Butterflies in Ologbo Forest
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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. -
Original Research Article DOI - 10.26479/2017.0206.01 BIOLOGY of FEW BUTTERFLY SPECIES of AGRICULTURE ECOSYSTEMS of ARID REGIONS of KARNATAKA, INDIA Santhosh S
Santhosh & Basavarajappa RJLBPCS 2017 www.rjlbpcs.com Life Science Informatics Publications Original Research Article DOI - 10.26479/2017.0206.01 BIOLOGY OF FEW BUTTERFLY SPECIES OF AGRICULTURE ECOSYSTEMS OF ARID REGIONS OF KARNATAKA, INDIA Santhosh S. & S. Basavarajappa* Entomology Laboratory, DOS in Zoology, University of Mysore, Manasagangotri, Mysore-570 006, India ABSTRACT: Agriculture ecosystems have provided congenial habitat for various butterfly species. The Papilionidae and Nymphalidae family member’s most of their life cycle is depended on natural plant communities amidst agriculture ecosystems. To record few butterflies viz., Papilio polytes, Graphium agamemnon, Ariadne merione and Junonia hierta, agriculture ecosystems were selected randomly and visited frequently by adapting five-hundred-meter length line transects during 2014 to 2016. Study sites were visited during 0800 to 1700 hours and recorded the ovipositing behaviour of gravid female of these butterfly species by following standard methods. Eggs along with the host plant leaves / shoot / twigs were collected in a sterilized Petri dish and brought to the laboratory for further studies. Eggs were maintained under sterilized laboratory conditions till hatching. Newly hatched larvae were fed with their preferred host plants foliage and reared by following standard methods. P. polytes and G. agamemnon and A. merione and J. hierta developmental stages included egg, larva, pupa and adult and these stages have showed significant variation (F=21.35; P>0.01). Further, all the four species had four moults and five instars in their larval stage. However, including larval period, pupal duration was also varied considerably among these species. Further, overall life cycle completed in 43, 32.5 to 40, 21 to 30 and 21 to 29 days by P. -
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. -
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. -
Phylogeny of the Aphnaeinae: Myrmecophilous African Butterflies
Systematic Entomology (2015), 40, 169–182 DOI: 10.1111/syen.12098 Phylogeny of the Aphnaeinae: myrmecophilous African butterflies with carnivorous and herbivorous life histories JOHN H. BOYLE1,2, ZOFIA A. KALISZEWSKA1,2, MARIANNE ESPELAND1,2,3, TAMARA R. SUDERMAN1,2, JAKE FLEMING2,4, ALAN HEATH5 andNAOMI E. PIERCE1,2 1Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, U.S.A., 2Museum of Comparative Zoology, Harvard University, Cambridge, MA, U.S.A., 3Museum of Natural History and Archaeology, Norwegian University of Science and Technology, Trondheim, Norway, 4Department of Geography, University of Wisconsin, Madison, WI, U.S.A. and 5Iziko South African Museum, Cape Town, South Africa Abstract. The Aphnaeinae (Lepidoptera: Lycaenidae) are a largely African subfamily of 278 described species that exhibit extraordinary life-history variation. The larvae of these butterflies typically form mutualistic associations with ants, and feed on awide variety of plants, including 23 families in 19 orders. However, at least one species in each of 9 of the 17 genera is aphytophagous, parasitically feeding on the eggs, brood or regurgitations of ants. This diversity in diet and type of symbiotic association makes the phylogenetic relations of the Aphnaeinae of particular interest. A phylogenetic hypothesis for the Aphnaeinae was inferred from 4.4 kb covering the mitochondrial marker COI and five nuclear markers (wg, H3, CAD, GAPDH and EF1) for each of 79 ingroup taxa representing 15 of the 17 currently recognized genera, as well as three outgroup taxa. Maximum Parsimony, Maximum Likelihood and Bayesian Inference analyses all support Heath’s systematic revision of the clade based on morphological characters. -
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. -
Tropical Phenology: Bi-Annual Rhythms and Interannual Variation in an Afrotropical Butterfly Assemblage 1, 2 3 4 ANU VALTONEN, FREERK MOLLEMAN, COLIN A
Tropical phenology: bi-annual rhythms and interannual variation in an Afrotropical butterfly assemblage 1, 2 3 4 ANU VALTONEN, FREERK MOLLEMAN, COLIN A. CHAPMAN, JAMES R. CAREY, 5 1 MATTHEW P. AYRES, AND HEIKKI ROININEN 1Department of Biology, University of Eastern Finland, Joensuu FI-80101 Finland 2Institute of Ecology and Earth Sciences, University of Tartu, Tartu EE-51014 Estonia 3Department of Anthropology and McGill School of Environment, McGill University, Montreal, Quebec H3A 2T7 Canada 4Department of Entomology, University of California, Davis, California 95616 USA 5Department of Biological Sciences, Dartmouth College, Hanover, New Hampshire 03755 USA Citation: Valtonen, A., F. Molleman, C. A. Chapman, J. R. Carey, M. P. Ayres, and H. Roininen. 2013. Tropical phenology: bi-annual rhythms and interannual variation in an Afrotropical butterfly assemblage. Ecosphere 4(3):36. http://dx.doi. org/10.1890/ES12-00338.1 Abstract. Temporal variation and phenology of tropical insect communities and the role of environmental factors controlling this variation is poorly understood. A better understanding is needed, for example, to predict the effects of climate change on tropical insect communities and to assess the long- term persistence of tropical communities. We studied seasonal and inter-annual variation in tropical fruit- feeding butterflies by exploiting a unique 137-month abundance time series of .100 species, sampled at 22 locations in the medium altitude montane rain forest of Kibale National Park, western Uganda. Precipitation peaked twice per year, about 20 d after each equinox. Vegetation greenness peaked approximately 33 d later. Species richness and abundance of butterflies peaked about 2 and 3 months, respectively, after the greenness peak. -
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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. -
Biodiversiteitsopname Biodiversity Assessment
Biodiversiteitsopname Biodiversity Assessment Bome - Trees (77 sp) Veldblomme - Flowering veld plants (65 sp) Grasse - Grasses (41 sp) Naaldekokers - Dragonflies (46 sp) Skoenlappers - Butterflies (81 sp) Motte - Moths (95 sp) Nog insekte - Other insects (102 sp) Spinnekoppe - Spiders (53 sp) Paddas - Frogs (14 sp) Reptiele - Reptiles (22 sp) Voëls - Birds (185 sp) Soogdiere - Mammals (23 sp) 4de uitgawe: Jan 2015 Plante/Plants Diere/Animals (24 000 spp in SA) Anthropoda Chordata (>150 000 spp in SA) Arachnida Insecta (spinnekoppe/spiders, 2020 spp in SA) Neuroptera – mayflies, lacewings, ant-lions (385 spp in SA) Odonata – dragonflies (164 spp in SA) Blattodea – cockroaches (240 spp in SA) Mantodea – mantids (185 spp in SA) Isoptera – termites (200 spp in SA) Orthoptera – grasshoppers, stick insects (900 spp in SA) Phthiraptera – lice (1150 spp in SA) Hemiptera – bugs (>3500 spp in SA) Coleoptera – beetles (18 000 spp in SA) Lepidoptera – butterflies (794 spp in SA), moths (5200 spp in SA) Diptera – flies (4800 spp in SA) Siphonoptera – fleas (100 spp in SA) Hymenoptera – ants, bees, wasps (>6000 spp in SA) Trichoptera – caddisflies (195 spp in SA) Thysanoptera – thrips (230 spp in SA) Vertebrata Tunicata (sea creatures, etc) Fish Amphibia Reptiles Birds Mammals (115 spp in SA) (255 spp in SA) (858 spp in SA) (244 spp in SA) Bome – Trees (n=77) Koffiebauhinia - Bauhinia petersiana - Dainty bauhinia Rooi-ivoor - Berchemia zeyheri - Red ivory Witgat - Boscia albitrunca - Shepherd’s tree Bergvaalbos - Brachylaena rotundata - Mountain silver-oak -
Male Secondary Sexual Characters in Aphnaeinae Wings (Lepidoptera: Lycaenidae)
Opusc. Zool. Budapest, 2017, 48(1): 27–34 Male secondary sexual characters in Aphnaeinae wings (Lepidoptera: Lycaenidae) 1 2 3 4 5 ZS. BÁLINT , A. HEATH , G. KATONA , K. KERTÉSZ & SZ. SÁFIÁN 1Zsolt Bálint, Department of Zoology, Hungarian Natural History Museum, Budapest, Baross u. 13, H-1088, Hungary. E-mail: [email protected] 2Alan Heath, Iziko South African Museum, Cape Town, South Africa. E-mail: [email protected] 3Katona Gergely, Department of Zoology, Hungarian Natural History Museum, Budapest, Baross u. 13, -1088, Hungary. E-mail: [email protected] 4Krisztián Kertész, Nanostructures Department, Institute of Technical Physics and Materials Sciences, Centre for Energy Research, Hungarian Academy of Sciences, Budapest, POB 49, H-1515 Hungary. E-mail: [email protected] 5Szabolcs Sáfián, Faculty of Forestry, University of West Hungary, Bajcsy-Zsilinszky u. 4, Sopron H-9400, Hungary. E-mail: [email protected] Abstract. Male secondary sexual characters have been discovered on the hindwing verso of genera Aphnaeus Hübner, [1819], Cigaritis Donzel, 1847, Lipaphnaeus Aurivillius, 1916 and Pseudaletis Druce, 1888 representing the Palaeotropical subfamily Aphnaeinae (Lycaenidae: Lepidoptera). Relevant wing parts are illustrated, described, and some observations on the organs are briefly annotated. With an appendix and 14 figures. Keywords. Androconia, hair tuft, classification, Palaeotropics, scaling. INTRODUCTION and Eliot 1990). However, Eliot did not indicate any male secondary sexual characters in this ne of the most characteristic features of Lepi- subfamily, nor did any of the previous or sub- O doptera is the scaled membranous wing sur- sequent workers (eg. Stempffer 1954, Heath 1997, face of the imagines. The scales covering the Libert 2013). -
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.