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11 results for “longitudinal connectivity”

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zenodo40/100

Text-fig. 27. Scanning electron microscope (SEM) images of stamens and pollen of Valvidistemon globiferus gen. et sp. nov.; Catefica locality, Portugal. a) Stamen in oblique lateral view showing laterally hinged valves, massive connective between the thecae and prominent, globular, apical extension of the connective; b) Stamen in oblique lateral view on the opposite side from (a) showing broken laterally hinged valves and distinct endothecium cells; c) Detail of stamen showing the large, longitudinally aligned cells of the massive connective, broad, poorly defined stamen base, and the laterally hinged valves of one of the thecae; d) Reticulate pollen attached to the inside of the anther wall. Specimen, Catefica 49-S107779 (holotype, a–d). Scale bars = 600 Μm (a, b), 100 Μm (c), 20 Μm (d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms

Text-fig. 27. Scanning electron microscope (SEM) images of stamens and pollen of Valvidistemon globiferus gen. et sp. nov.; Catefica locality, Portugal. a) Stamen in oblique lateral view showing laterally hinged valves, massive connective between the thecae and prominent, globular, apical extension of the connective; b) Stamen in oblique lateral view on the opposite side from (a) showing broken laterally hinged valves and distinct endothecium cells; c) Detail of stamen showing the large, longitudinally aligned cells of the massive connective, broad, poorly defined stamen base, and the laterally hinged valves of one of the thecae; d) Reticulate pollen attached to the inside of the anther wall. Specimen, Catefica 49-S107779 (holotype, a–d). Scale bars = 600 Μm (a, b), 100 Μm (c), 20 Μm (d).

opencc-by-4.0Dec 2022View details →
dryad32/100

Data from: Seascape genomics reveals adaptive divergence in a connected and commercially important mollusc, the greenlip abalone (Haliotis laevigata), along a longitudinal environmental gradient

Populations of broadcast spawning marine organisms often have large sizes and are exposed to reduced genetic drift. Under such scenarios, strong selection associated with spatial environmental heterogeneity is expected to drive localized adaptive divergence, even in the face of connectivity. We tested this hypothesis using a seascape genomics approach in the commercially important greenlip abalone (Haliotis laevigata). We assessed how its population structure has been influenced by environmental heterogeneity along a zonal coastal boundary in southern Australia linked by strong oceanographic connectivity. Our datasets include 9,109 filtered SNPs for 371 abalones from 13 localities and environmental mapping across ~800 km. Genotype-environment association analyses and outlier tests defined 8,786 putatively neutral and 323 candidate adaptive loci. From a neutral perspective, the species is better represented by a metapopulation with very low differentiation (global FST=0.0081) and weak isolation by distance following a stepping stone model. For the candidate adaptive loci, however, model-based and model-free approaches indicated five divergent population clusters. After controlling for spatial distance, the distribution of putatively adaptive variation was strongly correlated to selection linked to minimum sea surface temperature and oxygen concentration. Around 80 candidates were annotated to genes with functions related to high temperature and/or low oxygen tolerance, including genes that influence the resilience of abalone species found in other biogeographic regions. Our study includes a documented example about the uptake of genomic information in fisheries management and supports the hypothesis of adaptive divergence due to coastal environmental heterogeneity in a connected metapopulation of a broadcast spawner.

opencc-zeroDec 2016View details →
zenodo32/100

FIGURE. Flowers and longitudinal sections of ovaries of Hylaeaicum and Neoregelia. A–K. Hylaeaicum. A. H. eleutheropetalum (Leme 4491). B. H. myrmecophilum (Leme 2555). C. H. aff. myrmecophilum (Leme 3487). D. H. levianum (Leme 2777). E. H. wurdackii (Leme 2567). F. H. pendulum (Leme 1979). G. H. wurdackii (Leme 2567). H. H. aff. myrmecophilum (Leme 2553). I. H. pendulum (Leme 1979). J. H. eleutheropetalum (Leme 4491). K. H. levianum (Leme 5639-A) highlighting the immature seeds connected to the placenta. L–P. Neoregelia subg. Neoregelia. L–M. N. binotii (Leme 3482). N. N. ampullacea (Leme 9299). O–P. N. pontualii (Leme 5520). Q–S. Neoregelia subg. Longipetalopsis. Q–R. N. rubrovittata (Leme 1865). S. N. pernambucana (Leme 4407). Bars = 10 mm (A–F, L–S), 5 mm (G–K). in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence

FIGURE. Flowers and longitudinal sections of ovaries of Hylaeaicum and Neoregelia. A–K. Hylaeaicum. A. H. eleutheropetalum (Leme 4491). B. H. myrmecophilum (Leme 2555). C. H. aff. myrmecophilum (Leme 3487). D. H. levianum (Leme 2777). E. H. wurdackii (Leme 2567). F. H. pendulum (Leme 1979). G. H. wurdackii (Leme 2567). H. H. aff. myrmecophilum (Leme 2553). I. H. pendulum (Leme 1979). J. H. eleutheropetalum (Leme 4491). K. H. levianum (Leme 5639-A) highlighting the immature seeds connected to the placenta. L–P. Neoregelia subg. Neoregelia. L–M. N. binotii (Leme 3482). N. N. ampullacea (Leme 9299). O–P. N. pontualii (Leme 5520). Q–S. Neoregelia subg. Longipetalopsis. Q–R. N. rubrovittata (Leme 1865). S. N. pernambucana (Leme 4407). Bars = 10 mm (A–F, L–S), 5 mm (G–K).

opennotspecifiedMay 2021View details →
zenodo32/100

FIGURE. Seeds of genera and subgenera of Bromelioideae. A–C. Bromelia aff. reversacantha (Leme 4609). A. Longitudinal section of the fruits with seeds connected to placenta by the funicular appendage. B. Seeds with the funicular appendage manually detached. C. Frontal view of the distal funicular pole of the seeds with the funicular appendage backwardly inrolled to the seeds and attached under an aril-like coat. D. Disteganthus lateralis (Leme 9390). E. Aechmea of the "Streptocalycoid complex": A. nidularioides (Leme 2150). F. Aechmea subg. Chevaliera s.l.: A. digitata (Leme 4019). G. Araeococcus subg. Araeococcus: A. flagellifolius (Leme 9501). H. Pseudaraeococcus lageniformis (Leme 9603). I. Cryptanthus pickelii (Leme 3873). J. Fernseea bocainensis (Leme 1422). K. Greigia stenolepis (Leme 9738). L. Neoglaziovia variegata (Leme 9631). M. Aechmea subg. Chevaliera s.l.: A. ornata (Leme 6760). N. Billbergia subg. Billbergia: B. amoena var. stolonifera (Leme 215-B). O. Billbergia subg. Helicodea: B. zebrina (Leme 128). P. Quesnelia subg. Quesnelia: Q. quesneliana (Leme 107). Q. Portea petropolitana var. noetiigii (Leme 5277). R. Billbergia subg. Billbergia: B. tweedieana (Leme 278). S. Quesnelia subg. Billbergiopsis: Q. liboniana (Leme 2361). T. Wittmackia lingulatoides (Leme 9585). Bars = 1 mm. in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence

FIGURE. Seeds of genera and subgenera of Bromelioideae. A–C. Bromelia aff. reversacantha (Leme 4609). A. Longitudinal section of the fruits with seeds connected to placenta by the funicular appendage. B. Seeds with the funicular appendage manually detached. C. Frontal view of the distal funicular pole of the seeds with the funicular appendage backwardly inrolled to the seeds and attached under an aril-like coat. D. Disteganthus lateralis (Leme 9390). E. Aechmea of the "Streptocalycoid complex": A. nidularioides (Leme 2150). F. Aechmea subg. Chevaliera s.l.: A. digitata (Leme 4019). G. Araeococcus subg. Araeococcus: A. flagellifolius (Leme 9501). H. Pseudaraeococcus lageniformis (Leme 9603). I. Cryptanthus pickelii (Leme 3873). J. Fernseea bocainensis (Leme 1422). K. Greigia stenolepis (Leme 9738). L. Neoglaziovia variegata (Leme 9631). M. Aechmea subg. Chevaliera s.l.: A. ornata (Leme 6760). N. Billbergia subg. Billbergia: B. amoena var. stolonifera (Leme 215-B). O. Billbergia subg. Helicodea: B. zebrina (Leme 128). P. Quesnelia subg. Quesnelia: Q. quesneliana (Leme 107). Q. Portea petropolitana var. noetiigii (Leme 5277). R. Billbergia subg. Billbergia: B. tweedieana (Leme 278). S. Quesnelia subg. Billbergiopsis: Q. liboniana (Leme 2361). T. Wittmackia lingulatoides (Leme 9585). Bars = 1 mm.

opennotspecifiedMay 2021View details →
zenodo32/100

FIGURE. Fruits and seeds of Hylaeaicum. A–B. H. myrmecophilum (Leme 2555). A. Longitudinal section of the fruits preserving attached sepals. B. Longitudinal section of the fruits with seeds exposed and yet connected to the placenta by the funicular appendage. C. Ovules and seeds of H. margaretae connected to the placenta by the funicular appendage (Leme 2331). D. H. eleutheropetalum (Leme 9736). E. H. myrmecophilum (Leme 2555). F. H. wurdackii (Leme 2567). G. H. levianum (Leme 2777). H. H. levianum (Leme 5639-A). I. H. eleutheropetalum (Leme 4491). J. H. tarapotoense (Leme 1977). K. H. pendulum (Leme 1979). Bars = 5 mm. in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence

FIGURE. Fruits and seeds of Hylaeaicum. A–B. H. myrmecophilum (Leme 2555). A. Longitudinal section of the fruits preserving attached sepals. B. Longitudinal section of the fruits with seeds exposed and yet connected to the placenta by the funicular appendage. C. Ovules and seeds of H. margaretae connected to the placenta by the funicular appendage (Leme 2331). D. H. eleutheropetalum (Leme 9736). E. H. myrmecophilum (Leme 2555). F. H. wurdackii (Leme 2567). G. H. levianum (Leme 2777). H. H. levianum (Leme 5639-A). I. H. eleutheropetalum (Leme 4491). J. H. tarapotoense (Leme 1977). K. H. pendulum (Leme 1979). Bars = 5 mm.

opennotspecifiedMay 2021View details →
ClinicalTrials.gov32/100

Longitudinal Study of the Default-mode Network Connectivity in Brain Injured Patients Recovering From Coma

ClinicalTrials.gov study NCT01620957. IPD Sharing: Not stated. Countries: 1. Publications: 2.

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

Longitudinal Changes of Brain Functional Connectivity in Migraine

ClinicalTrials.gov study NCT03487978. IPD Sharing: Not stated. Countries: 1. Publications: 0.

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

Maternal Risk, Fetal-Neonatal Brain Connectivity, and Early Neurodevelopment: A Longitudinal Observational Study

ClinicalTrials.gov study NCT07059286. IPD Sharing: NO. Countries: 1. Publications: 7.

closedIPD-NOFeb 2026View details →
dryad32/100

Data from: Seascape genomics reveals adaptive divergence in a connected and commercially important mollusc, the greenlip abalone (Haliotis laevigata), along a longitudinal environmental gradient

Open the record for dataset details and reuse information.

publicDec 2017View details →
ClinicalTrials.gov24/100

Longitudinal Assessment of Functional Connectivity in Treatment Engaged Cocaine Users

ClinicalTrials.gov study NCT03554928. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

Longitudinal Monitoring of Cerebral Connectivity 3T MRI in Patients With a Transcient Global Amnesia

ClinicalTrials.gov study NCT02796287. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →

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Allen Brain Atlas

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allen-brain-atlas
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Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

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abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

ibl
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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