CBD First National Report
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Superior National Forest
Admirals & Relatives Subfamily Limenitidinae Skippers Family Hesperiidae £ Viceroy Limenitis archippus Spread-wing Skippers Subfamily Pyrginae £ Silver-spotted Skipper Epargyreus clarus £ Dreamy Duskywing Erynnis icelus £ Juvenal’s Duskywing Erynnis juvenalis £ Northern Cloudywing Thorybes pylades Butterflies of the £ White Admiral Limenitis arthemis arthemis Superior Satyrs Subfamily Satyrinae National Forest £ Common Wood-nymph Cercyonis pegala £ Common Ringlet Coenonympha tullia £ Northern Pearly-eye Enodia anthedon Skipperlings Subfamily Heteropterinae £ Arctic Skipper Carterocephalus palaemon £ Mancinus Alpine Erebia disa mancinus R9SS £ Red-disked Alpine Erebia discoidalis R9SS £ Little Wood-satyr Megisto cymela Grass-Skippers Subfamily Hesperiinae £ Pepper & Salt Skipper Amblyscirtes hegon £ Macoun’s Arctic Oeneis macounii £ Common Roadside-Skipper Amblyscirtes vialis £ Jutta Arctic Oeneis jutta (R9SS) £ Least Skipper Ancyloxypha numitor Northern Crescent £ Eyed Brown Satyrodes eurydice £ Dun Skipper Euphyes vestris Phyciodes selenis £ Common Branded Skipper Hesperia comma £ Indian Skipper Hesperia sassacus Monarchs Subfamily Danainae £ Hobomok Skipper Poanes hobomok £ Monarch Danaus plexippus £ Long Dash Polites mystic £ Peck’s Skipper Polites peckius £ Tawny-edged Skipper Polites themistocles £ European Skipper Thymelicus lineola LINKS: http://www.naba.org/ The U.S. Department of Agriculture (USDA) prohibits discrimination http://www.butterfliesandmoths.org/ in all its programs and activities on the basis of race, color, national -
SOME NOTES on BOLORIA in CENTRAL COLORADO (NYMPHALIDJE) by F. MARTIN BROWN Six Species of Boloria Are Found in Colorado, And
64 Val.S: nos.3-4 SOME NOTES ON BOLORIA IN CENTRAL COLORADO (NYMPHALIDJE) by F. MARTIN BROWN Six species of Boloria are found in Colorado, and there is the possibility that three others fly in the state but as yet have not been discovered. To avoid nomenclatorial confusion while awaiting KLOTS' promised revision of the genus I use here the names for species accepted by McDUNNOUGH in his J 938 Checklist. Boloria myrina ( = selene) tollandensis Barnes & Benjamin My experience with this insect is limited to three areas and all-too-brief collecting. The butterfly is on the wing early in July and by the last week of the month is in rather shabby condition. It seems to prefer open grassy meadows much like those in which its eastern counterpart flies. Altitudinally it seems to be narrowly restricted to a few hundred feet, either way, from 9000 feet. I know of colonies in the Front Range north of the South Fork of the Platte River, the Park Range, the Collegiate Range, and the Rabbit ears Range. DISTRIBUTION OF COLORADO WILLOW-BOG BOLOR/A. Boloria apbirape alticola Barnes & McDunnough This is one of three species closely associated with willow bogs in Colorado. There is good reason to believe that it flies in all of the mountain ranges of the state, although I have nor seen specimens from the Sange do Cristos. It first appears during the last week of June in bogs around 9600 feet, and the last specimens to be taken are found at about 12,000 feet late in August. -
BRUSH-FOOTED BUTTERFLIES OR FOUR-FOOTED BUTTERFLIES NYMPHALIDAE (RAFINESQUE, 1815) Classification Kingdom
BRUSH-FOOTED BUTTERFLIES OR FOUR-FOOTED BUTTERFLIES NYMPHALIDAE (RAFINESQUE, 1815) NATURAL HISTORY SUMMARY BY JACOB EGGE, PHD Classification Kingdom: Animalia Phylum: Arthropoda Class: Insecta Order: Lepidoptera Family: Nymphalidae Description The family Nymphalidae includes some 6,000 species of butterflies. Most species in this family have greatly reduced forelegs and stand on only four legs. The vestigial forelegs have a brush-like set of hairs. Antennae always have two grooves on the underside. Many have brightly colored wings with cryptic undersides that help provide camouflage among leaves and brush. Familiar species in the family include the Monarch (Danaus plexippus) and fritillaries (Speyeria and Boloria). Distribution The family Nymphalidae has representative species on all continents except Antarctica, but they are most diverse in the Neotropics (DeVries 1987). Diet Nymphalid caterpillars feed exclusively on plants and many are host specific, while others are generalists. Adults generally feed on nectar from flowers they suck through a proboscis. However, some species feed on sap, fermenting fruit, or dung. (Hadley 2016). Habitat and Ecology Nyphalids inhabit a variety of habitats ranging from tropical rainforests to tundra environments of high elevation summits. Many species of Nymphalid, including the Monarch, have distasteful body fluids that deter predators. These distasteful compounds are derived from the plants they feed on as caterpillars. Most species are diurnal, with a few nocturnal species. Caterpillars are typically found associated with a particular host plant species or group of plants. Plant specializations range broadly across the family and include aster, violet, willow, elm, poplar, nettles, thistle, hackberry, and milkweed (Triplehorn and Johnson 2005). Reproduction and Life Cycle All butterflies undergo complete metamorphosis with both a larval (caterpillar) and pupal stage. -
Behavioural Thermoregulation by High Arctic Butterflies*
Behavioural Thermoregulation by High Arctic Butterflies* P. G. KEVAN AND J. D. SHORTHOUSE2s ABSTRACT. Behavioural thermoregulation is an important adaptation of the five high arctic butterflies found at Lake Hazen (81 “49‘N., 71 18’W.), Ellesmere Island, NorthwestTerritories. Direct insolation is used byarctic butterflies to increase their body temperatures. They select basking substrates andprecisely orientate their wings with respect to the sun. Some experiments illustrate the importance of this. Wing morphology, venation, colour, hairiness, and physiology are briefly discussed. RI~SUMÉ.Comportement thermo-régulatoire des papillons du haut Arctique. Chez cinq especes de papillons trouvés au lac Hazen (81”49’ N, 71” 18’ W), île d’Elles- mere, Territoires du Nord-Ouest, le comportement thermo-régulatoire est une im- portante adaptation. Ces papillons arctiques se servent de l’insolation directe pour augmenter la température de leur corps: ils choisissent des sous-strates réchauffantes et orientent leurs ailes de façon précise par rapport au soleil. Quelques expériences ont confirmé l’importance de ce fait. On discute brikvement de la morphologie alaire, de la couleur, de la pilosité et de la physiologie de ces insectes. INTRODUCTION Basking in direct sunlight has long been known to have thermoregulatory sig- nificance for poikilotherms (Gunn 1942), particularly reptiles (Bogert 1959) and desert locusts (Fraenkel 1P30;.Stower and Griffiths 1966). Clench (1966) says that this was not known before iwlepidoptera but Couper (1874) wrote that the common sulphur butterfly, Colias philodice (Godart) when resting on a flower leans sideways “as if to receive the warmth of the sun”. Later workers, noting the consistent settling postures and positions of many butterflies, did not attribute them to thermoregulation, but rather to display (Parker 1903) or concealment by shadow minimization (Longstaff 1905a, b, 1906, 1912; Tonge 1909). -
Pearl-Bordered Fritillary Boloria Euphrosyne Species Action Plan
Pearl-bordered Fritillary Boloria euphrosyne Species Action Plan 1. Introduction The pearl-bordered fritillary butterfly was listed as a UK BAP species and subsequently included within Section 41 of the Natural Environment and Rural Communities (NERC) Act 2006. 2. Current Status 2.1 Ecology and habitat requirements The pearl-bordered fritillary is one of the earliest fritillaries to emerge and can be found as early as April in woodland clearings or on rough hillsides with bracken where it feeds on spring flowers such as bugle (Ajuga reptans). The most widely used larval food plants are common dog-violet (Viola riviniana) and early dog-violet (V. reichenbachiana). In all habitats it requires abundant larval food plants growing in short, sparse vegetation where there is abundant leaf litter (Asher et al., 2001). 2.2 Population and distribution The pearl-bordered fritillary is widespread across Europe from northern Spain to Scandinavia and eastwards to Russia and Asia. It appears to be stable in many European countries but elsewhere has undergone serious declines (e.g. populations in Belgium and Denmark show >50% decreases in 25 years). The State of the UK's Butterflies 2015 report (Fox et al., 2015) shows that the pearl-bordered fritillary underwent a rapid decline between 1976-2014 with a -95% change in occurrence and -71% change in abundance. However, from 2005-2014 the changes in occurrence and abundance are +3% and +45% respectively, indicating a recovery that can in part be attributed to successful working at a landscape scale in places such as Wyre Forest. The Wyre Forest is a nationally important stronghold for the pearl-bordered fritillary. -
Boloria Frigga Saga (Frigga Fritillary)
Maine 2015 Wildlife Action Plan Revision Report Date: January 13, 2016 Boloria frigga saga (Frigga Fritillary) Priority 1 Species of Greatest Conservation Need (SGCN) Class: Insecta (Insects) Order: Lepidoptera (Butterflies, Skippers, And Moths) Family: Nymphalidae (Brushfooted Butterflies) General comments: proposed endangered 2014; only 1 known population; restricted to northern Maine and habitat specialized but still partially un- surveyed; absent at several seemingly appropriate locales Species Conservation Range Maps for Frigga Fritillary: Town Map: Boloria frigga saga_Towns.pdf Subwatershed Map: Boloria frigga saga_HUC12.pdf SGCN Priority Ranking - Designation Criteria: Risk of Extirpation: Maine Status: Endangered State Special Concern or NMFS Species of Concern: NA Recent Significant Declines: NA Regional Endemic: NA High Regional Conservation Priority: NA High Climate Change Vulnerability: Vulnerability: 3, Confidence: Medium, Reviewers: Decided in Workshop (W) Understudied rare taxa: Recently documented or poorly surveyed rare species for which risk of extirpation is potentially high (e.g. few known occurrences) but insufficient data exist to conclusively assess distribution and status. *criteria only qualifies for Priority 3 level SGCN* Notes: proposed endangered 2014; only 1 known population; restricted to northern Maine and habitat specialized but still relatively un-surveyed; absent at several seemingly appropriate locales Historical: NA Culturally Significant: NA Professional Discretion: Current criteria ranked Boloria frigga -
Boloria Selene) on the Ochoco National Forest
2015 Surveys for Silver-bordered Fritillary (Boloria selene) On the Ochoco National Forest Prepared by Dana Ross (Entomologist, Lepidoptera Specialist) November 2015 0 SUMMARY The silver-bordered fritillary (Boloria selene) is designated as an ISSSSP Special Status/Sensitive Species in Oregon. In June and July of 2015, surveys were performed for this regionally rare butterfly on public lands managed by the Ochoco National Forest and Bureau of Land Management where there was either historical occurrence or a likelihood of undiscovered populations of the insect. Populations were documented at 8 distinct locations from Big Summit Prairie south to Williams and Gray prairies. All observed populations were in the North Fork Crooked River drainage at sites that contained at least some seasonally wet or marshy habitats with violets (the Boloria selene larval hostplant). Three fairly sizeable populations were located – at Elliot Creek (north Big Summit Prairie), along the BLM North Fork Crooked River/lower Lookout Creek site immediately south of Big Summit Prairie, and at NW Williams Prairie. Comparatively few of the butterflies were observed elsewhere. Observed damage to fragile critical habitats, such as at Elliot Creek (off-road vehicles) and Williams Prairie (cattle grazing), must be avoided in the future to prevent habitat degradation, population decline and potential local extirpation of the insect. It is recommended that additional surveys for silver-bordered fritillary take place on National Forest and BLM lands to: 1)more completely document the species regional range and distribution; 2) to more accurately assess population/meta-population size; 3) to assess the impact to future generations from observed mid-season damage to critical habitats; 4) to verify benefits (increased abundance or local persistence) to populations from habitat protection or habitat restoration; 5) to determine butterfly response to short or long term environmental conditions such as drought. -
How Much Biodiversity Is in Natura 2000?
Alterra Wageningen UR Alterra Wageningen UR is the research institute for our green living environment. P.O. Box 47 We off er a combination of practical and scientifi c research in a multitude of How much Biodiversity is in Natura 2000? 6700 AA Wageningen disciplines related to the green world around us and the sustainable use of our living The Netherlands environment, such as fl ora and fauna, soil, water, the environment, geo-information The “Umbrella Eff ect” of the European Natura 2000 protected area network T +31 (0) 317 48 07 00 and remote sensing, landscape and spatial planning, man and society. www.wageningenUR.nl/en/alterra The mission of Wageningen UR (University & Research centre) is ‘To explore Technical report Alterra Report 2730B the potential of nature to improve the quality of life’. Within Wageningen UR, ISSN 1566-7197 nine specialised research institutes of the DLO Foundation have joined forces with Wageningen University to help answer the most important questions in the Theo van der Sluis, Ruud Foppen, Simon Gillings, Thomas Groen, René Henkens, Stephan Hennekens, domain of healthy food and living environment. With approximately 30 locations, 6,000 members of staff and 9,000 students, Wageningen UR is one of the leading Kim Huskens, David Noble, Fabrice Ottburg, Luca Santini, Henk Sierdsema, Andre van Kleunen, organisations in its domain worldwide. The integral approach to problems and Joop Schaminee, Chris van Swaay, Bert Toxopeus, Michiel Wallis de Vries and Lawrence Jones-Walters the cooperation between the various disciplines -
Fritillary, White Mountain
Appendix A: Insects White Mountain Fritillary Boloria titania montinus Federal Listing N/A State Listing E Global Rank State Rank S1 Regional Status Photo by © K.P. McFarland Justification (Reason for Concern in NH) White Mountain fritillary is limited to the 2,800 ac alpine zone of the White Mountain National Forest (WMNF). The natural communities used most frequently by White Mountain fritillary ranked S1 in New Hampshire. Climate change will likely alter alpine habitat structure, composition, phenology, and distribution, all of which directly impact White Mountain fritillary populations (Kimball and Weihrauch 2000, McFarland 2003, Lesica and McCune 2004). Habitat isolation further increases the species’ vulnerability (Halloy and Mark 2003, McFarland 2003). Interdependent responses to climate change could disrupt ecological interactions throughout the alpine community, reducing the ability of sensitive species to endure other environmental stresses, such as acid deposition and increased UV‐B radiation (McCarty 2001). Distribution White Mountain fritillary is a subspecies endemic to the 2,800 ac alpine zone of the Presidential Range of the WMNF (McFarland 2003). Habitat suitability depends on the abundance of host plants, particularly Alpine goldenrod, as well as ground temperature, moisture, and winter snow cover (Anthony 1970, McFarland 2003). White Mountain fritillary populations tend to be locally abundant, the northernmost occurrence is from Mt. Madison and the southernmost is Mt. Pierce at an elevation range of 1,220 to 1,860 m, with the highest densities at Cragway Spring and Wamsutta Trail (McFarland 2003). The only historical record occurring outside the Presidential Range alpine zone was a specimen collected by D. J. -
Chequamegon Nicolet National Forest
Monarchs Subfamily Danainae £ Monarch Danaus plexippus Butterflies of the Skippers Family Hesperiidae Chequamegon Spread-wing Skippers Subfamily Pyrginae £ Silver-spotted Skipper Epargyreus clarus Nicolet £ Dreamy Duskywing Erynnis icelus £ Juvenal’s Duskywing Erynnis juvenalis National Forest £ Columbine Duskywing Erynnis lucilius £ Northern Cloudywing Thorybes pylades Skipperlings Subfamily Heteropterinae £ Arctic Skipper Carterocephalus palaemon Henry’s Elfin Grass-Skippers Subfamily Hesperiinae £ Pepper & Salt Skipper Amblyscirtes hegon R9SS £ Common Roadside-Skipper Amblyscirtes vialis Callophrys henrici £ Delaware Skipper Anatrytone logan £ Least Skipper Ancyloxypha numitor £ Dusted Skipper Atrytonopsis hianna £ Two-spotted Skipper Euphyes bimaculata £ Dion Skipper Euphyes dion £ Dun Skipper Euphyes vestris £ Common Branded Skipper Hesperia comma £ Leonard’s Skipper Hesperia leonardus £ Cobweb Skipper Hesperia metea £ Indian Skipper Hesperia sassacus LINKS: £ Hobomok Skipper Poanes hobomok £ Long Dash Polites mystic http://www.naba.org/cw £ Crossline Skipper Polites origenes http://www.butterfliesandmoths.org/ £ Peck’s Skipper Polites peckius The U.S. Department of Agriculture (USDA) prohibits discrimination more…. £ Tawny-edged Skipper Polites themistocles in all its programs and activities on the basis of race, color, national origin, age, disability, and where applicable, sex, marital status, familial status, parental status, religion, sexual orientation, genetic information, political beliefs, reprisal, or because all or part -
Boloria Eunomia and Boloria Selene
RESEARCH ARTICLE Cross-continental phylogeography of two Holarctic Nymphalid butterflies, Boloria eunomia and Boloria selene 1,2 3 4 5 Jana MaresovaID *, Jan Christian Habel , Gabriel NeveID , Marcin SielezniewID , Alena Bartonova1,2, Agata Kostro-Ambroziak5, Zdenek Faltynek Fric1 1 Biology Centre of the Czech Academy of Sciences, Institute of Entomology, Ceske Budejovice, Czech Republic, 2 University of South Bohemia, Faculty of Sciences, Ceske Budejovice, Czech Republic, 3 Terrestrial Ecology Research Group, Department of Ecology and Ecosystem Management, School of Life Sciences Weihenstephan, Technische UniversitaÈt MuÈnchen, Freising, Germany, 4 IMBE, Aix Marseille a1111111111 UniversiteÂ, CNRS, IRD, Avignon UniversiteÂ, Marseille, France, 5 Laboratory of Insect Evolutionary Biology a1111111111 and Ecology, Institute of Biology, University of Biaøystok, Biaøystok, Poland a1111111111 a1111111111 * [email protected] a1111111111 Abstract Pleistocene glaciations had significant effects on the distribution and evolution of species OPEN ACCESS inhabiting the Holarctic region. Phylogeographic studies concerning the entire region are Citation: Maresova J, Habel JC, Neve G, Sielezniew still rare. Here, we compared global phylogeographic patterns of one boreo-montane and M, Bartonova A, Kostro-Ambroziak A, et al. (2019) one boreo-temperate butterflies with largely overlapping distribution ranges across the Cross-continental phylogeography of two Holarctic Nymphalid butterflies, Boloria eunomia and Boloria Northern Hemisphere, but with different levels of range fragmentation and food specializa- selene. PLoS ONE 14(3): e0214483. https://doi. tion. We reconstructed the global phylogeographic history of the boreo-montane specialist org/10.1371/journal.pone.0214483 Boloria eunomia (n = 223) and of the boreo-temperate generalist Boloria selene (n = 106) Editor: èukasz Kajtoch, Institute of Systematics based on mitochondrial and nuclear DNA markers, and with species distribution modelling and Evolution of Animals Polish Academy of (SDM). -
Sentinels on the Wing: the Status and Conservation of Butterflies in Canada
Sentinels on the Wing The Status and Conservation of Butterflies in Canada Peter W. Hall Foreword In Canada, our ties to the land are strong and deep. Whether we have viewed the coasts of British Columbia or Cape Breton, experienced the beauty of the Arctic tundra, paddled on rivers through our sweeping boreal forests, heard the wind in the prairies, watched caribou swim the rivers of northern Labrador, or searched for song birds in the hardwood forests of south eastern Canada, we all call Canada our home and native land. Perhaps because Canada’s landscapes are extensive and cover a broad range of diverse natural systems, it is easy for us to assume the health of our important natural spaces and the species they contain. Our country seems so vast compared to the number of Canadians that it is difficult for us to imagine humans could have any lasting effect on nature. Yet emerging science demonstrates that our natural systems and the species they contain are increas- ingly at risk. While the story is by no means complete, key indicator species demonstrate that Canada’s natural legacy is under pressure from a number of sources, such as the conversion of lands for human uses, the release of toxic chemicals, the introduction of new, invasive species or the further spread of natural pests, and a rapidly changing climate. These changes are hitting home and, with the globalization and expansion of human activities, it is clear the pace of change is accelerating. While their flights of fancy may seem insignificant, butterflies are sentinels or early indicators of this change, and can act as important messengers to raise awareness.