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opencc-by-4.0Dec 2020View details →

Data sets comparing Ca(2+) dynamics in whole-cell and β-escin-based perforated patch clamp recordings in adult mouse brain slices.

# Hess-et-al-beta-escin-2020 Data of the "Data in Brief" article concerning the added buffer approach with beta-escin perforated patch. A joint work by: Simon Hess (`simon.hess@uni-koeln.de`), Christophe Pouzat (`christophe.pouzat@math.unistra.fr`), and Peter Kloppenburg (`peter.kloppenburg@uni-koeln.de`). ## Content This repository contains: - Directory `data_whole_cell` contains the experimental data in [HDF5](https://en.wikipedia.org/wiki/Hierarchical_Data_Format) format. The data contains recordings of _Substantia nigra_ dopaminergic neurons recorded in the whole-cell configuration. - Directory `data_beta_escin` contains the experimental data in [HDF5](https://en.wikipedia.org/wiki/Hierarchical_Data_Format) format. The data contains recordings of _Substantia nigra_ dopaminergic neurons recorded in the β-escin perforated patch clamp configuration.

opencc-zeroJan 2022View details →

Community patch‐dynamics governs direct and indirect nutrient recycling by aggregated animals across spatial scales

Animals can have pervasive effects on ecosystems as they modify their biogeochemical and physical environments. In particular, when animals occur in high densities these effects can result in dramatic changes in the physical environment and biogeochemical hotspots or hot moments. While most research to date has focused on the direct role of animals in biogeochemical cycles, few have examined how animals indirectly influence biogeochemical cycles across scales. Freshwater mussels occur as spatially heterogeneous, dense and species-rich aggregations in many river ecosystems worldwide. Here we examined how mussel communities (1) directly influence the flux of particulate and dissolved nutrients and (2) indirectly effect the flux of N2 production, via denitrification, across a gradient of mussel biomass and differences in community composition at the patch- (0.25 m2) and stream reach-scales (60-80 m). We combined measurements of ammonia (N) and soluble reactive phosphorous (P) excretion and C, N, and P biodeposition rates for ten species with biomass and distribution estimates for seven mixed-species aggregations to quantify direct mussel contributions to biogeochemical cycling and the spatial heterogeneity of their impact. Additionally, we sampled sediments at a fine spatial scale to determine how mussel biomass and richness influence potential denitrification (indirect flux) rates at the patch- and reach-scales. We predicted that increasing mussel biomass would lead to greater direct and indirect fluxes of nutrients, manifesting in heterogeneous nutrient redistribution within and among stream reaches. We also predicted that variation in community composition would result in differential nutrient excretion and egestion stoichiometries. Our results indicate that mussel aggregations directly influence soluble and particulate nutrient fluxes with community composition, particularly phylogenetic tribe composition, controlling the stoichiometry. Mussel aggregations also indirectly influenced nutrient fluxes as greater mussel biomass and species richness resulted in higher denitrification rates as mediated by their interactions with the sediments and enhancement of nutrient availability. Our results underscore the importance of patchy communities in acting as biogeochemical control points.

opencc-zeroJan 2022View details →

A patch-dynamic metacommunity perspective on the persistence of mutualistic and antagonistic bipartite networks

The structure of interactions between species within a community plays a key role in maintaining biodiversity. Previous studies have found that the effects of these structures might substantially differ depending on interaction type, for example, a highly connected and nested architecture stabilizes mutualistic communities, while the stability of antagonistic communities is enhanced in modular and weakly connected structures. Here we show that, when network dynamics are modelled using a patch-dynamic metacommunity framework, the qualitative differences between antagonistic and mutualistic systems disappear, with nestedness and modularity interacting to promote metacommunity persistence. However, the interactive effects are significantly weaker in antagonistic metacommunities. Our model also predicts an increase in connectance, nestedness and modularity over time in both types of interaction, except in antagonistic networks where nestedness declines. At steady state, we find a strong negative correlation between nestedness and modularity in both mutualistic and antagonistic metacommunities. These predictions are consistent with the structural trends found in a large dataset of real-world antagonistic and mutualistic communities.

EOL Dynamic Hierarchy Lizards Patch (LIZ): EOL Dynamic Hierarchy Lizards Patch

Squamata sans Serpentes. Hierarchy (following Ananjeva 2019, Conrad & Norell 2007, Pyron 2017, Pyron et al. 2013, Reeder et al. 2015, Streicher & Wiens 2017, Zheng & Wiens 2016), extinct taxa (main source: <a href="http://www.paleobiodb.org/">Paleobiology Database</a>), additions & corrections for Recent taxa (main source: <a href="http://reptile-database.reptarium.cz/">Reptile Database</a>) to complement Catalogue of Life coverage. Data sources: Alifanov, V.R. 1988. The new lizards (Lacertilia: Teiidae) from the Upper Cretaceous of Mongolia. In F. Kurochkin (ed.), Fossil reptiles and birds of Mongolia. Alifanov, V.R. 1989. [New priscagamas (Lacertilia) from the Upper Cretaceous of Mongolia and their systematic position in the Iguania]. Paleontologiceskij Zhurnal 4:73-87. Alifanov, V.R. 1993. New lizards of the family Macrocephalosauridae (Sauria) from the Upper Cretaceous of Mongolia, critical remarks on the systematics of the Teiidae. Paleontological Journal 27(1):70-90. 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EOL Dynamic Hierarchy Vespoidea Patch (VSP)

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Aglaotilla, a new genus of Australian Mutillidae (Hymenoptera) with metallic coloration. Zootaxa 4415(2):357-368. doi: 10.11646/zootaxa.4415.2.6. Brothers, D.J., Carpenter, J.M. 1993. Phylogeny of Aculeata: Chrysidoidea and Vespoidea. Journal of Hymenoptera Research 2:227-304. Brothers, D.J. & Finnamore A.T. 1993. Superfamily Vespoidea pp. 161-278.. In GOULET, H. & HUBER, J. eds.. Hymenoptera of the World: an identification guide to families. Research Branch, Agriculture Canada, Ottawa, Canada, 668 pp. Brothers DJ, Lelej AS 2017. Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60:1-97. DOI:10.3897/jhr.60.20091 Brown, G.R. 1983. Pentazeleboria. A New Genus of Australian Thynnini (Hymenoptera: Tiphiidae). Australian Journal of Entomology 22:61–64. Brown, G.R. 1987. Revision of the Australian Genus Acanthothynnus Turner (Hymenoptera: Tiphiidae). Australian Journal of Entomology 26:181–188. Brown, G.R. 1989. Revision of the Australian Genus Doratithynnus Tuner (Hymenoptera: Tiphiidae). Australian Journal of Entomology 28:1–17. Brown, G.R. 1992. Bifidothynnus wubiniensis, a New Genus and Species of Australian Thynnini (Hymenoptera: Tiphiidae: Thynninae). Australian Journal of Entomology 31:215–217. Brown, G.R. 1995. New synonyms and combinations in the genus ‘Zeleboria’ Saussure (Hymenoptera: Tiphiidae). General and Applied Entomology: The Journal of the Entomological Society of New South Wales 26:9. Brown, G.R. 1995. Revision of the Australian wasp genus Macrothynnus Turner (Hymenoptera: Tiphiidae: Thynninae). Records of the Western Australian Museum 17:267–275. Brown, G.R. 1995. Tachyphron, a New Genus of Australian Thynninae (Hymenoptera: Tiphiidae). Australian Journal of Entomology 34:241–246. Brown, G.R. 1996. Arthrothynnus, a New Genus of Orchid-pollinating Thynninae (Hymenoptera: Tiphiidae). The Beagle: Records of the Museums and Art Galleries of the Northern Territory 13:73. Brown, G.R. 1996. Chilothynnus, a New Genus of Australian Thynninae (Hymenoptera: Tiphiidae) Associated with Orchids. The Beagle: Records of the Museums and Art Galleries of the Northern Territory 13:61. Brown, G.R. 1998. Revision of the Neozeleboria cryptoides species group of thynnine wasps (Hymenoptera: Tiphiidae): Pollinators of native orchids. Australian Journal of Entomology 37:193–205. Brown, G.R. 2000. Caetrathynnus, Nitidothynnus and Procerothynnus, New Genera of Thynninae (Hymenoptera: Tiphiidae) from Northern Australia. The Beagle: Records of the Museums and Art Galleries of the Northern Territory 16:107. Brown, G.R. 2001. Status of the Ariphron generic group (Hymenoptera: Tiphiidae): A critical review. Australian Journal of Entomology 40(1):23-40. Brown, G.R. 2005. A revision of Tachyphron Brown and description of two new genera within the Ariphron group (Hymenoptera: Tiphiidae). Journal of Natural History 39: 197–239. Brown, G.R. 2008. Umbothynnus, a newly recognised genus for the Rhagigaster alexius Guérin group of species (Hymenoptera: Tiphiidae: Thynninae: Rhagigasterini) from northern Australia. Zootaxa 1933:43–58. Brown, G.R. 2009. Description of Two New Pseudaposematic Species with a Review of Defensive Adaptations in the Subfamily Thynninae (Hymenoptera: Thynnidae). The Beagle: Records of the Museums and Art Galleries of the Northern Territory 25:69. Brown, G.R. 2010. ‘Curvothynnus’ gen. nov. erected for two unusual species of thynnine wasps (Hymenoptera: Thynnidae: Thynninae: Rhagigasterini). The Beagle: Records of the Museums and Art Galleries of the Northern Territory 26:89. Brown, G.R. 2011. ‘Dimorphothynnus’ (Hymenoptera: Thynnidae: Rhagigasterini) newly recorded from the Northern Territory, Australia. The Beagle: Records of the Museums and Art Galleries of the Northern Territory 27:107. Brown, G.R. 2015. Rugosothynnus gen. nov. (Hymenoptera: Tiphiidae: Thynninae: Rhagigasterini), a newly recognised Australian genus. Zootaxa 3925:361–386. Carnimeo, Fernando Henrique, Noll, Fernando Barbosa 2018. On the dumping ground genus Scotaena Klug, 1810 (Hymenoptera: Tiphiidae: Thynninae): Phylogeny, taxonomy and geographic distribution. Zootaxa 4399(4): 451-490, DOI:10.11646/zootaxa.4399.4.1 Durán-Moya, L. 1941. Die Thynniden von Chile. Archiv fur Naturgeschichte 1941:71–176. Elçin, G., Bariaçik, N. and M. Boni Bartalucci. 2013. New Myzinin wasps from Turkey (Hymenoptera Tiphiidae). Linzer biologische Beiträge 45(2):2155-2163. Genise, J. & Kimsey, L.S. 1991. New genera of South American Thynninae (Tiphiidae, Hymenoptera). Psyche: A Journal of Entomology 98:57–69. DOI:10.1155/1991/37156 Genise, J. & Kimsey, L.S. 1993. Revision of the South American Thynninae genus Elaphroptera Guérin-Méneville (Hymenoptera, Tiphiidae). Journal of Hymenoptera Research 2:195–220. Gess, S.K. & Gess, F.W. 2014. Wasps and bees in southern Africa. SANBI Biodiversity Series 24. South African National Biodiversity Institute, Pretoria. 320 pp. Given, B.B. 1953. Evolutionary Trends in the Thynninae (Hymenoptera: Tiphiidae) With Special Reference To Feeding Habits Of Australian Species. Transactions of the Royal Entomological Society of London 105:1–10. Justino, C.E.L. 2013. Análise Filogenética de Scotaenini (Hymenoptera, Vespoidea, Tiphiidae, Thynninae). Masters Dissertation, UNESP, São José do Rio Preto, São Paulo, 55 pp. Justino, C.E.L., dos Santos, E.F. & Noll, F.B. 2013. Geographic note on species of the genus Upa Kimsey, 1991 (Hymenoptera, Tiphiidae, Thynninae) in the Atlantic Forest, Brazil. Check List 9(5):1057–1061. DOI:10.15560/9.5.1057 Justino, C.E.L, dos Santos, E.F. & Noll, F.B. 2016. Diversity of Tiphiidae (Insecta, Hymenoptera) in the fragmented Brazilian semi-deciduous Atlantic Forest. Journal of Insect Conservation, 20(3):417–431. DOI:10.1007/s10841-016-9875-9 Kimsey, L.S. 1991. Additional new genera and species of south american thynnine wasps (Hymenoptera, Tiphiidae). Psyche: A Journal of Entomology 98:71–80. DOI:10.1155/1991/83532 Kimsey, L.S. 1991. Relationships among the tiphiid wasp subfamilies (Hymenoptera). Systematic Entomology 16: 427-438. Kimsey, L.S. 1991. Revision of the South American wasp genus Aelurus (Hymenoptera, Tiphiidae, Thynninae). Systematic Entomology 16:223–237. DOI:10.1111/j.1365-3113.1991.tb00685.x Kimsey, L.S. 1992. Phylogenetic relations among the South American Thynninae Tiphiidae wasps. Systematic Entomology 17:133–144. DOI:10.1111/j.1365-3113.1992.tb00326.x Kimsey, L.S. 1996. Phylogenetic relationships of the thynnine wasp tribe Rhagigasterini (Hymenoptera: Tiphiidae). Journal of Hymenoptera Research 5:80–99. Kimsey, L.S. 1996. Revision of the South American thynnine genus Upa (Hymenoptera, Tiphiidae). Proceedings of the Entomological Society of Washington 98:55–63. Kimsey, L.S. 2000. Revision of the Australian Tiphiid Genus Leiothynnus (Hymenoptera: Tiphiidae: Thynninae). Journal of Hymenoptera Research 9:18–28. Kimsey, L.S. 2001. The New Western Australian Tiphiid Genus Dythynnus Kimsey (Hymenoptera: Tiphiidae: Thynninae). Journal of Hymenoptera Research 10:76–80. Kimsey, L.S. 2002. New genus and five new species of heat-tolerant tiphiid wasps from Western Australia (Hymenoptera: Tiphiidae: Thynninae). Australian Journal of Entomology 41:345–353. Kimsey, L.S. 2003. A Peculiar New Genus of Locally Abundant Australian Thynninae (Hymenoptera: Tiphiidae). Journal of Hymenoptera Research 12:102–124. Kimsey, L.S. 2004. Taxonomic changes and new generic synonymies in the tiphiid wasp subfamily Thynninae (Hymenoptera, Tiphiidae). Proceedings of the Entomological Society of Washington 106:508–512. Kimsey, L.S. 2004. Illustrated keys to the genera of the male wasps in the subfamily Thynninae (Hymenoptera, Tiphiidae). Proceedings of the Entomological Society of Washington 106:571–585. Kimsey, L.S. 2005. Revision of the Northern South American tiphiid genus Merithynnus Kimsey, 1991 (Hymenoptera, Tiphiidae, Thynninae). Proceedings of the Entomological Society of Washington 107:576–595. Kimsey, L.S. 2006. 14.2: Familia Tiphiidae. In: Hanson, P.Y. & Gauld, I.D. (Eds.), Hymenoptera de la Región Neotropical. Memoirs of the American Entomological Institute, Gainesville, pp. 575–583. Kimsey, L.S. 2011. Tiphiidae wasps of Madagascar (Hymenoptera, Tiphiidae). Journal of Hymenoptera Research 22:45–68. DOI:10.3897/JHR.22.1142 Kimsey, L.S. & Brothers, D.J. 2006. Capítulo 56: Familia Tiphiidae. In: Fernández, F.C. & Sharkey, M.J. (Eds.), Introducción a los Hymenoptera de La Región Neotropical. Sociedad Colombiana de Entomología, Colômiba, pp. 583–594. Kimsey, L.S. & Brown, G.R. 1993. Lectotype designations within the subfamily Thynninae (Hymenoptera, Tiphiidae). Journal of the Australian Entomological Society 32:317–326. DOI:10.1111/j.1440-6055.1993.tb00594.x Krombein, K.V. 1937. Studies in the Tiphiidae, I: a review of the genera of Myzininae. Annals of the Entomological Society of America 30:27–30. Krombein K.V. 1938. Studies in the Tiphiidae II. A revision of the Nearctic Myzininae. Transactions of the American Entomological Society 64:227-292. Krombein, K.V. 1949. Studies in the Tiphiidae. VII. The Madagascan species. Proceedings of the Entomological Society of Washington 51:45–73. Krombein K.V. 1968. Studies in the Tiphiidae. X. Hylomesa, a new genus of Myzininae wasp parasitic on larvae of longicorn beetles (Hymenoptera). Proceedings of the United States National Museum 124:1-22. Lelej, A.S. 2002. Catalogue of the Mutillidae Hymenoptera. of the Palaearctic Region. Vladivostok: Dalnauka, 172 p. Lelej, A.S. 2005. Catalogue of the Mutillidae (Hymenoptera) of the Oriental Region. Dalnauka, Vladivostok, 1–252. Lelej, A.S. & Brothers, D.J. 2008. The genus-group names of Mutillidae Hymenoptera. and their type species, with a new genus, new name, new synonymies, new combinations and lectotypifications. Zootaxa 1889:1–79. Lelej, A.S., T. Osten, 2004. To the knowledge of the mutillid and bradynobaenid wasps of Iran (Hymenoptera: Mutililidae, Bradynobaenidae). Proceeding of the Russian Entomological Society, St. Petersburg 75(1):253–262. Lelej, A.S. & van Harten, A. 2006. A review of the Mutillidae (Hymenoptera) of Yemen. Zootaxa 1226:1-50. Pagliano, G., Romano, M., World list of all known species of Bradynobaenidae (Hymenoptera) [WWW Document]. ResearchGate. URL <a href="https://www.researchgate.net/publication/329782449_World_list_of_all_known_species_of_Bradynobaenidae_Hymenoptera" target="_blank" rel="nofollow noopener">https://www.researchgate.net/publication/329782449_World_list_of_all_known_species_of_Bradynobaenidae_Hymenoptera</a> (accessed 1.20.19). Pate, V.S.L. 1947. A Conspectus of the Tiphiidæ, with Particular Reference to the Nearctic Forms (Hymenoptera, Aculeata). Journal of the New York Entomological Society 55:115–145. Torréns, J., Fidalgo, P., Roig-Alsina, A., Brothers, D.J., 2014. Review of the genus Eotilla Schuster, 1949 (Hymenoptera: Bradynobaenidae: Typhoctinae: Eotillini) and description of new species from Argentina. Zootaxa 3878, 1. DOI:10.11646/zootaxa.3878.1.1 Torrens, J. and Roig-Alsina, A., 2009. Description of a new species of Bradynobaenus (Hymenoptera: Bradynobaenidae) from Argentina, with a key to the females of the genus. Zootaxa 2047:63-68. Turrisi, G.F., M. Matteini Palmerini, and D.J. Brothers. 2015. Systematic Revision and Phylogeny of the Genera Blakeius Ashmead, 1903 and Liomutilla André, 1907, with Description of Two New Genera (Hymenoptera: Mutillidae, Myrmillinae). Zootaxa 4010(1):1–78. <a href="https://doi.org/10.11646/zootaxa.4010.1.1" target="_blank" rel="nofollow noopener">https://doi.org/10.11646/zootaxa.4010.1.1</a>. van Noort, S. 2020. WaspWeb: Hymenoptera of the Afrotropical region. URL: <a href="https://www.waspweb.org">www.waspweb.org</a>

EOL Dynamic Hierarchy Coccinelloidea Patch (COC): EOL Coccinelloidea Patch

Taxonomic hierarchies & species lists for Akalyptoischiidae, Alexiidae, Anamorphidae, Bothrideridae, Cerylonidae, and Endomychidae to complement Catalogue of Life coverage. Compiled from multiple sources: Andrews, F.G. 1976: Akalyptoischion, a new genus of Lathridiidae from western North America (Coleoptera). Occasional papers in entomology, California Department of Agriculture (22) Hartley, C.S.; Andrews, F.G.; McHugh, J.V. 2008: A taxonomic revision of the genus Akalyptoischion Andrews (Coleoptera: Latridiidae). Coleopterists Society monograph, (6) doi: <a href="https://doi.org/10.1649/0010-065X(2008)61[1:ATROTG]2.0.CO;2">10.1649/0010-065X(2008)61[1:ATROTG]2.0.CO;2 </a> Robertson, J.A., Slipinski, A., Moulton, M., Shockley, F.W., Giorgi, A., Lord, N.P., Mckenna, D.D., Tomaszewska, W., Forrester, J., Miller, K.B. and Whiting, M.F., 2015. Phylogeny and classification of Cucujoidea and the recognition of a new superfamily Coccinelloidea (Coleoptera: Cucujiformia). Systematic Entomology, 40(4), pp.745-778. Shockley F., Tomaszewska, K. and McHugh, J., 1999. An annotated checklist of the handsome fungus beetles of the world (Coleoptera: Cucujoidea: Endomychidae). Zootaxa, 113, p.30. Tomaszewska, W. (2011) On African Eupsilobiinae (Coleoptera: Endomychidae) with descriptions of new genus and species. Journal of Insect Science, 11, 1–14.

EOL Dynamic Hierarchy Erebidae Patch (ERE)

Updated Erebidae classification covering subfamilies, tribes, subtribes, and genera. Compiled from multiple sources: Da Costa, MA, Weller, SJ (2005). Phylogeny and classification of Callimorphini (Lepidoptera: Arctiidae: Arctiinae). Zootaxa 1025:1–94. De Prins J. & De Prins W. 2011–2019. Afromoths, online database of Afrotropical moth species (Lepidoptera). World Wide Web electronic publication: <a href="http://www.afromoths.net/" target="_blank" rel="nofollow noopener">http://www.afromoths.net</a> de Vos, R. 2011. Nicetosoma Gen. Nov., a New Genus for the ‘Spilosoma’ Niceta Group of Species East of the Weber Line (Lepidoptera: Erebidae, Arctiinae, Arctiini). Suara Serangga Papua 5 (4): 109-144. Dubatolov, VV (2010). Tiger-moths of Eurasia (Lepidoptera, Arctiidae) (Nyctemerini by Rob de Vos & Vladimir V. Dubatolov). Neue Entomologische Nachrichten 65:1–106. Edwards, ED (1996). Arctiidae. In: Nielsen E.S., Edwards E.D. & Rangsi T.V. (eds) Checklist of the Lepidoptera of Australia, Monographs on Australian Lepidoptera: 278–286. Ferguson DC, Opler PA (2006) Checklist of the Arctiidae (Lepidoptera: Insecta) of the continental United States and Canada. Zootaxa 1299:1–33. Fibiger, Michael (2007). Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 1, Taxonomy of the Pollexinae. Zootaxa 1567:1-116. Fibiger, Michael (2008). Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 2, Taxonomy of the Belluliinae, Magninae and Parachrostiinae. Zootaxa 1867:1-136. Fibiger, Michael (2010). Revision of the Micronoctuidae (Lepidoptera: Noctuoidea) Part 3, Taxonomy of the Tactusinae. Zootaxa 2583:1–119. Fibiger, Michael (2011). Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 4, Taxonomy of the subfamilies Tentaxinae and Micronoctuinae. Zootaxa 2842:1–188. Fibiger, Michael, Hacker, Hermann (2005). Systematic List of the Noctuoidea of Europe (Notodontidae, Nolidae, Arctiidae, Lymantriidae, Erebidae, Micronoctuidae, and Noctuidae). Esperlana 11:93–205. Fibiger, Michael, Han, Hui-Lin & Kononenko, Vladimir S. (2011). Five new species and one new subspecies of Micronoctuidae from China, with a checklist of Chinese species, including Taiwan (Lepidoptera: Noctuoidea, Micronoctuidae). Zootaxa. 2777: 1–13. Fibiger, Michael, Kononenko, Vladimir S. (2008). Revision of the Micronoctuidae species occurring in the Russian Far East and neighbouring countries with description of a new species (Lepidoptera, Noctuoidea). Zootaxa 1890:50-58. Fibiger, Michael, Lafontaine, J. Donald (2005). A review of the higher classification of the Noctuoidea (Lepidoptera) with special reference to the Holarctic fauna. Esperiana 11:7-92. Goodger DT, Watson A (1995) The Afrotropical Tiger-Moths. An illustrated catalogue, with generic diagnosis and species distribution, of the Afrotropical Arctiinae (Lepidoptera: Arctiidae). Apollo Books Aps.: Denmark, 55 pp. Han, H. L., & Kononenko, V. S. (2017). Two replacement names of the genus group of Micronoctuini and a new species of the genus Tentaxus Han & Kononenko from Sabah, East Malaysia (Lepidoptera, Erebidae, Hypenodinae). Taxonomic study of Micronoctuini. Contribution I. Zootaxa, 4362(2), 259. doi:10.11646/zootaxa.4362.2.5 Holloway, Jeremy D. (1988). The Moths of Borneo Part 6: Family Arctiidae, subfamilies Syntomine, Euchromiinae Arciinae; Noctuidae misplaced in Arctiidae. The Moths of Borneo. Southdene Sdn. Bhd. Holloway, Jeremy D. (1999). The Moths of Borneo: Family Lymantriidae. Malayan Nature Journal 53:1-188. Holloway, Jeremy D. (2001). The Moths of Borneo Part 7: Family Arctiidae, Subfamily Lithosiinae. The Moths of Borneo. Southdene Sdn. Bhd. Holloway, Jeremy D. (2005) The Moths of Borneo Parts 15 & 16: Family Noctuidae, Subfamily Catocalinae" The Moths of Borneo. Southdene Sdn. Bhd. Holloway, Jeremy D. (2008). The Moths of Borneo: family Noctuidae, subfamilies Rivulinae, Phytometrinae, Herminiinae, Hypeninae and Hypenodinae. Malayan Nature Journal 60:1-267. Homziak, Nicholas T., Breinholt, Jesse W., Kawahara, Akito Y. (2016). A historical review of the classification of Erebinae (Lepidoptera: Erebidae). Zootaxa 4189(3):516–542. doi:<a href="https://doi.org/10.11646/zootaxa.4189.3.4.">10.11646/zootaxa.4189.3.4.</a> Kaleka, AS, Rose, HS (2002). Inventory of species of Miltochrista Hübner (Lithosiinae: Arctiidae: Lepidoptera) from northwestern and northeastern India. Zoos__ Print Journal 17 (8):853-856. Kirti, J.S. & Singh, N. (2016) Arctiid Moths of India. Vol. 2. Nature Books India, New Delhi, 214 pp. Kononenko, VS, Pinratana, A (2013). Moths of Thailand Vol. 3, Part 2. Noctuoidea. An illustrated Catalogue of Erebidae, Nolidae, Euteliidae, and Noctuidae (Insecta: Lepidoptera) in Thailand. Bangkok: Brothers of St. Gabriel in Thailand. Lafontaine, J. Donald, Fibiger, Michael (2006). Revised higher classification of the Noctuoidea (Lepidoptera) Canadian Entomologist 138:610-635. Lafontaine, Donald; Walsh, J. Bruce (2010). A review of the subfamily Anobinae with the description of a new species of Baniana Walker from North and Central America (Lepidoptera, Erebidae, Anobinae). ZooKeys 39:3–11. doi:<a href="https://doi.org/10.3897/zookeys.39.428">10.3897/zookeys.39.428</a> Lafontaine, Donald, Schmidt, Christian (2010). Annotated check list of the Noctuoidea (Insecta, Lepidoptera) of North America north of Mexico. ZooKeys 40:1-239. doi:<a href="https://doi.org/10.3897/zookeys.40.414">10.3897/zookeys.40.414</a> Lafontaine, J. Donald; Schmidt, B. Christian (2013). Additions and corrections to the check list of the Noctuoidea (Insecta, Lepidoptera) of North America north of Mexico. ZooKeys. 264:227–236. doi:<a href="https://10.0.15.57/zookeys.264.4443">10.3897/zookeys.264.4443</a> Savela, Markku. 2020. Lepidoptera and Some Other Life Forms. World Wide Web electronic publication: <a href="https://ftp.funet.fi/pub/sci/bio/life/intro.html" target="_blank" rel="nofollow noopener">https://ftp.funet.fi/pub/sci/bio/life/intro.html</a> Van Nieukerken, E.J., Kaila, L., Kitching, I.J., Kristensen, N.P., Lees, D.C., Minet, J., Mitter, C., Mutanen, M., Regier, J.C., Simonsen, T.J. and Wahlberg, N., 2011. Order Lepidoptera Linnaeus, 1758. In: Zhang, Z.-Q.(Ed.) Animal biodiversity: an outline of higher-level classification and survey of taxonomic richness. Zootaxa, 3148(1):212-221. Volynkin, Anton V. 2016. On the generic placement and taxonomic status of some Miltochrista taxa described by Franz Daniel (Lepidoptera, Erebidae, Arctiinae) Zootaxa 4179(2):244-252. Volynkin, Anton V. 2017. Description of a New Species of Miltochrista Hübner from Vietnam, with Eight New Combinations (Lepidoptera, Erebidae, Arctiinae). Zootaxa 4286(1):145. <a href="https://doi.org/10.11646/zootaxa.4286.1.13" target="_blank" rel="nofollow noopener">https://doi.org/10.11646/zootaxa.4286.1.13</a>. Volynkin, Anton V., Singh, N., Cerný, K., Kirti, J. S., Datta, H. S. 2020. Revision of the Miltochrista obliquilinea species-group, with descriptions of four new species (Lepidoptera, Erebidae, Arctiinae, Lithosiini) Zootaxa 4780(3):448-470. Watson A (1971) An illustrated Catalog of the Neotropic Arctiinae type in the United States National Museum (Lepidoptera: Arctiidae) Part 1. Smithsonian Contributions to Zoology 50:1–361 Zahiri, Reza; et al. (2011). Molecular phylogenetics of Erebidae (Lepidoptera, Noctuoidea). Systematic Entomology 37:102–124. doi:<a href="https://doi.org/10.1111/j.1365-3113.2011.00607.x">10.1111/j.1365-3113.2011.00607.x</a> Zahiri, Reza; et al. (2011). A new molecular phylogeny offers hope for a stable family level classification of the Noctuoidea (Lepidoptera). Zoologica Scripta 40:158–173. doi:<a href="https://doi.org/10.1111/j.1463-6409.2010.00459.x">10.1111/j.1463-6409.2010.00459.x</a> Zahiri, Reza; et al. (2012). Molecular phylogenetics of Erebidae (Lepidoptera, Noctuoidea). Systematic Entomology 37:102–124. doi:<a href="https://doi.org/10.1111/j.1365-3113.2011.00607.x]">10.1111/j.1365-3113.2011.00607.x</a> Zahiri, Reza; et. al (2013). Relationships among the basal lineages of Noctuidae (Lepidoptera, Noctuoidea) based on eight gene regions. Zoologica Scripta 42:488–507. doi:<a href="https://doi.org/10.1111/zsc.12022">10.1111/zsc.12022</a> Zaspel, JM, Branham, MA (2008). World Checklist of Tribe Calpini (Lepidoptera: Noctuidae: Calpinae). Insecta Mundi 0047:1-15.

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A patch-dynamic metacommunity perspective on the persistence of mutualistic and antagonistic bipartite networks

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Community patch‐dynamics governs direct and indirect nutrient recycling by aggregated animals across spatial scales

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dryad32/100

Data from: A model for non-equilibrium metapopulation dynamics utilizing data on species occupancy, patch ages and landscape history

1. The distribution pattern of many species reflects the past rather than the current structure of landscapes. Consequently, species are most often not in equilibrium with the current landscape structure. Yet this is a well-known fact, there is no appropriate approach to estimate the colonization rate of non-equilibrium species based on only data on the species occurrence pattern in the landscape. 2. We present an approach to estimate the colonization rate of non-equilibrium metapopulations. The approach requires only data on species presence/absence among its patches (occurrence pattern), data on patch ages and data on the historic distribution of the patches in the landscape. By estimating the past occurrence patterns and colonization events leading to the current pattern of occupied and non-occupied patches, we estimate the colonization rate, including the dispersal kernel. We also show how to estimate effects of local patch conditions and how to include an independent estimate of the local extinction rate based on other data. We use nine epiphytic lichen species confined to beech trees to illustrate the method. 3. Five species had restricted dispersal range, between 200 and 4700 m, and their colonization rate decreased with increasing fragmentation. Species colonization rates were related to niche width. Among the demographic parameters, the force of colonization was more important than the dispersal range in explaining the colonization rates. Local patch conditions did not explain the colonization probability of any species. In metapopulation projections that did not account for restricted dispersal range, higher future metapopulation sizes were projected. 4. Synthesis. The presented approach uses data on only species occurrence, patch age and landscape history to estimate the species colonization rate and dispersal kernel. It can also utilize independent data on local extinction rate. Rather than identifying factors explaining the occurrence pattern, the model estimates the rate of change in the occurrence pattern. This dynamic modelling allows testing general and applied questions on the dynamics or viability of metapopulations of sessile species. The approach is applicable for species whose distribution pattern reflects the past rather than the current landscape structure, e.g. certain epiphytes and ground-floor plants.

opencc-zeroDec 2013View details →

dryad32/100

Patch size distribution affects species invasion dynamics in dendritic networks

<div class="page"> <div class="section"> <div class="layoutArea"> <div class="column"> Biological invasions are globally affecting ecosystems, causing local species loss and altering ecosystem functioning. Understanding how such biological invasions occur and succeed is thus of high priority. Both local properties and the spatial network structure have been shown to be determinants of invasion success, and the identification of spatial invasion hubs directly promoting invasion dynamics is gaining attention. Spatial dynamics, however, could also indirectly alter invasion success by shaping pre- invasion local community structure: in many ecosystems, such as riverine networks, regional properties such as patch size distribution are known drivers of local community structures, which themselves may affect the establishment success of invading species. Using microcosm experiments in dendritic networks, we disentangled how inherent patch size distribution and dispersal along specific network topologies shaped local resident communities, and, subsequently, affected the establishment success of invading species. After controlling for regional-scale effects of connectivity on pre-invasion diversity, we find that patch size distributions independently shaped pre-invasion community diversity and invasion success, with no direct effect of pre-invasion diversity on invasion success. Our results suggest that 1) landscape configuration plays an underestimated role in invasion success and that 2) invasion success should follow predictable landscape-scale patterns in riverine networks given non-random patch-size distribution. </div> </div> </div> </div>

opencc-zeroNov 2021View details →

FIG. 5 in Patch Dynamics Inform Management Decisions in a Threatened Frog Species

FIG. 5. (A) Crawfish Frog movement from Nate's Pond (Hillenbrand Fish and Wildlife Area-West, Greene County, Indiana). One-third of juvenile Crawfish Frogs that metamorphosed at Nate's Pond dispersed to nearby wetlands to breed. Two-thirds of juveniles returned to Nate's to breed. Numbers in parentheses represent counts of individuals. The sizes of the arrows are proportional to the number of individuals. (B) A subset of adult Crawfish Frogs shifted breeding wetlands between years. Colors match the initial wetland from which frogs emigrated. Numbers indicate counts of individuals moving between wetlands. Scale bar ¼ 500 m.

FIG. 4 in Patch Dynamics Inform Management Decisions in a Threatened Frog Species

FIG. 4. Retention of juvenile Crawfish Frogs released at artificial burrows west of Nate's Pond (Hillenbrand Fish and Wildlife AreaWest, Greene County, Indiana). From 24 June–1 August 2015, we used wildlife cameras to determine burrow occupancy. We defined snake predation as instances when frogs no longer appeared after a snake was photographed at burrows. Snake predation (n ¼ 10) and an unknown case of mortality (n¼ 1) are noted.

FIG. 1 in Patch Dynamics Inform Management Decisions in a Threatened Frog Species

FIG. 1. Crawfish Frog breeding wetlands (n ¼ 6) at Hillenbrand Fish and Wildlife Area-West (HFWA-W; Greene County, Indiana). We encircled Nate's and Cattail ponds (bolded text) with drift fence/pitfall trap arrays in 2009– 2016 and sampled at the remaining wetlands (Big, Erosion Control [EC], New, and Nate's Jr.) using funnel traps. We monitored Crawfish Frog breeding (late February through early May) and metamorphosis (mid-June through early August) at Nate's and Cattail, and only breeding at the remaining wetlands. The yellow outline indicates the boundary of HFWAW. Scale bar ¼ 1 km.

FIG. 2 in Patch Dynamics Inform Management Decisions in a Threatened Frog Species

FIG. 2. (A) Newly metamorphosed juvenile Crawfish Frogs at Nate's Pond (Hillenbrand Fish and Wildlife Area-West, Greene County, Indiana) exited with no specific directionality in 2009–2011 and 2014. Exiting frogs were captured by pitfall traps (indicated by yellow squares) positioned every 10 m along the drift fence. Sizes of trap squares are proportional to the number of juveniles exiting from each trap. Numbers next to the traps show the proportion of juveniles exiting from that trap, averaged across the years. (B) Post-breeding adult Crawfish Frogs exhibited a strong tendency to exit Nate's Pond towards the southeast, presumably in the direction of their primary burrow (Heemeyer and Lannoo, 2012). A smaller subset of adults exited east; a much smaller subset exited west. Sizes of trap squares are proportional to the ratio of adults versus juveniles exiting from each trap. We included adults that originated from Nate's Pond and were captured in 2013–2016, and excluded those from 2012 (small sample size, n ¼ 14). We included juveniles captured in 2009–2011 and 2014, and excluded years with small sample sizes (2013, n ¼ 8) and no recruitment (2012 and 2015). Scale bar ¼ 50 m.