Package of Practices for Horticultural Crops of Assam, 2021
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346 Genus Spalgis Moore
AFROTROPICAL BUTTERFLIES 17th edition (2018). MARK C. WILLIAMS. http://www.lepsocafrica.org/?p=publications&s=atb Genus Spalgis Moore, 1879 Proceedings of the Zoological Society of London 1879: 137 (136-144). Type-species: Geridus epeus Westwood, by monotypy [extralimital]. The genus Spalgis belongs to the Family Lycaenidae Leach, 1815; Subfamily Miletinae Reuter, 1896; Tribe Spalgini Toxopeus, 1929. There is no other genus in the Tribe Spalgini in the Afrotropical Region. Spalgis (Harvesters) is a genus containing three Afrotropical and one Oriental species (the type species of the genus). None of the Afrotropical species has a distribution that extends extralimitally. Females oviposit among coccid prey. Oecophylla ants are thought to prevent egg-laying when they are attending coccids. Larvae live among colonies of prey which may be without ants or might be attended by a wide variety of different genera including Crematogaster, Oecophylla and Anaplocnemis. Larvae may actually enter Crematogaster nests to prey on intranidal coccids. Larvae are not apparently attended by ants and seem to be largely ignored by them. Usually larvae are covered with debris composed of the waxy secretions and the cuticles of prey that have become entangled in their setae. This covering apparently serves as a protection against ants since artificially denuded larvae are attacked when introduced into ant-tended colonies whereas larvae with their covering intact are not. A scarcity of larvae in Oecophylla attended coccid colonies is probably due to prevention of oviposition in the vicinity of these colonies. Larvae introduced into such colonies can survive and feed in them. The DNO and TOs are absent. -
Biology, Predatory Activity and Peoples'perceptions Towards Apefly
The Nelson Mandela AFrican Institution of Science and Technology NM-AIST Repository https://dspace.mm-aist.ac.tz Life sciences and Bio-engineering PhD Theses and Dissertations [LiSBE] 2020-05 Biology, predatory activity and peoples’perceptions towards apefly (spalgis spp.) in Tanzania Nasari, Sayuni P. https://dspace.nm-aist.ac.tz/handle/20.500.12479/927 Provided with love from The Nelson Mandela African Institution of Science and Technology BIOLOGY, PREDATORY ACTIVITY AND PEOPLES’ PERCEPTIONS TOWARDS APEFLY (Spalgis spp.) IN TANZANIA Sayuni P. Nasari A Dissertation Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Life Sciences of the Nelson Mandela African Institution of Science and Technology Arusha, Tanzania May, 2020 ABSTRACT In June 2017, farmers in central and northern Tanzania reported the occurrence of what they called an unusual insect with a human-like facial appearance that they referred to as “Kidudu-mtu.” The reports prompted the need to assess the identity and occurrence of the insect in Tanzania. This research was conducted between March and August 2018 in Iringa, Morogoro, Shinyanga, Geita and Arusha regions. A total of 89 people in the study regions were purposely interviewed to determine their knowledge, perceptions and reactions towards the insect. Insect samples were collected and submitted to the Tropical Pesticide Research Institute (TPRI) for preliminary identification and toxicity test. Molecular identification was done at the Nelson Mandela African Institution of Science and Technology (NM-AIST) laboratory. The insect’s predatory activity against the papaya mealybug (Paracoccus marginatus Williams and Granara de Willink) was assessed at Tanzania Agricultural Research Institute (TARI) Tengeru. -
Lycaenidae): Phylogeny, Ecology, and Conservation John Mathew Old Dominion University
Old Dominion University ODU Digital Commons Biological Sciences Theses & Dissertations Biological Sciences Summer 2003 Aphytophagy in the Miletinae (Lycaenidae): Phylogeny, Ecology, and Conservation John Mathew Old Dominion University Follow this and additional works at: https://digitalcommons.odu.edu/biology_etds Part of the Ecology and Evolutionary Biology Commons, Entomology Commons, and the Genetics Commons Recommended Citation Mathew, John. "Aphytophagy in the Miletinae (Lycaenidae): Phylogeny, Ecology, and Conservation" (2003). Doctor of Philosophy (PhD), dissertation, Biological Sciences, Old Dominion University, DOI: 10.25777/v7rh-mb21 https://digitalcommons.odu.edu/biology_etds/74 This Dissertation is brought to you for free and open access by the Biological Sciences at ODU Digital Commons. It has been accepted for inclusion in Biological Sciences Theses & Dissertations by an authorized administrator of ODU Digital Commons. For more information, please contact [email protected]. APHYTOPHAGY IN THE MILETINAE (LYCAENIDAE): PHYLOGENY, ECOLOGY, AND CONSERVATION by John Mathew B.Sc. June 1990, Madras Christian College M.Sc. June 1992, Madras Christian College M.Phil. May 1994, Madras University A Dissertation Submitted to the Faculty of Old Dominion University in Partial Fulfillment of the Requirement for the Degree of DOCTOR OF PHILOSOPHY ECOLOGICAL SCIENCES OLD DOMINION UNIVERSITY August 2003 Approved by: Deborah A. Waller (Co-Director) »mi E. Pierce (Co-Director) H. Savitzky (Member) Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. ABSTRACT APHYTOPHAGY IN THE MILETINAE (LYCAENIDAE): PHYTOGENY, ECOLOGY AND CONSERVATION John Mathew Old Dominion University, 2003 Co-Directors of Advisory Committee: Dr. Deborah A. Waller Dr. Naomi E. Pierce Less than 1% of all Lepidoptera are aphytophagous; of these, a considerable proportion is found in the family Lycaenidae. -
Bionomics of the African Apefly (Spalgis Lemolea)
sustainability Article Bionomics of the African Apefly (Spalgis lemolea) as A Potential Natural Enemy of the Papaya Mealybug (Paracoccus marginatus) in Tanzania Sayuni P. Nasari 1,*, Anna C. Treydte 1, Patrick A. Ndakidemi 1 and Ernest R. Mbega 1 Department of Sustainable Agriculture, Biodiversity and Ecosystems Management, Nelson Mandela African Institution of Science and Technology, Arusha P. O. Box 447, Tanzania * Correspondence: [email protected] Received: 20 February 2020; Accepted: 2 April 2020; Published: 14 April 2020 Abstract: The African apefly (Spalgis lemolea Druce) is a potential natural enemy of the papaya mealybug (Paracoccus marginatus Williams and Granara de Willink). We studied the life history of apeflies in the laboratory at a temperature of 25–27 ◦C and a relative humidity of 55%–65% under a 12 h photoperiod condition. The papaya mealybugs and apefly larvae were collected from papaya plants in Tengeru, Arusha, Tanzania. The papaya mealybugs were introduced and allowed to multiply on potted sprouting potato plants in screened cages. In order to study the life cycle and predation of apeflies, an apefly egg was placed on an open screen-covered petri dish containing a moist blotter paper and observed for larva emergence. After the apefly larva emergence, a mixture of mealybug eggs (up to 1500), nymphs (200–250) and adults (100–150) was introduced in the petri dish each day and the consumption rate by the apefly larvae was quantified until the larvae reached pupal stage. Then, the apefly adults were collected and put into cages 30 cm 30 cm 30 cm containing × × cotton wool soaked in water, for observation of pre-mating, mating, egg-laying and life span. -
Protective Devices of the Carnivorous Butterfly, Spalgis Epius (Westwood) (Lepidoptera: Lycaenidae)
SCIENTIFIC CORRESPONDENCE Protective devices of the carnivorous butterfly, Spalgis epius (Westwood) (Lepidoptera: Lycaenidae) The apefly, Spalgis epius is a rare butter- and hidden. Aitken6 described the larva leaf and pupates after firmly attaching on fly and an inhabitant of wooded areas. and pupa of S. epius. The larvae were its ventral side to the leaf. Usually most observers miss it due to its found feeding voraciously on the egg The length, width and height of the retiring nature, small size and rather drab masses, nymphs and adults of mealybugs. pupa are 5.0–6.1 mm (5.6 ± 0.44), 3.5– colour. The species is known to occur in As the young larvae of S. epius simulate 4.2 mm (3.90 ± 0.19) and 3.2–4.1 mm Sikkim, Kolkata, Malda, South India, mealybugs, it is difficult to recognize them (3.55 ± 0.32) respectively. The bold pat- Burma and Sri Lanka1–3. Lycaenids are amidst the host population. Similarly, the tern on the hard dorsal side of the pupa unique in their larval stage as they eat young larvae of S. lemolea (Holl.) in of S. epius resembles the face of a rhesus unrelated food, including flowering plants, Africa24 and S. substrigata (Snell) in Philip- monkey (Figure 2 b). The pupa shows fungi, lichens, cycads, ferns, conifers, ant pines25 are camouflaged with the mea- clear spots of eyes, nose, mouth, cheeks larvae and homopterans4,5. The larva of lybug population. The mature larva of and forehead on the dorsal side. S. epius S. epius has been recorded as a predator S. -
Uncovering Host-Microbiome Interactions In
F1000Research 2020, 9:1478 Last updated: 02 SEP 2021 SOFTWARE TOOL ARTICLE Uncovering host-microbiome interactions in global systems with collaborative programming: a novel approach integrating social and data sciences [version 1; peer review: 1 approved with reservations] Jenna Oberstaller1, Swamy Rakesh Adapa1, Guy W. Dayhoff II1, Justin Gibbons1, Thomas E. Keller1, Chang Li1, Jean Lim 1, Minh Pham 1, Anujit Sarkar1, Ravi Sharma1, Agaz H. Wani1, Andrea Vianello 1, Linh M. Duong1, Chenggi Wang1, Celine Grace F. Atkinson1, Madeleine Barrow1, Nathan W. Van Bibber1, Jan Dahrendorff1, David A. E. Dean1, Omkar Dokur1, Gloria C. Ferreira1, Mitchell Hastings1, Gregory S. Herbert 1, Khandaker Tasnim Huq1, Youngchul Kim1,2, Xiangyun Liao3, XiaoMing Liu1, Fahad Mansuri1, Lynn B. Martin1, Elizabeth M. Miller 1, Ojas Natarajan 1, Jinyong Pang1, Francesca Prieto1, Peter W. Radulovic1, Vyoma Sheth1, Matthew Sumpter 1, Desirae Sutherland1, Nisha Vijayakumar1, Rays H. Y. Jiang1 1University of South Florida, Tampa, FL, 33612, USA 2Moffit Cancer Center, Tampa, FL, 33612, USA 3Texas A&M, College Station, TX, USA v1 First published: 17 Dec 2020, 9:1478 Open Peer Review https://doi.org/10.12688/f1000research.26459.1 Latest published: 17 Dec 2020, 9:1478 https://doi.org/10.12688/f1000research.26459.1 Reviewer Status Invited Reviewers Abstract Microbiome data are undergoing exponential growth powered by 1 rapid technological advancement. As the scope and depth of microbiome research increases, cross-disciplinary research is urgently version 1 needed for interpreting and harnessing the unprecedented data 17 Dec 2020 report output. However, conventional research settings pose challenges to much-needed interdisciplinary research efforts due to barriers in 1. -
Bacterial Communities Within Phengaris (Maculinea) Alcon
Received: 26 November 2018 | Revised: 30 January 2019 | Accepted: 1 February 2019 DOI: 10.1002/ece3.5010 ORIGINAL RESEARCH Bacterial communities within Phengaris (Maculinea) alcon caterpillars are shifted following transition from solitary living to social parasitism of Myrmica ant colonies Mark A. Szenteczki1 | Camille Pitteloud1 | Luca P. Casacci2,3 | Lucie Kešnerová4 | Melissa R.L. Whitaker5 | Philipp Engel4 | Roger Vila6* | Nadir Alvarez1,7* 1Department of Ecology and Evolution, University of Lausanne, Lausanne, Switzerland 2Museum and Institute of Zoology, Polish Academy of Sciences, Warsaw, Poland 3Department of Life Sciences and Systems Biology, University of Turin, Turin, Italy 4Department of Fundamental Microbiology, University of Lausanne, Switzerland 5Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts 6Institut de Biologia Evolutiva (CSIC‐UPF), Barcelona, Spain 7Unit of Research and Collections, Museum of Natural History, Geneva, Switzerland Correspondence Mark A. Szenteczki, Laboratory of Functional Ecology, Institute of Biology, University of Neuchâtel, Neuchâtel, Switzerland. Email: [email protected] Nadir Alvarez, Unit of Research and Collection, Museum of Natural History, Geneva, Switzerland. Email: nadir.alvarez@ville‐ge.ch Present Address Camille Pitteloud, Department of Environmental Systems Sciences, Institute of Terrestrial Ecosystems, ETHZ, Zürich, Switzerland Funding information AEI/FEDER, UE, Grant/Award Number: Abstract CGL2016‐76322‐P; Université de Bacterial symbionts are known -
Lepidoptera: Lycaenidae) on Planococcus Citri (Risso) (Homoptera: Pseudococcidae)
J Pest Sci DOI 10.1007/s10340-010-0303-8 ORIGINAL PAPER Development, life history characteristics and behaviour of mealybug predator, Spalgis epius (Westwood) (Lepidoptera: Lycaenidae) on Planococcus citri (Risso) (Homoptera: Pseudococcidae) Anegunda S. Dinesh • Melally G. Venkatesha • Sompalyam Ramakrishna Received: 1 November 2009 / Accepted: 1 April 2010 Ó Springer-Verlag 2010 Abstract The development of immature stages, life his- Introduction tory and behaviour of mealybug predator, Spalgis epius (Westwood) (Lepidoptera: Lycaenidae) reared on mealy- More than 99% of Lepidoptera survive solely on living bugs, Planococcus citri (Risso) (Homoptera: Pseudococ- plants (Pierce 1995). Among the aphytophagous Lepidop- cidae) was studied in the laboratory. Larvae of S. epius are tera, about 120 species in the subfamily Miletinae (Lepi- a potential predator of different species of mealybugs in doptera: Lycaenidae) feed on ant brood or Hemiptera India. The predator completed its life cycle in 23.8 days (Pierce 1995). Most of the aphytophagous butterflies are with four larval instars. Mean incubation period of egg was extremely rare, and several are endangered (Pierce 1995; 3.9 days. Mean duration of development of larval stages, Wynhoff et al. 1998). The genera Spalgis Moore, Tharaka prepupa and pupa was 9.4, 0.9 and 9.5 days, respectively. Doherty and Feniseca Grote of Miletinae feed on ant-ten- The first and last instar larvae measured 1.9 and 11.4 mm ded Hemiptera (including Homoptera). These hemipteran- in length, respectively. Length and width were not signif- feeders live among their prey without provoking an escape icantly correlated in larvae. Head capsule width was not response or an attack response from the ant mutualists of significantly correlated with larval length in any instar. -
Westwood) in the Indian Himalaya
HALTERES, Volume 4, 53-58, 2013 ISSN 0973-1555 © CHARN KUMAR Status of the Genus Spalgis Moore with taxonomic notes on the type species, Spalgis epeus (Westwood) in the Indian Himalaya Charn Kumar A.S. College, Khanna, Samrala Road Khanna, Ludhiana, Punjab, India - 141401 (e-mail: [email protected]) Abstract As per the earlier records, genus Spalgis Moore is represented by two species viz., epeus Westwood and baiongus Cantlie and Norman in India, the latter one being very rare and restricted to Assam. During the repeated surveys undertaken in an ICAR, New Delhi sponsored project, only the type-species of this genus, Spalgis epeus (Westwood) has been reported from the Himalayan region in India. The diagnosis of the genus has been updated by inclusion of the characters of the male and the female genitalia. The survey work shows that the species is quite rare in the Himalaya. Keywords: Himalaya, male genitalia, female gentalia, Lycaenidae, Spalgis. Introduction From the Indian region, about 1438 Out of these, the former two species have species of butterflies have been been reported from India and according documented and out of these, more than to Cantlie and Norman (1960) and Cantlie 438 species belong to the family (1963), the species, baiongus restricted to Lycaenidae which makes about 30% of Assam is very rare one. Further, d' this total butterfly diversity (Evans, Abrera (loc. cit.), who advocated the 1932; Wynter-Blyth, 1957; Haribal, 1992; taxonomic revision of the other species Khoshoo, 1994 and Kehimkar, 2008). i.e., epeus Westwood has reported eight Owing to small size, less attractive subspecies viz., e. -
Arthropod Management in Vineyards
Arthropod Management in Vineyards Noubar J. Bostanian • Charles Vincent Rufus Isaacs Editors Arthropod Management in Vineyards: Pests, Approaches, and Future Directions Editors Dr. Noubar J. Bostanian Dr. Charles Vincent Agriculture and Agri-Food Canada Agriculture and Agri-Food Canada Horticultural Research and Horticultural Research and Development Center Development Center 430 Gouin Blvd. 430 Gouin Blvd. Saint-Jean-sur-Richelieu, QC, Canada Saint-Jean-sur-Richelieu, QC, Canada Dr. Rufus Isaacs Department of Entomology Michigan State University East Lansing, MI, USA ISBN 978-94-007-4031-0 ISBN 978-94-007-4032-7 (eBook) DOI 10.1007/978-94-007-4032-7 Springer Dordrecht Heidelberg New York London Library of Congress Control Number: 2012939840 © Springer Science+Business Media B.V. 2012 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifi cally the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfi lms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. Exempted from this legal reservation are brief excerpts in connection with reviews or scholarly analysis or material supplied specifi cally for the purpose of being entered and executed on a computer system, for exclusive use by the purchaser of the work. Duplication of this publication or parts thereof is permitted only under the provisions of the Copyright Law of the Publisher’s location, in its current version, and permission for use must always be obtained from Springer. -
Diversity of Butterflies
川 TTERFLIES PhilipJ. DeVries Center for BiodiversityStudies, Milwaukee PublicMuseum Overview of Butterfly Taxonomic Diversity BUTTERFLIES LIKELY REPRESENT the most familiar I1. Early Stages and Host Relationships and best known group of all insects. Within the II1. Butterfly-Ant Symbioses context of human society, butterflies serve as center ツ IV. Butterfly Mimicry and Diversity pieces in educational media, they are used extensively V. GeographicalPatterns of Butterfly Diversity in the arts, including nature and commercial advertis ツ V1. Butterfly Diversity and Habitat Destruction ing, and they are used as symbols for religious and social groups. Within the field of biology, studies on butterflies have been fundamental to the development GLOSSARY of biogeography, behavior, coevolution, conservation, development, ecological genetics, evolution,global warming, mimicry, ツ aposematic Describing an organism that is rendered population ecology, sexual selec tion, speciation, symbiotic associations, and systemat- less susceptible to predation by advertising its obvi ツ ics. In summary, butterflies have been important to ous unpalatability. Batesian mimicry A form of mimicry in which the how we perceive biodiversity. target organism is rendered less susceptible to preda ツ tion by its resemblancein morphologyor coloration to a different species that is unpalatable. 1.OVERVIEW OF BUTTERFLY cryptic Describing an organism that is concealed or TAXONOMICDIVERSITY obscured by the similarity of its appearance to the surrounding environment. Although butterflies may be the best known group of Mullenan mimicry A form of mimicry in which two insects, our understandingof their taxonomic diversity or more unpalatable species resemble each other, has two fundamentalweaknesses. The first regards the with the effect that predators are more likely to avoid recent declineof professional butterflytaxonomists and any species with this appearance. -
Lepidoptera: Lycaenidae)
ORIGINAL ARTICLE doi:10.1111/evo.12599 When caterpillars attack: Biogeography and life history evolution of the Miletinae (Lepidoptera: Lycaenidae) Zofia A. Kaliszewska,1,∗ David J. Lohman,1,2,3,4,∗ Kathrin Sommer,1,5 Glenn Adelson,1,6 Douglas B. Rand,1 John Mathew,1,7,8 Gerard Talavera,1,9,10 and Naomi E. Pierce1,11 1Department of Organismic and Evolutionary Biology and Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts 02138 2Biology Department, City College of New York, City University of New York, New York, New York 10031 3Graduate Center, City University of New York, New York, New York 10016 4Entomology Section, National Museum of the Philippines, Manila 1000, Philippines 5Institut fur¨ Pathologie, Bonner Forum Biomedizin, Universitats¨ Klinikum Bonn, 53127 Bonn, Germany 6Environmental Studies Program, Lake Forest College, Lake Forest, Illinois 60045 7Department of Biological Sciences, Old Dominion University, Norfolk, Virginia 23529 8Department of Humanities and Social Science, Indian Institute of Science Education and Research, Pune, Maharashtra 411 008, India 9Institut de Biologia Evolutiva (CSIC-UPF), Passeig Marıtim´ de la Barceloneta, 37-49, 08003 Barcelona, Spain 10Faculty of Biology & Soil Science, St. Petersburg State University, 199034 St. Petersburg, Russia 11E-mail: [email protected] Received May 10, 2011 Accepted December 18, 2014 Of the four most diverse insect orders, Lepidoptera contains remarkably few predatory and parasitic species. Although species with these habits have evolved multiple times in moths and butterflies, they have rarely been associated with diversification. The wholly aphytophagous subfamily Miletinae (Lycaenidae) is an exception, consisting of nearly 190 species distributed primarily throughout the Old World tropics and subtropics.