Journal Vol 9 No 1, April 1993
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Spatiotemporal Pattern of Phenology Across Geographic Gradients in Insects
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2017 Spatiotemporal pattern of phenology across geographic gradients in insects Khelifa, Rassim Abstract: Phenology – the timing of recurrent biological events – influences nearly all aspects of ecology and evolution. Phenological shifts have been recorded in a wide range of animals and plants worldwide during the past few decades. Although the phenological responses differ between taxa, they may also vary geographically, especially along gradients such as latitude or elevation. Since changes in phenology have been shown to affect ecology, evolution, human health and the economy, understanding pheno- logical shifts has become a priority. Although phenological shifts have been associated with changes in temperature, there is still little comprehension of the phenology-temperature relationship, particularly the mechanisms influencing its strength and the extent to which it varies geographically. Such ques- tions would ideally be addressed by combining controlled laboratory experiments on thermal response with long-term observational datasets and historical temperature records. Here, I used odonates (drag- onflies and damselflies) and Sepsid scavenger flies to unravel how temperature affects development and phenology at different latitudes and elevations. The main purpose of this thesis is to provide essential knowledge on the factors driving the spatiotemporal phenological dynamics by (1) investigating how phenology changed in time and space across latitude and elevation in northcentral Europe during the past three decades, (2) assessing potential temporal changes in thermal sensitivity of phenology and (3) describing the geographic pattern and usefulness of thermal performance curves in predicting natural responses. -
1 June 2021 Researchgate: Researchgate.Net/Profile
DAVID OUTOMURO PRIEDE, PH.D. CURRICULUM VITAE June 2021 Researchgate: researchgate.net/profile/David_Outomuro ORCID: orcid.org/0000-0002-1296-7273 EDUCATION Ph.D. 2011 University of Oviedo, Spain (Biology). Summa cum laude. (Dr. Francisco J. Ocharan) B.S. 2005 University of Oviedo, Spain (Biology). Valedictorian. PROFESSIONAL EXPERIENCE Aug 2017- Aug 2021 Postdoctoral researcher, Dept. Biological Sciences, University of Cincinnati, USA (Dr. Nathan Morehouse) Jul 2015-Jun 2017 Postdoctoral researcher, Evolutionary Biology Centre, Uppsala University, Sweden (Drs. Frank Johansson, Anders Ödeen, & Karin Nordström) Jul 2014-Jul 2015 Visiting Professor, Dept. Ciencias Biológicas, Universidad de los Andes, Colombia Nov 2011-Dec 2013 Postdoctoral researcher, Evolutionary Biology Centre, Uppsala University, Sweden (Dr. Frank Johansson) Jun 2006-May 2010 Graduate researcher and Teaching assistant, Dept. Biología de Organismos y Sistemas, University of Oviedo, Spain (Dr. Francisco J. Ocharan) Jul 2005-Aug 2005 Intern, Servicio Regional de Investigación y Desarrollo Agroalimentario de Asturias (SERIDA), Spain (Dr. Isabel Feito Díaz) Sep 2004-Jun 2005 Undergraduate research fellow, Dept. Biología de Organismos y Sistemas, University of Oviedo, Spain (Dr. Francisco J. Ocharan) RESEARCH INTERESTS I am a behavioral ecologist, interested in the micro- and macroevolutionary processes that promote diversity. My research has explored questions on the evolution of color signals, color vision, and flight morphology. I am particularly interested in understanding the evolution of color signals, how they are perceived by intended and unintended receivers and the role of these audiences in driving population and species divergence. I also study the evolution of flight morphology because wings are large conspicuous body surfaces that can be also used as motion signal vehicles for intra- and interspecific communication. -
Subarctic Darner Aeshna Subarctica
Natural Heritage Subarctic Darner & Endangered Species Aeshna subarctica Program State Status: Endangered www.mass.gov/nhesp Federal Status: None Massachusetts Division of Fisheries & Wildlife DESCRIPTION OF ADULT: The Subarctic Darner is a stunning insect species in the order Odonata, suborder Anisoptera (the dragonflies), and family Aeshnidae (the darners). The adult is a large dragonfly magnificently colored with greens, blues, and rich browns. The thorax (winged and legged segment behind the head) is mostly brown, with two green to blue dorsal stripes and two blue-green to yellowish lateral stripes. The abdominal segments are predominantly brown with green to blue markings. The Subarctic Darner has black legs and transparent to amber-tinged wings. The face is yellow with a thin black cross-line, and the eyes are dull blue- gray to green in color. Subarctic Darners range from 2.6 to almost 3 inches (66-76 mm) in overall length, with the females averaging somewhat larger. Wingspread ranges from 3.1 to 3.6 inches (78-92 mm). SIMILAR SPECIES: Ten species of blue darners (genus Aeshna) occur regularly in Massachusetts and the Subarctic Darner closely resembles many of them in appearance. The slight differences in pattern and and can be distinguished from other Aeshna using coloration distinguish the various species. The face of characteristics as per the keys in Walker (1958). the adult Subarctic Darner is yellow with a black cross- line. In addition, the lateral thoracic stripes are bent HABITAT: Sphagnum bogs and deep fens with wet forward in their upper halves, with the top of the stripe sphagnum. -
Recent Range Shifts of European Dragonflies Provide Support for An
Global Ecology and Biogeography, (Global Ecol. Biogeogr.) (2013) 22, 403–409 bs_bs_banner RESEARCH Recent range shifts of European PAPER dragonflies provide support for an inverse relationship between habitat predictability and dispersal Yannic Grewe1, Christian Hof 2,3, D. Matthias Dehling2, Roland Brandl1 and Martin Brändle1* 1Department of Ecology – Animal Ecology, ABSTRACT Faculty of Biology, Philipps-Universität Aim We compared the effects of recent shifts of northern range boundaries of Marburg, Marburg, Germany, 2Biodiversity and Climate Research Centre (BiK-F) and odonates adapted to either lentic (standing water) or lotic (running water) habitats Senckenberg Gesellschaft für Naturforschung, in Europe. Lentic species are thought to have a higher dispersal propensity than Frankfurt (Main), Germany, 3Center for lotic species because of the lower spatial and temporal persistence of lentic habitats Macroecology, Evolution and Climate, on average. Hence, we expected shifts in the range boundaries particularly of lentic Department of Biology, University of species. Copenhagen, Copenhagen, Denmark Location Europe. Methods Our analyses are based on odonate distribution maps from two field guides that present the European ranges of dragonflies and damselflies in 1988 and 2006. We categorized species according to their preference for lentic or lotic habi- tats, and then assigned each species to a southern or a northern group according to the centre of its distribution. Shifts in northern range boundaries were calculated as the average distance between the 10 northernmost grid cells in 1988 and 2006. Range boundary shifts were also analysed with regard to prevalence, phenology, body size and wing size. Results Lentic species of the southern group expanded their range boundaries on average 115 km northwards per decade, whereas lotic species of the southern group on average did not change their range boundaries. -
Dragonflies and Damselflies in Your Garden
Natural England works for people, places and nature to conserve and enhance biodiversity, landscapes and wildlife in rural, urban, coastal and marine areas. Dragonflies and www.naturalengland.org.uk © Natural England 2007 damselflies in your garden ISBN 978-1-84754-015-7 Catalogue code NE21 Written by Caroline Daguet Designed by RR Donnelley Front cover photograph: A male southern hawker dragonfly. This species is the one most commonly seen in gardens. Steve Cham. www.naturalengland.org.uk Dragonflies and damselflies in your garden Dragonflies and damselflies are Modern dragonflies are tiny by amazing insects. They have a long comparison, but are still large and history and modern species are almost spectacular enough to capture the identical to ancestors that flew over attention of anyone walking along a prehistoric forests some 300 million river bank or enjoying a sunny years ago. Some of these ancient afternoon by the garden pond. dragonflies were giants, with This booklet will tell you about the wingspans of up to 70 cm. biology and life-cycles of dragonflies and damselflies, help you to identify some common species, and tell you how you can encourage these insects to visit your garden. Male common blue damselfly. Most damselflies hold their wings against their bodies when at rest. BDS Dragonflies and damselflies belong to Dragonflies the insect order known as Odonata, Dragonflies are usually larger than meaning ‘toothed jaws’. They are often damselflies. They are stronger fliers and referred to collectively as ‘dragonflies’, can often be found well away from but dragonflies and damselflies are two water. When at rest, they hold their distinct groups. -
Damselflies & Dragonflies of the Tees and Humber Industrial Sites
Damselflies & Dragonflies of the Tees and Humber Industrial Sites Introduction Damselflies and dragonflies belong to the same ‘order’ of insects called the Odonata. Although the adults are flying insects, the other stages of their life cycle are spent in water. Adults lay their eggs on aquatic plants or in the mud of still or slow moving freshwater. The larval or ‘nymph’ form is the immature stage which is wingless. Nymphs eat other aquatic insects and small animals such as tadpoles and small fish. They shed their skin as they grow and larger species can take several years to reach the point Damsel or Dragon? where they become full-grown. At this point The following key points will give an they climb out of the water onto surrounding indication of the main differences vegetation and after a short period the adult between dragonflies and damselflies: insect emerges from the old larval skin. The adults are also fearsome predators, catching • Both have two large ‘compound’ eyes at other flying insects on the wing. Damselflies the front of their head. A dragonfly’s eyes eat smaller species, such as greenfly or are so large that they meet in the middle midges, but a dragonfly’s diet includes larger or at the top of the head, but those of a flying insects such as butterflies, moths and damselfly are smaller and always separate. even smaller dragonflies and damselflies! • Both have four wings, but when resting, damselflies fold their wings back This leaflet is a useful field guide, that covers along their bodies or at 45 degrees, the Odonata species which can be seen in whereas dragonflies rest with their the Tees and Humber industrial areas. -
An Anomalous Connection in the Genus Aeshna Fabricius, 1775 (Odonata: Aeshnidae) with an Additional Record of Aeshna Cyanea (Müller, 1764) from Turkish Thrace
Acta entomologica serbica, 2010, 15(1): 1-6 UDC 595.733(560) AN ANOMALOUS CONNECTION IN THE GENUS AESHNA FABRICIUS, 1775 (ODONATA: AESHNIDAE) WITH AN ADDITIONAL RECORD OF AESHNA CYANEA (MÜLLER, 1764) FROM TURKISH THRACE NURTEN HACET Trakya University, Faculty of Arts and Sciences, Department of Biology, TR-22030 Edirne, Turkey E-mail: [email protected] Abstract A heterospecific tandem between a male Aeshna affinis Vander Linden, 1820 and a female Aeshna cyanea (Müller, 1764) is reported from İğneada (Longos Forest) in Kırklareli province in the Turkish Thrace Region. The locality, where the tandem was observed, is the second recording locality for A. cyanea from the region. KEY WORDS: Odonata, dragonfly, heterospecific tandem, Aeshnidae, Aeshna, Turkish Thrace, Turkey Introduction Recent studies have indicated that heterospecific tandems within Odonata are not unusual (BICK & BICK, 1981; UTZERI & BELFIORE, 1990; CORBET, 1999). However, the difficulty in detection of females in heterospecific pairs for some genera restricts the number of records of such pairs (BICK & BICK, 1981; CORBET, 1999). Thus, it is probable that there are unreported or unpublished records of heterospecific pairs among dragonflies, and it is possible that the total number of all records is greater than the amount of available data. Heterosexual heterospecific tandems were recorded and observed more often in Anisoptera than Zygoptera, and most of the known records showed that heterospecific pairs consist of individuals of the same genus (CORBET, 1999). Aeshnidae from Anisoptera is one of the families for which heterospecific pairings were recorded, and Sympetrum and Gomphus are Anisopteran genera including the highest record numbers of mixed pairings (BICK & BICK, 1981; CORBET, 1999). -
Predictive Modelling of Spatial Biodiversity Data to Support Ecological Network Mapping: a Case Study in the Fens
Predictive modelling of spatial biodiversity data to support ecological network mapping: a case study in the Fens Christopher J Panter, Paul M Dolman, Hannah L Mossman Final Report: July 2013 Supported and steered by the Fens for the Future partnership and the Environment Agency www.fensforthefuture.org.uk Published by: School of Environmental Sciences, University of East Anglia, Norwich, NR4 7TJ, UK Suggested citation: Panter C.J., Dolman P.M., Mossman, H.L (2013) Predictive modelling of spatial biodiversity data to support ecological network mapping: a case study in the Fens. University of East Anglia, Norwich. ISBN: 978-0-9567812-3-9 © Copyright rests with the authors. Acknowledgements This project was supported and steered by the Fens for the Future partnership. Funding was provided by the Environment Agency (Dominic Coath). We thank all of the species recorders and natural historians, without whom this work would not be possible. Cover picture: Extract of a map showing the predicted distribution of biodiversity. Contents Executive summary .................................................................................................................... 4 Introduction ............................................................................................................................... 5 Methodology .......................................................................................................................... 6 Biological data ................................................................................................................... -
Informes Individuales IUCN 2018.Indd
IUCN SSC Dragonfly Specialist Group 2018 Report Viola Clausnitzer Geert de Knijf Co-Chairs Mission statement completing the remaining assessments of ca. Viola Clausnitzer (1) The mission of the IUCN SSC Dragonfly 1,000 dragonflies globally; (5) gather data in Geert de Knijf (2) Specialist Group (DSG) is to increase the knowl- North America through OdonataCentral to feed edge on taxonomy, ecology and biogeography into global Red List assessments. Red List Authority Coordinator of all Odonata (damselflies and dragonflies). Research activities: (1) gain more informa- Viola Clausnitzer (1) Based on this information, we are currently tion on Lestes umbrinus to assist conserva- working on the final steps towards assessing all tion planning; (2) research and scientific publi- Location/Affiliation species globally against the criteria of The IUCN cation on dragonflies in Tatamá National Park and its buffer area in Colombian western (1) Senckenberg Research Institute, Red List of Threatened Species, while outdated Andes; (3) contribute to the process of delin- Goerlitz, Germany assessments are updated. In parallel, we help eating Key Biodiversity Areas (KBAs) for fresh- (2) Inbo, Belgium conservationists and countries to protect threatened species. water conservation; (4) delineate KBAs for freshwater conservation in Lake Tanganyika Number of members Projected impact for the 2017-2020 Catchment, Africa; (5) develop an Atlas of the 54 quadrennium dragonflies of Bhutan/the Eastern Himalaya; (6) use the atlas to develop a Dragonfly Biotic Social networks By the end of 2020, we want to see all Odonata Index for the Eastern Himalaya; (7) develop a assessed on the IUCN Red List of Threat- Facebook: field guide for the odonates in Tatamá region; ened Species. -
By the Lepidoptera (Eg Patterns Are Frequently Used
Odonatologica 15(3): 335-345 September I, 1986 A survey of some Odonata for ultravioletpatterns* D.F.J. Hilton Department of Biological Sciences, Bishop’s University, Lennoxville, Quebec, J1M 1Z7, Canada Received May 8, 1985 / Revised and Accepted March 3, 1986 series of 338 in families A museum specimens comprising spp. 118 genera and 16 were photographed both with and without a Kodak 18-A ultraviolet (UV) filter. These photographs revealed that only Euphaeaamphicyana reflected UV from its other wings whereas all spp. either did not absorb UV (e.g. 94.5% of the Coenagri- did In with flavescent. onidae) or so to varying degrees. particular, spp. orange or brown UV these wings (or wing patches) exhibited absorption for same areas. However, other spp. with nearly transparent wings (especially certain Gomphidae) Pruinose also had strong UV absorption. body regions reflected UV but the standard acetone treatment for color preservation dissolves thewax particles of the pruinosity and destroys UV reflectivity. As is typical for arthropod cuticle, non-pruinosebody regions absorbed UV and this obscured whatever color patterns might otherwise be visible without the camera’s UV filter. Frequently there is sexual dimorphismin UV and and these role various of patterns (wings body) differences may play a in aspects mating behavior. INTRODUCTION Considerable attention has been paid to the various ultraviolet (UV) patterns exhibited by the Lepidoptera (e.g. SCOTT, 1973). Studies have shown (e.g. RUTOWSKI, 1981) that differing UV-reflectance patterns are frequently used as visual in various of behavior. few insect cues aspects mating Although a other groups have been investigated for the presence of UV patterns (HINTON, 1973; POPE & HINTON, 1977; S1LBERGL1ED, 1979), little informationis available for the Odonata. -
Dragonfly Report
The Dragonflies & Damselflies of Rye Harbour Rye Harbour Fauna and Flora Volume 4 By Chris Bentley Published by East Sussex County Council and The Friends of Rye Harbour Nature Reserve Rye Harbour Nature Reserve 2 Watch Cottages Winchelsea, East Sussex TN36 4LU [email protected] www.WildRye.info February 2010 RYE HARBOUR FLORA & FAUNA Dragonflies & Damselflies RYE HARBOUR FLORA & FAUNA Dragonflies & Damselflies Introduction In 1965 East Sussex County Council published a report on the future development of the East Sussex Coast which included proposals to encourage the establishment of a Nature Reserve over the whole of the 728 hectares (c.1,800 acres) of the Rye Harbour Site This report should of Special Scientific Interest (SSSI). In 1970 the shingle beach, now owned by the Environment Agency , was declared a Local Nature print out in booklet Reserve (LNR) by the County Council, who also appointed a form so that you can Management Committee to administer the LNR. This was the beginning of Rye Harbour Local Nature Reserve. Since then further make your own. land has been added by agreement with neighbouring landowners and the County Council and by purchase of land by the Sussex Wildlife Trust with the help of the Friends of Rye Harbour Print on both sides of Nature Reserve . It is hoped that further areas of the SSSI will become part of the Nature Reserve and so this report covers the 14 sheets of A4 paper. whole area. The present extent of the Nature Reserve includes the seaward shingle ridges extending inland to, and including, the gravel pit known as Ternery Pool and the nearby excavation known as the Quarry (Beach Reserve), a large gravel pit (Castle Water), a large area of meadow land and shingle ridges around Camber Castle (Castle Farm) and a small area of saltmarsh fringing the western bank of the River Rother between Rye Harbour and the river mouth. -
Volume 38, No 1 Summer 2019
Newsletter of the Biological Survey of Canada Vol. 38(1) Summer 2019 The Newsletter of the BSC is published twice a year by the Biological Survey of Canada, an incorporated not-for-profit In this issue group devoted to promoting biodiversity science in Canada. From the editor’s desk.......2 Seeking a new webmaster for the BSC..........................2 Feature Article: Information on Are dragonflies moving into the western tundra? Membership ......................3 Paul M. Catling, Brenda Kostiuk, Robert A. Cannings, President’s Report .............4 Ryan Lucas, Donna Giberson, Sydney Cannings, and Cameron Eckert.......................................................10 BSC on facebook & twitter .............................................6 Contributing to the BSC Newsletter...........................6 Report on the 2019 AGM....7 Project Update Biota of Canada: Terrestrial Arthropods - first volume of the Biota of Canada project published ..............................................8 Project Update Request for specimens: Biota of Canada Project: Publication of Terres- Carabidae from across Canada; trial Arthropods Volume from Kevin Floate .....................9 Dave Langor and Cory Sheffield.................................8 Feature Article Are dragonflies moving into the western tundra? by PM Catling, B Kostiuk, RA National Biodiversity Cryobank of Canada Cannings, R Lucas, D Giber- Robert Anderson, Canadian Museum of Nature........18 son, S Cannings, and C Eck- ert........................................10 Request for specimens: Carabidae