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665 results for “ant diversity”
Ant Diversity and Vegetation Composition in Hemlock Removal Experiment at Harvard Forest 2006
Ants comprise a considerable amount of animal biomass in terrestrial ecosystems and play major roles in ecological processes ranging from seed dispersal to soil turnover. Invasion by the hemlock woolly adelgid will transform late-successional hemlock forests into earlier successional mixed hardwood-white pine forests or red-maple wetlands. Understanding how ant assemblages vary in different habitat types allows for predictions of how hemlock decline could alter the composition of ant assemblages, with implications for a wide range of ecosystem processes. An ongoing study at the Simes Tract of Harvard Forest is documenting the effects of invasion and land-use history on ant biodiversity. Surveys from 2003 to 2005 focused on ant structure in hemlock and hardwood microhabitats in the Harvard Forest Hemlock Removal Experiment, in which hemlock forest response to deforestation by the hemlock woolly adelgid (Adelges tsugae) and to selective logging is being examined (Ellison et al. 2005). In the summer of 2006, we surveyed a greater range of microhabitat types with two objectives. First, to collect rare or elusive species in hemlock and hardwood stands that may have gone uncollected in previous years. Second, to sample forest communities not included in previous years - white pine, swamp, and rocky slope - for ant species unique to these microhabitats. We found fourteen newly documented species of ants in the Simes Tract - nine of which were in an open, swamp. Aphaenogaster rudis and Camponotus pennsylvanicus were the only ant species found in all microhabitat types. In a canonical correspondence analysis, A. rudis and C. pennsylvanicus were associated most strongly with hemlock stands and low species richness of understory plants.
Ant Functional Diversity in Temperate Zone Forests: A Comparison with Neotropical Ants 2010
Predicted impacts of climatic change on ant functional diversity and distributions in eastern North American forests Aims--Climatic change is expected to rearrange species assemblages and ultimately affect organism-mediated ecosystem processes. We focus on identifying patterns and relationships between common ant species (representing 99% of total ant records) richness and functional diversity; modelling how these patterns may change at local and regional scales in future climatic conditions; and interpreting how these changes might influence ant-mediated ecosystem processes. Location--Forested ecosystems of eastern North America. Methods--We used a previously published dataset to evaluate functional diversity at 67 sites in the eastern U.S. and quantified 14 taxonomic, morphometric and natural history traits for 70 common ant species in the region. We used functional diversity metrics, functional groups and species distribution modelling methods to address our aims. We used stacked species distribution models and stacked functional group models to predict species assemblages and functional richness at the 67 sites and at a regional scale for current and future climatic conditions. Results--Species richness and functional diversity are positively correlated throughout the region. Under future climate scenarios, species richness and functional group richness were predicted to decrease in southern ecoregions and increase in northern ecoregions. This may be due to increased thermal stress for species in the southern extent of their ranges and increased habitat suitability in the northern ecoregions. Decomposers, arthropod community regulators and seed dispersers are forecast to be the most threatened ant functional groups. Main Conclusions--Climate change will likely lead to major changes in ant species richness and functional group richness in the forests of the north-eastern United States, and this may substantially alter ant-mediated ecosystem processes and services
Fig. 25 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 25. Habitat of Tachydromia ebejeri Gonçalves, Grootaert & Andrade sp. nov. in a forest of Quercus pyrenaica Willd. in Portugal, Arganil, Benfeita (Mata da Margaraça), a region under submediterranean influence.
Fig. 24 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 24. Forest of Fagus sylvatica L. in the Apennine Mountains, where Tachydromia apterygon Plant & Deeming, 2006 can be found.
Fig. 21 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 21. Drawings of the tip of stenopterous wings and images obtained by scanning electron microscope (SEM) of the micropterous wings. Males are pictured in the left column, females in the right. A, C. T. pandellei (Séguy, 1941). B–C. T. pieltaini (Gil Collado, 1936). D–E. T. semiaptera (Gil Collado, 1923). F–G. T. stenoptera Gonçalves, Grootaert & Andrade sp. nov. Scale bars: A–D, F = 50 µm; E, G = 10 µm.
Fig. 19 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 19. Images obtained by scanning electron microscopy of the spur-like structures present on the apical portion of the male mid tibia. A. T. lusitanica (Grootaert, Shamshev & Andrade, 2009). B. T. pandellei (Séguy, 1941). C. T. pieltaini (Gil Collado, 1936). D. T. ebejeri Gonçalves, Grootaert & Andrade sp. nov. E–F. T. semiaptera (Gil Collado, 1923). G. T. stenoptera Gonçalves, Grootaert & Andrade sp. nov. H. T. cantabrica Gonçalves, Grootaert & Andrade sp. nov. I. T. nigrohirta Gonçalves, Grootaert & Andrade sp. nov. J. T. apterygon Plant & Deeming, 2006. Scale bars: 10 µm.
Fig. 17 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 17. Mounted specimens of the Iberian ant-like Tachydromia Meigen, 1803. Males are pictured in the left column, females in the right. A–B. T. lusitanica (Grootaert, Shamshev & Andrade, 2009). C–D. T. nigrohirta Gonçalves, Grootaert & Andrade sp. nov. E–F. T. ebejeri Gonçalves, Grootaert & Andrade sp. nov. G–H. T. stenoptera Gonçalves, Grootaert & Andrade sp. nov. Scale bars: 1 mm.
Fig. 23 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 23. Distribution of Tachydromia apterygon Plant & Deeming, 2006 in Italy. Nine localities are currently known.
Fig. 15 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 15. Habitus of live specimens of the Iberian ant-like Tachydromia Meigen, 1803. Males are pictured in the left column, females in the right. A–B. T. lusitanica (Grootaert, Shamshev & Andrade, 2009). C–D. T. nigrohirta Gonçalves, Grootaert & Andrade sp. nov. E–F. T. ebejeri Gonçalves, Grootaert & Andrade sp. nov. G–H. T. stenoptera Gonçalves, Grootaert & Andrade sp. nov. I–J. T. cantabrica Gonçalves, Grootaert & Andrade sp. nov.
Fig. 18 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 18. Mounted specimens of the Iberian ant-like Tachydromia Meigen, 1803. Males are pictured in the left column, females in the right. A–B. T. cantabrica Gonçalves, Grootaert & Andrade sp. nov. C–D. T. iberica (Arias, 1919). E–F. T. semiaptera (Gil Collado, 1923). G–H. T. pieltaini (Gil Collado, 1936). I–J. T. pandellei (Séguy, 1941). Scale bars: 1 mm.
Fig. 16 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 16. Habitus of live specimens of the Iberian ant-like Tachydromia Meigen, 1803 and the Italian flightless Tachydromia. Males are pictured in the left column, females in the right. A–B. T. iberica (Arias, 1919). C–D. T. semiaptera (Gil Collado, 1923). E–F. T. pieltaini (Gil Collado, 1936). G–H. T. pandellei (Séguy, 1941). I–J. T. apterygon Plant & Deeming, 2006 (Italy).
Fig. 11 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 11. Terminalia of the topotype ofTachydromia pandellei (Séguy, 1941) from France, Hautes-Pyrénées, Arrens-Marsous, lectotype (RBINS). A. Right surstylus and right epandrial lamella. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. D. Right surstylus. Scale bar: 0.1 mm.
Fig. 14 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 14. Terminalia of Tachydromia stenoptera Gonçalves, Grootaert & Andrade sp. nov., holotype (RBINS). A. Right surstylus and right epandrial lamella. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. D–E. Right surstylus. Scale bar: 0.1 mm.
Fig. 13 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 13. Terminalia of Tachydromia semiaptera (Gil Collado, 1923) (RBINS). A. Right surstylus and right epandrial lamella. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. D. Right surstylus. Scale bar: 0.1 mm.
Fig. 12 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 12. Terminalia of Tachydromia pieltaini (Gil Collado, 1936) from Spain, Asturias, Covadonga (RBINS). A. Right surstylus and right epandrial lamella. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. D. Right surstylus. Scale bar: 0.1 mm.
Fig. 9 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 9. Terminalia of the holotype of Tachydromia lusitanica (Grootaert, Shamshev & Andrade, 2009) from Portugal, Braga, Gilmonde (RBINS). A. Right surstylus. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. Figure adapted from Grootaert et al. 2009.
Fig. 8 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 8. Terminalia of Tachydromia iberica (Arias, 1919) from Portugal, Leiria, Porto de Mós (RBINS). A. Right surstylus and right epandrial lamella. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. D. Right surstylus. Scale bar: 0.1 mm
Fig. 7 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 7. Terminalia of Tachydromia iberica (Arias, 1919) from Spain, Segovia, El Espinar (Central System) (RBINS). A. Right surstylus and right epandrial lamella. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. D. Right surstylus. Scale bar: 0.1 mm.
Fig. 6 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 6. Terminalia of Tachydromia iberica (Arias, 1919) from Spain, Madrid (RBINS). A. Right surstylus and right epandrial lamella. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. D. Right surstylus. Scale bar: 0.1 mm.
Fig. 5 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 5. Terminalia of the holotype of Tachydromia ebejeri Gonçalves, Grootaert & Andrade sp. nov., holotype (RBINS). A. Right surstylus and right epandrial lamella. B. Epandrium with cerci. C. Left epandrial lamella and left surstylus. D. Right surstylus. Scale bar: 0.1 mm.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.