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383 results for “growth analysis”

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zenodo32/100

Figure 9 in Cranial anatomy and systematics of Hypacrosaurus altispinus, and a comparative analysis of skull growth in lambeosaurine hadrosaurids (Dinosauria: Ornithischia)

Figure 9. Incomplete squamosal of Hypacrosaurus altispinus (AMNH 5248) in caudal (A), lateral (B), and medial (C) views. See text for list of anatomical abbreviations. Scale bar: 3 cm.

opennotspecifiedMay 2010View details →
zenodo32/100

Figure 12 in Cranial anatomy and systematics of Hypacrosaurus altispinus, and a comparative analysis of skull growth in lambeosaurine hadrosaurids (Dinosauria: Ornithischia)

Figure 12. Left dentary of Hypacrosaurus altispinus, ROM 702, in medial view (A); detailed view of dentary teeth from inset (B). Scale bars: 5 cm in (A); 1 cm in (B).

opennotspecifiedMay 2010View details →
zenodo32/100

Figure 7 in Cranial anatomy and systematics of Hypacrosaurus altispinus, and a comparative analysis of skull growth in lambeosaurine hadrosaurids (Dinosauria: Ornithischia)

Figure 7. Cranial bones of Hypacrosaurus altispinus. A, incomplete jugal of CMN 8674 in lateral view. B and C, incomplete quadratojugal of ROM 702 in lateral and medial views. D, vomer of CMN 2246 in?labial view. Scale bars: 2 cm.

opennotspecifiedMay 2010View details →
zenodo32/100

Figure 8 in Cranial anatomy and systematics of Hypacrosaurus altispinus, and a comparative analysis of skull growth in lambeosaurine hadrosaurids (Dinosauria: Ornithischia)

Figure 8. Incomplete pterygoid of Hypacrosaurus altispinus (ROM 702), in lateral (A), medial (B), and caudal (C) views. Scale bar: 5 cm.

opennotspecifiedMay 2010View details →
zenodo32/100

Figure 14 in Cranial anatomy and systematics of Hypacrosaurus altispinus, and a comparative analysis of skull growth in lambeosaurine hadrosaurids (Dinosauria: Ornithischia)

Figure 14. Bivariate plots of cranial growth exclusive of the cranial crest in lambeosaurine hadrosaurids. Blue (dotted) lines represent regression for Corythsaurus, red (solid) lines represent regression for Hypacrosaurus, and green (dashed) lines represent regression for Lambeosaurus. The log of skull length is the standard variable (x) in all comparisons. •, Corythosaurus casuarius; O, Corythosaurus intermedius morph; ¥, Hypacrosaurus altispinus; +, Hypacrosaurus stebingeri,

opennotspecifiedMay 2010View details →
zenodo32/100

Figure 16 in Cranial anatomy and systematics of Hypacrosaurus altispinus, and a comparative analysis of skull growth in lambeosaurine hadrosaurids (Dinosauria: Ornithischia)

Figure 16. Results of phylogenetic analyses conducted in this study using a modified version of the data matrix presented in Evans & Reisz (2007). Top: strict consensus of three most parsimonious trees (MPTs) recovered from the phylogenetic analysis of Lambeosaurinae. The data resulted in three MPTs of 112 steps, each with a consistency index of 0.9, a rescaled consistency index of 0.83, and a retention index of 0.92. See Evans & Reisz (2007) for a character list. Bottom: majority rule consensus tree resulting from Bayesian analysis (Mk+gamma model) of the same data matrix. Abbreviations: bd, bremer decay value; bs, bootstrap value; us, unambiguous synamorphies; prob, posterior probability values.

opennotspecifiedMay 2010View details →
zenodo32/100

Figure 15 in Cranial anatomy and systematics of Hypacrosaurus altispinus, and a comparative analysis of skull growth in lambeosaurine hadrosaurids (Dinosauria: Ornithischia)

Figure 15. Bivariate plots of cranial crest variables in lambeosaurine hadrosaurids. The log of skull length is the standard variable (x) in all comparisons. Blue (dotted) lines represent regression for Corythsaurus, red (solid) lines represent regression for Hypacrosaurus, and green (dashed) lines represent regression for Lambeosaurus. •, Corythosaurus casuarius; O, Corythosaurus intermedius morph; ¥, Hypacrosaurus altispinus; +, Hypacrosaurus stebingeri,, Lambeosaurus lambei, Z, Lambeosaurus clavinitialis morph; °, Lambeosaurus magnicristatus; z, Parasaurolophus walkeri.

opennotspecifiedMay 2010View details →
zenodo32/100

FIG. 1 in Effect of Season on Analysis of Growth in a Population of the Western Lesser Siren, Siren intermedia nettingi, in Northwestern Louisiana

FIG. 1. First season capture SVL (mm) frequency (n ¼ 881) for all individuals of Siren intermedia over the seven years of the study (1992– 1998).

opennotspecifiedApr 2022View details →
zenodo32/100

FIG. 2 in Effect of Season on Analysis of Growth in a Population of the Western Lesser Siren, Siren intermedia nettingi, in Northwestern Louisiana

FIG. 2. Graph of interaction among years, seasons, and sex on growth in mass of Siren intermedia as calculated by increase in g per day. See Table 3 for statistics.

opennotspecifiedApr 2022View details →
zenodo32/100

FIG. 4 in Effect of Season on Analysis of Growth in a Population of the Western Lesser Siren, Siren intermedia nettingi, in Northwestern Louisiana

FIG. 4. Number of Siren intermedia captured per season and year over the five years of the study that sampled all four seasons.

opennotspecifiedApr 2022View details →
zenodo32/100

FIG. 3 in Effect of Season on Analysis of Growth in a Population of the Western Lesser Siren, Siren intermedia nettingi, in Northwestern Louisiana

FIG. 3. Graph of interaction among years, seasons, and sex on growth in SVL of Siren intermedia as calculated by increase in mm per day. See Table 4 for statistics.

opennotspecifiedApr 2022View details →
zenodo32/100

IsoCloud4 Data Sets for Depositional Ice Growth Analysis

<p>Data sets used in the publication</p> <p><strong>Re-evaluating cloud chamber constraints on depositional ice growth in cirrus clouds--<br> Part 1: Model description and sensitivity tests&nbsp;</strong><br> K.D. Lamb, J. Harrington, B.W. Clouser, E.J. Moyer, L. Sarkozy, V. Ebert, O. M&ouml;hler, H. Saathoff.<br> <em>Atmospheric Chemistry and Physics </em>(2023)</p>

opencc-by-4.0May 2023View details →
ClinicalTrials.gov32/100

Goat Milk-Derived Formula vs. Undiluted Goat Milk in Infants Unable to Exclusively Breastfeed: Growth and Biomarker Analysis

ClinicalTrials.gov study NCT07225153. IPD Sharing: UNDECIDED. Countries: 1. Publications: 21.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

A Prospective Analysis of Long-Term Clinical Outcomes and 3D Spine Growth in Anterior Vertebral Body Tethering

ClinicalTrials.gov study NCT04914507. IPD Sharing: NO. Countries: 2. Publications: 9.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Efficacy Analysis of Cetuximab Plus Irinotecan in Patients With Wild-type KRAS Without Regard to Epidermal Growth Factor Receptor (EGFR) Expressions

ClinicalTrials.gov study NCT00637091. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Three Dimensional Facial Growth Analysis

ClinicalTrials.gov study NCT03514563. IPD Sharing: Not stated. Countries: 1. Publications: 9.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Data from: Effects of growth rate, size, and light availability on tree survival across life stages: a demographic analysis accounting for missing values and small sample sizes

Open the record for dataset details and reuse information.

publicMar 2015View details →
dryad32/100

Impacts of growth form and phylogenetic relatedness on seed germination: a large-scale analysis of a subtropical regional flora

Open the record for dataset details and reuse information.

publicDec 2021View details →
dryad28/100

Data from: Meta-analysis indicates that oxidative stress is both a constraint on and a cost of growth

Oxidative stress (OS) as a proximate mechanism for life-history trade-offs is widespread in the literature. One such resource allocation trade-off involves growth rate, and theory suggests that OS might act as both a constraint on and a cost of growth, yet studies investigating this have produced conflicting results. Here, we use meta-analysis to investigate whether increased OS levels impact on growth (OS as a constraint on growth) and whether greater growth rates can increase OS (OS as a cost of growth). The role of OS as a constraint on growth was supported by the meta-analysis. Greater OS, in terms of either increased damage or reduced levels of antioxidants, was associated with reduced growth although the effect depended on the experimental manipulation used. Our results also support an oxidative cost of growth, at least in terms of increased oxidative damage, although faster growth was not associated with a change in antioxidant levels. These findings that OS can act as a constraint on growth support theoretical links between OS and animal life histories and provide evidence for a growth–self-maintenance trade-off. Furthermore, the apparent oxidative costs of growth imply individuals cannot alter this trade-off when faced with enhanced growth. We offer a starting platform for future research and recommend the use of oxidative damage biomarkers in nonlethal tissue to investigate the growth–OS relationship further.

opencc-zeroDec 2015View details →
dryad28/100

Data from: Meta-analysis reveals enhanced growth of marine harmful algae from temperate regions with warming and elevated CO2 levels

Elevated pCO2 and warming may promote algal growth and toxin production, and thereby possibly support the proliferation and toxicity of HABs. Here, we tested whether empirical data supports this hypothesis using a meta-analytic approach and investigated the responses of growth rate and toxin content or toxicity of numerous marine and estuarine HAB species to elevated pCO2 and warming. Most of the available data on HAB responses towards the two tested climate change variables concerns dinoflagellates, as many members of this phytoplankton group are known to cause HAB outbreaks. Toxin content and toxicity did not reveal a consistent response towards both tested climate change variables, while growth rate increased consistently with elevated pCO2 . Warming also led to higher growth rates, but only for species isolated at higher latitudes. The observed gradient in temperature growth responses shows the potential for enhanced development of HABs at higher latitudes. Increases in growth rates with more CO2 may present an additional competitive advantage for HAB species, particularly as CO2 was not shown to enhance growth rate of other non-HAB phytoplankton species. However, this may also be related to the difference in representation of dinoflagellate and diatom species in the respective HAB and non-HAB phytoplankton groups. Since the proliferation of HAB species may strongly depend on their growth rates, our results warn for a greater potential of dinoflagellate HAB development in future coastal waters, particularly in temperate regions.

opencc-zeroDec 2018View details →

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Allen Brain Atlas

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allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
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behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
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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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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