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1 ng particles, and finally sequestered in the deep ocean.
2 aditional beliefs that POPs do not reach the deep ocean.
3 pollutants between the coastal ocean and the deep ocean.
4 persistent organic pollutants (POPs) in the deep ocean.
5 rticulate organic carbon (POC) fluxes to the deep ocean.
6 onments, including lakes, rather than in the deep ocean.
7 ly efficient at sequestering carbon into the deep ocean.
8 r enhance export of picophytoplankton to the deep ocean.
9 export of carbon and other nutrients to the deep ocean.
10 of which 5 to 15 per cent is exported to the deep ocean.
11 presents 4-31% of the oil sequestered in the deep ocean.
12 e a precursor of micro-blebs observed in the deep ocean.
13 ce of ash/pumice deposit distribution in the deep ocean.
14 the near-inertial energy penetrates into the deep ocean.
15 rtance of H(2) as a key energy source in the deep ocean.
16 arbon northward, and from the surface to the deep ocean.
17 n or uptake, sequestration and export to the deep ocean.
18 production and carbon sequestration into the deep ocean.
19 pable of delta(13)C(CH4) measurements in the deep ocean.
20 e marine habitats, from the surf zone to the deep ocean.
21 c was home to a globally sulphidic (euxinic) deep ocean.
22 on is transferred from the atmosphere to the deep ocean.
23 soon enough to avoid transfer of heat to the deep ocean.
24 have directly enhanced carbon export to the deep ocean.
25 sults in enhanced organic carbon flux to the deep ocean.
26 d subtle slope breaks located far out in the deep ocean.
27 the globe and regulates their storage in the deep ocean.
28 it serves as a lid to a larger volume of the deep ocean.
29 ates, and may have led to oxygenation of the deep ocean.
30 ent iron can alter the flux of carbon to the deep ocean.
31 it occurs on long unknown time scales in the deep ocean.
32 rn Ocean contained the saltiest water in the deep ocean.
33 o sustained and widespread freshening of the deep ocean.
34 ion concentration existed in the glacial-age deep ocean.
35 e will have inhibited transport of O2 to the deep ocean.
36 ents acting as a source of old carbon to the deep ocean.
37 organic material from surface waters to the deep ocean.
38 ontribution of different water masses to the deep ocean.
39 y and distribution of nektonic carbon in the deep ocean.
40 look its relevance as a carbon source to the deep ocean.
41 between benthic and pelagic habitats in the deep ocean.
42 retching from high montane lakes down to the deep ocean.
43 of sinking particulate organic matter in the deep ocean.
44 regarding the oil's fate and effects in the deep ocean.
45 om predators, particularly for fishes of the deep ocean.
46 ne food webs and the flux of carbon into the deep ocean.
47 supports numerous ecosystem services in the deep ocean.
48 r of carbon to higher trophic levels and the deep ocean.
49 ochthonous FDOM, which may accumulate in the deep ocean.
50 e of aquatic habitats from shallow rivers to deep oceans.
51 ccessible to humans, from distant planets to deep oceans.
52 s key step of the global carbon cycle in the deep oceans.
53 enzymes that underpin chemosynthesis in the deep oceans.
54 ources and transformations of mercury in the deep oceans.
55 k of environmental regulatory policy for the deep oceans.
56 s and man-made structures in the shallow and deep oceans.
57 variables among five scientific areas of the deep ocean: (1) biodiversity; (2) ecosystem functions; (
62 the carbon cycle and solar forcing modulates deep ocean acidity as well as the production and burial
63 city intensity and enhance the mixing in the deep ocean, also have potential implication for deep-sea
64 penetration of near-inertial energy into the deep ocean and a hotspot for the diapycnal mixing in win
65 -3) Wm(-2) radiates into the thermocline and deep ocean and accounts for 42%-58% of the energy requir
66 gin of sulfur-depleted organic matter in the deep ocean and cannot adequately reproduce our observed
67 oceanic reservoir due to oxygenation of the deep ocean and corresponding decrease in sulphidic condi
69 biological pump drives carbon storage in the deep ocean and is thought to function via gravitational
70 organic carbon from the ocean surface to the deep ocean and its subsequent burial through biogeochemi
71 e of the most abundant microorganisms in the deep ocean and responsible for much of the ammonia oxida
73 tion of a substantial fraction of DOC in the deep ocean and that this dilution acts as an alternative
75 conditions proposed previously for Ediacaran deep oceans and helps to explain the patchy temporal rec
77 gene and its transcription is greater in the deep ocean, and is highest in the sediment.s DMSP catabo
79 an is the principal means of ventilating the deep oceans, and is therefore a key element of the globa
81 t radiocarbon variations in the intermediate/deep ocean are associated with roughly synchronous chang
82 cale releases of methane from hydrate in the deep ocean are likely to be met by a similarly rapid met
84 ed carbon is transferred from the surface to deep ocean as sinking particles or dissolved organic car
86 sess the impact of mixing processes on these deep ocean bacterial communities and their capacity for
88 n the deep-ocean water for 1.8 years for the deep-ocean bacterioplankton to grow to the 2.4x higher c
89 present observations from the Scotia Sea, a deep ocean basin between the Antarctic peninsula and the
90 pping tectonic structures, especially in the deep ocean basins where the topography remains unmapped
94 Deep-sea coral communities are hotspots of deep ocean biomass and biodiversity, providing critical
95 The photochemical reaction cycle of Hawaiian deep ocean BPR in cells is 10-fold slower than that of G
96 hermal heating of young rift sediments alter deep-ocean budgets of bioavailable DOM, creating organic
97 s is among the highest found anywhere in the deep ocean, but constraints on microbial growth and meta
98 e near future by trapping natural CO2 in the deep ocean, but ultimately may limit oceanic uptake of a
99 observed estimates of vertical mixing in the deep ocean by presenting a revised view of the thermohal
101 rect quantification of the contribution from deep ocean carbon sources to community production in the
102 supports the view that the ventilation of a deep-ocean carbon reservoir in the Southern Ocean had a
103 t, during deglaciations, an isolated glacial deep-ocean carbon reservoir is reconnected with the atmo
104 eglacial injection of very old waters from a deep-ocean carbon reservoir that was previously well iso
105 ump almost doubles the previous estimates of deep-ocean carbon sequestration by biological processes
106 atmospheric CO2 variations invoke changes in deep-ocean carbon storage, probably modulated by process
107 e, match the shape of the CIE and pattern of deep ocean carbonate dissolution as recorded in sediment
109 ermine the population structure of a cryptic deep ocean cetacean, the Gray's beaked whale (Mesoplodon
110 ngly suggests that the sequenced surface and deep ocean changes were forced by pulsed meltwater outbu
111 etal enrichment record implies a Proterozoic deep ocean characterized by pervasive anoxia relative to
113 This suggests that on millennial timescales deep ocean circulation and iron fertilization in the Sou
114 y shows that various inferred changes in the deep ocean circulation and stratification between glacia
115 associated with major rearrangements in the deep ocean circulation and stratification, which have li
119 strong polar halocline fundamentally altered deep ocean circulation, which enhanced interhemispheric
120 he atmosphere--probably linked to changes in deep ocean circulation--occurred during the last deglaci
121 ever, understanding the relationship between deep-ocean circulation and ancient climate is complicate
122 eenhouse conditions can thus initiate abrupt deep-ocean circulation changes in less than a few thousa
125 e we present evidence for an abrupt shift in deep-ocean circulation using carbon isotope records from
126 ate climate model inferences that a shift in deep-ocean circulation would deliver relatively warmer w
131 may be related to iron-rich and sulfate-poor deep-ocean conditions facilitated by an increase in the
133 ains Southern Ocean surface water and global deep ocean cooling in the apparent absence of (sub-) equ
136 isotope (delta(13)C) megasplice, documenting deep-ocean delta(13)C evolution since 35 million years a
142 enomena suggests that the overturn of anoxic deep oceans during the Late Permian introduced high conc
143 An enigmatic mass extinction occurred in the deep oceans during the Mid Pleistocene, with a loss of o
144 ffective management of increasing use of the deep ocean (e.g., for bottom fishing, oil and gas extrac
145 s and virtually no in situ productivity, the deep oceans, Earth's largest ecosystem, are especially e
147 ed food supply), is projected to affect most deep-ocean ecosystems concomitantly with increasing dire
148 have revealed unexpectedly large changes in deep-ocean ecosystems significantly correlated to climat
151 .5-year record of photographic data from the Deep-ocean Environmental Long-term Observatory Systems s
154 with shallow tropical seas; however, recent deep-ocean exploration using advanced acoustics and subm
155 oto-degradation behaviour when compared with deep-ocean FDOM, further strengthening the similarity be
157 r petroleum hydrocarbons that settled to the deep ocean floor following release from the damaged Maco
160 rease occurred in the amplitude of change of deep-ocean foraminiferal oxygen isotopic ratios, traditi
161 cal dissolved inorganic carbon fluxes to the deep ocean from the organic-poor, metalliferous sediment
163 here on glacial-interglacial timescales, the deep ocean has been implicated as the likely location of
167 the volcano-induced dynamic chemistry of the deep ocean, here we demonstrate the Leidenfrost dynamic
169 t patterns of microbial succession following deep ocean hydrocarbon blowouts are predictable and prim
170 However, as our methods for exploring the deep ocean improve, common assumptions about dispersal,
172 here convection exports surface water to the deep ocean in winter as part of the thermohaline circula
173 reservoir of organic carbon suspended in the deep ocean, indicating that this event may have had a ke
175 hydrothermal chemical and heat flux into the deep-ocean interior and for dispersing propagules hundre
177 ubmerged oil thought to have been trapped in deep-ocean intrusion layers at depths of approximately 1
178 escales are dominated by slow changes in the deep ocean inventory of biologically sequestered carbon
180 cline suggest that P remineralization in the deep ocean is a byproduct of microbial carbon and energy
181 es through the mesopelagic zone and into the deep ocean is a critical determinant of the atmosphere-o
184 ogeochemical methane cycling dynamics in the deep ocean is hampered by a number of challenges, especi
189 the diapycnal mixing in the thermocline and deep ocean is tightly related to the shear variance of w
190 constraint the organic carbon export to the deep ocean is unable to compensate for the outgassing of
192 otope composition ((187)Os/(188)Os ratio) of deep oceans is 1.05, reflecting a balance between inputs
196 of the global ocean is critically shaped by deep-ocean mixing, which transforms cold waters sinking
198 ropose this elevation is due to increases in deep-ocean O(2) and marine sulfate concentrations betwee
199 age maximum at mid-depths and depriving the deep ocean of a fast escape route for accumulating respi
200 ation as rising atmospheric pO(2) sweeps the deep ocean of the ferrous iron substrate for photoferrot
201 of deglaciation include ice albedo feedback, deep-ocean out-gassing during post-glacial oceanic overt
204 bal ice volume proxy(3) (as derived from the deep-ocean oxygen isotope record) and sea-level cycles a
205 models linking drastic isotope excursions to deep ocean oxygenation and the opening of environments c
206 ide a reconstruction of transient changes in deep ocean oxygenation and, by inference, respired carbo
207 an between these two steps and the timing of deep-ocean oxygenation have important implications for t
208 rmations and marine red beds, which indicate deep-ocean oxygenation occurred in the middle Ediacaran,
209 of marine red beds constrains the timing of deep-ocean oxygenation.The evolution of oceanic redox st
212 organic carbon (POC) from the surface to the deep ocean, plays an important role in regulating atmosp
214 loss, indicating that biodegradation in the deep ocean progresses similarly to other environments.
215 from these two widely separated areas of the deep ocean provide compelling evidence that changes in c
216 nued international interest in exploring the deep ocean provides impetus to increase our understandin
217 in the Southern Ocean, we show that existing deep-ocean radiocarbon records from the glacial period a
218 rease in the residence time of carbon in the deep ocean, rather than an increase in biological carbon
220 Here we show, using new 2.4-Myr-long Eocene deep ocean records, that the comparatively modest hypert
222 l connections between surface waters and the deep ocean remain poorly studied despite the high biomas
227 ~38 to 28 million years ago), accompanied by deep-ocean reorganization attributed to gradual Antarcti
228 Climate Change (UNFCCC) could help to expand deep-ocean research and observation and to protect the i
229 as no upwelling of Se oxyanions from an oxic deep-ocean reservoir, which is consistent with previous
231 are present around hydrothermal vents in the deep ocean seafloor, this process might be relevant, at
232 ctinomycete strain CNQ-418, retrieved from a deep ocean sediment sample off the coast of La Jolla, CA
234 deglaciation, and the relative importance of deep ocean sequestration in regulating millennial-timesc
237 in the Chicxulub crater sediments and at two deep ocean sites indicate a fossil carbon source that ex
238 s, we hypothesize, initial conditions of the deep ocean state that are consistent with observations o
239 rine rejection leads to a strongly increased deep ocean stratification, consistent with high abyssal
241 ant decline in high-latitude sea surface and deep ocean temperature and enhanced seasonality in middl
242 e we present an orbitally resolved record of deep ocean temperature derived from benthic foraminifera
243 We present evidence that their record of deep ocean temperature is not reliable, thus raising dou
244 ghtly lead) global changes in ice volume and deep ocean temperature over the past 3.5 million years.
245 heric carbon dioxide, Antarctic temperature, deep ocean temperature, and global ice volume correlated
247 e introduce a method that infers basin-scale deep-ocean temperature changes from the travel times of
248 present a detailed record of North Atlantic deep-ocean temperature, global sea-level, and ice-volume
253 2 million years ago for both the surface and deep ocean that are consistent with an approximately 200
254 uations of species diversity in the tropical deep ocean that are correlated with orbital-scale oscill
255 ight their versatile metabolic strategies in deep oceans that might play a critical role in global ca
257 ow light levels-a pervasive condition in the deep ocean, the largest inhabitable space on the planet.
259 Along with recent measurements of Hg in the deep ocean, these archives indicate that atmospheric Hg
262 pwelling and associated carbon flux from the deep ocean to the atmosphere, a positive feedback loop n
265 sistent with the transfer of carbon from the deep ocean to the surface ocean and atmosphere via a Sou
267 and 400 Ma is thought to have oxygenated the deep oceans, ushered in modern biogeochemical cycles, an
268 ous records have hinted at a partitioning of deep ocean ventilation across the two major intervals of
272 ecosystem were facilitated by restoration of deep ocean ventilation linked mechanistically to a chang
276 tion rate together with plausible changes in deep-ocean ventilation and the global carbon cycle durin
277 biological export of carbon and increases in deep-ocean ventilation via southern-sourced water masses
278 make unlikely suggestions that a slowdown in deep-ocean ventilation was responsible for a sizable fra
279 he Earth's albedo, ongoing changes in global deep-ocean ventilation, and the evolution of Southern Oc
281 rge genomic fragments from both surface- and deep-ocean viruses sampled during the Tara Oceans and Ma
282 efore the Bolling-Allerod interstadial), the deep ocean was about three degrees Celsius warmer than s
283 strial-scale dumping of organic waste to the deep ocean was once common practice, leaving a legacy of
286 Therefore, the seamount should retain the deep-ocean water for 1.8 years for the deep-ocean bacter
287 cale ventilation of Southern Ocean CO2-rich, deep-ocean water masses is thought to have been fundamen
290 sants stimulate microbial oil degradation in deep ocean waters and instead highlights that dispersant
292 scale dynamical instabilities by the flow of deep-ocean waters along a steep topographic boundary.
293 usly undocumented mixing mechanism, by which deep-ocean waters are efficiently laundered through inte
295 rface ocean conditions are translated to the deep ocean, where decadal peaks in supply, remineralizat
296 le in furnishing the diapycnal mixing in the deep ocean which affects the uptake of heat and carbon b
297 ents 20% of total organic carbon flux to the deep ocean, which constitutes a primary control on atmos
299 eparates the productive upper ocean from the deep ocean, yet little is known of its long-term dynamic
300 ces of dissolved organic carbon (DOC) to the deep ocean, yet the contribution from advective settings