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84 results for “Common model”
Supplementary material 6 from: Lommen STE, Jongejans E, Leitsch-Vitalos M, Tokarska-Guzik B, Zalai M, Müller-Schärer H, Karrer G (2018) Time to cut: population models reveal how to mow invasive common ragweed cost-effectively. NeoBiota 39: 53-78. https://doi.org/10.3897/neobiota.39.23398
Stochastic population growth for alternative seed bank scenarios (graphic results, population dynamics) :
Supplementary material 8 from: Lommen STE, Jongejans E, Leitsch-Vitalos M, Tokarska-Guzik B, Zalai M, Müller-Schärer H, Karrer G (2018) Time to cut: population models reveal how to mow invasive common ragweed cost-effectively. NeoBiota 39: 53-78. https://doi.org/10.3897/neobiota.39.23398
r-cost curves for different seed survival scenarios and reference data sets (graphic results, population dynamics) :
Datasets for "Global Assessment of Atmospheric Forcing Uncertainties in The Common Land Model 2024 Simulations"
<p>This repository provides the datasets for the publication "Global Assessment of Atmospheric Forcing Uncertainties in The Common Land Model 2024 Simulations".</p>
High quality figures of "Global Assessment of Atmospheric Forcing Uncertainties in The Common Land Model 2024 Simulations"
<p>This repository provides the figures for the publication "Global Assessment of Atmospheric Forcing Uncertainties in The Common Land Model 2024 Simulations" in their original resolution, ensuring clarity the high-quality visual representations for readers.</p>
Data from: A unified model explains commonness and rarity on coral reefs
Abundance patterns in ecological communities have important implications for biodiversity maintenance and ecosystem functioning. However, ecological theory has been largely unsuccessful at capturing multiple macroecological abundance patterns simultaneously. Here, we propose a parsimonious model that unifies widespread ecological relationships involving local aggregation, species-abundance distributions, and species associations, and we test this model against the metacommunity structure of reef-building corals and coral reef fishes across the western and central Pacific. For both corals and fishes, the unified model simultaneously captures extremely well local species-abundance distributions, interspecific variation in the strength of spatial aggregation, patterns of community similarity, species accumulation, and regional species richness, performing far better than alternative models also examined here and in previous work on coral reefs. Our approach contributes to the development of synthetic theory for large-scale patterns of community structure in nature, and to addressing ongoing challenges in biodiversity conservation at macroecological scales.
Inlists for paper: Stellar response after stripping as a model for common-envelope outcomes
<p>MESA (r11554) inlists for the models shown the "Stellar response after stripping as a model for common-envelope outcomes" paper (2107.14526). The inlists reproduce both the pre-stripped and stripped stellar models.</p> <p>Contents:</p> <p>strippedStars_MESA_inlists.zip</p> <ul> <li>single_star_evolution<br> - inlist_project<br> - run_star_extras.f</li> <li>stripped_star<br> - inlist_project<br> - run_star_extras.f</li> </ul>
Figure 1 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 1. Diagram of Mediterranean Islands showing endemic genera and species of soricids from the Plio–Quaternary to the present: white shrew silhouettes, current species; grey shrew silhouettes, extinct or with presence in the fossil record. From west to east: species of Nesiotites (extinct) from the Gymnesic Islands; species of Asoriculus (extinct) from the Corso-Sardinian complex; Asoriculus burgioi (extinct) from Sicily; Crocidura sicula sicula (present in the fossil record and extant) and Crocidura sicula esuae (extinct) from the Sicilian–Maltese archipelago; Crocidura zimmermanni (present in the fossil record and extant) from Crete; and Crocidura suaveolens praecypria (extinct) from Cyprus. See text for references.
Figure 2 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 2. Chronological framework of the species used in the study: in black, species related to the tribe Nectogalini; in grey, Crocidura species. The circles highlight the species analysed from different sites sorted biochronologically (connected by a thick line), the squares highlight the species analysed from only one site, and the empty squares highlight the mainland (ancestor) species. Below the species: the site, locality, and molar/s used for estimating body mass are listed.
Figure 4 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 4. Estimations of body masses (in g) of Nesiotites species (row A, lower molars) and Crocidura zimmermanni (row B, lower molars; and row C, upper molars) from different sites ordered chronologically (see Table 2 for site acronyms). The first column shows the predictions of body mass using all of the estimators (white square, LM1; black circle, WM1; grey circle, TRLM1; grey square, AAM1; white circle, TRAAM1) and the following columns represent each measurement separately (LM1, WM1, TRLM1, AAM1, and TRAAM1, respectively). In order to observe the fluctuation of the points, we linked the points with a line. Dotted lines in Nesiotites diagrams (row A) separate the three statistically different subgroups.
Figure 3 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 3. Measurements of mandible, cranium, and postcranial bones. A, cranium: WOC, width of the occipital condyles. B, mandible: TRLM/1, tooth row length of lower molars. C, femur: FL, femur length; FTDp, proximal femoral transversal diameter; FAPDd, distal femoral anteroposterior diameter; FTDd, distal femoral transversal diameter. D, humerus: HL, humerus length; HAPDp, proximal humeral anteroposterior diameter; HAPDd, distal humeral anteroposterior diameter; HTDd, distal humeral transversal diameter. E, tibia: TL, tibia length; TAPDp, proximal tibia anteroposterior diameter; TTDp, proximal tibia transversal diameter; TTDd, distal tibia transversal diameter.
Figure 5 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 5. Diagrams comparing the body mass (in g) of extant relatives and fossil species: A, extinct Asoriculus and Nesiotites species and the extant species of the tribe Nectogalini; B, extinct and extant Crocidura species. Lines indicate the body mass range of groups. See the legend for symbols.
dataset related to article "Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human Patients"
<p> CINZIA CAGNOLI 0000-0001-6863-6687, MICHELA TAIANA 0000-0001-8257-8831, MONICA NIZZARDO 0000-0001-5447-0882, STEFANIA CORTI 0000-0001-5425-969X, VIVIANA PENSATO 0000-0001-9798-2669, ANNA VENERANDO <a href="https://orcid.org/0000-0002-7489-1833">0000-0002-7489-1833</a>, CINZIA GELLERA <a href="https://orcid.org/0000-0002-3582-665X">0000-0002-3582-665X</a>, SILVIA FENU 0000-0002-5233-6580, DAVIDE PAREYSON 0000-0001-6854-765X, RICCARDO MASSON 0000-0002-9311-452X, LORENZO MAGGI 0000-0002-0932-5173, ELEONORA DALLA BELLA 0000-0001-6267-9651, GIUSEPPE LAURIA 0000-0001-9773-020X, RENATO MANTEGAZZA 0000-0002-9810-5737, PIA BERNASCONI 0000-0003-0869-2104, ANGELO POLETTI 0000-0002-8883-0468, SILVIA BONANNO 0000-0002-8823-6821, STEFANIA MARCUZZO 0000-0001-6893-6372.</p>
Highly variable (no clear pattern). All portions of the dorsal views were equally used. In head images the area around the eye, the top of the head, the snout and the throat were all used in similar proportions. P. carbonelli Variable for both views. Snout and middle of the dorsum used in dorsal view. Top of the head most frequently (but not strictly) used in lateral view. P. guadarramae Whole body used for dorsal view (but variable); either throat (most common) or ear region used in head lateral views. P. hispanicus Variable. Anterior portion of snout used more frequently than in other species for both dorsal and head lateral views. P. liolepis Highly variable. Whole body used in most dorsal images, area around the eye and throat used in head lateral views, but other patterns common. P. lusitanicus Highly variable. All parts of the dorsum used (but frequently the most posterior part); area around the ear frequently used in head lateral images. P. tunesiacus Highly variable. Dorsal area near the insertion of the posterior limbs used more frequently than in other species; different regions of the head used, often simultaneously. P. Ʋaucheri Highly variable. Different regions of dorsum (from head to the posterior region) used in dorsal images, all portions of the head, but most frequently the throat, used in lateral images. P. Ʋirescens Highly variable. All parts of both images used. Head and anterior part of the dorsum more used than in other species. in Identification of morphologically cryptic species with computer vision models: wall lizards (Squamata: Lacertidae: Podarcis) as a case study
Highly variable (no clear pattern). All portions of the dorsal views were equally used. In head images the area around the eye, the top of the head, the snout and the throat were all used in similar proportions. P. carbonelli Variable for both views. Snout and middle of the dorsum used in dorsal view. Top of the head most frequently (but not strictly) used in lateral view. P. guadarramae Whole body used for dorsal view (but variable); either throat (most common) or ear region used in head lateral views. P. hispanicus Variable. Anterior portion of snout used more frequently than in other species for both dorsal and head lateral views. P. liolepis Highly variable. Whole body used in most dorsal images, area around the eye and throat used in head lateral views, but other patterns common. P. lusitanicus Highly variable. All parts of the dorsum used (but frequently the most posterior part); area around the ear frequently used in head lateral images. P. tunesiacus Highly variable. Dorsal area near the insertion of the posterior limbs used more frequently than in other species; different regions of the head used, often simultaneously. P. Ʋaucheri Highly variable. Different regions of dorsum (from head to the posterior region) used in dorsal images, all portions of the head, but most frequently the throat, used in lateral images. P. Ʋirescens Highly variable. All parts of both images used. Head and anterior part of the dorsum more used than in other species.
Data from: Towards a common methodology for developing logistic tree mortality models based on ring-width data
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Data from: A unified model explains commonness and rarity on coral reefs
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Data from: Can opportunistically-collected Citizen Science data fill a data gap for habitat suitability models of less common species?
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Data from: Microhabitat selection in the common lizard: implications of biotic interactions, age, sex, local processes, and model transferability among populations
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Integrating laboratory experiments and biogeographic modelling approaches to understand sensitivity to ocean warming in rare and common marine annelids
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The effects of exploratory behavior on physical activity in a common animal model of human disease, zebrafish (Danio rerio)
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R code from: Diagnosing common sources of lack of fit to composition data in fisheries stock assessment models using One-Step-Ahead (OSA) residuals
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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.