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C10 Beano1senn.Mimosa.Amo-Des
LEGUMINOSAE PART ONE Caesalpinioideae, Mimosoideae, Papilionoideae, Amorpha to Desmodium Revised 04 May 2015 BEAN FAMILY 1 Amphicarpaea CAESALPINIACEAE Cassia Anthyllis Cercis Apios Chamaecrista Astragalus Gleditsia Baptisia Gymnocladus Caragana Senna Cladrastus MIMOSACEAE Desmanthus Coronilla Mimosa Crotalaria Schrankia Dalea PAPILIONACEAE Amorpha Desmodium un-copyrighted draught --- “No family of the vegetable kingdom possesses a higher claim to the attention of the naturalist than the Leguminosae, wether we regard them as objects of ornament or utility. Of the former, we might mention the splendid varieties of Cercis, with their purple flowers, the Acacias, with their airy foliage and silky stamens, the Pride of India, Colutea, and Cæsalpina, with a host of others, which, like the Sweet Pea, are redolent with perfume. Of the latter, the beans, peas, lentils, clover, and lucerne, are too well known to require recommendation. Among timber trees, the Rosewood (a Brazilian species of Mimosa), the Laburnum, whose wood is durable and of an olive-green color, and the Locust of our own country are preëminent. The following are a few important officinal products of this order. In medicine; liquorice is the product of the root of Glycyrrhiza glabra of S. Europe. The purgative senna consists of leaves of Cassia Senna, C. acutifolia, C. Æthiopica, and other species of Egypt and Arabia. C. Marilandica is also a cathartic, but more mild than the former. The sweet pulp tamarind, is the product of a large and beautiful tree (Tamarindus Indica) of the E. and W. Indies. Resins and Balsams: Gum Senegal is yielded by Acacia Verek of the River Senegal; Gum Arabic, by several species of Acacia of Central Africa; Gum Tragacynth, by Astragalus verus, &c., Persia. -
Arthropods of Elm Fork Preserve
Arthropods of Elm Fork Preserve Arthropods are characterized by having jointed limbs and exoskeletons. They include a diverse assortment of creatures: Insects, spiders, crustaceans (crayfish, crabs, pill bugs), centipedes and millipedes among others. Column Headings Scientific Name: The phenomenal diversity of arthropods, creates numerous difficulties in the determination of species. Positive identification is often achieved only by specialists using obscure monographs to ‘key out’ a species by examining microscopic differences in anatomy. For our purposes in this survey of the fauna, classification at a lower level of resolution still yields valuable information. For instance, knowing that ant lions belong to the Family, Myrmeleontidae, allows us to quickly look them up on the Internet and be confident we are not being fooled by a common name that may also apply to some other, unrelated something. With the Family name firmly in hand, we may explore the natural history of ant lions without needing to know exactly which species we are viewing. In some instances identification is only readily available at an even higher ranking such as Class. Millipedes are in the Class Diplopoda. There are many Orders (O) of millipedes and they are not easily differentiated so this entry is best left at the rank of Class. A great deal of taxonomic reorganization has been occurring lately with advances in DNA analysis pointing out underlying connections and differences that were previously unrealized. For this reason, all other rankings aside from Family, Genus and Species have been omitted from the interior of the tables since many of these ranks are in a state of flux. -
Insects That Feed on Trees and Shrubs
INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture, -
Io Moth Automeris Io (Fabricius) (Insecta: Lepidoptera: Saturniidae)1 Donald W
EENY608 Io Moth Automeris io (Fabricius) (Insecta: Lepidoptera: Saturniidae)1 Donald W. Hall2 Introduction The beautiful Io moth, Automeris io (Fabricius), is one of our most recognizable moths. It is distinctive because of its prominent hind wing eyespots. The Io moth, like many of the other saturniid moths, is less common now in parts of its range. With the exception of Cape Cod and some of the Massachusetts islands, it is now rare in New England where it was once common, and its populations have declined in the Gulf States (with the exception of Louisiana) since the 1970s (Manley 1993). The attractive Io moth caterpillar is also well-known because of its painful sting. Figure 1. Male Io moth, Automeris io (Fabricius). Automeris is a large genus with about 145 species (Heppner Credits: Donald W. Hall, University of Florida 1996). All Automeris species are characterized by large eyespots in the middle of the hind wings. Most species Synonymy are found in Central and South America. There are seven Fabricius (1775, p.560) described the Io moth and named species in the United States. Five of these, Automeris it Bombyx io. Abbott and Smith (1797, p.97) published zephyria Grote (New Mexico and western Texas), Automeris the first account of the Io moth’s life cycle under the cecrops (Boisduval), Automeris iris (Walker), Automeris name Phalaena io. Some early references used the genus patagoniensis Lemaire, and Automeris randa Druce name Hyperchiria (e.g., Eliot & Soule 1902, Lintner 1872, (southeastern Arizona) are found only in the western U.S. Stratton-Porter 1921, Strecker 1872). -
Moths of Ohio Guide
MOTHS OF OHIO field guide DIVISION OF WILDLIFE This booklet is produced by the ODNR Division of Wildlife as a free publication. This booklet is not for resale. Any unauthorized INTRODUCTION reproduction is prohibited. All images within this booklet are copyrighted by the Division of Wildlife and it’s contributing artists and photographers. For additional information, please call 1-800-WILDLIFE. Text by: David J. Horn Ph.D Moths are one of the most diverse and plentiful HOW TO USE THIS GUIDE groups of insects in Ohio, and the world. An es- Scientific Name timated 160,000 species have thus far been cata- Common Name Group and Family Description: Featured Species logued worldwide, and about 13,000 species have Secondary images 1 Primary Image been found in North America north of Mexico. Secondary images 2 Occurrence We do not yet have a clear picture of the total Size: when at rest number of moth species in Ohio, as new species Visual Index Ohio Distribution are still added annually, but the number of species Current Page Description: Habitat & Host Plant is certainly over 3,000. Although not as popular Credit & Copyright as butterflies, moths are far more numerous than their better known kin. There is at least twenty Compared to many groups of animals, our knowledge of moth distribution is very times the number of species of moths in Ohio as incomplete. Many areas of the state have not been thoroughly surveyed and in some there are butterflies. counties hardly any species have been documented. Accordingly, the distribution maps in this booklet have three levels of shading: 1. -
Weevils) of the George Washington Memorial Parkway, Virginia
September 2020 The Maryland Entomologist Volume 7, Number 4 The Maryland Entomologist 7(4):43–62 The Curculionoidea (Weevils) of the George Washington Memorial Parkway, Virginia Brent W. Steury1*, Robert S. Anderson2, and Arthur V. Evans3 1U.S. National Park Service, 700 George Washington Memorial Parkway, Turkey Run Park Headquarters, McLean, Virginia 22101; [email protected] *Corresponding author 2The Beaty Centre for Species Discovery, Research and Collection Division, Canadian Museum of Nature, PO Box 3443, Station D, Ottawa, ON. K1P 6P4, CANADA;[email protected] 3Department of Recent Invertebrates, Virginia Museum of Natural History, 21 Starling Avenue, Martinsville, Virginia 24112; [email protected] ABSTRACT: One-hundred thirty-five taxa (130 identified to species), in at least 97 genera, of weevils (superfamily Curculionoidea) were documented during a 21-year field survey (1998–2018) of the George Washington Memorial Parkway national park site that spans parts of Fairfax and Arlington Counties in Virginia. Twenty-three species documented from the parkway are first records for the state. Of the nine capture methods used during the survey, Malaise traps were the most successful. Periods of adult activity, based on dates of capture, are given for each species. Relative abundance is noted for each species based on the number of captures. Sixteen species adventive to North America are documented from the parkway, including three species documented for the first time in the state. Range extensions are documented for two species. Images of five species new to Virginia are provided. Keywords: beetles, biodiversity, Malaise traps, national parks, new state records, Potomac Gorge. INTRODUCTION This study provides a preliminary list of the weevils of the superfamily Curculionoidea within the George Washington Memorial Parkway (GWMP) national park site in northern Virginia. -
Notes on Lixus Concavus
434 JOURNAL OF ECONOMIC ENTOMOLOGY [Vol. 5 NOTES ON LIXUS CONCAVUS By HARRY B. WEISS, New Brunswick, N. J. This beetle commonly known as the rhubarb curculio emerges from its winter quarters about the last week of May in the latitude of New Brunswick. It hibernates, presumably under debris commonly found in the field, inasmuch as two specimens were taken last December from under dead leaves and rubbish and one from under a loose piece' of bark at the base of a stump. Careful searches at different times later in the winter resulted in none being found. Egg deposition commences soon after emergence, as eggs were col- Downloaded from lected in the field on the first of June in the stems of Rumex crispus, which is undoubtedly the favorite food plant of the larvre. Sun- flower and thistle were examined for egg punctures with negative results and in one instance only, eggs were found in a species of poly- gonum or smartweed. http://jee.oxfordjournals.org/ In dock the egg punctures occur from the base of the stem all the way to the tip of the plant and it is not uncommon to find from fif- teen to twenty punctures in a stem three feet high. Occasionally . they occur in the leaf petiole. Not all of these punctures, however, contain eggs, only a comparatively few. Upon cutting into some stems, many egg cavities were found to be empty and the surround- ing tissue showed no evidence of larval activity. Other stems showed by guest on June 9, 2016 many empty egg cavities together with channels eaten by the first hatched larv::e. -
Io Moth (Automeris Io)
CLOSE ENCOUNTERS WITH THE ENVIRONMENT What’s Eating You? Io Moth (Automeris io) Eric W. Hossler, MD; Dirk M. Elston, MD; David L. Wagner, PhD f the 7 species of Automeris moths (order, About 10 days after being deposited, minute 2- to Lepidoptera; family, Saturniidae) found in the 3-mm larvae emerge from the ova and feed gregari- O United States, Automeris io often is the most ously upon their host plant. Favorite foods of the Io common and familiar. Its range extends as far north caterpillars include azaleas, birch, blackberry, cherry, as Quebec, Ontario, and southern Manitoba, Canada; clover, cotton, currant, elm, hackberry, hibiscus, west to Utah, Colorado, Nebraska, and Texas; and mesquite, oak, pear, poplar, redbud, rose, sassafras, south to Florida, eastern Mexico, and Costa Rica.1-3 and willow.1,2,4 In addition, larvae frequently feed on Across much of its range, the moths and their lar- grasses such as corn or Bermuda grass.2,4 Io moths are vae are among the most common giant silk moths around in deciduous woodlands, forests, and fields; encountered by the public. In Louisiana, the closely along power line rights-of-way; and in orchards, related Automeris louisiana largely replaces the Io parks, and suburban yards.2,5 moth in coastal areas.2 The sexually dimorphic adults have a wingspan The Io moth has 4 life stages: egg, larva (or cat- of 2.0 to 3.5 in and are easily recognized by the pres- erpillar), pupa, and adult. Eclosion of Io moths from ence of prominent black to blue eyespots with white cocoons occurs during late morning or early evening. -
Impacts of Native and Non-Native Plants on Urban Insect Communities: Are Native Plants Better Than Non-Natives?
Impacts of Native and Non-native plants on Urban Insect Communities: Are Native Plants Better than Non-natives? by Carl Scott Clem A thesis submitted to the Graduate Faculty of Auburn University in partial fulfillment of the requirements for the Degree of Master of Science Auburn, Alabama December 12, 2015 Key Words: native plants, non-native plants, caterpillars, natural enemies, associational interactions, congeneric plants Copyright 2015 by Carl Scott Clem Approved by David Held, Chair, Associate Professor: Department of Entomology and Plant Pathology Charles Ray, Research Fellow: Department of Entomology and Plant Pathology Debbie Folkerts, Assistant Professor: Department of Biological Sciences Robert Boyd, Professor: Department of Biological Sciences Abstract With continued suburban expansion in the southeastern United States, it is increasingly important to understand urbanization and its impacts on sustainability and natural ecosystems. Expansion of suburbia is often coupled with replacement of native plants by alien ornamental plants such as crepe myrtle, Bradford pear, and Japanese maple. Two projects were conducted for this thesis. The purpose of the first project (Chapter 2) was to conduct an analysis of existing larval Lepidoptera and Symphyta hostplant records in the southeastern United States, comparing their species richness on common native and alien woody plants. We found that, in most cases, native plants support more species of eruciform larvae compared to aliens. Alien congener plant species (those in the same genus as native species) supported more species of larvae than alien, non-congeners. Most of the larvae that feed on alien plants are generalist species. However, most of the specialist species feeding on alien plants use congeners of native plants, providing evidence of a spillover, or false spillover, effect. -
Rhubarb Curculio Lixus Concavus Say; Family: Curculionidae
IDL INSECT DIAGNOSTIC LABORATORY Cornell University, Dept. of Entomology, 2144 Comstock Hall, Ithaca NY 14853-2601 Rhubarb Curculio Lixus concavus Say; Family: Curculionidae Adult rhubarb curculio, with yellowish coating present. Size: about 1/2 inch long. Photo by M. Malkin. Injury Rhubarb is a hardy perennial that is not usually seriously affected by insect pests. However, attacks of the rhubarb curculio occasionally do occur. The leaf stalks of the rhubarb may show exuding sap and partial decay from late-May through early summer, due to the feeding and egg laying punctures of the rhubarb curculio. Feeding injury appears as notches in the stem and on the leaf edges. Sap exudes from wounds of either type and collects as glistening drops of gum when fresh. Fortunately, the eggs of this insect do not hatch when deposited in rhubarb. Description The rhubarb curculio (or rhubarb weevil) is a large snout beetle, about 1/2 inch long. It is dark colored, with a yellow powdery material dusted on its back. The yellowish covering easily rubs off when the insect is handled. The head has a downwardly curved snout, at the end of which are the mandibles (the chewing mouth parts). The eggs are oblong and yellow- white in color. The mature larva is a legless grub about 3/4 inch in length, with a brown head. Life History The curculio overwinters as an adult, in piles of debris or in other protected places near the rhubarb planting. In about mid-May the adults appear, and are seen resting on the stalks and leaves of rhubarb, dock, thistle or sunflower. -
The Pennsylvania State University
The Pennsylvania State University The Graduate School College of the Liberal Arts ANCIENT HUMAN BEHAVIORAL ECOLOGY AND COLONIZATION IN GRENADA, WEST INDIES A Dissertation in Anthropology by Jonathan Andrew Hanna © 2018 Jonathan Andrew Hanna Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy December 2018 The dissertation of Jonathan Andrew Hanna was reviewed and approved* by the following: Douglas J. Kennett Professor of Anthropology Head of the Department of Anthropology Dissertation Adviser Chair of Committee Douglas W. Bird Associate Professor of Anthropology Kristina G. Douglass Assistant Professor of Anthropology Peter B. Newman Professor of Recreation, Park, and Tourism Management Lee A. Newsom Associate Professor Emeritus of Anthropology Professor of Anthropology, Flagler College Special Member William F. Keegan Curator of Caribbean Archaeology, Florida Museum of Natural History Professor of Anthropology, University of Florida Special Member Mary K. Shenk Associate Professor of Anthropology & Demography Director of Graduate Studies *Signatures on file in the Graduate School ABSTRACT The pre-Columbian colonization of the Caribbean is traditionally described as a series of migrations from coastal South America moving northward, island to island, as “stepping-stones.” As the southernmost island in the Antilles archipelago, just 90 miles off Venezuela, the island of Grenada is assumed to be the crucial first “step” in these migrations. However, too little archaeological data was available to substantiate this claim. This dissertation project was designed to fill the gap. Using the Ideal Free Distribution (IFD), a heuristic from Human Behavioral Ecology, a predictive model was built to test areas of high-probability for early settlement on Grenada via an island-wide “radiocarbon survey” that collected artifactual, soil, and radiocarbon samples. -
Bioblitz Results
BioBlitz Results Eagle Marsh May 31 and June 1 2014 RESULTS FROM THE 2014 EAGLE MARSH BIODIVERSITY SURVEY ALLEN COUNTY, INDIANA Compiled from the Science Team Reports Assembled by Don Ruch (Indiana Academy of Science) Table of Contents Title Page………………………………………………………………………….………………. 1 Table of Contents……………………………………………………………………………......... 2 General Introduction ……..………………………………………………………..……………... 3-4 Maps…………………………………………………………………………………….………… 5-7 The Story of Eagle Marsh by Judy Nelsen………………………………….……………….…… 8-9 History and Physical Setting of Eagle Marsh by Tony Fleming…………………………………. 10-20 Table 1: Birds ..………………………………….…………………………..………….……….. 22-27 Table 2: Fish .…………………………………………………...……………………………….. 28-34 Table 3: Herpetofauna (Amphibians and Reptiles) …………………………………………….. 35-38 Table 4: Mammals ……………………………………………………….……………………… 39-40 Table 5: Beetles (Coleoptera) …………………………………………………………………... 41-46 Table 6: Butterflies ………………………………………………............................................... 47-50 Table 7: Dragonflies and Damselflies (Odonata) ………………………………………….…… 51-52 Table 8: Singing Insects ……………………………………………………............................... 53-55 Table 9: Snail-killing Flies (Sciomyzidae) ………………………..…….................................... 56-57 Table 10: Aquatic Macroinvertebrates ………………………………………………………… 58-62 Table 11: Freshwater Mussels …………………………………………………………….…… 63-64 Table 12: Mushrooms and Fungi ……………………………………………………................ 65-67 Table 13: Vascular Plants …………………………..……......................................................... 68-92