Mare Basalt Thickness in Sinus Aestuum and Sinus Medii J
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Perspective Where Might Be Many Tropical Insects?
Biological Conservation 233 (2019) 102–108 Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Perspective Perspective: Where might be many tropical insects? T ⁎ Daniel H. Janzen , Winnie Hallwachs Department of Biology, University of Pennsylvania, Philadelphia 19104, United States of America ABSTRACT I have been watching the gradual and very visible decline of Mexican and Central American insect density and species richness since 1953 and Winnie since 1978. The loss is very real for essentially all higher taxa, and the reasons are very evident: intense forest and agricultural simplification of very large areas, massive use of pesticides, habitat fragmentation, and at least since the 1980's, ever-increasing climate change in temperature, rainfall, and synchronization of seasonal cues. There is no ecological concept suggesting that this biodiversity and habitat impoverishment is restricted to this portion of the Neotropics, and our 50 years of occasional visits to other parts of the tropics suggest the same. We are losing most of the insect community that is still in the cloud forests due to the drying of the tops of tropical mountains, just as we are losing the huge expanses of insect communities that once occupied the fertile soils, weather, and water of the lowland tropics. Today we have unimaginable access to the world's biodiversity through the internet, roads, dwellings, education, bioliterate societies, DNA barcoding, genome sequencing, and human curiosity. The wild world gains from our understanding that it needs large and diverse terrain, relief from hunting trees and animals, site-specific restoration, profit-sharing with its societies, and tolerance of humans and our extended genomes. -
Lepidoptera Sphingidae:) of the Caatinga of Northeast Brazil: a Case Study in the State of Rio Grande Do Norte
212212 JOURNAL OF THE LEPIDOPTERISTS’ SOCIETY Journal of the Lepidopterists’ Society 59(4), 2005, 212–218 THE HIGHLY SEASONAL HAWKMOTH FAUNA (LEPIDOPTERA SPHINGIDAE:) OF THE CAATINGA OF NORTHEAST BRAZIL: A CASE STUDY IN THE STATE OF RIO GRANDE DO NORTE JOSÉ ARAÚJO DUARTE JÚNIOR Programa de Pós-Graduação em Ciências Biológicas, Departamento de Sistemática e Ecologia, Universidade Federal da Paraíba, 58059-900, João Pessoa, Paraíba, Brasil. E-mail: [email protected] AND CLEMENS SCHLINDWEIN Departamento de Botânica, Universidade Federal de Pernambuco, Av. Prof. Moraes Rego, s/n, Cidade Universitária, 50670-901, Recife, Pernambuco, Brasil. E-mail:[email protected] ABSTRACT: The caatinga, a thorn-shrub succulent savannah, is located in Northeastern Brazil and characterized by a short and irregular rainy season and a severe dry season. Insects are only abundant during the rainy months, displaying a strong seasonal pat- tern. Here we present data from a yearlong Sphingidae survey undertaken in the reserve Estação Ecológica do Seridó, located in the state of Rio Grande do Norte. Hawkmoths were collected once a month during two subsequent new moon nights, between 18.00h and 05.00h, attracted with a 160-watt mercury vapor light. A total of 593 specimens belonging to 20 species and 14 genera were col- lected. Neogene dynaeus, Callionima grisescens, and Hyles euphorbiarum were the most abundant species, together comprising up to 82.2% of the total number of specimens collected. These frequent species are residents of the caatinga of Rio Grande do Norte. The rare Sphingidae in this study, Pseudosphinx tetrio, Isognathus australis, and Cocytius antaeus, are migratory species for the caatinga. -
Lake Worth Lagoon
TABLE OF CONTENTS INTRODUCTION ................................................................................ 1 PURPOSE AND SIGNIFICANCE OF THE PARK ...................................... 1 Park Significance .............................................................................. 1 PURPOSE AND SCOPE OF THE PLAN ................................................... 2 MANAGEMENT PROGRAM OVERVIEW ................................................. 7 Management Authority and Responsibility ............................................ 7 Park Management Goals .................................................................... 8 Management Coordination ................................................................. 8 Public Participation ........................................................................... 9 Other Designations ........................................................................... 9 RESOURCE MANAGEMENT COMPONENT INTRODUCTION .............................................................................. 15 RESOURCE DESCRIPTION AND ASSESSMENT ................................... 15 Natural Resources .......................................................................... 16 Topography ............................................................................... 20 Geology .................................................................................... 21 Soils ......................................................................................... 21 Minerals ................................................................................... -
Invertebrate Distribution and Diversity Assessment at the U. S. Army Pinon Canyon Maneuver Site a Report to the U
Invertebrate Distribution and Diversity Assessment at the U. S. Army Pinon Canyon Maneuver Site A report to the U. S. Army and U. S. Fish and Wildlife Service G. J. Michels, Jr., J. L. Newton, H. L. Lindon, and J. A. Brazille Texas AgriLife Research 2301 Experiment Station Road Bushland, TX 79012 2008 Report Introductory Notes The invertebrate survey in 2008 presented an interesting challenge. Extremely dry conditions prevailed throughout most of the adult activity period for the invertebrates and grass fires occurred several times throughout the summer. By visual assessment, plant resources were scarce compared to last year, with few green plants and almost no flowering plants. Eight habitats and nine sites continued to be sampled in 2008. The Ponderosa pine/ yellow indiangrass site was removed from the study after the low numbers of species and individuals collected there in 2007. All other sites from the 2007 survey were included in the 2008 survey. We also discontinued the collection of Coccinellidae in the 2008 survey, as only 98 individuals from four species were collected in 2007. Pitfall and malaise trapping were continued in the same way as the 2007 survey. Sweep net sampling was discontinued to allow time for Asilidae and Orthoptera timed surveys consisting of direct collection of individuals with a net. These surveys were conducted in the same way as the time constrained butterfly (Papilionidea and Hesperoidea) surveys, with 15-minute intervals for each taxanomic group. This was sucessful when individuals were present, but the dry summer made it difficult to assess the utility of these techniques because of overall low abundance of insects. -
Location #1: Peary/Whipple Crater
Location, Location, Location A Lunar Investment Strategy Hoyt Davidson Near Earth LLC June 2017 ISU's International Institute of Space Commerce Lunar Economic Action Plan (LEAP) Space and Questions from 1960 Still Relevant Today Economic Development • How can we utilize our dynamic system of competitive private enterprise in space, as on earth, to make newly discovered resources useful to man? • How can private enterprise and private capital make their maximum contribution? Philosophy and Policy The ultimate goal is not to impress others, or merely to explore our planetary system, but to use accessible space for the benefit of humankind. It is a goal that is not confined to a decade or a century. Nor is it confined to a single nearby destination, or to a fleeting dash to plant a flag. The idea is to begin preparing now for a future in which the material trapped in the Sun's vicinity is available for incorporation into our way of life. Dr. John Marburger, Head of the Office of Science and Technology Policy 2006 3 The Investment Premise • Just as on Earth, lunar real estate “value” is driven by location, location, location Rank Location Why Valuable 1 Peary Crater Best 1st industrial base and settlement 2 Sinus Medii Good cargo port & space elevator site 3 Largest skylights / lava tubes Best large scale settlements 4 Tsiolkovskiy crater, dark side Prime radio astronomy site 5 High helium-3 concentrations Potential high value mining 6 Lipsky Crater Space elevator site for Earth-Moon L2 7 Aristillus High Thorium concentrations • Lunar real -
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes Akito Y. Kawahara1*, Andre A. Mignault1, Jerome C. Regier2, Ian J. Kitching3, Charles Mitter1 1 Department of Entomology, College Park, Maryland, United States of America, 2 Center for Biosystems Research, University of Maryland Biotechnology Institute, College Park, Maryland, United States of America, 3 Department of Entomology, The Natural History Museum, London, United Kingdom Abstract Background: The 1400 species of hawkmoths (Lepidoptera: Sphingidae) comprise one of most conspicuous and well- studied groups of insects, and provide model systems for diverse biological disciplines. However, a robust phylogenetic framework for the family is currently lacking. Morphology is unable to confidently determine relationships among most groups. As a major step toward understanding relationships of this model group, we have undertaken the first large-scale molecular phylogenetic analysis of hawkmoths representing all subfamilies, tribes and subtribes. Methodology/Principal Findings: The data set consisted of 131 sphingid species and 6793 bp of sequence from five protein-coding nuclear genes. Maximum likelihood and parsimony analyses provided strong support for more than two- thirds of all nodes, including strong signal for or against nearly all of the fifteen current subfamily, tribal and sub-tribal groupings. Monophyly was strongly supported for some of these, including Macroglossinae, Sphinginae, Acherontiini, Ambulycini, Philampelini, Choerocampina, and Hemarina. Other groupings proved para- or polyphyletic, and will need significant redefinition; these include Smerinthinae, Smerinthini, Sphingini, Sphingulini, Dilophonotini, Dilophonotina, Macroglossini, and Macroglossina. The basal divergence, strongly supported, is between Macroglossinae and Smerinthinae+Sphinginae. All genes contribute significantly to the signal from the combined data set, and there is little conflict between genes. -
The Mcguire Center for Lepidoptera and Biodiversity
Supplemental Information All specimens used within this study are housed in: the McGuire Center for Lepidoptera and Biodiversity (MGCL) at the Florida Museum of Natural History, Gainesville, USA (FLMNH); the University of Maryland, College Park, USA (UMD); the Muséum national d’Histoire naturelle in Paris, France (MNHN); and the Australian National Insect Collection in Canberra, Australia (ANIC). Methods DNA extraction protocol of dried museum specimens (detailed instructions) Prior to tissue sampling, dried (pinned or papered) specimens were assigned MGCL barcodes, photographed, and their labels digitized. Abdomens were then removed using sterile forceps, cleaned with 100% ethanol between each sample, and the remaining specimens were returned to their respective trays within the MGCL collections. Abdomens were placed in 1.5 mL microcentrifuge tubes with the apex of the abdomen in the conical end of the tube. For larger abdomens, 5 mL microcentrifuge tubes or larger were utilized. A solution of proteinase K (Qiagen Cat #19133) and genomic lysis buffer (OmniPrep Genomic DNA Extraction Kit) in a 1:50 ratio was added to each abdomen containing tube, sufficient to cover the abdomen (typically either 300 µL or 500 µL) - similar to the concept used in Hundsdoerfer & Kitching (1). Ratios of 1:10 and 1:25 were utilized for low quality or rare specimens. Low quality specimens were defined as having little visible tissue inside of the abdomen, mold/fungi growth, or smell of bacterial decay. Samples were incubated overnight (12-18 hours) in a dry air oven at 56°C. Importantly, we also adjusted the ratio depending on the tissue type, i.e., increasing the ratio for particularly large or egg-containing abdomens. -
2009 Pinon Canyon Invertebrate Survey Report
"- - 70.096 60.096 50.096 40.096 30.096 20.096 10.096 0.0% Fig. 1 Most abundant Apiformes species calculated as a proportion of the total abundance of Apiformes in the collection period. Pinon Canyon Maneuver Site, 2008. 04% 1 j 0.391> 0.2% 0.1% 0.0% Fig. 2 Least abundant Apiformes species calculated as a proportion of the total abundance of Apiformes in the collection period. Pinon Canyon Maneuver Site, 2008.7 Fig. 3 Most abundant Carabidae species calculated as a proportion of the total abundance of Carabidae in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 4 Least abundant Carabidae species calculated as a proportion of the total abundance of Carabidae in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 5 Asilidae species abundance calculated as a proportion of the total abundace of Asilidae in the collection period. Pinon Canyon Maneuver Site, 2008. 30.0% 25.0% 20.0% 15.0% 10.0% 5.0% 0.0% Fig. 6 Butterfly species abundance calculated as a proportion of the total abundance of butterflies in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 7 Most abundant Orthoptera species calculated as a proportion of the total abundance of Orthoptera in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 8 Moderately abundant Orthoptera species calculated as a proportion of the total abundance of Orthoptera in the collection period. Pinon Canyon Maneuver Site, 2008. Fig. 9 Least abundant Orthoptera species calculated as a proportion of the total abundance of Orthoptera in the collection period. -
Surveyor 1 Space- Craft on June 2, 1966 As Seen by the Narrow Angle Camera of the Lunar Re- Connaissance Orbiter Taken on July 17, 2009 (Also See Fig
i “Project Surveyor, in particular, removed any doubt that it was possible for Americans to land on the Moon and explore its surface.” — Harrison H. Schmitt, Apollo 17 Scientist-Astronaut ii Frontispiece: Landing site of the Surveyor 1 space- craft on June 2, 1966 as seen by the narrow angle camera of the Lunar Re- connaissance Orbiter taken on July 17, 2009 (also see Fig. 13). The white square in the upper photo outlines the area of the enlarged view below. The spacecraft is ca. 3.3 m tall and is casting a 15 m shadow to the East. (NASA/LROC/ ASU/GSFC photos) iii iv Surveyor I: America’s First Moon Landing by William F. Mellberg v © 2014, 2015 William F. Mellberg vi About the author: William Mellberg was a marketing and public relations representative with Fokker Aircraft. He is also an aerospace historian, having published many articles on both the development of airplanes and space vehicles in various magazines. He is the author of Famous Airliners and Moon Missions. He also serves as co-Editor of Harrison H. Schmitt’s website: http://americasuncommonsense.com Acknowledgments: The support and recollections of Frank Mellberg, Harrison Schmitt, Justin Rennilson, Alexander Gurshstein, Paul Spudis, Ronald Wells, Colin Mackellar and Dwight Steven- Boniecki is gratefully acknowledged. vii Surveyor I: America’s First Moon Landing by William F. Mellberg A Journey of 250,000 Miles . December 14, 2013. China’s Chang’e 3 spacecraft successfully touched down on the Moon at 1311 GMT (2111 Beijing Time). The landing site was in Mare Imbrium, the Sea of Rains, about 25 miles (40 km) south of the small crater, Laplace F, and roughly 100 miles (160 km) east of its original target in Sinus Iridum, the Bay of Rainbows. -
CHECKLIST of WISCONSIN MOTHS (Superfamilies Mimallonoidea, Drepanoidea, Lasiocampoidea, Bombycoidea, Geometroidea, and Noctuoidea)
WISCONSIN ENTOMOLOGICAL SOCIETY SPECIAL PUBLICATION No. 6 JUNE 2018 CHECKLIST OF WISCONSIN MOTHS (Superfamilies Mimallonoidea, Drepanoidea, Lasiocampoidea, Bombycoidea, Geometroidea, and Noctuoidea) Leslie A. Ferge,1 George J. Balogh2 and Kyle E. Johnson3 ABSTRACT A total of 1284 species representing the thirteen families comprising the present checklist have been documented in Wisconsin, including 293 species of Geometridae, 252 species of Erebidae and 584 species of Noctuidae. Distributions are summarized using the six major natural divisions of Wisconsin; adult flight periods and statuses within the state are also reported. Examples of Wisconsin’s diverse native habitat types in each of the natural divisions have been systematically inventoried, and species associated with specialized habitats such as peatland, prairie, barrens and dunes are listed. INTRODUCTION This list is an updated version of the Wisconsin moth checklist by Ferge & Balogh (2000). A considerable amount of new information from has been accumulated in the 18 years since that initial publication. Over sixty species have been added, bringing the total to 1284 in the thirteen families comprising this checklist. These families are estimated to comprise approximately one-half of the state’s total moth fauna. Historical records of Wisconsin moths are relatively meager. Checklists including Wisconsin moths were compiled by Hoy (1883), Rauterberg (1900), Fernekes (1906) and Muttkowski (1907). Hoy's list was restricted to Racine County, the others to Milwaukee County. Records from these publications are of historical interest, but unfortunately few verifiable voucher specimens exist. Unverifiable identifications and minimal label data associated with older museum specimens limit the usefulness of this information. Covell (1970) compiled records of 222 Geometridae species, based on his examination of specimens representing at least 30 counties. -
A Homeowner's Guide to Pollinator Garden
LIVING IN THE DUNES A HOMEOWNER’S GUIDE TO POLLINATOR GARDEN LANDSCAPING IN INDIANA’S COASTAL COMMUNITIES VOLUME 2 Acknowledgments This project would not have been possible without our supportive staff, expert advisory committee, skilled project team, and generous funding partners. Save the Dunes greatly appreciates those who dedicated their time, knowledge and energy to complete this guide. Advisory Committee Name Affiliation Karl Ackermann Wild Ones - Gibson Woods Chapter Eric Bird Shirley Heinze Land Trust Laura Henderson Naturalist/Member - Indiana Native Plant Society Susan Kirt Susan Kirt Photography and Chicago State University Brianne Lowe USDA - Natural Resource Conservation Service Laura Milkert The Field Museum Joel Perez-Castaneda The Nature Conservancy Desi Robertson-Thompson, Ph.D. Indiana Dunes National Park Steve Sass Indiana Nature LLC Ron Trigg Naturalist/Photographer Project Team Name Affiliation Victoria Wittig, Ph.D. Save the Dunes (Project Lead) Gina Altieri Phenix7 Mktg, Inc. Joel Baldin Hitchcock Design Group Kate Bulin Hitchcock Design Group Nathanael Pilla Orbis Environmental Consulting Barbara Spies Labus Artist/Illustrator Betsy Serdar Phenix7 Mktg, Inc. This publication was made possible by a grant from the National Oceanic and Atmospheric Administration and the Indiana Department of Natural Resources Lake Michigan Coastal Program. Matching support was generously provided by BP, the McDougal Family Foundation, NIPSCO and the Unity Foundation. Printing and outreach support was provided in part by a grant from -
Alberta Wild Species General Status Listing 2010
Fish & Wildlife Division Sustainable Resource Development Alberta Wild Species General Status Listing - 2010 Species at Risk ELCODE Group ID Scientific Name Common Name Status 2010 Status 2005 Status 2000 Background Lichens Cladonia cenotea Powdered Funnel Lichen Secure Cladonia cervicornis Lichens Ladder Lichen Secure verticillata Lichens Cladonia chlorophaea Mealy Pixie-cup Lichen Secure Lichens Cladonia coccifera Eastern Boreal Pixie-cup Lichen Undetermined Lichens Cladonia coniocraea Common Pixie Powderhorn Secure Lichens Cladonia cornuta Bighorn Pixie Lichen Secure Lichens Cladonia cornuta cornuta Bighorn Pixie Lichen Secure Lichens Cladonia crispata Organpipe Lichen Secure Lichens Cladonia cristatella British Soldiers Lichen Secure Cladonia Lichens Mealy Pixie-cup Lichen Undetermined cryptochlorophaea Lichens Cladonia cyanipes Blue-footed Pixie Lichen Sensitive Lichens Cladonia deformis Lesser Sulphur-cup Lichen Secure Lichens Cladonia digitata Fingered Pixie-cup Lichen May Be At Risk Lichens Cladonia ecmocyna Orange-footed Pixie Lichen Secure Lichens Cladonia fimbriata Trumpeting Lichen Secure Lichens Cladonia furcata Forking Lichen Sensitive Lichens Cladonia glauca Glaucous Pixie Lichen May Be At Risk Lichens Cladonia gracilis gracilis Gracile Lichen May Be At Risk Lichens Cladonia gracilis turbinata Bronzed Lichen Secure Lichens Cladonia grayi Gray's Pixie-cup Lichen May Be At Risk Lichens Cladonia humilis Humble Pixie-cup Lichen Undetermined Lichens Cladonia macilenta Lipstick Powderhorn Lichen Secure Cladonia macilenta Lichens