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184 results for “barbs”
Figure 8 in Life history traits and exploitation of Hampala barb (Hampala macrolepidota - Cyprinidae) in a subtropical reservoir (Lao PDR)
Figure 8. – Percentage of catches during 2016 according to size class of Hampala macrolepidota from the Nam Theun 2 Reservoir in Lao PDR.
Figure 9 in Life history traits and exploitation of Hampala barb (Hampala macrolepidota - Cyprinidae) in a subtropical reservoir (Lao PDR)
Figure 9. – Percentage of catches during 2016 according to age group (year) of Hampala macrolepidota from the Nam Theun 2 Reservoir in Lao PDR.
Fig. 2 in Tolerância à dessecação e armazenamento em temperatura sub-zero de sementes de Butia odorata (Barb. Rodr.) Noblick
Fig. 2. Germinação (G%) e formação de plântulas completas (P%) a partir de sementes de Butia odorata escarificadas pelo método de abertura total da cavidade embrionária, após armazenadas em ambiente de laboratório por 120 dias (teor de água de 6,14%) (controle); após armazenadas em ambiente de laboratório por 120 dias seguido de 24h em estufa com circulação de ar forçada a 30 ºC constantes (teor de água de 3,8%); e seguido de 120 dias sob temperatura negativa (sub-zero). Médias seguidas de letras minúsculas para G% e maiúsculas para P% não diferem estatisticamente pelo teste LSD de Fisher.
Fig. 1 in Tolerância à dessecação e armazenamento em temperatura sub-zero de sementes de Butia odorata (Barb. Rodr.) Noblick
Fig. 1. Teor de água de diásporos inteiros e de sementes isoladas de Butia odorata logo após a coleta; após dez dias em ambiente de laboratório; após 120 dias; após 120 dias seguido de 120 dias sob temperatura negativa; e após 120 dias em ambiente de laboratório seguido de 24h em estufa com circulação de ar forçada a 30 ºC constantes. Médias seguidas de letras minúsculas para sementes e maiúsculas para diásporos, não diferem estatisticamente pelo teste LSD de Fisher.
Figs. 2A-C in Impacto de las concentraciones de ANA y sacarosa en el enraizamiento in vitro de Butia odorata (Barb. Rodr.) Noblick
Figs. 2A-C. Enraizamiento in vitro de plantas de Butia odorata sometidos a los medios de cultivo con diferentes concentraciones del ácido naftalenacético. A. porcentaje de plantas con callo; B. porcentaje de plantas enraizadas; C. masa fresca de plantas.
FIGURE 5 in A new small barb (Cyprininae: Smiliogastrini) from the N'sele and Mayi Ndombe rivers in the lower reaches of the middle Congo basin (Democratic Republic of Congo, Central Africa)
FIGURE 5. Principle components (PC) 1 and 2 displaying variation in body shape for mature male (stars) and female (circles) specimens of "Barbus" validus. Visualization of shape variation is provided as warped grids of (A) minimum and (B) maximum PC 1 values relative to mean shape.
Continuous Locked Non-barbed Suture for Mesh Fixation During Laparoscopic Ventral Rectopexy for Severe Rectal Prolapse
ClinicalTrials.gov study NCT05254860. IPD Sharing: Not stated. Countries: 0. Publications: 1.
Effect of Barbed Suture Fascia Closure on Incisional Hernia in Midline Laparotomy for Gynecological Diseases (BARBHER)
ClinicalTrials.gov study NCT04643197. IPD Sharing: UNDECIDED. Countries: 0. Publications: 2.
Barbed Suture vs Smooth Suture for Vaginal Cuff Closure
ClinicalTrials.gov study NCT01262573. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a Conventional Absorbable Suture
ClinicalTrials.gov study NCT00959374. IPD Sharing: Not stated. Countries: 2. Publications: 0.
Data from: Barb geometry of asymmetrical feathers reveals a transitional morphology in the evolution of avian flight
Open the record for dataset details and reuse information.
Genomic structure of the Sicklefin Barb, Puntioplites falcifer (Cyprinidae), in the lower Mekong River basin reveals patterns of both migration and population partitioning
<p>Effective management of the Sicklefin Barb, <i>Puntioplites falcifer</i>, with the planned construction of several dams in the Mekong River Basin depends upon disentangling conflicting reports of isolated populations and highly migratory behavior. We investigated patterns of population genomic structure, relatedness, and inferred connectivity among three locations on the Mekong and a fourth at Attapeu on the Sekong tributary. The results supported both isolation of populations and migratory behavior. STRUCTURE, AMOVA, and PCA revealed three distinct nDNA clusters. The most divergent nDNA cluster (pairwise <i>F</i><sub>ST</sub> ≥ 0.43, <i>p < </i>0.0001) exhibited negligible inferred relative migration rates with the other samples (<i>m</i> ≤ 0.02), including those from common sampling locations, and was likely a different species - putatively <i>P. proctozysron </i>(Ppr). However, mtDNA barcoding suggested differentiation between Ppr and a published mtDNA genome for this species. Most of the fish from the Sekong tributary belonged to a second distinct nDNA cluster and the sample from that location was differentiated from the Mekong sites (pairwise <i>F</i><sub>ST</sub> = 0.02 - 0.03, <i>p</i> < 0.0001). Supporting migration, a third nDNA cluster exhibited high rates of migration among the Mekong locations (<i>m</i> = 0.6 - 1) and was found in small numbers at the Sekong location which was characterized by intermediate migration rates with the Mekong (<i>m</i> = 0.3 - 0.4). Mitochondrial DNA barcoding indicated that the fish comprising the Mekong and Sekong nDNA clusters were differentiated from a <i>P. falcifer </i>mtDNA genome sampled well upstream of the Mekong locations in this study. Estimates of <i>N</i><sub>e</sub> by both location and nDNA cluster were near or below the minimal sustainable size (173-1651), suggesting susceptibility to over-exploitation or population fragmentation. Together, these results suggest that proposed hydropower dams could subdivide connected Mekong populations, isolate and split the Sekong population, and further drive down <i>N</i><sub>e</sub> if accommodations are not made to facilitate connectivity. Additionally, the combined pattern of nDNA and mtDNA diversity is consistent with substantial cryptic diversity and a <i>P. falcifer</i> – <i>P. proctozysron</i> species complex that could be further described with rigorous population genomic surveys and expanded geographic sampling.</p>
Figure 3 in Pethia arunachalensis, a new species of small barb (Teleostei: Cyprinidae) from Arunachal Pradesh, India
Figure 3. Noa-dhing River, type locality of Pethia arunachalensis.
Symmcora® Long-term Bidirectional Barbed Suture for Anastomosis in Patients Undergoing Robot Assisted Radical Prostatectomy
ClinicalTrials.gov study NCT06055946. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Unidirectional Barbed Sutures in Mucogingival Procedures
ClinicalTrials.gov study NCT04937114. IPD Sharing: NO. Countries: 1. Publications: 0.
To Show the Safety and Effectiveness of the Demetech Barbed Polydioxanone (PDO) Suture
ClinicalTrials.gov study NCT06404372. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Barbed Reposition Pharyngoplasty in Patients Complaining of Unilevel Palatal Snoring
ClinicalTrials.gov study NCT05643352. IPD Sharing: NO. Countries: 1. Publications: 0.
Clinical Impact of Uterine Repair During Cesarean Section with Barbed Suture on the Incidence of Isthmocele
ClinicalTrials.gov study NCT06691750. IPD Sharing: NO. Countries: 1. Publications: 0.
Knotless Barbed Suture Closure of the Uterus at Caesarean Section
ClinicalTrials.gov study NCT06979687. IPD Sharing: YES. Countries: 1. Publications: 0.
Comparison of Barbed and Conventional Sutures in Adhesion Formation Following Cesarean Section
ClinicalTrials.gov study NCT03183362. IPD Sharing: NO. Countries: 1. Publications: 0.
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International Brain Laboratory public data
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OpenNeuro
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