BOLD Taxonid Tree

Total Page:16

File Type:pdf, Size:1020Kb

BOLD Taxonid Tree BOLD TaxonID Tree Title : Tree Result - Search (2626 records) Date : 29-Nov-2016 Data Type : Nucleotide Distance Model : Kimura 2 Parameter Marker : COI-5P Colourization : Taxonomy: Order Label : Process ID Label : Order Label : Family Label : Subfamily Label : Taxon Label : Barcode Cluster (BIN) Sequence Count : 2626 Species count : 697 Genus count : 721 Family count : 247 Unidentified : 1893 BIN Count : 2626 Cover Page 1/1 Search Tue Nov 29 11:16:49 2016 Page 1 of 27 20 % Eupodidae|[1]|SSECC1138-15|Trombidiformes|Eupodidae||BOLD:ACB5424 Eupodidae|[2]|SSECC1152-15|Trombidiformes|Eupodidae||BOLD:AAL8146 Eupodidae|[3]|SSBCA1628-15|Trombidiformes|Eupodidae||BOLD:ACG6712 Eupodidae|[4]|SSECC1128-15|Trombidiformes|Eupodidae||BOLD:ACK5087 Eupodidae|[5]|SSECC1115-15|Trombidiformes|Eupodidae||BOLD:ACV9427 Trombidiformes|[6]|SSECC379-15|Trombidiformes|||BOLD:ACX3248 Eupodidae|[7]|SSKNA3783-15|Trombidiformes|Eupodidae||BOLD:AAF9119 Eupodidae|[8]|SSKNA8175-15|Trombidiformes|Eupodidae||BOLD:ACY4643 Tydeidae|[9]|SSKNA9914-15|Trombidiformes|Tydeidae||BOLD:ACZ3130 Trombidiidae|[10]|SSBCA1542-15|Trombidiformes|Trombidiidae||BOLD:AAU6281 Trombidiidae|[11]|SSBCA4915-15|Trombidiformes|Trombidiidae||BOLD:AAZ0397 Trombidiidae|[12]|SSECC824-15|Trombidiformes|Trombidiidae||BOLD:ACU3750 Trombidiidae|[13]|SSECC175-15|Trombidiformes|Trombidiidae||BOLD:ACU3554 Trombidiidae|[14]|SSECC722-15|Trombidiformes|Trombidiidae||BOLD:ACX4628 Trombidiformes|[15]|SSBCA1550-15|Trombidiformes|||BOLD:ACX4840 Microtrombidiidae|[16]|SSBCA1554-15|Trombidiformes|Microtrombidiidae||BOLD:ACX5647 Lebertia|[17]|SSKNA3764-15|Trombidiformes|Lebertiidae||BOLD:ACG5337 Lebertiidae|[18]|SSBCA1544-15|Trombidiformes|Lebertiidae||BOLD:ACX4954 Leptus|[19]|SSBCA5715-15|Trombidiformes|Erythraeidae|Leptinae|BOLD:AAF9230 Leptus|[20]|SSBCA1548-15|Trombidiformes|Erythraeidae|Leptinae|BOLD:AAU6288 Erythraeidae|[21]|SSBCA5695-15|Trombidiformes|Erythraeidae||BOLD:ACG5252 Erythraeidae|[22]|SSBCA3673-15|Trombidiformes|Erythraeidae||BOLD:AAF9122 Erythraeidae|[23]|SSKNA9447-15|Trombidiformes|Erythraeidae||BOLD:ACX6503 Bdellidae|[24]|SSECC375-15|Trombidiformes|Bdellidae||BOLD:ACG4744 Bdellidae|[25]|SSKNA9406-15|Trombidiformes|Bdellidae||BOLD:ACV8109 Bdellidae|[26]|SSKNA8268-15|Trombidiformes|Bdellidae||BOLD:ACE2588 Bdellidae|[27]|SSECC495-15|Trombidiformes|Bdellidae||BOLD:ACW0371 Bdellidae|[28]|SSKNA8113-15|Trombidiformes|Bdellidae||BOLD:ACW0679 Rhagidiidae|[29]|SSECC376-15|Trombidiformes|Rhagidiidae||BOLD:ACX1773 Rhagidiidae|[30]|SSECC374-15|Trombidiformes|Rhagidiidae||BOLD:ACX2381 Rhagidiidae|[31]|SSECC1181-15|Trombidiformes|Rhagidiidae||BOLD:ACX3591 Rhagidiidae|[32]|SSKNA10035-15|Trombidiformes|Rhagidiidae||BOLD:AAF9282 Rhagidiidae|[33]|SSKNA9552-15|Trombidiformes|Rhagidiidae||BOLD:ACK8322 Rhagidiidae|[34]|SSECC809-15|Trombidiformes|Rhagidiidae||BOLD:ACV7879 Rhagidiidae|[35]|SSECC868-15|Trombidiformes|Rhagidiidae||BOLD:ACX3501 Rhagidiidae|[36]|SSKNA9335-15|Trombidiformes|Rhagidiidae||BOLD:AAF9084 Rhagidiidae|[37]|SSKNA8284-15|Trombidiformes|Rhagidiidae||BOLD:AAF9267 Rhagidiidae|[38]|SSECC703-15|Trombidiformes|Rhagidiidae||BOLD:ACV6836 Rhagidiidae|[39]|SSECC1140-15|Trombidiformes|Rhagidiidae||BOLD:ACX3517 Rhagidiidae|[40]|SSECC1143-15|Trombidiformes|Rhagidiidae||BOLD:ACX4617 Rhagidiidae|[41]|SSECC1093-15|Trombidiformes|Rhagidiidae||BOLD:ACX5173 Rhagidiidae|[42]|SSECC1092-15|Trombidiformes|Rhagidiidae||BOLD:ACX6177 Rhagidiidae|[43]|SSECC768-15|Trombidiformes|Rhagidiidae||BOLD:ACX5841 Rhagidiidae|[44]|SSKNA9551-15|Trombidiformes|Rhagidiidae||BOLD:ACX6789 Anystidae|[45]|SSKNA1167-15|Trombidiformes|Anystidae||BOLD:AAH6549 Anystidae|[46]|SSBCA6337-15|Trombidiformes|Anystidae||BOLD:AAL8164 Anystidae|[47]|SSBCA1537-15|Trombidiformes|Anystidae||BOLD:AAF1092 Anystidae|[48]|SSKNA1800-15|Trombidiformes|Anystidae||BOLD:ACC0995 Anystidae|[49]|SSKNA5892-15|Trombidiformes|Anystidae||BOLD:ACK5255 Anystidae|[50]|SSBCA4442-15|Trombidiformes|Anystidae||BOLD:ABW5642 Anystidae|[51]|SSBCA1538-15|Trombidiformes|Anystidae||BOLD:ABW5662 Anystidae|[52]|SSBCA1660-15|Trombidiformes|Anystidae||BOLD:AAF9123 Anystidae|[53]|SSBCA4498-15|Trombidiformes|Anystidae||BOLD:ACE1288 Anystidae|[54]|SSBCA4894-15|Trombidiformes|Anystidae||BOLD:ACE1374 Anystidae|[55]|SSBCA5705-15|Trombidiformes|Anystidae||BOLD:AAF9255 Anystidae|[56]|SSBCA5309-15|Trombidiformes|Anystidae||BOLD:ACM8527 Calyptostomatidae|[57]|SSBCA5717-15|Trombidiformes|Calyptostomatidae||BOLD:ACY6900 Proctophyllodidae|[58]|SSKNA3793-15|Sarcoptiformes|Proctophyllodidae||BOLD:ACM8457 Brachychthoniidae|[59]|SSBCA1632-15|Sarcoptiformes|Brachychthoniidae||BOLD:AAZ4682 Brachychthoniidae|[60]|SSBCA1622-15|Sarcoptiformes|Brachychthoniidae||BOLD:ACX5297 Sarcoptiformes|[61]|SSBCA4225-15|Sarcoptiformes|||BOLD:ACX5948 Phthiracaridae|[62]|SSBCA1564-15|Sarcoptiformes|Phthiracaridae||BOLD:ACX4883 Atropacarus striculus|[63]|SSBCA4256-15|Sarcoptiformes|Phthiracaridae||BOLD:AAL5699 Hoplophthiracarus illinoisensis|[64]|SSBCA4282-15|Sarcoptiformes|Phthiracaridae||BOLD:ACT6604 Phthiracarus|[65]|SSKNA9852-15|Sarcoptiformes|Phthiracaridae||BOLD:ACZ3970 Hypochthonius rufulus|[66]|SSBCA4254-15|Sarcoptiformes|Hypochthoniidae||BOLD:AAH6471 Eniochthonius crosbyi|[67]|SSBCA1702-15|Sarcoptiformes|Eniochthoniidae||BOLD:AAH6518 Damaeidae|[68]|SSECC1151-15|Sarcoptiformes|Damaeidae||BOLD:ACV1086 Damaeidae|[69]|SSECC1186-15|Sarcoptiformes|Damaeidae||BOLD:ACX3852 Damaeidae|[70]|SSBCA1704-15|Sarcoptiformes|Damaeidae||BOLD:ACX5646 Scheloribatidae|[71]|SSBCA4912-15|Sarcoptiformes|Scheloribatidae||BOLD:ACG5401 Pergalumna|[72]|SSBCA1661-15|Sarcoptiformes|Galumnidae||BOLD:AAD9459 Scheloribates pallidulus|[73]|SSBCA1593-15|Sarcoptiformes|Scheloribatidae||BOLD:AAD7099 Scheloribates|[74]|SSBCA1592-15|Sarcoptiformes|Scheloribatidae||BOLD:AAV2447 Scheloribatidae|[75]|SSECC1220-15|Sarcoptiformes|Scheloribatidae||BOLD:ACX3656 Phenopelopidae|[76]|SSKNA10051-15|Sarcoptiformes|Phenopelopidae||BOLD:ACZ3036 Oppiidae|[77]|SSECC1205-15|Sarcoptiformes|Oppiidae||BOLD:ACX3864 Megeremaeus|[78]|SSKNA5879-15|Sarcoptiformes|Megeremaeidae||BOLD:ACC1118 Cymbaeremaeidae|[79]|SSECC174-15|Sarcoptiformes|Cymbaeremaeidae||BOLD:ACE1409 Gymnodamaeus|[80]|SSECC1111-15|Sarcoptiformes|Gymnodamaeidae||BOLD:ACG5501 Eremaeidae|[81]|SSECC1206-15|Sarcoptiformes|Eremaeidae||BOLD:ACX3706 Anachipteria|[82]|SSBCA1761-15|Sarcoptiformes|Achipteriidae||BOLD:ACX5661 Suctobelbidae|[83]|SSECC1131-15|Sarcoptiformes|Suctobelbidae||BOLD:ACX3943 Suctobelbella|[84]|SSBCA4249-15|Sarcoptiformes|Suctobelbidae||BOLD:AAH6599 Suctobelbidae|[85]|SSBCA4475-15|Sarcoptiformes|Suctobelbidae||BOLD:ACX3563 Suctobelbidae|[86]|SSBCA4394-15|Sarcoptiformes|Suctobelbidae||BOLD:ACY6743 Suctobelbidae|[87]|SSBCA4508-15|Sarcoptiformes|Suctobelbidae||BOLD:AAU6076 Suctobelbidae|[88]|SSECC1195-15|Sarcoptiformes|Suctobelbidae||BOLD:ACX3479 Suctobelbidae|[89]|SSBCA4352-15|Sarcoptiformes|Suctobelbidae||BOLD:ACY7524 Oribatulidae|[90]|SSKNA5878-15|Sarcoptiformes|Oribatulidae||BOLD:ACD8939 Oribatulidae|[91]|SSECC180-15|Sarcoptiformes|Oribatulidae||BOLD:ACT9894 Tectocepheidae|[92]|SSECC1196-15|Sarcoptiformes|Tectocepheidae||BOLD:ACW1977 Tectocepheidae|[93]|SSECC1210-15|Sarcoptiformes|Tectocepheidae||BOLD:ACX3775 Tectocepheus|[94]|SSBCA1724-15|Sarcoptiformes|Tectocepheidae||BOLD:ACG6714 Tectocepheus|[95]|SSBCA1759-15|Sarcoptiformes|Tectocepheidae||BOLD:ACX5298 Sarcoptiformes|[96]|SSBCA1712-15|Sarcoptiformes|||BOLD:ACX4358 Sarcoptiformes|[97]|SSBCA4314-15|Sarcoptiformes|||BOLD:ACY7575 Sarcoptiformes|[98]|SSKNA9362-15|Sarcoptiformes|||BOLD:ACX6701 Search Tue Nov 29 11:16:49 2016 Page 2 of 27 Tectocepheus|[95]|SSBCA1759-15|Sarcoptiformes|Tectocepheidae||BOLD:ACX5298 Sarcoptiformes|[96]|SSBCA1712-15|Sarcoptiformes|||BOLD:ACX4358 Sarcoptiformes|[97]|SSBCA4314-15|Sarcoptiformes|||BOLD:ACY7575 Sarcoptiformes|[98]|SSKNA9362-15|Sarcoptiformes|||BOLD:ACX6701 Ceratoppia quadridentata|[99]|SSKNA9394-15|Sarcoptiformes|Peloppiidae||BOLD:AAC4607 Ceratoppia|[100]|SSBCA3001-15|Sarcoptiformes|Peloppiidae||BOLD:AAW4451 Ceratoppia|[101]|SSKNA9461-15|Sarcoptiformes|Peloppiidae||BOLD:ACD8994 Ceratoppia|[102]|SSBCA3004-15|Sarcoptiformes|Peloppiidae||BOLD:ACE1872 Eremaeidae|[103]|SSKNA5915-15|Sarcoptiformes|Eremaeidae||BOLD:ACT1778 Ametroproctus|[104]|SSECC1185-15|Sarcoptiformes|Cymbaeremaeidae||BOLD:ACI4478 Neoliodidae|[105]|SSECC082-15|Sarcoptiformes|Neoliodidae||BOLD:ACI6337 Oribatellidae|[106]|SSECC1203-15|Sarcoptiformes|Oribatellidae||BOLD:ACW2556 Ceratozetidae|[107]|SSECC1200-15|Sarcoptiformes|Ceratozetidae||BOLD:ACX4061 Mycobatidae|[108]|SSBCA4250-15|Sarcoptiformes|Mycobatidae||BOLD:AAZ5801 Oppiidae|[109]|SSECC1211-15|Sarcoptiformes|Oppiidae||BOLD:ACV9776 Oppiidae|[110]|SSBCA4357-15|Sarcoptiformes|Oppiidae||BOLD:AAM7997 Oppiidae|[111]|SSECC1177-15|Sarcoptiformes|Oppiidae||BOLD:ACX3500 Oppiidae|[112]|SSBCA4340-15|Sarcoptiformes|Oppiidae||BOLD:AAF9155 Sarcoptiformes|[113]|SSBCA1716-15|Sarcoptiformes|||BOLD:ACX4970 Sarcoptiformes|[114]|SSBCA4471-15|Sarcoptiformes|||BOLD:ACX5196 Sarcoptiformes|[115]|SSBCA1673-15|Sarcoptiformes|||BOLD:ACX6000 Sarcoptiformes|[116]|SSBCA4342-15|Sarcoptiformes|||BOLD:ACX6056 Diapterobates humeralis|[117]|SSKNA5897-15|Sarcoptiformes|Ceratozetidae||BOLD:AAE0813 Neogymnobates luteus|[118]|SSKNA10199-15|Sarcoptiformes|Ceratozetidae||BOLD:AAF9171 Ceratozetidae|[119]|SSBCA3435-15|Sarcoptiformes|Ceratozetidae||BOLD:AAL7981 Ceratozetidae|[120]|SSECC504-15|Sarcoptiformes|Ceratozetidae||BOLD:ACX4863 Eupelops|[121]|SSKNA9851-15|Sarcoptiformes|Phenopelopidae||BOLD:ACE1427 Sphodrocepheus|[122]|SSECC858-15|Sarcoptiformes|Cepheidae||BOLD:ACR1929 Eremaeidae|[123]|SSECC1221-15|Sarcoptiformes|Eremaeidae||BOLD:ACF0235
Recommended publications
  • Dipterists Digest
    Dipterists Digest 2019 Vol. 26 No. 1 Cover illustration: Eliozeta pellucens (Fallén, 1820), male (Tachinidae) . PORTUGAL: Póvoa Dão, Silgueiros, Viseu, N 40º 32' 59.81" / W 7º 56' 39.00", 10 June 2011, leg. Jorge Almeida (photo by Chris Raper). The first British record of this species is reported in the article by Ivan Perry (pp. 61-62). Dipterists Digest Vol. 26 No. 1 Second Series 2019 th Published 28 June 2019 Published by ISSN 0953-7260 Dipterists Digest Editor Peter J. Chandler, 606B Berryfield Lane, Melksham, Wilts SN12 6EL (E-mail: [email protected]) Editorial Panel Graham Rotheray Keith Snow Alan Stubbs Derek Whiteley Phil Withers Dipterists Digest is the journal of the Dipterists Forum . It is intended for amateur, semi- professional and professional field dipterists with interests in British and European flies. All notes and papers submitted to Dipterists Digest are refereed. Articles and notes for publication should be sent to the Editor at the above address, and should be submitted with a current postal and/or e-mail address, which the author agrees will be published with their paper. Articles must not have been accepted for publication elsewhere and should be written in clear and concise English. Contributions should be supplied either as E-mail attachments or on CD in Word or compatible formats. The scope of Dipterists Digest is: - the behaviour, ecology and natural history of flies; - new and improved techniques (e.g. collecting, rearing etc.); - the conservation of flies; - reports from the Diptera Recording Schemes, including maps; - records and assessments of rare or scarce species and those new to regions, countries etc.; - local faunal accounts and field meeting results, especially if accompanied by ecological or natural history interpretation; - descriptions of species new to science; - notes on identification and deletions or amendments to standard key works and checklists.
    [Show full text]
  • Tri-Ology Vol 58, No. 1
    FDACS-P-00124 April - June 2020 Volume 59, Number 2 TRI- OLOGY A PUBLICATION FROM THE DIVISION OF PLANT INDUSTRY, BUREAU OF ENTOMOLOGY, NEMATOLOGY, AND PLANT PATHOLOGY Division Director, Trevor R. Smith, Ph.D. BOTANY ENTOMOLOGY NEMATOLOGY PLANT PATHOLOGY Providing information about plants: Identifying arthropods, taxonomic Providing certification programs and Offering plant disease diagnoses native, exotic, protected and weedy research and curating collections diagnoses of plant problems and information Florida Department of Agriculture and Consumer Services • Division of Plant Industry 1 Phaenomerus foveipennis (Morimoto), a conoderine weevil. Photo by Kyle E. Schnepp, DPI ABOUT TRI-OLOGY TABLE OF CONTENTS The Florida Department of Agriculture and Consumer Services- Division of Plant Industry’s (FDACS-DPI) Bureau of Entomology, HIGHLIGHTS 03 Nematology, and Plant Pathology (ENPP), including the Botany Noteworthy examples from the diagnostic groups Section, produces TRI-OLOGY four times a year, covering three throughout the ENPP Bureau. months of activity in each issue. The report includes detection activities from nursery plant inspections, routine and emergency program surveys, and BOTANY 04 requests for identification of plants and pests from the public. Samples are also occasionally sent from other states or countries Quarterly activity reports from Botany and selected plant identification samples. for identification or diagnosis. HOW TO CITE TRI-OLOGY Section Editor. Year. Section Name. P.J. Anderson and G.S. Hodges ENTOMOLOGY 07 (Editors). TRI-OLOGY Volume (number): page. [Date you accessed site.] Quarterly activity reports from Entomology and samples reported as new introductions or interceptions. For example: S.E. Halbert. 2015. Entomology Section. P.J. Anderson and G.S.
    [Show full text]
  • The Nestling Diet of Svalbard Snow Buntings Identified by DNA Metabarcoding
    Faculty of Biosciences, Fisheries and Economics, Department of Arctic and Marine Biology The nestling diet of Svalbard snow buntings identified by DNA metabarcoding — Christian Stolz BIO-3950 Master thesis in Biology, Northern Populations and Ecosystems, May 2019 Faculty of Biosciences, Fisheries and Economics, Department of Arctic and Marine Biology The nestling diet of Svalbard snow buntings identified by DNA metabarcoding Christian Stolz, UiT The Arctic University of Norway, Tromsø, Norway and The University Centre in Svalbard (UNIS), Longyearbyen, Norway BIO-3950 Master Thesis in Biology, Northern Populations and Ecosystems, May 2018 Supervisors: Frode Fossøy, Norwegian Institute for Nature Research (NINA), Trondheim, Norway Øystein Varpe, The University Centre in Svalbard (UNIS), Longyearbyen, Norway Rolf Anker Ims, UiT The Arctic University of Norway, Tromsø, Norway i Abstract Tundra arthropods have considerable ecological importance as a food source for several bird species that are reproducing in the Arctic. The actual arthropod taxa comprising the chick diet are however rarely known, complicating assessments of ecological interactions. In this study, I identified the nestling diet of Svalbard snow bunting (Plectrophenax nivalis) for the first time. Faecal samples of snow bunting chicks were collected in Adventdalen, Svalbard in the breeding season 2018 and analysed via DNA metabarcoding. Simultaneously, the availability of prey arthropods was measured via pitfall trapping. The occurrence of 32 identified prey taxa in the nestling diet changed according to varying abundances and emergence patterns within the tun- dra arthropod community: Snow buntings provisioned their offspring mainly with the most abundant prey items which were in the early season different Chironomidae (Diptera) taxa and Scathophaga furcata (Diptera: Scathophagidae), followed by Spilogona dorsata (Diptera: Mus- cidae).
    [Show full text]
  • High Consistency of Trophic Niches in Soil Microarthropod Species
    1 Supplementary materials 2 High consistency of trophic niches in soil microarthropod species 3 (Oribatida, Acari) across soil depth and forest type 4 Authors: Jing-Zhong Lu1*, Peter Cordes1, Mark Maraun1, Stefan Scheu1,2 5 6 Affiliations: 7 1. Johann-Friedrich-Blumenbach Institute of Zoology and Anthropology, Universität Göttingen, 8 Untere Karspüle 2, 37073 Göttingen, Germany 9 2. Center of Biodiversity and Sustainable Land Use, Universität Göttingen, Büsgenweg 1, 37077 10 Göttingen, Germany 11 * Corresponding author (E-mail: [email protected]) 12 13 Supplementary Tables 14 Table S1 15 Species list Oribatida (n = 40). Trophic guilds were assigned according to litter calibrated δ13C and 16 δ15N values: primary decomposer, secondary decomposer, endophagous Oribatida and 17 scavenger/predator. Total number of animals for each species used for stable isotopes and their 18 ranges (min - max) are given. Total number Trophic Oribatid taxa Family (range) δ13C δ15N guilds Ceratozetes minimus Sellnick, 1928 Ceratozetidae 10 (10-10) 2.95 ± 0.06 11.02 ± 0.17 predator Hypochthonius rufulus C. L. Koch, 1835 Hypochthoniidae 4 (2-7) 3.15 ± 0.77 6.23 ± 0.96 predator Metabelba pulverosa Strenzke, 1953 Damaeidae 3 (3-3) 3.08 ± 0.25 6.29 ± 2.40 predator Microppia minus (Paoli, 1908) Oppiidae 19 (7-25) 2.42 ± 0.28 8.74 ± 2.42 predator Oppiella nova (Oudemans, 1902) Oppiidae 14 (8-17) 2.70 ± 1.84 6.73 ± 2.79 predator Oppiella subpectinata (Oudemans, 1900) Oppiidae 9 (3-16) 2.93 ± 0.93 7.28 ± 1.96 predator Suctobelbella spp Jacot, 1937 Suctobelbidae 22 (18-26) 3.00 ± 0.74 6.69 ± 0.72 predator Acrogalumna longipluma (Berlese, 1904) Galumnidae 4 (3-5) 4.41 ± 0.18 5.06 ± 0.12 endophagous Carabodes ornatus Storkan, 1925 Carabodidae 2 (1-3) 3.26 ± 1.79 0.68 ± 0.52 endophagous Liacarus coracinus (C.
    [Show full text]
  • Muscidae (Insecta: Diptera) of Latin America and the Caribbean: Geographic Distribution and Check-List by Country
    Zootaxa 3650 (1): 001–147 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3650.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:E9059441-5893-41E4-9134-D4AD7AEB78FE ZOOTAXA 3650 Muscidae (Insecta: Diptera) of Latin America and the Caribbean: geographic distribution and check-list by country PETER LÖWENBERG-NETO1 & CLAUDIO J. B. DE CARVALHO2 1Universidade Federal da Integração Latino-Americana, C.P. 2064, CEP 85867-970, Foz do Iguaçu, PR, Brasil. E-mail: [email protected] 2Departamento de Zoologia, Universidade Federal do Paraná, C.P. 19020, CEP 81.531–980, Curitiba, PR, Brasil. E-mail: [email protected] Magnolia Press Auckland, New Zealand Accepted by S. Nihei: 14 Mar. 2013; published: 14 May 2013 PETER LÖWENBERG-NETO & CLAUDIO J. B. DE CARVALHO Muscidae (Insecta: Diptera) of Latin America and the Caribbean: geographic distribution and check-list by country (Zootaxa 3650) 147 pp.; 30 cm. 14 May 2013 ISBN 978-1-77557-156-8 (paperback) ISBN 978-1-77557-157-5 (Online edition) FIRST PUBLISHED IN 2013 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2013 Magnolia Press All rights reserved. No part of this publication may be reproduced, stored, transmitted or disseminated, in any form, or by any means, without prior written permission from the publisher, to whom all requests to reproduce copyright material should be directed in writing. This authorization does not extend to any other kind of copying, by any means, in any form, and for any purpose other than private research use.
    [Show full text]
  • Xavier Pons Catedràtic D'universitat
    Xavier Pons Catedràtic d'Universitat Dades personals Descaregar imagen Categoria: Catedràtic d'Universitat Àrea de coneixement: Entomologia Adreça: ETSEA, Edifici Principal B, despatx 1.13.2 Telèfon: +34 973 702824 E-mail: [email protected] [ mailto:[email protected] ] Formació Acadèmica · Doctorat, Universitat Politèecnica de Catalunya (UPC), 1986 · Enginyer Agrònom, UPC, 1983 · Enginyer Tècnic en Explotacions Agropecuàries, 1978 Experiència Professional · 2002 – Actualitat: Catedràtic d’Universitat, Universitat de Lleida (UdL), Departament de Producció Vegetal i Ciència Forestal · 1996 – 2002: Professor Titular d’Universitat, UdL, Departament de Producció Vegetal i Ciència Forestal · 1986 – 1996: Profesor Titular d’Escola Universitària, UdL, Departament de Producció Vegetal i Ciència Forestal · 1982 – 1986: Profesor Associat, UPC, Escola Universitària d’Enginyeria Tècnica Agrícola de Lleida Recerca · Control integrat de plagues de cultius herbacis extensius: panís, alfals i altres. · Biologia, ecologia i control de pugons. 1 · Control integrat de plagues en espais verds urbans. Docència · INCENDIS I SANITAT FORESTAL Grau en Enginyeria Forestal · SALUT SELS BOSCOS Grau en Enginyeria Forestal · PROTECCIÓ VEGETAL Grau en Enginyeria Agrària i Alimentària · ENTOMOLOGIA AGRÍCOLA Màster Universitari en Protecció Integrada de Cultius · PROGRAMES DE PROTECCIÓ INTEGRADA DE CULTIUS Màster Universitari en Protecció Integrada de Cultius Publicacions Recents Madeira F, di Lascio, Costantini ML, Rossi L, Pons X. 2019. Intercrop movement of heteropteran predators between alfalfa and maize examined by stable isotope analysis. Jorunal of Pest Science 92: 757-76. DOI: 10.1007/s10340-018-1049-y Karp D, Chaplin-Kramer R, Meehan TD, Martin EA, DeClerck F, et al. 2018. Crop pest and predators exhibit inconsistent responses to surrounding landscape composition.
    [Show full text]
  • The Armoured Mite Fauna (Acari: Oribatida) from a Long-Term Study in the Scots Pine Forest of the Northern Vidzeme Biosphere Reserve, Latvia
    FRAGMENTA FAUNISTICA 57 (2): 141–149, 2014 PL ISSN 0015-9301 © MUSEUM AND INSTITUTE OF ZOOLOGY PAS DOI 10.3161/00159301FF2014.57.2.141 The armoured mite fauna (Acari: Oribatida) from a long-term study in the Scots pine forest of the Northern Vidzeme Biosphere Reserve, Latvia 1 2 1 Uģis KAGAINIS , Voldemārs SPUNĢIS and Viesturs MELECIS 1 Institute of Biology, University of Latvia, 3 Miera Street, LV-2169, Salaspils, Latvia; e-mail: [email protected] (corresponding author) 2 Department of Zoology and Animal Ecology, Faculty of Biology,University of Latvia, 4 Kronvalda Blvd., LV-1586, Riga, Latvia; e-mail: [email protected] Abstract: In 1992–2012, a considerable amount of soil micro-arthropods has been collected annually as a part of a project of the National Long-Term Ecological Research Network of Latvia at the Mazsalaca Scots Pine forest sites of the North Vidzeme Biosphere Reserve. Until now, the data on oribatid species have not been published. This paper presents a list of oribatid species collected during 21 years of ongoing research in three pine stands of different age. The faunistic records refer to 84 species (including 17 species new to the fauna of Latvia), 1 subspecies, 1 form, 5 morphospecies and 18 unidentified taxa. The most dominant and most frequent oribatid species are Oppiella (Oppiella) nova, Tectocepheus velatus velatus and Suctobelbella falcata. Key words: species list, fauna, stand-age, LTER, Mazsalaca INTRODUCTION Most studies of Oribatida or the so-called armoured mites (Subías 2004) have been relatively short term and/or from different ecosystems simultaneously and do not show long- term changes (Winter et al.
    [Show full text]
  • Species List
    The species collected in all Malaise traps are listed below. They are organized by group and are listed in the order of the 'Species Image Library'. ‘New’ refers to species that are brand new to our DNA barcode library. 'Rare' refers to species that were only collected in one trap out of all 59 that were deployed for the program.
    [Show full text]
  • Woolly Oak Aphids Stegophylla Brevirostris Quednau and Diphyllaphis Microtrema Quednau (Insecta: Hemiptera: Aphididae)1 Susan E
    EENY574 Woolly oak aphids Stegophylla brevirostris Quednau and Diphyllaphis microtrema Quednau (Insecta: Hemiptera: Aphididae)1 Susan E. Halbert2 The Featured Creatures collection provides in-depth profiles flocculent wax. Two genera of woolly oak aphids occur in of insects, nematodes, arachnids and other organisms Florida, each including one known native Florida species. relevant to Florida. These profiles are intended for the use of One species, Stegophylla brevirostris Quednau, is common, interested laypersons with some knowledge of biology as well and the other, Diphyllaphis microtrema Quednau, is rare. as academic audiences. Distribution Introduction Both species occur in eastern North America. Stegophylla brevirostris is a pest only in Florida. Description Florida woolly oak aphids can be recognized easily by the large quantities of woolly wax that they secrete (Figs. 1, 2). Beneath the wax, the aphid bodies are pale. Young nymphs can be pale green, and they tend to be more mobile than adults. Excreted honeydew forms brown droplets in the wax. Separation of the two species is based on microscopic characters. Both species have short appendages and pore- like siphunculi. They lack the tubular siphunculi present in many species of aphids. Species of Stegophylla have larger siphuncular pores, with a ring of setae surrounding them (Figs. 3, 4). Species of Diphyllaphis have minute siphuncular Figure 1. Stegophylla brevirostris Quednau colony on oak. pores that lack setae (Figs. 5, 6). The majority (59%) of DPI Credits: Susan E. Halbert records for Stegophylla brevirostris indicate that live oak (Quercus virginiana Mill.) was the host. A few records came Woolly oak aphids are conspicuous pests on oak (Quercus from other species of oaks.
    [Show full text]
  • Hotspots of Mite New Species Discovery: Sarcoptiformes (2013–2015)
    Zootaxa 4208 (2): 101–126 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Editorial ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4208.2.1 http://zoobank.org/urn:lsid:zoobank.org:pub:47690FBF-B745-4A65-8887-AADFF1189719 Hotspots of mite new species discovery: Sarcoptiformes (2013–2015) GUANG-YUN LI1 & ZHI-QIANG ZHANG1,2 1 School of Biological Sciences, the University of Auckland, Auckland, New Zealand 2 Landcare Research, 231 Morrin Road, Auckland, New Zealand; corresponding author; email: [email protected] Abstract A list of of type localities and depositories of new species of the mite order Sarciptiformes published in two journals (Zootaxa and Systematic & Applied Acarology) during 2013–2015 is presented in this paper, and trends and patterns of new species are summarised. The 242 new species are distributed unevenly among 50 families, with 62% of the total from the top 10 families. Geographically, these species are distributed unevenly among 39 countries. Most new species (72%) are from the top 10 countries, whereas 61% of the countries have only 1–3 new species each. Four of the top 10 countries are from Asia (Vietnam, China, India and The Philippines). Key words: Acari, Sarcoptiformes, new species, distribution, type locality, type depository Introduction This paper provides a list of the type localities and depositories of new species of the order Sarciptiformes (Acari: Acariformes) published in two journals (Zootaxa and Systematic & Applied Acarology (SAA)) during 2013–2015 and a summary of trends and patterns of these new species. It is a continuation of a previous paper (Liu et al.
    [Show full text]
  • Biology and Ecology of Leptographium Species and Their Vectos As Components of Loblolly Pine Decline Lori G
    Louisiana State University LSU Digital Commons LSU Doctoral Dissertations Graduate School 2003 Biology and ecology of Leptographium species and their vectos as components of loblolly pine decline Lori G. Eckhardt Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_dissertations Part of the Plant Sciences Commons Recommended Citation Eckhardt, Lori G., "Biology and ecology of Leptographium species and their vectos as components of loblolly pine decline" (2003). LSU Doctoral Dissertations. 2133. https://digitalcommons.lsu.edu/gradschool_dissertations/2133 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Doctoral Dissertations by an authorized graduate school editor of LSU Digital Commons. For more information, please [email protected]. BIOLOGY AND ECOLOGY OF LEPTOGRAPHIUM SPECIES AND THEIR VECTORS AS COMPONENTS OF LOBLOLLY PINE DECLINE A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Plant Pathology & Crop Physiology by Lori G. Eckhardt B.S., University of Maryland, 1997 August 2003 © Copyright 2003 Lori G. Eckhardt All rights reserved ii ACKNOWLEDGMENTS I gratefully acknowledge the invaluable input provided by my dissertation advisor, Dr. John P. Jones. Among many other things, he has demonstrated his patients, enthusiasm and understanding as I struggled to pursue my graduate studies. I am indebted to Dr. Marc A. Cohn, for his guidance, encouragement, support and most of all, his friendship.
    [Show full text]
  • Kenai National Wildlife Refuge Species List, Version 2018-07-24
    Kenai National Wildlife Refuge Species List, version 2018-07-24 Kenai National Wildlife Refuge biology staff July 24, 2018 2 Cover image: map of 16,213 georeferenced occurrence records included in the checklist. Contents Contents 3 Introduction 5 Purpose............................................................ 5 About the list......................................................... 5 Acknowledgments....................................................... 5 Native species 7 Vertebrates .......................................................... 7 Invertebrates ......................................................... 55 Vascular Plants........................................................ 91 Bryophytes ..........................................................164 Other Plants .........................................................171 Chromista...........................................................171 Fungi .............................................................173 Protozoans ..........................................................186 Non-native species 187 Vertebrates ..........................................................187 Invertebrates .........................................................187 Vascular Plants........................................................190 Extirpated species 207 Vertebrates ..........................................................207 Vascular Plants........................................................207 Change log 211 References 213 Index 215 3 Introduction Purpose to avoid implying
    [Show full text]