Butlletí 82 (2018)

Total Page:16

File Type:pdf, Size:1020Kb

Butlletí 82 (2018) 82 Butlletí de la Institució Catalana d’Història Natural 82 Barcelona 2018 Butlletí de la Institució Catalana d’HistòriaButlletí de la Institució Catalana Natural 2018 Butlletí de la Institució Catalana d’Història Natural, 82: 3-4. 2018 ISSN 2013-3987 (online edition): ISSN: 1133-6889 (print edition)3 nota BREU NOTA BREU Torymus sinensis Kamijo, 1982 (Hymenoptera, Torymidae) has arrived in Spain Torymus sinensis Kamijo, 1982 (Hymenoptera, Torymidae) ha arribat a Espanya Juan Luis Jara-Chiquito* & Juli Pujade-Villar* * Universitat de Barcelona. Facultat de Biologia. Departament de Biologia Evolutiva, Ecologia i Ciències Ambientals (Secció invertebrats). Diagonal, 643. 08028 Barcelona (Catalunya). A/e: [email protected], [email protected] Rebut: 25.11.2017. Acceptat: 12.12.2017. Publicat: 08.01.2018 a b Figure 1. SEM pictures of Torymus sinensis collected in Catalonia: (a) male antenna, (b) female habitus. Dryocosmus kuriphilus Yasumatsu, 1951 (Hym., Cynipi- untries took this initiative as well: France from 2011-2013 dae), an Oriental pest in chestnut (Castanea spp), was detect- (Borowiec et al., 2014), Croatia and Hungary in 2014-2015 ed for the first time in the Iberian Peninsula in 2012 (Pujade- (Matoševič et al., 2015) and Slovenia in 2015 (Matošević et Villar et al., 2013). It was introduced accidentally in Europe, al., 2015). Once released this species does not only occupy via Italy in 2002, according to (Brussino et al., 2002). the area of liberation but spreads into others due to its gre- Torymus sinensis Kamijo, 1982 (Fig. 1) is a parasitoid, nati- at mobility. There have been some test-releases in Spain and ve from China, and a specific species attackingD. kuriphilus. Portugal as well (Paparella et al., 2016). In the case of Spain, It has already been used in America and Oriental Palaearctic these tests were carried out in the South (Andalusia) and the successfully. In Europe, the first releases of this species took Northwest (Galicia and Asturias) of the country, according to place in Italy in 2005 (Quacchia et al., 2008) which also ser- Gerardo Sánchez Peña (pers. com., Biocastanea-2017).. ved as a testing ground. Among the many studies conducted Torymus sinensis has shown high dispersal ability, spre- in Italy with T. sinensis, Matošević et al. (2015) mention that ading over short distance by active flight and over long dis- after 6-7 years parasitism, this parasitoid reduced the popula- tance aided by wind, being able to cover more than 70 km in tions of D. kuriphilus to tolerable levels (infestation less than only a few days (Colombari & Battisti, 2015). In the northe- 30 %). Later, several years after releasing T. sinensis in Italy ast of the Iberian Peninsula, the locations where T. sinensis and probably pressured by tree economic losses, different co- were collected emerging (in 2016) from D. kuriphilus galls Butlletí ICHN 82, 2018 4 J. L. JARA-CHIQUITO & J. PUJADE-VILLAR NOTA BREU Bibliography BARTLETT, D. 2016. Viewpoint: Partnerships in action – Europe and beyond. Inpractice [Bulletin of the Chartered Institute of Ecology and Environmental Management. CIEEM (Chartered Institute of Ecology and Environmental Management)], 94: 13-15. BOROWIEC, N., THAON, M., BRANCACCIO, L., WAROT, S., VERCKEN, E., FAUVERGUE, X., RIS, N. & MALAUSA, J. C. 2014. Classical biological control against the chestnut gall wasp Dryocosmus kuriphilus (Hymenoptera, Cynipidae) in France. Plant Protection Quarterly, 29 (1): 7-10. BRUSSINO, G., BOSIO, G., BAUDINO, M., GIORDANO, R., RAMELLO, F. & MELIKA, G. 2002. Nuovo cinipide galligeno in Piemonte. Pericoloso insetto esotico per il castagno europeo. L’Informatore Agrario, 37: 59-61. COLOMBARI, F. & BATTISTI, A. 2015. Spread of the introduced biocontrol agent Torymus sinensis in north-eastern Italy: dispersal through active flight or assisted by wind?Biocontrol , 61: 127-139. MATOŠEVIĆ, D., LACKOVIČ, N., MELIKA, G., KOS, K., FRANIČ, I., KRISTON, E., BOZSO, M., SELJAK, G. & ROT, Figure 2. Distribution of Castanea sativa in Eastern Europe (obtained M. 2015. Biological control of invasive Dryocosmus kuriphilus from http://www.euforgen.org/fileadmin/templates/euforgen.org/upload/ with introduced parasitoid Torymus sinensis in Croatia, Slovenia Documents/Maps/JPG/Castanea_sativa.jpg) including the points of T. sinensis release in France (obtained from https://www6.inra.fr/cynips- and Hungary. Periodicum Biologorum, 117: 471-477. chataignier/Principaux-resultats) and the point where this parasitoid was MATOŠEVIĆ, D., LACKOVIČ, N., KOS, K., KRISTON, E., collected in Dryocosmus kuriphilus Catalonian galls. MELIKA, G., ROT, M. & PERNEK, M. 2017a. Success of classical biocontrol agent Torymus sinensis within its expanding range in Europe. Journal of Applied Entomology, 141 (9): 758-767. are: Olot (La Garrotxa, Girona): 12 ♀ 9 ♂; Celrà (El Gironès, DOI: https://doi.org/10.1111/jen.12388. Girona): 13 ♀ 5 ♂; and Montseny (La Selva, Girona): 5 ♀ MATOŠEVIĆ, D., MUJEZINOVIĆ, O. & DAUTBAŠIĆ, M. 2017b. First record of biocontrol agent Torymus sinensis 1 ♂. All these localities are around 300-400 km far from the (Hymenoptera; Torymidae) in Bosnia and Herzegovina. South- closest T. sinensis releasing sites in France (Fig. 2). Conside- east European forestry, 8 (2): 147-149. DOI: https://doi. ring the data mentioned above, they have had enough time to org/10.15177/seefor.17-14. reach the Catalan territory (4-7 years), so we have no doubt PAPARELLA F., FERRACINI C., PORTALURI A., MANZO A. that this has been the most possible way for T. sinensis to & ALMA, A. 2016. Biological control of the chestnut gall wasp reach Catalonia. We must also keep in mind that the border with T. sinensis: a mathematical model. Ecological Modelling, between Spain and France is a windy place where the heights 338: 17-36. of the mountains (via Girona near the sea) are by no means PUJADE-VILLAR, J., TORRELL, A. & ROJO, M. 2013. Primeres in any case a geographical barrier, while winds are strong troballes a la península Ibèrica de Dryocosmus kuriphilus (Hym., Cynipidae), una espècie de cinípid d’origen asiàtic altament and abundant in this mentioned area. We must also menti- perillosa per al castanyer (Fagaceae). Orsis, 27: 295-301. on that cinipids (and by extension Chalcidoidea) can travel QUACCHIA, A., MORIYA, S., BOSIO, G., SCAPIN, I. & ALMA, long distances thanks to air currents; Ros-Farré & Pujade-Vi- A. 2008. Rearing, release and settlement prospect in Italy of llar (1988) showed that Plagiotrochus amenti Kieffer, 1901 Torymus sinensis, the biological control agent of the chestnut gall (Hym.: Cynipidae) was displaced off in an annuity about 200 wasp Dryocosmus kuriphilus. BioControl, 53: 829-839. km. On the other hand, a nearly continuous distribution of C. ROS-FARRÉ, P. & PUJADE-VILLAR, J. 1998. Estudio mediante sativa with presence of D. kuriphilus favours the implantati- una trampa Malaise de la comunidad de cinípidos cecidógenos e on of T. sinensis in areas far from the liberation site (Fig. 2). inquilinos de Santa Coloma, Andorra (Hymenoptera, Cynipidae). In fact, the present populations of T. sinensis in Hungary are Ecología, 12: 441-454. due not only because of the releasing but also by the natural migrating of specimens from Italy (Matošević et al., 2017a). Records of T. sinensis in countries where no release has yet been made have already been mentioned in Switzerland in 2013, in England in 2015 (Bartlett, 2016), in Bosnia and Her- zegovina in 2016 (Matošević et al., 2017b) and now (since 2016) in Catalonia (Girona province). Acknowledgements We thank Dick Askew for sending us some specimens of Torymus sinensis to compare with our material. Butlletí ICHN 82, 2018 Butlletí de la Institució Catalana d’Història Natural, 82: 5-7. 2018 ISSN 2013-3987 (online edition): ISSN: 1133-6889 (print edition)5 nota BREU NOTA BREU Notes sobre plantes aŀlòctones al NE de Catalunya, amb especial atenció a males herbes dels arrossars Notes on alien plants in NE Catalonia, with special attention to weeds of rice fields Lluís Vilar*, Jordi Bou Manobens*, Josep Gesti* & Joan Font** * LAGP-Flora i Vegetació. Institut de Medi Ambient. Universitat de Girona. Campus Montilivi. 17003 Girona. ** Grup de Recerca en Biodiversitat. Ecologia, Tecnologia i Gestió Ambiental (BETA). Universitat de Vic - Universitat Central de Catalunya (UVIC-UCC). Campus Torre dels Frares. C/ de la Laura, 13. 08500 Vic. Autor per a la correspondència: [email protected] Rebut: 05.12.2017. Acceptat: 29.01.2018. Publicat: 28.02.2018 Es donen noves cites de plantes aŀlòctones rares o poc ci- 1989). Després es va anar enrarint i fins i tot es va donar tades a Catalunya. Alguns d’aquests tàxons s’han recoŀlectat per extingida en algunes d’aquestes localitats (Bolòs et al., en arrossars de l’Empordà i són plantes de les quals no es 1993), però des de fa uns anys s’ha tornat a expandir a Cata- tenia coneixement de la seva presència o bé no s’havien re- lunya (Álvarez et al., 2016; Batriu et al., 2012; Curcó, 2007), trobat en els darrers anys. a tota la península ibèrica i fins i tot a les Illes Balears (Sáez et al., 2011). Aquesta planta creix als marges dels arrossars, Diplachne fusca Roem. & Schult. subsp. uninervia (J. Presl) però també es fa a les vores dels embassaments, com el de P.M. Peterson & N. Snow [Leptochloa fusca subsp. uni­ Sau (Batriu et al., 2012), on aprofita els sòls fangosos humits nervia (J. Presl) N. Snow] que es formen a finals d’estiu, ja que és una espècie que flo- Alt Empordà: Castelló d’Empúries, arrossars a les closes de reix pel setembre i octubre. De l’Alt Empordà n’existeix un la Gallinera, EG0575, 3 m, 28-VII-2017, L. Vilar & J. Bou plec a l’herbari Vayreda de Figueres sense data i una cita de Casasayas (1989) a Sant Pere Pescador, però la planta no fou (HGI 23811). retrobada posteriorment (Gesti, 2006). Segons la revisió taxonòmica de Snow et al.
Recommended publications
  • Coleoptera, Carabidae) 517 Doi: 10.3897/Zookeys.100.1543 Research Article Launched to Accelerate Biodiversity Research
    A peer-reviewed open-access journal ZooKeys 100: 517–532What (2011)do we know about winter active ground beetles (Coleoptera, Carabidae) 517 doi: 10.3897/zookeys.100.1543 RESEARCH ARTICLE www.zookeys.org Launched to accelerate biodiversity research What do we know about winter active ground beetles (Coleoptera, Carabidae) in Central and Northern Europe? Radomir Jaskuła, Agnieszka Soszyńska-Maj Department of Invertebrate Zoology & Hydrobiology, University of Łódź, Banacha 12/16, 90-237 Łódź, Poland Corresponding authors: Radomir Jaskuła ([email protected]), Agnieszka Soszyńska-Maj ([email protected]) Academic editor: J. Noordijk | Received 26 November 2009 | Accepted 8 April 2010 | Published 20 May 2011 Citation: Jaskuła R, Soszyńska-Maj A (2011) What do we know about winter active ground beetles (Coleoptera, Carabidae) in Central and Northern Europe? In: Kotze DJ, Assmann T, Noordijk J, Turin H, Vermeulen R (Eds) Carabid Beetles as Bioindicators: Biogeographical, Ecological and Environmental Studies. ZooKeys 100: 517–532. doi: 10.3897/ zookeys.100.1543 Abstract This paper summarizes the current knowledge on winter active Carabidae in Central and Northern Eu- rope. In total 73 winter active species are listed, based on literature and own observations. Ground beetles are among the three most numerous Coleoptera families active during the autumn to spring period. The winter community of Carabidae is composed both of larvae (mainly autumn breeding species) and adults, as well as of epigeic species and those inhabiting tree trunks. Supranivean fauna is characterized by lower species diversity than the subnivean fauna. The activity of ground beetles decreases in late autumn, is lowest during mid-winter and increases in early spring.
    [Show full text]
  • The Lichens' Microbiota, Still a Mystery?
    fmicb-12-623839 March 24, 2021 Time: 15:25 # 1 REVIEW published: 30 March 2021 doi: 10.3389/fmicb.2021.623839 The Lichens’ Microbiota, Still a Mystery? Maria Grimm1*, Martin Grube2, Ulf Schiefelbein3, Daniela Zühlke1, Jörg Bernhardt1 and Katharina Riedel1 1 Institute of Microbiology, University Greifswald, Greifswald, Germany, 2 Institute of Plant Sciences, Karl-Franzens-University Graz, Graz, Austria, 3 Botanical Garden, University of Rostock, Rostock, Germany Lichens represent self-supporting symbioses, which occur in a wide range of terrestrial habitats and which contribute significantly to mineral cycling and energy flow at a global scale. Lichens usually grow much slower than higher plants. Nevertheless, lichens can contribute substantially to biomass production. This review focuses on the lichen symbiosis in general and especially on the model species Lobaria pulmonaria L. Hoffm., which is a large foliose lichen that occurs worldwide on tree trunks in undisturbed forests with long ecological continuity. In comparison to many other lichens, L. pulmonaria is less tolerant to desiccation and highly sensitive to air pollution. The name- giving mycobiont (belonging to the Ascomycota), provides a protective layer covering a layer of the green-algal photobiont (Dictyochloropsis reticulata) and interspersed cyanobacterial cell clusters (Nostoc spec.). Recently performed metaproteome analyses Edited by: confirm the partition of functions in lichen partnerships. The ample functional diversity Nathalie Connil, Université de Rouen, France of the mycobiont contrasts the predominant function of the photobiont in production Reviewed by: (and secretion) of energy-rich carbohydrates, and the cyanobiont’s contribution by Dirk Benndorf, nitrogen fixation. In addition, high throughput and state-of-the-art metagenomics and Otto von Guericke University community fingerprinting, metatranscriptomics, and MS-based metaproteomics identify Magdeburg, Germany Guilherme Lanzi Sassaki, the bacterial community present on L.
    [Show full text]
  • Megachile (Callomegachile) Sculpturalis Smith, 1853 (Apoidea: Megachilidae): a New Exotic Species in the Iberian Peninsula, and Some Notes About Its Biology
    Butlletí de la Institució Catalana d’Història Natural, 82: 157-162. 2018 ISSN 2013-3987 (online edition): ISSN: 1133-6889 (print edition)157 GEA, FLORA ET fauna GEA, FLORA ET FAUNA Megachile (Callomegachile) sculpturalis Smith, 1853 (Apoidea: Megachilidae): a new exotic species in the Iberian Peninsula, and some notes about its biology Oscar Aguado1, Carlos Hernández-Castellano2, Emili Bassols3, Marta Miralles4, David Navarro5, Constantí Stefanescu2,6 & Narcís Vicens7 1 Andrena Iniciativas y Estudios Medioambientales. 47007 Valladolid. Spain. 2 CREAF. 08193 Cerdanyola del Vallès. Spain. 3 Parc Natural de la Zona Volcànica de la Garrotxa. 17800 Olot. Spain. 4 Ajuntament de Sant Celoni. Bruc, 26. 08470 Sant Celoni. Spain. 5 Unitat de Botànica. Universitat Autònoma de Barcelona. 08193 Cerdanyola del Vallès. Spain. 6 Museu de Ciències Naturals de Granollers. 08402 Granollers. Spain. 7 Servei de Medi Ambient. Diputació de Girona. 17004 Girona. Spain. Corresponding author: Oscar Aguado. A/e: [email protected] Rebut: 20.09.2018; Acceptat: 26.09.2018; Publicat: 30.09.2018 Abstract The exotic bee Megachile sculpturalis has colonized the European continent in the last decade, including some Mediterranean countries such as France and Italy. In summer 2018 it was recorded for the first time in Spain, from several sites in Catalonia (NE Iberian Peninsula). Here we give details on these first records and provide data on its biology, particularly of nesting and floral resources, mating behaviour and interactions with other species. Key words: Hymenoptera, Megachilidae, Megachile sculpturalis, exotic species, biology, Iberian Peninsula. Resum Megachile (Callomegachile) sculpturalis Smith, 1853 (Apoidea: Megachilidae): una nova espècie exòtica a la península Ibèrica, amb notes sobre la seva biologia L’abella exòtica Megachile sculpturalis ha colonitzat el continent europeu en l’última dècada, incloent alguns països mediterranis com França i Itàlia.
    [Show full text]
  • An Annotated Checklist of Wisconsin Scarabaeoidea (Coleoptera)
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida March 2002 An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera) Nadine A. Kriska University of Wisconsin-Madison, Madison, WI Daniel K. Young University of Wisconsin-Madison, Madison, WI Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons Kriska, Nadine A. and Young, Daniel K., "An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera)" (2002). Insecta Mundi. 537. https://digitalcommons.unl.edu/insectamundi/537 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, Vol. 16, No. 1-3, March-September, 2002 3 1 An annotated checklist of Wisconsin Scarabaeoidea (Coleoptera) Nadine L. Kriska and Daniel K. Young Department of Entomology 445 Russell Labs University of Wisconsin-Madison Madison, WI 53706 Abstract. A survey of Wisconsin Scarabaeoidea (Coleoptera) conducted from literature searches, collection inventories, and three years of field work (1997-1999), yielded 177 species representing nine families, two of which, Ochodaeidae and Ceratocanthidae, represent new state family records. Fifty-six species (32% of the Wisconsin fauna) represent new state species records, having not previously been recorded from the state. Literature and collection distributional records suggest the potential for at least 33 additional species to occur in Wisconsin. Introduction however, most of Wisconsin's scarabaeoid species diversity, life histories, and distributions were vir- The superfamily Scarabaeoidea is a large, di- tually unknown.
    [Show full text]
  • New Or Interesting Lichens and Lichenicolous Fungi from Belgium, Luxembourg and Northern France
    New or interesting lichens and lichenicolous fungi from Belgium, Luxembourg and northern France. X Emmanuël SÉRUSIAUX1, Paul DIEDERICH2, Damien ERTZ3, Maarten BRAND4 & Pieter VAN DEN BOOM5 1 Plant Taxonomy and Conservation Biology Unit, University of Liège, Sart Tilman B22, B-4000 Liège, Belgique ([email protected]) 2 Musée national d’histoire naturelle, 25 rue Munster, L-2160 Luxembourg, Luxembourg ([email protected]) 3 Jardin Botanique National de Belgique, Domaine de Bouchout, B-1860 Meise, Belgium ([email protected]) 4 Klipperwerf 5, NL-2317 DX Leiden, the Netherlands ([email protected]) 5 Arafura 16, NL-5691 JA Son, the Netherlands ([email protected]) Sérusiaux, E., P. Diederich, D. Ertz, M. Brand & P. van den Boom, 2006. New or interesting lichens and lichenicolous fungi from Belgium, Luxembourg and northern France. X. Bul- letin de la Société des naturalistes luxembourgeois 107 : 63-74. Abstract. Review of recent literature and studies on large and mainly recent collections of lichens and lichenicolous fungi led to the addition of 35 taxa to the flora of Belgium, Lux- embourg and northern France: Abrothallus buellianus, Absconditella delutula, Acarospora glaucocarpa var. conspersa, Anema nummularium, Anisomeridium ranunculosporum, Artho- nia epiphyscia, A. punctella, Bacidia adastra, Brodoa atrofusca, Caloplaca britannica, Cer- cidospora macrospora, Chaenotheca laevigata, Collemopsidium foveolatum, C. sublitorale, Coppinsia minutissima, Cyphelium inquinans, Involucropyrenium squamulosum, Lecania fructigena, Lecanora conferta, L. pannonica, L. xanthostoma, Lecidea variegatula, Mica- rea micrococca, Micarea subviridescens, M. vulpinaris, Opegrapha prosodea, Parmotrema stuppeum, Placynthium stenophyllum var. isidiatum, Porpidia striata, Pyrenidium actinellum, Thelopsis rubella, Toninia physaroides, Tremella coppinsii, Tubeufia heterodermiae, Verru- caria acrotella and Vezdaea stipitata.
    [Show full text]
  • Taxonomic Notes and Type Designations of Gall Inducing Cynipid Wasps Described by G.Mayr (Insecta: Hymenoptera: Cynipidae)
    ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Annalen des Naturhistorischen Museums in Wien Jahr/Year: 2001 Band/Volume: 103B Autor(en)/Author(s): Bechtold M., Melika George Artikel/Article: Taxonomic notes and type designations of gall inducing cynipid wasps described by G.Mayr (Insecta: Hymenoptera: Cynipidae). 327-339 ©Naturhistorisches Museum Wien, download unter www.biologiezentrum.at Ann. Naturhist. Mus. Wien 103 B 327 - 339 Wien, Dezember 2001 Taxonomic notes and type designations of gall inducing cynipid wasps described by G. Mayr (Insecta: Hymenoptera: Cynipidae) G. Melika & M. Bechtold* Abstract Lectotypes for twelve of Mayr's cynipid gall wasp species (Hymenoptera: Cynipidae: Cynipinae) are desi- gnated. From twenty cynipid gall wasp species, described by Mayr, seven have already been synonymized, and thirteen species are still valid. Andricus insana (WESTWOOD, 1837) syn.n. is a new synonym of Andricus quercustozae (Bosc, 1792). Key words: Cynipidae, gall wasps, Hymenoptera, lectotype designation, Gustav Mayr, new synonymy, taxonomy. Zusammenfassung Lectotypen für zwölf der von Mayr beschriebenen Gallwespenarten (Hymenoptera: Cynipidae: Cynipinae) werden designiert. Mayr hat zwanzig Gallwespenarten beschrieben, davon sind sieben bereits synonymi- siert worden, dreizehn Arten sind noch gültig. Andricus insana (WESTWOOD, 1837) syn.n. ist ein neues Synonym von Andricus quercustozae (Bosc, 1792). Introduction Gustav Mayr, a famous Austrian entomologist, described eleven genera of gall inducing Cynipidae and twenty species from twelve genera (Hymenoptera: Cynipoidea). Seven of them have already been synonymized, while thirteen species are still valid. However, he never designated types for his newly described species. All the specimens are syn- or cotypes and usually these specimens were marked with "Type" or even not so.
    [Show full text]
  • The Beetle Fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and Distribution
    INSECTA MUNDI, Vol. 20, No. 3-4, September-December, 2006 165 The beetle fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and distribution Stewart B. Peck Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada stewart_peck@carleton. ca Abstract. The beetle fauna of the island of Dominica is summarized. It is presently known to contain 269 genera, and 361 species (in 42 families), of which 347 are named at a species level. Of these, 62 species are endemic to the island. The other naturally occurring species number 262, and another 23 species are of such wide distribution that they have probably been accidentally introduced and distributed, at least in part, by human activities. Undoubtedly, the actual numbers of species on Dominica are many times higher than now reported. This highlights the poor level of knowledge of the beetles of Dominica and the Lesser Antilles in general. Of the species known to occur elsewhere, the largest numbers are shared with neighboring Guadeloupe (201), and then with South America (126), Puerto Rico (113), Cuba (107), and Mexico-Central America (108). The Antillean island chain probably represents the main avenue of natural overwater dispersal via intermediate stepping-stone islands. The distributional patterns of the species shared with Dominica and elsewhere in the Caribbean suggest stages in a dynamic taxon cycle of species origin, range expansion, distribution contraction, and re-speciation. Introduction windward (eastern) side (with an average of 250 mm of rain annually). Rainfall is heavy and varies season- The islands of the West Indies are increasingly ally, with the dry season from mid-January to mid- recognized as a hotspot for species biodiversity June and the rainy season from mid-June to mid- (Myers et al.
    [Show full text]
  • Decline of Six Native Mason Bee Species Following the Arrival of an Exotic Congener Kathryn A
    www.nature.com/scientificreports OPEN Decline of six native mason bee species following the arrival of an exotic congener Kathryn A. LeCroy1*, Grace Savoy‑Burke2, David E. Carr1, Deborah A. Delaney2 & T’ai H. Roulston1 A potential driver of pollinator declines that has been hypothesized but seldom documented is the introduction of exotic pollinator species. International trade often involves movement of many insect pollinators, especially bees, beyond their natural range. For agricultural purposes or by inadvertent cargo shipment, bee species successfully establishing in new ranges could compete with native bees for food and nesting resources. In the Mid‑Atlantic United States, two Asian species of mason bee (Osmia taurus and O. cornifrons) have become recently established. Using pan‑trap records from the Mid‑Atlantic US, we examined catch abundance of two exotic and six native Osmia species over the span of ffteen years (2003–2017) to estimate abundance changes. All native species showed substantial annual declines, resulting in cumulative catch losses ranging 76–91% since 2003. Exotic species fared much better, with O. cornifrons stable and O. taurus increasing by 800% since 2003. We characterize the areas of niche overlap that may lead to competition between native and exotic species of Osmia, and we discuss how disease spillover and enemy release in this system may result in the patterns we document. International trade creates opportunities for plant and animal species to be intentionally or inadvertently intro- duced into novel ecosystems where they may interact with native species. One outcome of species introductions is the potential for competitive interactions with native species, especially those that are most closely related to the introduced species.
    [Show full text]
  • Old Woman Creek National Estuarine Research Reserve Management Plan 2011-2016
    Old Woman Creek National Estuarine Research Reserve Management Plan 2011-2016 April 1981 Revised, May 1982 2nd revision, April 1983 3rd revision, December 1999 4th revision, May 2011 Prepared for U.S. Department of Commerce Ohio Department of Natural Resources National Oceanic and Atmospheric Administration Division of Wildlife Office of Ocean and Coastal Resource Management 2045 Morse Road, Bldg. G Estuarine Reserves Division Columbus, Ohio 1305 East West Highway 43229-6693 Silver Spring, MD 20910 This management plan has been developed in accordance with NOAA regulations, including all provisions for public involvement. It is consistent with the congressional intent of Section 315 of the Coastal Zone Management Act of 1972, as amended, and the provisions of the Ohio Coastal Management Program. OWC NERR Management Plan, 2011 - 2016 Acknowledgements This management plan was prepared by the staff and Advisory Council of the Old Woman Creek National Estuarine Research Reserve (OWC NERR), in collaboration with the Ohio Department of Natural Resources-Division of Wildlife. Participants in the planning process included: Manager, Frank Lopez; Research Coordinator, Dr. David Klarer; Coastal Training Program Coordinator, Heather Elmer; Education Coordinator, Ann Keefe; Education Specialist Phoebe Van Zoest; and Office Assistant, Gloria Pasterak. Other Reserve staff including Dick Boyer and Marje Bernhardt contributed their expertise to numerous planning meetings. The Reserve is grateful for the input and recommendations provided by members of the Old Woman Creek NERR Advisory Council. The Reserve is appreciative of the review, guidance, and council of Division of Wildlife Executive Administrator Dave Scott and the mapping expertise of Keith Lott and the late Steve Barry.
    [Show full text]
  • The Population Biology of Oak Gall Wasps (Hymenoptera:Cynipidae)
    5 Nov 2001 10:11 AR AR147-21.tex AR147-21.SGM ARv2(2001/05/10) P1: GSR Annu. Rev. Entomol. 2002. 47:633–68 Copyright c 2002 by Annual Reviews. All rights reserved THE POPULATION BIOLOGY OF OAK GALL WASPS (HYMENOPTERA:CYNIPIDAE) Graham N. Stone,1 Karsten Schonrogge,¨ 2 Rachel J. Atkinson,3 David Bellido,4 and Juli Pujade-Villar4 1Institute of Cell, Animal, and Population Biology, University of Edinburgh, The King’s Buildings, West Mains Road, Edinburgh EH9 3JT, United Kingdom; e-mail: [email protected] 2Center of Ecology and Hydrology, CEH Dorset, Winfrith Technology Center, Winfrith Newburgh, Dorchester, Dorset DT2 8ZD, United Kingdom; e-mail: [email protected] 3Center for Conservation Science, Department of Biology, University of Stirling, Stirling FK9 4LA, United Kingdom; e-mail: [email protected] 4Departamento de Biologia Animal, Facultat de Biologia, Universitat de Barcelona, Avenida Diagonal 645, 08028 Barcelona, Spain; e-mail: [email protected] Key Words cyclical parthenogenesis, host alternation, food web, parasitoid, population dynamics ■ Abstract Oak gall wasps (Hymenoptera: Cynipidae, Cynipini) are characterized by possession of complex cyclically parthenogenetic life cycles and the ability to induce a wide diversity of highly complex species- and generation-specific galls on oaks and other Fagaceae. The galls support species-rich, closed communities of inquilines and parasitoids that have become a model system in community ecology. We review recent advances in the ecology of oak cynipids, with particular emphasis on life cycle characteristics and the dynamics of the interactions between host plants, gall wasps, and natural enemies. We assess the importance of gall traits in structuring oak cynipid communities and summarize the evidence for bottom-up and top-down effects across trophic levels.
    [Show full text]
  • Domenico Puntillo & Sonia Ravera Naetrocymbe Mori
    Fl. Medit. 23: 5-9 doi: 10.7320/FlMedit23.005 Version of Record published online on 30 December 2013 Domenico Puntillo & Sonia Ravera Naetrocymbe mori-albae, a new species from Calabria (Southern Italy) Abstract Puntillo, D. & Ravera S.: Naetrocymbe mori-albae, a new species from Calabria (Southern Italy). — Fl. Medit. 23: 5-9. 2013. — ISSN: 1120-4052 printed, 2240-4538 online. The new taxon belongs to the group Arthopyrenia rhyponta-A. punctiformis, recently trans- ferred to the problematic genus Naetrocymbe Korb. (Naetrocymbaceae Höhn. ex R.C. Harris), as it is a non or weakly lichenized group. This species is characterized by tadpole-shaped 1-sep- tate ascospores with a conical lower cell and perithecia which are 4-8 linearly arranged. Key words: Naetrocymbe, Lichenes, Italy. Introduction Naetrocymbe is a genus of pyrenocarpous ascomycetes belonging to the family Naetrocymbaceae establish by Harris (1995). This family includes species usually not lichen-forming and characterized by short-celled paraphyses with refractive bodies near the septa, obpyriform asci with a distinctive apical region lacking a nasse and short rod- shaped microconidia. It has a mainly temperate/boreal distribution. Because of some Naetrocymbe species can be lichenized (Keissler 1938; Knudsen & Lendemer 2009; Roux 2009), Aptroot (1998, 2002), Coppins (2002) and Coppins & Orange (2009) consider unnecessary a separation between Naetrocymbe and Arthopyrenia. They disagree with Harris (1973, 1975, 1995), Tucker & Harris (1980) and Coppins (1988), about the impor- tance of the hamathecial tissues as valuable character. In Aptroot’s opinion, the cosmopol- itan genus Arthopyrenia s.l. should be considered in its original wide concept: character- ized by branched pseudoparaphyses, which may disappear, and sole-shaped ascospores.
    [Show full text]
  • Mycosphere Notes 225–274: Types and Other Specimens of Some Genera of Ascomycota
    Mycosphere 9(4): 647–754 (2018) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/9/4/3 Copyright © Guizhou Academy of Agricultural Sciences Mycosphere Notes 225–274: types and other specimens of some genera of Ascomycota Doilom M1,2,3, Hyde KD2,3,6, Phookamsak R1,2,3, Dai DQ4,, Tang LZ4,14, Hongsanan S5, Chomnunti P6, Boonmee S6, Dayarathne MC6, Li WJ6, Thambugala KM6, Perera RH 6, Daranagama DA6,13, Norphanphoun C6, Konta S6, Dong W6,7, Ertz D8,9, Phillips AJL10, McKenzie EHC11, Vinit K6,7, Ariyawansa HA12, Jones EBG7, Mortimer PE2, Xu JC2,3, Promputtha I1 1 Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand 2 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, 132 Lanhei Road, Kunming 650201, China 3 World Agro Forestry Centre, East and Central Asia, 132 Lanhei Road, Kunming 650201, Yunnan Province, People’s Republic of China 4 Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biological Resource and Food Engineering, Qujing Normal University, Qujing, Yunnan 655011, China 5 Shenzhen Key Laboratory of Microbial Genetic Engineering, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China 6 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 7 Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, Thailand 8 Department Research (BT), Botanic Garden Meise, Nieuwelaan 38, BE-1860 Meise, Belgium 9 Direction Générale de l'Enseignement non obligatoire et de la Recherche scientifique, Fédération Wallonie-Bruxelles, Rue A.
    [Show full text]