AR-120: 2007 KAES Annual Report
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CHESTNUT (CASTANEA Spp.) CULTIVAR EVALUATION for COMMERCIAL CHESTNUT PRODUCTION
CHESTNUT (CASTANEA spp.) CULTIVAR EVALUATION FOR COMMERCIAL CHESTNUT PRODUCTION IN HAMILTON COUNTY, TENNESSEE By Ana Maria Metaxas Approved: James Hill Craddock Jennifer Boyd Professor of Biological Sciences Assistant Professor of Biological and Environmental Sciences (Director of Thesis) (Committee Member) Gregory Reighard Jeffery Elwell Professor of Horticulture Dean, College of Arts and Sciences (Committee Member) A. Jerald Ainsworth Dean of the Graduate School CHESTNUT (CASTANEA spp.) CULTIVAR EVALUATION FOR COMMERCIAL CHESTNUT PRODUCTION IN HAMILTON COUNTY, TENNESSEE by Ana Maria Metaxas A Thesis Submitted to the Faculty of the University of Tennessee at Chattanooga in Partial Fulfillment of the Requirements for the Degree of Master of Science in Environmental Science May 2013 ii ABSTRACT Chestnut cultivars were evaluated for their commercial applicability under the environmental conditions in Hamilton County, TN at 35°13ꞌ 45ꞌꞌ N 85° 00ꞌ 03.97ꞌꞌ W elevation 230 meters. In 2003 and 2004, 534 trees were planted, representing 64 different cultivars, varieties, and species. Twenty trees from each of 20 different cultivars were planted as five-tree plots in a randomized complete block design in four blocks of 100 trees each, amounting to 400 trees. The remaining 44 chestnut cultivars, varieties, and species served as a germplasm collection. These were planted in guard rows surrounding the four blocks in completely randomized, single-tree plots. In the analysis, we investigated our collection predominantly with the aim to: 1) discover the degree of acclimation of grower- recommended cultivars to southeastern Tennessee climatic conditions and 2) ascertain the cultivars’ ability to survive in the area with Cryphonectria parasitica and other chestnut diseases and pests present. -
Seed Germination of the Halophyte Anabasis Setifera (Amaranthaceae) from Saudi Arabia
Botany Seed germination of the halophyte Anabasis setifera (Amaranthaceae) from Saudi Arabia. Journal: Botany Manuscript ID cjb-2018-0053.R1 Manuscript Type: Article Date Submitted by the Author: 19-May-2018 Complete List of Authors: Basahi, Mohammed; Shaqra University College of Science and Arts Sajir, biology; Anabasis setifera,Draft halophyte, Temperature, Germination, seed germination Keyword: recovery Is the invited manuscript for consideration in a Special Not applicable (regular submission) Issue? : https://mc06.manuscriptcentral.com/botany-pubs Page 1 of 27 Botany Seed germination of the halophyte Anabasis setifera (Amaranthaceae) from Saudi Arabia. Mohammed A Basahi College of Science and Arts Sajir Shaqra University P.O. Box 33, Shaqra 11961 Saudi Arabia [email protected] Draft00966582223689 1 https://mc06.manuscriptcentral.com/botany-pubs Botany Page 2 of 27 Abstract The main objective of this study was to determine the effects of temperature, light/darkness, and salinity (NaCl) on seed germination of Anabasis setifera Moq. and the effects of alleviating salinity stress using distilled water. One-hundred percent of seeds completed germination at 15/5, 20/10, and 20°C, and a higher percentage of seeds completed germinationin light than in the dark at 20/10 and 25/15°C. The percentage of seeds that completed the germination decreased as salinity increased from 0 to 700 mM NaCl. Seeds that did not complete germination in the 800 or 700 mM NaCl solutions completed its germinationDraft after being transferred to distilled water, with a recovery rate of 94.5% and 75.5%, respectively, at 25/15°C. The inhibitory effect of NaCl on the completion of germination in this species probably occurs via an osmotic effect. -
Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2
Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) by Boris C. Kondratieff, Paul A. Opler, Matthew C. Garhart, and Jason P. Schmidt C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 March 15, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration (top to bottom): Widow Skimmer (Libellula luctuosa) [photo ©Robert Behrstock], Stonefly (Perlesta species) [photo © David H. Funk, White- lined Sphinx (Hyles lineata) [photo © Matthew C. Garhart] ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences, Colorado State University, Fort Collins, Colorado 80523 Copyrighted 2004 Table of Contents EXECUTIVE SUMMARY……………………………………………………………………………….…1 INTRODUCTION…………………………………………..…………………………………………….…3 OBJECTIVE………………………………………………………………………………………….………5 Site Descriptions………………………………………….. METHODS AND MATERIALS…………………………………………………………………………….5 RESULTS AND DISCUSSION………………………………………………………………………..…...11 Dragonflies………………………………………………………………………………….……..11 -
ECO-Ssls for Pahs
Ecological Soil Screening Levels for Polycyclic Aromatic Hydrocarbons (PAHs) Interim Final OSWER Directive 9285.7-78 U.S. Environmental Protection Agency Office of Solid Waste and Emergency Response 1200 Pennsylvania Avenue, N.W. Washington, DC 20460 June 2007 This page intentionally left blank TABLE OF CONTENTS 1.0 INTRODUCTION .......................................................1 2.0 SUMMARY OF ECO-SSLs FOR PAHs......................................1 3.0 ECO-SSL FOR TERRESTRIAL PLANTS....................................4 5.0 ECO-SSL FOR AVIAN WILDLIFE.........................................8 6.0 ECO-SSL FOR MAMMALIAN WILDLIFE..................................8 6.1 Mammalian TRV ...................................................8 6.2 Estimation of Dose and Calculation of the Eco-SSL ........................9 7.0 REFERENCES .........................................................16 7.1 General PAH References ............................................16 7.2 References Used for Derivation of Plant and Soil Invertebrate Eco-SSLs ......17 7.3 References Rejected for Use in Derivation of Plant and Soil Invertebrate Eco-SSLs ...............................................................18 7.4 References Used in Derivation of Wildlife TRVs .........................25 7.5 References Rejected for Use in Derivation of Wildlife TRV ................28 i LIST OF TABLES Table 2.1 PAH Eco-SSLs (mg/kg dry weight in soil) ..............................4 Table 3.1 Plant Toxicity Data - PAHs ..........................................5 Table 4.1 -
Complex Patterns of Phenotypic Plasticity: Interactive Effects of Temperature During Rearing and Oviposition
Ecology, 86(4), 2005, pp. 924±934 q 2005 by the Ecological Society of America COMPLEX PATTERNS OF PHENOTYPIC PLASTICITY: INTERACTIVE EFFECTS OF TEMPERATURE DURING REARING AND OVIPOSITION R. CRAIG STILLWELL1 AND CHARLES W. F OX Department of Entomology, University of Kentucky, S-225 Ag Science Center North, Lexington, Kentucky 40546-0091 USA Abstract. Temperature profoundly affects growth and life history traits in ectothermic animals through selection (i.e., genetic) and through direct effects on the phenotype (i.e., nongenetic/plasticity). We examined the effects of rearing temperature (248,308, and 368C) on adult body size and development time and the interactive effects of temperature ex- perienced during rearing and oviposition on several life history traits (age-at-®rst-repro- duction, fecundity, egg size, egg development, and egg hatching) in two populations of the seed beetle, Stator limbatus, collected at different elevations. The higher elevation popu- lation was larger and matured sooner than the low-elevation population when raised at the lower temperature, but the reverse was true at the higher temperature suggesting that these populations have adapted to local temperature. There were interactions between the effects of rearing temperature and oviposition temperature for age-at-®rst-reproduction, fecundity, egg development, egg hatching, and two composite measures of ®tness, generating complex reaction norms. The most dramatic example of this was a large maternal effect on egg hatching; females raised at low temperature produced eggs that had substantially reduced hatching when laid at high temperature. Our experimental design also allowed us to explore the adaptive signi®cance of acclimation. Beetles reared at intermediate or low temperature had the highest ®tness at multiple oviposition temperatures. -
Hymenoptera, Braconidae) from India
A peer-reviewed open-access journal ZooKeys 889: 23–35 (2019) Two new species of Braconidae from India 23 doi: 10.3897/zookeys.889.36436 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Two new species of braconid wasps (Hymenoptera, Braconidae) from India Zubair Ahmad1,2,4, Hamed A. Ghramh1,2,3, Anjum Ansari5 1 Research Center for Advanced Materials Science (RCAMS), King Khalid University, 9004, Abha 61413, Saudi Arabia 2 Unit of Bee Research and Honey Production, Faculty of Science, King Khalid University, P.O. Box 9004, Abha 61413, Saudi Arabia 3 Biology Department, Faculty of Science, King Khalid University, P.O. Box 9004, Abha 61413, Saudi Arabia 4 Biology Department, Faculty of Sciences and Arts, Dhahran Al Janoub, King Khalid University, Saudi Arabia 5 Department of Zoology, Aligarh Muslim University, Aligarh, 202002, UP., India Corresponding author: Zubair Ahmad ([email protected]) Academic editor: J. Fernandez-Triana | Received 22 May 2019 | Accepted 26 August 2019 | Published 14 November 2019 http://zoobank.org/D1E6D6F0-B26A-4091-81F8-2BD43F563F4F Citation: Ahmad Z, Ghramh HA, Ansari A (2019) Two new species of braconid wasps (Hymenoptera, Braconidae) from India. ZooKeys 889: 23–35. https://doi.org/10.3897/zookeys.889.36436 Abstract Two new species viz., Pambolus (Phaenodus) shujai sp. nov., and Parachremylus trachysi sp. nov., of braco- nid wasps are described as new to science. Parachremylus trachysi sp. nov., is reared from larvae of the leaf miner Trachys sp. (Coleoptera, Buprestidae) on Corchorus sp. (Wild Jute Plant). A new species of Pambolus Haliday along with two known species is also recorded. -
Fauna Europaea: Hymenoptera – Symphyta & Ichneumonoidea Van Achterberg, K.; Taeger, A.; Blank, S.M.; Zwakhals, K.; Viitasaari, M.; Yu, D.S.K.; De Jong, Y
UvA-DARE (Digital Academic Repository) Fauna Europaea: Hymenoptera – Symphyta & Ichneumonoidea van Achterberg, K.; Taeger, A.; Blank, S.M.; Zwakhals, K.; Viitasaari, M.; Yu, D.S.K.; de Jong, Y. DOI 10.3897/BDJ.5.e14650 Publication date 2017 Document Version Final published version Published in Biodiversity Data Journal License CC BY Link to publication Citation for published version (APA): van Achterberg, K., Taeger, A., Blank, S. M., Zwakhals, K., Viitasaari, M., Yu, D. S. K., & de Jong, Y. (2017). Fauna Europaea: Hymenoptera – Symphyta & Ichneumonoidea. Biodiversity Data Journal, 5, [e14650]. https://doi.org/10.3897/BDJ.5.e14650 General rights It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons). Disclaimer/Complaints regulations If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: https://uba.uva.nl/en/contact, or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible. UvA-DARE is a service provided by the library of the University of Amsterdam (https://dare.uva.nl) Download date:27 Sep 2021 Biodiversity Data Journal 5: e14650 doi: 10.3897/BDJ.5.e14650 Data Paper Fauna Europaea: Hymenoptera – Symphyta & Ichneumonoidea Kees van Achterberg‡, Andreas Taeger§, Stephan M. -
Origin and Age of Australian Chenopodiaceae
ARTICLE IN PRESS Organisms, Diversity & Evolution 5 (2005) 59–80 www.elsevier.de/ode Origin and age of Australian Chenopodiaceae Gudrun Kadereita,Ã, DietrichGotzek b, Surrey Jacobsc, Helmut Freitagd aInstitut fu¨r Spezielle Botanik und Botanischer Garten, Johannes Gutenberg-Universita¨t Mainz, D-55099 Mainz, Germany bDepartment of Genetics, University of Georgia, Athens, GA 30602, USA cRoyal Botanic Gardens, Sydney, Australia dArbeitsgruppe Systematik und Morphologie der Pflanzen, Universita¨t Kassel, D-34109 Kassel, Germany Received 20 May 2004; accepted 31 July 2004 Abstract We studied the age, origins, and possible routes of colonization of the Australian Chenopodiaceae. Using a previously published rbcL phylogeny of the Amaranthaceae–Chenopodiaceae alliance (Kadereit et al. 2003) and new ITS phylogenies of the Camphorosmeae and Salicornieae, we conclude that Australia has been reached in at least nine independent colonization events: four in the Chenopodioideae, two in the Salicornieae, and one each in the Camphorosmeae, Suaedeae, and Salsoleae. Where feasible, we used molecular clock estimates to date the ages of the respective lineages. The two oldest lineages both belong to the Chenopodioideae (Scleroblitum and Chenopodium sect. Orthosporum/Dysphania) and date to 42.2–26.0 and 16.1–9.9 Mya, respectively. Most lineages (Australian Camphorosmeae, the Halosarcia lineage in the Salicornieae, Sarcocornia, Chenopodium subg. Chenopodium/Rhagodia, and Atriplex) arrived in Australia during the late Miocene to Pliocene when aridification and increasing salinity changed the landscape of many parts of the continent. The Australian Camphorosmeae and Salicornieae diversified rapidly after their arrival. The molecular-clock results clearly reject the hypothesis of an autochthonous stock of Chenopodiaceae dating back to Gondwanan times. -
Santalales: Opiliaceae) in Taiwan
Biodiversity Data Journal 8: e51544 doi: 10.3897/BDJ.8.e51544 Taxonomic Paper First report of the root parasite Cansjera rheedei (Santalales: Opiliaceae) in Taiwan Po-Hao Chen‡, An-Ching Chung§, Sheng-Zehn Yang| ‡ Graduate Institute of Bioresources, National Pingtung University of Science and Technology, Neipu Township, Pintung, Taiwan § Liouguei Research Center, Taiwan Forest Research Institute, Liouguei District, Kaohsiung, Taiwan | Department of Forestry, National Pingtung University of Science and Technology, Neipu Township, Pintung, Taiwan Corresponding author: Sheng-Zehn Yang ([email protected]) Academic editor: Yasen Mutafchiev Received: 27 Feb 2020 | Accepted: 08 Apr 2020 | Published: 10 Apr 2020 Citation: Chen P-H, Chung A-C, Yang S-Z (2020) First report of the root parasite Cansjera rheedei (Santalales: Opiliaceae) in Taiwan. Biodiversity Data Journal 8: e51544. https://doi.org/10.3897/BDJ.8.e51544 Abstract Background The family Opiliaceae in Santalales comprises approximately 38 species within 12 genera distributed worldwide. In Taiwan, only one species of the tribe Champereieae, Champereia manillana, has been recorded. Here we report the first record of a second member of Opiliaceae, Cansjera in tribe Opilieae, for Taiwan. New information The newly-found species, Cansjera rheedei J.F. Gmelin (Opiliaceae), is a liana distributed from India and Nepal to southern China and western Malaysia. This is the first record of both the genus Cansjera and the tribe Opilieae of Opiliaceae in Taiwan. In this report, we provide a taxonomic description for the species and colour photographs to facilitate identification in the field. © Chen P et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. -
The Canadian Ent~~S&O'gis T
The Canadian Ent~~s&o'gist - - Vol. 100 Ottawa, Canada, October 1 29 1968 No. 10 NOTES ON BRUCHIDAE OF AMERICA NORWFMEXICO WITH A LIST OF WORLD GEI^~^^~'~^ L. J. BOTTIMER' Entomology Research Institute, Canada Department of Agriculture, Ottawa Abstract Can. Ent. 100: 1009-1049 (1968) This paper contains notes affecting the classification of the Bruchidae of United States and Canada, a list of all species found north of AfIexico, and a list of World genera and their type-species. The Mexican Merobrzichzis vacillator (Sharp) is added to the fauna of this area. Transferred from our list to that of Latin America are: Acanthoscelides ca1ifornicu.r (Boheman), Megacerus ez~genie new name for Brucbus micornis Boheman nec Erichson, and Mimosestes innotatits (Pic.). The following are synonynlizecl: Spernwpl~gzis (Zabrotes) se~fiicinctzisHorn (1894) with Zabrotes snbfasciatzis (Bohenlan 1833) ; Brzicbus siibserripes Fall (1910) with Acanthoscelides compressicornis (Schaeffer 1907); Litl~raeus electus Bridwell (1952) with Litbraens elegans (Blanchard 1851); Brzicbus a/lioguttatus Motschoulsky (1874) with Meibomeus in-iisculiis (Say 1831) ; Britcbzis bivzilneratus Horn ( 1873) with Brzicbus abbreviates, inadvertently validated by Say = Sennius abbreviates (Say 1824); Br-nc/~zisnigrinus Horn (1873), B. nictitans Motschoulsliy (1874), and B. depresses Fall (1912) with Sennius cmentatits (Horn 1873) ; Br-nchus pytboniciis Pic (191 3) with Stator midialis (Schaeffer 1907) ; and Brzicl7zis bigzittatus Fabricius (1801) = Bruclms bignttellzis Schocnherr (1833) with Callosobr-ncbus chinensis (Linnaeus 1758). Original spellings of the specific names of two species are revived: Megacerus pygidatis (Mot~~h~~l~liy)nec pygidialis Pic, and Megacms discoidus (Say) nec discoidens: authors. Knichus lividus J. E. LeContc 1824 is placed in our list as an unrccogni~cdspecies. -
A New Symbiotic Lineage Related to Neisseria and Snodgrassella Arises from the Dynamic and Diverse Microbiomes in Sucking Lice
bioRxiv preprint doi: https://doi.org/10.1101/867275; this version posted December 6, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. A new symbiotic lineage related to Neisseria and Snodgrassella arises from the dynamic and diverse microbiomes in sucking lice Jana Říhová1, Giampiero Batani1, Sonia M. Rodríguez-Ruano1, Jana Martinů1,2, Eva Nováková1,2 and Václav Hypša1,2 1 Department of Parasitology, Faculty of Science, University of South Bohemia, České Budějovice, Czech Republic 2 Institute of Parasitology, Biology Centre, ASCR, v.v.i., České Budějovice, Czech Republic Author for correspondence: Václav Hypša, Department of Parasitology, University of South Bohemia, České Budějovice, Czech Republic, +42 387 776 276, [email protected] Abstract Phylogenetic diversity of symbiotic bacteria in sucking lice suggests that lice have experienced a complex history of symbiont acquisition, loss, and replacement during their evolution. By combining metagenomics and amplicon screening across several populations of two louse genera (Polyplax and Hoplopleura) we describe a novel louse symbiont lineage related to Neisseria and Snodgrassella, and show its' independent origin within dynamic lice microbiomes. While the genomes of these symbionts are highly similar in both lice genera, their respective distributions and status within lice microbiomes indicate that they have different functions and history. In Hoplopleura acanthopus, the Neisseria-related bacterium is a dominant obligate symbiont universally present across several host’s populations, and seems to be replacing a presumably older and more degenerated obligate symbiont. -
Journal of Hymenoptera Research
c 3 Journal of Hymenoptera Research . .IV 6«** Volume 15, Number 2 October 2006 ISSN #1070-9428 CONTENTS BELOKOBYLSKIJ, S. A. and K. MAETO. A new species of the genus Parachremylus Granger (Hymenoptera: Braconidae), a parasitoid of Conopomorpha lychee pests (Lepidoptera: Gracillariidae) in Thailand 181 GIBSON, G. A. P., M. W. GATES, and G. D. BUNTIN. Parasitoids (Hymenoptera: Chalcidoidea) of the cabbage seedpod weevil (Coleoptera: Curculionidae) in Georgia, USA 187 V. Forest GILES, and J. S. ASCHER. A survey of the bees of the Black Rock Preserve, New York (Hymenoptera: Apoidea) 208 GUMOVSKY, A. V. The biology and morphology of Entedon sylvestris (Hymenoptera: Eulophidae), a larval endoparasitoid of Ceutorhynchus sisymbrii (Coleoptera: Curculionidae) 232 of KULA, R. R., G. ZOLNEROWICH, and C. J. FERGUSON. Phylogenetic analysis Chaenusa sensu lato (Hymenoptera: Braconidae) using mitochondrial NADH 1 dehydrogenase gene sequences 251 QUINTERO A., D. and R. A. CAMBRA T The genus Allotilla Schuster (Hymenoptera: Mutilli- dae): phylogenetic analysis of its relationships, first description of the female and new distribution records 270 RIZZO, M. C. and B. MASSA. Parasitism and sex ratio of the bedeguar gall wasp Diplolqjis 277 rosae (L.) (Hymenoptera: Cynipidae) in Sicily (Italy) VILHELMSEN, L. and L. KROGMANN. Skeletal anatomy of the mesosoma of Palaeomymar anomalum (Blood & Kryger, 1922) (Hymenoptera: Mymarommatidae) 290 WHARTON, R. A. The species of Stenmulopius Fischer (Hymenoptera: Braconidae, Opiinae) and the braconid sternaulus 316 (Continued on back cover) INTERNATIONAL SOCIETY OF HYMENOPTERISTS Organized 1982; Incorporated 1991 OFFICERS FOR 2006 Michael E. Schauff, President James Woolley, President-Elect Michael W. Gates, Secretary Justin O. Schmidt, Treasurer Gavin R.