Collembola, Neanuridae, Pseudachorutinae) with the Description of a New Brazilian Species
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Unexpected Diversity in Neelipleona Revealed by Molecular Phylogeny Approach (Hexapoda, Collembola)
S O I L O R G A N I S M S Volume 83 (3) 2011 pp. 383–398 ISSN: 1864-6417 Unexpected diversity in Neelipleona revealed by molecular phylogeny approach (Hexapoda, Collembola) Clément Schneider1, 3, Corinne Cruaud2 and Cyrille A. D’Haese1 1 UMR7205 CNRS, Département Systématique et Évolution, Muséum National d’Histoire Naturelle, CP50 Entomology, 45 rue Buffon, 75231 Paris cedex 05, France 2 Genoscope, Centre National de Sequençage, 2 rue G. Crémieux, CP5706, 91057 Evry cedex, France 3 Corresponding author: Clément Schneider (email: [email protected]) Abstract Neelipleona are the smallest of the four Collembola orders in term of species number with 35 species described worldwide (out of around 8000 known Collembola). Despite this apparent poor diversity, Neelipleona have a worldwide repartition. The fact that the most commonly observed species, Neelus murinus Folsom, 1896 and Megalothorax minimus Willem, 1900, display cosmopolitan repartition is striking. A cladistic analysis based on 16S rDNA, COX1 and 28S rDNA D1 and D2 regions, for a broad collembolan sampling was performed. This analysis included 24 representatives of the Neelipleona genera Neelus Folsom, 1896 and Megalothorax Willem, 1900 from various regions. The interpretation of the phylogenetic pattern and number of transformations (branch length) indicates that Neelipleona are more diverse than previously thought, with probably many species yet to be discovered. These results buttress the rank of Neelipleona as a whole order instead of a Symphypleona family. Keywords: Collembola, Neelidae, Megalothorax, Neelus, COX1, 16S, 28S 1. Introduction 1.1. Brief history of Neelipleona classification The Neelidae family was established by Folsom (1896), who described Neelus murinus from Cambridge (USA). -
Reviews of the Genera Schaefferia Absolon, 1900, Deuteraphorura
TAR Terrestrial Arthropod Reviews 5 (2012) 35–85 brill.nl/tar Reviews of the genera Schaefferia Absolon, 1900, Deuteraphorura Absolon, 1901, Plutomurus Yosii, 1956 and the Anurida Laboulbène, 1865 species group without eyes, with the description of four new species of cave springtails (Collembola) from Krubera-Voronya cave, Arabika Massif, Abkhazia Rafael Jordana1, Enrique Baquero1*, Sofía Reboleira2 and Alberto Sendra3 1Department of Zoology and Ecology, University of Navarra, 31080 Pamplona, Spain e-mails: [email protected]; [email protected] *Corresponding author. 2Department of Biology, Universidade de Aveiro and CESAM Campus Universitário de Santiago, 3810-193 Aveiro, Portugal e-mail: [email protected] 3Museu Valencià d’Història Natural (Fundación Entomológica Torres Sala) Paseo de la Pechina 15. 46008 Valencia, Spain e-mail: [email protected] Received on November 4, 2011. Accepted on November 21, 2011 Summary Krubera-Voronya cave and other deep systems in Arabika Massif are being explored during many speleological expeditions. A recent Ibero-Russian exploration expedition (summer of 2010) took place in this cave with the aim of providing a study of the biocenosis of the deepest known cave in the world. Four new species of Collembola were found at different depths: Schaefferia profundissima n. sp., Anurida stereoodorata n. sp., Deuteraphorura kruberaensis n. sp., and Plutomurus ortobalaganensis n. sp., the last one at -1980 m deep. The identification and description of the new species have required the careful study of all congeneric species, implying a revision of each genus. As a result of this work tables and keys to all significant characters for each species are presented. -
Collembola: Neanuridae) from Peru
Biodiversity Data Journal 8: e57743 doi: 10.3897/BDJ.8.e57743 Taxonomic Paper A new species of the genus Neotropiella Handschin, 1942 (Collembola: Neanuridae) from Peru José G. Palacios-Vargas‡, Yony T. Callohuari§,| ‡ Universidad Nacional Autónoma de México, México, D. F., Mexico § University of Illinois at Urbana-Champaign, Urbana, United States of America | Universidad Nacional Agraria La Molina, Lima, Peru Corresponding author: Yony T. Callohuari ([email protected]) Academic editor: Ľubomír Kováč Received: 18 Aug 2020 | Accepted: 15 Nov 2020 | Published: 25 Nov 2020 Citation: Palacios-Vargas JG, Callohuari YT (2020) A new species of the genus Neotropiella Handschin, 1942 (Collembola: Neanuridae) from Peru. Biodiversity Data Journal 8: e57743. https://doi.org/10.3897/BDJ.8.e57743 ZooBank: urn:lsid:zoobank.org:pub:570D8CC8-6869-464E-8358-08CDE5B3FD53 Abstract Background Neotropiella is a genus of springtails which can be of medium size (2 mm) or relatively long (5 mm). These springtails live in leaf litter, under the bark of dead trees or in decomposing wood, mainly in the Neotropical Region and are often collected by litter samples on Berlese funnels or by pitfall traps. Most species have been described, based on relatively few specimens and chaetotaxy of several species is incomplete. New information A new species within Neotropiella was discovered in recent pitfall trap collections from Peru. Neotropiella peruana sp. n. was taxonomically treated and studied under both phase contrast and scanning electron microscopy. It is similar to N. insularis from Brazil, but smaller with only 4 mandibular teeth (vs. 5) and with well-developed unguis lateral teeth. © Palacios-Vargas J, Callohuari Y. -
Why Are There So Many Exotic Springtails in Australia? a Review
90 (3) · December 2018 pp. 141–156 Why are there so many exotic Springtails in Australia? A review. Penelope Greenslade1, 2 1 Environmental Management, School of School of Health and Life Sciences, Federation University, Ballarat, Victoria 3353, Australia 2 Department of Biology, Australian National University, GPO Box, Australian Capital Territory 0200, Australia E-mail: [email protected] Received 17 October 2018 | Accepted 23 November 2018 Published online at www.soil-organisms.de 1 December 2018 | Printed version 15 December 2018 DOI 10.25674/y9tz-1d49 Abstract Native invertebrate assemblages in Australia are adversely impacted by invasive exotic plants because they are replaced by exotic, invasive invertebrates. The reasons have remained obscure. The different physical, chemical and biotic characteristics of the novel habitat seem to present hostile conditions for native species. This results in empty niches. It seems the different ecologies of exotic invertebrate species may be better adapted to colonise these novel empty niches than native invertebrates. Native faunas of other southern continents that possess a highly endemic fauna, such as South America, South Africa and New Zealand, may have suffered the same impacts from exotic species but insufficient survey data and unreliable and old taxonomy makes this uncertain. Here I attempt to discover what particular characteristics of these novel habitats are hostile to native invertebrates. I chose the Collembola as a target taxon. They are a suitable group because the Australian collembolan fauna consists of a high percentage of endemic taxa, but also exotic, non-native, species. Most exotic Collembola species in Australia appear to have originated from Europe, where they occur at low densities (Fjellberg 1997, 2007). -
Cravens Peak Scientific Study Report
Geography Monograph Series No. 13 Cravens Peak Scientific Study Report The Royal Geographical Society of Queensland Inc. Brisbane, 2009 The Royal Geographical Society of Queensland Inc. is a non-profit organization that promotes the study of Geography within educational, scientific, professional, commercial and broader general communities. Since its establishment in 1885, the Society has taken the lead in geo- graphical education, exploration and research in Queensland. Published by: The Royal Geographical Society of Queensland Inc. 237 Milton Road, Milton QLD 4064, Australia Phone: (07) 3368 2066; Fax: (07) 33671011 Email: [email protected] Website: www.rgsq.org.au ISBN 978 0 949286 16 8 ISSN 1037 7158 © 2009 Desktop Publishing: Kevin Long, Page People Pty Ltd (www.pagepeople.com.au) Printing: Snap Printing Milton (www.milton.snapprinting.com.au) Cover: Pemberton Design (www.pembertondesign.com.au) Cover photo: Cravens Peak. Photographer: Nick Rains 2007 State map and Topographic Map provided by: Richard MacNeill, Spatial Information Coordinator, Bush Heritage Australia (www.bushheritage.org.au) Other Titles in the Geography Monograph Series: No 1. Technology Education and Geography in Australia Higher Education No 2. Geography in Society: a Case for Geography in Australian Society No 3. Cape York Peninsula Scientific Study Report No 4. Musselbrook Reserve Scientific Study Report No 5. A Continent for a Nation; and, Dividing Societies No 6. Herald Cays Scientific Study Report No 7. Braving the Bull of Heaven; and, Societal Benefits from Seasonal Climate Forecasting No 8. Antarctica: a Conducted Tour from Ancient to Modern; and, Undara: the Longest Known Young Lava Flow No 9. White Mountains Scientific Study Report No 10. -
Forest Disturbance and Arthropods: Small‐Scale Canopy Gaps Drive
Forest disturbance and arthropods: Small-scale canopy gaps drive invertebrate community structure and composition 1, 2,3 4 1,5 KAYLA I. PERRY , KIMBERLY F. WALLIN, JOHN W. WENZEL, AND DANIEL A. HERMS 1Department of Entomology, Ohio Agricultural Research and Development Center, The Ohio State University, 1680 Madison Avenue, Wooster, Ohio 44691 USA 2Rubenstein School of Environment and Natural Resources, University of Vermont, 312H Aiken Center, Burlington, Vermont 05405 USA 3USDA Forest Service, Northern Research Station, 312A, Aiken, Burlington, Vermont 05405 USA 4Powdermill Nature Reserve, Carnegie Museum of Natural History, 1847 PA-381, Rector, Pennsylvania 15677 USA 5The Davey Tree Expert Company, 1500 Mantua Street, Kent, Ohio 44240 USA Citation: Perry, K. I., K. F. Wallin, J. W. Wenzel, and D. A. Herms. 2018. Forest disturbance and arthropods: Small-scale canopy gaps drive invertebrate community structure and composition. Ecosphere 9(10):e02463. 10.1002/ecs2.2463 Abstract. In forest ecosystems, disturbances that cause tree mortality create canopy gaps, increase growth of understory vegetation, and alter the abiotic environment. These impacts may have interacting effects on populations of ground-dwelling invertebrates that regulate ecological processes such as decom- position and nutrient cycling. A manipulative experiment was designed to decouple effects of simultane- ous disturbances to the forest canopy and ground-level vegetation to understand their individual and combined impacts on ground-dwelling invertebrate communities. We quantified invertebrate abundance, richness, diversity, and community composition via pitfall traps in response to a factorial combination of two disturbance treatments: canopy gap formation via girdling and understory vegetation removal. For- mation of gaps was the primary driver of changes in invertebrate community structure, increasing activity- abundance and taxonomic richness, while understory removal had smaller effects. -
With Special Emphasis on the Equatorial Oceanic Islands
insects Article Synthesis of the Brazilian Poduromorpha (Collembola: Hexapoda) with Special Emphasis on the Equatorial Oceanic Islands Estevam C. A. de Lima 1,2,* , Maria Cleide de Mendonça 1, Gabriel Costa Queiroz 1 , Tatiana Cristina da Silveira 1 and Douglas Zeppelini 2 1 Laboratório de Apterygotologia, Departamento de Entomologia, Museu Nacional, Universidade Federal do Rio de Janeiro, Rio de Janeiro 20940-040, Brazil; [email protected] (M.C.d.M.); [email protected] (G.C.Q.); [email protected] (T.C.d.S.) 2 Laboratório de Sistemática de Collembola e Conservação—Coleção de Referência de Fauna de Solo—CCBSA—Universidade Estadual da Paraíba Campus V, João Pessoa 58070-450, Brazil; [email protected] * Correspondence: [email protected] Simple Summary: Endemic Collembola species are bioindicators of environmental quality since native species abundance is particularly sensitive to environmental disturbances. Oceanic island biota generally present high percentages of endemic species, and the vulnerability of these species is higher than those of the continents. The objective of this work was to carry out a survey of the Collembola species of the order Poduromorpha in the Brazilian oceanic islands and synthesize a distribution list of this order for Brazil. Our results reveal four new species of Collembola Poduromorpha for Brazilian oceanic islands that may be useful for the conservation strategies of these island regions and a contributor to the knowledge of the order in Brazil. Citation: de Lima, E.C.A.; de Mendonça, M.C.; Queiroz, G.C.; da Silveira, T.C.; Abstract: We present new species and records of Poduromorpha for the Brazilian oceanic islands and Zeppelini, D. -
A New Species of Deutonura (Collembola: Neanuridae: Neanurinae) from North-Eastern Algeria, and Characterisation of Two Intraspecific Lineages by Their Barcodes
Zootaxa 3920 (2): 281–290 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2015 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3920.2.4 http://zoobank.org/urn:lsid:zoobank.org:pub:6AC3DAB1-9D75-4833-9610-91FC5EC3C35C A new species of Deutonura (Collembola: Neanuridae: Neanurinae) from north-eastern Algeria, and characterisation of two intraspecific lineages by their barcodes LOUIS DEHARVENG1,4, ABDELMALEK ZOUGHAILECH2, SALAH HAMRA-KROUA2 & DAVID PORCO3 1Institut de Systématique, Evolution, Biodiversité, ISYEB - UMR 7205 - CNRS, MNHN, UPMC, EPHE, Museum national d'Histoire naturelle, Sorbone Universités, 55 rue Cuvier, CP50, F-75005 Paris, France. E-mail: [email protected] 2Laboratoire de Biosystématique et Ecologie des Arthropodes, Faculté des Sciences de la Nature et de la Vie, Université Constantine 1, Route de Ain El-Bey, 25000 Constantine, Algeria. E-mail: [email protected] 3Laboratoire ECODIV, Université de Rouen, Bâtiment IRESE A, Place Emile Blondel, 76821 Mont Saint Aignan Cedex, France. E-mail: [email protected] 4Corresponding author Abstract A new species of Deutonura, D. zana sp. nov., is described from north-eastern Algeria. It is morphologically similar in most characters to D. deficiens meridionalis and to D. luberonensis, both members of the D. phlegraea group, differing from the former by the absence of chaeta O on head, and from the later by the separation of tubercles Di and De on Th. I. The muscular insertion pattern of the new species is figured, and suggested as a potential new character for the taxonomy of Neanurinae. Deutonura zana sp. -
Biodiversity of Compost Mesofauna and Its Potential As an Indicator of the Composting Process Status
® Dynamic Soil, Dynamic Plant ©2011 Global Science Books Biodiversity of Compost Mesofauna and its Potential as an Indicator of the Composting Process Status Hanne Steel* • Wim Bert Nematology Unit, Department of Biology, Ghent University, K.L. Ledeganckstraat 35, 9000 Ghent, Belgium Corresponding author : * [email protected] ABSTRACT One of the key issues in compost research is to assess the quality and maturity of the compost. Biological parameters, especially based on mesofauna, have multiple advantages for monitoring a given system. The mesofauna of compost includes Isopoda, Myriapoda, Acari, Collembola, Oligochaeta, Tardigrada, Hexapoda, and Nematoda. This wide spectrum of organisms forms a complex and rapidly changing community. Up to the present, none of the dynamics, in relation to the composting process, of these taxa have been thoroughly investigated. However, from the mesofauna, only nematodes possess the necessary attributes to be potentially useful ecological indicators in compost. They occur in any compost pile that is investigated and in virtually all stages of the compost process. Compost nematodes can be placed into at least three functional or trophic groups. They occupy key positions in the compost food web and have a rapid respond to changes in the microbial activity that is translated in the proportion of functional (feeding) groups within a nematode community. Further- more, there is a clear relationship between structure and function: the feeding behavior is easily deduced from the structure of the mouth cavity and pharynx. Thus, evaluation and interpretation of the abundance and function of nematode faunal assemblages or community structures offers an in situ assessment of the compost process. -
Collembola of Canada 187 Doi: 10.3897/Zookeys.819.23653 REVIEW ARTICLE Launched to Accelerate Biodiversity Research
A peer-reviewed open-access journal ZooKeys 819: 187–195 (2019) Collembola of Canada 187 doi: 10.3897/zookeys.819.23653 REVIEW ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Collembola of Canada Matthew S. Turnbull1, Sophya Stebaeva2 1 Unaffiliated, Kingston, Ontario, Canada2 The Severtsov Institute of Ecology and Evolution, Russian Aca- demy of Sciences, Leninskii pr. 33, Moscow 119071, Russia Corresponding author: Matthew S. Turnbull ([email protected]) Academic editor: D. Langor | Received 16 January 2018 | Accepted 8 May 2018 | Published 24 January 2019 http://zoobank.org/3A331779-19A1-41DA-AFCF-81AAD4CB049F Citation: Turnbull MS, Stebaeva S (2019) Collembola of Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment. Part 1: The Terrestrial Arthropods. ZooKeys 819: 187–195.https://doi. org/10.3897/zookeys.819.23653 Abstract The state of knowledge of diversity of Collembola in Canada was assessed by examination of literature and DNA barcode data. There are 474 described extant Collembola species known from Canada, a significant change compared to the 520 species estimated to occur in Canada in 1979 (Richards 1979) and the 341 reported in the most recent national checklist (Skidmore 1993). Given the number of indeterminate or cryptic species records, the dearth of sampling in many regions, and the growing use of genetic biodiversity assessment methods such as Barcode Index Numbers, we estimate the total diversity of Collembola in Canada to be approximately 675 species. Advances in Collembola systematics and Canadian research are discussed. Keywords biodiversity assessment, Biota of Canada, Collembola, springtails Collembola, commonly known as springtails, is a class of small, entognathous, wing- less hexapods that is a sister group to Insecta. -
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). -
The Springtails (Insecta: Collembola) Fauna at Different Microhabitats of Bečići Beach, Montenegro
UNIVERSITY THOUGHT doi:10.5937/univtho8-14774 Publication in Natural Sciences, Vol. 8, No. 1, 2018, pp. 5-9. Original Scientific Paper THE SPRINGTAILS (INSECTA: COLLEMBOLA) FAUNA AT DIFFERENT MICROHABITATS OF BEČIĆI BEACH, MONTENEGRO TATJANA R. JAKŠIĆ1*, PREDRAG S. VASIĆ1, NENAD Đ. LABUS1, OLIVERA M. PAPOVIĆ1, MILOŠ R. STANOJEVIĆ1, NIKOLA N. ĐUKIĆ1 1Faculty of Sciences and Mathematics, University of Pristina, Kosovska Mitrovica, Serbia ABSTRACT Collembola fauna has been investigated at different microhabitats near the beach in Bečići, Montenegro. Samples were collected from four locations: Hotel “Tara”, “Sveti Toma” Church (St. Thomas), Hotel “Naftagas” and “Zelena Stena” (Green Rock). Each of the location presented different microhabitat: under the palm tree, cypresses tree, larch tree and white pine tree. Samples were taken in May and September 2015 and results presented as qualitative findings. Total number of 30 Collembola species was identified, classified into six families and 17 genera. Representatives of the family Hypogastruridae and Isotomidae were recorded at all of the studied sites, while representatives of the families: Naenuridae, Onychiuridae, Entomobryidae and Sminthuridae were present on some of locations. The biggest number of species and the highest Collembola population density was found at the Green Stone site, 24 species in total, microhabitat- white pine, and the smallest number of species, 6 on site “St. Thomas” Church, microhabitat- cypresses trees. Keywords: Collembola, microhabitats, Bečići Beach, Montenegro. 7 families. 28 species and subspecies are endemic for Serbia INTRODUCTION (12,02%) and 11 for Montenegro (12,36%). Most of the endemic and relict forms live in caves, but some of them inhabits forests Springtails (Insecta: Collembola) communities have been and cultivated steppe.