Biology of Proserpinus Clarkiae (Sphingidae)
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Natural Communities of Michigan: Classification and Description
Natural Communities of Michigan: Classification and Description Prepared by: Michael A. Kost, Dennis A. Albert, Joshua G. Cohen, Bradford S. Slaughter, Rebecca K. Schillo, Christopher R. Weber, and Kim A. Chapman Michigan Natural Features Inventory P.O. Box 13036 Lansing, MI 48901-3036 For: Michigan Department of Natural Resources Wildlife Division and Forest, Mineral and Fire Management Division September 30, 2007 Report Number 2007-21 Version 1.2 Last Updated: July 9, 2010 Suggested Citation: Kost, M.A., D.A. Albert, J.G. Cohen, B.S. Slaughter, R.K. Schillo, C.R. Weber, and K.A. Chapman. 2007. Natural Communities of Michigan: Classification and Description. Michigan Natural Features Inventory, Report Number 2007-21, Lansing, MI. 314 pp. Copyright 2007 Michigan State University Board of Trustees. Michigan State University Extension programs and materials are open to all without regard to race, color, national origin, gender, religion, age, disability, political beliefs, sexual orientation, marital status or family status. Cover photos: Top left, Dry Sand Prairie at Indian Lake, Newaygo County (M. Kost); top right, Limestone Bedrock Lakeshore, Summer Island, Delta County (J. Cohen); lower left, Muskeg, Luce County (J. Cohen); and lower right, Mesic Northern Forest as a matrix natural community, Porcupine Mountains Wilderness State Park, Ontonagon County (M. Kost). Acknowledgements We thank the Michigan Department of Natural Resources Wildlife Division and Forest, Mineral, and Fire Management Division for funding this effort to classify and describe the natural communities of Michigan. This work relied heavily on data collected by many present and former Michigan Natural Features Inventory (MNFI) field scientists and collaborators, including members of the Michigan Natural Areas Council. -
Emergence of Parasitic Flies from Adult Actinote Diceus (Nymphalidae: Acraeinae) in Ecuador
VOLUME 55, NUMI:lEH 2 79 Larvae began to bllrrow in soil in preparation for pupation 36-4.5 Hodges ( 197l) stated that adults can be coll ected during the day days aftPf egg hatch. Mortality was high at this stagp: of 4.5 larvae while nectaring on flowers. T suspect this report to bp in error since that burrowed. on Iy 18 pupated. I .arvae pupated under dead leaves all collections throughout the range of the moth. that I have been and pieces 0[" wood. just under the soil surface. and up to 16 ..5 em able to document, were made at lights, and none of the moths I underground in tbe rootball of senescing hostplants. Pupation usu reared was active cluring the day. Moreover, the adults do not feed. ally occurred in firmly packed ovate cells. The cremaster possesses a I thank M. Caterino, J. Herbeck, J. Kruse, F. Sperling, J Tuttle bifurcate tip as depicted by Osborne ( 199.5 ) for Proserpinus clarkiae and especially J. Powell for comments which greatly improved the (Hoi sduval ) (Sphingidae). quality of this work aud J. Kruse [or his assistance in the field. J. The 18 pupae were maintained outside in a ventilated plastic tub Powell and J. DeBenedictis helped with museum tallies. This work in Berkeley until November when they were placed in a refrigcrator was supported in part by an ARCS foundation fellowship, the M. C. at 1.7°C ± 1°C. No development was evident in the pupae until they Walker fund, and a grant hom the California Agricultural Experi had been moved £l'om refrigeration to outside tf'mperatures (be ment Station to F. -
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. -
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. -
Moths & Butterflies of Grizzly Peak Preserve
2018 ANNUAL REPORT MOTHS & BUTTERFLIES OF GRIZZLY PEAK PRESERVE: Inventory Results from 2018 Prepared and Submi�ed by: DANA ROSS (Entomologist/Lepidoptera Specialist) Corvallis, Oregon SUMMARY The Grizzly Peak Preserve was sampled for butterflies and moths during May, June and October, 2018. A grand total of 218 species were documented and included 170 moths and 48 butterflies. These are presented as an annotated checklist in the appendix of this report. Butterflies and day-flying moths were sampled during daylight hours with an insect net. Nocturnal moths were collected using battery-powered backlight traps over single night periods at 10 locations during each monthly visit. While many of the documented butterflies and moths are common and widespread species, others - that include the Western Sulphur (Colias occidentalis primordialis) and the noctuid moth Eupsilia fringata - represent more locally endemic and/or rare taxa. One geometrid moth has yet to be identified and may represent an undescribed (“new”) species. Future sampling during March, April, July, August and September will capture many more Lepidoptera that have not been recorded. Once the site is more thoroughly sampled, the combined Grizzly Peak butterfly-moth fauna should total at least 450-500 species. INTRODUCTION The Order Lepidoptera (butterflies and moths) is an abundant and diverse insect group that performs essential ecological functions within terrestrial environments. As a group, these insects are major herbivores (caterpillars) and pollinators (adults), and are a critical food source for many species of birds, mammals (including bats) and predacious and parasitoid insects. With hundreds of species of butterflies and moths combined occurring at sites with ample habitat heterogeneity, a Lepidoptera inventory can provide a valuable baseline for biodiversity studies. -
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. -
British Lepidoptera (/)
British Lepidoptera (/) Home (/) Anatomy (/anatomy.html) FAMILIES 1 (/families-1.html) GELECHIOIDEA (/gelechioidea.html) FAMILIES 3 (/families-3.html) FAMILIES 4 (/families-4.html) NOCTUOIDEA (/noctuoidea.html) BLOG (/blog.html) Glossary (/glossary.html) Family: SPHINGIDAE (3SF 13G 18S) Suborder:Glossata Infraorder:Heteroneura Superfamily:Bombycoidea Refs: Waring & Townsend, Wikipedia, MBGBI9 Proboscis short to very long, unscaled. Antenna ~ 1/2 length of forewing; fasciculate or pectinate in male, simple in female; apex pointed. Labial palps long, 3-segmented. Eye large. Ocelli absent. Forewing long, slender. Hindwing ±triangular. Frenulum and retinaculum usually present but may be reduced. Tegulae large, prominent. Leg spurs variable but always present on midtibia. 1st tarsal segment of mid and hindleg about as long as tibia. Subfamily: Smerinthinae (3G 3S) Tribe: Smerinthini Probably characterised by a short proboscis and reduced or absent frenulum Mimas Smerinthus Laothoe 001 Mimas tiliae (Lime Hawkmoth) 002 Smerinthus ocellata (Eyed Hawkmoth) 003 Laothoe populi (Poplar Hawkmoth) (/002- (/001-mimas-tiliae-lime-hawkmoth.html) smerinthus-ocellata-eyed-hawkmoth.html) (/003-laothoe-populi-poplar-hawkmoth.html) Subfamily: Sphinginae (3G 4S) Rest with wings in tectiform position Tribe: Acherontiini Agrius Acherontia 004 Agrius convolvuli 005 Acherontia atropos (Convolvulus Hawkmoth) (Death's-head Hawkmoth) (/005- (/004-agrius-convolvuli-convolvulus- hawkmoth.html) acherontia-atropos-deaths-head-hawkmoth.html) Tribe: Sphingini Sphinx (2S) -
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. -
MOTHS and BUTTERFLIES LEPIDOPTERA DISTRIBUTION DATA SOURCES (LEPIDOPTERA) * Detailed Distributional Information Has Been J.D
MOTHS AND BUTTERFLIES LEPIDOPTERA DISTRIBUTION DATA SOURCES (LEPIDOPTERA) * Detailed distributional information has been J.D. Lafontaine published for only a few groups of Lepidoptera in western Biological Resources Program, Agriculture and Agri-food Canada. Scott (1986) gives good distribution maps for Canada butterflies in North America but these are generalized shade Central Experimental Farm Ottawa, Ontario K1A 0C6 maps that give no detail within the Montane Cordillera Ecozone. A series of memoirs on the Inchworms (family and Geometridae) of Canada by McGuffin (1967, 1972, 1977, 1981, 1987) and Bolte (1990) cover about 3/4 of the Canadian J.T. Troubridge fauna and include dot maps for most species. A long term project on the “Forest Lepidoptera of Canada” resulted in a Pacific Agri-Food Research Centre (Agassiz) four volume series on Lepidoptera that feed on trees in Agriculture and Agri-Food Canada Canada and these also give dot maps for most species Box 1000, Agassiz, B.C. V0M 1A0 (McGugan, 1958; Prentice, 1962, 1963, 1965). Dot maps for three groups of Cutworm Moths (Family Noctuidae): the subfamily Plusiinae (Lafontaine and Poole, 1991), the subfamilies Cuculliinae and Psaphidinae (Poole, 1995), and ABSTRACT the tribe Noctuini (subfamily Noctuinae) (Lafontaine, 1998) have also been published. Most fascicles in The Moths of The Montane Cordillera Ecozone of British Columbia America North of Mexico series (e.g. Ferguson, 1971-72, and southwestern Alberta supports a diverse fauna with over 1978; Franclemont, 1973; Hodges, 1971, 1986; Lafontaine, 2,000 species of butterflies and moths (Order Lepidoptera) 1987; Munroe, 1972-74, 1976; Neunzig, 1986, 1990, 1997) recorded to date. -
Restoration Objectives and Strategies for Terrestrial Habitats and Species of the Willamette Sub-Basin
Protection, Restoration, and Management of Terrestrial Habitats and Species of the Willamette Sub-Basin Technical Appendix 1 Contents 1. Introduction 1 1.1 Purpose and Objectives 1 1.2 Scope and Scale of the Report 2 1.3 Principal Sources of Data 5 1.4 Analytical Approaches 7 1.5 Building Upon Previous Efforts 11 1.6 How to Apply this Report and Databases to Decision-making 14 2. Focal Habitats and Associated Focal Species 31 2.1 Introduction 31 2.2 Focal Habitat: Oak Woodlands 37 2.2.1 Definition 37 2.2.2 Recognition of Importance 37 2.2.3 Status and Distribution 37 2.2.4 Past Impacts, Limiting Factors, and Future Threats 38 2.2.5 Protection, Restoration, and Management 39 2.2.6 Compatibility of Oak Woodland Management and Stream Habitat Management. 40 2.2.7 Contribution of Oak Woodlands to Regional Biodiversity 40 2.2.8 Selected Focal Species 40 2.2.9 Synthesis: Indicators of Oak Woodland Ecological Condition and Sustainability 53 2.3 Focal Habitat: Upland Prairie, Savanna, and Rock Outcrops 55 2.3.1 Description 55 2.3.2 Recognition of Importance 55 2.3.3 Status and Distribution 56 2.3.4 Past Impacts, Limiting Factors, and Future Threats 57 2.3.5 Protection, Restoration, and Management 58 2.3.6 Compatibility of Upland Prairie-Savanna Management and Stream Management 58 2.3.7 Contribution of Upland Prairie-Savanna to Regional Biodiversity 59 2.3.8 Selected Focal Species 59 2.3.9 Synthesis: Indicators of Ecological Condition and Sustainability for Upland Prairie- Savanna 77 2.4 Focal Habitat: Wetland Prairie and Seasonal Marsh 81 2.4.1 -
Butterflies and Moths of Yavapai County, Arizona, United States
Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail -
Reptiles and Amphibians
A good book for beginners is Himmelman’s (2002) book “Discovering Moths’. Winter Moths (2000) describes several methods for By Dennis Skadsen capturing and observing moths including the use of light traps and sugar baits. There are Unlike butterflies, very little fieldwork has a few other essential books listed in the been completed to determine species suggested references section located on composition and distribution of moths in pages 8 & 9. Many moth identification northeast South Dakota. This is partly due guides can now be found on the internet, the to the fact moths are harder to capture and North Dakota and Iowa sites are the most study because most adults are nocturnal, and useful for our area. Since we often identification to species is difficult in the encounter the caterpillars of moths more field. Many adults can only be often than adults, having a guide like differentiated by studying specimens in the Wagners (2005) is essential. hand with a good understanding of moth taxonomy. Listed below are just a few of the species that probably occur in northeast South Although behavior and several physiological Dakota. The list is compiled from the characteristics separate moths from author’s personnel collection, and specimens butterflies including flight periods (moths collected by Gary Marrone or listed in Opler are mainly nocturnal (night) and butterflies (2006). Common and scientific names diurnal (day)); the shapes of antennae and follow Moths of North Dakota (2007) or wings; each have similar life histories. Both Opler (2006). moths and butterflies complete a series of changes from egg to adult called metamorphosis.