Find research datasets worth reusing

opencc-by-4.0Feb 2022View details →

Beyond depression and anxiety; a systematic review about the role of corticotropin-releasing hormone antagonists in diseases of the pelvic and abdominal organs-Worksheets

This file has several worksheets corresponding to the data used for the review with the same table as indicated in the file

opencc-by-4.0Mar 2022View details →

Influences of the 1855 AD Huanghe (Yellow River) Relocation on Sedimentary Organic Carbon Burial in the Southern Yellow Sea

This is the original data used in the manuscript titled "Influences of the 1855 AD Huanghe (Yellow River) Relocation on Sedimentary Organic Carbon Burial in the Southern Yellow Sea" which has been accepted by Frontiers in Marine Science. The data is from a box-core HH12 recovered from the southern Yellow Sea (123.50°E, 35.00°N; core length: 48 cm; water depth: 77 m; time span: ~300 yr). This excel includes depth, year, TOC, TN, biomarkers and other proxy record. Full Article at: <a href="https://www.frontiersin.org/articles/10.3389/fmars.2022.824617/full">https://www.frontiersin.org/articles/10.3389/fmars.2022.824617/full</a>

opencc-by-4.0Mar 2022View details →

Glacier shrinkage will accelerate downstream decomposition of organic matter and alters microbiome structure and function

Two datasets supporting the publication, "Glacier shrinkage will accelerate downstream decomposition of organic matter and alters microbiome structure and function" in Global Change Biology. DATA S1 Detailed metadata for sampled glacier-fed streams, including sample date and time, GPS coordinates, elevation, physical streamwater measurements, glacier characteristics, nutrient chemistry, and a column indicating samples used in metagenomics analyses. DATA S2 Full patch-level dataset of extracellular enzyme activities (nmol h-1 g-1 DM sediment) and chlorophyll a (µg chlorophyll a g-1 DM).

opencc-by-4.0Jan 2021View details →

Characterization of legacy persistent organic pollutants (POPs) in northern bottlenose whales of the Western North-Atlantic

Dataset associated with the Canadian Technical Report of Fisheries and Aquatic Sciences entitled "Characterization of legacy persistent organic pollutants (POPs) in northern bottlenose whales of the Western North-Atlantic". Presents lipid weight corrected persistent organic pollutant concentrations (microgram per gram) in the blubber of northern bottlenose whales samples in the western North Atlantic.

Fig. 2 in The Influence Of Fixatives On The Validity Of Histological Preparations Of Olfactory Organ In Teleostei

Fig. 2. Cross-section through the olfactory organ of Misgurnus fossilis at developmental stage 36 (А, В), developmental stage 37 (C, D), stage of early larva (E, F), stage of late larva (G, H). Arrowheads indicate the artifacts "anlage of lamellae"; arrows indicate the rises of epithelium (artifacts); b — brain; e — eye; oe — olfactory epithelium; ol — olfactory lamella; o — olfactory pit; op — olfactory placode. Left images correspond to Bouin's solution, right images correspond to 10 % formalin fixation.

Fig. 1 in The Influence Of Fixatives On The Validity Of Histological Preparations Of Olfactory Organ In Teleostei

Fig. 1. Section levels through the olfactory organ of European weatherfish Misgurnus fossilis: A — cross-section (prolarva); B — frontal section (larva).

Fig. 5 in The Features Of The Structural Organization Of Spinal Ganglia In A Subphylum Of Vertebtates

Fig. 5. Fragment of microscopic structure of spinal ganglion of domestic dog: a — cytoplasma of neurocyte; b — nucleus and nucleolus; c — cores of glial cells. Hematoxilin and eosin. ×640.

Fig. 2 in The Features Of The Structural Organization Of Spinal Ganglia In A Subphylum Of Vertebtates

Fig. 2. Fragment of microscopical structure of spinal ganglion of pond frog: a— nervous cell; b — the core and kernel; c — nervous fibers. Bilshovskiy-Gros. ×128.

Fig. 3 in The Features Of The Structural Organization Of Spinal Ganglia In A Subphylum Of Vertebtates

Fig. 3. Fragment of microscopical structure of spinal ganglion of domestic hen: a — neurocyte; b — nucleus and nucleolus; c — cores of gliocytes; d — nerval fibers. Bilshovskiy-Gros. ×400.

Fig. 1 in The Features Of The Structural Organization Of Spinal Ganglia In A Subphylum Of Vertebtates

Fig. 1. Microscopical structure of spinal ganglion of carp: a — large neurocyte; b — middle neyrocyte; c — small neurocytes; d — process of neurocyte; e — the core. Ramon-Kahal. ×320.

Fig. 6 in The Features Of The Structural Organization Of Spinal Ganglia In A Subphylum Of Vertebtates

Fig. 6. Fragment of microscopic structure of spinal ganglion of domestic bull: a — neurocytes; b — cores if glial cells; c — nerval fibers. Hematoxilin and eosin. ×120.

Fig. 4 in The Features Of The Structural Organization Of Spinal Ganglia In A Subphylum Of Vertebtates

Fig. 4. Fragment of microscopic structure of spinal ganglion of european rabbit: a — light neurocytes; b — dark neurocytes; c — cores of mantle gliocytes; d — nerval fibers. Ramon-Kahal. ×280.

Fig. 1 in The Plasticity And Morphofunctional Organization Of The Digestive System Of Waders (Charadrii) As Migrants

Fig. 1. The esophagus wall Tringa ochropus, cross cut, caudal section. Histopreparation (hematoxylin and eosin, х100). 1 — folds; 2 — epithelial layer; 3 — esophageal glands; 4 — muscle plate; 5 — submucosal basis; 6 — muscle (а — inner longitudinal layer; b — outer circle layer); 7 — layers of connective tissue.

Fig. 5 in The Plasticity And Morphofunctional Organization Of The Digestive System Of Waders (Charadrii) As Migrants

Fig. 5. The wall of the cecum Philomachus pugnax, the area of the body, cross cut. Histopreparation (hematoxylin and eosin, х100). 1 — mucosal plates; 2 — crypt; 3 — lymphoid tissue; 4 — submucosal basis; 5 — muscle.

Fig. 4 in The Plasticity And Morphofunctional Organization Of The Digestive System Of Waders (Charadrii) As Migrants

Fig. 4. Crypt in the wall of the duodenum Tringa nebularia, cross cut. Histopreparation (hematoxylin and eosin, ×250). 1 — crypt; 2 — corpuscle enterocytes; 3 — alveolar extension of the bottom part of the crypt; 4 — separate muscle cell myocytes; 5 — submucosal basis; 6 — muscle (а — inner longitudinal layer; b — outer circle layer); 7 — gray serum.

Fig. 3 in The Plasticity And Morphofunctional Organization Of The Digestive System Of Waders (Charadrii) As Migrants

Fig. 3. The wall of the jejunum Calidris ferruginea, cross cut, cranial section. Histopreparation (hematoxylin and eosin, х100). 1 — plates of the mucous, located zigzag; 2 — goblet cells; 3 — intestinal crypt; 4 — muscle.

Fig. 2 in The Plasticity And Morphofunctional Organization Of The Digestive System Of Waders (Charadrii) As Migrants

Fig. 2. The wall of the muscular stomach Tringa nebularia cross cut. Histopreparation (hematoxylin and eosin, х40). 1 — cuticle, 2 — tubular glands; 3 — muscle (а — inner longitudinal layer; b — outer thick circle layer); 4 — layers of connective tissue; 5 — blood vessels,

Fig. 6 in The Plasticity And Morphofunctional Organization Of The Digestive System Of Waders (Charadrii) As Migrants

Fig. 6. The wall of the rectum Tringa glareola, cross cut, cranial section. Histopreparation (hematoxylin and eosin, ×100). 1 — fold of the wall; 2 — mucosal plates; 3 — crypt; 4 — muscle plate; 5 — submucosal basis; 6 — muscle (а — inner circle layer; б — outer longitudinal layer).

opencc-by-4.0Sep 2016View details →

Fig. 1 in Histological, Topographical And Ultrastructural Organization Of Different Cells Lining The Olfactory Epithelium Of Red Piranha, Pygocentrus Nattereri (Characiformes, Serrasalmidae)

Fig. 1. Photomicrographs of the olfactory epithelium of Pygocentrus nattereri by scanning electron microscopy (SEM) and histological architecture stained with Delafield's Haematoxylin-Eosin (HE) and Mallory's triple (MT) stain. A — oval shaped olfactory rosette showing olfactory lamellae (OL) radiating from median raphe (R). Note tongue shaped structure (arrow heads) on the apical end of the lamellae (SEM) ×50. B — sensory olfactory epithelium (OEP) lined with receptor cells. Note the presence of blood vessels (BV) in the central core (CC) which is distinguished from OEP by basement membrane (BM). Arrow heads indicate basal cells above BM (MT) ×400. C — higher magnification of OEP showing a large number of primary receptor cells (RC) with conspicuous nuclei (N), secondary recptor cells (broken arrows), microvillous cells (MV) intermingled with supporting cells (SC). Note the presence of BV in CC and BC (arrow heads) near CC. Solid arrow indicates the axons of secondary RC communicate to CC (MT) ×1000. D — OEP exhibiting cylindrical RC with knob like vesicles (black arrow heads), ciliated supporting cells (solid arrows), non-ciliated supporting cells (white arrow heads) and BC above CC. Broken arrows mark the cilia of supporting cells on the epithelial surface (HE) ×400. E — tuft of receptor cells (RC) in between supporting cells (SC) (SEM) ×4000. F — dendrite patches of RC (broken arrows) and microvillous cells (solid arrows) in between stratified epithelial cells (SEC). Note the opening of mucous cells (arrow heads) in between SEC (SEM) ×2500.