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361 results for “proportions”
Figure. The proportion of benthic abundance for different invertebrate orders relative to the total benthic abundance [%] of the Munzur and Pülümür rivers, representing the mean value of the 2 sites per river. in Macroinvertebrate composition in the metarhithral zones of the Munzur and Pülümür rivers: a preliminary study
Figure. The proportion of benthic abundance for different invertebrate orders relative to the total benthic abundance [%] of the Munzur and Pülümür rivers, representing the mean value of the 2 sites per river.
Fig. 3. Proportions and 95 in Metamasius callizona (Coleoptera: Curculionidae): fertility and larval survival to the third instar in the laboratory
Fig. 3. Proportions and 95% confidence intervals for egg eclosion per 10 d from eggs laid inside leaves by Metamasius callizona. Confidence intervals were calculated using Wilson score intervals (α = 0.05; Wilson 1927).
Figs 2, 3 in Susceptibility of targets to the vampire bat Desmodus rotundus are proportional to their abundance in Atlantic Forest fragments?
Figs 2, 3. Two records of the approach of Desmodus rotundus (É. Geoffroy, 1810): 2, a bat landing on a trunk near a deer (Mazama americana); 3, a bat on the ground very close to a tapir (Tapirus terrestris).
Fig. 1 in Susceptibility of targets to the vampire bat Desmodus rotundus are proportional to their abundance in Atlantic Forest fragments?
Fig. 1. Study area located in the municipalities of ItajÁ and Aporé, state of GoiÁs, BraZil. Black dots represent the sites where the camera traps were set up.
Fig. 7 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 7. Pectoral girdle and forelimb of choristodere reptile Khurendukhosaurus sp. (MPC-MX 1/107) from middle–late Albian (Early Cretaceous), Khuren-Dukh, Mongolia. A. Interclavicle in ventral (A1, A2) and dorsal (A3) views, clavicle facets (A4, A5). B. Right scapulocoracoid in ventral (B1), dorsal (B2, B3), and lateral (B4–B5) views. C. Right humerus, proximal end in proximal view (C1) and dorsal (C2) views, distal end in distal view (C3) and ventral (C4) views. D. Left humerus in dorsal (D1) and ventral (D2) views. E. Right radius in proximal (E1), anterior (E2), posterior (E3), distal (E4), and lateral (E5) views. F. Left radius in anterior (F1), posterior (F2), and lateral (F3) views. Photographs (A1, A3, A4, B1, B2, B4, C, E); explanatory drawings A2, A5, B3, B5, D, F). Scale bars 10 mm.
Fig. 2 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 2. All elements of the newly discovered specimen of the choristoderan reptile Khurendukhosaurus sp. (MPC-MX 1/107) from middle–late Albian (Early Cretaceous), Khuren-Dukh, Mongolia. The bones are disarticulated but preserved in close association. This image shows the elements arranged in anatomical position.
Fig. 6 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 6. Ribs and gastralia of choristodere reptile Khurendukhosaurus sp. (MPC-MX 1/107, A–C, E) from middle–late Albian (Early Cretaceous), Khuren-Dukh, Mongolia and Champsosaurus gigas (D) from Late Paleocene, Wannagan Creek Quarry, USA. A. A cervical rib in dorsal (A1), anterior (A2), and medial (A3) views, reconstruction of cervical rib articulated with a cervical vertebra in lateral view (A4). B. Dorsal ribs (B1–B3) in anterior view. C, D. Sections through the trunk of dorsal vertebrae (number unknown) (C) and eighth dorsal vertebra (D, modified from Erickson 1985). E. Gastralia in anterior view (E1), with an enlargement of their articular surfaces (E2). Scale bars 10 mm. C, D not to scale.
Fig. 9 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 9. Phylogenetic relationships of Khurendukhosaurus within Choristodera based on data from all available specimens. Strict consensus of five most parsimonious trees (MPTs) obtained by TNT (length = 329). Numbers in brackets indicate Bremer branch supports, followed by Bootstrap values. Abbreviations: CBU, Claude Bernard University no. Re 437, coll. Gennevaux 92813; IGM, Geological Institute of the Mongolian Academy of Sciences, Ulan Bataar, Mongolia; MNHN, Muséum National d'Histoire Naturelle, Paris; PKUP, Peking University Paleontological Collections, Beijing, China; SMM, Science Museum Minnesota, USA; TMP, Royal Tyrrell Museum of Palaeontology, Drumheller, Alberta, Canada.
Fig. 8 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 8. Pelvic girdle and hind limbs of choristodere reptile Khurendukhosaurus sp. (MPC-MX 1/107) from middle–late Albian (Early Cretaceous), Khuren-Dukh, Mongolia. A. Associated ilium, pubis, and ischium in dorsal (A1), ventral (A2), lateral (A3, A4), and medial (A5, A6) views. B. Left femur in ventral (B1) and anterior (B2) views. C. Right tibia in lateral (C1), anterior (C2), and medial (C3) views. D. Left fibula in proximal (D1), medial (D2, D4), distal (D3), anterior (D4), and lateral (D5) views. Photographs (A1, A3, A5, B, C, D1–D3), explanatory drawings (A2, A4, A6, D4–D6).
Fig. 1 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 1. Map showing Khuren-Dukh Formation, Mongolia and localities where long-necked choristoderes have been found. 1, Shokawa ikoi, Okurodani Formation, Barremian–Aptian (Evans and Manabe 1999); 2, Hyphalosaurus baitaigouensis, Baitaigou, Yixian Formation, Barremian–Aptian (Ji et al. 2004); 3, Hyphalosaurus sp., Luojiagou, Yixian Formation, Barremian–Aptian (Zhang et al. 2012; the Tianyu specimens with locality information are all from Badaoyingzi, Luojiagou); 4, Hyphalosaurus lingyuanensis, Dawangzhangzi, Yixian Formation, Barremian–Aptian (Fanzhangzi) (Gao et al. 1999; Gao and Ksepka, 2008); 5, Khurendukhosaurus orlovi and Khurendukhosaurus sp., Khuren-Dukh Formation, middle–late Albian (Sigogneau-Russell and Efimov 1984; Efimov and Storrs 2000); 6, Khurendukhosaurus sp., Mogoito, Murtoi Formation, Barremian?–Aptian (Efimov 1996; Skutschas 2008; Skutschas and Vitenko 2017); 7, cf. Khurendukhosaurus sp., Bol'shoi Kemchung 3, Ilek Formation, Early Cretaceous (Skutschas and Vitenko 2017).
Fig. 4 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 4. Dorsal vertebrae (A–F) of choristodere reptile Khurendukhosaurus sp. (MPC-MX 1/107) from middle–late Albian (Early Cretaceous), KhurenDukh, Mongolia; in anterior (A1–F1), lateral (A2–F2), posterior (A3–F3), dorsal (A4–F4), and ventral (A5–F5) views.
Fig. 5 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 5. Caudal vertebrae (A–F) of choristodere reptile Khurendukhosaurus sp. (MPC-MX 1/107) from middle–late Albian (Early Cretaceous), KhurenDukh, Mongolia; in anterior (A1–F1), lateral (A2–F2), posterior (A3–F3), dorsal (A4–F4), and ventral (A5–F5) views. Based on morphology, the vertebrae are arranged in an approximate proximal to distal sequence.
Fig. 3 in Revealing body proportions of the enigmatic choristodere reptile Khurendukhosaurus from Mongolia
Fig. 3. Cervical vertebrae (A–G) of choristodere reptile Khurendukhosaurus sp. (MPC-MX 1/107) from middle–late Albian (Early Cretaceous), KhurenDukh, Mongolia; in anterior (A1–G1), lateral (A2–G2), posterior (A3–G3), dorsal (A4–G4), and ventral (A5–G5) views. The precise anatomical order of these seven cervical vertebrae is uncertain, but vertebrae D, E, and F may be associated.
Decadal Diatom Decline - Proportions for diatoms, haptophytes and cryptophytes
<div> <div> <div> <div> <p>This dataset is associated with the "Decadal Diatom Decline" preprint. It includes files that represent the proportion of total chlorophyll <em>a</em> attributed to different phytoplankton groups.</p> <ul> <li><strong>PDiatom</strong>: The percentage of total chlorophyll <em>a</em> contributed by diatoms.</li> <li><strong>PHapto</strong>: The percentage of total chlorophyll <em>a</em> contributed by haptophytes.</li> <li><strong>PCrypto</strong>: The percentage of total chlorophyll <em>a</em> contributed by cryptophytes.</li> </ul> <p>Each file (PDiatom, PHapto, PCrypto) follows the same format, showing the chlorophyll contribution percentages for these specific groups.</p> </div> </div> </div> </div> <div> <div> <div> </div> </div> </div>
ATACSeq fastq files associated with the manuscript entitled 'Interspecies transcriptome analyses identify genes that control the development and evolution of limb skeletal proportion'
<p>This next-generation sequencing dataset is associated with the research manuscript entitled ‘<em>Interspecies transcriptome analyses identify genes that control the development and evolution of limb skeletal proportion</em>’ (https://www.biorxiv.org/content/10.1101/754002v2).</p> <p>The zipped folder ‘<strong>Zenodo_Saxena_etal_2021_ATACSeq_FastqFiles</strong>’ contains raw/unprocessed ATACSeq Fatsq read files for postnatal day 5 (P5) mouse (Mus) and jerboa (Jac) cartilage samples (Metatarsal = MT; Radius/Ulna = RU).</p> <p>> The <strong>Jac_P5</strong> subfolder contains paired-end reads (R1 and R2) for three jerboa metatarsals (MT1-3) and radius/ulna (RU1-3) biological replicates.</p> <p>> The <strong>Mus_P5</strong> subfolder contains paired-end reads (R1 and R2) for two mouse metatarsals (MT1-2) and radius/ulna (RU1-2) biological replicates.</p>
Text-fig. 5. The generic composition of the rodent faunas on the family and subfamily level. The black line sets apart subfamilies of the Muridae (right side) from other rodents (left). The proportion of murid genera increases over time. in Generically Speaking, A Survey On Neogene Rodent Diversity At The Genus Level In The Now Database
Text-fig. 5. The generic composition of the rodent faunas on the family and subfamily level. The black line sets apart subfamilies of the Muridae (right side) from other rodents (left). The proportion of murid genera increases over time.
Text-fig. 6. Boxplots showing the proportion of mf2 in relation to the sum of the occlusal area in the five families of extinct sloths. in Unexpected Inhibitory Cascade In The Molariforms Of Sloths (Folivora, Xenarthra): A Case Study In Xenarthrans Honouring Gerhard Storch'S Open-Mindedness
Text-fig. 6. Boxplots showing the proportion of mf2 in relation to the sum of the occlusal area in the five families of extinct sloths.
Figure 5 in Locomotion in terrestrial mammals: the influence of body mass, limb length and bone proportions on speed
Figure 5. Regression plots of anatomical variables to log running speed in km h-1, showing the distinct curvilinearity of some of the samples, in this case, log forelimb length in mm (a) and olecranon process/radius ratio (b). The polynomial regression model yielded a significantly better fit to the data than ordinary least squares regression lines. For equation see Table 5.
Figure 1. Phylogenetic relationships between the 76 in Locomotion in terrestrial mammals: the influence of body mass, limb length and bone proportions on speed
Figure 1. Phylogenetic relationships between the 76 species of mammals used in the study. Numbers adjacent to the nodes refer to split ages in units of millions of years. Total height of tree is 85 million years. Literature sources used in constructing the tree are Kielan-Jaworowska et al. (1979), Bennett (1980), Janis (1982), Savage & Russel (1983), Lanave et al. (1985), Shoshani (1986), Janis & Scott (1987), Wayne & O'Brien (1987), Gentry & Hooker (1988), Flynn et al. (1988), Novacek et al. (1988), Padmadisastra (1988), Prothero et al. (1988), Tassy & Shoshani (1988), Georgiadis et al. (1990), Marshall (1990), Miyamoto et al. (1990), Nowak (1991), Geffen et al. (1992), Novacek (1992a,b), Garland & Janis (1993), Wyss & Flynn (1993), Flynn (1996), Hunt (1996), Foote et al. (1999) and Penny et al. (1999).
Figure 3 in Locomotion in terrestrial mammals: the influence of body mass, limb length and bone proportions on speed
Figure 3. Regression plots of independent contrasts for fore limb parameters. Log running speed is in km h-1. a, Fore limb length in mm/3÷body mass in kg; b, radius/humerus ratio; c, metacarpus/humerus ratio; d, olecranon process length in mm/ 3÷body mass in kg. Regression lines fitted to the contrasts by means of least squares (model I) analysis.
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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.