038 Genus Eretis Mabille

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AFROTROPICAL BUTTERFLIES 17th edition (2018). MARK C. WILLIAMS. http://www.lepsocafrica.org/?p=publications&s=atb Genus Eretis Mabille, 1891 Bulletin de la Société Entomologique de Belgique 35: 71 (59-88, 106-121, 168-187). Type-species: Eretis melania Mabille, by monotypy. The genus Eretis belongs to the Family Hesperiidae Latreille, 1809; Subfamily Pyrginae Burmeister, 1878; Tribe Celaenorrhinini Swinhoe, 1912. Other genera of the Tribe Celaenorrhini in the Afrotropical Region are Ortholexis, Katreus, Celaenorrhinus, Scopulifera, Bettonula, Apallaga, Sarangesa, Alenia and Triskelionia. Eretis (Elfs) is an Afrotropical genus of 12 species. Most closely related to the genus Sarangesa but are mostly smaller, and the forewings have an irregular outline (Larsen, 1991c). Some of the species can only be identified by reference to the genitalia (Evans, 1937; Larsen, 1991c). In the males of some species of Eretis there is a ventral hair fringe on the first abdominal segment (Larsen & Cock, 2011: 15). *Eretis artorius Larsen & Cock, 2011 Eretis artorius Larsen & Cock, 2011. Tropical Lepidoptera Research 21 (1): 12 (12-16). Top: Male holotype ex Kakamega Forest (left – upperside; right – underside) Below: Female paratype ex Kakamega Forest (left – upperside; right – underside) Images from a PDF of the original publication courtesy Torben Larsen. Type locality: Kenya: Kakamega District, Kakamega Forest, D257 at Ikuywa Stream, 18 June 1991, photo 91.9.34, M.J.W. Cock (ex coll. T.B. Larsen). Holotype (male) in the Natural History Museum, London. Etymology: The specific name is a latinized version of Arthur, Cock’s domestic cat (Larsen & Cock, 2011). Distribution: Democratic Republic of Congo (Larsen pers comm, 2011), Uganda, Rwanda, Kenya. Specific localities: 1 Democratic Republic of Congo – Ruwenzori (Larsen pers comm, 2011); North Kivu (Larsen pers comm, 2011). Uganda – Impenetrable Forest (Larsen & Cock, 2011); Kigezi area (Larsen & Cock, 2011). Rwanda – Bugoie Forest (Larsen & Cock, 2011); Nyungwe Forest (Larsen & Cock, 2011). Kenya – Kakamega Forest at Ikuywa Stream (TL); Yala River [= Kakamega] (Larsen & Cock, 2011); Mau Forest (Larsen & Cock, 2011); Nandi Hills (Larsen & Cock, 2011). Habitat: Submontane rainforest (Larsen & Cock, 2011). Habits: It is a fairly common skipper, at least in Kakamega, that flies in somewhat open areas within or adjacent to forest. The flight is fast and usually low down and they often settle with flattened wings on the upper surface of green leaves. They freely come to nectar at small flowers (Larsen & Cock, 2011). Early stages: Nothing published. Larval food: Nothing published. *Eretis buamba Evans, 1937 Male of Eretis buamba. Kibale Forest, Uganda. October, 2014. Image courtesy Raimund Schutte. Eretis buamba Evans, 1937. A catalogue of the African Hesperiidae indicating the classification and nomenclature adopted in the British Museum: 39 (212 pp.). Type locality: Uganda: “Bugoma Forest, Unyoro, 3,700 ft”. Distribution: Democratic Republic of Congo, Uganda (west). Specific localities: Uganda – Bugoma Forest (TL). Early stages: Nothing published. Larval food: Nothing published. *Eretis camerona Evans, 1937 Eretis camerona Evans, 1937. A catalogue of the African Hesperiidae indicating the classification and nomenclature adopted in the British Museum: 38 (212 pp.). Type locality: Cameroon: “Cameroons (Bitje)”. Distribution: Cameroon, Democratic Republic of Congo, Uganda (west). Recorded, in error, from Nigeria by Larsen, 1999 (CD of draft for Butterflies of West Africa) (Larsen, 2005a). Specific localities: Cameroon – Bitje (TL). Early stages: Nothing published. Larval food: Nothing published. 2 *Eretis djaelaelae (Wallengren, 1857)# Marbled Elf Perching males of the Marbled Elf (Eretis djaelaelae) Images courtesy Steve Woodhall. Male Marbled Elf (Eretis djaelaelae) displaying scent brush on leg. Image courtesy Steve Woodhall. Pterygospidea djaelaelae Wallengren, 1857. Öfversigt af Kongl. Vetenskaps-Akademiens Förhandlingar. Stockholm annis 1838-1845. Collecta (n.s.) 2 (4): 54 (55 pp.). Nisoniades djaelaelae Wallengren. Trimen, 1866a. Pterygospidea djaelaelae Wallengren, 1857. Trimen & Bowker, 1889. Eretis djaelaelae Wallengren. Swanepoel, 1953a. Eretis djaelaelae (Wallengren, 1857). Dickson & Kroon, 1978. Eretis djaelaelae (Wallengren, 1857). Pringle et al., 1994: 312. Eretis djaelaelale. Male (Wingspan 33 mm). Left – upperside; right – underside. Lekgalameetse N.R., Limpopo Province, South Africa. 20 October 2012. M. Williams. Images M.C. Williams ex Williams Collection. Type locality: [South Africa]: “Caffraria”. Holotype in the Swedish Natural History Museum (images available at www2.nrm.se/en/lep_nrm/d). Diagnosis: See Eretis umbra for differentiation. 3 Distribution: Tanzania (east-central), Malawi, Zambia, Mozambique, Zimbabwe, South Africa (Limpopo Province, Mpumalanga, North West Province, Gauteng, KwaZulu-Natal, Eastern Cape Province, Western Cape Province – south-east), Swaziland. Specific localities: Tanzania – Image Mountain (Kielland, 1990d); Ruaha National Park (Kielland, 1990d). Zambia – Nyika (Heath et al., 2002). Limpopo Province – Warmbaths (Swanepoel, 1953); Mica (Swanepoel, 1953); Polokwane (Swanepoel, 1953); Munnik (Swanepoel, 1953); Vivo (Swanepoel, 1953); Sibasa (Swanepoel, 1953); Messina (Swanepoel, 1953); Lekgalameetse Nature Reserve (“Malta Forest”). Mpumalanga – Komatipoort (Swanepoel, 1953); Sterkspruit Nature Reserve (Williams); Buffelspoort Nature Reserve (Williams); Kaapsehoop (male illustrated above). North West Province – Zeerust (Swanepoel, 1953). Gauteng – Pretoria (Swanepoel, 1953). KwaZulu-Natal – Margate (Swanepoel, 1953); Pietermaritzburg (Swanepoel, 1953); Greytown (Swanepoel, 1953); Estcourt (Swanepoel, 1953); Eshowe (Swanepoel, 1953); St Lucia Bay (Swanepoel, 1953); Rwayi, South Coast (S. Woodhall, unpublished, 2009). Eastern Cape Province – Port Elizabeth (Swanepoel, 1953); Somerset East (Swanepoel, 1953); Fort Beaufort (Swanepoel, 1953); King William’s Town (Swanepoel, 1953); Queenstown (Swanepoel, 1953); Stormberg (Swanepoel, 1953); Cathcart (Swanepoel, 1953); Stutterheim (Swanepoel, 1953); Kei River (Swanepoel, 1953); East London (Dickson & Kroon, 1978). Western Cape Province – Plettenberg Bay (Swanepoel, 1953); Mossel Bay (requires verification) (Pringle et al., 1994). Swaziland – Malolotja N. R. (www.sntc.org.sz). Habitat: Savanna woodland; rarely grassland. In Tanzania it is found in woodland and open montane grassland, from 700 to 2 100 m (Kielland, 1990d). Habits: Adults fly close to the ground, with a skipping flight. They alight frequently, with expanded wings, on low plants or on the ground. Both sexes often visit flowers. Males occasionally mud-puddle or imbibe moisture from fresh cow-dung (Pringle et al., 1994). Males may establish territories, usually centred on a small bush. Flight period: All year but in cooler areas from August to May. Commonest from September to March (Pringle et al., 1994). Early stages: Clark, in Dickson & Kroon, 1978: 216; plate 6 [as Eretis djaelaelae djaelaelae; Horse Shoe Valley, East London, Eastern Cape Province, South Africa. There is a possibility that this record may be that of the life history of Eretis umbra (Trimen)]. “Egg: Laid singly on a leaf or bud-cluster. Yellow when laid changing to red; 0,8 mm diameter over the ribs by 0,5 mm high. There are 14 to 16 upright ribs, only half of them reaching the micropyle, and some 10 cross-ribs, the lower not fully developed. Eggs hatch after 8 days. Shell is not eaten. Larva: 1st instar 1 to 2 mm in 19 days; 2nd instar 2 to 4 mm in 20 days; 3rd instar 4 to 6 mm in 19 days; 4th instar 6 to 10 mm in 22 days; 5th instar 10 to 16 or 17 mm in 65 days. The duration of instars varies with climatic conditions. Larva constructs a cache by binding leaves together and lives concealed in it, only emerging to feed. When this becomes too small for the larva another is made by it for furthr use. Moulting and pupation take place within the cache. Pupa: 11,5 mm ♂, 13,5 mm ♀. At first dull greenish-gray. After about 8 days thorax gradually turns brown, eyes become reddish and wing-cases whiten, while body becomes greener but is still pale. Emergence occurs after 10 or 11 days. Parasite: Apanteles species ex final larval instar. This species is multi-brooded.” Larval food: Asystasia sp. (Acanthaceae) [Sevastopulo, 1975]. Asystasia schimperi T.Anderson (Acanthaceae) [Van Someren, 1974: 325]. Barleria fissiflora Bojer ex Nees (= Barleria setigera Rendle) (Acanthaceae) [Kielland, 1990d: 231]. Dyschoriste setigera (Pers.) Vollesen (= Chaetacanthus setiger (Pers.) Lindl. (syn. persoonii C.B. Cl.) (Acanthaceae) [Murray, 1959; South Africa]. Justicia protracta (Nees) T.Anderson (Acanthaceae) [Henning, Henning, Joannou & Woodhall, 1997: 71]. Justicia sp. (Acanthaceae) [Dickson & Kroon, 1978: 183]. Phaulopsis imbricata (Forssk.) Sweet (Acanthaceae) [Dickson & Kroon, 1978: 183]. 4 *Eretis herewardi Riley, 1921 Eretis herewardi Riley, 1921. Transactions of the Entomological Society of London 1921: 255 (234-259). Eretis rotundimacula herewardi Riley, 1921. Evans, 1937. Eretis rotundimacula herewardi Riley, 1921. Pringle et al., 1994: 312. Eretis herewardi Riley, 1921. Ackery et al., 1995. Eretis herewardi herewardi. Male. Left – upperside; right – underside. Wingspan: 33mm. Wanzizi, Mpanda, Tanzania. 24/1/69. Kielland. (Henning collection – H10). Type locality: [Zambia]: “Solwezi”. Distribution: Angola, Democratic Republic of Congo, Uganda, Tanzania, Malawi, Zambia, Mozambique. According to
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  • A Handbook on the Rare, Threatened & Endemic Species of the Greater St Lucia Wetland Park

    A Handbook on the Rare, Threatened & Endemic Species of the Greater St Lucia Wetland Park

    f A HANDBOOK ON THE RARE, THREATENED & ENDEMIC SPECIES OF THE GREATER ST LUCIA WETLAND PARK A product of the Greater St Lucia Wetland Park Rare, Threatened & Endemic Species Project Combrink & Kyle June 2006 St Lucia Office: The Dredger Harbour, Private Bag x05, St Lucia 3936 Tel No. +27 35 590 1633, Fax No. +27 35 590 1602, e-mail [email protected] 2 “Suddenly, as rare things will, it vanished” Robert Browning A photograph taken in 2003 of probably the last known Bonatea lamprophylla, a recently (1976) described terrestrial orchid that was known from three small populations, all within the Greater St Lucia Wetland Park. Nothing was known on the biology or life history of this species, except that it produced spectacular flowers between September and October. This orchid might have to be reclassified in the future as extinct. Suggested citation for this product: Combrink, A.S. and Kyle, R. 2006. A Handbook on the Rare, Threatened & Endemic Species of the Greater St Lucia Wetland Park. A product of the Greater St Lucia Wetland Park - Rare, Threatened & Endemic Species Project. Unpublished internal report. 191 pp. 3 TABLE OF CONTENTS 1 FOREWORD............................................................................................................................................ 6 2 INTRODUCTION .................................................................................................................................... 7 3 EXECUTIVE SUMMARY .....................................................................................................................