L. ; IL Larentia bilineata L. — (2). Protoparce convolvuli. Entom. Zeitschr. Guben. 17. Jahrg. p. 22. — (3). Über Mimikry. Gaea. 39. Jhg. p. 166—170, 233—237. — (4). A mimicryröl. Rov. Lapok, vol. X, p. 28—34, 45—53 — (5). A Mimicry. Allat. Kozl. 1902, p. 117—126. — (6). (Über Mimikry). Allgem. Zeitschr. f. Entom. 7. Bd. (Schluß p. 405—409). Über Falterarten, welche auch gesondert von ihrer Umgebung, in ruhendem Zustande eine eigentümliche, das Auge täuschende Form annehmen (Lasiocampa quercifolia [dürres Blatt], Phalera bucephala [zerbrochenes Ästchen], Calocampa exoleta [Stück morschen Holzes]. — [Stabheuschrecke, Acanthoderus]. Raupen, die Meister der Mimikry sind. Nachahmung anderer Tiere. Die Mimik ist in vielen Fällen zwecklos. — Die wenn auch recht geistreichen Mimikry-Theorien sind doch vielleicht nur ein müßiges Spiel der Phantasie. Aitken u. Comber, E. A list of the butterflies of the Konkau. Journ. Bombay Soc. vol. XV. p. 42—55, Suppl. p. 356. Albisson, J. Notes biologiques pour servir ä l'histoire naturelle du Charaxes jasius. Bull. Soc. Etud. Sc. nat. Nimes. T. 30. p. 77—82. Annandale u. Robinson. Siehe unter S w i n h o e.
    [Show full text]
  • AGIDE Final Report
    COMPTE RENDU FINAL D’EXECUTION DE PROJET I. INFORMATIONS DE BASE Nom de l’organisation : Association pour la Gestion Intégrée et Durable de l'Environnement (AGIDE) Adresses Siège social : Tsévié, Préfecture de Zio, Région maritime, TOGO B.P. 149 Tsévié – TOGO Cel. :(00228) 909 05 84 E-mail : [email protected] Antennes : Kpalimé, Préfecture de Kloto, Région des plateaux E-mail : [email protected] Titre du projet : Inventory of Butterflies in the Missahoe Classified Forest in Togo, Upper Guinea Forest II. REMARQUES PRÉALABLES 1 – Présentation sommaire du Togo Situé dans la sous région Ouest africaine, le Togo est un petit pays effilé coincé entre le Bénin à l’Est et le Ghana à l’Ouest. Il est limité au Nord par le Burkina Faso et au Sud par le Golfe de Guinée. Sa superficie est de 56 600 km2. La population est de 4 500 000 habitants avec une densité moyenne de 25 habitants / Km2. La proportion de la femme est de 62%. La zone guinéenne du Togo qui comprend les régions Maritimes et des Plateaux compte 76,6% de pauvre dont 65,5% extrêmement pauvre1. Sur le plan économique, l’évolution du PIB par habitant du Togo en général a progressivement baissé depuis les années 1997 à la suite de la situation socio politique du pays, jointe aux problèmes climatiques qui ont eu des impacts négatifs sur la flore, la faune et la production agricole2. En vue de freiner la pression anthropique sur les ressources naturelles et réduire la pauvreté des populations tributaires des ressources animales et végétales, les divers programme de développement3 proposent dans leur plan d’action, le développement des activités génératrices de revenus afin d’orienter les activités de ces exploitants.
    [Show full text]
  • Deutsche Entomologische Zeitscrift
    © Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zobodat.at On a collection of Lepidoptera from Bangala*). By Euiily Mary Sliarpe. The following- is a list of the Butterflies collected by Mr. Herbert Ward at Bangala on the River C'oiigo. Mr. \\'ard, as is well known. was oiie of the officers of the Rear Guard of the Emin Pasha Relief Expedition, and as was the case with Mr. Janieson his ofiicial duties left him but iittle leisure for natural history studies. I have referred especially to the following- books and papers which deal with the Lepidoptera of the Congo Region, and other parts of West. Africa. Voijage de IM. Cli. Allmud dans le territoire d ' A s s i n i e (A f r i q u e o c c i d e n t a 1 e) en juillet et aoüt 1886. 4e Memoire (1). IJpklopÜrcs a Y e c des n o t e s s u r quelques a u t r e s e s p e c e s d ' A f r i q u e. Par M. Faul Malnllc, Ann. Soc. Ent. France, (6), X, pt. I, pp. 17—33, 1890. Cataloqne des Upidopteres de la cote occidejitale d'Afrique. Par. U Faul MihiUe, Bull. Soc. Zool. France, I, pp. 194—203, 1876. Jameson, 7. S. Storii of the Fear Cohimn of the Emin Fasha JEdpedition. I^epidoptera Fhopalocera. Bij I. Z). Godman, F. F. '^. and Oshert Salvin, F. R. S. pp. 426—445, 1890. ^1 list of the Butterflles collected by Mr.
    [Show full text]
  • Arise by Chance As the Result of Mutation. They Therefore Suggest
    THE EVOLUTION OF DOMINANCE UNDER DISRUPTIVE SELECTION C. A. CLARKE and P. Ni. SHEPPARD Department of Medicine and Department of Zoology, University of Liverpool Received6.iii.59 1.INTRODUCTION INa paper on the effects of disruptive selection, Mather (1955) pointed out that if there are two optimum values for a character and all others are less advantageous or disadvantageous there will be disruptive selection which can lead to the evolution of a polymorphism. Sheppard (1958) argued that where such selection is effective and the change from one optimum value to the other is switched by a single pair of allelomorphs there will be three genotypes but only two advantageous phenotypes. Consequently if dominance were absent initially it would be evolved as a result of the disruptive selection, the heterozygote and one of the homozygotes both coming to resemble one of the two optimum phenotypes (see Ford, 1955, on Tripharna comes). Thoday (1959) has shown by means of an artificial selection experiment that, even when a character is, at the beginning, controlled polygenically (sternopleural chaeta-number in Drosophila) and there is 50 per cent. gene exchange between the "high" and "low" selected sub-popu- lations, a polymorphism can evolve. The most fully understood examples of disruptive selection (other than sex) are provided by instances of Batesian Mimicry, where there are a number of distinct warningly coloured species, acting as models, which are mimicked by the polymorphic forms of a single more edible species. Fisher and Ford (see Ford, 1953) have argued that a suffi- ciently good resemblance between mimic and model is not likely to arise by chance as the result of mutation.
    [Show full text]
  • Spatial and Matrix Influences on the Biogeography of Insect Taxa in Forest Fragments in Central Uganda
    Spatial and matrix influences on the biogeography of insect taxa in forest fragments in central Uganda Perpetra Akite Dissertation for a cotutelle award of Doctor of Philosophy Degree of Makerere University, Uganda and University of Bergen, Norway Makerere University University of Bergen 2016 Department of Biological Sciences, Makerere University Department of Biology, University of Bergen ii DECLARATION OF ORIGINALITY This is my own work and it has never been submitted for any degree award in any University iii TABLE OF CONTENTS DECLARATION OF ORIGINALITY......................................................................................iii LIST OF CONTENTS...............................................................................................................iv ACKNOWLEDGEMENTS.......................................................................................................vi LIST OF PAPERS....................................................................................................................vii Declaration of authors’ contributions…………………….…...……………...……...viii ABSTRACT...............................................................................................................................x BACKGROUND........................................................................................................................1 Problem statement..........................................................................................................……….2 Objectives........................................................................................................................3
    [Show full text]
  • Butterfly Species Abundances by Site
    Main Bait Line Trap Captures ‐ Species Abundances by Site TOTAL Bobiri Owabi Kajease Bonwire Asantemanso Gyakye Kona Total Specimens 8453 1292 2684 596 746 1059 752 1324 Total Species 116 67 82 37 50 60 47 62 Species List Amauris niavius 20100 0 01 Amauris tartarea 10100 0 00 Andronymus hero 11000 0 00 Anthene locuples 10000 1 00 Anthene rubricinctus 10000 0 10 Ariadne enotrea 42100 0 01 Aterica galene 213 25 96 14 17 35 9 17 Bebearia absolon 66 36 15 2 3 7 0 3 Bebearia barce 40000 4 00 Bebearia cocalia 140540 0 05 Bebearia demetra 11000 0 00 Bebearia lucayensis 52000 0 21 Bebearia mandinga 132512 2 01 Bebearia mardania 47 1 22 0 3 10 0 11 Bebearia oxione 101601 2 00 Bebearia paludicola 80220 3 01 Bebearia phantasina 77000 0 00 Bebearia sophus 270 16 143 9 6 60 11 25 Bebearia tentyris 182 127 19 0 1 1 11 23 Bebearia zonara 44 31 3 0 1 0 1 8 Bicyclus abnormis 667 237 287 0 28 4 0 111 Bicyclus dorothea 68 0 15 21 0 10 7 15 Bicyclus funebris 593 149 147 21 80 48 21 127 Bicyclus madetes 440 25 134 7 71 63 53 87 Bicyclus martius 448 33 70 3 87 47 42 166 Bicyclus procora 67 8 57 0 1 0 1 0 Bicyclus safitza 35 2 12 12 1 3 3 2 Bicyclus sandace 229 2 38 50 4 69 39 27 Bicyclus sangmelinae 40 5 34 0 0 1 0 0 Bicyclus taenias 166 17 47 1 10 30 39 22 Bicyclus vulgaris 504 62 75 87 24 106 84 66 Bicyclus xeneas 41 19 8 0 2 0 0 12 Bicyclus zinebi 154 4 43 6 47 3 3 48 Catuna crithea 20200 0 00 Celaenorrhinus galenus 20 0 1 0 16 1 2 0 Celaenorrhinus meditrina 20000 2 00 Charaxes ameliae 10000 0 01 Charaxes anticlea 41200 1 00 Charaxes bipunctatus 110011
    [Show full text]
  • The Volta Region
    WILDLIFE DIVISION (FORESTRY COMMISSION) REPUBLIC OF GHANA Wildlife Division Support Project (WDSP) The Butterflies of Kyabobo National Park, Ghana, and those of the Volta Region by Torben B Larsen (WDSP Report No. 64) March 2006 In collaboration with: Butterflies of Kyabobo and Volta Region. WDSP Report no 64 March 2006 TABLE OF CONTENTS EXECUTIVE SUMMARY …………………………………… 4 ACKNOWLEDGEMENTS ………………………………….. 7 1. INTRODUCTION ………………………………………… 8 2. KYABOBO NATIONAL PARK …………………………. 9 2.1 Location and characteristics of Kyabobo National Park …… 9 2.1.1 Habitat types ………………………………………………… 9 2.2 The butterflies of Kyabobo National Park …………………. 10 2.2.1 Material and methods ……………………………………….. 10 2.2.2 Analysis of the Kyabobo butterflies ……………………….... 11 2.2.3 Conservation value of Kyabobo National Park ……..………. 14 2.3 Ecotourism potential ..……………………………………... 14 3. VOLTA REGION – ECOLOGY AND BIOGEOGRAPHY 17 3.1 The Volta Region setting …………………………………… 17 3.2 History of butterfly collecting in the Volta Region ………… 18 3.3 Review of the Volta Region butterfly fauna ………………… 19 3.3.1 Total butterfly fauna …………………………………………… 19 3.3.2 Endemics of Africa west of the Dahomey Gap ……………….. 21 3.3.3 Eastern species not found west of the Volta River ……………. 23 3.4 Biogeographical summary …………………………………… 25 3.5 Conservation priorities in the Volta Region ………...………. 25 3.6 Ecotourism …………………………………………………... 27 4. CONCLUDING REMARKS ……………………………… 29 REFERENCES ……………………………………………. 30 APPENDICES: Appendix 1 The butterflies of the Volta Region, Kyabobo, Wli Falls, and Kalakpa…………….….…………….. 33 Appendix 2 Butterflies recorded by Karsch (1893) from Adeli Mountains, German Togoland …………… 55 2 Butterflies of Kyabobo and Volta Region. WDSP Report no 64 March 2006 LIST OF TABLES: Table 2.2.2.
    [Show full text]