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165 results for “late life”
Data-driven model enhancement of late-life lithium-ion batteries
<p>Suplement dataset for the paper "Data-driven model enhancement of late-life lithium-ion batteries"</p>
Fig. 1 in Three shell types in Mardinella daviesi indicate the evolution of a paratrimorphic life cycle among late Paleocene soritid benthic foraminifera
Fig. 1. Measured column of the Qorban member in the study locality. A. Position of the Qorban section in the general map of Iran. B. Satellite image with the position of the section base (star). C. Qorban Member stratigraphy with indication of the four Mardinella-rich levels studied in this work. Abbreviations: Fm., Formation; Maas., Maastrichtian; SBZ, Shallow Benthic Zones; U.C., Upper Cretaceous.
Fig. 3 in Three shell types in Mardinella daviesi indicate the evolution of a paratrimorphic life cycle among late Paleocene soritid benthic foraminifera
Fig. 3. Megalospheric forms of soritid foraminifer Mardinella daviesi (Henson, 1950) from the Thanetian, Paleocene of Iran. A. Gmm13980F41b, centred section of a gamont (A2) individual. C, E, G. Gmm13980F39a, Gmm13980F39c, Gmm13980F41c, respectively, juvenile schizonts (A1) in equatorial (C, G) and axial (E) views. B, H. Gmm13980F40e, Gmm13980F41d, respectively, equatorial section of an adult schizont. D. Gmm13980F39b, subaxial sections of two adult schizonts. F. Gmm13980F39d, equatorial section of an adult schizont; note the crosswise oblique disposition of pillars. Scale bar 1 mm.
Fig. 2. Microspheric B in Three shell types in Mardinella daviesi indicate the evolution of a paratrimorphic life cycle among late Paleocene soritid benthic foraminifera
Fig. 2. Microspheric B forms (agamonts) of soritid foraminifer Mardinella daviesi (Henson, 1950) from the Thanetian, Paleocene of Iran. A. Gmm13980F40a, subaxial oblique section; note the brood chambers in the adult reproductive stage of growth (arrows). B. Gmm13980F40b, axial section showing empty brood chambers (two-headed arrow) on both sides of the specimen. C. Gmm13980F40c, subequatorial section. D. Gmm13980F40d, oblique section with some brood chambers (two-headed arrow). E. Gmm13980F41a, fragment of shell with five brood chambers; note the irregularly disposed beams. Scale bar 1 mm.
Figure 9 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 9. Phylogenetic relationships within Eryopidae as found in the present analysis, with the most important synapomorphies mapped onto nodes. See Appendix A for character definitions and a matrix, and see the text for a complete list of results.
Figure 8 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 8. Morphometrics of eryopiform skulls, depicting crucial skull proportions relative to size. Arrows in (a) highlight ontogeny in O. labyrinthicus and S. haeuseri.
Figure 6 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 6. Cranial morphology in eryopid temnospondyls, exemplified by reconstructed skull dorsal views. (a) Actinodon frossardi (after Werneburg, 1997), (b) Osteophorus roemeri (after Meyer, 1860), (c) Glaukerpeton avinoffi (after Werneburg and Berman, 2012), (d) Onchiodon labyrinthicus (after Boy, 1990), (e) Onchiodon thuringiensis (after Werneburg, 2008), (f) Clamorosaurus nocturnus (after Gubin, 1983, and photographs courteously provided by Ralf Werneburg), (g) Eryops sp. from the Moran Formation (MCZ 1914), (h) Eryops anatinus (AMNH 4310), (i) Eryops megacephalus (MCZ 1129). Darker shading figures depressions on the dorsal side of the skull roof.
Figure 7 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 7. Morphospace occupation of eryopiform skulls, showing differences in ontogenetic change and morphometric variance between Onchiodon labyrinthicus and Sclerocephalus spp. and adult skulls of other eryopids. (a) PC1–PC2 axes, (b) areas occupied by immature Onchiodon and Sclerocephalus compared, (c) close-up of (a) with focus on variation in O. labyrinthicus, and (d) PC1 plotted against size.
Figure 2 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 2. Larger juveniles of Onchiodon labyrinthicus Geinitz. (a) LFUG 13570, (b) LFUG 13501, (c) MMG SaP 356, (d) LFUG 13391, (e) LFUG 13398, (f) LFUG 13609, (g) LFUG 13047. Darker shading figures depressions on the dorsal side of the skull roof. Scale equals 10 mm.
Figure 4 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 4. Reconstruction of skulls in dorsal view Onchiodon labyrinthicus Geinitz. (a) MMG SaP 237, (b) LFUG 13343, (c) LFUG 13405, (d) MMG SaP 356, (e) LFUG 13391, (f) LFUG 13570, (g) LFUG 13501, (h) LFUG 13292. Darker shading figures depressions on dorsal side of skull roof. Scale equals 10 mm.
Figure 5 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 5. Palate of Onchiodon labyrinthicus Geinitz, in ventral view. (a) LFUG 13394, (b) LFUG 13514. Darker grey is the inner side of the skull roof. Scale equals 10 mm.
Figure 3 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 3. Ontogeny of the dermal ornament in Onchiodon labyrinthicus Geinitz. (a) LFUG 13343, (b) MMG SaP 390, (c) MMG SaP 356, (d) MMG SaP 361, (e) LFUG 13395, (f) LFUG 13391, (g) LFUG 13570, (h) LFUG 13292.
Single cell transcriptomics unveiled that early life BDE-99 exposure reprogrammed the gut-liver axis to promote a pro-inflammatory metabolic signature in male mice at late adulthood (Part 1/2)
Open the record for dataset details and reuse information.
Single cell transcriptomics unveiled that early life BDE-99 exposure reprogrammed the gut-liver axis to promote a pro-inflammatory metabolic signature in male mice at late adulthood (Part 2/2)
Open the record for dataset details and reuse information.
Early, typical, and late talkers: an exploratory study on predictors of language development in the first two years of life
<p>Background: The consensus in scientific literature is that each child undergoes a unique linguistic development path, albeit with shared developmental stages. Some children excel or lag behind their peers in language skills. Consequently, a key challenge in language acquisition research is pinpointing factors influencing individual differences in language development.</p> <p>Methods: We observed children longitudinally from 3 to 24 months of life to explore early predictors of vocabulary size. Based on the productive vocabulary size of children at 24 months, 30 children met our sample selection criteria: 10 late talkers and 10 early talkers, and we compared them with 10 typical talkers. We evaluated interactive behaviors at 3, 6, 9 and 12 months, considering vocal production, gaze at mother's face, and gestural production during mother-child interactions, and we considered mothers' report of children's actions and gestures and receptive-vocabulary size at 15 and 18 months.</p> <p>Results: Results indicated early precursors of language outcome at 24 months identifiable as early as 3 months in vocal productions, 6 months for gaze at mother's face and 12 months for gestural productions.</p> <p>Conclusions: Our research highlights both theoretical and practical implications. Theoretically, identifying the early indicators of belonging to the group of late or early talkers underscores the significant role of this developmental period for future studies. On a practical note, our findings emphasize the crucial need for early investigations to identify predictors of vocabulary development before the typical age at which lexical delay is identified.</p>
Data from: Trait-dependent associations between early- and late-life reproduction in a wild mammal
<p>Early- versus late-life trade-offs are a central prediction of life-history theory that are expected to shape the evolution of ageing. While ageing is widely observed in wild vertebrates, evidence that early–late trade-offs influence ageing rates remains limited. Vertebrate reproduction is a complex, multi-stage process, yet few studies have examined how different aspects of early-life reproductive allocation shape late-life performance and ageing. Here, we use longitudinal data from a 36-year study of wild Soay sheep to show that early-life reproduction predicts late-life reproductive performance in a trait-dependent manner. Females that started breeding earlier showed more rapid declines in annual fecundity with age, consistent with a trade-off. However, age-related declines in offspring first-year survival and birth weight were not associated with early-life reproduction. Selective disappearance was evident in all three late-life reproductive measures, with longer-lived females having higher average performance. Our results provide mixed support for early–late reproductive trade-offs and show that the way early-life reproduction shapes late-life performance and ageing can differ among reproductive traits.</p>
Antiglucocorticoid Therapy for Cognitive Impairment in Late-life Anxiety Disorders
ClinicalTrials.gov study NCT01333098. IPD Sharing: NO. Countries: 1. Publications: 1.
Telephone Psychotherapy for Late-Life Generalized Anxiety Disorder (GAD)
ClinicalTrials.gov study NCT01259596. IPD Sharing: NO. Countries: 1. Publications: 2.
Mechanisms of Antidepressant Non-Response in Late-Life Depression
ClinicalTrials.gov study NCT01931202. IPD Sharing: NO. Countries: 1. Publications: 1.
Neural Mechanisms of Monoaminergic Engagement in Late-life Depression Treatment Response (NEMO)
ClinicalTrials.gov study NCT03128021. IPD Sharing: YES. Countries: 1. Publications: 4.
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.