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Figure 8 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 8 Geographic map shows the distribution of the samples analyzed in this study. Blue dots: S. juliae, ocher dots: S. fugax, black dots: S. cypridis.
Figure 7 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 7 Principal component analyses of RAV data of Solenopsis queen individuals. Blue rectangles: S. juliae, ocher diamonds: S. fugax, black triangles: S. cypridis.
Figure 6 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 6 Principal component analyses of RAV data of Solenopsis workers. Each dot represents a colony sample. Blue rectangles: S. juliae, ocher diamonds: S. fugax, black triangles: S. cypridis.
Figure 5 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 5 Principal component analyses of residuals of Solenopsis worker morphometric data. Each small dot represents a colony sample. Large dots represent centroids. Double rings represent type specimens or type series. Note: four workers mounted on two different pins (3 and 1 workers respectively) of the S. cypridis syntype material appear separately in the plot as red circles.
Figure 4 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 4 Comparison of five exploratory data analyses with the final species hypothesis. Dendrogram showing NC Clustering using ward distance method. Ocher bars: Solenopsis fugax, blue bars: S. juliae. Data input: RAV-corrected values of workers in the character system of BS.
Figure 3 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 3 Dendrogram comparing the results of "kmeans", and "hclust" in NC Clustering using UPGMA distance method of Solenopsis workers' morphometric raw data. Ocher bars: S. fugax, blue bars: S. juliae. The type material of S. juliae was not available for measurements, not shown. Black bar represents the S. cypridis samples as outgroup. Data input: raw data within the character system of SC. The cypridis cluster (black bars) was assigned as outlier in 'hclust' but 'kmeans' assigned it in the fugax cluster. Note: four workers mounted on different pins (3 and 1 workers respectively) of the S. cypridis syntype material appear separately in the tree.
Figure 23 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 23 Head of worker of Solenopsis cypridis in full-face view (CASENT0913887). Photo: AntWeb.org, Photographer: Will Ericson.
Figure 24 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 24 Lateral view of Solenopsis cypridis worker (CASENT0913887). Photo: AntWeb.org, Photographer: Will Ericson.
Figure 22 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 22 Scatterplot for morphometric ratios of Solenopsis juliae workers and S. crivellarii type. Red triangles: S. juliae; black dot: S. crivellarii type (measured from drawings).
Figure 2 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 2 Definition of preocular distance (PROC) of the Solenopsis workers measured in this study (for details, see Table 1).
Figure 1 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
Figure 1 Definition of morphological characters of the Solenopsis workers measured in this study. Head in dorsal view with measurement lines for CL1, CL2, CW, FRS, ClSpD, ApS, SApS, and SL; frontal region of the head dorsum with measurement lines for FR, FL, ClSpLL, and ClSpLM; dorsal view of mesosoma with measurement lines for ML, PEH, PEL, NOH, and PPH (for definitions, see Table 1).
Supplementary material 1 from: Csősz S, Seifert B, László M, Yusupov ZM, Herczeg G (2023) Broadly sympatric occurrence of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region (Hymenoptera, Formicidae) is disclosed. ZooKeys 1187: 189-222. https://doi.org/10.3897/zookeys.1187.105866
List of morphometrically investigated samples
Fig. 2 in Current Distribution Of The European Grayling, Thymallus Thymallus, And Huchen, Hucho Hucho, In The Transcarpatian Region Of Ukraine
Fig. 2. Distribution of the huchen, Hucho hucho, in the Transcarpatian Region of Ukraine: potential distribution — information obtained from interviewing inspectors of the Transcarpathian Fish Protection Inspection, forestry inspectors, and local people; places of catches — sites, where huchen were actually caught and/or recorded during scientific surveys, in recreational or poacher's fishing gears, places of introduction — sites were huchen were released intentionally or escaped accidentally.
Dataset: Local management and landscape composition affect predatory mites in European wine-growing regions
<p>Data repository of the raw data for the data analysis of the article: "Local management and landscape composition affect predatory mites in European wine-growing regions" published in Agriculture, Ecosystems and Environment Volume 344, 1 March 2023, 108292.</p>
Dataset related to the article: Exploring the recent upsurge in productivity disparities among European regions
Open the record for dataset details and reuse information.
Supplementary material 2 from: Sieber I, Borges P, Burkhard B (2018) Hotspots of biodiversity and ecosystem services: the Outermost Regions and Overseas Countries and Territories of the European Union. One Ecosystem 3: e24719. https://doi.org/10.3897/oneeco.3.e24719
all studies were conducted between 1991 and 2017 .
Supplementary material 8 from: Sieber I, Borges P, Burkhard B (2018) Hotspots of biodiversity and ecosystem services: the Outermost Regions and Overseas Countries and Territories of the European Union. One Ecosystem 3: e24719. https://doi.org/10.3897/oneeco.3.e24719
Appendix of included literature
Fig. 7 in The Rhagionidae or Snipeflies of the Botanical Garden Jean Massart (Brussels-Capital Region, Belgium) with notes on the identity of the rare European species Archicera avarorum Szilády, 1934 and Ptiolina obscura (Fallén, 1814) (Diptera: Rhagionidae)
Fig. 7. Ptiolina obscura (Fallén, 1814), male habitus. © Camille Locatelli.
Fig. 3 in The Rhagionidae or Snipeflies of the Botanical Garden Jean Massart (Brussels-Capital Region, Belgium) with notes on the identity of the rare European species Archicera avarorum Szilády, 1934 and Ptiolina obscura (Fallén, 1814) (Diptera: Rhagionidae)
Fig. 3. Archicera avarorum Szilády, 1934. Female habitus. © Patrick Grootaert.
Turning old foes into new allies – harnessing drainage canals for biodiversity conservation in a desiccated European lowland region
<p>1. Drainage canals are widespread components of agricultural landscapes. Although canals have greatly contributed to biodiversity loss by desiccating wetlands, they have recently attracted conservation attention due to their potential to function as refugia for native species in intensively managed landscapes. However, their conservation role in complex landscapes composed of agricultural fields and desiccated but otherwise untransformed, semi-natural habitats, on which canals still pose a heavy burden, is unknown. Improved understanding of drainage canals and related biodiversity in these landscapes could help unlock their potential and support synergistic land management for nature conservation and water resource management.</p> <p>2. We applied a multitaxon approach, including plants, butterflies, true bugs, spiders and birds, to (1) assess the conservation value of drainage canals with temporary water cover in a heavily drained European lowland region, (2) to test landscape-level and local canal parameters for aiding prioritization among canals, and (3) to propose a reconciliation-based management framework that suits the interest of all stakeholders.</p> <p>3. We found that drainage canals and their banks concentrate more species across most taxa than semi-natural, mostly grassland habitats, possibly due to micro-environmental heterogeneity and the absence of low-intensity annual management compared to grasslands. Canals traversing semi-natural grasslands concentrate particularly high numbers of native species, but agricultural canals also support remarkable species richness. However, agricultural canals are important dispersal corridors for non-native invasive plants, which may negatively affect native biodiversity. Canal size has little effect on biodiversity but habitat stress is an important determinant. The higher the stress (due to sandiness and salinity), the higher is the added value of canals to landscape-wide biodiversity.</p> <p><i>Synthesis and applications.</i> We show that drainage canals can harbour high biodiversity and should therefore be recognized as important novel ecosystems with high conservation value, even when cutting through semi-natural grassland habitats. Canals have previously been considered detrimental to nature conservation due to their association with loss of wetlands. However, by reducing water loss with reversible obstructions, controlling invasive species and applying specific conservation measures, they may be turned into conservation allies without compromising long-term interests of water management and agricultural land use.</p>
ScienceDex guides
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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.