Identifying the State of Knowledge: Farmer’S Knowledge in Kenya Rachel Kagoiya
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Review of the Potential for Biological Control of Wild Radish (Raphanus Raphanistrum) Based on Surveys in the Mediterranean Region
Thirteenth Australian Weeds Conference Review of the potential for biological control of wild radish (Raphanus raphanistrum) based on surveys in the Mediterranean region John K. Scott1,2,3, Janine Vitou2 and Mireille Jourdan2 1 Cooperative Research Centre for Australian Weed Management 2 CSIRO European Laboratory, Campus International de Baillarguet, 34980 Montferrier sur Lez, France 3 Present Address: CSIRO Entomology, Private Bag 5, PO Wembley, Western Australia 6913, Australia Summary Wild radish (Raphanus raphanistrum) BIOLOGICAL CONTROL STRATEGY (Brassicaceae) is one of southern Australia’s worst Classical biological control of wild radish is a diffi cult weeds of cropping. The potential for biological objective. In the sections below are summarised the control of this weed in Australia is being investigated main issues, which are mainly to do with the safety of in the weed’s original distribution, southern Europe biological control because of the shared evolution be- and the circum-Mediterranean region. Surveys for tween wild radish and some important crop species. insects and pathogens have been made throughout the Mediterranean region, concentrating on southern Genetics and evolution of Raphanus Wild radish Portugal, northern Tunisia, the Mediterranean coast relatives in the family Brassicaceae comprises about of France, and southern Greece. While many of 13 tribes, 375 genera and 3200 species (Hewson the organisms found are specialists on the family 1982, Schulz 1936). The genus Raphanus is included Brassicaceae, most of these are not suffi ciently host in the tribe Brassiceae, which is regarded as a natural specifi c to exclude the risk to canola (Brassica napus), grouping. Within the Brassiceae, most phylogenetic the most important crop related to wild radish. -
Pest Management of Small Grains—Weeds
PUBLICATION 8172 SMALL GRAIN PRODUCTION MANUAL PART 9 Pest Management of Small Grains—Weeds MICK CANEVARI, University of California Cooperative Extension Farm Advisor, San Joaquin County; STEVE ORLOFF, University of California Cooperative Extension Farm Advisor, Siskiyou County; RoN VARGAS, University of California Cooperative Extension Farm Advisor, UNIVERSITY OF Madera County; STEVE WRIGHT, University of California Cooperative Extension Farm CALIFORNIA Advisor, Tulare County; RoB WILsoN, University of California Cooperative Extension Farm Division of Agriculture Advisor, Lassen County; DAVE CUDNEY, Extension Weed Scientist Emeritus, Botany and and Natural Resources Plant Sciences, University of California, Riverside; and LEE JACKsoN, Extension Specialist, http://anrcatalog.ucdavis.edu Small Grains, Department of Plant Sciences, University of California, Davis This publication, Pest Management of Small Grains—Weeds, is the ninth in a fourteen- part series of University of California Cooperative Extension online publications that comprise the Small Grain Production Manual. The other parts cover specific aspects of small grain production practices in California: • Part 1: Importance of Small Grain Crops in California Agriculture, Publication 8164 • Part 2: Growth and Development, Publication 8165 • Part 3: Seedbed Preparation, Sowing, and Residue Management, Publication 8166 • Part 4: Fertilization, Publication 8167 • Part 5: Irrigation and Water Relations, Publication 8168 • Part 6: Pest Management—Diseases, Publication 8169 • Part 7: -
Taxonomic Revision of the Afrotropical Hover Fly Genus Senaspis Macquart (Diptera, Syrphidae)
ZooKeys 1003: 83–160 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.1003.56557 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research Taxonomic revision of the Afrotropical hover fly genus Senaspis Macquart (Diptera, Syrphidae) Marc De Meyer1, Georg Goergen2, Kurt Jordaens1 1 Royal Museum for Central Africa, Invertebrates Section and JEMU, Leuvensesteenweg 13, B3080 Tervuren, Belgium 2 International Institute of Tropical Agriculture, Biodiversity Centre, 08 BP 0932 Tri Postal, Cotonou, Benin Corresponding author: Marc De Meyer ([email protected]) Academic editor: X. Mengual | Received 15 July 2020 | Accepted 20 October 2020 | Published 14 December 2020 http://zoobank.org/5D883EC6-5306-4AC3-A0D7-8CA867324596 Citation: De Meyer M, Goergen G, Jordaens K (2020) Taxonomic revision of the Afrotropical hover fly genus Senaspis Macquart (Diptera, Syrphidae). ZooKeys 1003: 83–160. https://doi.org/10.3897/zookeys.1003.56557 Abstract The representatives of the Afrotropical hover fly genus Senaspis Macquart (Diptera) are revised. In total, ten species are recognized. Senaspis apophysata (Bezzi) is herewith placed as junior synonym of S. flaviceps Macquart, S. livida (Bezzi) is herewith placed as junior synonym of S. dentipes (Macquart) and S. griseifaci- es (Bezzi) is herewith placed as junior synonym of S. haemorrhoa (Gerstaecker). All species are redescribed and an identification key is provided. DNA barcoding analysis (7 species, 64 barcodes) showed that the technique can be used to unambiguously identify the species. The relationships among the different Se- naspis species are discussed based on morphological and DNA data. Keywords Africa, DNA barcoding, Eristalinae, flower fly Copyright Marc De Meyer et al. -
SPECIES COMPOSITION and POLLINATOR EFFICIENCY of Ocimum Kilimandscharicum FLOWER VISITORS ALONG KAKAMEGA FOREST ECOSYSTEM
SPECIES COMPOSITION AND POLLINATOR EFFICIENCY OF Ocimum Kilimandscharicum FLOWER VISITORS ALONG KAKAMEGA FOREST ECOSYSTEM BY HELLEN MANDELA KUTWA A Research Thesis Submitted in Partial Fulfillment of the Requirements for the Award of the Degree of Masters of Science in Environmental Biology, School of Biological and Physical Sciences MOI UNIVERSITY ELDORET 2017 2 ECLARATION 3 DEDICATION I dedicate this work to my parents who have supported me throughout, Dr Amos Kutwa and Mrs. Phillisters Kutwa. To my siblings Alice, Erastus and Fred I hope this serves as a source of inspiration and reassurance that hard work and persistence pays out. My grandparents Alice, Hellen and Silvanas for their prayers and encouragement. 4 ACKNOWLEDGEMENT I am grateful to Professor Mugatsia Tsingalia for having accepted to be my University supervisor and providing me with high quality assistance and guidance. You have been a source of motivation from the beginning and I truly appreciate your patience especially when I had no sense of direction and you guided me and molded me into a better researcher. I am thankful as you have always been that academic lighthouse for me. I also recognize the Moi University fraternity especially School of Biological and Physical science for seeing potential in me and accepting my postgraduate application. I am also greatly indebted to Professor Mary Gikungu. You have always been encouraging from the beginning setting a fine example for me as a strong independent woman. You helped instill in me the importance of being resilient and humble no matter what you have achieved. You encouraged me even when I was about to give up, taking your time to go through my drafts and giving critical and up building comments. -
Hymenoptera, Apidae)
A peer-reviewed open-access journal ZooKeys 428: 29–40A new (2014) species of the cleptoparasitic bee genus Thyreus from northern Yemen... 29 doi: 10.3897/zookeys.428.7821 RESEARCH ARTICLE www.zookeys.org Launched to accelerate biodiversity research A new species of the cleptoparasitic bee genus Thyreus from northern Yemen and southwestern Saudi Arabia (Hymenoptera, Apidae) Abdulaziz S. Alqarni1, Mohammed A. Hannan1,2, Michael S. Engel3 1 Department of Plant Protection, College of Food and Agriculture Sciences, King Saud University, P.O. Box 2460, Riyadh 11451, Kingdom of Saudi Arabia 2 Current address: 60-125 Cole Road, Guelph, Ontario N1G 4S8, Canada 3 Division of Entomology, Natural History Museum, and Department of Ecology & Evolutionary Biology, 1501 Crestline Drive – Suite 140, University of Kansas, Lawrence, Kansas 66045, USA Corresponding author: Abdulaziz S. Alqarni ([email protected]) Academic editor: Michael Ohl | Received 30 April 2014 | Accepted 3 July 2014 | Published 23 July 2014 http://zoobank.org/151D6C5F-F54A-45EF-95C5-D89C301EDE10 Citation: Alqarni AS, Hannan MA, Engel MS (2014) A new species of the cleptoparasitic bee genus Thyreus from northern Yemen and southwestern Saudi Arabia (Hymenoptera, Apidae). ZooKeys 428: 29–40. doi: 10.3897/zookeys.428.7821 Abstract A new species of cleptoparasitic bee of the genus Thyreus Panzer (Apinae: Melectini) is described and figured from northern Yemen and southwestern Saudi Arabia. Thyreus shebicus Engel, sp. n. is a relatively small species superficially similar to the widespread and polytypic species T. ramosus (Lepeletier de Saint Fargeau) and T. ramosellus (Cockerell) but more closely allied to various African forms on the basis of the male genitalia. -
Pollination of Cultivated Plants in the Tropics 111 Rrun.-Co Lcfcnow!Cdgmencle
ISSN 1010-1365 0 AGRICULTURAL Pollination of SERVICES cultivated plants BUL IN in the tropics 118 Food and Agriculture Organization of the United Nations FAO 6-lina AGRICULTUTZ4U. ionof SERNES cultivated plans in tetropics Edited by David W. Roubik Smithsonian Tropical Research Institute Balboa, Panama Food and Agriculture Organization of the United Nations F'Ø Rome, 1995 The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. M-11 ISBN 92-5-103659-4 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying or otherwise, without the prior permission of the copyright owner. Applications for such permission, with a statement of the purpose and extent of the reproduction, should be addressed to the Director, Publications Division, Food and Agriculture Organization of the United Nations, Viale delle Terme di Caracalla, 00100 Rome, Italy. FAO 1995 PlELi. uion are ted PlauAr David W. Roubilli (edita Footli-anal ISgt-iieulture Organization of the Untled Nations Contributors Marco Accorti Makhdzir Mardan Istituto Sperimentale per la Zoologia Agraria Universiti Pertanian Malaysia Cascine del Ricci° Malaysian Bee Research Development Team 50125 Firenze, Italy 43400 Serdang, Selangor, Malaysia Stephen L. Buchmann John K. S. Mbaya United States Department of Agriculture National Beekeeping Station Carl Hayden Bee Research Center P. -
Fish, Various Invertebrates
Zambezi Basin Wetlands Volume II : Chapters 7 - 11 - Contents i Back to links page CONTENTS VOLUME II Technical Reviews Page CHAPTER 7 : FRESHWATER FISHES .............................. 393 7.1 Introduction .................................................................... 393 7.2 The origin and zoogeography of Zambezian fishes ....... 393 7.3 Ichthyological regions of the Zambezi .......................... 404 7.4 Threats to biodiversity ................................................... 416 7.5 Wetlands of special interest .......................................... 432 7.6 Conservation and future directions ............................... 440 7.7 References ..................................................................... 443 TABLE 7.2: The fishes of the Zambezi River system .............. 449 APPENDIX 7.1 : Zambezi Delta Survey .................................. 461 CHAPTER 8 : FRESHWATER MOLLUSCS ................... 487 8.1 Introduction ................................................................. 487 8.2 Literature review ......................................................... 488 8.3 The Zambezi River basin ............................................ 489 8.4 The Molluscan fauna .................................................. 491 8.5 Biogeography ............................................................... 508 8.6 Biomphalaria, Bulinis and Schistosomiasis ................ 515 8.7 Conservation ................................................................ 516 8.8 Further investigations ................................................. -
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. -
Hoverflies of Assam (Diptera: Syrphidae): New JEZS 2019; 7(4): 965-969 © 2019 JEZS Records and Their Diversity Received: 10-05-2019 Accepted: 12-06-2019
Journal of Entomology and Zoology Studies 2019; 7(4): 965-969 E-ISSN: 2320-7078 P-ISSN: 2349-6800 Hoverflies of Assam (Diptera: Syrphidae): New JEZS 2019; 7(4): 965-969 © 2019 JEZS records and their diversity Received: 10-05-2019 Accepted: 12-06-2019 Rojeet Thangjam Rojeet Thangjam, Veronica Kadam, Kennedy Ningthoujam and Mareena College of Agriculture, Central Sorokhaibam Agricultural University, Kyrdemkulai, Meghalaya, India Abstract Veronica Kadam Hoverflies, generally known as Syrphid flies belongs to family Syrphidae, which is one of the largest College of Post Graduate Studies families of order Diptera. The adults use to feed on nectar and pollen of many flowering plants and larval in Agricultural Sciences, Umiam stages of some species are predaceous to homopteran insects. The objective of the present investigation (CAU-Imphal) Meghalaya, India was focused on the assessment of the diversity and abundance of hoverfly at Assam Agricultural University, Jorhat, Assam during 2015-16. A total of 225 individual hoverflies were recorded during the Kennedy Ningthoujam study out of which 23 species belonging to 16 genera under 2 sub-families viz., Eristalinae and Syrphinae College of Post Graduate Studies were observed. Among them, ten species viz., Eristalinus tristriatus, Eristalis tenax, Eristalodes paria, in Agricultural Sciences, Umiam (CAU-Imphal) Meghalaya, India Lathyrophthalmus arvorum, Lathyrophthalmus megacephalus, Lathyrophthalmus obliquus, Phytomia errans, Pandasyopthalmus rufocinctus, Metasyrphus bucculatus and Sphaerophoria macrogaster were Mareena Sorokhaibam newly recorded from Assam. Among the species, Episyrphus viridaureus and Lathyrophthalmus College of Agriculture, Central arvorum were found to be the most abundant species with the relative abundance of 16.89 and 10.22% Agricultural University, Imphal, respectively. -
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 -
Lepidoptera Fauna of Namibia. I. Seasonal Distribution of Moths of the Koakoland (Mopane) Savanna in Ogongo, Northern Namibia
FRAGMENTA FAUNISTICA 57 (2): 117–129, 2014 PL ISSN 0015-9301 © MUSEUM AND INSTITUTE OF ZOOLOGY PAS DOI 10.3161/00159301FF2014.57.2.117 Lepidoptera fauna of Namibia. I. Seasonal distribution of moths of the Koakoland (Mopane) Savanna in Ogongo, northern Namibia Grzegorz KOPIJ Department of Wildlife Management, University of Namibia, Katima Mulilio Campus, Private Bag 1096, Katima Mulilo, Namibia; e-mail: [email protected] Abstract: During the years 2011–2013, moths were collected in Koakoland (Mopane) Savanna in the Cuvelai Drainage System, Ovamboland, northern Namibia. In total, 77 species from 13 families have been identified. Their seasonal occurrence in this habitat was also investigated, with most species recorded in wet season between September and April, but with clear peak in February and March. The family Noctuidae was by far the most speciose (38 recorded species), followed by Crambidae (8 spp.), Sphingidae (6 spp.) and Arctiidae (4 spp.). All other families were represented by 1–3 species. For each species listed date of collection is given, and data on its global distribution. Key words: Lepidoptera, check-list, biodiversity, distribution, moths, Ovamboland INTRODUCTION According to recent quite precise estimate, there are 15 5181 species, 16 650 genera and 121 families of Lepidoptera worldwide (Pouge 2009). Lepidoptera fauna of Namibia has recently attracted attention of European entomologists. However, thorough surveys were conducted hitherto in a few areas only, such as Brandberg and Hobatere. The northern regions of the country were especially badly neglected. In southern Africa (south of Zambezi and Kunene Rivers) – 8 511 species, 2 368 genera and 89 families were recently catalogued (Vári et al. -
Apocynaceae: Asclepiadoideae) ⁎ A
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Available online at www.sciencedirect.com South African Journal of Botany 75 (2009) 689–698 www.elsevier.com/locate/sajb New records of insect pollinators for South African asclepiads (Apocynaceae: Asclepiadoideae) ⁎ A. Shuttleworth, S.D. Johnson School of Biological and Conservation Sciences, University of KwaZulu-Natal Pietermaritzburg, Private Bag X01, Scottsville 3209, South Africa Received 1 April 2009; received in revised form 21 July 2009; accepted 27 July 2009 Abstract Studies of pollination in southern African asclepiads (aside from the stapeliads and members of the genus Ceropegia) are remarkably scarce given the diversity of asclepiad species in the region. In this study, we report new observations of insect flower visitors and their pollen loads for 15 species of South African asclepiads in the genera Asclepias, Aspidoglossum, Miraglossum, Pachycarpus, Periglossum, Woodia and Xysmalobium. Nectar properties are also presented for some species. Four specialized pollination systems are suggested by these observations: (1) pollination by wasps in the genus Hemipepsis (Hymenoptera: Pompilidae) in eight species, (2) pollination by chafer beetles (Scarabaeidae: Cetoniinae) in three species, (3) pollination by honeybees, Apis mellifera (Hymenoptera: Apidae) in two species, and (4) pollination by flies from various families in one species. The pollination system of Asclepias crispa remains unclear but appears to be one of generalized insect pollination. Future research is likely to confirm the preponderance of specialized pollination systems within this group of plants in southern Africa. © 2009 SAAB. Published by Elsevier B.V. All rights reserved.