Abhandlungen Und Berichte
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Comparative Functional Morphology of Attachment Devices in Arachnida
Comparative functional morphology of attachment devices in Arachnida Vergleichende Funktionsmorphologie der Haftstrukturen bei Spinnentieren (Arthropoda: Arachnida) DISSERTATION zur Erlangung des akademischen Grades doctor rerum naturalium (Dr. rer. nat.) an der Mathematisch-Naturwissenschaftlichen Fakultät der Christian-Albrechts-Universität zu Kiel vorgelegt von Jonas Otto Wolff geboren am 20. September 1986 in Bergen auf Rügen Kiel, den 2. Juni 2015 Erster Gutachter: Prof. Stanislav N. Gorb _ Zweiter Gutachter: Dr. Dirk Brandis _ Tag der mündlichen Prüfung: 17. Juli 2015 _ Zum Druck genehmigt: 17. Juli 2015 _ gez. Prof. Dr. Wolfgang J. Duschl, Dekan Acknowledgements I owe Prof. Stanislav Gorb a great debt of gratitude. He taught me all skills to get a researcher and gave me all freedom to follow my ideas. I am very thankful for the opportunity to work in an active, fruitful and friendly research environment, with an interdisciplinary team and excellent laboratory equipment. I like to express my gratitude to Esther Appel, Joachim Oesert and Dr. Jan Michels for their kind and enthusiastic support on microscopy techniques. I thank Dr. Thomas Kleinteich and Dr. Jana Willkommen for their guidance on the µCt. For the fruitful discussions and numerous information on physical questions I like to thank Dr. Lars Heepe. I thank Dr. Clemens Schaber for his collaboration and great ideas on how to measure the adhesive forces of the tiny glue droplets of harvestmen. I thank Angela Veenendaal and Bettina Sattler for their kind help on administration issues. Especially I thank my students Ingo Grawe, Fabienne Frost, Marina Wirth and André Karstedt for their commitment and input of ideas. -
BÖCEKLERİN SINIFLANDIRILMASI (Takım Düzeyinde)
BÖCEKLERİN SINIFLANDIRILMASI (TAKIM DÜZEYİNDE) GÖKHAN AYDIN 2016 Editör : Gökhan AYDIN Dizgi : Ziya ÖNCÜ ISBN : 978-605-87432-3-6 Böceklerin Sınıflandırılması isimli eğitim amaçlı hazırlanan bilgisayar programı için lütfen aşağıda verilen linki tıklayarak programı ücretsiz olarak bilgisayarınıza yükleyin. http://atabeymyo.sdu.edu.tr/assets/uploads/sites/76/files/siniflama-05102016.exe Eğitim Amaçlı Bilgisayar Programı ISBN: 978-605-87432-2-9 İçindekiler İçindekiler i Önsöz vi 1. Protura - Coneheads 1 1.1 Özellikleri 1 1.2 Ekonomik Önemi 2 1.3 Bunları Biliyor musunuz? 2 2. Collembola - Springtails 3 2.1 Özellikleri 3 2.2 Ekonomik Önemi 4 2.3 Bunları Biliyor musunuz? 4 3. Thysanura - Silverfish 6 3.1 Özellikleri 6 3.2 Ekonomik Önemi 7 3.3 Bunları Biliyor musunuz? 7 4. Microcoryphia - Bristletails 8 4.1 Özellikleri 8 4.2 Ekonomik Önemi 9 5. Diplura 10 5.1 Özellikleri 10 5.2 Ekonomik Önemi 10 5.3 Bunları Biliyor musunuz? 11 6. Plocoptera – Stoneflies 12 6.1 Özellikleri 12 6.2 Ekonomik Önemi 12 6.3 Bunları Biliyor musunuz? 13 7. Embioptera - webspinners 14 7.1 Özellikleri 15 7.2 Ekonomik Önemi 15 7.3 Bunları Biliyor musunuz? 15 8. Orthoptera–Grasshoppers, Crickets 16 8.1 Özellikleri 16 8.2 Ekonomik Önemi 16 8.3 Bunları Biliyor musunuz? 17 i 9. Phasmida - Walkingsticks 20 9.1 Özellikleri 20 9.2 Ekonomik Önemi 21 9.3 Bunları Biliyor musunuz? 21 10. Dermaptera - Earwigs 23 10.1 Özellikleri 23 10.2 Ekonomik Önemi 24 10.3 Bunları Biliyor musunuz? 24 11. Zoraptera 25 11.1 Özellikleri 25 11.2 Ekonomik Önemi 25 11.3 Bunları Biliyor musunuz? 26 12. -
Biodiversity and Threats in Non-Protected Areas: a Multidisciplinary and Multi-Taxa Approach Focused on the Atlantic Forest
Heliyon 5 (2019) e02292 Contents lists available at ScienceDirect Heliyon journal homepage: www.heliyon.com Biodiversity and threats in non-protected areas: A multidisciplinary and multi-taxa approach focused on the Atlantic Forest Esteban Avigliano a,b,*, Juan Jose Rosso c, Dario Lijtmaer d, Paola Ondarza e, Luis Piacentini d, Matías Izquierdo f, Adriana Cirigliano g, Gonzalo Romano h, Ezequiel Nunez~ Bustos d, Andres Porta d, Ezequiel Mabragana~ c, Emanuel Grassi i, Jorge Palermo h,j, Belen Bukowski d, Pablo Tubaro d, Nahuel Schenone a a Centro de Investigaciones Antonia Ramos (CIAR), Fundacion Bosques Nativos Argentinos, Camino Balneario s/n, Villa Bonita, Misiones, Argentina b Instituto de Investigaciones en Produccion Animal (INPA-CONICET-UBA), Universidad de Buenos Aires, Av. Chorroarín 280, (C1427CWO), Buenos Aires, Argentina c Grupo de Biotaxonomía Morfologica y Molecular de Peces (BIMOPE), Instituto de Investigaciones Marinas y Costeras, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata (CONICET), Dean Funes 3350, (B7600), Mar del Plata, Argentina d Museo Argentino de Ciencias Naturales “Bernardino Rivadavia” (MACN-CONICET), Av. Angel Gallardo 470, (C1405DJR), Buenos Aires, Argentina e Laboratorio de Ecotoxicología y Contaminacion Ambiental, Instituto de Investigaciones Marinas y Costeras, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Mar del Plata (CONICET), Dean Funes 3350, (B7600), Mar del Plata, Argentina f Laboratorio de Biología Reproductiva y Evolucion, Instituto de Diversidad -
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. -
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. -
Phylogeny of Endopterygote Insects, the Most Successful Lineage of Living Organisms*
REVIEW Eur. J. Entomol. 96: 237-253, 1999 ISSN 1210-5759 Phylogeny of endopterygote insects, the most successful lineage of living organisms* N iels P. KRISTENSEN Zoological Museum, University of Copenhagen, Universitetsparken 15, DK-2100 Copenhagen 0, Denmark; e-mail: [email protected] Key words. Insecta, Endopterygota, Holometabola, phylogeny, diversification modes, Megaloptera, Raphidioptera, Neuroptera, Coleóptera, Strepsiptera, Díptera, Mecoptera, Siphonaptera, Trichoptera, Lepidoptera, Hymenoptera Abstract. The monophyly of the Endopterygota is supported primarily by the specialized larva without external wing buds and with degradable eyes, as well as by the quiescence of the last immature (pupal) stage; a specialized morphology of the latter is not an en dopterygote groundplan trait. There is weak support for the basal endopterygote splitting event being between a Neuropterida + Co leóptera clade and a Mecopterida + Hymenoptera clade; a fully sclerotized sitophore plate in the adult is a newly recognized possible groundplan autapomorphy of the latter. The molecular evidence for a Strepsiptera + Díptera clade is differently interpreted by advo cates of parsimony and maximum likelihood analyses of sequence data, and the morphological evidence for the monophyly of this clade is ambiguous. The basal diversification patterns within the principal endopterygote clades (“orders”) are succinctly reviewed. The truly species-rich clades are almost consistently quite subordinate. The identification of “key innovations” promoting evolution -
Habitat Divergence Shapes the Morphological Diversity Of
www.nature.com/scientificreports OPEN Habitat divergence shapes the morphological diversity of larval insects: insights from scorpionfies Received: 5 March 2018 Lu Jiang1,2, Yuan Hua1,3, Gui-Lin Hu1 & Bao-Zhen Hua1 Accepted: 21 August 2019 Insects are the most diverse group of organisms in the world, but how this diversity was achieved is Published: xx xx xxxx still a disputable and unsatisfactorily resolved issue. In this paper, we investigated the correlations of habitat preferences and morphological traits in larval Panorpidae in the phylogenetic context to unravel the driving forces underlying the evolution of morphological traits. The results show that most anatomical features are shared by monophyletic groups and are synapomorphies. However, the phenotypes of body colorations are shared by paraphyletic assemblages, implying that they are adaptive characters. The larvae of Dicerapanorpa and Cerapanorpa are epedaphic and are darkish dorsally as camoufage, and possess well-developed locomotory appendages as adaptations likely to avoid potential predators. On the contrary, the larvae of Neopanorpa are euedaphic and are pale on their trunks, with shallow furrows, reduced antennae, shortened setae, fattened compound eyes on the head capsules, and short dorsal processes on the trunk. All these characters appear to be adaptations for the larvae to inhabit the soil. We suggest that habitat divergence has driven the morphological diversity between the epedaphic and euedaphic larvae, and may be partly responsible for the divergence of major clades within the Panorpidae. Insects are the most diverse organisms on the earth, exhibiting the most diverse morphological features and occupying a wide range of ecological niches1,2. -
Evolution of the Insects David Grimaldi and Michael S
Cambridge University Press 0521821495 - Evolution of the Insects David Grimaldi and Michael S. Engel Index More information INDEX 12S rDNA, 32, 228, 269 Aenetus, 557 91; general, 57; inclusions, 57; menageries 16S rDNA, 32, 60, 237, 249, 269 Aenigmatiinae, 536 in, 56; Mexican, 55; parasitism in, 57; 18S rDNA, 32, 60, 61, 158, 228, 274, 275, 285, Aenne, 489 preservation in, 58; resinite, 55; sub-fossil 304, 307, 335, 360, 366, 369, 395, 399, 402, Aeolothripidae, 284, 285, 286 resin, 57; symbioses in, 303; taphonomy, 468, 475 Aeshnoidea, 187 57 28S rDNA, 32, 158, 278, 402, 468, 475, 522, 526 African rock crawlers (see Ambermantis wozniaki, 259 Mantophasmatodea) Amblycera, 274, 278 A Afroclinocera, 630 Amblyoponini, 446, 490 aardvark, 638 Agaonidae, 573, 616: fossil, 423 Amblypygida, 99, 104, 105: in amber, 104 abdomen: function, 131; structure, 131–136 Agaoninae, 423 Amborella trichopoda, 613, 620 Abies, 410 Agassiz, Alexander, 26 Ameghinoia, 450, 632 Abrocomophagidae, 274 Agathiphaga, 560 Ameletopsidae, 628 Acacia, 283 Agathiphagidae, 561, 562, 567, 630 American Museum of Natural History, 26, 87, acalyptrate Diptera: ecological diversity, 540; Agathis, 76 91 taxonomy, 540 Agelaia, 439 Amesiginae, 630 Acanthocnemidae, 391 ages, using fossils, 37–39; using DNA, 38–40 ametaboly, 331 Acari, 99, 105–107: diversity, 101, fossils, 53, Ageniellini, 435 amino acids: racemization, 61 105–107; in-Cretaceous amber, 105, 106 Aglaspidida, 99 ammonites, 63, 642 Aceraceae, 413 Aglia, 582 Amorphoscelidae, 254, 257 Acerentomoidea, 113 Agrias, 600 Amphientomidae, -
Fossil Calibrations for the Arthropod Tree of Life
bioRxiv preprint doi: https://doi.org/10.1101/044859; this version posted June 10, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. FOSSIL CALIBRATIONS FOR THE ARTHROPOD TREE OF LIFE AUTHORS Joanna M. Wolfe1*, Allison C. Daley2,3, David A. Legg3, Gregory D. Edgecombe4 1 Department of Earth, Atmospheric & Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA 2 Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK 3 Oxford University Museum of Natural History, Parks Road, Oxford OX1 3PZ, UK 4 Department of Earth Sciences, The Natural History Museum, Cromwell Road, London SW7 5BD, UK *Corresponding author: [email protected] ABSTRACT Fossil age data and molecular sequences are increasingly combined to establish a timescale for the Tree of Life. Arthropods, as the most species-rich and morphologically disparate animal phylum, have received substantial attention, particularly with regard to questions such as the timing of habitat shifts (e.g. terrestrialisation), genome evolution (e.g. gene family duplication and functional evolution), origins of novel characters and behaviours (e.g. wings and flight, venom, silk), biogeography, rate of diversification (e.g. Cambrian explosion, insect coevolution with angiosperms, evolution of crab body plans), and the evolution of arthropod microbiomes. We present herein a series of rigorously vetted calibration fossils for arthropod evolutionary history, taking into account recently published guidelines for best practice in fossil calibration. -
Curriculum Vitae (PDF)
CURRICULUM VITAE Steven J. Taylor April 2020 Colorado Springs, Colorado 80903 [email protected] Cell: 217-714-2871 EDUCATION: Ph.D. in Zoology May 1996. Department of Zoology, Southern Illinois University, Carbondale, Illinois; Dr. J. E. McPherson, Chair. M.S. in Biology August 1987. Department of Biology, Texas A&M University, College Station, Texas; Dr. Merrill H. Sweet, Chair. B.A. with Distinction in Biology 1983. Hendrix College, Conway, Arkansas. PROFESSIONAL AFFILIATIONS: • Associate Research Professor, Colorado College (Fall 2017 – April 2020) • Research Associate, Zoology Department, Denver Museum of Nature & Science (January 1, 2018 – December 31, 2020) • Research Affiliate, Illinois Natural History Survey, Prairie Research Institute, University of Illinois at Urbana-Champaign (16 February 2018 – present) • Department of Entomology, University of Illinois at Urbana-Champaign (2005 – present) • Department of Animal Biology, University of Illinois at Urbana-Champaign (March 2016 – July 2017) • Program in Ecology, Evolution, and Conservation Biology (PEEC), School of Integrative Biology, University of Illinois at Urbana-Champaign (December 2011 – July 2017) • Department of Zoology, Southern Illinois University at Carbondale (2005 – July 2017) • Department of Natural Resources and Environmental Sciences, University of Illinois at Urbana- Champaign (2004 – 2007) PEER REVIEWED PUBLICATIONS: Swanson, D.R., S.W. Heads, S.J. Taylor, and Y. Wang. A new remarkably preserved fossil assassin bug (Insecta: Heteroptera: Reduviidae) from the Eocene Green River Formation of Colorado. Palaeontology or Papers in Palaeontology (Submitted 13 February 2020) Cable, A.B., J.M. O’Keefe, J.L. Deppe, T.C. Hohoff, S.J. Taylor, M.A. Davis. Habitat suitability and connectivity modeling reveal priority areas for Indiana bat (Myotis sodalis) conservation in a complex habitat mosaic. -
Functional Morphology of the Larval Mouthparts of Panorpodidae Compared with Bittacidae and Panorpidae (Insecta: Mecoptera)
Org Divers Evol (2015) 15:671–679 DOI 10.1007/s13127-015-0225-7 ORIGINAL ARTICLE Functional morphology of the larval mouthparts of Panorpodidae compared with Bittacidae and Panorpidae (Insecta: Mecoptera) Lu Jiang1 & Bao-Zhen Hua1 Received: 10 February 2015 /Accepted: 15 June 2015 /Published online: 27 June 2015 # Gesellschaft für Biologische Systematik 2015 Abstract In Mecoptera, the larvae of Bittacidae and morphological and biological diversity (Byers and Thornhill Panorpidae are saprophagous, but the feeding habit of larval 1983; Byers 1987, 1991; Grimaldi and Engel 2005;Maetal. Panorpodidae remains largely unknown. Here, we compare 2009, 2012). The feeding habits of adult Mecoptera vary the ultramorphology of the mouthparts of the larvae among among families (Palmer 2010): predacious in Bittacidae (Tan the hangingfly Bittacus planus Cheng, 1949, the scorpionfly and Hua 2006;Maetal.2014b), phytophagous in Boreidae Panorpa liui Hua, 1997, and the short-faced scorpionfly and Panorpodidae (Carpenter 1953; Russell 1982;Beuteletal. Panorpodes kuandianensis Zhong, Zhang & Hua, 2011 to 2008;Maetal.2013), and saprophagous in Panorpidae, infer the feeding habits of Panorpodidae. The molar region Apteropanorpidae, Choristidae, Eomeropidae, and of Panorpodidae is glabrous, lacking the long spines for filter- Meropidae (Palmer and Yeates 2005; Palmer 2010; Huang ing (preventing larger particles from entering the pharynx) as and Hua 2011). The knowledge of the feeding habits of larval found in Bittacidae or the tuberculate teeth for grinding as Mecoptera, however, is still fragmentary. present in Panorpidae. The mandibles of Panorpodidae are The larvae of Mecoptera are morphologically diverse unsuitable for grinding, and most likely, larval Panorpodidae and inhabit a wide range of habitats (Byers 1987, 1991). -
Diversity and Distribution of Mites (Acari: Ixodida, Mesostigmata, Trombidiformes, Sarcoptiformes) in the Svalbard Archipelago
Article Diversity and Distribution of Mites (Acari: Ixodida, Mesostigmata, Trombidiformes, Sarcoptiformes) in the Svalbard Archipelago Anna Seniczak 1,*, Stanisław Seniczak 2, Marla D. Schwarzfeld 3 and Stephen J. Coulson 4,5 and Dariusz J. Gwiazdowicz 6 1 Department of Natural History, University Museum of Bergen, University of Bergen, Postboks 7800, 5020 Bergen, Norway 2 Department Evolutionary Biology, Faculty of Biological Sciences, Kazimierz Wielki University, J.K. Chodkiewicza 30, 85-064 Bydgoszcz, Poland; [email protected] 3 Canadian National Collection of Insects, Arachnids and Nematodes, Agriculture and Agri-food Canada, 960 Carling Avenue, Ottawa, ON K1A 0C6, Canada; [email protected] 4 Swedish Species Information Centre, Swedish University of Agricultural Sciences, SLU Artdatabanken, Box 7007, 75007 Uppsala, Sweden; [email protected] 5 Department of Arctic Biology, University Centre in Svalbard, P.O. Box 156, 9171 Longyearbyen, Svalbard, Norway 6 Faculty of Forestry, Poznań University of Life Sciences, Wojska Polskiego 71c, 60-625 Poznań, Poland; [email protected] * Correnspondence: [email protected] Received: 21 July 2020; Accepted: 19 August 2020; Published: 25 August 2020 Abstract: Svalbard is a singular region to study biodiversity. Located at a high latitude and geographically isolated, the archipelago possesses widely varying environmental conditions and unique flora and fauna communities. It is also here where particularly rapid environmental changes are occurring, having amongst the fastest increases in mean air temperature in the Arctic. One of the most common and species-rich invertebrate groups in Svalbard is the mites (Acari). We here describe the characteristics of the Svalbard acarofauna, and, as a baseline, an updated inventory of 178 species (one Ixodida, 36 Mesostigmata, 43 Trombidiformes, and 98 Sarcoptiformes) along with their occurrences.