Papers and New Species of Minor Insect Orders Published in Zootaxa, 2001– 2020
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The Mitochondrial Genomes of Palaeopteran Insects and Insights
www.nature.com/scientificreports OPEN The mitochondrial genomes of palaeopteran insects and insights into the early insect relationships Nan Song1*, Xinxin Li1, Xinming Yin1, Xinghao Li1, Jian Yin2 & Pengliang Pan2 Phylogenetic relationships of basal insects remain a matter of discussion. In particular, the relationships among Ephemeroptera, Odonata and Neoptera are the focus of debate. In this study, we used a next-generation sequencing approach to reconstruct new mitochondrial genomes (mitogenomes) from 18 species of basal insects, including six representatives of Ephemeroptera and 11 of Odonata, plus one species belonging to Zygentoma. We then compared the structures of the newly sequenced mitogenomes. A tRNA gene cluster of IMQM was found in three ephemeropteran species, which may serve as a potential synapomorphy for the family Heptageniidae. Combined with published insect mitogenome sequences, we constructed a data matrix with all 37 mitochondrial genes of 85 taxa, which had a sampling concentrating on the palaeopteran lineages. Phylogenetic analyses were performed based on various data coding schemes, using maximum likelihood and Bayesian inferences under diferent models of sequence evolution. Our results generally recovered Zygentoma as a monophyletic group, which formed a sister group to Pterygota. This confrmed the relatively primitive position of Zygentoma to Ephemeroptera, Odonata and Neoptera. Analyses using site-heterogeneous CAT-GTR model strongly supported the Palaeoptera clade, with the monophyletic Ephemeroptera being sister to the monophyletic Odonata. In addition, a sister group relationship between Palaeoptera and Neoptera was supported by the current mitogenomic data. Te acquisition of wings and of ability of fight contribute to the success of insects in the planet. -
A New Insect Trackway from the Upper Jurassic—Lower Cretaceous Eolian Sandstones of São Paulo State, Brazil: Implications for Reconstructing Desert Paleoecology
A new insect trackway from the Upper Jurassic—Lower Cretaceous eolian sandstones of São Paulo State, Brazil: implications for reconstructing desert paleoecology Bernardo de C.P. e M. Peixoto1,2, M. Gabriela Mángano3, Nicholas J. Minter4, Luciana Bueno dos Reis Fernandes1 and Marcelo Adorna Fernandes1,2 1 Laboratório de Paleoicnologia e Paleoecologia, Departamento de Ecologia e Biologia Evolutiva, Universidade Federal de São Carlos (UFSCar), São Carlos, São Paulo, Brazil 2 Programa de Pós Graduacão¸ em Ecologia e Recursos Naturais, Centro de Ciências Biológicas e da Saúde, Universidade Federal de São Carlos (UFSCar), São Carlos, São Paulo, Brazil 3 Department of Geological Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada 4 School of the Environment, Geography, and Geosciences, University of Portsmouth, Portsmouth, Hampshire, United Kingdom ABSTRACT The new ichnospecies Paleohelcura araraquarensis isp. nov. is described from the Upper Jurassic-Lower Cretaceous Botucatu Formation of Brazil. This formation records a gigantic eolian sand sea (erg), formed under an arid climate in the south-central part of Gondwana. This trackway is composed of two track rows, whose internal width is less than one-quarter of the external width, with alternating to staggered series, consisting of three elliptical tracks that can vary from slightly elongated to tapered or circular. The trackways were found in yellowish/reddish sandstone in a quarry in the Araraquara municipality, São Paulo State. Comparisons with neoichnological studies and morphological inferences indicate that the producer of Paleohelcura araraquarensis isp. nov. was most likely a pterygote insect, and so could have fulfilled one of the Submitted 6 November 2019 ecological roles that different species of this group are capable of performing in dune Accepted 10 March 2020 deserts. -
Insecta: Phasmatodea) and Their Phylogeny
insects Article Three Complete Mitochondrial Genomes of Orestes guangxiensis, Peruphasma schultei, and Phryganistria guangxiensis (Insecta: Phasmatodea) and Their Phylogeny Ke-Ke Xu 1, Qing-Ping Chen 1, Sam Pedro Galilee Ayivi 1 , Jia-Yin Guan 1, Kenneth B. Storey 2, Dan-Na Yu 1,3 and Jia-Yong Zhang 1,3,* 1 College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004, China; [email protected] (K.-K.X.); [email protected] (Q.-P.C.); [email protected] (S.P.G.A.); [email protected] (J.-Y.G.); [email protected] (D.-N.Y.) 2 Department of Biology, Carleton University, Ottawa, ON K1S 5B6, Canada; [email protected] 3 Key Lab of Wildlife Biotechnology, Conservation and Utilization of Zhejiang Province, Zhejiang Normal University, Jinhua 321004, China * Correspondence: [email protected] or [email protected] Simple Summary: Twenty-seven complete mitochondrial genomes of Phasmatodea have been published in the NCBI. To shed light on the intra-ordinal and inter-ordinal relationships among Phas- matodea, more mitochondrial genomes of stick insects are used to explore mitogenome structures and clarify the disputes regarding the phylogenetic relationships among Phasmatodea. We sequence and annotate the first acquired complete mitochondrial genome from the family Pseudophasmati- dae (Peruphasma schultei), the first reported mitochondrial genome from the genus Phryganistria Citation: Xu, K.-K.; Chen, Q.-P.; Ayivi, of Phasmatidae (P. guangxiensis), and the complete mitochondrial genome of Orestes guangxiensis S.P.G.; Guan, J.-Y.; Storey, K.B.; Yu, belonging to the family Heteropterygidae. We analyze the gene composition and the structure D.-N.; Zhang, J.-Y. -
ENTOMOLOGY 322 LABS 13 & 14 Insect Mouthparts
ENTOMOLOGY 322 LABS 13 & 14 Insect Mouthparts The diversity in insect mouthparts may explain in part why insects are the predominant form of multicellular life on earth (Bernays, 1991). Insects, in one form or another, consume essentially every type of food on the planet, including most terrestrial invertebrates, plant leaves, pollen, fungi, fungal spores, plant fluids (both xylem and phloem), vertebrate blood, detritus, and fecal matter. Mouthparts are often modified for other functions as well, including grooming, fighting, defense, courtship, mating, and egg manipulation. This tremendous morphological diversity can tend to obscure the essential appendiculate nature of insect mouthparts. In the following lab exercises we will track the evolutionary history of insect mouthparts by comparing the mouthparts of a generalized insect (the cricket you studied in the last lab) to a variety of other arthropods, and to the mouthparts of some highly modified insects, such as bees, butterflies, and cicadas. As mentioned above, the composite nature of the arthropod head has lead to considerable debate as to the true homologies among head segments across the arthropod classes. Table 13.1 is presented below to help provide a framework for examining the mouthparts of arthropods as a whole. 1. Obtain a specimen of a horseshoe crab (Merostoma: Limulus), one of the few extant, primitively marine Chelicerata. From dorsal view, note that the body is divided into two tagmata, the anterior Figure 13.1 (Brusca & Brusca, 1990) prosoma (cephalothorax) and the posterior opisthosoma (abdomen) with a caudal spine (telson) at its end (Fig. 13.1). In ventral view, note that all locomotory and feeding appendages are located on the prosoma and that all except the last are similar in shape and terminate in pincers. -
The Evolution of Zoraptera
Systematic Entomology (2020), 45, 349–364 DOI: 10.1111/.12400 The evolution of Zoraptera YOKOMATSUMURA 1,2,ROLFG.BEUTEL 1*,JOSÉA.RAFAEL 3*, IZUMIYAO 4*,JOSENIRT.CÂMARA 5*,SHEILAP.LIMA 3 KAZUNORIYOSHIZAWA 4 1E G,I ü Z Evh,Fh Sh Uv J,J,G, 2D F Mh Bh,Z I,K Uv,K,G, 3I N P Az,M,Bz, 4S E,Sh A,Hkk Uv,S,J 5Uv F Pí, B J,Pí, Bz Abstract. Z h .B w x wh h kw, w h h DNA -v h. Th h hw h Z v h , h w . Th h h h v h . Th v h P. P h h h Z w h v, h h . Th h h P , v h k Gw L . Th x v f v h , hv, k hh v h.W v v h h v.O v / h , hk . Introduction B et al., 2014; Mh et al., 2014; Ch, 2018). I h h v (vw Z h h I Mh- Mh et al., 2014;K et al., 2016; B et al., 2017), G. Th wh h wh Z (G &E, 2005; h P - v (Yhzw, 2011; M et al., 2014; C:Yk M,E G,I ü Z Evh,Fh Sh Uv W &P, 2014; Mh et al., 2014, 2015; M J,E. 1, 07743 J,G &D F- et al., 2015; W et al., 2019). R,W et al. Mh Bh,Z I,K (2019) h h h - Uv, Bh G 1–9, 24118, K,G. P v v, E-: k..h@.;R G. -
Insect Life Histories and Diversity Outline HOW MANY SPECIES OF
Insect Life Histories and Diversity Outline 1. There are many kinds of insects 2. Why, how? 3. The Orders HOW MANY SPECIES OF INSECTS ARE THERE? Insect Diversity • Distribution spread primarily between 5 orders 1. Coleoptera (beetles) = 350,000 2. Lepidoptera (butterflies and moths) = 150,000 3. Hymenoptera (wasps, ants and bees) = 125,000 4. Diptera (flies) = 120,000 5. Hemiptera (bugs etc) =90,000 1 There has never been more insect diversity than now WHY DO INSECTS DOMINATE THE NUMBER OF SPECIES? 540 Why? Insects were the first animals to • Insects have been around over 400 million years adapt to and diversify on land First insect fossils Land becomes habitable Why is the basis of Why? high rates of speciation? • Their geologic age • High speciation rates • High fecundity (many offspring) • Short generation time (more chances • One estimate: Lepidoptera for mutation) in the last 100 million years added 2-3 species • These combine to produce huge # of every thousand years individuals, increased range of variation • = more variation for natural selection 2 Combined with low rates of natural Why? extinction • Geologic age • Fossil evidence • Capacity for high speciation rates that insects • Low rates of extinction were not affected (much) by • Design previous mass extinction events •Why? DESIGN Insect Size –size and life span Wide range of insect sizes.... –diversity of characteristics of insect cuticle –flight –modularity at many levels –holometabolous larvae But most are small 3 Small size Life Span • Wide variation 1. Shorter generation time 2. More ecological niches available than to larger animals Life Span • Wide variation but most are relatively short insect cuticle Flight • Takes on diversity of shapes, colors, textures • A composite material: variations are tough enough to cut hardwood, have high plasticity, delicate enough gases will diffuse through it. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Zoraptera: Zorotypidae), with Discussion on Relationships of and Within the Order
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Revistes Catalanes amb Accés Obert ACTA GEOLOGICA HISPANICA, v. 35 (2000), nº 1,p. 149-164 AWinged Zorotypusin Miocene Amber from the Dominican Republic (Zoraptera: Zorotypidae), with Discussion on Relationships of and within the Order M.S. ENGEL(1) and D.A. GRIMALDI(2) (1) Division of Entomology, Natural History Museum and Biodiversity Research Center, and Department of Ecology and Evolutionary Biology, 1460 Jayhawk Boulevard, Snow Hall, University of Kansas, Lawrence, Kansas 66045-7523, U.S.A. E-mail: [email protected] (2) Department of Entomology, American Museum of Natural History, Central Park West at 79th Street, New York, New York 10024-5192, U.S.A. E-mail: [email protected] ABSTRACT A new fossil zorapteran is described and figured in Miocene Dominican amber. The specimen is the first winged Zo ro t y p u s fo s s i l , and is described as Zo r otypus goe l e t i n.sp. The species is distinguished from the only other fossil zorapteran, Z. palaeus also in Do- minican amber, as well as an extant species to which it appears most similar, Z. snyd e r i . The new fossil is significant in the possession of segmented cerci, a plesiomorphic character unique for the order. The classification of the order is briefly summarized and genera pro- posed by Kuk a l ov á - P eck and Peck (1993) and Chao and Chen (2000) are newl y synonymized under Zo ro t y p u s . -
Changes to the Fossil Record of Insects Through Fifteen Years of Discovery
This is a repository copy of Changes to the Fossil Record of Insects through Fifteen Years of Discovery. White Rose Research Online URL for this paper: https://eprints.whiterose.ac.uk/88391/ Version: Published Version Article: Nicholson, David Blair, Mayhew, Peter John orcid.org/0000-0002-7346-6560 and Ross, Andrew J (2015) Changes to the Fossil Record of Insects through Fifteen Years of Discovery. PLosOne. e0128554. https://doi.org/10.1371/journal.pone.0128554 Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ RESEARCH ARTICLE Changes to the Fossil Record of Insects through Fifteen Years of Discovery David B. Nicholson1,2¤*, Peter J. Mayhew1, Andrew J. Ross2 1 Department of Biology, University of York, York, United Kingdom, 2 Department of Natural Sciences, National Museum of Scotland, Edinburgh, United Kingdom ¤ Current address: Department of Earth Sciences, The Natural History Museum, London, United Kingdom * [email protected] Abstract The first and last occurrences of hexapod families in the fossil record are compiled from publications up to end-2009. -
Embioptera (PDF)
Embioptera EMBIOPTERA Webspinners / Embiids The name Embioptera, derived from the Greek "embio" meaning lively and "ptera" meaning wings refers to the fluttery movement of wings that was observed in the first male Embioptera described. Classification Life History & Ecology Distribution Physical Features Economic Importance Major Families Fact File Hot Links Life History & Ecology: The order Embioptera (webspinners or embiids) is another group within the Orthopteroid complex that probably appeared early in the Carboniferous period. Many insect taxonomists believe webspinners represent another evolutionary "dead end" that diverged about the same time as Plecoptera. Determining phylogenetic relationships for this group is unusually difficult because the Embioptera have a number of adaptations not found in any other insects. The tarsi of the front legs, for example, are enlarged and contain glands that produce silk. No other group of insects, fossil or modern, have silk-producing glands in http://www.cals.ncsu.edu/course/ent425/compendium/webspi~1.html (1 of 5) [10/24/2007 12:08:15 PM] Embioptera the legs. The silk is used to construct elaborate nests and tunnels under leaves or bark. Webspinners live gregariously within these silken nests, feeding on grass, dead leaves, moss, lichens, or bark. Nymphs and adults are similar in appearance. Embiids rarely leave their silken tunnels; a colony grows by expanding its tunnel system to new food resources. Well-developed muscles in the hind legs allow these insects to run backward through their tunnels as easily as they run forward. Only adult males have wings. Front and hind wings are similar in shape and unusually flexible; they fold over the head when the insect runs backward through its tunnels. -
100 Years Zoraptera – a Phantom in Insect Evolution and the History Of
1 100 years Zoraptera – a phantom in insect evolution and the 1 2 3 2 4 history of its investigation 5 6 3 7 8 9 4 Mashimo, Y., Y. Matsumura, R. Machida, R. Dallai, M. Gottardo, K. Yoshizawa, F. 10 11 5 Friedrich, B. Wipfler & R.G. Beutel 12 13 6 14 15 16 7 Y. Mashimo, R. Machida, Sugadaira Montane Research Center, University of Tsukuba, 17 18 8 Sugadaira Kogen, Ueda, Nagano 386-2204, Japan 19 20 21 9 R. Dallai, M. Gottardo, Department of Life Sciences, University of Siena, Via A. Moro 2, I- 22 23 10 53100 Siena, Italy 24 25 26 11 Y. Yoshizawa, Systematic Entomology, Hokkaido University, Sapporo, Hokkaido 060-8589, 27 28 12 Japan 29 30 13 F. Friedrich, Biozentrum Grindel und Zoologisches Museum Hamburg, , Martin-Luther-King- 31 32 33 14 Platz 3, Universität Hamburg, 20146 Hamburg, Germany 34 35 15 R.G. Beutel, B. Wipfler, Y. Matsumura, Institut für Spezielle Zoologie und 36 37 38 16 Evolutionsbiologie, Erbertstr. 1, FSU Jena, 07743 Jena, Germany ([email protected]) 39 40 17 41 42 43 18 Zoraptera are a cryptic and enigmatic group of insects. The species diversity is 44 45 19 lower than in almost all other groups of Hexapoda, but may be distinctly higher 46 47 48 20 than presently known. Several new species were described from different regions 49 50 21 recently. The systematic placement was discussed controversially since the group 51 52 22 was discovered 100 years ago. Affinities with Isoptera and Psocoptera were 53 54 55 23 discussed in earlier studies. -
Grooming Behavior in Embioptera and Zoraptera (Insecta)1
Grooming Behavior in Embioptera and Zoraptera (Insecta)1 BARRY D. VALENTINE, Faculty of Zoology, The Ohio State University, Columbus, OH 43210-1293 ABSTRACT. Embiid grooming (based on Oligembia (D.) vandykei Ross, and two unidentified species) includes five acts, all involving the mouth as the effector organ: Antenna Clean, Foreleg Clean, Midleg Clean, Hindleg Clean, and Abdomen Clean. Of these, only Antenna Clean is unusual because the antenna is unassisted by a foreleg, and is turned under the body and supported by the substrate as the head dips to reach it. Zorapteran grooming (Zorotypus hubbardi Caudell) includes 10 acts which can be performed in 13 ways. Alternate ways occur in Midleg Clean and Palpus Clean. The remaining eight acts are: Antenna Clean, Foreleg Clean, Hindleg Clean, Abdomen Clean, Antenna-Foreleg Rub, Head-Foreleg Rub, Body-Foreleg Rub, and Body-Substrate Rub. Modes unknown in other insects occur in Midleg Clean (with both forelegs raised), and Abdomen Clean (body forming a closed upside-down U, on a 4-point stance, the forelegs raised). Grooming behavior of embiids and zorapterans does not suggest relationships with other insect orders, and emphasizes their isolation. OHIO J. SCI. 86 (4): 150-152, 1986 INTRODUCTION microscope light. An alate male Oligembia (Dilobocera) vandykei Ross, 1944 (Family Oligembiidae) was collected in Florida, Monroe Grooming behavior for most insect orders is poorly County, Bahia Honda Key, Sandspur Beach, on 25 December 1979, known, despite the insight it provides by relating struc- by the author after a light rain, and was observed in a vial immediately ture to function. Of the two orders described here, zo- after capture from 0900 to 0945 hrs.