COPTOTERMES ACINACIFORMIS (Froggatt) COPTOTERMES
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Isoptera Book Chapter
Isoptera 535 See Also the Following Articles Biodiversity ■ Biogeographical Patterns ■ Cave Insects ■ Introduced Insects Further Reading Carlquist , S. ( 1974 ) . “ Island Biology . ” Columbia University Press , New York and London . Gillespie , R. G. , and Roderick , G. K. ( 2002 ) . Arthropods on islands: Colonization, speciation, and conservation . Annu. Rev. Entomol. 47 , 595 – 632 . Gillespie , R. G. , and Clague , D. A. (eds.) (2009 ) . “ Encyclopedia of Islands. ” University of California Press , Berkeley, CA . Howarth , F. G. , and Mull , W. P. ( 1992 ) . “ Hawaiian Insects and Their Kin . ” University of Hawaii Press , Honolulu, HI . MacArthur , R. H. , and Wilson , E. O. ( 1967 ) . “ The Theory of Island Biogeography . ” Princeton University Press , Princeton, NJ . Wagner , W. L. , and Funk , V. (eds.) ( 1995 ) . “ Hawaiian Biogeography Evolution on a Hot Spot Archipelago. ” Smithsonian Institution Press , Washington, DC . Whittaker , R. J. , and Fern á ndez-Palacios , J. M. ( 2007 ) . “ Island Biogeography: Ecology, Evolution, and Conservation , ” 2nd ed. Oxford University Press , Oxford, U.K . I Isoptera (Termites) Vernard R. Lewis FIGURE 1 Castes for Isoptera. A lower termite group, University of California, Berkeley Reticulitermes, is represented. A large queen is depicted in the center. A king is to the left of the queen. A worker and soldier are he ordinal name Isoptera is of Greek origin and refers to below. (Adapted, with permission from Aventis Environmental the two pairs of straight and very similar wings that termites Science, from The Mallis Handbook of Pest Control, 1997.) Thave as reproductive adults. Termites are small and white to tan or sometimes black. They are sometimes called “ white ants ” and can be confused with true ants (Hymenoptera). -
Haviland's Subterranean Termite, Coptotermes Havilandi Holmgren (Insecta: Isoptera: Rhinotermitidae)1
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. EENY-128 Haviland's Subterranean Termite, Coptotermes havilandi Holmgren (Insecta: Isoptera: Rhinotermitidae)1 Rudolf H. Scheffrahn and Nan-Yao Su2 Introduction Barbuda, Cuba, Grand Turk, Guadeloupe, Little Cayman, Montserrat, Nevis, Providenciales, Puerto Coptotermes havilandi is a very damaging Rico (San Juan), and St. Kitts. It has also been termite and a threat to wooden structures wherever it collected in southern Mexico and possibly occurs on occurs. As one might expect, Coptotermes havilandi Jamaica and Virgin Gorda, B.V.I. is similar in many respects to C. formosanus Shiraki, the Formosan subterranean termite. General In 1996, C. havilandi was collected for the first information related to the life history, damage, and time in the continental United States from a storefront management of C. formosanus is applicable to C. and a church in Miami, Florida. In 1999, a colony of havilandi and can be obtained from our sister C. havilandi was discovered infesting a waterfront publication on C. formosanus. This report highlights house in Key West, Florida. Dade County, Florida, is important distinguishing characteristics of C. the only known locality where C. formosanus and C. havilandi. havilandi have both become established. In 2000, three additional homes in another neighborhood of Distribution Key West were found to be infested with C. havilandi. Elsewhere in the world, these two widely Coptotermes havilandi is endemic to Southeast introduced species are geographically isolated. Asia. Over the last century, human activity has spread Coptotermes formosanus usually invades mildly this termite far beyond its native range. -
Coptotermes Gestroi (WASMANN) (BLATTODEA: RHINOTERMITIDAE)
MOLECULAR SYSTEMATICS OF SUBTERRANEAN TERMITES COPTOTERMES SPP., MICROSATELLITE DEVELOPMENT AND POPULATION GENETICS OF Coptotermes gestroi (WASMANN) (BLATTODEA: RHINOTERMITIDAE) YEAP BENG KEOK UNIVERSITI SAINS MALAYSIA 2010 MOLECULAR SYSTEMATICS OF SUBTERRANEAN TERMITES COPTOTERMES SPP., MICROSATELLITE DEVELOPMENT AND POPULATION GENETICS OF Coptotermes gestroi (WASMANN) (BLATTODEA: RHINOTERMITIDAE) BY YEAP BENG KEOK Thesis submitted in fulfillment of the requirements for the degree of Doctor of Philosophy March 2010 ACKNOWLEDGEMENTS This work would not have been completed without the generosity, support, and encouragement of many people. Utmost thanks must extend to my mentors, Professor Dr. Lee Chow Yang and Associate Professor Dr. Ahmad Sofiman Othman. Prof. Lee, my main supervisor, constantly guided and lifted me with his wisdom. He introduced me to termites and gave me a lot of encouragement by providing me many opportunities to attend seminars and conferences throughout Asia countries. He has continued to support and promote my work tirelessly and widen my vision in this ground. Dr. Sofiman, my co-supervisor, gave me a very friendly and valuable advices and guidance, supported me to many useful workshops, and provided a well-equipped laboratory for my molecular study. I extend my sincerest gratitude to Professor Abu Hassan, for being the ever helpful and generous Dean of School of Biological Sciences. To Dr. Zairi Jaal, thank you for being the very supportive, cheerful and bighearted coordinator of Vector Control Research Unit. To Dr. Siti Azizah, for her support and always put a lot of effort organizing very informative workshops. To all staff of School of Biological Sciences and VCRU who have help me in one way and another, thank you for your assistance throughout my research. -
Morphometric Analysis of Coptotermes Spp. Soldier Caste (Blattodea: Rhinotermitidae) in Indonesia and Evidence of Coptotermes Gestroi Extreme Head-Capsule Shapes
insects Article Morphometric Analysis of Coptotermes spp. Soldier Caste (Blattodea: Rhinotermitidae) in Indonesia and Evidence of Coptotermes gestroi Extreme Head-Capsule Shapes Bramantyo Wikantyoso 1,2,*, Shu-Ping Tseng 3, Setiawan Khoirul Himmi 2 , Sulaeman Yusuf 2 and Tsuyoshi Yoshimura 1 1 Research Institute for Sustainable Humanosphere (RISH), Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan; [email protected] 2 Research Center for Biomaterials, Indonesian Institute of Sciences (LIPI) Jl. Raya Bogor km 46 Cibinong, Bogor 16911, Indonesia; [email protected] (S.K.H.); [email protected] (S.Y.) 3 Department of Entomology, University of California, 900 University Avenue, Riverside, CA 92521, USA; [email protected] * Correspondence: [email protected] Simple Summary: The morphological characteristics of the soldier caste in termites provide valuable taxonomic information at the species level. Head-shape variation in soldiers was often used as an indicative characteristic in some genera. While species with egg-shaped and waterdrop-shaped head capsule (HC), Coptotermes gestroi and C. curvignathus, respectively, are familiar in Indonesia, neither a measurement nor head index may avoid the subjectivity of shape interpretation. We conducted linear Citation: Wikantyoso, B.; Tseng, S.-P.; and geometric morphometrics analyses of soldiers’ HC of Coptotermes spp. obtained from various Himmi, S.K.; Yusuf, S.; Yoshimura, T. locations in Indonesia. Although subtle differences were observed, the posterior parts of the HC Morphometric Analysis of laterally expanded in a gradual manner in C. gestroi, C. sepangensis, and C. curvignathus in that order. Coptotermes spp. Soldier Caste Furthermore, three extreme head-shape variations of C. -
Catalogue of Protozoan Parasites Recorded in Australia Peter J. O
1 CATALOGUE OF PROTOZOAN PARASITES RECORDED IN AUSTRALIA PETER J. O’DONOGHUE & ROBERT D. ADLARD O’Donoghue, P.J. & Adlard, R.D. 2000 02 29: Catalogue of protozoan parasites recorded in Australia. Memoirs of the Queensland Museum 45(1):1-164. Brisbane. ISSN 0079-8835. Published reports of protozoan species from Australian animals have been compiled into a host- parasite checklist, a parasite-host checklist and a cross-referenced bibliography. Protozoa listed include parasites, commensals and symbionts but free-living species have been excluded. Over 590 protozoan species are listed including amoebae, flagellates, ciliates and ‘sporozoa’ (the latter comprising apicomplexans, microsporans, myxozoans, haplosporidians and paramyxeans). Organisms are recorded in association with some 520 hosts including mammals, marsupials, birds, reptiles, amphibians, fish and invertebrates. Information has been abstracted from over 1,270 scientific publications predating 1999 and all records include taxonomic authorities, synonyms, common names, sites of infection within hosts and geographic locations. Protozoa, parasite checklist, host checklist, bibliography, Australia. Peter J. O’Donoghue, Department of Microbiology and Parasitology, The University of Queensland, St Lucia 4072, Australia; Robert D. Adlard, Protozoa Section, Queensland Museum, PO Box 3300, South Brisbane 4101, Australia; 31 January 2000. CONTENTS the literature for reports relevant to contemporary studies. Such problems could be avoided if all previous HOST-PARASITE CHECKLIST 5 records were consolidated into a single database. Most Mammals 5 researchers currently avail themselves of various Reptiles 21 electronic database and abstracting services but none Amphibians 26 include literature published earlier than 1985 and not all Birds 34 journal titles are covered in their databases. Fish 44 Invertebrates 54 Several catalogues of parasites in Australian PARASITE-HOST CHECKLIST 63 hosts have previously been published. -
Formosan Subterranean Termite
Formosan subterranean termite By Sylvia Kenmuir Photograph with Permission from: National Pest Management Association Common Name: Formosan subterranean termite Scientific name: Coptotermes formosanus. The Formosan subterranean termite is in the order Blattodea and in the family Rhinotermitidae. Identifying Characteristics: Formosan termites are a subterranean termite with an incomplete metamorphosis. There are three distinctive castes or body forms which include workers, soldiers and reproductives (king, queen and alates). The workers are the most numerous, having a small whitish beige soft body and are not useful in identification. Alates resemble worker termites but are winged and soldiers have an orange-brown oval shaped head, curved mandibles and a whitish body. Both alates and soldiers are useful in identification. Host range: Taiwan, southern China, and Japan. In the US they were discovered in Hawaii in the late 1800’s and spread through the southeast from 1960 through the 1980’s. Description of Damage: Formosan termites have the largest colony size. One colony may contain several million termites whose tunnels can extend up to 300 ft across. Because of these two factors any structures in their path can be threatened. Life History: Coptotermes formosanus can produce 70,000 alates. After mating, the males and females shed their wings and search for a nesting site. After finding a suitable site with wood, the female lays a small clutch of eggs. These termites become the first workers and care for the next batch. These are eusocial insects and have cooperative care for overlapping generations. As the numbers in the colony increase, soldiers are produced to defend the growing colony. -
The Formosan Subterranean Termite
The Formosan Subterranean Termite The Formosan subterranean termite, Coptotermes formosanus, is a pest of major economic importance in New Orleans, Louisiana and other areas of the southeastern United States. This exotic pest was introduced into United States port cities, such as New Orleans and Lake Charles, Louisiana, from eastern Asia after World War II by way of infested wooden cargo crates and pallets (La Fage 1987). In the continental United States, the first specimen of the Formosan subterranean termite was collected in Charleston, South Carolina in 1957 (Su 2003), but it was not positively identified until 1969.The Formosan subterranean termite was first identified in Houston, Texas in 1966 (Beal 1987). Documentation of infestations followed in New Orleans and Lake Charles, Louisiana and Galveston, Texas (La Fage 1987). In New Orleans, Formosan subterranean termite populations are well-established in the metro area. This species has replaced the native subterranean termite species as the primary structural pest in the greater New Orleans area. Worldwide, the Formosan subterranean termite is located in temperate and subtropical regions (Su 2003). This species’ distribution is limited by its temperature and humidity requirements. Populations of Formosan subterranean termites are typically located within the global area 35° north and south of the equator (Su and Tamashiro 1987). # # 30 # ## # ## ##### # # # # ## # # ##### # # # # Equator # 30 # Worldwide, Formosan subterranean termite populations are established throughout China, Taiwan, Japan, Midway, Hawaii, South Africa, and in multiple locations within the continental United States. Currently, established populations of Formosan subterranean termites have been reported in the states of Texas, Florida, California, Mississippi, Alabama, Tennessee, North Carolina, South Carolina, Georgia, and Louisiana (Su and Tamashiro 1987, Scheffrahn et al. -
TAXONOMIC REVISION of the TERMITOPHILOUS SUBTRIBE COPTOTERMOECIINA (Coleoptera : Staphylinidae)
Pacific Insects 12 (1): 85-115 20 May 1970 TAXONOMIC REVISION OF THE TERMITOPHILOUS SUBTRIBE COPTOTERMOECIINA (Coleoptera : Staphylinidae) with a description of some integumentary glands and a numerical analysis of their relationships1 By David H. Kistner2 and Jacques M. Pasteels' Abstract: The single previously known genus of the Subtribe Coptotermoeciina is herein redescribed and illustrated. Three new genera are herein described, Coptophilus, Philobrunneus, and Coptolimulus. Both previously known species are herein redescribed. In addition 7 new species are described: Coptophilus greavesi (Australian Capital Ter ritory) ; Coptotermoecia seeversi (Australian Capital Territory); C. flava (West Aus tralia) ; C. pilosa (New South Wales) ; C. robusta (West Australia) ; Philobrunneus gayi (West Australia) ; and Coptolimulus calabyi (West Australia). Many new geographic and host data of previously described species are presented. The integumentary glands are described for Coptophilus and Coptotermoecia. In both genera, the post-pleural glands are reduced. The tergal glands are reduced and modi fied but differently in each genus. Both genera possess large gland cells beneath the pronotum and additionally Coptophilus possesses numerous type 3 cells. Since the gland cells of the pronotum and the type 3 cells are not found in free-living species of sta phylinids, they perhaps act during host-guest interactions. The relationships between the genera and species are analyzed numerically and a den drogram produced which matches what is thought to be the phylogeny derived by tra ditional means. When this phylogeny is matched to the host relationships, the relation ships between the species of termitophiles match the relationships between their termite hosts as derived by F. J. -
The Complete Mitochondrial Genome of Coptotermes ‘Suzhouensis’ (Syn
Journal of Insect Science, (2018) 18(2): 26; 1–10 doi: 10.1093/jisesa/iey018 Research The Complete Mitochondrial Genome of Coptotermes ‘suzhouensis’ (syn. Coptotermes formosanus) (Isoptera: Rhinotermitidae) and Molecular Phylogeny Analysis Juan Li,1 Jin-long Zhu,1 Shi-di Lou,1 Ping Wang,1 You-sen Zhang,2 Lin Wang,1 Ruo-chun Yin,1 and Ping-ping Zhang1 1School of Life Sciences, Anhui University, Hefei 230601, Anhui, China, 2Hefei Termite Control Institute, Hefei 230001, Anhui, China, and Corresponding author, e-mail: [email protected] Received 7 November 2017; Editorial decision 30 January 2018 Abstract Coptotermes suzhouensis (Isoptera: Rhinotermitidae) is a significant subterranean termite pest of wooden structures and is widely distributed in southeastern China. The complete mitochondrial DNA sequence of C. suzhouensis was analyzed in this study. The mitogenome was a circular molecule of 15,764 bp in length, which contained 13 protein-coding genes (PCGs), 22 transfer RNA genes, two ribosomal RNA genes, and an A+T-rich region with a gene arrangement typical of Isoptera mitogenomes. All PCGs were initiated by ATN codons and terminated by complete termination codons (TAA), except COX2, ND5, and Cytb, which ended with an incomplete termination codon T. All tRNAs displayed a typical clover-leaf structure, except for tRNASer(AGN), which did not contain the stem- loop structure in the DHU arm. The A+T content (69.23%) of the A+T-rich region (949 bp) was higher than that of the entire mitogenome (65.60%), and two different sets of repeat units (A+B) were distributed in this region. -
CHECKLIST of PROTOZOA RECORDED in AUSTRALASIA O'donoghue P.J. 1986
1 PROTOZOAN PARASITES IN ANIMALS Abbreviations KINGDOM PHYLUM CLASS ORDER CODE Protista Sarcomastigophora Phytomastigophorea Dinoflagellida PHY:din Euglenida PHY:eug Zoomastigophorea Kinetoplastida ZOO:kin Proteromonadida ZOO:pro Retortamonadida ZOO:ret Diplomonadida ZOO:dip Pyrsonymphida ZOO:pyr Trichomonadida ZOO:tri Hypermastigida ZOO:hyp Opalinatea Opalinida OPA:opa Lobosea Amoebida LOB:amo Acanthopodida LOB:aca Leptomyxida LOB:lep Heterolobosea Schizopyrenida HET:sch Apicomplexa Gregarinia Neogregarinida GRE:neo Eugregarinida GRE:eug Coccidia Adeleida COC:ade Eimeriida COC:eim Haematozoa Haemosporida HEM:hae Piroplasmida HEM:pir Microspora Microsporea Microsporida MIC:mic Myxozoa Myxosporea Bivalvulida MYX:biv Multivalvulida MYX:mul Actinosporea Actinomyxida ACT:act Haplosporidia Haplosporea Haplosporida HAP:hap Paramyxea Marteilidea Marteilida MAR:mar Ciliophora Spirotrichea Clevelandellida SPI:cle Litostomatea Pleurostomatida LIT:ple Vestibulifera LIT:ves Entodiniomorphida LIT:ent Phyllopharyngea Cyrtophorida PHY:cyr Endogenida PHY:end Exogenida PHY:exo Oligohymenophorea Hymenostomatida OLI:hym Scuticociliatida OLI:scu Sessilida OLI:ses Mobilida OLI:mob Apostomatia OLI:apo Uncertain status UNC:sta References O’Donoghue P.J. & Adlard R.D. 2000. Catalogue of protozoan parasites recorded in Australia. Mem. Qld. Mus. 45:1-163. 2 HOST-PARASITE CHECKLIST Class: MAMMALIA [mammals] Subclass: EUTHERIA [placental mammals] Order: PRIMATES [prosimians and simians] Suborder: SIMIAE [monkeys, apes, man] Family: HOMINIDAE [man] Homo sapiens Linnaeus, -
Areawide Field Study on Effect of Three Chitin Synthesis Inhibitor Baits on Populations of Coptotermes Formosanus and Reticulite
HOUSEHOLD AND STRUCTURAL INSECTS Areawide Field Study on Effect of Three Chitin Synthesis Inhibitor Baits on Populations of Coptotermes formosanus and Reticulitermes flavipes (Isoptera: Rhinotermitidae) 1 WESTE L. A. OSBRINK, MARY L. CORNELIUS, AND ALAN R. LAX Southern Regional Research Center, USDAÐARS, 1100 Robert E. Lee Boulevard, New Orleans, LA 70124 J. Econ. Entomol. 104(3): 1009Ð1017 (2011); DOI: 10.1603/EC10217 ABSTRACT Periodic sampling of 43 independent monitors, initially active with Formosan subter- ranean termite, Coptotermes formosanus Shiraki, or the eastern subterranean termite, Reticulitermes flavipes (Kollar) (Isoptera: Rhinotermitidae), was conducted to evaluate the effects of cellulose baits containing one of three chitin synthesis inhibitors (CSIs)Ñdißubenzuron, hexaßumuron, or chlor- ßuazuronÑon termite populations. Dißubenzuron at 0.1% active ingredient (AI, wt:wt) had no noticeable effect on termite populations. Chlorßuazuron (0.25% [AI]) signiÞcantly reduced termite populations in Ϸ3 yr. Chlorßuazuron used after Ͼ2-yr dißubenzuron treatment signiÞcantly reduced termite populations within months. This suggests dißubenzuron exposure increased the termiteÕs sensitivity to chlorßuazuron accelerating population collapse. Hexaßumuron (0.5% [AI]) also reduced termite populations in Ϸ2 yr. The process of removing most detectable termite populations from the Ϸ160,000-m2 campus of the Southern Regional Research Center, New Orleans, LA, with CSIs baits required Ϸ3 yr. Adjustments in the speciÞc bait formulations and application -
Preferences of Coptotermes Formosanus Shiraki and Coptotermes Gestroi (Wasmann) (Blattodea: Rhinotermitidae) Among Three Commercial Wood Species Nirmala K
Insects 2011, 2, 499-508; doi:10.3390/insects2040499 OPEN ACCESS insects ISSN 2075-4450 www.mdpi.com/journal/insects/ Article Preferences of Coptotermes formosanus Shiraki and Coptotermes gestroi (Wasmann) (Blattodea: Rhinotermitidae) among Three Commercial Wood Species Nirmala K. Hapukotuwa * and J. Kenneth Grace College of Tropical Agriculture & Human Resources, University of Hawaii at Manoa, 3050 Maile Way, Gilmore Hall 310, Honolulu, HI 96822, USA; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +1-808-956-2462; Fax: +1-808-956-2460. Received: 13 October 2011; in revised form: 3 November 2011 / Accepted: 8 November 2011 / Published: 25 November 2011 Abstract: The Formosan subterranean termite, Coptotermes formosanus Shiraki, and the Asian subterranean termite, Coptotermes gestroi (Wasmann), are both pests of wood in service in Hawaii and Florida. We conducted a laboratory study using method modified from those described in standard E1-09 of the American Wood Protection Association (AWPA 2009) to assess the termite resistance of three commercially available wood species used in regions of the USA where both termite species occur: Douglas fir, Pseudotsuga menziessii, southern yellow pine, Pinus spp. and redwood, Sequoia sempervirens. A multiple-choice (three-choice) assay was used for four weeks (28 days) in order to simulate field conditions of food choice and assess termite feeding preferences under 28 °C and 72–80% RH. 400 termites (360 workers: 40 soldiers) were released into each test jar. Five replicates and two controls of each wood species were used with each termite species. Termite mortality was recorded at the end of the test; and wood wafers were oven-dried and weighed before and after termite exposure to determine the mass loss due to termite feeding, and rated visually on a 0 (failure) to 10 (sound) scale.