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Fig. 3 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species
Fig. 3. Lateral (A) and dorsal (B) views of head of Parascorpaena poseidon (NSMT-P 17865, 97.8 mm SL). Bars indicate 5 mm.
Fig. 4 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species
Fig. 4. Relationships between body width (A); head width (B); snout length (C); interorbital width at vertical midline of eye (D); upper-jaw length (E); maxilla depth (F); postorbital length (G); orbit diameter (H); and separation between opercular spine tips (I) (all as % of SL) and standard length (mm) in Parascorpaena poseidon, showing ontogenetic changes. Star indicates holotype [except for snout length, interorbital width at vertical midline of eye, and upper-jaw length—see text regarding measurements by Chou and Liao (2022)].
Fig. 2 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species
Fig. 2. Variously-sized preserved specimens of Parascorpaena poseidon. A, FMNH 75818, 1 of 27 specimens, 35.3 mm SL, Galle, Sri Lanka; B, FMNH 75818, 1 of 27 specimens, 65.3 mm SL, Galle, Sri Lanka; C, NSMT-P 17865, 97.8 mm SL, Yaku-shima Island, Osumi Islands, Kagoshima, Japan; D, BPBM 27680, 1 of 2 specimens, 115.4 mm SL, Kovalam, Kerala India.
Fig. 1 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species
Fig. 1. Fresh specimen of Parascorpaena poseidon from Kovalam, Kerala, India (BPBM 27680, 1 of 2 specimens, 115.4 mm SL). Photo by J. E. Randall (BPBM).
Fig. 5 in Distributional Range Extension of the Shallow Water Scorpionfish Parascorpaena poseidon (Perciformes: Scorpaenidae), with a Revised Diagnosis of the Species
Fig. 5. Distributional records of Parascorpaena poseidon, based on original description (triangles and star), literature record as P. mossambica (closed circle), and present study (open circles). Star indicates type locality.
Fig. 6 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 6. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model for 2041–2060 (all distribution data and bioclimatic variables; point-wise
Fig. 3 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 3. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model (all distribution data and bioclimatic variables for 1970–2000; point-wise
Fig. 5 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 5. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model for 2021–2040 (all distribution data and bioclimatic variables; point-wise
The Adult Adansonia digitata L. (baobab tree) distribution map derived from very high resolution satelite imagery for 2010s across the Sahel at 1km resolution
<p>The baobab tree (<em>Adansonia digitata</em> <em>L.</em>) is an integral part of rural livelihoods throughout the African continent. However, the combined effects of climate change and increasing global demand for baobab products are currently exerting pressure on the sustainable utilization of these resources. Here we employ sub-meter resolution satellite imagery to identify nearly 3 million baobab trees in the Sahel, a dryland region of 1.5 million km<sup>2</sup>. This achievement is considered an essential step towards improving valuable woody species' management and monitoring system. The map's overall underestimate bias is 0.27. To prevent mismanagement of this specific tree species, we aggregated every single adult baobab tree map to 1 × 1 km grids. We also classified the baobab trees using the tree crown diameters( small: 3-9m; medium 9m-13m; large: >13m). The baobab tree count map is also available for these three different size classes. </p>
F I G U R E 6 in Current and future potential geographical distribution of Bactericera cockerelli: an invasive pest of increasing global importance
F I G U R E 6 Predicted future climatic suitability for tomato potato psyllid (TPP; Bactericera cockerelli) in (a) its native range in North America, and (b) its invasive regions in Australia under a future climate change scenario predicted to the year 2090 in CLIMEX using the general circular model (GCM) CSIRO Mark 3.0, run with the A1B emissions scenario the known global distributions denoted by green colour dots.
F I G U R E 5 in Current and future potential geographical distribution of Bactericera cockerelli: an invasive pest of increasing global importance
F I G U R E 5 Predicted global climatic suitability for tomato potato psyllid (TPP; Bactericera cockerelli) under a future climate change scenario predicted to the year 2090 in CLIMEX using the general circular model (GCM) CSIRO Mark 3.0, run with the A1B emissions scenario.
F I G U R E 2 in Current and future potential geographical distribution of Bactericera cockerelli: an invasive pest of increasing global importance
F I G U R E 2 Predicted global climatic suitability for tomato potato psyllid (TPP; Bactericera cockerelli) under current climatic conditions in its native region in North America. The known global distributions are denoted by green colour dots.
F I G U R E 4 in Current and future potential geographical distribution of Bactericera cockerelli: an invasive pest of increasing global importance
F I G U R E 4 Predicted climatic suitability for tomato potato psyllid (TPP; Bactericera cockerelli) under current climatic conditions in New Zealand under current climatic conditions. The known global distributions are denoted by green colour dots.
F I G U R E 1 in Current and future potential geographical distribution of Bactericera cockerelli: an invasive pest of increasing global importance
F I G U R E 1 Predicted global climatic suitability (ecoclimatic index) for tomato potato psyllid (TPP; Bactericera cockerelli under current climatic conditions using the adjusted parameters given in Table 1 under (a) natural rainfall and (b) as composite of natural rainfall and irrigation based on areas identified by Siebert et al. (2013). The known global distributions are denoted by green colour dots.
F I G U R E 3 in Current and future potential geographical distribution of Bactericera cockerelli: an invasive pest of increasing global importance
F I G U R E 3 Predicted climatic suitability for tomato potato psyllid (TPP; Bactericera cockerelli) under current climatic conditions in Australia current climatic conditions. The known global distributions are denoted by green colour dots.
F I G U R E 7 in Current and future potential geographical distribution of Bactericera cockerelli: an invasive pest of increasing global importance
F I G U R E 7 Predicted future climatic suitability for tomato potato psyllid (TPP; Bactericera cockerelli) in New Zealand under a future climate change scenario predicted to the year 2090 in CLIMEX using the general circular model (GCM) CSIRO Mark 3.0, run with the A1B emissions scenario. The known global distributions denoted by green colour dots.
Fig. 4 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 4. Reliability test for the Miramiola pusilla. Maxent distribution model (bioclimatic variables for 1970–2000; 25 replicates with cross-validation).
Fig. 3 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 3. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model (all distribution data and bioclimatic variables for 1970–2000; point-wise mean for 25 replicates).
Fig. 6 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 6. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model for 2041–2060 (all distribution data and bioclimatic variables; point-wise mean for 25 replicates; CNRM-ESM2-1 (Séférian et al., 2019) climatic model for 3-7.0 Shared Socioeconomic Pathway (Meinshausen et al., 2020).
Fig. 5 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 5. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model for 2021–2040 (all distribution data and bioclimatic variables; point-wise mean for 25 replicates; CNRM-ESM2-1 (Séférian et al., 2019) climatic model for 3-7.0 Shared Socioeconomic Pathway (Meinshausen et al., 2020).
ScienceDex guides
Understand access before you commit
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.