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The Life Cycle of Heteropoda Venatoria (Linnaeus) (Araneae: Heteropodidae)I, by John Ross 3, David B
THE LIFE CYCLE OF HETEROPODA VENATORIA (LINNAEUS) (ARANEAE: HETEROPODIDAE)I, BY JOHN ROSS 3, DAVID B. RICHMAN 3, FADEL MANSOUR4, ANNE TRAMBARULO3, AND W. H. WHITCOMB The giant crab spider, Heteropoda venatoria (L.), is known to occur throughout much of the tropics and subtropics of the world where it is valued as a predator of cockroaches (Guthrie and Tindall 1968, Hughes 1977, Edwards 1979). Its feeding habits, like those of most spiders, vary somewhat and it has also been known to eat scorpions and bats (Bhattacharya 1941), although it is questionable as to whether it normally attacks such prey. This spider is often found associated with human habitation, possibly due to the abun- dance of prey (Subrahamanyam 1944, Edwards 1979). Although biological notes on H. venatoria have been published by several workers (Lucas 1871, Minchin 1904, Bristowe 1924, Bonnet 1930, Ori 1974, 1977), the only life history work to date was published by Bonnet (1932) and Sekiguchi (1943, 1944a,b, 1945). Bonnet (1932) based his study on only 12 spiders (of which seven matured) and lacked data on the postembryonic stages. Sekiguchi (1943, 1944a,b, 1945) presented a more nearly complete study, but the papers are difficult to translate and they still lack some data, especially in regard to variation in the number of instars and carapace width. We have raised H. venatoria in the laboratory and present here our data on life cycle of this important beneficial arthropod. MATERIALS AND METHODS Spiders were obtained from avocado groves in south Florida, near Homestead, Dade County. Egg sacs taken from our laboratory This study was partially supported by the United States-lsrael BARD Fund as Research Project No. -
The Sphingidae (Lepidoptera) of the Philippines
©Entomologischer Verein Apollo e.V. Frankfurt am Main; download unter www.zobodat.at Nachr. entomol. Ver. Apollo, Suppl. 17: 17-132 (1998) 17 The Sphingidae (Lepidoptera) of the Philippines Willem H o g e n e s and Colin G. T r e a d a w a y Willem Hogenes, Zoologisch Museum Amsterdam, Afd. Entomologie, Plantage Middenlaan 64, NL-1018 DH Amsterdam, The Netherlands Colin G. T readaway, Entomologie II, Forschungsinstitut Senckenberg, Senckenberganlage 25, D-60325 Frankfurt am Main, Germany Abstract: This publication covers all Sphingidae known from the Philippines at this time in the form of an annotated checklist. (A concise checklist of the species can be found in Table 4, page 120.) Distribution maps are included as well as 18 colour plates covering all but one species. Where no specimens of a particular spe cies from the Philippines were available to us, illustrations are given of specimens from outside the Philippines. In total we have listed 117 species (with 5 additional subspecies where more than one subspecies of a species exists in the Philippines). Four tables are provided: 1) a breakdown of the number of species and endemic species/subspecies for each subfamily, tribe and genus of Philippine Sphingidae; 2) an evaluation of the number of species as well as endemic species/subspecies per island for the nine largest islands of the Philippines plus one small island group for comparison; 3) an evaluation of the Sphingidae endemicity for each of Vane-Wright’s (1990) faunal regions. From these tables it can be readily deduced that the highest species counts can be encountered on the islands of Palawan (73 species), Luzon (72), Mindanao, Leyte and Negros (62 each). -
4 Reproductive Biology of Cerambycids
4 Reproductive Biology of Cerambycids Lawrence M. Hanks University of Illinois at Urbana-Champaign Urbana, Illinois Qiao Wang Massey University Palmerston North, New Zealand CONTENTS 4.1 Introduction .................................................................................................................................. 133 4.2 Phenology of Adults ..................................................................................................................... 134 4.3 Diet of Adults ............................................................................................................................... 138 4.4 Location of Host Plants and Mates .............................................................................................. 138 4.5 Recognition of Mates ................................................................................................................... 140 4.6 Copulation .................................................................................................................................... 141 4.7 Larval Host Plants, Oviposition Behavior, and Larval Development .......................................... 142 4.8 Mating Strategy ............................................................................................................................ 144 4.9 Conclusion .................................................................................................................................... 148 Acknowledgments ................................................................................................................................. -
The Reproductive Behaviour of an Aphidophagous Ladybeetle,Coccinella Septempunctata (Coleoptera: Coccinellidae)
Eur. J. Entomol. 99: 465-470, 2002 ISSN 1210-5759 The reproductive behaviour of an aphidophagous ladybeetle,Coccinella septempunctata (Coleoptera: Coccinellidae) OMKAR* and Sh e f a l i SRIVASTAVA Department ofZoology, University ofLucknow, Lucknow-226 007 India; e-mail:[email protected] Key words. Coccinellids, Coccinella septempunctata, reproductive behaviour, courtship and mating, mating duration, mate recognition Abstract. The reproductive behaviour of a ladybeetle,Coccinella septempunctata was studied in detail. Males became sexually mature within 8.8 ± 0.3 days at 27°C, while females took 11.2 ± 0.4 days. Males exhibited courtship display in five steps: approach, watch, examine, mount and copulatory attempt. A prominent rejection display was shown by certain females who had not matured sexually, had recently mated or were about to oviposit. Males appeared to recognize females through chemical and some visual cues, such as size and body shape, with the chemical cues possibly playing a more significant role. Multiple matings took place within the same day. There was a gradual decrease with time in reproductive parametres, such as the duration of copulation, the number of copulatory bouts and the latent period from first to subsequent matings on the same day. The interval between mating bouts slightly increased from first to subsequent matings. The sexual status of males and females affected the duration of copulation, which was greatest in the case of unmated males and virgin females. Multiple matings increased the oviposition period, fecundity and percent hatching of eggs. INTRODUCTION MATERIALS AND METHODS Mating and reproduction are essential to assure the sur To determine the pre-mating period vival of a species (Omkar et al., 2000; Omkar & Pervez, Pupae ofC. -
Nansei Islands Biological Diversity Evaluation Project Report 1 Chapter 1
Introduction WWF Japan’s involvement with the Nansei Islands can be traced back to a request in 1982 by Prince Phillip, Duke of Edinburgh. The “World Conservation Strategy”, which was drafted at the time through a collaborative effort by the WWF’s network, the International Union for Conservation of Nature (IUCN), and the United Nations Environment Programme (UNEP), posed the notion that the problems affecting environments were problems that had global implications. Furthermore, the findings presented offered information on precious environments extant throughout the globe and where they were distributed, thereby providing an impetus for people to think about issues relevant to humankind’s harmonious existence with the rest of nature. One of the precious natural environments for Japan given in the “World Conservation Strategy” was the Nansei Islands. The Duke of Edinburgh, who was the President of the WWF at the time (now President Emeritus), naturally sought to promote acts of conservation by those who could see them through most effectively, i.e. pertinent conservation parties in the area, a mandate which naturally fell on the shoulders of WWF Japan with regard to nature conservation activities concerning the Nansei Islands. This marked the beginning of the Nansei Islands initiative of WWF Japan, and ever since, WWF Japan has not only consistently performed globally-relevant environmental studies of particular areas within the Nansei Islands during the 1980’s and 1990’s, but has put pressure on the national and local governments to use the findings of those studies in public policy. Unfortunately, like many other places throughout the world, the deterioration of the natural environments in the Nansei Islands has yet to stop. -
The Mcguire Center for Lepidoptera and Biodiversity
Supplemental Information All specimens used within this study are housed in: the McGuire Center for Lepidoptera and Biodiversity (MGCL) at the Florida Museum of Natural History, Gainesville, USA (FLMNH); the University of Maryland, College Park, USA (UMD); the Muséum national d’Histoire naturelle in Paris, France (MNHN); and the Australian National Insect Collection in Canberra, Australia (ANIC). Methods DNA extraction protocol of dried museum specimens (detailed instructions) Prior to tissue sampling, dried (pinned or papered) specimens were assigned MGCL barcodes, photographed, and their labels digitized. Abdomens were then removed using sterile forceps, cleaned with 100% ethanol between each sample, and the remaining specimens were returned to their respective trays within the MGCL collections. Abdomens were placed in 1.5 mL microcentrifuge tubes with the apex of the abdomen in the conical end of the tube. For larger abdomens, 5 mL microcentrifuge tubes or larger were utilized. A solution of proteinase K (Qiagen Cat #19133) and genomic lysis buffer (OmniPrep Genomic DNA Extraction Kit) in a 1:50 ratio was added to each abdomen containing tube, sufficient to cover the abdomen (typically either 300 µL or 500 µL) - similar to the concept used in Hundsdoerfer & Kitching (1). Ratios of 1:10 and 1:25 were utilized for low quality or rare specimens. Low quality specimens were defined as having little visible tissue inside of the abdomen, mold/fungi growth, or smell of bacterial decay. Samples were incubated overnight (12-18 hours) in a dry air oven at 56°C. Importantly, we also adjusted the ratio depending on the tissue type, i.e., increasing the ratio for particularly large or egg-containing abdomens. -
Faunal Makeup of Macrolepidopterous Moths in Nopporo Forest Park, Hokkaido, Northern Japan, with Some Related Title Notes
Faunal Makeup of Macrolepidopterous Moths in Nopporo Forest Park, Hokkaido, Northern Japan, with Some Related Title Notes Author(s) Sato, Hiroaki; Fukuda, Hiromi Environmental science, Hokkaido : journal of the Graduate School of Environmental Science, Hokkaido University, Citation Sapporo, 8(1), 93-120 Issue Date 1985-07-31 Doc URL http://hdl.handle.net/2115/37177 Type bulletin (article) File Information 8(1)_93-120.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP 93 Environ. Sci., Hokkaiclo 8 (1) 93-v120 I June 1985 Faunal Makeup of Macrolepidopterous Moths in Nopporo Forest Park, Hokkaido, Northern Japan, with Some Related Notes Hiroaki Sato and Hiromi Ful<uda Department of Biosystem Management, Division of Iinvironmental Conservation, Graciuate Schoo! of Environmental Science, Hokkaido University, Sapporo, 060, Japan Abstraet Macrolepidopterous moths were collected in Nopporo Forest Park to disclose the faunal mal<eup. By combining this survey with other from Nopporo, 595 species "rere recorded, compris- ing of roughly 45% of all species discovered in }{{okkaiclo to clate. 'irhe seasonal fiuctuations of a species diversity were bimodal, peal<ing in August and November. The data obtained had a good correlation to both lognormal and logseries clistributions among various species-abundance models. In summer, it was found that specialistic feeders dominated over generalistic feeders. However, in autumn, generalistic feeders clominated, most lil<ely because low temperature shortened hours for seel<ing host plants on which to lay eggs. - Key Words: NopporQ Forest Park, Macrolepidoptera, Species diversity, Species-abundance model, Generalist, Specialist 1. Introduction Nopporo Forest Park, which has an area of approximately 2,OOO ha and is adjacent to the city of Sapporo, contains natural forests representing the temperate and boreal features of vegetation. -
Mai Po Nature Reserve Management Plan: 2019-2024
Mai Po Nature Reserve Management Plan: 2019-2024 ©Anthony Sun June 2021 (Mid-term version) Prepared by WWF-Hong Kong Mai Po Nature Reserve Management Plan: 2019-2024 Page | 1 Table of Contents EXECUTIVE SUMMARY ................................................................................................................................................... 2 1. INTRODUCTION ..................................................................................................................................................... 7 1.1 Regional and Global Context ........................................................................................................................ 8 1.2 Local Biodiversity and Wise Use ................................................................................................................... 9 1.3 Geology and Geological History ................................................................................................................. 10 1.4 Hydrology ................................................................................................................................................... 10 1.5 Climate ....................................................................................................................................................... 10 1.6 Climate Change Impacts ............................................................................................................................. 11 1.7 Biodiversity ................................................................................................................................................ -
Chapter 13 Arachnids As
CHAPTER THIRTEEN ARACHNIDS 13.1 The arachnid fauna of south central Seram As with insects, only a very few specimens compared with the total number of known species were collected in the field. Nevertheless, they do cover most species commonly encountered and named by the Nuaulu. A checklist of arachnid specimens recorded in the Nuaulu area during field- work is presented in table 22. 13.2 Nuaulu categories applied to arachnids excepting Acarida 13.2.1 kanopone Scorpions (SCORPIONIDA) and possibly also whip-scorpions ( URO- PYGI ). 13.2.2 riko-riko, nau asue The first term is consistently applied to harvestmen ( PHALANGIDA ). In the second, nau is a general term for augury and divination; asu = 'dog', asu- = 'cheek' + non-human possessive pronominal suffix. Nau asue is applied to the harvestman Altobunus formosus. It is probably a synonym for riko-riko, being used as a nick-name in circumstances in which it seems auspicious. 13.2.3 kahuneke hatu nohu inae Hatu nohu(e), meaning 'cavernous rock outcrop, cave', indicates the habitat of this spider; inae = 'mother'. As kahunekete is the generic term for spider we thus have 'mother cave spider'. Applied quite specifically to tailess whip scorpions, and generally encountered in rock fissures when hunting bats. 13.2.4 kahuneke ai ukune Ai ukune = 'treetop', far forest. Applied to various kinds of long- bodied spider, including Theridion and possibly Nephilia. It therefore seems to be applied to both hunters and spinners of irregular webs in forest habi- tats. - 201 - 13.2.5 kahuneke titie Titie = 'hot', so-called on account of the ability of this round-bodied spider to bite humans and cause a painful swelling. -
Far Eastern Entomologist Number 429: 8-11 April 2021
Far Eastern Entomologist ISSN 1026-051X (print edition) Number 429: 8-11 ISSN 2713-2196 (online edition) April 2021 https://doi.org/10.25221/fee.429.2 http://zoobank.org/References/36A71DD0-FE2B-4D2B-BBEC-9BA2C73FA989 FIRST RECORD OF NOCTUID MOTH CALLOPISTRIA AETHIOPS BUTLER, 1878 (LEPIDOPTERA: NOCTUIDAE) FROM SOUTHERN PRIMORYE AS AN EXAMPLE OF THE EAST ASIAN SPECIES PENETRATING IN RUSSIAN FAUNA V. V. Dubatolov1, 2) 1) Federal State Institution "Zapovednoe Priamurye", Yubileinaya street, 8, Bychikha village, Khabarovskii Krai, 680502, Russia. E-mail: [email protected] 2) Institute of Systematics and Ecology of Animals, Siberian Branch of Russian Academy of Sciences, Frunze str. 11, Novosibirsk, 630091, Russia. Summary. An East Asian-Oriental noctuid species Callopistria aethiops Butler, 1878 is recorded from Russia for the first time. The trend of invasions of the southern Macroheterocera species into the Russian Far East has existed at least during last century but is noticeably increased during last 20 years. Key words: Lepidoptera, Noctuidae, fauna, new record, invasion, Primorskii Krai, Russia. В. В. Дубатолов. Первая находка совки Callopistria aethiops Butler, 1878 (Lepidoptera: Noctuidae) в Южном Приморье как пример внедрения восточноазиатских видов в фауну России // Дальневосточный энтомолог. 2021. N 429. С. 8-11. Резюме. Восточноазиатско-ориентальная совка Callopistria aethiops Butler, 1878 впервые найдена в России. Показано, что тенденция проникновения южных видов макрочешуекрылых на Дальний Восток России отмечена, по крайней мере, в течение ста лет, но наиболее ярко она выражена в последние два десятилетия. INTRODUCTION During an excursion to Vitjaz Bay (Khasan District in Primorskii Krai) in September 2020, a new for Russian fauna noctuid moth was collected among other 73 late summer and autumn Macroheterocera species. -
その他の昆虫類 Other Miscellaneous Insects 高橋和弘 1) Kazuhiro Takahashi
丹沢大山総合調査学術報告書 丹沢大山動植物目録 (2007) その他の昆虫類 Other Miscellaneous Insects 高橋和弘 1) Kazuhiro Takahashi 要 約 今回の目録に示した各目ごとの種数は, 次のとおりである. カマアシムシ目 10 種 ナナフシ目 5 種 ヘビトンボ目 3 種 トビムシ目 19 種 ハサミムシ目 5 種 ラクダムシ目 2 種 イシノミ目 1 種 カマキリ目 3 種 アミメカゲロウ目 55 種 カゲロウ目 61 種 ゴキブリ目 4 種 シリアゲムシ目 13 種 トンボ目 62 種 シロアリ目 1 種 チョウ目 (ガ類) 1756 種 カワゲラ目 52 種 チャタテムシ目 11 種 トビケラ目 110 種 ガロアムシ目 1 種 カメムシ目 (異翅亜目除く) 501 種 バッタ目 113 種 アザミウマ目 19 種 凡 例 清川村丹沢山 (Imadate & Nakamura, 1989) . 1. 本報では、 カゲロウ目を石綿進一、 カワゲラ目を石塚 新、 トビ ミヤマカマアシムシ Yamatentomon fujisanum Imadate ケラ目を野崎隆夫が執筆し、 他の丹沢大山総合調査報告書生 清川村丹沢堂平 (Imadate, 1994) . 物目録の昆虫部門の中で諸般の事情により執筆者がいない分類 群について,既存の文献から,データを引用し、著者がまとめた。 文 献 特に重点的に参照した文献は 『神奈川県昆虫誌』(神奈川昆虫 Imadate, G., 1974. Protura Fauna Japonica. 351pp., Keigaku Publ. 談話会編 , 2004)※である. Co., Tokyo. ※神奈川昆虫談話会編 , 2004. 神奈川県昆虫誌 . 1438pp. 神 Imadate, G., 1993. Contribution towards a revision of the Proturan 奈川昆虫談話会 , 小田原 . Fauna of Japan (VIII) Further collecting records from northern 2. 各分類群の記述は, 各目ごとに分け, 引用文献もその目に関 and eastern Japan. Bulletin of the Department of General するものは, その末尾に示した. Education Tokyo Medical and Dental University, (23): 31-65. 2. 地名については, 原則として引用した文献に記されている地名 Imadate, G., 1994. Contribution towards a revision of the Proturan とした. しがって, 同一地点の地名であっても文献によっては異 Fauna of Japan (IX) Collecting data of acerentomid and なった表現となっている場合があるので, 注意していただきたい. sinentomid species in the Japanese Islands. Bulletin of the Department of General Education Tokyo Medical and Dental カマアシムシ目 Protura University, (24): 45-70. カマアシムシ科 Eosentomidae Imadate, G. & O. Nakamura, 1989. Contribution towards a revision アサヒカマアシムシ Eosentomon asahi Imadate of the Proturan Fauna of Japan (IV) New collecting records 山 北 町 高 松 山 (Imadate, 1974) ; 清 川 村 宮 ヶ 瀬 (Imadate, from the eastern part of Honshu. -
Trees, Shrubs, and Perennials That Intrigue Me (Gymnosperms First
Big-picture, evolutionary view of trees and shrubs (and a few of my favorite herbaceous perennials), ver. 2007-11-04 Descriptions of the trees and shrubs taken (stolen!!!) from online sources, from my own observations in and around Greenwood Lake, NY, and from these books: • Dirr’s Hardy Trees and Shrubs, Michael A. Dirr, Timber Press, © 1997 • Trees of North America (Golden field guide), C. Frank Brockman, St. Martin’s Press, © 2001 • Smithsonian Handbooks, Trees, Allen J. Coombes, Dorling Kindersley, © 2002 • Native Trees for North American Landscapes, Guy Sternberg with Jim Wilson, Timber Press, © 2004 • Complete Trees, Shrubs, and Hedges, Jacqueline Hériteau, © 2006 They are generally listed from most ancient to most recently evolved. (I’m not sure if this is true for the rosids and asterids, starting on page 30. I just listed them in the same order as Angiosperm Phylogeny Group II.) This document started out as my personal landscaping plan and morphed into something almost unwieldy and phantasmagorical. Key to symbols and colored text: Checkboxes indicate species and/or cultivars that I want. Checkmarks indicate those that I have (or that one of my neighbors has). Text in blue indicates shrub or hedge. (Unfinished task – there is no text in blue other than this text right here.) Text in red indicates that the species or cultivar is undesirable: • Out of range climatically (either wrong zone, or won’t do well because of differences in moisture or seasons, even though it is in the “right” zone). • Will grow too tall or wide and simply won’t fit well on my property.