Lepidopteran Biodiversity of Ethiopia: Current Knowledge and Future Perspectives
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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 -
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. -
Lepidoptera: Lycaenidae: Polyommatinae)
Zootaxa 3860 (2): 195–200 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3860.2.6 http://zoobank.org/urn:lsid:zoobank.org:pub:CDDB0DDD-3904-457F-B77E-4AEC414B654A Neurellipes rhoko sp. n. from the Cross River Loop, Eastern Nigeria (Lepidoptera: Lycaenidae: Polyommatinae) SZABOLCS SÁFIÁN Institute of Silviculture and Forest Protection, University of West Hungary. Bajcsy-Zsilinszky út 4. H-9400 Sopron, Hungary Butterfly Conservation Society, Ghana, TDC Serviced plot E-109. Community 14 Lashibi-Tema, Ghana. E-mail: [email protected] Abstract A new species belonging to the recently revised Neurellipes mahota-group has been found in the Cross River Loop, East- ern Nigeria. It resembles the recently described Liberian N. georgiadisi Larsen, 2009, but differs from it by the wing shape and the extent and shape of orange patches on the hindwing, also on the forewing, especially in the discoidal cell. The species is described as N. rhoko sp. n.; a detailed comparison with the other species in the N. mahota-group is given, as well as notes on the biogeography of N. rhoko and its Liberian sub-region vicariant N. georgiadisi. Key words: Neurellipes, mahota-group, N. mahota, N. gola, N. georgiadisi, West Africa, Liberian sub-region, biogeog- raphy, allopatry Introduction All African species with orange spotting previously placed in the genus Anthene Doubleday, were removed by Libert (2010), who transferred them to Neurellipes, a genus previously comprising many fewer species, including a group of smaller sized orange-spotted species. -
Wetlands of the Nile Basin the Many Eco for Their Liveli This Chapt Distribution, Functions and Contribution to Contribution Livelihoods They Provide
important role particular imp into wetlands budget (Sutch 11 in the Blue N icantly 1110difi Wetlands of the Nile Basin the many eco for their liveli This chapt Distribution, functions and contribution to contribution livelihoods they provide. activities, ane rainfall (i.e. 1 Lisa-Maria Rebelo and Matthew P McCartney climate chan: food securit; currently eX' arc under tb Key messages water resour support • Wetlands occur extensively across the Nile Basin and support the livelihoods ofmillions of related ;;ervi people. Despite their importance, there are big gaps in the knowledge about the current better evalu: status of these ecosystems, and how populations in the Nile use them. A better understand systematic I ing is needed on the ecosystem services provided by the difl:erent types of wetlands in the provide. Nile, and how these contribute to local livelihoods. • While many ofthe Nile's wetlands arc inextricably linked to agricultural production systems the basis for making decisions on the extent to which, and how, wetlands can be sustainably used for agriculture is weak. The Nile I: • Due to these infi)fl11atio!1 gaps, the future contribution of wetlands to agriculture is poorly the basin ( understood, and wetlands are otten overlooked in the Nile Basin discourse on water and both the E agriculture. While there is great potential for the further development of agriculture and marsh, fen, fisheries, in particular in the wetlands of Sudan and Ethiopia, at the same time many that is stat wetlands in the basin are threatened by poor management practices and populations. which at \, In order to ensure that the future use of wetlands for agriculture will result in net benefits (i.e. -
Title Lorem Ipsum Dolor Sit Amet, Consectetur Adipiscing Elit
Volume 26: 102–108 METAMORPHOSIS www.metamorphosis.org.za ISSN 1018–6490 (PRINT) LEPIDOPTERISTS’ SOCIETY OF AFRICA ISSN 2307–5031 (ONLINE) Classification of the Afrotropical butterflies to generic level Published online: 25 December 2015 Mark C. Williams 183 van der Merwe Street, Rietondale, Pretoria, South Africa. E-mail: [email protected] Copyright © Lepidopterists’ Society of Africa Abstract: This paper applies the findings of phylogenetic studies on butterflies (Papilionoidea) in order to present an up to date classification of the Afrotropical butterflies to genus level. The classification for Afrotropical butterflies is placed within a worldwide context to subtribal level. Taxa that still require interrogation are highlighted. Hopefully this classification will provide a stable context for researchers working on Afrotropical butterflies. Key words: Lepidoptera, Papilionoidea, Afrotropical butterflies, classification. Citation: Williams, M.C. (2015). Classification of the Afrotropical butterflies to generic level. Metamorphosis 26: 102–108. INTRODUCTION Suborder Glossata Fabricius, 1775 (6 infraorders) Infraorder Heteroneura Tillyard, 1918 (34 Natural classifications of biological organisms, based superfamilies) on robust phylogenetic hypotheses, are needed before Clade Obtectomera Minet, 1986 (12 superfamilies) meaningful studies can be conducted in regard to their Superfamily Papilionoidea Latreille, 1802 (7 evolution, biogeography, ecology and conservation. families) Classifications, dating from the time of Linnaeus in the Family Papilionidae Latreille, 1802 (32 genera, 570 mid seventeen hundreds, were based on morphology species) for nearly two hundred and fifty years. Classifications Family Hedylidae Guenée, 1858 (1 genus, 36 species) based on phylogenies derived from an interrogation of Family Hesperiidae Latreille, 1809 (570 genera, 4113 the genome of individual organisms began in the late species) 20th century. -
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. -
Local History of Ethiopia Ma - Mezzo © Bernhard Lindahl (2008)
Local History of Ethiopia Ma - Mezzo © Bernhard Lindahl (2008) ma, maa (O) why? HES37 Ma 1258'/3813' 2093 m, near Deresge 12/38 [Gz] HES37 Ma Abo (church) 1259'/3812' 2549 m 12/38 [Gz] JEH61 Maabai (plain) 12/40 [WO] HEM61 Maaga (Maago), see Mahago HEU35 Maago 2354 m 12/39 [LM WO] HEU71 Maajeraro (Ma'ajeraro) 1320'/3931' 2345 m, 13/39 [Gz] south of Mekele -- Maale language, an Omotic language spoken in the Bako-Gazer district -- Maale people, living at some distance to the north-west of the Konso HCC.. Maale (area), east of Jinka 05/36 [x] ?? Maana, east of Ankar in the north-west 12/37? [n] JEJ40 Maandita (area) 12/41 [WO] HFF31 Maaquddi, see Meakudi maar (T) honey HFC45 Maar (Amba Maar) 1401'/3706' 1151 m 14/37 [Gz] HEU62 Maara 1314'/3935' 1940 m 13/39 [Gu Gz] JEJ42 Maaru (area) 12/41 [WO] maass..: masara (O) castle, temple JEJ52 Maassarra (area) 12/41 [WO] Ma.., see also Me.. -- Mabaan (Burun), name of a small ethnic group, numbering 3,026 at one census, but about 23 only according to the 1994 census maber (Gurage) monthly Christian gathering where there is an orthodox church HET52 Maber 1312'/3838' 1996 m 13/38 [WO Gz] mabera: mabara (O) religious organization of a group of men or women JEC50 Mabera (area), cf Mebera 11/41 [WO] mabil: mebil (mäbil) (A) food, eatables -- Mabil, Mavil, name of a Mecha Oromo tribe HDR42 Mabil, see Koli, cf Mebel JEP96 Mabra 1330'/4116' 126 m, 13/41 [WO Gz] near the border of Eritrea, cf Mebera HEU91 Macalle, see Mekele JDK54 Macanis, see Makanissa HDM12 Macaniso, see Makaniso HES69 Macanna, see Makanna, and also Mekane Birhan HFF64 Macargot, see Makargot JER02 Macarra, see Makarra HES50 Macatat, see Makatat HDH78 Maccanissa, see Makanisa HDE04 Macchi, se Meki HFF02 Macden, see May Mekden (with sub-post office) macha (O) 1. -
RECENT LITERATURE on LEPIDOPTERA (Under the Supervision of PETER F
1960 .loumal of the Lepidopterists' Society 161 RECENT LITERATURE ON LEPIDOPTERA (Under the supervision of PETER F. BELLINGER) F. BIOLOGY AND IMMATURE STAGES Comstock, John Adams, "Notes on metamorphoses of the Giant Skippers (LepidopTera: Megathymimc) and (he life history of an Arizona species." Rull. southern Calif. Acad. Sri., vol.55: pp.19-27, 3 figs. 1956. Describes mature larva & pupa of Mega thymus evalls;. [P B.] Comstock, John Adams, "Notes on the life history of a rare Arizona sphinx moth, Xylophanes faito Walker." Bull. southerll Calif. Acad. Sci., vo1.55: pp.102-106. 5 figs. 1956. Describes mature larva & pupa; foodplant B01lvardia glaberrima. LP.B.] Comstock, John A., "Brief notes on the life histories of two Arizona geometrid moths." Bull. southem Calif. A (ad. Sci., vol. 56 : pp.99-100 1957. Describes larva & pupa of Philobia aspirata (from Black Walnut), & egg & young larva of Pero modest1ls. [P.B.] Com';tock, John Adams, "Life histories of two southern Arizona moths of the genus Caripeta." Bull. southern Calif. Ilrad. Sci., vol. 56 : pp.88-96, 4 pIs. 1957. De£cribes & figures early stages of C. hilumaria (reared on willow, probably not the normal food plant) & C. macularia (reared on oak). [Po B.] Comstock, John Adams, "Notes on the early stages of two western American moths." Bull. southern Calif. Acad. Sci., vol.56: pp.42-47, 6 figs. 1957. Describes mature larva; & pupa; of Cisthene nexa & Agriopodes viridata; both feed on the lichen Ramalina combeoides. [Po B J Comstock, John Adams, "Notes on the metamorphosis of an Agave-boring butterfly from Baja California, Mexico." Trans. -
Noctuoidea: Erebidae: Others
Staude et al. / Metamorphosis 27: S165–S188 S165 ____________________________________________________________________________________________________________________________ Noctuoidea: Erebidae: Others Reference/ Lepidoptera Host plant Locality rearing no. Taxon Subfamily Family Taxon Family M1148 Anoba angulilinea Anobinae Erebidae Dalbergia Fabaceae Tshukudu Game melanoxylon Reserve, Hoedspruit M998 Anoba atripuncta Anobinae Erebidae Ormocarpum Fabaceae Tshukudu Game trichocarpum Reserve, Hoedspruit Gv71 Baniana arvorum Anobinae Erebidae Elephantorrhiza Fabaceae Steenkoppies, farm, elephantina Magaliesburg 14HSS52 Baniana arvorum Anobinae Erebidae Elephantorrhiza Fabaceae Steenkoppies, farm, elephantina Magaliesburg 13HSS84 Plecoptera arctinotata Anobinae Erebidae Senegalia caffra Fabaceae Steenkoppies, farm, Magaliesburg M1020a Plecoptera flaviceps Anobinae Erebidae Dalbergia Fabaceae Casketts, farm, melanoxylon Hoedspruit M317 Bareia incidens Calpinae Erebidae Ficus lutea Moraceae Casketts, farm, (unplaced as to Hoedspruit tribe) 14HSS87 Egnasia vicaria Calpinae Erebidae Afrocanthium Rubiaceae Dlinsa Forest, (unplaced as to mundianum Eshowe tribe) 12HSS163 Exophyla multistriata Calpinae Erebidae Celtis africana Cannabaceae Golden Valley, (unplaced as to Magaliesburg tribe) M416 Exophyla multistriata Calpinae Erebidae Trema orientalis Cannabaceae Sekororo, Tzaneen (unplaced as to (Fed on Celtis tribe) africana) M743 Lacera alope Calpinae Erebidae Pterolobium Fabaceae Moholoholo Rehab (unplaced as to stellatum Centre, Hoedspruit tribe) -
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. -
Comparative Morphology of the Male Genitalia in Lepidoptera
COMPARATIVE MORPHOLOGY OF THE MALE GENITALIA IN LEPIDOPTERA. By DEV RAJ MEHTA, M. Sc.~ Ph. D. (Canta.b.), 'Univefsity Scholar of the Government of the Punjab, India (Department of Zoology, University of Oambridge). CONTENTS. PAGE. Introduction 197 Historical Review 199 Technique. 201 N ontenclature 201 Function • 205 Comparative Morphology 206 Conclusions in Phylogeny 257 Summary 261 Literature 1 262 INTRODUCTION. In the domains of both Morphology and Taxonomy the study' of Insect genitalia has evoked considerable interest during the past half century. Zander (1900, 1901, 1903) suggested a common structural plan for the genitalia in various orders of insects. This work stimulated further research and his conclusions were amplified by Crampton (1920) who homologized the different parts in the genitalia of Hymenoptera, Mecoptera, Neuroptera, Diptera, Trichoptera Lepidoptera, Hemiptera and Strepsiptera with those of more generalized insects like the Ephe meroptera and Thysanura. During this time the use of genitalic charac ters for taxonomic purposes was also realized particularly in cases where the other imaginal characters had failed to serve. In this con nection may be mentioned the work of Buchanan White (1876), Gosse (1883), Bethune Baker (1914), Pierce (1909, 1914, 1922) and others. Also, a comparative account of the genitalia, as a basis for the phylo genetic study of different insect orders, was employed by Walker (1919), Sharp and Muir (1912), Singh-Pruthi (1925) and Cole (1927), in Orthop tera, Coleoptera, Hemiptera and the Diptera respectively. It is sur prising, work of this nature having been found so useful in these groups, that an important order like the Lepidoptera should have escaped careful analysis at the hands of the morphologists. -
Native Versus Exotic Crotalaria Species (Fabaceae) As Host Plants of the Ornate Bella Moth, Utetheisa Ornatrix (Lepidoptera: Erebidae: Arctiinae) Andrei Sourakov*
Journal of Natural History, 2015 Vol. 49, Nos. 39–40, 2397–2415, http://dx.doi.org/10.1080/00222933.2015.1006700 You are what you eat: native versus exotic Crotalaria species (Fabaceae) as host plants of the Ornate Bella Moth, Utetheisa ornatrix (Lepidoptera: Erebidae: Arctiinae) Andrei Sourakov* McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL, USA (Received 9 April 2014; accepted 2 January 2015; first published online 3 March 2015) Crotalaria plants and Utetheisa ornatrix are closely linked to each other: the larvae destroy the seeds, while the moth depends on hostplants for alkaloids. To better understand the ongoing co-evolution, the present study examines how native hos- tplants compare to exotic ones. Leaf-feeding on Crotalaria pumila, C. rotundifolia,and C. incana,nativetothemoth’s range, led to faster larval development than on the exotic C. lanceolata, C. spectabilis,andC. pallida. Seed-feeding on all species of Crotalaria led to accelerated larval development and a resultant larger adult moth, and correlates with a higher nitrogen content in the plant tissues. These results add a novel dimension to the previous studies of reproductive biology of this model organ- ism. In controlled settings, mature larvae showed preference for leaves of C. spectabilis over those of other species, perhaps due to the higher alkaloid content. Differences in morphology and phenology of Crotalaria determine the ecology of U. ornatrix popu- lations in Florida. The introduction of novel hostplants, on which U. ornatrix can have a significant negative effect and which are of concern to humans as invasive toxic weeds, has greatly expanded the niche occupied by this moth.