Mecoptera of Ontario
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Topic Paper Chilterns Beechwoods
. O O o . 0 O . 0 . O Shoping growth in Docorum Appendices for Topic Paper for the Chilterns Beechwoods SAC A summary/overview of available evidence BOROUGH Dacorum Local Plan (2020-2038) Emerging Strategy for Growth COUNCIL November 2020 Appendices Natural England reports 5 Chilterns Beechwoods Special Area of Conservation 6 Appendix 1: Citation for Chilterns Beechwoods Special Area of Conservation (SAC) 7 Appendix 2: Chilterns Beechwoods SAC Features Matrix 9 Appendix 3: European Site Conservation Objectives for Chilterns Beechwoods Special Area of Conservation Site Code: UK0012724 11 Appendix 4: Site Improvement Plan for Chilterns Beechwoods SAC, 2015 13 Ashridge Commons and Woods SSSI 27 Appendix 5: Ashridge Commons and Woods SSSI citation 28 Appendix 6: Condition summary from Natural England’s website for Ashridge Commons and Woods SSSI 31 Appendix 7: Condition Assessment from Natural England’s website for Ashridge Commons and Woods SSSI 33 Appendix 8: Operations likely to damage the special interest features at Ashridge Commons and Woods, SSSI, Hertfordshire/Buckinghamshire 38 Appendix 9: Views About Management: A statement of English Nature’s views about the management of Ashridge Commons and Woods Site of Special Scientific Interest (SSSI), 2003 40 Tring Woodlands SSSI 44 Appendix 10: Tring Woodlands SSSI citation 45 Appendix 11: Condition summary from Natural England’s website for Tring Woodlands SSSI 48 Appendix 12: Condition Assessment from Natural England’s website for Tring Woodlands SSSI 51 Appendix 13: Operations likely to damage the special interest features at Tring Woodlands SSSI 53 Appendix 14: Views About Management: A statement of English Nature’s views about the management of Tring Woodlands Site of Special Scientific Interest (SSSI), 2003. -
Insect Orders V: Panorpida & Hymenoptera
Insect Orders V: Panorpida & Hymenoptera • The Panorpida contain 5 orders: the Mecoptera, Siphonaptera, Diptera, Trichoptera and Lepidoptera. • Available evidence clearly indicates that the Lepidoptera and the Trichoptera are sister groups. • The Siphonaptera and Mecoptera are also closely related but it is not clear whether the Siponaptera is the sister group of all of the Mecoptera or a group (Boreidae) within the Mecoptera. If the latter is true, then the Mecoptera is paraphyletic as currently defined. • The Diptera is the sister group of the Siphonaptera + Mecoptera and together make up the Mecopteroids. • The Hymenoptera does not appear to be closely related to any of the other holometabolous orders. Mecoptera (Scorpionflies, hangingflies) • Classification. 600 species worldwide, arranged into 9 families (5 in the US). A very old group, many fossils from the Permian (260 mya) onward. • Structure. Most distinctive feature is the elongated clypeus and labrum that together form a rostrum. The order gets its common name from the gential segment of the male in the family Panorpodiae, which is bulbous and often curved forward above the abdomen, like the sting of a scorpion. Larvae are caterpillar-like or grub- like. • Natural history. Scorpionflies are most common in cool, moist habitats. They get the name “hangingflies” from their habit of hanging upside down on vegetation. Larvae and adult males are mostly predators or scavengers. Adult females are usually scavengers. Larvae and adults in some groups may feed on vegetation. Larvae of most species are terrestrial and caterpillar-like in body form. Larvae of some species are aquatic. In the family Bittacidae males attract females for mating by releasing a sex pheromone and then presenting the female with a nuptial gift. -
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. -
Nuptial Food Gifts Influence Female Egg Production in the Scorpionfly
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Publications at Bielefeld University Ecological Entomology (2007), 32, 327–332 DOI: 10.1111/j.1365-2311.2006.00835.x SHORT COMMUNICATION Nuptial food gifts infl uence female egg production in the scorpionfl y Panorpa cognata LEIF ENGQVIST Department of Evolutionary Biology and Ecology, University of Bonn, Germany Abstract . 1. Before copulation, male Panorpa cognata scorpionflies offer females a salivary secretion, which is consumed by the female during copulation. It has previously been demonstrated that this nuptial food gift functions as mating effort by increasing male attractiveness and by increasing ejaculate transfer during copulation. 2. In this study, the effect of saliva consumption on female reproductive output was investigated, and thus the possibility that nuptial food gifts also serve as paternal investment. The experimental design enabled the effect of nuptial gift consumption to be disentangled from other possible effects of multiple mating or increased copula duration. 3. The results showed that saliva consumption increases female egg production by on average 8% (4.5 eggs) per consumed salivary mass, whereas mean egg weight was not influenced. 4. These results have important implications for the evolution and maintenance of both male nuptial gifts and female polyandry in this and other species. Key words . Female fecundity , mating effort , Mecoptera , nuptial food gifts , paternal investment , sexual selection . Introduction number or size of nuptial gifts on the female fitness traits stud- ied (e.g. Gwynne et al. , 1984; Jones et al. , 1986; Svärd & The traditional view that female fitness should be maximized Wiklund, 1988; Wedell & Arak, 1989; Will & Sakaluk, 1994; with only one or a few matings ( Bateman, 1948 ) is often chal- Ward & Landolt, 1995; Vahed & Gilbert, 1997; Cook, 1999; lenged by the observation of female multiple matings in many Maxwell, 2000; Ryne et al. -
Arthropods of Elm Fork Preserve
Arthropods of Elm Fork Preserve Arthropods are characterized by having jointed limbs and exoskeletons. They include a diverse assortment of creatures: Insects, spiders, crustaceans (crayfish, crabs, pill bugs), centipedes and millipedes among others. Column Headings Scientific Name: The phenomenal diversity of arthropods, creates numerous difficulties in the determination of species. Positive identification is often achieved only by specialists using obscure monographs to ‘key out’ a species by examining microscopic differences in anatomy. For our purposes in this survey of the fauna, classification at a lower level of resolution still yields valuable information. For instance, knowing that ant lions belong to the Family, Myrmeleontidae, allows us to quickly look them up on the Internet and be confident we are not being fooled by a common name that may also apply to some other, unrelated something. With the Family name firmly in hand, we may explore the natural history of ant lions without needing to know exactly which species we are viewing. In some instances identification is only readily available at an even higher ranking such as Class. Millipedes are in the Class Diplopoda. There are many Orders (O) of millipedes and they are not easily differentiated so this entry is best left at the rank of Class. A great deal of taxonomic reorganization has been occurring lately with advances in DNA analysis pointing out underlying connections and differences that were previously unrealized. For this reason, all other rankings aside from Family, Genus and Species have been omitted from the interior of the tables since many of these ranks are in a state of flux. -
Insects of Larose Forest (Excluding Lepidoptera and Odonates)
Insects of Larose Forest (Excluding Lepidoptera and Odonates) • Non-native species indicated by an asterisk* • Species in red are new for the region EPHEMEROPTERA Mayflies Baetidae Small Minnow Mayflies Baetidae sp. Small minnow mayfly Caenidae Small Squaregills Caenidae sp. Small squaregill Ephemerellidae Spiny Crawlers Ephemerellidae sp. Spiny crawler Heptageniiidae Flatheaded Mayflies Heptageniidae sp. Flatheaded mayfly Leptophlebiidae Pronggills Leptophlebiidae sp. Pronggill PLECOPTERA Stoneflies Perlodidae Perlodid Stoneflies Perlodid sp. Perlodid stonefly ORTHOPTERA Grasshoppers, Crickets and Katydids Gryllidae Crickets Gryllus pennsylvanicus Field cricket Oecanthus sp. Tree cricket Tettigoniidae Katydids Amblycorypha oblongifolia Angular-winged katydid Conocephalus nigropleurum Black-sided meadow katydid Microcentrum sp. Leaf katydid Scudderia sp. Bush katydid HEMIPTERA True Bugs Acanthosomatidae Parent Bugs Elasmostethus cruciatus Red-crossed stink bug Elasmucha lateralis Parent bug Alydidae Broad-headed Bugs Alydus sp. Broad-headed bug Protenor sp. Broad-headed bug Aphididae Aphids Aphis nerii Oleander aphid* Paraprociphilus tesselatus Woolly alder aphid Cicadidae Cicadas Tibicen sp. Cicada Cicadellidae Leafhoppers Cicadellidae sp. Leafhopper Coelidia olitoria Leafhopper Cuernia striata Leahopper Draeculacephala zeae Leafhopper Graphocephala coccinea Leafhopper Idiodonus kelmcottii Leafhopper Neokolla hieroglyphica Leafhopper 1 Penthimia americana Leafhopper Tylozygus bifidus Leafhopper Cercopidae Spittlebugs Aphrophora cribrata -
About the Book the Format Acknowledgments
About the Book For more than ten years I have been working on a book on bryophyte ecology and was joined by Heinjo During, who has been very helpful in critiquing multiple versions of the chapters. But as the book progressed, the field of bryophyte ecology progressed faster. No chapter ever seemed to stay finished, hence the decision to publish online. Furthermore, rather than being a textbook, it is evolving into an encyclopedia that would be at least three volumes. Having reached the age when I could retire whenever I wanted to, I no longer needed be so concerned with the publish or perish paradigm. In keeping with the sharing nature of bryologists, and the need to educate the non-bryologists about the nature and role of bryophytes in the ecosystem, it seemed my personal goals could best be accomplished by publishing online. This has several advantages for me. I can choose the format I want, I can include lots of color images, and I can post chapters or parts of chapters as I complete them and update later if I find it important. Throughout the book I have posed questions. I have even attempt to offer hypotheses for many of these. It is my hope that these questions and hypotheses will inspire students of all ages to attempt to answer these. Some are simple and could even be done by elementary school children. Others are suitable for undergraduate projects. And some will take lifelong work or a large team of researchers around the world. Have fun with them! The Format The decision to publish Bryophyte Ecology as an ebook occurred after I had a publisher, and I am sure I have not thought of all the complexities of publishing as I complete things, rather than in the order of the planned organization. -
The Evolution of Animal Nuptial Gifts
ADVANCES IN THE STUDY OF BEHAVIOR, VOL. 44 The Evolution of Animal Nuptial Gifts Sara Lewis and Adam South department of biology, tufts university, medford, massachusetts, usa Rich gifts wax poor when givers prove unkind William Shakespeare, Hamlet, Prince of Denmark (3.1.101) I. INTRODUCTION A. WHAT ARE NUPTIAL GIFTS? Nuptial arrangements in many human cultures include gift-giving tradi- tions (Cronk and Dunham, 2007; Mehdi, 2003), and this behavior plays an important role in the mating systems of other creatures as well (Boggs, 1995; Fabre, 1918; Gwynne, 2008; Lack, 1940; Thornhill, 1976; Vahed, 1998, 2007; Zeh and Smith, 1985). In species widely distributed across the animal kingdom, males transfer many different non-gametic materials to females during courtship and mating. Such materials can include lipids, carbo- hydrates, proteins, peptides, amino acids, uric acid, minerals, water, anti- predator defensive compounds, anti-aphrodisiac pheromones, and neuroendocrine modulators of recipient physiology. These nuptial gifts are an important aspect of reproductive behavior and animal mating sys- tems (Andersson, 1994; Thornhill and Alcock, 1983). However, when com- pared to more conspicuous sexually selected traits such as male weaponry or ornamentation, such gifts have received relatively little attention from behavioral, ecological, and evolutionary research. Nuptial gifts heighten male reproductive investment, thus limiting male mating rates and altering courtship sex roles and sexual size dimorphism (Boggs, 1995; Gwynne and Simmons, 1990; Leimar et al., 1994). Selection acts on both gift-givers and receivers to shape nuptial gift structure and biochemical composition, as well as gift-giving behaviors. Not only do nuptial gifts form the basis for dynamic coevolutionary interactions between the sexes, but they also link 53 0065-3454/12 $35.00 Copyright 2012, Elsevier Inc. -
Hypothesis on Monochromatic Vision in Scorpionflies Questioned by New
www.nature.com/scientificreports OPEN Hypothesis on monochromatic vision in scorpionfies questioned by new transcriptomic data Received: 7 July 2017 Alexander Böhm 1, Karen Meusemann2,3,4, Bernhard Misof3 & Günther Pass1 Accepted: 12 June 2018 In the scorpionfy Panorpa, a recent study suggested monochromatic vision due to evidence of only a Published: xx xx xxxx single opsin found in transcriptome data. To reconsider this hypothesis, the present study investigates opsin expression using transcriptome data of 21 species including representatives of all major lineages of scorpionfies (Mecoptera) and of three families of their closest relatives, the feas (Siphonaptera). In most mecopteran species investigated, transcripts encode two opsins with predicted peak absorbances in the green, two in the blue, and one in the ultraviolet spectral region. Only in groups with reduced or absent ocelli, like Caurinus and Apteropanorpa, less than four visual opsin messenger RNAs have been identifed. In addition, we found a Rh7-like opsin in transcriptome data derived from larvae of the mecopteran Nannochorista, and in two fea species. Peropsin expression was observed in two mecopterans. In light of these new data, we question the hypothesis on monochromatic vision in the genus Panorpa. In a broader phylogenetic perspective, it is suggested that the common ancestor of the monophyletic taxon Antliophora (Diptera, Mecoptera and Siphonaptera) possessed the full set of visual opsins, a Rh7-like opsin, and in addition a pteropsin as well as a peropsin. In the course of evolution individual opsins were likely lost in several lineages of this clade. Colour vision has two prerequisites1,2: receptors with diferent spectral responses and a neural system that can process their output in a way that preserves colour information. -
Mecoptera: Meropeidae): Simply Dull Or Just Inscrutable?
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 8-24-2007 Etymology of the earwigfly, Merope tuber Newman (Mecoptera: Meropeidae): Simply dull or just inscrutable? Louis A. Somma University of Florida, [email protected] James C. Dunford University of Florida, Gainesville, FL Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons Somma, Louis A. and Dunford, James C., "Etymology of the earwigfly, Merope tuber Newman (Mecoptera: Meropeidae): Simply dull or just inscrutable?" (2007). Insecta Mundi. 65. https://digitalcommons.unl.edu/insectamundi/65 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI A Journal of World Insect Systematics 0013 Etymology of the earwigfly, Merope tuber Newman (Mecoptera: Meropeidae): Simply dull or just inscrutable? Louis A. Somma Department of Zoology PO Box 118525 University of Florida Gainesville, FL 32611-8525 [email protected] James C. Dunford Department of Entomology and Nematology PO Box 110620, IFAS University of Florida Gainesville, FL 32611-0620 [email protected] Date of Issue: August 24, 2007 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Louis A. Somma and James C. Dunford Etymology of the earwigfly, Merope tuber Newman (Mecoptera: Meropeidae): Simply dull or just inscrutable? Insecta Mundi 0013: 1-5 Published in 2007 by Center for Systematic Entomology, Inc. P. O. Box 147100 Gainesville, FL 32604-7100 U. -
Ours to Save: the Distribution, Status & Conservation Needs of Canada's Endemic Species
Ours to Save The distribution, status & conservation needs of Canada’s endemic species June 4, 2020 Version 1.0 Ours to Save: The distribution, status & conservation needs of Canada’s endemic species Additional information and updates to the report can be found at the project website: natureconservancy.ca/ourstosave Suggested citation: Enns, Amie, Dan Kraus and Andrea Hebb. 2020. Ours to save: the distribution, status and conservation needs of Canada’s endemic species. NatureServe Canada and Nature Conservancy of Canada. Report prepared by Amie Enns (NatureServe Canada) and Dan Kraus (Nature Conservancy of Canada). Mapping and analysis by Andrea Hebb (Nature Conservancy of Canada). Cover photo credits (l-r): Wood Bison, canadianosprey, iNaturalist; Yukon Draba, Sean Blaney, iNaturalist; Salt Marsh Copper, Colin Jones, iNaturalist About NatureServe Canada A registered Canadian charity, NatureServe Canada and its network of Canadian Conservation Data Centres (CDCs) work together and with other government and non-government organizations to develop, manage, and distribute authoritative knowledge regarding Canada’s plants, animals, and ecosystems. NatureServe Canada and the Canadian CDCs are members of the international NatureServe Network, spanning over 80 CDCs in the Americas. NatureServe Canada is the Canadian affiliate of NatureServe, based in Arlington, Virginia, which provides scientific and technical support to the international network. About the Nature Conservancy of Canada The Nature Conservancy of Canada (NCC) works to protect our country’s most precious natural places. Proudly Canadian, we empower people to safeguard the lands and waters that sustain life. Since 1962, NCC and its partners have helped to protect 14 million hectares (35 million acres), coast to coast to coast. -
Ancient Rapid Radiations of Insects: Challenges for Phylogenetic Analysis
ANRV330-EN53-23 ARI 2 November 2007 18:40 Ancient Rapid Radiations of Insects: Challenges for Phylogenetic Analysis James B. Whitfield1 and Karl M. Kjer2 1Department of Entomology, University of Illinois, Urbana, Illinois 61821; email: jwhitfi[email protected] 2Department of Ecology, Evolution and Natural Resources, Rutgers University, New Brunswick, New Jersey 08901; email: [email protected] Annu. Rev. Entomol. 2008. 53:449–72 Key Words First published online as a Review in Advance on diversification, molecular evolution, Palaeoptera, Orthopteroidea, September 17, 2007 fossils The Annual Review of Entomology is online at ento.annualreviews.org Abstract by UNIVERSITY OF ILLINOIS on 12/18/07. For personal use only. This article’s doi: Phylogenies of major groups of insects based on both morphological 10.1146/annurev.ento.53.103106.093304 and molecular data have sometimes been contentious, often lacking Copyright c 2008 by Annual Reviews. the data to distinguish between alternative views of relationships. Annu. Rev. Entomol. 2008.53:449-472. Downloaded from arjournals.annualreviews.org All rights reserved This paucity of data is often due to real biological and historical 0066-4170/08/0107-0449$20.00 causes, such as shortness of time spans between divergences for evo- lution to occur and long time spans after divergences for subsequent evolutionary changes to obscure the earlier ones. Another reason for difficulty in resolving some of the relationships using molecu- lar data is the limited spectrum of genes so far developed for phy- logeny estimation. For this latter issue, there is cause for current optimism owing to rapid increases in our knowledge of comparative genomics.