Section Reports Following Are a Few of the Notable Entries from This Volume of TRI-OLOGY
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Natural Heritage Program List of Rare Plant Species of North Carolina 2016
Natural Heritage Program List of Rare Plant Species of North Carolina 2016 Revised February 24, 2017 Compiled by Laura Gadd Robinson, Botanist John T. Finnegan, Information Systems Manager North Carolina Natural Heritage Program N.C. Department of Natural and Cultural Resources Raleigh, NC 27699-1651 www.ncnhp.org C ur Alleghany rit Ashe Northampton Gates C uc Surry am k Stokes P d Rockingham Caswell Person Vance Warren a e P s n Hertford e qu Chowan r Granville q ot ui a Mountains Watauga Halifax m nk an Wilkes Yadkin s Mitchell Avery Forsyth Orange Guilford Franklin Bertie Alamance Durham Nash Yancey Alexander Madison Caldwell Davie Edgecombe Washington Tyrrell Iredell Martin Dare Burke Davidson Wake McDowell Randolph Chatham Wilson Buncombe Catawba Rowan Beaufort Haywood Pitt Swain Hyde Lee Lincoln Greene Rutherford Johnston Graham Henderson Jackson Cabarrus Montgomery Harnett Cleveland Wayne Polk Gaston Stanly Cherokee Macon Transylvania Lenoir Mecklenburg Moore Clay Pamlico Hoke Union d Cumberland Jones Anson on Sampson hm Duplin ic Craven Piedmont R nd tla Onslow Carteret co S Robeson Bladen Pender Sandhills Columbus New Hanover Tidewater Coastal Plain Brunswick THE COUNTIES AND PHYSIOGRAPHIC PROVINCES OF NORTH CAROLINA Natural Heritage Program List of Rare Plant Species of North Carolina 2016 Compiled by Laura Gadd Robinson, Botanist John T. Finnegan, Information Systems Manager North Carolina Natural Heritage Program N.C. Department of Natural and Cultural Resources Raleigh, NC 27699-1651 www.ncnhp.org This list is dynamic and is revised frequently as new data become available. New species are added to the list, and others are dropped from the list as appropriate. -
"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
Biosecurity Plan for the Vegetable Industry
Biosecurity Plan for the Vegetable Industry A shared responsibility between government and industry Version 3.0 May 2018 Plant Health AUSTRALIA Location: Level 1 1 Phipps Close DEAKIN ACT 2600 Phone: +61 2 6215 7700 Fax: +61 2 6260 4321 E-mail: [email protected] Visit our web site: www.planthealthaustralia.com.au An electronic copy of this plan is available through the email address listed above. © Plant Health Australia Limited 2018 Copyright in this publication is owned by Plant Health Australia Limited, except when content has been provided by other contributors, in which case copyright may be owned by another person. With the exception of any material protected by a trade mark, this publication is licensed under a Creative Commons Attribution-No Derivs 3.0 Australia licence. Any use of this publication, other than as authorised under this licence or copyright law, is prohibited. http://creativecommons.org/licenses/by-nd/3.0/ - This details the relevant licence conditions, including the full legal code. This licence allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to Plant Health Australia (as below). In referencing this document, the preferred citation is: Plant Health Australia Ltd (2018) Biosecurity Plan for the Vegetable Industry (Version 3.0 – 2018) Plant Health Australia, Canberra, ACT. This project has been funded by Hort Innovation, using the vegetable research and development levy and contributions from the Australian Government. Hort Innovation is the grower-owned, not for profit research and development corporation for Australian horticulture Disclaimer: The material contained in this publication is produced for general information only. -
Arachnids (Excluding Acarina and Pseudoscorpionida) of the Wichita Mountains Wildlife Refuge, Oklahoma
OCCASIONAL PAPERS THE MUSEUM TEXAS TECH UNIVERSITY NUMBER 67 5 SEPTEMBER 1980 ARACHNIDS (EXCLUDING ACARINA AND PSEUDOSCORPIONIDA) OF THE WICHITA MOUNTAINS WILDLIFE REFUGE, OKLAHOMA JAMES C. COKENDOLPHER AND FRANK D. BRYCE The Wichita Mountains are located in eastern Greer, southern Kiowa, and northwestern Comanche counties in Oklahoma. Since their formation more than 300 million years ago, these rugged mountains have been fragmented and weathered, until today the highest peak (Mount Pinchot) stands only 756 meters above sea level (Tyler, 1977). The mountains are composed predominantly of granite and gabbro. Forests of oak, elm, and walnut border most waterways, while at elevations from 153 to 427 meters prair ies are the predominant vegetation type. A more detailed sum mary of the climatic and biotic features of the Wichitas has been presented by Blair and Hubbell (1938). A large tract of land in the eastern range of the Wichita Moun tains (now northeastern Comanche County) was set aside as the Wichita National Forest by President McKinley during 1901. In 1905, President Theodore Roosevelt created a game preserve on those lands managed by the Forest Service. Since 1935, this pre serve has been known as the Wichita Mountains Wildlife Refuge. Numerous papers on Oklahoma spiders have been published (Bailey and Chada, 1968; Bailey et al., 1968; Banks et al, 1932; Branson, 1958, 1959, 1966, 1968; Branson and Drew, 1972; Gro- thaus, 1968; Harrel, 1962, 1965; Horner, 1975; Rogers and Horner, 1977), but only a single, comprehensive work (Banks et al., 1932) exists covering all arachnid orders in the state. Further additions and annotations to the arachnid fauna of Oklahoma can be found 2 OCCASIONAL PAPERS MUSEUM TEXAS TECH UNIVERSITY in recent revisionary studies. -
SPIDERS of WASHINGTON COUNTY, MISSISSIPPI Orrey P. Young Southern Field Crop Insect Management Laboratory USDA-ARS, P.O. Box
Young, O . P., T. C . Lockley and G . B . Edwards . 1989 . Spiders of Washington County, Mississippi . J . Arachnol ., 17 :27-41 . SPIDERS OF WASHINGTON COUNTY, MISSISSIPPI Orrey P. Young Southern Field Crop Insect Management Laboratory USDA-ARS, P.O. Box 346 Stoneville, Mississippi 38776 USA Timothy C. Lockley Imported Fire Ant Station USDA-APHIS-PPQ 3505 25th Avenue Gulfport, Mississippi 39501 USA and G. B. Edwards Florida State Collection of Arthropods Division of Plant Industry Florida Dept. Agric. & Cons . Serv. P.O. Box 1269 Gainesville, Florida 32602 USA ABSTRACT Over a seven-year period, approximately 35,000 spiders representing 26 families, 133 genera, and 234 species were captured in Washington County, Mississippi, by pitfall, sweepnet, vacuum, bag, and hand. Specimens were collected in 10 different habitat types and in four vegetational strata . Old-field habitats yielded the most species (152) and residential lawns the fewest (14) . Considering all habitats sampled, the ground layer produced 111 species, the herbaceous strata 133, the shrub layer 49, and the tree strata 30 species . The sweepnet method of capture obtained 128 species, pitfall 95, hand 61, vacuum 53, and bagging 19 species. The largest number of species were obtained in spring and early summer (maximum of 125 in May), with the fewest in mid-winter (Jan . = 24) . Twenty-one species were considered abundant, 51 common, 67 uncommon, and 95 rare . Additions to the state list of Dorris (1972) number 102 species, for a new state total of 364 species . A comparison with the North American fauna and with other surveys indicates that Washington County is underrepresented both in cursorial forms active on the soil surface and web-spinning forms typical of undisturbed habitats . -
Wiesław Krzemiński—A Man of a Great Passion for Fossil Flies
Palaeoentomology 003 (5): 434–444 ISSN 2624-2826 (print edition) https://www.mapress.com/j/pe/ PALAEOENTOMOLOGY PE Copyright © 2020 Magnolia Press Editorial ISSN 2624-2834 (online edition) https://doi.org/10.11646/palaeoentomology.3.5.1 http://zoobank.org/urn:lsid:zoobank.org:pub:72BA5A28-1CE2-4C20-8DA0-B9E4DA3D0354 Wiesław Krzemiński—a man of a great passion for fossil flies AGNIESZKA SOSZYŃSKA-MAJ1, KORNELIA SKIBIŃSKA2 & KATARZYNA KOPEĆ2 1University of Lodz, Faculty of Biology and Environmental Protection, Department of Invertebrate Zoology and Hydrobiology, 90-237 Lodz, Poland 2Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, 31-016 Krakow, Poland [email protected]; https://orcid.org/0000-0002-2661-6685 [email protected]; https://orcid.org/0000-0002-5971-9373 [email protected]; https://orcid.org/0000-0001-6449-3412 FIGURE 1. Wiesław Krzemiński, Natural History Museum in London, 2014 (photo A. Soszyńska-Maj). Wiesław Krzemiński was born on 26 October 1948, Polish Academy of Sciences in Kraków (ISEA PAS) and in Oświęcim, south of Poland. In his youth he was an the Pedagogical University in Kraków. addicted book reader and developed his love for nature. In 1976, Wiesław finished his master’s degree at After few years of playing in a big beat band he eventually the Department of Biology and Earth Sciences at the focused on biology. Currently, he is a full time Professor Jagiellonian University in Kraków under the supervision of and works in the Institute of Systematics and Evolution Dr. Janusz Wojtusiak. His thesis considered the taxonomy 434 Submitted: 6 May. -
The Non-Photosynthetic Algae Helicosporidium Spp.: Emergence of a Novel Group of Insect Pathogens
Insects 2013, 4, 375-391; doi:10.3390/insects4030375 OPEN ACCESS insects ISSN 2075-4450 www.mdpi.com/journal/insects/ Review The Non-Photosynthetic Algae Helicosporidium spp.: Emergence of a Novel Group of Insect Pathogens Aurélien Tartar Division of Math, Science, and Technology, Nova Southeastern University, 3301 College Avenue, Fort Lauderdale, FL 33314, USA; E-Mail: [email protected]; Tel.: +1-954-262-8148; Fax: +1-954-262-3931 Received: 30 May 2013; in revised form: 4 July 2013 / Accepted: 8 July 2013 / Published: 17 July 2013 Abstract: Since the original description of Helicosporidium parasiticum in 1921, members of the genus Helicosporidium have been reported to infect a wide variety of invertebrates, but their characterization has remained dependent on occasional reports of infection. Recently, several new Helicosporidium isolates have been successfully maintained in axenic cultures. The ability to produce large quantity of biological material has led to very significant advances in the understanding of Helicosporidium biology and its interactions with insect hosts. In particular, the unique infectious process has been well documented; the highly characteristic cyst and its included filamentous cell have been shown to play a central role during host infection and have been the focus of detailed morphological and developmental studies. In addition, phylogenetic analyses inferred from a multitude of molecular sequences have demonstrated that Helicosporidium are highly specialized non-photosynthetic algae (Chlorophyta: Trebouxiophyceae), and represent the first described entomopathogenic algae. This review provides an overview of (i) the morphology of Helicosporidium cell types, (ii) the Helicosporidium life cycle, including the entire infectious sequence and its impact on insect hosts, (iii) the phylogenetic analyses that have prompted the taxonomic classification of Helicosporidium as green algae, and (iv) the documented host range for this novel group of entomopathogens. -
Paecilomyces Niveus Stolk & Samson, 1971 (Ascomycota
http://dx.doi.org/10.1590/1519-6984.08014 Original Article Paecilomyces niveus Stolk & Samson, 1971 (Ascomycota: Thermoascaceae) as a pathogen of Nasonovia ribisnigri (Mosley, 1841) (Hemiptera, Aphididae) in Brazil M. A. C. Zawadneaka*, I. C. Pimentelb, D. Roblb, P. Dalzotob, V. Vicenteb, D. R. Sosa-Gómezc, M. Porsanib and F. L. Cuqueld aLaboratório de Entomologia Prof. Ângelo Moreira da Costa Lima, Departamento de Patologia Básica, Universidade Federal do Paraná – UFPR, CP 19020, CEP 81531-980, Curitiba, PR, Brazil bLaboratório de Microbiologia, Departamento de Patologia Básica, Universidade Federal do Paraná – UFPR, CP 19020, CEP 81531-980, Curitiba, PR, Brazil cLaboratório de Entomologia, Embrapa Soja, CP 231, CEP 86001-970, Londrina, PR, Brazil dDepartamento de Fitotecnia e Fitossanitarismo, Universidade Federal do Paraná – UFPR, Rua dos Funcionários, CP 1540, CEP 80035-050, Curitiba, PR, Brazil *e-mail: [email protected] Received: May 2, 2014 – Accepted: August 27, 2014 – Distributed: November 30, 2015 (With 2 figures) Abstract Nasonovia ribisnigri is a key pest of lettuce (Lactuca sativa L.) in Brazil that requires alternative control methods to synthetic pesticides. We report, for the first time, the occurrence of Paecilomyces niveus as an entomopathogen of the aphid Nasonovia ribisnigri in Pinhais, Paraná, Brazil. Samples of mummified aphids were collected from lettuce crops. The fungus P. niveus (PaePR) was isolated from the insect bodies and identified by macro and micromorphology. The species was confirmed by sequencing Internal Transcribed Spacer (ITS) rDNA. We obtained a sequence of 528 bp (accession number HQ441751), which aligned with Byssochlamys nivea strains (100% identities). In a bioassay, 120 h after inoculation of N. -
Natural Enemies of the Currant Lettuce Aphid, Nasonovia Ribisnigri (Mosely) (Hemiptera: Aphididae) and Their Population Fluctuations in Ahvaz, Iran
J. Crop Prot. 2014, 3 (4):487-497_______________________________________________________ Research Article Natural enemies of the currant lettuce aphid, Nasonovia ribisnigri (Mosely) (Hemiptera: Aphididae) and their population fluctuations in Ahvaz, Iran Afrooz Farsi1*, Farhan Kocheili1, Mohammad Saeed Mossadegh1, Arash Rasekh1 and Mehrzad Tavoosi2 1. Department of Plant Protection, Faculty of Agriculture, Shahid Chamran University of Ahvaz, Ahvaz, Iran. 2. Agriculture and Natural Resources Research Center of Khuzestan-Ahvaz. Abstract: Nasonovia ribisnigri (Mosely) is one of the most important pests of the lettuce plant and it was reported for the first time in Ahvaz in 2008. In order to investigate the dominant species of its natural enemies and their population fluctuations, sample were taken arbitrarily from fifty plants twice a week during the growing season in 2010-2012. In this study, ten species of predators, three species of parasitoids and two species of hyperparasitoids were collected and identified. Hoverflies with a relative frequency of 55% were the dominant predators. Peaks of lacewings and subsequently ladybird beetles were more coincident with peaks of aphid population in mid-March in the first year of studies. But their densities in the second year were very low. Also, hoverflies and parasitoids were mainly observed in the high densities in late March-early April, in both years. Regression analysis indicated that populations of aphids were mainly affected by ladybird beetles and lacewings in the first year of study, as well as by ladybird beetles, hoverflies and parasitoids in the second year. Therefore, additional studies are required for further evaluation on the potential abilities of these natural enemies being a good candidates for the future biological control programs. -
Upland & Pollinator Plants Flip Book
Pictures Ilex opaca Callicarpa americana American Holly Beautyberry Prunus serotina Pteridium aquilinum Black Cherry Bracken Fern Descriptions Callicarpa americana Ilex opaca The American beautyberry is a shrub, 6-9 ft in height. Shoot This tree grows to be 35 to 50 ft tall and 15 to 25 ft wide. growth occurs throughout much of the season. It is It has a dense, pyramid-shaped crown. characterized by its attractive foliage and clusters of flowers or fruit around the leaf nodes. Leaves Leaves Alternate, simple and laceolate or elliptic in shape, 2-4 inches long and 1-1.5 inches wide. Medium to dark, Simple, opposite or subopposite, and deciduous. 3-5” long green in color, and shiny or flat. Leaf margins are usually and 1-3” wide, oval shaped, with an acute apex. Leaf bases spiny and will be flat or wavy. are tapered, margins are serrate. Surfaces are green and usually glabrous above, paler and pubescent below. Flowers Petioles are short and slender. Small, green or white in color, fragrant and found in Flowers clusters in the leaf axils. Perfect, in sessile clusters around the leaf nodes Bark Fruit The bark is light gray and may be covered by wart-like growths. Because the bark is very thin, it is easily A 4-pitted lavender-pink, magenta, or violet drupe, about 1/4 damaged. inch in diameter. Lasts long into winter and is eaten by a variety of birds. Interesting Facts Trunk The preserved berries of this tree were used by American Indians as decorative buttons. Historically, the Older stems have a thin protective, light-brown bark. -
What We Have Learned About the Bermudagrass Stem Maggot
WHAT WE HAVE LEARNED ABOUT THE BERMUDAGRASS STEM MAGGOT D.W. Hancock, W.G. Hudson, L.L. Baxter, and J.T. McCullers1 Abstract Since first being discovered in southern Georgia in July 2010, the bermudagrass stem maggot (BSM; Atherigona reversura Villeneuve) has infested and damaged forage bermudagrass (Cynodon dactylon) throughout the southeastern United States. Our objectives for this presentation were to summarize the available literature on this new, invasive species and provide additional insight from what is currently known about other Atherigona spp. The BSM, along with other Atherigona spp., are small, muscid flies native to Central and Southeast Asia. The adult fly of the BSM lays its eggs on bermudagrass leaves. Upon hatching, the BSM larva slips into the sheath, down the tiller, and penetrates the pseudostem at the first node. The BSM larva then feeds on the vascular tissue, sap, and (potentially) the subsequent decaying plant material before exiting the tiller, pupating in the soil, and emerging as a fly. As a result of the larval feeding, bermudagrass exhibits senescence and necrosis of the terminal leaves on the affected shoots. The affected leaves are easily pulled out of the sheath and show obvious damage near the affected node. In severe infestations, over 80% of the tillers in a given area may be affected. There is a paucity of information about the lifecycle of A. reversura and how it can be managed or controlled, but some information is available on basic larva behavior, fly physiology, and the potential differences in resistance among some bermudagrass varieties. Additional research is underway to better understand the lifecycle of this species, confirm and quantify the degree of preference A. -
A Protocol for Online Documentation of Spider Biodiversity Inventories Applied to a Mexican Tropical Wet Forest (Araneae, Araneomorphae)
Zootaxa 4722 (3): 241–269 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2020 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4722.3.2 http://zoobank.org/urn:lsid:zoobank.org:pub:6AC6E70B-6E6A-4D46-9C8A-2260B929E471 A protocol for online documentation of spider biodiversity inventories applied to a Mexican tropical wet forest (Araneae, Araneomorphae) FERNANDO ÁLVAREZ-PADILLA1, 2, M. ANTONIO GALÁN-SÁNCHEZ1 & F. JAVIER SALGUEIRO- SEPÚLVEDA1 1Laboratorio de Aracnología, Facultad de Ciencias, Departamento de Biología Comparada, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Colonia Copilco el Bajo. C. P. 04510. Del. Coyoacán, Ciudad de México, México. E-mail: [email protected] 2Corresponding author Abstract Spider community inventories have relatively well-established standardized collecting protocols. Such protocols set rules for the orderly acquisition of samples to estimate community parameters and to establish comparisons between areas. These methods have been tested worldwide, providing useful data for inventory planning and optimal sampling allocation efforts. The taxonomic counterpart of biodiversity inventories has received considerably less attention. Species lists and their relative abundances are the only link between the community parameters resulting from a biotic inventory and the biology of the species that live there. However, this connection is lost or speculative at best for species only partially identified (e. g., to genus but not to species). This link is particularly important for diverse tropical regions were many taxa are undescribed or little known such as spiders. One approach to this problem has been the development of biodiversity inventory websites that document the morphology of the species with digital images organized as standard views.