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Biological indicator records (diatoms, chrysophyte cysts, freshwater inverteb...
Here, we present diatom (Bacillariophyceae), chrysophyte (Chrysophyceae), and zoological indicator (Chironomidae, other aquatic insect, planktonic crustaceans, Bryozoa,... -
Nonmarine diatom counts for IODP Hole 381-M0080A
This dataset has no description
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Nonmarine diatom counts for IODP Hole 381-M0079A
This dataset has no description
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6000-year diatom and ostracod record of Son Kol, Kyrgyzstan (Central Asia)
6000-year-old lake sediment core from Son Kol (Central Kyrgyzstan) show distinct and repeated changes in diatom and ostracod species assemblages. Supplement to: Schwarz, Anja;... -
Results of diatom analysis of Hole 302-M0004A
Abundance: A = abundant, C = common, R = rare, B = barren. Preservation: G = good, P = poor. -
Results of diatom analysis of Hole 302-M0002A
Relative abundance: A = abundant, C = common, F = few, R = rare, B=barren (numerical values are abundance in counts) / + = ? -
Diatom assemblage in surface sediments of the Laptev Sea
This dataset has no description
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Realtive abundance of diatom species in sediment core IK9373-10
This dataset has no description
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Relative abundance of diatom species in sediment core PM9462-4
This dataset has no description
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(Table S3) Diatom species counts of IODP Hole 318-U1361A
DEPTH, sediment/rock [m] is given in mbsf. -
Diatom fragment composition in the back-scattered electron images obtained fr...
The dataset of diatom fragment composition in the back-scattered electron images (BSEI) of cross thin section of laminated sediments and lamina thickness for Sections... -
Diatom analysis in subsample smear slides from IODP Hole 323-U1340A
The dataset of diatom analysis in the subsample smear slides obtained from Sections IODP323-U1340A-10H-1W, 134-149cm, 10H-2W, 001-116cm, and 14H-1W, 60-88cm. -
(Table 2) Key diatom species of IODP Hole 323-U1340A
DEPTH, sediment/rock [m] is given in mcd. -
Under-ice export flux measurements by short-term drifting sediment traps at 2...
A critical question regarding the organic carbon cycle in the Arctic Ocean is whether the decline in ice extent and thickness and the associated increase in solar irradiance in... -
Spin Coherent Transport in Organic Spin-Valves
We have recently performed a `proof-of-principle' Low Energy Muon Spin Rotation experiment on an organic spin valve. In an extension to our muon measurements and an attempt to... -
Investigation of the effect of increased spin-orbit coupling on the performan...
We wish to perform PNR measurements on organic spin valve devices to assess the effect on the device performances of the spin relaxation mechanisms related to spin-orbit... -
Investigation of the relevancy of the ¿strong coupling hot-spot¿ model of org...
A recent theoretical model has been proposed [Nat Phys 6, 615 (2011)] to explain MR in organic spin valves. It describes a coupling between the spacer and the FM electrode that... -
Spatially profiling internal microstructure changes during redox driven rapid...
The redox driven swelling and deswelling of conducting polymers has been termed Electronic Muscle actuation. One application of this property is as a sphincter-like valve in a... -
Characterication of metals in hemolymph and tissues of the Antarctic bivalve ...
A high input of lithogenic sediment from glaciers was assumed to be responsible for high Fe and Mn contents in the Antarctic soft shell clam Laternula elliptica at King George... -
Export fluxes (diatom abundances, particulate organic carbon (POC), diatom ca...
Satellite‐derived data suggest an increase in annual primary production following the loss of summer sea ice in the Arctic Ocean. The scarcity of field data to corroborate this...
