FUDMA Journal of Sciences (FJS) Vol. 4 No. 2, June, 2020, Pp 92 - 100 92 EFFECT of PHYSICO-CHEMICAL… Akpan, Et Al., FJS
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Comparative Analyses of Venoms from American and African Sicarius Spiders That Differ in Sphingomyelinase D Activity
This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository. Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Toxicon 55 (2010) 1274–1282 Contents lists available at ScienceDirect Toxicon journal homepage: www.elsevier.com/locate/toxicon Comparative analyses of venoms from American and African Sicarius spiders that differ in sphingomyelinase D activity Pamela A. Zobel-Thropp*, Melissa R. Bodner 1, Greta J. Binford Department of Biology, Lewis and Clark College, 0615 SW Palatine Hill Road, Portland, OR 97219, USA article info abstract Article history: Spider venoms are cocktails of toxic proteins and peptides, whose composition varies at Received 27 August 2009 many levels. Understanding patterns of variation in chemistry and bioactivity is funda- Received in revised form 14 January 2010 mental for understanding factors influencing variation. The venom toxin sphingomyeli- Accepted 27 January 2010 nase D (SMase D) in sicariid spider venom (Loxosceles and Sicarius) causes dermonecrotic Available online 8 February 2010 lesions in mammals. Multiple forms of venom-expressed genes with homology to SMase D are expressed in venoms of both genera. -
Evaluation of the Chemical Defense Fluids of Macrotermes Carbonarius
www.nature.com/scientificreports OPEN Evaluation of the chemical defense fuids of Macrotermes carbonarius and Globitermes sulphureus as possible household repellents and insecticides S. Appalasamy1,2*, M. H. Alia Diyana2, N. Arumugam2 & J. G. Boon3 The use of chemical insecticides has had many adverse efects. This study reports a novel perspective on the application of insect-based compounds to repel and eradicate other insects in a controlled environment. In this work, defense fuid was shown to be a repellent and insecticide against termites and cockroaches and was analyzed using gas chromatography-mass spectrometry (GC– MS). Globitermes sulphureus extract at 20 mg/ml showed the highest repellency for seven days against Macrotermes gilvus and for thirty days against Periplaneta americana. In terms of toxicity, G. sulphureus extract had a low LC50 compared to M. carbonarius extract against M. gilvus. Gas chromatography–mass spectrometry analysis of the M. carbonarius extract indicated the presence of six insecticidal and two repellent compounds in the extract, whereas the G. sulphureus extract contained fve insecticidal and three repellent compounds. The most obvious fnding was that G. sulphureus defense fuid had higher potential as a natural repellent and termiticide than the M. carbonarius extract. Both defense fuids can play a role as alternatives in the search for new, sustainable, natural repellents and termiticides. Our results demonstrate the potential use of termite defense fuid for pest management, providing repellent and insecticidal activities comparable to those of other green repellent and termiticidal commercial products. A termite infestation could be silent, but termites are known as destructive urban pests that cause structural damage by infesting wooden and timber structures, leading to economic loss. -
Arthropod Envenomation
Arthropod Envenomation Michael R. Loomis, DVM, MA, DACZM North Carolina Zoological Park Hymenoptera Envenomation Order Hymenoptera Family Vespidae- wasps Family Formicidae- ants Familt Mutillidae- velvet ants Family Apidae- bees • Stinger is a modified ovipositor Bee and Wasp Venom Components • Proteins, peptides and • Apitoxin – 52% Melitten (potent anti- amines inflammatory agent that – Phospholipase increases production of cortisol) – Histamine – 10-12% Phospholipase A2 – Bradykinin – 2-5% Aldolapin (blocks – cyclooxygenase) Acetylcholine – 1-3% Hyuronidase – Dopamine – 0.5-2% Histamine – Seratonin – 1-2% Dopamine and noradrenaline – Mast cell degranulating – 2% Protease-inhibitors peptide – Apamine increases cortisol – Mastoparan production, mild neurotoxin Ant Venom Components • Fire ants- 95% alkaloid (Unique among ants) • Most other ants, similar to bee and wasp venom • Harvester ant venom contains a hemolysin Venom Toxicity Family Common Name LD 50 (mg/kg) Apidae Honey bee 2.8 Mutillidae Velvet ant 71.0 Vespidae Paper wasp 2.4 Vespidae Yellowjacket 3.5 Formicidae Harvester ant 0.66 Formicidae Maricopa Harvester ant 0.12 Morbidity and Mortality Bees and Wasps • In US, 9.3 million ant • 17-56% produce local stings and 1 million reactions stings of other • Hymenoptera/year 1-2% produce generalized reactions • More deaths/year than any other type of • 5% seek medical care envenomation • 30-120 deaths from • Most deaths are the wasp and bee result of Anaphylaxis stings/year Local Reactions • Pain • Edema which may extend 10 cm from -
Pilbara Project Short-Range Endemic Invertebrate Fauna Survey
Short-Range Endemic Invertebrate Fauna Report: FerrAus Pilbara Project Prepared for FerrAus Ltd Final Report 5HY October 2010 Phoenix Environmental Sciences Pty Ltd 1 Short-range Endemic Invertebrate Fauna Survey Final Report FerrAus Pilbara Project FerrAus Ltd Short-range Endemic Invertebrate Fauna Survey 3URMHFW)HUU$XV3LOEDUD3URMHFW )LQDO5HSRUW5HY October 2010 Authors: Conor O’Neill and Jarrad Clark Reviewer: Melanie White Prepared for FerrAus Ltd Prepared by: Phoenix Environmental Sciences Pty Ltd © 2010 Phoenix Environmental Sciences Pty Ltd The information contained in this report is solely for the use of the Client for the purpose in which it has been prepared and Phoenix Environmental Sciences Pty Ltd accepts no responsibility for use beyond this purpose. Any person or organisation wishing to quote or reproduce any section of this report may only do so with the written permission of Phoenix Environmental Sciences Pty Ltd or FerrAus Ltd. Phoenix Environmental Sciences Pty Ltd 1/511 Wanneroo Road BALCATTA WA 6021 P: 08 9345 1608 F: 08 6313 0680 E: [email protected] Project code: 952-DC-FER-SRE Phoenix Environmental Sciences Pty Ltd i Short-range Endemic Invertebrate Fauna Survey Final Report FerrAus Pilbara Project FerrAus Ltd TABLE OF CONTENTS EXECUTIVE SUMMARY ................................................................................................................................... iv 1.0 INTRODUCTION ....................................................................................................................................... -
Intracolonial Demography of the Mound-Building Termite Macrotermes Natalensis (Haviland) (Isoptera, Termitidae) in the Northern Kruger National Park, South Africa
Insectes soc. 47 (2000) 390–397 0020-1812/00/040390-08 $ 1.50+0.20/0 Insectes Sociaux © Birkhäuser Verlag, Basel, 2000 Research article Intracolonial demography of the mound-building termite Macrotermes natalensis (Haviland) (Isoptera, Termitidae) in the northern Kruger National Park, South Africa V.W. Meyer 1, *, R.M. Crewe 1,L.E.O.Braack2, H.T. Groeneveld 3 and M.J. van der Linde 3 1 Department of Zoology and Entomology, University of Pretoria, Pretoria, 0002, South Africa, e-mail: [email protected]; [email protected] 2 Department of Conservation Development, Kruger National Park, Skukuza, 1350, South Africa, e-mail: [email protected] 3 Department of Statistics, University of Pretoria, Pretoria, 0002, South Africa, e-mail: [email protected]; [email protected] * Correspondence address: PO Box 1969, Wingate Park, 0153, South Africa Received 14 January 2000; revised 18 September 2000; accepted 26 September 2000. Summary. This paper reports on the number of individuals todeally (from the rectum). Secondly, termites have been in Macrotermes natalensis (Hav.) colonies of different sized shown to fix nitrogen (Curtis and Waller, 1998). If the nitro- mounds in the northern Kruger National Park. Mounds were gen fixation rate per individual termite is known, caste num- fully excavated, termites collected by means of vacuuming, bers and proportions provided by the present study can be and colony size estimated by sub-sampling. The proportion used to accurately derive overall nitrogen fixation, as rates of of termites in the mound (above and underground sections) fixation vary among species and castes via microbes and amounts to more than 70% of the colony; the rest being pre- fungi (e.g., Matsumoto and Abe, 1979; Collins, 1983). -
Complementary Symbiont Contributions to Plant Decomposition in a Fungus-Farming Termite
Complementary symbiont contributions to plant decomposition in a fungus-farming termite Michael Poulsena,1,2, Haofu Hub,1, Cai Lib,c, Zhensheng Chenb, Luohao Xub, Saria Otania, Sanne Nygaarda, Tania Nobred,3, Sylvia Klaubaufe, Philipp M. Schindlerf, Frank Hauserg, Hailin Panb, Zhikai Yangb, Anton S. M. Sonnenbergh, Z. Wilhelm de Beeri, Yong Zhangb, Michael J. Wingfieldi, Cornelis J. P. Grimmelikhuijzeng, Ronald P. de Vriese, Judith Korbf,4, Duur K. Aanend, Jun Wangb,j, Jacobus J. Boomsmaa, and Guojie Zhanga,b,2 aCentre for Social Evolution, Department of Biology, University of Copenhagen, DK-2100 Copenhagen, Denmark; bChina National Genebank, BGI-Shenzen, Shenzhen 518083, China; cCentre for GeoGenetics, Natural History Museum of Denmark, University of Copenhagen, DK-1350 Copenhagen, Denmark; dLaboratory of Genetics, Wageningen University, 6708 PB, Wageningen, The Netherlands; eFungal Biodiversity Centre, Centraalbureau voor Schimmelcultures, Royal Netherlands Academy of Arts and Sciences, NL-3584 CT, Utrecht, The Netherlands; fBehavioral Biology, Fachbereich Biology/Chemistry, University of Osnabrück, D-49076 Osnabrück, Germany; gCenter for Functional and Comparative Insect Genomics, Department of Biology, University of Copenhagen, DK-2100 Copenhagen, Denmark; hDepartment of Plant Breeding, Wageningen University and Research Centre, NL-6708 PB, Wageningen, The Netherlands; iDepartment of Microbiology, Forestry and Agricultural Biotechnology Institute, University of Pretoria, Pretoria SA-0083, South Africa; and jDepartment of Biology, University of Copenhagen, DK-2100 Copenhagen, Denmark Edited by Ian T. Baldwin, Max Planck Institute for Chemical Ecology, Jena, Germany, and approved August 15, 2014 (received for review October 24, 2013) Termites normally rely on gut symbionts to decompose organic levels-of-selection conflicts that need to be regulated (12). -
Spatial Distribution and Density of Termite Mounds in a Protected Habitat in the South of Cote D’Ivoire: Case of National Floristic Center (Cnf) of Ufhb of Abidjan
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by European Scientific Journal (European Scientific Institute) European Scientific Journal January 2015 edition vol.11, No.3 ISSN: 1857 – 7881 (Print) e - ISSN 1857- 7431 SPATIAL DISTRIBUTION AND DENSITY OF TERMITE MOUNDS IN A PROTECTED HABITAT IN THE SOUTH OF COTE D’IVOIRE: CASE OF NATIONAL FLORISTIC CENTER (CNF) OF UFHB OF ABIDJAN Boga Jean-Pierre, PhD Assistant-Prof. Akpesse Akpa Alexandre Moise, PhD Assistant-Prof. Ouali-N’goran San-Whouli Mauricette, PhD Associate-Prof. Laboratory of Zoology and Animal Biology, UFR-Biosciences, Félix Houphouët-Boigny University of Abidjan, Côte d’Ivoire Trabi Crolaud Sylvain, PhD Assistant Laboratory of Animal Biology, UFR of agroforestery, Jean-Lourougnon Guédé University of Daloa, Côte d'Ivoire Kouassi Kouassi Philippe, PhD Prof. Tano Yao, PhD Prof. Yapi Ahoua, PhD Associate-Prof. Laboratory of Zoology and Animal Biology, UFR-Biosciences, Félix Houphouët-Boigny University of Abidjan, Côte d’Ivoire Abstract The spatial distribution and termite mounds density and their activity were studies in order to assess to the biological restoration level in a protected area, knowing that termites are considered as tropical ecosystem engineers. The CNF area was subdivided into 4 sectors (SW, SE, NW and NE). In every sector of 1.75 ha, 20 transects (5 m x 100 m) were sampled. Termite nests were counted. Their dimensions and geographical coordinates were recorded. The superposition of spatial distribution maps of the 3 types of termite mounds showed an impressive abundance of termite mounds in all CNF area. In total, there were recorded 165 termite mounds. -
Telling Time with Termite Mounds: Termite Mound Declination, Azimuth, and Structure in Tarangire National Park
Telling Time with Termite Mounds: Termite mound declination, azimuth, and structure in Tarangire National Park Erin Frankson St. Olaf College Macrotermes michaelseni termites are found in savannah habitats throughout sub-Saharan Africa. Macrotermes michaelseni differ from other species of termites in that they construct chimney-shaped mounds in order to house their colonies (Turner 2001). These mounds are com- plex structures which utilize the sun as a tool for thermoregulation. By building their mounds at an angle, Macrotermes michaelseni are able to control air flow and regulate temperature within the inner chambers of their mounds. This study examined the zenith (heading on the hori- zon to which the mound points) and azimuth (the angle of tilt from ver- tical) of Macrotermes michaelseni termite mounds in Northern Tanza- nia. A total of 62 termite mounds were studied in and around Tarangi- re National Park during the month of October. Overall, the average zenith of Macrotermes michaelseni mounds was found to be 29.4 °, how- ever, average angle decreased as termite mound height increased. Of the 62 mounds studied, 59 faced northwest, with an average azimuth of 61.7 ° west of north. These results suggest that one can indeed use a termite mound in order to tell time. We tested this idea by constructing a sundial which mimicked the average angle and direction of the Ma- crotermes michaelseni termite mounds. We recorded the shadow cast by the mound for every hour of daylight and ultimately produced a chart which can be used to determine time using a Macrotermes michaelseni termite mound. Overall, termites provide vital ecosystem services for the surrounding environment. -
Termite Communities Along a Disturbance Gradient in a West African Savanna
insects Article Termite Communities along A Disturbance Gradient in a West African Savanna Janine Schyra 1,* and Judith Korb 1,2 1 Behavioral Biology, University of Osnabrueck, Barbarastr. 11, D-49076 Osnabrueck, Germany; [email protected] 2 Evolution and Ecology, Albert-Ludwigs-University Freiburg, Hauptstr. 1, D-79104 Freiburg im Breisgau, Germany * Correspondence: [email protected] Received: 23 November 2018; Accepted: 30 December 2018; Published: 8 January 2019 Abstract: (1) Background: Termites are important ecosystem engineers, crucial for the maintenance of tropical biodiversity and ecosystem functioning. But they are also pests which cause billions of dollars in damage annually to humans. Currently, our understanding of the mechanisms influencing species occurrences is limited and we do not know what distinguishes pest from non-pest species. (2) Method: We analyzed how anthropogenic disturbance (agriculture) affects species occurrences. We tested the hypothesis that strong disturbance functions as a habitat filter and selects for a subset of species which are major pests of crop. Using a cross-sectional approach, we studied termite assemblage composition along a disturbance gradient from fields to 12-year-old fallows in a West African savanna. (3) Results: We reliably identified 19 species using genetic markers with a mean of about 10 species—many of them from the same feeding type—co-occurring locally. Supporting our hypothesis, disturbance was associated with environmental filtering of termites from the regional species pool, maybe via its effect on vegetation type. The most heavily disturbed sites were characterized by a subset of termite species which are well-known pests of crop. -
Activity of Mound-Building Macrotermes Bellicosus
Animal Research International (2018) 15(1): 2918 – 2925 2918 ACTIVITY OF MOUND - BUILDING MACROTERMES BELLICOSUS (ISOPTERA: TERMITIDAE) AROUND KWARA STATE UNIVERSITY CAMPUS GUINEA SAVANNAH ECOZONE, NIGERIA 1 AJAO, Adeyemi Mufutau, 2 OLADIMEJI, Yusuf Usman, 1 OLADIPO, Segun Olayinka and 1 ADEPOJU, Suraju Adeshina 1 Department of Bioscience and Biotechnology, Kwara State University, Malete, Kwara State, Nigeria. 2 Department of Agricultural Economics and Rural Sociology, Ahmadu Bello University, PMB 1044 , Zaria, Kaduna State, Nigeria . Corresponding Author: Ajao, A. M. Department of Bioscience and Biotechnology, Kwara State University, Malete, Kwara State, Nigeria. Email : [email protected] Phone: +234 8035058904 ABSTRACT This study was designed to investigate Macrotermes bellicosus , nes ting mounds, abundance and activity in the savannah ecological zone of Kwara State, North - Central, Nigeria. The research was conducted at four randomly selected villages around and including Kwara S tate U niversity. A systematic survey of visible mounds of M. bellicosus was carried out over the entire study area. Also, the heights of mounds were measured using a measuring tape. M. bellicosus collection was conducted using bait ed traps consisting of cardboard, toilet tissue, wooden stakes and wood shaving . These were embedded or placed on ground within plots at a regular distance of 10 m and checked twice weekly. The samples collected per bait ed trap per plot per location were pre served in 90 % ethanol and identified. Similarly, survey of physically damaged items was conducted and recorded to observe termite activity. The result from the four diff erent locations of the study show ed that the number of M. -
Araneae: Mygalomorphae: Actinopodidae: Missulena) from the Pilbara Region, Western Australia
Zootaxa 3637 (5): 521–540 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3637.5.2 http://zoobank.org/urn:lsid:zoobank.org:pub:447D8DF5-F922-4B3A-AC43-A85225E56C57 New species of Mouse Spiders (Araneae: Mygalomorphae: Actinopodidae: Missulena) from the Pilbara region, Western Australia DANILO HARMS1, 2, 3, 4 & VOLKER W. FRAMENAU1, 2, 3 1 School of Animal Biology, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia. 2 Department of Terrestrial Zoology, Western Australian Museum, Locked Bag 49, Welshpool DC, Western Australia 6986, Australia. 3 Phoenix Environmental Sciences Pty Ltd, 1/511 Wanneroo Road, Balcatta, Western Australia 6021, Australia. 4 Corresponding author. E-mail: [email protected] Abstract Two new species of Mouse Spiders, genus Missulena, from the Pilbara region in Western Australia are described based on morphological features of males. Missulena faulderi sp. nov. and Missulena langlandsi sp. nov. are currently known from a small area in the southern Pilbara only. Mitochondrial cytochrome c oxidase subunit I (COI) sequence divergence failed in clearly delimiting species in Missulena, but provided a useful, independent line of evidence for taxonomic work in addition to morphology. Key words: taxonomy, systematics, barcoding, mitochondrial DNA, short-range endemism, Actinopus, Plesiolena Introduction The Actinopodidae Simon, 1892 is a small family of mygalomorph spiders with a Gondwanan distribution that includes three genera: Actinopus Perty, 1833 (27 species), Missulena Walckenaer, 1805 (11 species) and Plesiolena Goloboff & Platnick, 1987 (two species). Actinopus and Plesiolena are known only from South and Central America (Platnick 2012). -
Australian Funnel-Web Spiders Evolved Human-Lethal Δ-Hexatoxins for Defense Against Vertebrate Predators
Australian funnel-web spiders evolved human-lethal δ-hexatoxins for defense against vertebrate predators Volker Herziga,b,1,2, Kartik Sunagarc,1, David T. R. Wilsond,1, Sandy S. Pinedaa,e,1, Mathilde R. Israela, Sebastien Dutertref, Brianna Sollod McFarlandg, Eivind A. B. Undheima,h,i, Wayne C. Hodgsonj, Paul F. Alewooda, Richard J. Lewisa, Frank Bosmansk, Irina Vettera,l, Glenn F. Kinga,2, and Bryan G. Frym,2 aInstitute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia; bGeneCology Research Centre, School of Science and Engineering, University of the Sunshine Coast, Sippy Downs, QLD 4556, Australia; cEvolutionary Venomics Lab, Centre for Ecological Sciences, Indian Institute of Science, Bangalore 560012, India; dCentre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Smithfield, QLD 4878, Australia; eBrain and Mind Centre, University of Sydney, Camperdown, NSW 2052, Australia; fInstitut des Biomolécules Max Mousseron, UMR 5247, Université Montpellier, CNRS, 34095 Montpellier Cedex 5, France; gSollod Scientific Analysis, Timnath, CO 80547; hCentre for Advanced Imaging, The University of Queensland, St Lucia, QLD 4072, Australia; iCentre for Ecology and Evolutionary Synthesis, Department of Biosciences, University of Oslo, 0316 Oslo, Norway; jMonash Venom Group, Department of Pharmacology, Monash University, Clayton, VIC 3800, Australia; kBasic and Applied Medical Sciences Department, Faculty of Medicine, Ghent University, 9000 Ghent, Belgium; lSchool