Guide to Biological Control to Some Common Yard and Garden Pests
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False Black Widows and Other Household Spiders
False Black Widows and Other Household Spiders Spiders can quite unnecessarily evoke all kinds of dread and fear. The Press does not help by publishing inaccurate and often alarmist stories about them. Spiders are in fact one of our very important beneficial creatures. Spiders in the UK devour a weight of insect 'pests' equivalent to that of the nation's human population! During the mid-late summer, many spiders mature and as a result become more obvious as they have then grown to their full size. One of these species is Steatoda nobilis. It came from the Canary and Madeiran Islands into Devon over a 100 years ago, being first recorded in Britain near Torquay in 1879! However it was not described from Britain until 1993, when it was known to have occurred since at least 1986 and 1989 as flourishing populations in Portsmouth (Hampshire) and Swanage (Dorset). There was also a population in Westcliff-on-Sea (Essex) recorded in 1990, and another in Littlehampton and Worthing (West Sussex). Its distribution is spreading more widely along the coast in the south and also inland, with confirmed records from South Devon, East Sussex, Kent, Surrey and Warwick. The large, grape-like individuals are the females and the smaller, more elongate ones, the males. These spiders are have become known as False Widows and, because of their colour, shape and size, are frequently mistaken for the Black Widow Spider that are found in warmer climes, but not in Britain (although some occasionally come into the country in packaged fruit and flowers). Black Widow Spiders belong to the world-wide genus Latrodectus. -
The Behavioural Ecology of Latrodectus Hasselti (Thorell), the Australian Redback Spider (Araneae: Theridiidae): a Review
Records of the Western Australian MIISellnl Supplement No. 52: 13-24 (1995). The behavioural ecology of Latrodectus hasselti (Thorell), the Australian Redback Spider (Araneae: Theridiidae): a review Lyn Forster McMasters Road, RD 1, Saddle Hill, Dunedin, New Zealand Abstract - Aspects of the biogeographical history and behavioural ecology of the AustralIan Latrodectus hasseIti provide support for the endemic status of this species. Cannibalism, prey stealing and short instar lengths are growth strategies for. female spiders whereas early maturation, small size, hiding and scavengmg are useful survival tactics for males. Moreover male complicity is an important component of sexual cannibalism which is ~hown to be a highly predictable event. Latrodectus hasseIti males hybridize with female L. katlpo (a New Zealand species) and fertile Fl and F2 generations Imply genetic relatedness. Hence, it is likely that L. hasselti and L. katipo evolv~d from a common ancestor in ancient Pangaea, a feasible explanation only If L. hasseItl IS endemic to Australia. It is concluded that L. hasseIti would have been able to persist in outback Australia for millions of years, with ItS mtraspeClfJc predatory habits aiding subsistence and the evolution of sexual cannibalism providing a way of coping with infrequent meeting and matmg opportunities. INTRODUCTION indigenous status, Main (1993) notes that, (as a Many stories and articles have been written consequence of its supposed introduction), "the about the redback spider (McKeown 1963; Raven absence of Latrodectus in the Australian region, 1992) with considerable attention being devoted to prior to human habitation, poses a curious its venomous nature (Southcott 1978; Sutherland zoogeographic dilemma". This comment raises an and Trinca 1978). -
Cambridge University Press 978-1-107-11607-8 — a Natural History of Ladybird Beetles M. E. N. Majerus , Executive Editor H. E. Roy , P
Cambridge University Press 978-1-107-11607-8 — A Natural History of Ladybird Beetles M. E. N. Majerus , Executive Editor H. E. Roy , P. M. J. Brown Index More Information Index 2-isopropyl-3-methoxy-pyrazine, 238 281, 283, 285, 287–9, 291–5, 297–8, 2-phenylethylamine, 237 301–3, 311, 314, 316, 319, 325, 327, 329, 335 abdomen, 17, 20, 22, 24, 28–9, 32, 38, 42, 110, Adalia 4-spilota,80 114, 125, 128, 172, 186, 189, 209–10, Adalia conglomerata, 255 218 adaline, 108, 237, 241 Acacia, 197, 199 adalinine, 237 acaricides, 316 adelgids, 29, 49, 62, 65, 86, 91, 176, 199, 308, Acaridae, 217 310, 322 Acarina, 205, 217 Adonia, 44, 71 Acer pseudoplatanus, 50, 68, 121 aggregations, 163, 165, 168, 170, 178, 184, Acraea, 228, 297, 302 221, 312, 324 Acraea encedana, 302 Aiolocaria, 78, 93, 133, 276 Acraea encedon, 297, 302 Aiolocaria hexaspilota,78 Acyrthosiphon nipponicum, 101 Aiolocaria mirabilis, 133, 276 Acyrthosiphon pisum, 75, 77, 90, 92, 97–101, albino, 273 116, 239 Alces alces,94 Adalia, 5–6, 10, 22, 34, 44, 64, 70, 78, 80, 86, Aleyrodidae, 91, 310 123, 125, 128, 130, 132, 140, 143, 147, alfalfa, 119, 308, 316, 319, 325 159–60, 166–7, 171, 180–1, 218, 222, alimentary canal, 29, 35, 221 234, 237, 239, 241, 255, 259–60, 262, alkaloids, x, 99–100, 195–7, 202, 236–9, 241–2, 269, 279, 281, 284, 286, 298, 311, 325, 245–6 327, 335 Allantonematidae, 220 Adalia 10-punctata, 22, 70, 80, 86, 98–100, anal cremaster, 38, 40 104, 108, 116, 132, 146–7, 149, Anatis, 4, 17, 23, 41, 44, 66, 76, 89, 102, 131, 154, 156, 160, 174, 181–3, 188, 148, 165, 186, 191, 193, -
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Revista Brasileira de Entomologia 62 (2018) 288–291 REVISTA BRASILEIRA DE Entomologia A Journal on Insect Diversity and Evolution www.rbentomologia.com Biology, Ecology and Diversity Filling gaps in species distributions through the study of biological collections: 415 new distribution records for Neotropical Cryptinae (Hymenoptera, Ichneumonidae) a,∗ b Bernardo F. Santos , João Paulo M. Hoppe a National Museum of Natural History, Department of Entomology, Washington, DC, USA b Universidade Federal do Espírito Santo, Departamento de Ciências Biológicas, Vitória, ES, Brazil a r a b s t r a c t t i c l e i n f o Article history: Filling gaps in species distributions is instrumental to increase our understanding of natural environ- Received 30 June 2018 ments and underpin efficient conservation policies. For many hyperdiverse groups, this knowledge is Accepted 1 September 2018 hampered by insufficient taxonomic information. Herein we provide 415 new distribution records for Available online 28 September 2018 the parasitic wasp subfamily Cryptinae (Hymenoptera, Ichneumonidae) in the Neotropical region, based Associate Editor: Rodrigo Gonc¸ alves on examination of material from 20 biological collections worldwide. Records span across 227 sites in 24 countries and territories, and represent 175 species from 53 genera. Of these, 102 represent new coun- Keywords: try records for 74 species. A distinct “road pattern” was detected in the records, at least within Brazil, Atlantic Forest where 50.2% of the records fall within 10 km of federal roads, an area that occupies only 11.9% of the biodiversity Cryptini surface of the country. The results help to identify priority areas that remain poorly sampled and should database be targeted for future collecting efforts, and highlight the importance of biological collections in yielding parasitoid wasp new information about species distributions that is orders of magnitude above what is provided in most individual studies. -
Tachinidae, Tachinid Flies
Beneficial Insects Class Insecta, Insects Order Diptera, Flies, gnats, and midges Diptera means “two wings,” and true flies bear only one pair of functional wings. Flies are one of the largest insect groups, with approximately 35 families that contain predatory or parasitic species. All flies have piercing/sucking/sponging mouthparts. Tachinid flies Family Tachinidae Description and life history: This is a large and important family, with up to 1300 native parasitoid species in North America and additional introduced species to help control foreign pests. These flies vary in color, size, and shape but most resemble houseflies. Adults are usually gray, black, or striped, and hairy. Adults lay eggs on plants to be consumed by hosts, or they glue eggs to the outside of hosts, so the maggots can burrow into the host. Rarely will tachinids insert eggs into host bodies. Tachinid flies develop rapidly within their host and pupate in 4–14 days. By the time they emerge, they have killed their host. Many species have several generations a year, although some are limited by hosts with a single annual generation. Prey species: Most tachinid flies attack caterpillars and adult and larval beetles, although others specialize on Tachinid fly adult. (327) sawfly larvae, true bugs, grasshoppers, or other insects. Photo: John Davidson Lydella thompsoni is a parasitoid of European corn borer, Voria ruralis attacks cabbage looper caterpillars, Myiopharus doryphorae attacks Colorado potato beetle larvae, and Istocheta aldrichi parasitizes adult Japanese beetles. Although these are very important natural en- emies, none is available commercially. IPM of Midwest Landscapes 263. -
COLEOPTERA COCCINELLIDAE) INTRODUCTIONS and ESTABLISHMENTS in HAWAII: 1885 to 2015
AN ANNOTATED CHECKLIST OF THE COCCINELLID (COLEOPTERA COCCINELLIDAE) INTRODUCTIONS AND ESTABLISHMENTS IN HAWAII: 1885 to 2015 JOHN R. LEEPER PO Box 13086 Las Cruces, NM USA, 88013 [email protected] [1] Abstract. Blackburn & Sharp (1885: 146 & 147) described the first coccinellids found in Hawaii. The first documented introduction and successful establishment was of Rodolia cardinalis from Australia in 1890 (Swezey, 1923b: 300). This paper documents 167 coccinellid species as having been introduced to the Hawaiian Islands with forty-six (46) species considered established based on unpublished Hawaii State Department of Agriculture records and literature published in Hawaii. The paper also provides nomenclatural and taxonomic changes that have occurred in the Hawaiian records through time. INTRODUCTION The Coccinellidae comprise a large family in the Coleoptera with about 490 genera and 4200 species (Sasaji, 1971). The majority of coccinellid species introduced into Hawaii are predacious on insects and/or mites. Exceptions to this are two mycophagous coccinellids, Calvia decimguttata (Linnaeus) and Psyllobora vigintimaculata (Say). Of these, only P. vigintimaculata (Say) appears to be established, see discussion associated with that species’ listing. The members of the phytophagous subfamily Epilachninae are pests themselves and, to date, are not known to be established in Hawaii. None of the Coccinellidae in Hawaii are thought to be either endemic or indigenous. All have been either accidentally or purposely introduced. Three species, Scymnus discendens (= Diomus debilis LeConte), Scymnus ocellatus (=Scymnobius galapagoensis (Waterhouse)) and Scymnus vividus (= Scymnus (Pullus) loewii Mulsant) were described by Sharp (Blackburn & Sharp, 1885: 146 & 147) from specimens collected in the islands. There are, however, no records of introduction for these species prior to Sharp’s descriptions. -
Crop Profile for Apples in California General Production
Crop Profile for Apples in California General Production Information ● Apple production in California represents 8.5% of the national production (1). ● California has over 38,500 bearing acres of apples (1). ● Yield per acre varies from 2 to 18 tons per acre throughout California’s growing regions, primarily due to irrigation and varietal differences (13). ● From 1995 to 1997, California apple growers average production was 920,000,000 pounds. In 1997, 962,000,000 pounds of apples were produced (1). ● The average value of apples produced in the state between 1995 and 1997 was $158,918,000. The value of apples produced in 1997 was $162,655,000 (1). ● The average cost to produce an acre of apples in California amounts to $4,523 per acre for irrigated orchards and $3,947 per acre for non-irrigated orchards (11, 12). Production Regions There are five major regions in which apples are grown in California. Historically, apple production was limited to the coastal mountains north and south of San Francisco Bay, in the Sierra foothills east of Sacramento, and in the Southern California mountains. Recently apple production has expanded into the Central Valley, with new plantings of Granny Smith, Fuji, Gala, and other varieties. Important coastal apple producing counties are Sonoma in the North Coast, and Santa Cruz and San Luis Obispo in the Central Coast region. However the major apple production areas are now in the San Joaquin Valley with Kern, Fresno, San Joaquin, and Madera counties being the leading producers (3). Southern California mountain regions still have a few orchards. -
Arthropods of Elm Fork Preserve
Arthropods of Elm Fork Preserve Arthropods are characterized by having jointed limbs and exoskeletons. They include a diverse assortment of creatures: Insects, spiders, crustaceans (crayfish, crabs, pill bugs), centipedes and millipedes among others. Column Headings Scientific Name: The phenomenal diversity of arthropods, creates numerous difficulties in the determination of species. Positive identification is often achieved only by specialists using obscure monographs to ‘key out’ a species by examining microscopic differences in anatomy. For our purposes in this survey of the fauna, classification at a lower level of resolution still yields valuable information. For instance, knowing that ant lions belong to the Family, Myrmeleontidae, allows us to quickly look them up on the Internet and be confident we are not being fooled by a common name that may also apply to some other, unrelated something. With the Family name firmly in hand, we may explore the natural history of ant lions without needing to know exactly which species we are viewing. In some instances identification is only readily available at an even higher ranking such as Class. Millipedes are in the Class Diplopoda. There are many Orders (O) of millipedes and they are not easily differentiated so this entry is best left at the rank of Class. A great deal of taxonomic reorganization has been occurring lately with advances in DNA analysis pointing out underlying connections and differences that were previously unrealized. For this reason, all other rankings aside from Family, Genus and Species have been omitted from the interior of the tables since many of these ranks are in a state of flux. -
Insects and Related Arthropods Associated with of Agriculture
USDA United States Department Insects and Related Arthropods Associated with of Agriculture Forest Service Greenleaf Manzanita in Montane Chaparral Pacific Southwest Communities of Northeastern California Research Station General Technical Report Michael A. Valenti George T. Ferrell Alan A. Berryman PSW-GTR- 167 Publisher: Pacific Southwest Research Station Albany, California Forest Service Mailing address: U.S. Department of Agriculture PO Box 245, Berkeley CA 9470 1 -0245 Abstract Valenti, Michael A.; Ferrell, George T.; Berryman, Alan A. 1997. Insects and related arthropods associated with greenleaf manzanita in montane chaparral communities of northeastern California. Gen. Tech. Rep. PSW-GTR-167. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Dept. Agriculture; 26 p. September 1997 Specimens representing 19 orders and 169 arthropod families (mostly insects) were collected from greenleaf manzanita brushfields in northeastern California and identified to species whenever possible. More than500 taxa below the family level wereinventoried, and each listing includes relative frequency of encounter, life stages collected, and dominant role in the greenleaf manzanita community. Specific host relationships are included for some predators and parasitoids. Herbivores, predators, and parasitoids comprised the majority (80 percent) of identified insects and related taxa. Retrieval Terms: Arctostaphylos patula, arthropods, California, insects, manzanita The Authors Michael A. Valenti is Forest Health Specialist, Delaware Department of Agriculture, 2320 S. DuPont Hwy, Dover, DE 19901-5515. George T. Ferrell is a retired Research Entomologist, Pacific Southwest Research Station, 2400 Washington Ave., Redding, CA 96001. Alan A. Berryman is Professor of Entomology, Washington State University, Pullman, WA 99164-6382. All photographs were taken by Michael A. Valenti, except for Figure 2, which was taken by Amy H. -
E0020 Common Beneficial Arthropods Found in Field Crops
Common Beneficial Arthropods Found in Field Crops There are hundreds of species of insects and spi- mon in fields that have not been sprayed for ders that attack arthropod pests found in cotton, pests. When scouting, be aware that assassin bugs corn, soybeans, and other field crops. This publi- can deliver a painful bite. cation presents a few common and representative examples. With few exceptions, these beneficial Description and Biology arthropods are native and common in the south- The most common species of assassin bugs ern United States. The cumulative value of insect found in row crops (e.g., Zelus species) are one- predators and parasitoids should not be underes- half to three-fourths of an inch long and have an timated, and this publication does not address elongate head that is often cocked slightly important diseases that also attack insect and upward. A long beak originates from the front of mite pests. Without biological control, many pest the head and curves under the body. Most range populations would routinely reach epidemic lev- in color from light brownish-green to dark els in field crops. Insecticide applications typical- brown. Periodically, the adult female lays cylin- ly reduce populations of beneficial insects, often drical brown eggs in clusters. Nymphs are wing- resulting in secondary pest outbreaks. For this less and smaller than adults but otherwise simi- reason, you should use insecticides only when lar in appearance. Assassin bugs can easily be pest populations cannot be controlled with natu- confused with damsel bugs, but damsel bugs are ral and biological control agents. -
Coleoptera: Coccinellidae): Influence of Subelytral Ultrastructure
Experimental & Applied Acarology, 23 (1999) 97–118 Review Phoresy by Hemisarcoptes (Acari: Hemisarcoptidae) on Chilocorus (Coleoptera: Coccinellidae): influence of subelytral ultrastructure M.A. Houck* Department of Biological Sciences, Texas Tech University, Lubbock, TX 79409–3131, USA (Received 9 January 1997; accepted 17 April 1998) ABSTRACT The non-phoretic stages of mites of the genus Hemisarcoptes are predators of the family Diaspididae. The heteromorphic deutonymph (hypopus) maintains a stenoxenic relationship with beetles of the genus Chilocorus. The mites attach to the subelytral surface of the beetle elytron during transport. There is variation in mite density among species of Chilocorus. Both Hemisarcoptes and Chilocorus have been applied to biological control programmes around the world. The objective of this study was to determine whether subelytral ultrastructure (spine density) plays a role in the evolution of symbiosis between the mite and the beetle. The subelytral surfaces of 19 species of Chilocorus and 16 species of Exochomus were examined. Spine density was determined for five subelytral zones: the anterior pronotal margin, medial central region, caudoventral tip, lateral distal margin and epipleural region. Spine density on the subelytral surface of Chilocorus and Exochomus was inversely correlated with the size of the elytron for all zones except the caudoventral tip. This suggests that an increase in body size resulted in a redistribution of spines and not an addition of spines. The pattern of spine density in Exochomus and Chilocorus follows a single size–density trajectory. The pattern of subelytral ultrastructure is not strictly consistent with either beetle phylogeny or beetle allometry. The absence of spines is not correlated with either beetle genus or size and species of either Chilocorus or Exochomus may be devoid of spines in any zone, irrespective of body size. -
Centomologica: -'F
:1 |II || ISSN 0001-561X AdTA| CENTOMOLOGICA: -'F. NNICA I A:_:1 $-** ; R. E. Linn vuori | Heteortera of Yemen and Siouth Yemenll 0 ,~~~~~~~~~~~~~~~~~~~I Vo41.4 1989 : ANNALES ENTOMOLOGICI FEMNNICI ACTA ENTOMOLOGICA FENNICA Published since 1935, four numbers a year. Published since 1947, monographs Annual subscription FIM 150, in Finland at irregular intervals. FIM 120. Price variable. Address: Zoological Museum, P. Rautatiek. 13, SF-00100 Helsinki, Finland. Publishers Suomen Hy6nteistieteellinen Seura Entomological Society of Finland - Societas Entomologica Fennica Entomologiska Foreningen i Helsingfors - Helsingin Hyonteistieteellinen Yhdistys Societas Entomologica Helsingforsiensis Editorial Board Chairman: A. Jansson (chief editor) Other members: K. Heliovaara (assistant editor of Acta), L. Hulddn (secretary, assistant editor), R. livarinen (treasurer), H. Krogerus, i. Mannerkoski, H. Silfverberg (editor of Acta) Board of Trustees President: E. Kangas Other members: 0. Bistrom, 1. Terds, A. Pekkarinen, R. Rosengren (vice president) Annales Entomologici Fennici publishes scientific papers, notes and reviews based principally on Finnish entomological investigations. Monographs and other longer articles are directed to Acta Entomologica Fennica, articles of mainly Nordic interest to Notulae Entomologicae. Contributors are requested to take into consideration the style and format of articles in recently published volumes. Two copies of each manuscript must be submitted with the original. As modern techniques often allow printing directly from computer diskettes, the editor should be informed if the manuscript is written on a word processor. The journals are cited selectively by Bibliographie der Pflanzenschutz-Literatur of Biologische Bundesanstaft for Land- und Forstwirtschaft, Biological Abstracts of the Biosciences Information Service, Current Contents (Series Agriculture, Biology & Environmental Sciences) of Institute for Scientific Information, Entomology Abstracts of Information Retrieval Limited, and Review of Applied Entomology (Series A.