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1 edge kelp forests on both sides of the North Atlantic.
2 influences on hydroclimate over the tropical Atlantic.
3 n the upper Porcupine Bank Canyon (uPBC), NE Atlantic.
4 whales (Megaptera novaeangliae) in the North Atlantic.
5 austion of excess carbonate in the Northeast Atlantic.
6 res the multidecadal variability seen in the Atlantic.
7 , Gulf of Mexico and western North and South Atlantic.
8 iction of ISOW pathways throughout the North Atlantic.
9 iological productivity in the tropical North Atlantic.
10 termining the salinity of the subpolar North Atlantic.
11 uth of Greenland, cooling the subpolar North Atlantic.
12 curately the temperature change in the North Atlantic.
13 nnected to lower latitudes through the North Atlantic.
14 onized the already existing rookeries of the Atlantic.
15 Sharks were collected from the North-East Atlantic.
16 ic diversity within a major ocean basin (the Atlantic), a regional rookery (Cabo Verde Archipelago) a
17 duals in the Americas and populations across Atlantic Africa, yielding a more comprehensive understan
18 nucleotide polymorphisms clearly resolved an Atlantic and a Norwegian group within P. maximus as well
21 6 times larger to protect the same number of Atlantic and Caribbean species, which occur at lower abu
23 Here, we show that along the North American Atlantic and Gulf coasts the meridional distributions of
25 als AESs around sub-Antarctic islands in the Atlantic and Indian Oceans and over the Antarctic contin
28 ch is critically endangered in the Northeast Atlantic and landings have been prohibited (although the
30 s of potential teleconnections between North Atlantic and mid-to-low latitudes at the transition from
31 eef fish trophic interactions in the Western Atlantic and modeled projections of changes in fish occu
34 vironmental conditions in the tropical North Atlantic and North Pacific and significantly correlated
35 e anticorrelation of TUTTs between the North Atlantic and North Pacific makes the TC activity indices
36 alysis of surge extremes covering the entire Atlantic and North Sea coasts of Europe for the period 1
38 15%-30% (+/-12%-17%) in the North and South Atlantic and Pacific, and the Indian Ocean by 2100, wher
41 red laminarin along transects in the Arctic, Atlantic, and Pacific oceans and during three time serie
45 ported from the Norwegian Sea into the North Atlantic as part of the global Meridional Overturning Ci
46 on (the leading mode of variability in North Atlantic atmospheric circulation) by an order of magnitu
47 . counties for all land-falling or near-land Atlantic basin storms, covering 1996-2011 for all metric
48 ropical cyclone intensification rates in the Atlantic basin that are highly unusual compared to model
50 cyclone ecology is biased towards the North Atlantic Basin, because cyclone effects do differ across
52 tal mercury in muscle tissue from 268 reared Atlantic bluefin tuna in the Mediterranean Sea, detects
53 ies investigated (blue marlin, white marlin, Atlantic bluefin tuna, yellowfin tuna) frequently crosse
54 encephalitis virus has been detected in wild Atlantic bottlenose dolphins, and captive orcas have bee
55 p boundary current around the subpolar North Atlantic, but this single-boundary-following pathway is
56 mited climate refugia locations in the North Atlantic by 2100 for scleractinian corals (30%-42% of pr
58 a substantial warming over much of the North Atlantic, caused by increasing greenhouse gases over the
61 ons are in agreement with multidecadal North Atlantic climate variability derived from independent pr
62 blue crab (Callinectes sapidus) along the US Atlantic coast and found that their intrinsic dynamics w
64 Scotia to Georgia winter exclusively on the Atlantic coast of northern South America and share commo
66 the northern Amazon and then directly to the Atlantic coast, or heading south into the continent and
67 ecognized across the Southeast, Midwest, and Atlantic Coast, with many providers in this area managin
69 ted 12.5 million people from ports along the Atlantic coastline of Africa between the 16th and 19th c
70 ng and autumn through the Gulf of Mexico and Atlantic coasts of the south-eastern US, the most promin
76 ransformation limits and the central role of Atlantic cod, which is the main target species but canno
79 ta, ruggedness, and backscatter from a trans-Atlantic corridor along the Vema Fracture Zone, covering
81 circulation, including slowing of the North Atlantic Current and diversion of Arctic freshwater from
82 importantly, we show evidence that the North Atlantic current and its variability shape the spatial d
83 reveal an increase, up to two-fold, in North Atlantic current surface velocities over the last 24 yea
85 m, the West Atlantic D. antillarum, the East Atlantic D. africanum, and the Indo-Pacific D. paucispin
86 n in the East Pacific D. mexicanum, the West Atlantic D. antillarum, the East Atlantic D. africanum,
87 emperature (SST) estimates from southwestern Atlantic Deep Sea Drilling Project Site 516 (paleolatitu
89 Here we present a detailed record of North Atlantic deep-ocean temperature, global sea-level, and i
91 imply a larger fraction of NADW in the deep Atlantic during the LGM and deglaciation than reconstruc
94 warmer, higher-salinity water from the North Atlantic entering the Arctic (260 +/- 20 pg/L versus 190
95 Over the past century, the subpolar North Atlantic experienced slight cooling or suppressed warmin
97 We extrapolated our findings to the entire Atlantic Forest and found that just 19.4% of the total e
99 uence, An. cruzii moves to the border of the Atlantic Forest nearing urban areas seeking resources, i
101 by northern (lowland) and southern (montane) Atlantic Forest species, triggered by the joint impact o
102 focused on the globally threatened Brazilian Atlantic Forest, where commitments have been made to res
109 (2) of rock habitats potentially occur along Atlantic fracture zones alone, significantly increasing
111 d to much greater depths than those at Trans-Atlantic Geotraverse and Logachev-1 hydrothermal fields
112 metabolomes of five mother and pup pairs of Atlantic grey seals, Halichoerus grypus, from birth to w
113 two species) inhabits the eastern equatorial Atlantic, Gulf of Mexico and western North and South Atl
114 ries Study (BATS) in the Sargasso Sea (North Atlantic gyre) provides a unique opportunity to explore
117 modeling experiments to show that the North Atlantic has also strongly influenced the Extratropical
118 etic models suggests the colonization of the Atlantic has occurred in two distinct waves, each corres
121 n hurricane-associated rainfall in the North Atlantic highlight the need to consider how such shifts,
122 This suggests that spatial heterogeneity in Atlantic hurricane activity since 1850 CE could have per
123 ing examples from Hawaiian volcanic and West Atlantic hurricane interactions, this work illustrates h
124 ined the effects of the most energetic North Atlantic hurricane season in 50 years on the genetic div
127 ucted climate variables characterizing North Atlantic: i.e. sea surface temperatures (SST) from the t
130 apor transport from the tropical Pacific and Atlantic increased high-altitude atmospheric humidity an
131 n the Pacific sector and deceleration in the Atlantic-Indian Sectors, forming a bi-polar spatial patt
132 r taxa under a future scenario of increasing Atlantic influence, but the eukaryote response is more c
133 and slow) have different frequencies across Atlantic intertidal zones due to selection on postsettle
135 Here, the chemical status of the Northeast Atlantic is examined by means of a high-quality database
136 ayer, the carbonate content in the Northeast Atlantic is maintained by the interplay between the nort
137 elected Tropic Seamount in the North-Eastern Atlantic is representative for the majority of isolated
138 e may be having a larger impact on the North Atlantic jet stream than previously thought. The increas
140 g this deep water cycle because hydration in Atlantic lithosphere, produced by slow spreading, is exp
141 shelf-life of mechanically filleted well-fed Atlantic mackerel during frozen storage at -25 degrees C
143 et molecules from the most abundant species (Atlantic mackerel) both in real-time and from the archiv
147 w PGE data for volcanic rocks of the Central Atlantic Magmatic Province (CAMP) in Morocco and show th
150 basaltic rocks from the end-Triassic Central Atlantic Magmatic Province (CAMP), through investigation
152 prioritization strategies, the Northeastern Atlantic marine terebellid Eupolymnia nebulosa was selec
153 re, continued ocean warming in the northeast Atlantic may reduce primary productivity of this foundat
154 ttribute to invigoration or weakening of the Atlantic meridional overturning circulation (AMOC) and a
156 ep convection, affecting the strength of the Atlantic Meridional Overturning Circulation (AMOC) and t
157 limate anomalies in response to slow-down of Atlantic meridional overturning circulation (AMOC) durin
158 y effective during glacial periods, when the Atlantic Meridional Overturning Circulation (AMOC) exper
159 mportant diagnostic for the stability of the Atlantic Meridional Overturning Circulation (AMOC).
162 k Channel and supplies the lower limb of the Atlantic Meridional Overturning Circulation, a critical
163 ordic Seas comprises the deepest limb of the Atlantic Meridional Overturning Circulation, yet questio
164 n in accordance with stronger (weaker) South Atlantic mid- to high-latitudes mean sea-level pressure
165 equent records from other parts of the North Atlantic, minke whales have never been acoustically reco
166 s they provide, under predicted increases of Atlantic mixing and warming within the Arctic region.
167 highlight the potential role of other North Atlantic modes of variability (i.e., East Atlantic patte
168 ISM rainfall appears to be modulated by the Atlantic Multi-decadal Oscillation (AMO) via changes in
169 Nino-Southern Oscillation (ENSO), the North Atlantic Multidecadal Oscillation (AMO), and tropical cy
173 g dominated the distribution of deep glacial Atlantic Nd isotopes, our results would imply a larger f
174 sharks, Cetorhinus maximus, in the Northeast Atlantic (NEA) affords an opportunity to resolve individ
177 nditions are found during warm states of the Atlantic Ocean and positive phases of the North Atlantic
178 ses biological productivity in the Subarctic Atlantic Ocean as increasing ocean surface buoyancy supp
179 ored by a uranium-lead chronology with North Atlantic ocean data to show that the first two deglaciat
180 titude ~36 degrees S) and western equatorial Atlantic Ocean Drilling Project Site 929 (paleolatitude
183 fects, in seagrass ecosystems of the western Atlantic Ocean spanning 30 degrees of latitude from the
184 hat, during 1955-2017, up to one-half of the Atlantic Ocean warming and thermosteric sea-level rise a
185 ies are found in the temperate western North Atlantic Ocean, with limited information existing on the
194 nd in the Pacific, Indian and southern South Atlantic Oceans, comprising five previously allopatric s
195 associating with warmer northern Pacific and Atlantic oceans, leading mostly to global supply shortag
196 teleconnections to regions beyond the North Atlantic offer the prospect of reconstructing AMV from h
200 ance from the coast, elevation and the North Atlantic Oscillation (NAO) using PEP725 leafout data for
201 g El Nino Southern Oscillation (ENSO), North Atlantic Oscillation (NAO), and Pacific Decadal Oscillat
202 ction of the total variability) of the North Atlantic Oscillation (the leading mode of variability in
203 (a) negatively associated with lagged North Atlantic Oscillation for seals at NR and (b) positively
204 just the variance of the ensemble-mean North Atlantic Oscillation forecast to match the observed vari
206 are also improved, suggesting that the North Atlantic Oscillation is not driven solely by Atlantic mu
208 d use only the ensemble members with a North Atlantic Oscillation sufficiently close to the variance-
215 th Atlantic modes of variability (i.e., East Atlantic pattern) on the non-stationary behaviour of the
216 nce of the predicted(5) collapse of northern Atlantic planktonic stocks in response to a weakened Atl
217 to distinct assemblages across a gradient of Atlantic-Polar Water influence in the Norwegian Sea.
218 ent OSNAP (Overturning in the Subpolar North Atlantic Program) data with respect to estimates from cl
219 th high spatial resolution in the North-East Atlantic provides a unique opportunity to assess the abi
221 ures were widely dispersed through the North Atlantic reducing their overlap with breeding adults.
222 m 1982 to 2004 for Chesapeake Bay in the mid-Atlantic region of the United States supported estimates
224 of sea-surface pressure changes in the North Atlantic region, whose waters are among the world's fast
227 ture alkaline hydrothermal vents off the Mid-Atlantic Ridge axis nearly 20 y ago, the observation tha
229 n created during 26 Ma at a 11 degrees N Mid-Atlantic Ridge segment, and exposed along the Vema Trans
235 iated with probabilities of endangered North Atlantic right whales Eubalaena glacialis migrating to a
236 , we derived thermal affinities for European Atlantic rocky intertidal species by matching their know
237 and report 15,483 high-confidence SVs in 492 Atlantic salmon (Salmo salar L.) sampled from a broad ph
238 despread decline in marine survival rates of Atlantic salmon (Salmo salar) over the last four decades
240 investigated the genetic basis of growth in Atlantic salmon by exploiting the high level of genetic
241 ates the potential for production of further Atlantic salmon clonal lines, potentially with distinct
243 ice abundance after 38 EMB treatments on six Atlantic salmon farms, in a small archipelago in British
246 he differences between wild and domesticated Atlantic salmon may provide insights into some of the ge
247 Functional divergence of tshbeta paralogs in Atlantic salmon supports a specific role of tshbetab in
248 me of the offspring of wild and domesticated Atlantic salmon were compared using a common-garden expe
253 ts can occur within a single year (e.g., the Atlantic seaboard due to tropical cyclones and atmospher
254 ication of megalithic architecture along the Atlantic seaboard, culminating in the great passage tomb
256 -ice and the ice-associated ecosystem in the Atlantic Sector lasts far beyond their short lifespan.
257 ntimately links conditions on the North West Atlantic shelf and slope region with the eastern subpola
260 o large climate-induced changes in the North Atlantic simultaneously impacting populations from dista
262 n flows surround the edges of the Rivera and Atlantic slabs, while escape flows are inferred through
263 ese refugia, the Cantabrian region (northern Atlantic Spain), was intensively occupied throughout the
264 High-Arctic proxy and other highly resolved Atlantic SST proxies demonstrate that it shares the mult
265 eric-only model, that anomalously warm North Atlantic SSTs enhance heatwave activity through an assoc
266 recedented time resolution, indicating North Atlantic SSTs were coldest from ~1400-1800 CE, while cur
268 ences in pstS between the ETNP and the North Atlantic stations were consistent with differences in ph
269 establish baseline information on endangered Atlantic Sturgeon in the New York Wind Energy Area (NY W
272 The Gulf Stream front separates the North Atlantic subtropical and subpolar ocean gyres, water mas
273 In contrast to the ETNP, in the oxic North Atlantic T4-like cyanophages encoded psbA and pstS throu
276 tuce, is a fast growing seaweed in the North Atlantic that chefs are bringing into the local cuisine.
277 Along the Gulf Stream front in the North Atlantic, these observations further suggest that shear
279 o synchronize ocean sediments from the North Atlantic to correlate major climate events in a common t
280 experiments were performed in the northwest Atlantic to elucidate connectivity among areas closed to
281 anistic path by which a climatic driver, the Atlantic trade winds, determines the viability of a bird
284 es because they are known to influence North Atlantic tropical cyclone activity and because their und
286 We show that the eastern subpolar North Atlantic underwent extreme freshening during 2012 to 201
294 % of in- and outflow takes place), the North Atlantic Waters transport most of the ocean heat, but al
295 sea surface temperatures (SSTs) in the North Atlantic which vary on a multidecadal scale (Atlantic mu
296 ideo transects in the eastern tropical North Atlantic, which features a mild but intensifying midwate
297 of AChE in the hippocampal formation of the Atlantic white-sided dolphin (AWSD) with the view to und
298 es and show that decadal variations in North Atlantic winter climate are highly predictable, despite
299 tending from the Bering Sea to the northwest Atlantic, with high levels of genetic diversity in the e