Thysanoptera (Insecta) of Barrow Island, Western Australia
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Bean Thrips Surveys
Blackwell Publishing AsiaMelbourne, AustraliaAENAustralian Journal of Entomology1326-6756© 2006 The Authors; Journal compilation © 2006 Australian Entomological SocietyMay 2006452122129Original ArticleSurvey for Caliothrips fasciatus in Australia M S Hoddle et al. Australian Journal of Entomology (2006) 45, 122–129 Populations of North American bean thrips, Caliothrips fasciatus (Pergande) (Thysanoptera: Thripidae: Panchaetothripinae) not detected in Australia Mark S Hoddle,1* Christina D Stosic1 and Laurence A Mound2 1Department of Entomology, University of California, Riverside, CA 92521, USA. 2Australian National Insect Collection, CSIRO Entomology, Canberra, ACT 2601, Australia. Abstract Caliothrips fasciatus is native to the USA and western Mexico and overwintering adults are regular contaminants in the ‘navel’ of navel oranges exported from California, USA to Australia, New Zealand and elsewhere. Due to the long history of regular interceptions of C. fasciatus in Australia, a survey for this thrips was undertaken around airports, seaports, public recreational parks and major agricul- tural areas in the states of Queensland, New South Wales, Victoria, South Australia and Western Australia to determine whether C. fasciatus has successfully invaded Australia. Host plants that are known to support populations of C. fasciatus, such as various annual and perennial agricultural crops, urban ornamentals and weeds along with native Australian flora, were sampled for this thrips. A total of 4675 thrips specimens encompassing at least 76 species from a minimum of 47 genera, and three families were collected from at least 159 plant species in 67 families. Caliothrips striatopterus was collected in Queensland, but the target species, C. fasciatus, was not found anywhere. An undescribed genus of Thripidae, Panchaetothripinae, was collected from ornamental Grevillea (var. -
Thrips Pollination of Mesozoic Gymnosperms
Thrips pollination of Mesozoic gymnosperms Enrique Peñalvera, Conrad C. Labandeirab,c,1, Eduardo Barróna, Xavier Delclòsd, Patricia Nele, André Nele, Paul Tafforeauf, and Carmen Sorianof aMuseo Geominero, Instituto Geológico y Minero de España, Madrid E-28003, Spain; bDepartment of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013; cDepartment of Entomology and Behavior, Ecology, Evolution and Systematics Program, University of Maryland, College Park, MD 20742; dDepartament d’Estratigrafia, Paleontologia i Geociències Marines, Facultat de Geologia, Universitat de Barcelona, E-08071, Spain; eCentre National de la Recherche Scientifique Unité Mixte de Recherche 7205, Entomologie, Muséum National d’Histoire Naturelle, Paris F-75005; Département Sciences de la Vie et Santé, AgroParisTech, Paris F-75231, France; and fEuropean Synchrotron Radiation Facility, Grenoble, F-38000, France Edited by David L. Dilcher, Indiana University, Bloomington, IN, and approved April 10, 2012 (received for review December 13, 2011) Within modern gymnosperms, conifers and Ginkgo are exclusively several to a few hundred pollen grains to flowers (18) or cones wind pollinated whereas many gnetaleans and cycads are insect (Table S1); for example, Cycadothrips chadwicki can deliver up to pollinated. For cycads, thrips are specialized pollinators. We report 5,700 pollen grains per ovule to Macrozamia communis cycad such a specialized pollination mode from Early Cretaceous amber of cones in an afternoon (8). Several species of Cycadothrips are ef- Spain, wherein four female thrips representing a genus and two ficient pollinators of endemic Australian Macrozamia cycads (7, 8, species in the family Melanthripidae were covered by abundant 21). Besides pollination of gnetaleans and cycads, thrips species Cycadopites pollen grains. -
Ficus Microcarpa Chinese Banyan Moraceae
Ficus microcarpa Chinese banyan Moraceae Forest Starr, Kim Starr, and Lloyd Loope United States Geological Survey--Biological Resources Division Haleakala Field Station, Maui, Hawai'i January, 2003 OVERVIEW Ficus microcarpa is a popular ornamental tree grown widely in many tropical regions of the world. The pollinator wasp has been introduced to a number of places where the tree is cultivated, including Hawai'i, allowing this species to spread beyond initial plantings. F. microcarpa is a notorious invader in Hawai'i, Florida, Bermuda, and from Central to South America. Tiny seeds within small sized fruit are ingested by many fruit eating animals, such as birds. Seeds are capable of germinating and growing almost anywhere they land, even in cracks in concrete or in the crotch of other trees. The small seedling begins to grow on its host, sending down aerial roots, and eventually strangling and replacing the host tree or structure. In Hawai'i, most of the main islands are infested with F. microcarpa. Typically, this species invades disturbed urban sites to degraded secondary forests in areas nearby initial plantings. It has recently been observed growing on native wiliwili (Erythrina sandwicense) in lowland dry forests of Maui. On the main islands of Hawai'i, rapid containment once inside natural area boundaries may be the only feasible action, given the widespread distribution. On Midway Atoll, the wasp was introduced later than on the main islands and, as a result, F. microcarpa has only recently begun to spread there. With limited distribution, control here seems more feasible than on the main islands. To decrease the potential for this species to spread, it should not be introduced to new areas and could be removed in natural areas where it is limited in distribution. -
Phlaeothripidae: Thysanoptera
Vol. XXII, No. 3, December, 1977 495 A Review of the Hawaiian Species of Idolothripinae (Phlaeothripidae: Thysanoptera) K. Sakimura and F. A. Bianchi BISHOP MUSEUM, HONOLULU, HAWAII Published knowledge of the Hawaiian tubuliferous thrips fauna is meager. This is largely due to the limited extent to which our findings have been reported in the past. Those accumulated findings are being jointly reported in this paper and in others to follow. The primary objective of these papers is to assemble all the information on these thrips together in a ready reference available for local use. All the Hawaiian literatures will be completely cited. Recent innovations in the systematics of the suborder Tubulifera, specifically the two major contributions by Mound (1974a, b) on the Pacific Idolothripinae, provided impetus to the study of the Hawaiian species. The last review of the Hawaiian Thysanoptera (Zimmerman 1948) is in need of extensive clarifications and additions. It listed only six idolothripine species. In the present review, one synonymy and two nomenclatural changes are reported, and four more species, including one new to science, are added. A new idolothripine species described subsequent to the last review was found to have been misplaced in this subfamily. Among nine species listed here, only three are considered endemic to the Hawaiian Islands. Materials accumulated in the Sakimura Collection and the Bishop Museum Collection are all pooled in this work. The Bianchi Collection, which included the HSPA Collection and the Hawaiian Entomological Society Collection, is now deposited in the Bernice P. Biship Museum. In our listings of "Material Studied" and "Earlier Collection Recorded", specimens from the Sakimura Collection are all specified by his accession numbers, and those from the Bishop Museum Collection are marked with an asterisk. -
Idolothripinae
Index | Glossary A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Idolothripinae Introduction The sub-order Tubulifera comprises a single family of living thrips, the Phlaeothripidae, and in this two subfamilies are recognised (ThripsWiki, 2020). Subfamily Phlaeothripinae includes 2990 described species in 370 genera worldwide, and the Idolothripinae 735 species in 83 genera. An alternative classification proposed by Bhatti (1992, 1994) recognised an Head & pronotumWingless female Male head & fore leg Order Tubulifera in which eight small families were distinguished from Phlaeothripidae. There is no general introduction to the Phlaeothripidae of Australia, but introductions are available to the taxa in this Family from the Neotropics (Mound & Marullo, 1996) and also from Japan (Okajima, 2006). An introduction to the Idolothripinae of Australia that included 70 species in 23 genera is well out-of- Female Male Female Head & pronotum date (Mound, 1974), but a revision is available of the taxa related to the genus Nesothrips (Eow et al., 2014), as is a key to world genera of this subfamily (Mound & Palmer, 1983). Currently, just over 100 species in 25 genera of Idolothripinae are listed from Australia, but only six of the genera are endemic, with most having wide distributions across Asia and the Pacific. Wingless & winged females These spore-feeding thrips live on the surface of dead twigs and Head & pronotum (wingless branches, and also in leaf-litter on the ground (Tree & Walter, female) 2012). Thrips on dead bark in Australia are exposed to desiccation, and also to a wide range of predators including birds, lizards, ants and spiders. -
Thysanoptera: Phlaeothripinae, Leeuweniini), with Comments on Related Old World Taxa
Blackwell Science, LtdOxford, UKAENAustralian Journal of Entomology1326-67562004 Australian Entomological SocietyMarch 20044312837Original ArticleAustralian long-tailed gall thripsLaurence A Mound Australian Journal of Entomology (2004) 43, 28–37 Australian long-tailed gall thrips (Thysanoptera: Phlaeothripinae, Leeuweniini), with comments on related Old World taxa Laurence A Mound CSIRO Entomology, GPO Box 1700, Canberra, ACT 2601, Australia. Abstract The Tribe Leeuweniini is a group of Old World Phlaeothripinae species that feed and usually induce irregular galls on the leaves of rainforest trees. These thrips all have the last abdominal segment unusually elongate, but this is a variable and homoplastic character state, and the tribe remains ill- defined. Worldwide, 27 species in three genera are now recognised, with five other generic names here included as synonyms of Leeuwenia Karny. From Australia, six species in two genera are recorded here occurring in the eastern rainforests. Four newly described Australian species and their host plants are: Leeuwenia diospyri sp. n. (Diospyros pentamera–Ebenaceae); L. polyosmae sp. n. (Polyosma cunninghamii–Grossulariaceae); L. scolopiae sp. n. (Scolopia braunii–Flacourtiaceae); and L. tetrastigmae sp. n. (Tetrastigma nitens–Vitaceae). The host association of L. convergens Hood is not known, but the sixth species, Neohoodiella jennibeardae Mound and Williams, breeds on two unrelated plants of which the leaves are similar in texture – Ficus coronata (Moraceae) and Rhipogonum elseyanum (Smilacaceae). Key words galls, Leeuwenia, Neohoodiella, rainforest trees. INTRODUCTION that was found living in an abandoned weevil mine on an Acacia phyllode in Queensland. In contrast to other insects, adults of the 3500 named species This paper gives some account of the six Australian mem- in the thysanopteran family Phlaeothripidae have the tenth bers of an Old World group of 27 described thrips species in abdominal segment forming a complete tube. -
Heteroptera: Anthocoridae, Lasiochilidae)
2018 ACTA ENTOMOLOGICA 58(1): 207–226 MUSEI NATIONALIS PRAGAE doi: 10.2478/aemnp-2018-0018 ISSN 1804-6487 (online) – 0374-1036 (print) www.aemnp.eu RESEARCH PAPER Annotated catalogue of the fl ower bugs from India (Heteroptera: Anthocoridae, Lasiochilidae) Chandish R. BALLAL1), Shahid Ali AKBAR2,*), Kazutaka YAMADA3), Aijaz Ahmad WACHKOO4) & Richa VARSHNEY1) 1) National Bureau of Agricultural Insect Resources, Bengaluru, India; e-mail: [email protected] 2) Central Institute of Temperate Horticulture, Srinagar, 190007 India; e-mail: [email protected] 3) Tokushima Prefectural Museum, Bunka-no-Mori Park, Mukoterayama, Hachiman-cho, Tokushima, 770–8070 Japan; e-mail: [email protected] 4) Department of Zoology, Government Degree College, Shopian, Jammu and Kashmir, 192303 India; e-mail: [email protected] *) Corresponding author Accepted: Abstract. The present paper provides a checklist of the fl ower bug families Anthocoridae th 6 June 2018 and Lasiochilidae (Hemiptera: Heteroptera) of India based on literature and newly collected Published online: specimens including eleven new records. The Indian fauna of fl ower bugs is represented by 73 5th July 2018 species belonging to 26 genera under eight tribes of two families. Generic transfers of Blap- tostethus pluto (Distant, 1910) comb. nov. (from Triphleps pluto Distant, 1910) and Dilasia indica (Muraleedharan, 1978) comb. nov. (from Lasiochilus indica Muraleedharan, 1978) are provided. A lectotype is designated for Blaptostethus pluto. Previous, as well as new, distribu- -
Hoplothrips Karnyi Distinguishing Features Both Sexes Either Fully Winged Or with Wings Shorter Than Thorax Width
Hoplothrips karnyi Distinguishing features Both sexes either fully winged or with wings shorter than thorax width. Body and legs brown, tarsi and much of fore tibiae yellow, also hind tibiae sometimes yellow at base; antennal segment III mainly yellow, IV–VI variably yellow at base; fore wings weakly Pelta & tergite II shaded toward apex. Antennae 8-segmented; sense Female Antenna cones longer in winged than wingless individuals, segment III with 3 sense cones, IV with 4 sense cones; VIII constricted to base. Head longer than wide, slightly wider across cheeks than across eyes, cheeks without prominent tubercles, but with several small setae in wingless individuals; postocular setae long Male sternite VIII and pointed, wide apart; maxillary stylets retracted to eyes, close together medially. Pronotum without sculpture medially; with four pairs of slender pointed major setae, anteromarginal setae Male head, pronotum & fore legs small. Fore tarsal tooth small in winged but large in wingless individuals. Metanotum without sculpture medially. Fore wing parallel sided, with about 10 duplicated cilia. Abdominal tergites II–VII with two pairs of sigmoid wing-retaining setae, even in wingless individuals, marginal setae S1 long and pointed; tergite IX setae S1 pointed, almost as long as tube. Male varying in size, large males with fore femora swollen; tergite IX setae S2 short and stout; sternite VIII with transverse pore plate extending full width of sternite. Related species This species is not known from California, but is included here as one specimen has been seen from British Colombia. H. karnyi from North America is possibly the same species as the European H. -
(Thysanoptera: Melanthripidae) in Baghdad - Iraq
Awatif A. Hamodi Bull. Iraq nat. Hist. Mus. (2012) 12 (1): 11-17 NEW RECORD OF PREDATOR MELANTHRIPS PALLIDIOR PRIESNER (THYSANOPTERA: MELANTHRIPIDAE) IN BAGHDAD - IRAQ Awatif Abdul-Fatah Hamodi Dept. of Plant Protection - College of Agriculture Baghdad University - Baghdad - IRAQ ABSTRACT The predator Melanthrips pallidior Priesner regarded as a new record in Baghdad. The specimens were collected from alfalfa field during April 2010 to April 2011 in Abu-Gharib. Morphological characters of different body parts were studied and compared with other specimens by using taxonomic keys. INTRODUCTION Alfalfa Medicage sativa L. one of perennial plant that regarded as a good media for pests and their natural enemies in the world. The natural enemies are an important biological factors that balancing and limiting the outbreak of pests. Thrips belong to the order Thysanoptera are divided into two suborders, suborder Terebrantia and suborder Tubuilifera (Haliday, 1836) depending on number of antennal segments and shape of sense cones, shape a tip of fore wing and number of setae on the two veins, these two suborders include over 6000 species belong to 9 families and six subfamilies (Mound & Marullo. 1996; Mound & Morris. 2007a; Mound. 2007). There are many species of thrips feed on insects and mites and small size arthropods. Melanthrips pallidior Priesner was record a predator on insects of bean flowers in Turkey (Akakan.2008), also in Europe, Africa and North America on wheat (Alavie & Zurstrasn & Bagherami. 2007) and on Tulipa gesneriana L. and Pyrus zommunis L. (Kirk. 2007; Mound and Morris, 2oo7; Nichle, 2003, Raspudic, Ivezic,. Brmez, Trdan, 2009) the pupate found under the soil inside a fine cocoon (De Borbon, 2009). -
Terrestrial Arthropod Surveys on Pagan Island, Northern Marianas
Terrestrial Arthropod Surveys on Pagan Island, Northern Marianas Neal L. Evenhuis, Lucius G. Eldredge, Keith T. Arakaki, Darcy Oishi, Janis N. Garcia & William P. Haines Pacific Biological Survey, Bishop Museum, Honolulu, Hawaii 96817 Final Report November 2010 Prepared for: U.S. Fish and Wildlife Service, Pacific Islands Fish & Wildlife Office Honolulu, Hawaii Evenhuis et al. — Pagan Island Arthropod Survey 2 BISHOP MUSEUM The State Museum of Natural and Cultural History 1525 Bernice Street Honolulu, Hawai’i 96817–2704, USA Copyright© 2010 Bishop Museum All Rights Reserved Printed in the United States of America Contribution No. 2010-015 to the Pacific Biological Survey Evenhuis et al. — Pagan Island Arthropod Survey 3 TABLE OF CONTENTS Executive Summary ......................................................................................................... 5 Background ..................................................................................................................... 7 General History .............................................................................................................. 10 Previous Expeditions to Pagan Surveying Terrestrial Arthropods ................................ 12 Current Survey and List of Collecting Sites .................................................................. 18 Sampling Methods ......................................................................................................... 25 Survey Results .............................................................................................................. -
Thysanoptera, Phlaeothripidae) 1 Doi: 10.3897/Zookeys.345.6167 RESEARCH ARTICLE Launched to Accelerate Biodiversity Research
A peer-reviewed open-access journal ZooKeys 345:Review 1–28 (2013)of the spore-feeding Idolothripinae from China (Thysanoptera, Phlaeothripidae) 1 doi: 10.3897/zookeys.345.6167 RESEARCH ARTICLE www.zookeys.org Launched to accelerate biodiversity research Review of the spore-feeding Idolothripinae from China (Thysanoptera, Phlaeothripidae) Li-Hong Dang1,2, Ge-Xia Qiao1 1 Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, No. 1 Beichen West Road, Chaoyang District, Beijing 100101, P.R.China 2 University of Chinese Academy of Sciences, No. 19, Yuquan Road, Shijingshan District, Beijing 100049, P.R.China Corresponding author: Ge-Xia Qiao ([email protected]) Academic editor: L. Mound | Received 28 August 2013 | Accepted 2 October 2013 | Published 29 October 2013 Citation: Dang L-H, Qiao G-X (2013) Review of the spore-feeding Idolothripinae from China (Thysanoptera, Phlaeothripidae). ZooKeys 345: 1–28. doi: 10.3897/zookeys.345.6167 Abstract An illustrated key is provided to the 19 genera of the subfamily Idolothripinae from China, and a checklist given to 62 named species, of which six species are newly recorded from China, together with the genus Bolothrips that is represented by two un-named species. A generic diagnosis is given for each genus, along with some discussion of systematic relationship problems and species diversity. Identification keys to species of 11 genera are provided, and Megathrips antennatus Guo, Feng & Duan is considered as a new synonym of Megathrips lativentris (Heeger). Keywords Idolothripinae, genera, illustrated keys, species checklist, new records, China Introduction The insect order Thysanoptera, comprises more than 6000 species, and is classified into two suborders, Terebrantia and Tubulifera (ThripsWiki 2013). -
An Updated Checklist of Thrips from Slovakia with Emphasis on Economic Species
Original Paper Plant Protection Science, 56, 2020 (4): 292–304 https://doi.org/10.17221/87/2020-PPS An updated checklist of thrips from Slovakia with emphasis on economic species Martina Zvaríková, Rudolf Masarovič, Pavol Prokop; Peter Fedor* Department of Environmental Ecology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia *Corresponding author: [email protected] Citation: Zvaríková M., Masarovič R., Prokop P., Fedor P. (2020): An updated checklist of thrips from Slovakia with emphasis on economic species. Plant Protect. Sci., 56: 292–304. Abstract: Almost sixty years after the first published plea for more systematic research on thrips in Slovakia, the checklist undisputedly requires an appropriate revision with a special emphasis on the economic consequences of climate change and biological commodity trade globalisation synergic effects, followed by the dynamic and significant changes in the native biodiversity due to alien species introduction. The updated checklist contains 189 species recorded from the area of Slovakia, from three families: Aeolothripidae Uzel, 1895 (15 species), Thripidae Stephens, 1829 (113 species) and Phlaeothripidae Uzel, 1895 (61 species), including 7 beneficiary and 35 economic pest elements, such as one A2 EPPO quarantine pest (Frankliniella occidentalis) and five potential transmitters of tospoviruses (F. occidentalis, F. intonsa, F. fusca, Thrips tabaci, Dictyothrips betae). Several species (e.g., Hercinothrips femoralis, Microcephalothrips abdomi- nalis, F. occidentalis, T. flavus, T. tabaci, Limothrips cerealium, L. denticornis, etc.) may possess a heavy introduction and invasion potential with well-developed mechanisms for successful dispersion. Keywords: alien species; biodiversity; globalisation; invasions; crop pests; tospoviruses Thrips (Thysanoptera) are generally known as crop a synergy of factors may support the fact that exot- pests throughout the world (Lewis 1997).