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4. Deep-Sea Misconceptions Cause Underestimation of Seabed-Mining Impacts

14. Evaluating deep-sea communities' susceptibility to mining plumes using shallow-water data.

15. Mercury isotopic evidence for the importance of particles as a source of mercury to marine organisms.

16. Microbiomes of Hadal Fishes across Trench Habitats Contain Similar Taxa and Known Piezophiles.

17. Abyssal deposit feeders are secondary consumers of detritus and rely on nutrition derived from microbial communities in their guts.

19. Mercury isotopes identify near-surface marine mercury in deep-sea trench biota.

20. Deep-Sea Misconceptions Cause Underestimation of Seabed-Mining Impacts.

21. Climate change considerations are fundamental to management of deep-sea resource extraction.

22. Evidence for long-term seamount-induced chlorophyll enhancements.

24. Differences in the trophic ecology of micronekton driven by diel vertical migration.

25. Microbial Community Diversity Within Sediments from Two Geographically Separated Hadal Trenches.

26. Gut Microbial Divergence between Two Populations of the Hadal Amphipod Hirondellea gigas.

27. Genome Reduction in Psychromonas Species within the Gut of an Amphipod from the Ocean's Deepest Point.

28. Molecular adaptation to high pressure in cytochrome P450 1A and aryl hydrocarbon receptor systems of the deep-sea fish Coryphaenoides armatus.

29. Distribution, composition and functions of gelatinous tissues in deep-sea fishes.

30. Carbon, Nitrogen, and Mercury Isotope Evidence for the Biogeochemical History of Mercury in Hawaiian Marine Bottomfish.

31. Pseudoliparis swirei sp. nov.: A newly-discovered hadal snailfish (Scorpaeniformes: Liparidae) from the Mariana Trench.

32. Megafauna of the UKSRL exploration contract area and eastern Clarion-Clipperton Zone in the Pacific Ocean: Annelida, Arthropoda, Bryozoa, Chordata, Ctenophora, Mollusca.

33. Climate change is projected to reduce carrying capacity and redistribute species richness in North Pacific pelagic marine ecosystems.

34. Dining in the Deep: The Feeding Ecology of Deep-Sea Fishes.

35. Depth as a driver of evolution in the deep sea: Insights from grenadiers (Gadiformes: Macrouridae) of the genus Coryphaenoides.

36. Near-island biological hotspots in barren ocean basins.

37. Characterizing a Foraging Hotspot for Short-Finned Pilot Whales and Blainville's Beaked Whales Located off the West Side of Hawai'i Island by Using Tagging and Oceanographic Data.

38. Mercury sources and trophic ecology for Hawaiian bottomfish.

39. Paraliparis hawaiiensis, a new species of snailfish (Scorpaeniformes: Liparidae) and the first described from the Hawaiian Archipelago.

40. Marine fish may be biochemically constrained from inhabiting the deepest ocean depths.

41. Understanding the scale of Marine protection in Hawai'i: from community-based management to the remote Northwestern Hawaiian Islands.

42. Red muscle proportions and enzyme activities in deep-sea demersal fishes.

43. Global trophic position comparison of two dominant mesopelagic fish families (Myctophidae, Stomiidae) using amino acid nitrogen isotopic analyses.

44. The role of carrion supply in the abundance of deep-water fish off California.

45. Decreasing urea∶trimethylamine N-oxide ratios with depth in chondrichthyes: a physiological depth limit?

46. Metabolism and enzyme activities of hagfish from shallow and deep water of the Pacific Ocean.

47. The influence of depth on mercury levels in pelagic fishes and their prey.

48. Lipid, sterols and fatty acid composition of abyssal holothurians and ophiuroids from the North-East Pacific Ocean: food web implications.

49. The rate of metabolism in marine animals: environmental constraints, ecological demands and energetic opportunities.

50. Correlation of trimethylamine oxide and habitat depth within and among species of teleost fish: an analysis of causation.

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