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Fig. 4 in Effects of trap locations, pheromone source, and temperature on red palm weevil surveillance (Coleoptera: Dryophthoridae)
Fig. 4. Mean number of captured red palm weevils (± SE) using 5 and 8 d fermented dates as kairomones. Bars marked with different letters are significantly different (ANOVA, GLM procedure, followed by LSD at P <0.05).
Fig. 3 in Effects of trap locations, pheromone source, and temperature on red palm weevil surveillance (Coleoptera: Dryophthoridae)
Fig. 3. Mean number of captured male and female red palm weevils (± SE) per trap per wk in Ferrolure and Rhylure traps. Bars marked with different letters are significantly different (ANOVA, GLM procedure, followed by LSD at P <0.05).
Fig. 2 in Effects of trap locations, pheromone source, and temperature on red palm weevil surveillance (Coleoptera: Dryophthoridae)
Fig. 2. Mean temperature and mean number of captured weevils per trap per wk in Ferrolure and Rhylure traps.
Baseline and Future (2050s and 2090s) Climate Suitability Scores for 116 Useful Tree Species and 220 locations from Côte d'Ivoire, Ghana and Guinea
<p>Climate suitability scores were calculated for 116 Useful Tree Species identified by filtering Top830+ native tree species from Côte d'Ivoire, Ghana and Guinea via the <a href="https://patspo.shinyapps.io/GlobalUsefulTrees/">GlobalUsefulNativeTrees</a> database and checking for the availability of globally observed environmental ranges from the <a href="https://doi.org/10.5281/zenodo.13132613">TreeGOER</a> database.</p> <ul> <li>Score = 3 means that in 'environmental space' the planting site occurs within the 25% - 75% species's range (as documented in the <a href="https://onlinelibrary.wiley.com/doi/full/10.1111/gcb.16914" target="_blank" rel="noopener">TreeGOER</a> ) for all variables</li> <li>Score = 2 corresponds to the 5% - 95% species's range for all variables. For some variables, the planting site occurs outside the 25% - 75% species's range.</li> <li>Score = 1 corresponds to the 0% - 100% species's range for all variables. For some variables, the planting site occurs outside the 5% - 95% species's range.</li> <li>Score = 0 means that the planting site occurs outside the 0% - 100% species's range for some of the variables</li> <li>Score = -1 means that the species is not documented by TreeGOER</li> </ul> <p>Locations corresponded to cities and weather stations from the three target countries sourced from the <a href="https://doi.org/10.5281/zenodo.10004594">CitiesGOER</a> and <a href="https://doi.org/10.5281/zenodo.12679832">ClimateForecasts</a> databases, respectively. Both these databases provide bioclimatic conditions for the historical (baseline) and three future climate change scenarios. Bioclimatic variables for future climates correspond to the median values from 24 Global Climate Models (GCMs) for Shared Socio-Economic Pathway (SSP) 1-2.6 for the 2050s (2041-2060), from 21 GCMs for SSP 3-7.0 for the 2050s and from 13 GCMs for SSP 5-8.5 for the 2090s.</p> <p>Investigations were made for two different sets of bioclimatic variables, allowing for sensitivity analysis:</p> <ul> <li>One set of bioclimatic variables included BIO01 (mean annual temperature), BIO12 (total annual precipitation), climaticMoistureIndex, monthCountByTemp10 (number of months with average temperature above 10 degrees), growingDegDays5, BIO05 (maximum temperature of the warmest month), BIO06 (minimum temperature of teh coldest month), BIO16 (precipitation of the wettest quarter), BIO17 (precipitation of the driest quarter) and MCWD (Maximum Climatological Water Deficit). These are the same bioclimatic variables available internally in the <a href="https://worldagroforestry.org/output/globalusefulnativetrees">GlobalUsefulNativeTrees</a> for climate filtering.</li> <li>One set only included BIO01 (mean annual temperature), which is the single bioclimatic variables available for the BGCI <a href="https://cat.bgci.org/">Climate Assessment Tool</a>.</li> </ul> <p>Calculations were made with similar scripting pipelines in the <em>R</em> statistical environment as documented here: <a href="https://rpubs.com/Roeland-KINDT/1168650">https://rpubs.com/Roeland-KINDT/1168650</a>. These scripts use similar calculations methods as those used for the global case studies of the TreeGOER manuscript (Kindt <a href="https://onlinelibrary.wiley.com/doi/10.1111/gcb.16914">2023</a>), and used internally in the <a href="https://worldagroforestry.org/output/globalusefulnativetrees">GlobalUsefulNativeTrees</a> online database. Interested readers should especially refer to the manuscript for further details on methods used and their justification.</p> <p>The maps show the frequency distribution of tree species with climate scores 3, 2, 1 and 0, excluding 18 species not documented by the TreeGOER.</p> <p> </p> <p><strong>References</strong></p> <ul> <li>Kindt, R. (2023). TreeGOER: A database with globally observed environmental ranges for 48,129 tree species. Global Change Biology, 00, 1–16. <a href="https://onlinelibrary.wiley.com/doi/10.1111/gcb.16914">https://onlinelibrary.wiley.com/doi/10.1111/gcb.16914</a>.</li> <li>Kindt, R. (2024). TreeGOER: Tree Globally Observed Environmental Ranges (2024.07) [Data set]. Zenodo. <a href="https://doi.org/10.5281/zenodo.13132613" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.13132613</a></li> <li>Kindt, R., Graudal, L., Lillesø, JP.B. <em>et al.</em> (2023). GlobalUsefulNativeTrees, a database documenting 14,014 tree species, supports synergies between biodiversity recovery and local livelihoods in landscape restoration. <em>Sci Rep</em> <strong>13</strong>, 12640. <a href="https://doi.org/10.1038/s41598-023-39552-1">https://doi.org/10.1038/s41598-023-39552-1</a></li> <li>Kindt, R. (2023). CitiesGOER: Globally Observed Environmental Data for 52,602 Cities with a Population ≥ 5000 (2023.10) [Data set]. Zenodo. <a href="https://doi.org/10.5281/zenodo.10004594" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.10004594</a></li> <li>Kindt, R. (2024). ClimateForecasts: Globally Observed Environmental Data for 15,504 Weather Station Locations (2024.07) [Data set]. Zenodo. <a href="https://doi.org/10.5281/zenodo.12679832" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.12679832</a></li> <li>Fick, S. E., & Hijmans, R. J. (2017). WorldClim 2: New 1‐km spatial resolution climate surfaces for global land areas. <em>International Journal of Climatology</em>, <em>37</em>(12), 4302–4315. <a href="https://doi.org/10.1002/joc.5086">https://doi.org/10.1002/joc.5086</a></li> <li>Title, P. O., & Bemmels, J. B. (2018). ENVIREM: An expanded set of bioclimatic and topographic variables increases flexibility and improves performance of ecological niche modeling. <em>Ecography</em>, <em>41</em>(2), 291–307. <a href="https://doi.org/10.1111/ecog.02880">https://doi.org/10.1111/ecog.02880</a></li> <li>Opendatasoft (2023) Geonames - All Cities with a population > 1000. <a href="https://public.opendatasoft.com/explore/dataset/geonames-all-cities-with-a-population-1000/information/?disjunctive.cou_name_en&sort=name">https://public.opendatasoft.com/explore/dataset/geonames-all-cities-with-a-population-1000/information/?disjunctive.cou_name_en&sort=name</a> (accessed 22-JULY-2023)</li> <li>Meteostat (2024) Weather stations: Lite dump with active weather stations. <a href="https://github.com/meteostat/weather-stations">https://github.com/meteostat/weather-stations</a> (accessed 17-FEB-2024)</li> </ul> <p> </p> <p><strong>Funding</strong></p> <p>The data sets and maps available in this archive were created within the context of an agreement between The International Centre for Research in Agroforestry (ICRAF) and WORLD UNIVERSITY SERVICE OF CANADA (WUSC) for a <em><a href="https://ceci.org/en/projects/nature-based-climate-adaptation-guinean-forest-west-africa-sbn-guinean-forests">Nature-based climate adaptation project in the Guinean forests of West Africa (NbS Guinean Forests)</a></em> funded by <a href="https://www.international.gc.ca/global-affairs-affaires-mondiales/home-accueil.aspx?lang=eng">Global Affairs Canada</a>.</p>
Social Media Usage According to Different Locations
<p>This ai-generated dataset provides detailed information on how individuals allocate their time across various social media platforms, including Facebook, Twitter, Instagram, YouTube, Snapchat, TikTok, LinkedIn, WhatsApp, and Pinterest. Each entry represents the number of hours spent on each platform and includes location data to explore geographic trends in social media consumption.</p> <p>The dataset is ideal for analyzing:</p> <ul> <li>Time distribution across social platforms.</li> <li>Location-based patterns in social media usage.</li> <li>Comparative studies on platform preferences.</li> </ul> <p>Perfect for social behavior analysis and data-driven marketing insights!</p>
Image 1. Locations where Lanthanotus borneensis has been recorded. Green spots indicate findings from 1912 in First record of the Borneo Earless Monitor Lanthanotus borneensis (Steindachner, 1877) (Reptilia: Lanthanotidae) in West Kalimantan (Indonesian Borneo)
Image 1. Locations where Lanthanotus borneensis has been recorded. Green spots indicate findings from 1912-discoveries, yellow spots 1912–1966 and red spot 1966-present.
Locations where video evidence for the Ivory-billed Woodpecker was obtained in Louisiana
<p>This video confirms the locations where evidence for the persistence of the Ivory-billed Woodpecker was obtained in the Pearl River swamp in Louisiana in 2006 and 2008. A drone is launched from the locations where the videos were obtained. Trees that appear in the videos were still recognizable when the drone video was obtained in 2021. As the drone gains altitude, the rocket towers at Stennis Space Center and other recognizable landmarks come into view. This video debunks speculations that the bird in the 2006 video could be another <em>Camphephilus</em> woodpecker that was filmed in South America.</p>
Text-fig. 1. Location map and original field label of T 68, fragment of arsinoithere upper molar from Oued Grigema, Tunisia. in Arsinoitherium (Embrithopoda) And Other Large Mammals And Plants From The Oligocene Of Tunisia
Text-fig. 1. Location map and original field label of T 68, fragment of arsinoithere upper molar from Oued Grigema, Tunisia.
Text-fig. 13. Scatter diagram of m1 length vs SDQ for pre-Eemian (time slice 5) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain. in Independent Water Vole (Mimomys Savini, Arvicola: Rodentia, Mammalia) Lineages In Italy And Central Europe
Text-fig. 13. Scatter diagram of m1 length vs SDQ for pre-Eemian (time slice 5) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain.
Text-fig. 1. Location of Ivanovce Pliocene primate site in Slovakia within the wider area of the Carpathians-Pannonian Basin (white circle). The northern wall of the former limestone quarry at Ivanovce near Trenčín in western Slovakia. Several karst fillings provided a rich early Pliocene vertebrate assemblage. a: schematic sketch of the site showing the location of different karst fillings, b: photo of the same site during the palaeontological research in 1960s. in Allosorex Stenodus Fejfar, 1966 (Eulipotyphla, Soricidae): Re-Description Of Type Material And Re-Interpretation Of Its Fossil Record
Text-fig. 1. Location of Ivanovce Pliocene primate site in Slovakia within the wider area of the Carpathians-Pannonian Basin (white circle). The northern wall of the former limestone quarry at Ivanovce near Trenčín in western Slovakia. Several karst fillings provided a rich early Pliocene vertebrate assemblage. a: schematic sketch of the site showing the location of different karst fillings, b: photo of the same site during the palaeontological research in 1960s.
Text-fig. 11. Scatter diagram of m1 length vs SDQ for Würmian/Weichselian (time slice 3) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and extant Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain. in Independent Water Vole (Mimomys Savini, Arvicola: Rodentia, Mammalia) Lineages In Italy And Central Europe
Text-fig. 11. Scatter diagram of m1 length vs SDQ for Würmian/Weichselian (time slice 3) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and extant Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain.
Text-fig. 12. Scatter diagram of m1 length vs SDQ for Eemian (time slice 4) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain. in Independent Water Vole (Mimomys Savini, Arvicola: Rodentia, Mammalia) Lineages In Italy And Central Europe
Text-fig. 12. Scatter diagram of m1 length vs SDQ for Eemian (time slice 4) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain.
Text-fig. 4. Location Map of the examined water vole localities. From Masini et al. (2007), modified. 1: Madrid, surroundings, 2: Graz, 3: Eisfeld, 4: Langen, 5: Delta Po, 6: Rovigo, 7: Ferrara, 8: Calabria, 9: Caverna degli Orsi, 10: Arma delle Manie, 11: Riparo Mochi, 12: Grotta di Castelcivita, 13: Grotta della Serratura, 14: Grotta del Romito, 15: Scario Grotta Grande, 16: Grotta di Cucigliana, 17: Upper Valdarno Campitello, 18: Riparo di Visogliano, 19: Isernia La Pineta, 20: Baume Gigny, 21: Baume Moula Guercy, 22: Grotte de L'Eglise, 23: Grotte-Abri Suard, 24: Grotte d'Artenac, 25: Pié Lombard, 26: Abri Vaufrey, 27: Grotte du Lazaret, 28: Abri Gaudry, 29: Pisede, 30: Euerwanger Bühl, 31: Kemathenhöhle, 32: Krockstein (Rübeland 1), 33: Burgtonna, 34: Parkhöhle (Weimar), 35: Stuttgart- Untertürkheim, 36: Taubach, 37: Ehringsdorf, 38: Plaidter-Hummerich, 39: Mosbach, 40: Petersbuch 1, 41: Bilzingsleben, 42: Miesenheim 1, 43: Voigtstedt, 44: Untermassfeld. See Table 1 for symbol explanations. in Independent Water Vole (Mimomys Savini, Arvicola: Rodentia, Mammalia) Lineages In Italy And Central Europe
Text-fig. 4. Location Map of the examined water vole localities. From Masini et al. (2007), modified. 1: Madrid, surroundings, 2: Graz, 3: Eisfeld, 4: Langen, 5: Delta Po, 6: Rovigo, 7: Ferrara, 8: Calabria, 9: Caverna degli Orsi, 10: Arma delle Manie, 11: Riparo Mochi, 12: Grotta di Castelcivita, 13: Grotta della Serratura, 14: Grotta del Romito, 15: Scario Grotta Grande, 16: Grotta di Cucigliana, 17: Upper Valdarno Campitello, 18: Riparo di Visogliano, 19: Isernia La Pineta, 20: Baume Gigny, 21: Baume Moula Guercy, 22: Grotte de L'Eglise, 23: Grotte-Abri Suard, 24: Grotte d'Artenac, 25: Pié Lombard, 26: Abri Vaufrey, 27: Grotte du Lazaret, 28: Abri Gaudry, 29: Pisede, 30: Euerwanger Bühl, 31: Kemathenhöhle, 32: Krockstein (Rübeland 1), 33: Burgtonna, 34: Parkhöhle (Weimar), 35: Stuttgart- Untertürkheim, 36: Taubach, 37: Ehringsdorf, 38: Plaidter-Hummerich, 39: Mosbach, 40: Petersbuch 1, 41: Bilzingsleben, 42: Miesenheim 1, 43: Voigtstedt, 44: Untermassfeld. See Table 1 for symbol explanations.
FIG. 4 in Statistical comparisons of late Caradoc (Ordovician) brachiopod faunas around the Iapetus Ocean, and terranes located around Australia, Kazakhstan and China
FIG. 4. — Proposed palaeogeographic reconstruction; Kazakh terranes: 1, Altai-Sayan; 2, Chu-Ili; 3, Chingiz; limits of terranes unknown. Scale bar: 4000 km.
FIG. 3 in Statistical comparisons of late Caradoc (Ordovician) brachiopod faunas around the Iapetus Ocean, and terranes located around Australia, Kazakhstan and China
FIG. 3. — Assemblage scores on axes 1 and 2 of detrended correspondence analysis (DCA) based on presence/absence of genera. Key: same as Figure 2.
FIG. 2 in Statistical comparisons of late Caradoc (Ordovician) brachiopod faunas around the Iapetus Ocean, and terranes located around Australia, Kazakhstan and China
FIG. 2. — Cluster analysis on presence/absence data of 27 localities using 173 genera; UPGMA, Dice Index of similarity (values are displayed on the vertical axis). Data: see Appendix. Shaded areas represent the five clusters numbered 1 to 5. Key for assemblage: see Appendix.
Figure 14 Type locations. A in Paraquanothrus n. gen. from freshwater rock pools in the USA, with new diagnoses of Aquanothrus, Aquanothrinae, and Ameronothridae (Acari, Oribatida)
Figure 14 Type locations. A – type location of Paraquanothrus grahamin. sp., on barren sandstone ('slickrock fin') near Moab, Utah; B – same, closeup of dry 'pan' (shallow rock pool; cell phone and∼15 cm ruler for scale); C – same general location, small water-filled pan containing more than 100 individuals∼(10 cm pipette for scale); D-F – type location of Paraquanothrus spoonerin. sp., Heggie's Rock, Georgia, general view (D) and small dry rock pools (E-F) containing mites, vegetated by Black Rock Moss (Grimmia laevigata(Bird.)) and Elf Orpine (Diamorpha smalliiBritton ex Small). Photographs contributed by Tim Graham (A-C) and John Spooner (D-F).
Text-fig. 6. The riparian/swamp forest structure of the village of Sakarcaören in the late Miocene, location within the east part of GVP, and comparison with the other forest types from early Miocene of GVP (Akkemik et al. 2009, 2016, 2017, Bayam et al. 2018). in The First Glyptostroboxylon And Taxodioxylon Descriptions From The Late Miocene Of Turkey And Palaeoclimatological Evaluation
Text-fig. 6. The riparian/swamp forest structure of the village of Sakarcaören in the late Miocene, location within the east part of GVP, and comparison with the other forest types from early Miocene of GVP (Akkemik et al. 2009, 2016, 2017, Bayam et al. 2018).
Text-fig. 3. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori. a: part of fertile pinnule; b: one practically complete sorus located on the terminal part of a lateral vein; c: sorus with four visible sporangia; d: partly damaged sorus with three visible sporangia; e: two neighbouring sori. Locality: the borehole IK-675, depth 961.7 m. Scale 1 mm (a, b, e), 500 Μm (c), 100 Μm (d). in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 3. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori. a: part of fertile pinnule; b: one practically complete sorus located on the terminal part of a lateral vein; c: sorus with four visible sporangia; d: partly damaged sorus with three visible sporangia; e: two neighbouring sori. Locality: the borehole IK-675, depth 961.7 m. Scale 1 mm (a, b, e), 500 Μm (c), 100 Μm (d).
Text-fig. 1. Sampling areas in Çankırı province: the village of Sakarcaören near to the town of Orta (green circle) in the east of GVP, and the other sites (yellow circles), volcanic centers (red circles) and the border of GVP. The sites marked as yellow circles: ELM, Elmali village; SOG, Soguksu National Park; BUG, Bugralar village; INO, Inozu Valley South Side; INL, Inozu Valley North Side; KAR, Karasar village; MEN, Menceler Plateau; KIR, Kiraluc Site near Nuhhoca village; AGU, Asagiguney village; KUZ, Kuzca village (Bayam et al. 2018); PEL, Pelitcik village (Akkemik et al. 2009); GUD, Gudul (Akkemik et al. 2017); HOC, Hoçaş village and KOZ, Kozyaka village (Akkemik et al. 2016). The sites located in the western part (INO, INL, KAR, MEN, KIR, AGU, KUZ, HOC and KUZ) are from early – middle Burdigalian and Hancili Formation (Altun et al. 2002, Akbaş et al. 2002). The sites in the central part (GUD, BUG, ELM, PEL and SOG) are from middle – late Burdigalian, Pazar Formation (Kazancı 2012, Sen et al. 2017), and finally the fossil site in the east part of GVP is the late Miocene, Hüyükköy Formation (Sengüler 2007). in The First Glyptostroboxylon And Taxodioxylon Descriptions From The Late Miocene Of Turkey And Palaeoclimatological Evaluation
Text-fig. 1. Sampling areas in Çankırı province: the village of Sakarcaören near to the town of Orta (green circle) in the east of GVP, and the other sites (yellow circles), volcanic centers (red circles) and the border of GVP. The sites marked as yellow circles: ELM, Elmali village; SOG, Soguksu National Park; BUG, Bugralar village; INO, Inozu Valley South Side; INL, Inozu Valley North Side; KAR, Karasar village; MEN, Menceler Plateau; KIR, Kiraluc Site near Nuhhoca village; AGU, Asagiguney village; KUZ, Kuzca village (Bayam et al. 2018); PEL, Pelitcik village (Akkemik et al. 2009); GUD, Gudul (Akkemik et al. 2017); HOC, Hoçaş village and KOZ, Kozyaka village (Akkemik et al. 2016). The sites located in the western part (INO, INL, KAR, MEN, KIR, AGU, KUZ, HOC and KUZ) are from early – middle Burdigalian and Hancili Formation (Altun et al. 2002, Akbaş et al. 2002). The sites in the central part (GUD, BUG, ELM, PEL and SOG) are from middle – late Burdigalian, Pazar Formation (Kazancı 2012, Sen et al. 2017), and finally the fossil site in the east part of GVP is the late Miocene, Hüyükköy Formation (Sengüler 2007).
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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.