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The 2014 Golden Gate National Parks Bioblitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event
National Park Service U.S. Department of the Interior Natural Resource Stewardship and Science The 2014 Golden Gate National Parks BioBlitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event Natural Resource Report NPS/GOGA/NRR—2016/1147 ON THIS PAGE Photograph of BioBlitz participants conducting data entry into iNaturalist. Photograph courtesy of the National Park Service. ON THE COVER Photograph of BioBlitz participants collecting aquatic species data in the Presidio of San Francisco. Photograph courtesy of National Park Service. The 2014 Golden Gate National Parks BioBlitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event Natural Resource Report NPS/GOGA/NRR—2016/1147 Elizabeth Edson1, Michelle O’Herron1, Alison Forrestel2, Daniel George3 1Golden Gate Parks Conservancy Building 201 Fort Mason San Francisco, CA 94129 2National Park Service. Golden Gate National Recreation Area Fort Cronkhite, Bldg. 1061 Sausalito, CA 94965 3National Park Service. San Francisco Bay Area Network Inventory & Monitoring Program Manager Fort Cronkhite, Bldg. 1063 Sausalito, CA 94965 March 2016 U.S. Department of the Interior National Park Service Natural Resource Stewardship and Science Fort Collins, Colorado The National Park Service, Natural Resource Stewardship and Science office in Fort Collins, Colorado, publishes a range of reports that address natural resource topics. These reports are of interest and applicability to a broad audience in the National Park Service and others in natural resource management, including scientists, conservation and environmental constituencies, and the public. The Natural Resource Report Series is used to disseminate comprehensive information and analysis about natural resources and related topics concerning lands managed by the National Park Service. -
Lepidoptera of North America 5
Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera by Valerio Albu, 1411 E. Sweetbriar Drive Fresno, CA 93720 and Eric Metzler, 1241 Kildale Square North Columbus, OH 43229 April 30, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration: Blueberry Sphinx (Paonias astylus (Drury)], an eastern endemic. Photo by Valeriu Albu. 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 and Pest Management Colorado State University, Fort Collins, CO 80523 Abstract A list of 1531 species ofLepidoptera is presented, collected over 15 years (1988 to 2002), in eleven southern West Virginia counties. A variety of collecting methods was used, including netting, light attracting, light trapping and pheromone trapping. The specimens were identified by the currently available pictorial sources and determination keys. Many were also sent to specialists for confirmation or identification. The majority of the data was from Kanawha County, reflecting the area of more intensive sampling effort by the senior author. This imbalance of data between Kanawha County and other counties should even out with further sampling of the area. Key Words: Appalachian Mountains, -
Chionodes Scotodes
Chionodes scotodes Chionodes formosella-complex. Chionodes abitus Hodges, 1999. Chionodes argentipunctella (Ely, 1910). Chionodes bicostomaculella (Chambers, 1872). Chionodes formosella (Murtfeldt, 1881). Chionodes fuscomaculella (Chambers, 1872). Chionodes hapsus Hodges, 1999. Chionodes iridescens Clarke, 1947. Chionodes percultor Hodges, 1999. Chionodes powelli Hodges, 1999. Chionodes suasor Hodges, 1999. Chionodes gilvomaculella-complex. Chionodes scotodes (Walsingham, 1911). The obscurusella species-group. Chionodes thoraceochrella-complex. CHIONODES Hübner 1825 - Valid Name abdominella Busck 1903 - Valid Name abella Busck 1903 - Valid Name abradescens Braun 1921 - Valid Name acerella Sattler 1967 - Valid Name acrina Keifer 1933 - Valid Name agriodes Meyrick 1927 - Valid Name apolectella Walsingham 1900 - Valid Name arenella Forbes 1922 - Valid Name argentipunctella Ely 1910 - Valid Name argosema Meyrick 1917 - Valid Name aristella Busck 1903 - Valid Name bastuliella Rebel 1931 -. Valid Name bicolor Clarke 1947 - Valid Name bicostomaculella Chambers 1872 - Valid Name * gibbosella Chambers 1873 - Junior subjective synonym * querci... Original publication details: Scientific Name of Taxon: scotodes. Original Rank: ? Current Status: Valid Name. Current Rank: SPECIES. Original Combination Chionodes scotodes Walsingham 1911. urn:lsid:insecta.pro:taxonomy:655999. Authors. * Our website is multilingual. Some comments have been translated from other languages. Chionodes scotodes photos. There are no photos of this species on the website yet. You can offer your photo by logging into your account. Other species Chionodes. Chionodes abdominella Busck 1903. Chionodes abella Busck 1903. Chionodes abradescens Braun 1921. Chionodes acerella Sattler 1967. Chionodes acrina Keifer 1933. Chionodes agriodes Meyrick 1927. Chionodes apolectella (Walsingham, 1900). Chionodes aprilella (Huemer & Sattler, 1995). Chionodes arenella Forbes 1922. Chionodes argentipunctella Ely 1 Chionodes is a genus of moths of the family Gelechiidae. -
Insect Survey of Four Longleaf Pine Preserves
A SURVEY OF THE MOTHS, BUTTERFLIES, AND GRASSHOPPERS OF FOUR NATURE CONSERVANCY PRESERVES IN SOUTHEASTERN NORTH CAROLINA Stephen P. Hall and Dale F. Schweitzer November 15, 1993 ABSTRACT Moths, butterflies, and grasshoppers were surveyed within four longleaf pine preserves owned by the North Carolina Nature Conservancy during the growing season of 1991 and 1992. Over 7,000 specimens (either collected or seen in the field) were identified, representing 512 different species and 28 families. Forty-one of these we consider to be distinctive of the two fire- maintained communities principally under investigation, the longleaf pine savannas and flatwoods. An additional 14 species we consider distinctive of the pocosins that occur in close association with the savannas and flatwoods. Twenty nine species appear to be rare enough to be included on the list of elements monitored by the North Carolina Natural Heritage Program (eight others in this category have been reported from one of these sites, the Green Swamp, but were not observed in this study). Two of the moths collected, Spartiniphaga carterae and Agrotis buchholzi, are currently candidates for federal listing as Threatened or Endangered species. Another species, Hemipachnobia s. subporphyrea, appears to be endemic to North Carolina and should also be considered for federal candidate status. With few exceptions, even the species that seem to be most closely associated with savannas and flatwoods show few direct defenses against fire, the primary force responsible for maintaining these communities. Instead, the majority of these insects probably survive within this region due to their ability to rapidly re-colonize recently burned areas from small, well-dispersed refugia. -
List of Animal Species with Ranks October 2017
Washington Natural Heritage Program List of Animal Species with Ranks October 2017 The following list of animals known from Washington is complete for resident and transient vertebrates and several groups of invertebrates, including odonates, branchipods, tiger beetles, butterflies, gastropods, freshwater bivalves and bumble bees. Some species from other groups are included, especially where there are conservation concerns. Among these are the Palouse giant earthworm, a few moths and some of our mayflies and grasshoppers. Currently 857 vertebrate and 1,100 invertebrate taxa are included. Conservation status, in the form of range-wide, national and state ranks are assigned to each taxon. Information on species range and distribution, number of individuals, population trends and threats is collected into a ranking form, analyzed, and used to assign ranks. Ranks are updated periodically, as new information is collected. We welcome new information for any species on our list. Common Name Scientific Name Class Global Rank State Rank State Status Federal Status Northwestern Salamander Ambystoma gracile Amphibia G5 S5 Long-toed Salamander Ambystoma macrodactylum Amphibia G5 S5 Tiger Salamander Ambystoma tigrinum Amphibia G5 S3 Ensatina Ensatina eschscholtzii Amphibia G5 S5 Dunn's Salamander Plethodon dunni Amphibia G4 S3 C Larch Mountain Salamander Plethodon larselli Amphibia G3 S3 S Van Dyke's Salamander Plethodon vandykei Amphibia G3 S3 C Western Red-backed Salamander Plethodon vehiculum Amphibia G5 S5 Rough-skinned Newt Taricha granulosa -
Arthropod Diversity and Conservation in Old-Growth Northwest Forests'
AMER. ZOOL., 33:578-587 (1993) Arthropod Diversity and Conservation in Old-Growth mon et al., 1990; Hz Northwest Forests complex litter layer 1973; Lattin, 1990; JOHN D. LATTIN and other features Systematic Entomology Laboratory, Department of Entomology, Oregon State University, tural diversity of th Corvallis, Oregon 97331-2907 is reflected by the 14 found there (Lawtt SYNOPSIS. Old-growth forests of the Pacific Northwest extend along the 1990; Parsons et a. e coastal region from southern Alaska to northern California and are com- While these old posed largely of conifer rather than hardwood tree species. Many of these ity over time and trees achieve great age (500-1,000 yr). Natural succession that follows product of sever: forest stand destruction normally takes over 100 years to reach the young through successioi mature forest stage. This succession may continue on into old-growth for (Lattin, 1990). Fire centuries. The changing structural complexity of the forest over time, and diseases, are combined with the many different plant species that characterize succes- bances. The prolot sion, results in an array of arthropod habitats. It is estimated that 6,000 a continually char arthropod species may be found in such forests—over 3,400 different ments and habitat species are known from a single 6,400 ha site in Oregon. Our knowledge (Southwood, 1977 of these species is still rudimentary and much additional work is needed Lawton, 1983). throughout this vast region. Many of these species play critical roles in arthropods have lx the dynamics of forest ecosystems. They are important in nutrient cycling, old-growth site, tt as herbivores, as natural predators and parasites of other arthropod spe- mental Forest (HJ cies. -
Moths of the Malheur National Wildlife Refuge
MOTHS OF UMATILLA NATIONAL WILDLIFE REFUGE: Results from 10 sites Sampled May 22-23, 2017 Dana Ross 1005 NW 30th Street Corvallis, OR 97330 (541) 758-3006 [email protected] SUMMARY Macro-moths were sampled from the Umatilla National Wildlife Refuge for a third time 22-23 May, 2017 as part of an ongoing pollinator inventory. Blacklight traps were deployed for a single night at ten sites representative of major plant communities in the McCormack and Paterson Units. A grand total of 331 specimens and 36 moth species were sampled. Of those, 17 species (47%) were documented from the refuge for the first time. In a somewhat larger geographical context, 21 species were recorded for the first (8), second (7) or third (6) time from Morrow County, Oregon while 4 species were documented for the first (1) or second (3) time from Benton County, Washington. INTRODUCTION National Wildlife Refuges protect important habitats for many plant and animal species. Refuge inventories have frequently included plants, birds and mammals, but insects - arguably the most abundant and species-rich group in any terrestrial habitat - have largely been ignored. Small size, high species richness and a lack of identification resources have all likely contributed to their being overlooked. Certain groups such as moths, however, can be easily and inexpensively sampled using light traps and can be identified by regional moth taxonomists. Once identified, many moth species can be tied to known larval hostplant species at a given site, placing both insect and plant within a larger ecological context. Moths along with butterflies belong to the insect Order Lepidoptera. -
Big Creek Lepidoptera Checklist
Big Creek Lepidoptera Checklist Prepared by J.A. Powell, Essig Museum of Entomology, UC Berkeley. For a description of the Big Creek Lepidoptera Survey, see Powell, J.A. Big Creek Reserve Lepidoptera Survey: Recovery of Populations after the 1985 Rat Creek Fire. In Views of a Coastal Wilderness: 20 Years of Research at Big Creek Reserve. (copies available at the reserve). family genus species subspecies author Acrolepiidae Acrolepiopsis californica Gaedicke Adelidae Adela flammeusella Chambers Adelidae Adela punctiferella Walsingham Adelidae Adela septentrionella Walsingham Adelidae Adela trigrapha Zeller Alucitidae Alucita hexadactyla Linnaeus Arctiidae Apantesis ornata (Packard) Arctiidae Apantesis proxima (Guerin-Meneville) Arctiidae Arachnis picta Packard Arctiidae Cisthene deserta (Felder) Arctiidae Cisthene faustinula (Boisduval) Arctiidae Cisthene liberomacula (Dyar) Arctiidae Gnophaela latipennis (Boisduval) Arctiidae Hemihyalea edwardsii (Packard) Arctiidae Lophocampa maculata Harris Arctiidae Lycomorpha grotei (Packard) Arctiidae Spilosoma vagans (Boisduval) Arctiidae Spilosoma vestalis Packard Argyresthiidae Argyresthia cupressella Walsingham Argyresthiidae Argyresthia franciscella Busck Argyresthiidae Argyresthia sp. (gray) Blastobasidae ?genus Blastobasidae Blastobasis ?glandulella (Riley) Blastobasidae Holcocera (sp.1) Blastobasidae Holcocera (sp.2) Blastobasidae Holcocera (sp.3) Blastobasidae Holcocera (sp.4) Blastobasidae Holcocera (sp.5) Blastobasidae Holcocera (sp.6) Blastobasidae Holcocera gigantella (Chambers) Blastobasidae -
Macrolepidoptera Inventory of the Chilcotin District
Macrolepidoptera Inventory of the Chilcotin District Aud I. Fischer – Biologist Jon H. Shepard - Research Scientist and Crispin S. Guppy – Research Scientist January 31, 2000 2 Abstract This study was undertaken to learn more of the distribution, status and habitat requirements of B.C. macrolepidoptera (butterflies and the larger moths), the group of insects given the highest priority by the BC Environment Conservation Center. The study was conducted in the Chilcotin District near Williams Lake and Riske Creek in central B.C. The study area contains a wide variety of habitats, including rare habitat types that elsewhere occur only in the Lillooet-Lytton area of the Fraser Canyon and, in some cases, the Southern Interior. Specimens were collected with light traps and by aerial net. A total of 538 species of macrolepidoptera were identified during the two years of the project, which is 96% of the estimated total number of species in the study area. There were 29,689 specimens collected, and 9,988 records of the number of specimens of each species captured on each date at each sample site. A list of the species recorded from the Chilcotin is provided, with a summary of provincial and global distributions. The habitats, at site series level as TEM mapped, are provided for each sample. A subset of the data was provided to the Ministry of Forests (Research Section, Williams Lake) for use in a Flamulated Owl study. A voucher collection of 2,526 moth and butterfly specimens was deposited in the Royal BC Museum. There were 25 species that are rare in BC, with most known only from the Riske Creek area. -
Moths of North Carolina - Early Draft 1
Erebidae Clemensia albata Little White Lichen Moth 30 n=56 ••• • • • • • • 20 High Mt. •• • • • • N • • •• u 10 • • • • • • m • • • • • • • b • 0 • • • e • • • • • • • r 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 • • 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 NC counties: 56 • • Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec • o • • 30 • • • f n=152 • = Sighting or Collection Low Mt. High counts of: • • in NC since 2001 F 20 • = Not seen since 2001 l 130 - Martin - 1996-07-17 • i 10 126 - Onslow - 1995-07-05 g Status Rank h 110 - Martin - 1996-07-18 0 NC US NC Global t 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 D Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec a 30 30 t n=77 n=298 e 20 Pd 20 CP s 10 10 0 0 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Three periods to each month: 1-10 / 11-20 / 21-31 FAMILY: Erebidae SUBFAMILY: Arctiinae TRIBE: Lithosiini TAXONOMIC_COMMENTS: One of three species in this genus that occur in North America (Lafontaine and Schmidt, 2010). -
Zeitschrift Für Naturforschung / C / 42 (1987)
1352 Notes (Z)-3-TetradecenyI Acetate as a Sex-Attractant species feed on Picea, Rumex and Rubus, respective Component in Gelechiinae and Anomologinae ly, and their relative trap captures greatly varied (Lepidoptera: Gelechiidae) between test sites, depending on host abundance; Ernst Priesner which may explain why one species (A. micella) was missing from the test by Willemse et al. Max-Planek-Institut für Verhaltensphysiologie. D-8131 Seewiesen The outstanding effectiveness of the Z3-14:Ac for Z. Naturforsch. 42c, 1352—1355 (1987); males of these gelechiid species was supported by received August 25, 1987 electroantennogram measurements. These were Sex-Attractant, Attraction-Inhibitor, J3-Alkenyl made from males newly taken in Z3-14:Ac baited A cetates, Chionodes, Monochroa, Argolamprotes, traps (with antennae not yet glued to the adhesive), Aproaerema, Gelechiidae using technical procedures as in other Microlepido- The title compound, unreported as an insect pheromone ptera [3, 4], In the series of (Z)- and (£)-alkenyl ace component, effectively attracted certain male Gelechiidae tates, varied for chain length and double bond posi (genera Chionodes, Monochroa, Argolamprotes) as a sin gle chemical. Trap captures with this chemical decreased tion, the Z3-14:Ac, at the test amount of 1 |ig, elic on addition of either (E)-3-dodecenyl acetate, (£)-3-tetra- ited the greatest EAG response. This was followed decenyl acetate or (Z)-3-tetradecen-l-ol, the sexual attrac- by the geometric isomer (.O-MiAc), the corre tants of other, closely related species. Results on an Aproaerem a test species showing a synergistic attraction sponding alcohol analogue (Z3-14:OH) and some response to combinations of (Z)-3-tetradecenyl acetate positional isomers and shorter-chain homologues with its homologue (Z)-3-dodecenyl acetate are included. -
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.