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1 consistent with proxy evidence for the last glacial.
2 schger (D-O) climate changes during the last glacial.
7 itation, involving dissolution in ethanol or glacial acetic acid followed by precipitation by additio
11 western Greenland Ice Sheet (GIS) during the glacial advance of marine oxygen isotope stage 4 (MIS4).
14 has only been identified for the most recent glacial and deglacial periods and is thought to be absen
15 ocean circulation and stratification between glacial and interglacial climates can be interpreted as
16 ts were grounded below sea level during both glacial and interglacial periods, with grounding lines a
17 limate has undergone dramatic shifts between glacial and interglacial time periods, with high-latitud
18 indings support the hypothesis that repeated glacial and landslide damming in this region inhibited h
19 spread As and Mn contamination including the Glacial Aquifer in the U.S., the Ganges-Brahmaputra-Meht
20 -latitude climate variations during the last glacial are expected to propagate globally in a complex
21 bution of allochthonous migrants in the post-glacial assembly of Europe is unparalleled in other plan
22 coalescent simulations showed that the post-glacial assembly of European bryophytes involves a compl
23 ss mixing dominated the distribution of deep glacial Atlantic Nd isotopes, our results would imply a
26 his hypothesis, previous work has shown that glacial Ca limits vegetative growth in the wild progenit
28 m an iron and silicate mineral-rich basaltic glacial catchment were an order of magnitude higher than
30 netic diversity are likely influenced by the glacial climate cycle and recent history of whaling.
31 vier shells would need to be precipitated in glacial climates in order for these organisms to remain
33 Earth has experienced warm ice-free and cold glacial climates, but it is unknown whether transitions
37 deficit and temperature were decreased under glacial conditions at La Brea, and these have compensati
41 ht to constrain the magnitude and pattern of glacial cooling from palaeothermometers(1,2), but the un
42 set of climate model simulations of the last glacial cycle (120 kyr), that compares well against a co
43 ironmental histories that span the last full glacial cycle and are representative of regional change
44 onounced ice-sheet asymmetry within the last glacial cycle and significant variations in ice-marginal
45 treme Greenland shelf glaciation of the last glacial cycle occurred during MIS 4, with another promin
50 a warmer climate state with sawtooth-shaped glacial cycles in the Early Miocene was brought about by
53 Only with global cooling and the onset of glacial cycles some 3 Mya, toward the end of the Pliocen
54 Between about 2.8 and 1.2 million years ago, glacial cycles were smaller in magnitude and shorter in
55 c divergences relative to the timing of past glacial cycles, including collapses of the West Antarcti
62 Conversely, regions of bedrock confined by glacial deposits yielded significantly lower median N2O-
63 onstraint for the youngest Palaeoproterozoic glacial deposits, the Rietfontein diamictite in South Af
66 ween being primarily regulated by sea ice or glacial discharge from the surrounding grounded ice shee
70 e infer that reduced vegetation cover during glacials drove higher sediment flux from the rift flanks
72 ive that changes in snow and ice melt across glacial environments will influence the abundance and di
74 matic conditions, including interglacial and glacial episodes, between 670 and 650 (i.e., MIS17/MIS16
75 Miocene was brought about by subsidence and glacial erosion in West Antarctica during the Late Oligo
77 surface, but there is uncertainty about how glacial erosion should be parameterised in landscape evo
78 ecipitation has received little attention in glacial erosion studies, but our data illustrate its imp
79 ed by spatially heterogeneous Neoproterozoic glacial erosion totaling a global average of 3-5 vertica
80 to show that interactions between ice flow, glacial erosion, and sediment transport drive these cycl
82 ndings can be used to improve models of past glacial, eustatic, tectonic, and geomorphic processes on
84 n the deep Atlantic, similar in magnitude to glacial events, have been relatively common and occasion
88 We identify the location of immediate pre-glacial fluvially derived sandy systems where rivers fro
89 Centennial-scale mineral dust peaks in last glacial Greenland ice cores match the timing of lowest G
90 ture in the grass's western spread, although glacial history and environmental heterogeneity also cou
91 e is very low and is sourced from melting of glacial ice and direct release of occluded CO(2) gases i
93 nd modelling evidence indicate that the last glacial inception in North America was in NE Canada, lit
95 hat have remained more stable in response to glacial-interglacial changes in climate were also more s
100 el varied on average by 13 +/- 5 metres over glacial-interglacial cycles during the middle-to-late Pl
103 siderably across and within millennia during glacial-interglacial cycles of the Late Quaternary.
104 Over the past eight hundred thousand years, glacial-interglacial cycles oscillated with a period of
105 ive amplitude of sea-level variations within glacial-interglacial cycles remains poorly constrained.
106 nal hydroclimate records that cover multiple glacial-interglacial cycles(2,3) with different orbital
107 ficantly across decades and centuries during glacial-interglacial cycles, likely causing rapid region
111 ng by Earth's climatic precession, with each glacial-interglacial period spanning four or five cycles
113 er observed in pyrite, and are in phase with glacial-interglacial sea level and temperature changes.
114 ing the strength of the biological pump, the glacial-interglacial shift in the Si cycle may present a
115 drologic seesaw is apparent over orbital and glacial-interglacial timescales, but its existence over
116 of carbon exchanging with the atmosphere on glacial-interglacial timescales, the deep ocean has been
117 bfossil chironomid records spanning the last glacial-interglacial transition (~15,000-11,000 years ag
118 r, wetter, and more isolated during the last glacial-interglacial transition from approximately 15 to
119 lation bottleneck hypothesis during the Last Glacial-Interglacial transition, providing a demographic
121 ally significant difference between previous glacial-interglacial transitions and the very last one w
122 tion rests on two assumptions: that previous glacial-interglacial transitions were similar to the end
123 why did these large mammals survive previous glacial-interglacial transitions, only to vanish at the
124 Our results confirm that the amplitudes of glacial-interglacial variations in atmospheric greenhous
125 f applications, including ocean circulation, glacial/interglacial climates, and anthropogenic climate
127 Their area has varied dramatically over the glacial/interglacial cycles of the last million years, b
129 rk provides a clear sign of sea level-driven glacial/interglacial oscillations in biogeochemical flux
130 ies probably colonized Abaco during the last glacial interval but were eliminated when the island bec
131 50 to 35 ka, are surprisingly high for this glacial interval, and remain unexplained by previous mod
132 the plants that were present during the last glacial interval, including all of the arctic-alpines, a
134 es an independent constraint on the combined Glacial Isostatic Adjustment - the Earth's delayed visco
135 These records capture spatial variations in glacial isostatic adjustment and paleotidal range, yet b
137 is sea-level record using a revised model of glacial isostatic adjustment characterized by a peak glo
138 ences of penultimate and LIG deglaciation on glacial isostatic adjustment, this excess loss of polar
141 s to expand to a fully formed moraine-dammed glacial lake, the degradation of the ice core could have
143 ne the influence of surface debris cover and glacial lakes on glacier mass loss across the Himalaya s
144 oat and therefore shares similarities to sub-glacial lakes where they are sealed to the atmosphere.
147 variation in P. leucopus indicates two post-glacial lineages are separated by the St. Lawrence River
155 by the Laurentide ice sheet during the Last Glacial Maximum (18,000 years before present [YBP]); aft
156 )of cultural evidence that dates to the Last Glacial Maximum (26,500-19,000 years ago)(18), and which
157 reases the volume of the AIS during the Last Glacial Maximum (about 26,000 to 20,000 years ago), trig
158 efore, during and immediately after the Last Glacial Maximum (about 26.5-19 thousand years ago)(2,3)
159 eastern Ross Sea shelf edge during the Last Glacial Maximum (LGM) and eventually retreated 1000 km t
163 by heavy sea ice conditions during the Last Glacial Maximum (LGM) yielded genetic signatures of near
164 olf population that expanded during the last glacial maximum (LGM)(1-3) and replaced local wolf popul
166 more radiogenic than modern during the Last Glacial Maximum (LGM), and shifted towards modern values
170 owth potential of Trichodesmium for the last glacial maximum (LGM), the present (2006-2015) and the e
175 and two paleoclimatic environments, the Last Glacial Maximum (LGM, ~ 21 kya) and the Mid-Holocene (MH
177 arth's history, in particular since the Last Glacial Maximum 20,000 years ago, and are used in this s
178 ons of the extent of the AIS during the Last Glacial Maximum and subsequent ice-sheet retreat, and wi
179 ximus groups having diverged during the last glacial maximum and subsequently expanded, whereas P. ja
182 d drainage of Fe-rich waters during the Last Glacial Maximum could have reached the Southern Ocean.
183 wave of megafaunal turnover before the Last Glacial Maximum in Eurasia, in addition to the better-kn
185 or divergence prior to the onset of the last glacial maximum shaped the genetic diversity and structu
187 ated as tidal channels during the post- Last Glacial Maximum transgression, when the study area was a
188 che modeling to infer current and past (Last Glacial Maximum) environmental suitability across the sp
189 an and Epigravettian layers, across the Last Glacial Maximum, and dated between 31210-33103 and 18334
190 casted species distributions during the Last Glacial Maximum, we hypothesize that Arctic coastal syst
191 ntaining tropical grasslands during the last glacial maximum, which are possible centres of diversifi
192 ed dramatic range reductions during the Last Glacial Maximum, yet refugial populations from which mod
204 cal for understanding how current and future glacial melt seasons may influence downstream environmen
205 consumption in proglacial freshwaters due to glacial melt-enhanced weathering is likely a globally re
207 dicated that the pesticide concentrations in glacial meltwater and lake water were strongly correlate
208 aminants in suspended sediments suggest that glacial meltwater and the delivery of cryoconite have li
209 nt export of microbial assemblages alongside glacial meltwater is expected to impact the ecology of a
210 ic climate conditions and suggests that peak glacial meltwater production is imminent if not already
212 sticides were quantified in air, lake water, glacial meltwater, and streamwater in the catchment of L
219 .4 +/- 0.4 to 111.0 +/- 0.4 ka BP during the glacial onset and retreated from 12.1 +/- 0.1 to 9.0 +/-
221 mperature records, and estimates of the last glacial oxygen isotopic composition of precipitation bas
222 ved regional amount effect variability, last glacial paleotemperature records, and estimates of the l
223 d and Antarctic temperatures during the last glacial period (115,000 to 11,650 years ago) are thought
224 atterns of variability since the penultimate glacial period (140 ka), but the seasonality of this sig
225 Both tephra were erupted during the last glacial period and a widespread increase in subglacial v
226 t largely formed during the late Pleistocene glacial period and shrank in the Holocene Thermal Maximu
229 pheric CO2 (Ca ) experienced during the last glacial period is hypothesized to have been an important
230 of the region, suggests that during the last glacial period such ticks occupied distinct refugia, wit
232 his hydroclimatic transition from the wetter glacial period to more arid Holocene accompanies a surfa
233 jor atmospheric CO2 drawdown during the last glacial period were linked to iron (Fe) fertilization of
236 climatic episodes in Alaska during the last glacial period, when permafrost was absent, allowing wat
237 ed by the atmospheric conditions of the last glacial period, with important implications for the orig
238 the Amazon was widely drier during the last glacial period, with much less recycling of water and pr
245 er similar oscillations are typical of prior glacial periods, however, has not been well established.
246 rsist in the southern Atlantic Forest during glacial periods, particularly during the Last Glacial Ma
247 would have been especially effective during glacial periods, when the Atlantic Meridional Overturnin
250 nologies are only available for several Last Glacial pollen and rare speleothem archives principally
251 s for emplacing offshore groundwater include glacial processes that drove water into exposed continen
252 ur results indicate a stronger role for post-glacial range expansion, rather than isolation in allopa
255 ering of these distinctive features was in a glacial refuge zone on the southern coast 100-70 ka, wit
256 Long-lasting geographic isolation between glacial refugia could have been led to the allopatric sp
257 infer the precise latitude and longitude of glacial refugia in two widespread, codistributed hickori
261 e this issue, as it has been considered as a glacial refugium during critical periods of the Neandert
262 was in NE Canada, little is known about the glacial response of the nearby western Greenland Ice She
265 m, we found that weathering reactions in the glacial rivers actively consumed CO(2) up to 42 km downs
267 particulate and dissolved organic carbon in glacial runoff and near surface coastal waters was aged
268 sheet melting, suggests that their export in glacial runoff is likely to be important for biological
270 he existence of complex interactions between glacial sea level changes, volcanic degassing and atmosp
271 dionuclides (FRNs) and other contaminants in glacial sediments, especially cryoconite, in European gl
273 ts before these impacts suggests large-scale glacial silt production and supports the previously prop
276 the existence of refuge areas during intense glacial stages and raise questions concerning understudi
281 dary carotenoids, which cause a darkening of glacial surfaces leading to a decrease in surface albedo
282 cate that a surface-meltwater-rich sub-polar glacial system existed under climate conditions similar
287 ve remained spatially stable throughout post-glacial time, although with transform-affinity faults re
288 s substantially drier or remained wet during glacial times has been controversial, largely because mo
291 ved, boron isotope CO2 data to show that the glacial to interglacial CO2 difference increased from ap
292 se in unthreshed grain yield of 50% with the glacial to postglacial increase in Ca , which matched th
293 temperature in the 40k world are well above glacial values from the past eight hundred thousand year
294 e present an exceptionally well-dated annual glacial varve chronology recording the melting history o
296 ical and geological evidence shows that post-glacial warming released human populations from their va