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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). -
Biodiversidad De Collembola (Hexapoda: Entognatha) En México
Revista Mexicana de Biodiversidad, Supl. 85: S220-S231, 2014 220 Palacios-Vargas.- BiodiversidadDOI: 10.7550/rmb.32713 de Collembola Biodiversidad de Collembola (Hexapoda: Entognatha) en México Biodiversity of Collembola (Hexapoda: Entognatha) in Mexico José G. Palacios-Vargas Laboratorio de Ecología y Sistemática de Microartrópodos, Departamento de Ecología y Recursos Naturales, Facultad de Ciencias, Universidad Nacional Autónoma de México, Circuito exterior s/n, Cd. Universitaria, 04510 México, D. F. [email protected] Resumen. Se hace una breve evaluación de la importancia del grupo en los distintos ecosistemas. Se describen los caracteres morfológicos más distintivos, así como los biotopos donde se encuentran y su tipo de alimentación. Se hace una evaluación de la biodiversidad, encontrando que existen citados más de 700 taxa, muchos de ellos a nivel genérico, de 24 familias. Se discute su distribución geográfica por provincias biogeográficas, así como la diversidad de cada estado. Se presentan cuadros con la clasificación ecológica con ejemplos mexicanos; se indican las familias y su riqueza a nivel mundial y nacional, así como la curva acumulativa de especies mexicanas por quinquenio. Palabras clave: Collembola, biodiversidad, distribución, ecología, acumulación de especies. Abstract. A brief assessment of the importance of the group in different ecosystems is done. A description of the most distinctive morphological characters, as well as biotopes where they live is included. An evaluation of their biodiversity is presented; finding that more than 700 taxa have been cited, many of them at the generic level, in 24 families. Their geographical distribution is discussed and the state richness is pointed out. Tables of ecological classification applied to Mexican species are given. -
Redalyc.Biodiversidad De Collembola (Hexapoda: Entognatha) En México
Revista Mexicana de Biodiversidad ISSN: 1870-3453 [email protected] Universidad Nacional Autónoma de México México Palacios-Vargas, José G. Biodiversidad de Collembola (Hexapoda: Entognatha) en México Revista Mexicana de Biodiversidad, vol. 85, 2014, pp. 220-231 Universidad Nacional Autónoma de México Distrito Federal, México Disponible en: http://www.redalyc.org/articulo.oa?id=42529679040 Cómo citar el artículo Número completo Sistema de Información Científica Más información del artículo Red de Revistas Científicas de América Latina, el Caribe, España y Portugal Página de la revista en redalyc.org Proyecto académico sin fines de lucro, desarrollado bajo la iniciativa de acceso abierto Revista Mexicana de Biodiversidad, Supl. 85: S220-S231, 2014 220 Palacios-Vargas.- BiodiversidadDOI: 10.7550/rmb.32713 de Collembola Biodiversidad de Collembola (Hexapoda: Entognatha) en México Biodiversity of Collembola (Hexapoda: Entognatha) in Mexico José G. Palacios-Vargas Laboratorio de Ecología y Sistemática de Microartrópodos, Departamento de Ecología y Recursos Naturales, Facultad de Ciencias, Universidad Nacional Autónoma de México, Circuito exterior s/n, Cd. Universitaria, 04510 México, D. F. [email protected] Resumen. Se hace una breve evaluación de la importancia del grupo en los distintos ecosistemas. Se describen los caracteres morfológicos más distintivos, así como los biotopos donde se encuentran y su tipo de alimentación. Se hace una evaluación de la biodiversidad, encontrando que existen citados más de 700 taxa, muchos de ellos a nivel genérico, de 24 familias. Se discute su distribución geográfica por provincias biogeográficas, así como la diversidad de cada estado. Se presentan cuadros con la clasificación ecológica con ejemplos mexicanos; se indican las familias y su riqueza a nivel mundial y nacional, así como la curva acumulativa de especies mexicanas por quinquenio. -
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). -
(Collembola) in Meadows, Pastures and Road Verges in Central Finland
© Entomologica Fennica. 29 August 2017 Springtails (Collembola) in meadows, pastures and road verges in Central Finland Atte Komonen* & Saana Kataja-aho Komonen, A. & Kataja-aho, S. 2017: Springtails (Collembola) in meadows, pas- tures and road verges in Central Finland. — Entomol. Fennica 28: 157–163. Understanding of species distribution, abundance and habitat affinities is crucial for red-list assessment, conservation and habitat management. In Central Fin- land, we studied Collembola in three habitat types, namely non-grazed meadows, pastures and road verges using pitfall traps. Altogether, 9,630 Collembola indi- viduals were recorded. These belonged to 12 families, 34 genera and 60 species. The number of specimens was clearly higher in meadows than in pastures or road verges. The number of species, however, was higher in meadows and road verges (40 and 39 species, respectively) than in pastures (33 species). The overall spe- cies number is comparable to other large-scale sampling schemes in similar habi- tats. We recorded a few abundant species (Spatulosminthurus flaviceps, Smin- thurus viridis and Sminthurus nigromaculatus) that have been previously re- corded from very different biotopes. In conclusion, biodiversity inventories of soil fauna, as well as other biota, should also include marginal habitats, which of- ten host peculiar communities. A. Komonen, University of Jyväskylä, Department of Biological and Environ- mental Science, P.O. Box 35, FI-40014 University of Jyväskylä, Finland; *Cor- responding author’s e-mail: [email protected] S. Kataja-aho, University of Jyväskylä, Natural History Museum, P.O. Box 35, FI-40014 University of Jyväskylä, Finland; E-mail: [email protected] Received 15 November 2016, accepted 22 December 2016 1. -
First Survey of Collembola (Hexapoda: Entognatha) Fauna in Soil of Archipelago Fernando De Noronha, Brazil Estevam C
First survey of Collembola (Hexapoda: Entognatha) fauna in soil of Archipelago Fernando de Noronha, Brazil Estevam C. Araujo De Lima1, * and Douglas Zeppelini1,2, Collembola (Hexapoda: Entognatha) is one of the most abundant Table 1. Collembola recorded on the Fernando de Noronha archipelago, Brazil. and widely distributed taxa among terrestrial Hexapoda (Hopkin 1997). Collection localites were: a sandy beach (SB), soil on the slope of a cliff (SC) and the Soil in the forest at the hilltop (SF). World distribution was summarized for Collembola specimens are found in almost all habitats, excluding each species as follows: Boreal (Bor) include regions 1–8, Neotropical (Neo) re- aquatic environments below the surface firm where their occurrence is gions 24–30, South African (Saf) region 31, Paleotropical (Pal) regions 9–23, Aus- rare or accidental. The greatest diversity and abundance of these spe- tralian (Aus) regions 32–34, and Antarctic (Ant) regions 35–37. Species distributed cies occurs in soil and in adjacent microhabitats, especially where there in at least, in 4 of the major regions (Neo, Pal, etc.) are considered to be cosmo- is much organic matter (Zeppelini et al. 2008). The potential value of politan (Cos). Species distribution restricted to Northeast and Central Brazil (NCB), restricted to Fernando de Noronha (RFN) and doubtful distribution Record (?). Collembola as biological indicators of soil health and ecosystem quality is increasingly recognized and therefore knowledge of the diversity of Localities Collembola becomes useful in the development of conservation strate- World gies and environmental monitoring (Stork & Eggleton 1992; Zeppelini Taxa SB SC SF distribution et al. -
New Records of Springtail Fauna (Hexapoda: Collembola: Entomobryomorpha) from Ordu Province in Turkey
Turkish Journal of Zoology Turk J Zool (2017) 41: 24-32 http://journals.tubitak.gov.tr/zoology/ © TÜBİTAK Research Article doi:10.3906/zoo-1509-28 New records of springtail fauna (Hexapoda: Collembola: Entomobryomorpha) from Ordu Province in Turkey 1 2, 3 Muhammet Ali ÖZATA , Hasan SEVGİLİ *, Igor J. KAPRUS 1 Demir Karamancı Anatolian High School, Melikgazi, Kayseri, Turkey 2 Department of Biology, Faculty of Arts and Sciences, Ordu University, Ordu, Turkey 3 State Museum of Natural History, Ukrainian National Academy of Sciences, L’viv, Ukraine Received: 14.09.2015 Accepted/Published Online: 27.04.2016 Final Version: 25.01.2017 Abstract: This study aims to elucidate the Collembola fauna of the province of Ordu, which is situated between the Middle and Eastern Black Sea regions of Turkey. Although a large number of Collembolan specimens had been collected, only Entomobryomorpha species were given emphasis. From 44 different sampled localities of the province of Ordu, we recorded 6 families, 14 genera, and 28 species. Six of these species were previously recorded and 20 of them are new records for Turkey. The results were not surprising, considering that the sampled region had not been studied previously, quite like many habitats in Turkey. With our 20 new records (Entomobryomorpha), the grand total of the springtail fauna of Turkey is increased to 73 species. This represents an increase of almost 40% of the current list of known species. These numbers show us that the diversity of Collembola in Turkey is not thoroughly known and it is clear that numerous species remain undiscovered or undescribed. -
Two High-Quality De Novo Genomes from Single Ethanol-Preserved Specimens of Tiny Metazoans
GigaScience, 10, 2021, 1–12 doi: 10.1093/gigascience/giab035 Data Note DATA NOTE Downloaded from https://academic.oup.com/gigascience/article/10/5/giab035/6279595 by guest on 29 September 2021 Two high-quality de novo genomes from single ethanol-preserved specimens of tiny metazoans (Collembola) Clement´ Schneider 1,2,*, Christian Woehle 3,CarolaGreve 1, Cyrille A. D’Haese 4, Magnus Wolf 1,5,6, Michael Hiller 1,6,7,AxelJanke 1,5,6, † † Miklos´ Balint´ 1,5, and Bruno Huettel 3, 1LOEWE Centre for Translational Biodiversity Genomics (LOEWE-TBG), Senckenberganlage 25, 60325 Frankfurt am Main, Germany; 2Senckenberg Gesellschaft fur¨ Naturforschung, Abteilung Bodenzoologie, Am Museum 1, 02826 Gorlitz,¨ Germany; 3Max Planck Institute for Plant Breeding Research, Max Planck Genome-centre Cologne, Carl-von-Linne-Weg´ 10, 50829 Cologne, Germany; 4UniteM´ ecanismes´ adaptatifs & Evolution (MECADEV), CNRS, Museum´ national d’Histoire naturelle, 45 rue Buffon 75005 Paris, France; 5Senckenberg Biodiversity and Climate Research Centre, Senckenberganlage 25, 60325 Frankfurt am Main, Germany; 6Goethe University, Max-von-Laue-Str. 9, 60438 Frankfurt am Main, Germany and 7Senckenberg Research Institute, Senckenberganlage 25, 60325 Frankfurt, Germany ∗Correspondence address. Clement´ Schneider, LOEWE Centre for Translational Biodiversity Genomics (LOEWE-TBG), Senckenberganlage 25, 60325 Frankfurt am Main, Germany. Email: [email protected] http://orcid.org/0000-0003-3743-9319 †These authors contributed equally to the manuscript. Abstract Background: Genome sequencing of all known eukaryotes on Earth promises unprecedented advances in biological sciences and in biodiversity-related applied fields such as environmental management and natural product research. Advances in long-read DNA sequencing make it feasible to generate high-quality genomes for many non–genetic model species. -
A Synthesis of the Antarctic Springtail Phylogeographic Record
Insects 2011, 2, 62-82; doi:10.3390/insects2020062 OPEN ACCESS insects ISSN 2075-4450 www.mdpi.com/journal/insects/ Review Extreme Glacial Legacies: A Synthesis of the Antarctic Springtail Phylogeographic Record Angela McGaughran 1, Mark I. Stevens 2,*, Ian D. Hogg 3 and Antonio Carapelli 4 1 Max Planck Institute for Developmental Biology, Department for Evolutionary Biology, Spemannstr. 37-39/IV, Tübingen, D-72076, Germany; E-Mail: [email protected] 2 South Australian Museum, and School of Earth and Environmental Sciences, University of Adelaide, SA 5000, Adelaide, Australia 3 Centre for Biodiversity and Ecology Research, University of Waikato, Hamilton, New Zealand; E-Mail: [email protected] 4 Department of Evolutionary Biology, University of Siena, via A. Moro 2, 53100, Siena, Italy; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +61-8-8207-7685; Fax: +61-8-8207-7222. Received: 23 December 2010; in revised form: 15 February 2011 / Accepted: 2 April 2011 / Published: 6 April 2011 Abstract: We review current phylogeographic knowledge from across the Antarctic terrestrial landscape with a focus on springtail taxa. We describe consistent patterns of high genetic diversity and structure among populations which have persisted in glacial refugia across Antarctica over both short (<2 Mya) and long (>10 Mya) timescales. Despite a general concordance of results among species, we explain why location is important in determining population genetic patterns within bioregions. We complete our review by drawing attention to the main limitations in the field of Antarctic phylogeography, namely that the scope of geographic focus is often lacking within studies, and that large gaps remain in our phylogeographic knowledge for most terrestrial groups. -
A New Member of the Genus Isotomurus from the Kuril Islands (Collembola: Isotomidae): Returning to the Problem of ``Colour Patte
A new member of the genus Isotomurus from the Kuril Islands (Collembola: Isotomidae): returning to the problem of “colour pattern species” Mikhail Potapov, David Porco, Louis Deharveng To cite this version: Mikhail Potapov, David Porco, Louis Deharveng. A new member of the genus Isotomurus from the Kuril Islands (Collembola: Isotomidae): returning to the problem of “colour pattern species”. Zootaxa, Magnolia Press, 2018, 4394 (3), pp.383-394. 10.11646/zootaxa.4394.3.4. hal-01835310 HAL Id: hal-01835310 https://hal.sorbonne-universite.fr/hal-01835310 Submitted on 11 Jul 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. A new member of the genus Isotomurus from the Kuril Islands (Collembola: Isotomidae): returning to the problem of “colour pattern species” MIKHAIL POTAPOV1,4, DAVID PORCO2 & LOUIS DEHARVENG3 1Moscow State Pedagogical University, Kibalchicha str., 6, korp. 3, Moscow, 129278, Russia. 2Musée national d’histoire naturelle, 25 rue Munster, 2160 Luxembourg, Luxembourg. E-mail: [email protected] 3Institut de Systématique, Evolution, Biodiversité (ISYEB) UMR 7205 CNRS, MNHN, UPMC, EPHE, Museum national d'Histoire naturelle, Sorbonne Universités, 45 rue Buffon, CP50, F75005 Paris, France. E-mail: [email protected] 4Corresponding author. -
Diversity of Springtails (Hexapoda) According to a Altitudinal Gradient
Diversity of springtails (Hexapoda) according to a altitudinal gradient Arturo García-Gómez (1) , Gabriela Castaño-Meneses (1,2) and José G. Palacios-Vargas (1 ) (1) Universidad Nacional Autónoma de México (UNAM), Ecología y Sistemática de Microartrópodos, Departamento de Ecología y Recursos Naturales, Facultad de Ciencias, Ciudad Universitaria, 04510 México, D. F. E-mail: [email protected]; [email protected] (2) UNAM, Unidad Multidisciplinaria de Docencia e Investigación, Facultad de Ciencias, Campus Juriquilla, Boulevard Juriquilla, 3001, C.P. 76230, Querétaro, Querétaro, México. E-mail: [email protected] Abstract – The objective of this work was to elevate gradient effect on diversity of Collembola, in a temperate forest on the northeast slope of Iztaccíhuatl Volcano, Mexico. Four expeditions were organized from November 2003 to August 2004, at four altitudes (2,753, 3,015, 3,250 and 3,687 m a.s.l.). In each site, air temperature, CO 2 concentration, humidity, and terrain inclination were measured. The infl uence of abiotic factors on faunal composition was evaluated, at the four collecting sites, with canonical correspondence analyses (CCA). A total of 24,028 specimens were obtained, representing 12 families, 44 genera and 76 species. Mesaphorura phlorae , Proisotoma ca. tenella and Parisotoma ca. notabilis were the most abundant species. The highest diversity and evenness were recorded at 3,250 m (H’ = 2.85; J’ = 0.73). Canonical analyses axes 1 and 2 of the CCA explained 67.4% of the variance in species composition, with CO 2 and altitude best explaining axis 1, while slope and humidity were better correlated to axis 2. -
Invertebrate Monitoring As Measure of Ecosystem Change Mélissa Jane
Invertebrate monitoring as measure of ecosystem change Mélissa Jane Houghton B. Arts and Sciences M. Environmental Management A thesis submitted for the degree of Doctor of Philosophy at The University of Queensland in 2020 School of Biological Sciences Centre for Biodiversity and Conservation Science Abstract Islands and their biodiversity have high conservation value globally. Non-native species are largely responsible for island extinctions and island ecosystem disruption and are one of the major drivers of global biodiversity loss. Developing tools to effectively measure and understand island ecosystem change is therefore vital to future island conservation management, specifically island communities and the threatened species within them. One increasing utilised island conservation management tool is invasive mammal eradication. Such programs are increasing in number and success, with high biodiversity gains. Typically, it is assumed that the removal of target non-native species equates to management success and in some instances, recovery of a key threatened or charismatic species affected by the pest species are monitored. Yet to date, there are few published studies quantifying post- eradication ecosystem responses. Such monitoring helps to calculate return-on-investment, understand the conservation benefits of management and inform conservation decision- making associated with current and future restoration programs. Not only are there few studies providing empirical evidence of whole-of-ecosystem recovery following mammal eradications,