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1 e.g. factors linked to treeline position and glaciers).
2 of the total ice loss expected from Thwaites Glacier.
3 +/-0.2 muM) over a 14 day period at Leverett Glacier.
4 2 for Jakobshavn, Helheim, and Kangerlussuaq glacier.
5 ts and decreased with distance away from the glacier.
6 Jakobshavn Isbrae, Greenland's major outlet glacier.
7 nge can instigate surges of Arctic tidewater glaciers.
8 involve a transient increase due to melting glaciers.
9 community with the complete disappearance of glaciers.
10 rrent simulations of ice loss from tidewater glaciers.
11 ng increased discharge of marine-terminating glaciers.
12 ribution to sea level rise of PIG and nearby glaciers.
13 ils of known age exposed upon the retreat of glaciers.
14 vance and retreat of Pleistocene continental glaciers.
15 ive the retreat of modern marine-terminating glaciers.
16 of 8.1 +/- 1.1 millimetres from these three glaciers.
17 and climate from a global compilation of 38 glaciers.
18 erated by physical comminution of bedrock by glaciers.
19 athway of BC from distant regions to the HTP glaciers.
20 that may be present in many Arctic tidewater glaciers.
21 7 glaciers (85% of D) and indirectly for 110 glaciers (15%) using velocity-scaled reference fluxes.
22 anisms driving the observed retreat of these glaciers, 2 ~32-m-long ice cores to bedrock recovered in
23 grounding line migration of 38% for Thwaites Glacier 350 years in the future, or 26.8% reduction in c
24 trace metal ice core record from the Dasuopu glacier (7,200 m, central Himalayas), the highest drilli
25 ischarge, D, into the ocean directly for 107 glaciers (85% of D) and indirectly for 110 glaciers (15%
27 state-of-the-art ice sheet model of Thwaites Glacier, a marine-terminating glacier in West Antarctica
29 on (~10%), the recession of lake-terminating glaciers accounted for up to 32% of mass loss in differe
30 thropogenic black carbon (BC) to snowmelt in glacier accumulation zones of Central Asia based on in-s
32 e determined volume changes for 400 mountain glaciers across the Southern Alps, New Zealand for three
36 driven by the direct and indirect impacts of glacier algae on ice albedo, with a significant negative
37 the photophysiological mechanisms that allow glacier algae to thrive on and darken the bare ice surfa
38 e cellular content of chlorophyll a) enables glacier algae to tolerate extreme irradiance (up to ~4,0
41 ution Imaging Spectroradiometer [MODIS]) and glacier algal biomass (R (2) = 0.75, n = 149), indicatin
42 ased 50-fold by phenolic pigmentation, while glacier algal chloroplasts positioned beneath shading pi
44 eness of this event, we extend the record of glacier and ocean changes back 1700 years by analyzing a
51 ts in an increased flux of ice from adjacent glaciers and ice streams, thereby raising sea level glob
52 ade aggravates the BC pollution over the HTP glaciers and may cause significant climate change there.
53 haea) in distinct surface habitats and on 12 glaciers and permanent snow fields in Svalbard and Arcti
54 cover five to 15 times the area of permanent glaciers and snow, highlighting their eco-hydrological i
58 ely consumed CO(2) up to 42 km downstream of glaciers, and cumulatively transformed the High Arctic's
59 main contributors to sea-level rise (oceans, glaciers, and ice sheets) respond to climate change on t
64 makes this region vulnerable to drought, but glaciers are a uniquely drought-resilient source of wate
65 le economically and socially to drought, but glaciers are a uniquely drought-resilient source of wate
66 ems.The reason some of the Earth's tidewater glaciers are advancing despite increasing temperatures i
67 systems, and demonstrate that debris-covered glaciers are among the most sensitive recorders of obliq
71 mountain stream insects, particularly where glaciers are likely to vanish on contemporary timescales
77 functional genes was mainly associated with glacier area proportion, glacier source proportion, tota
79 arch needle within the ice of Schaufelferner glacier at 2,870 m asl (Stubai Alps, Austria) allows for
82 fer direct access to the stratigraphy at the glacier base and validation against existing age constra
83 up-glacier, mobilizing the entire 450 km(2) glacier basin over a few days as the till entered an uns
85 sported 4.8 x 10(6) m(3) of meltwater to the glacier bed in ~5 h, reducing the lake to a third of its
86 e 20(th) century high SSTs in magnitude, the glacier behaved differently during the 20(th) century.
88 involved the near-complete disappearance of glaciers below 4700 masl in the eastern Andean cordiller
89 ptobiosis during six centuries of cold-based glacier burial in Antarctica, 2) after re-exposure due t
90 he highest elevation streams primarily below glaciers, but also snowfields and groundwater springs.
91 e in these regions that currently have large glaciers, but few lakes, if future projected ice loss ge
94 e, we combine high-resolution biological and glacier change (ca. 1850-2015) datasets for Glacier Nati
97 demonstrates the potential for using alpine glacier chronologies in the Transantarctic Mountains as
98 iment and meltwater delivery from changes in glacier configuration may impact interpretations of mari
100 t a 70 km-diameter crater into a continental glacier could release between 8.7 x 10(13) to 5.0 x 10(1
104 ry inputs to arctic ecosystems downstream of glaciers despite recent reductions in global mercury emi
108 red to bedrock on the summit of one of these glaciers document a rapid pace in the loss of ice cover
109 largest Alaskan Cordilleran Ice Sheet outlet glacier during Last Glacial Maximum climate transitions.
110 eases in meltwater could induce a shift to a glacier dynamic regime characterised by seasonal-scale h
111 melting), and Greenland and Antarctic outlet glaciers (dynamic response to ocean melting) was partial
112 The mass loss is controlled at 66 +/- 8% by glacier dynamics (9.1 mm) and 34 +/- 8% by SMB (4.6 mm).
114 f young organic matter sources released from glacier ecosystems and their surrounding watersheds.
116 nthesis of the microbial ecology of mountain glacier ecosystems, and particularly those at low- to mi
117 Flow models of the ice sheet and till-bedded glaciers elsewhere require a law that relates slip resis
118 ra subglacial basin, that marine-terminating glaciers existed at the Sabrina Coast by the early to mi
119 a one-month period in early summer 2016, the glacier experienced essentially no calving, and was butt
120 onar surveys to image a subsurface tidewater glacier face and document a time-variable, three-dimensi
121 limnology, to conclusively show that certain glacier-fed freshwater ecosystems are important and prev
122 in the catchment of Lake Brewster, an alpine glacier-fed lake located in the Southern Alps of New Zea
126 en metabolic pathways and abiotic factors in glacier-fed streams in the Tianshan Mountains in Central
127 e microbial functions of benthic biofilms in glacier-fed streams, we predicted metagenomes from 16s r
132 results motivate a generalized slip law for glacier-flow models that combines processes of hard-bedd
135 and the preconditioning of land-terminating glaciers for new lake development increases the likeliho
142 mountains-have the highest concentration of glaciers globally, and 800 million people depend in part
143 esent on the ice shelf in front of Petermann Glacier, Greenland, but other systems, such as on the La
147 ormer tributary of the once larger Hasanabad Glacier (Hunza region), dammed the proglacial river of M
148 lect stick-slip motion which occurs when the glacier hydrological system is unable to accommodate the
149 re consistent with values measured from cold glacier ice and while this may be feasible, uncertaintie
153 sents the first documented advance of alpine glacier ice in the Dry Valleys during Marine Isotope Sta
156 nt of this method, all LA-ICP-MS analyses of glacier ice involved a single element per ablation pass
158 s recovered beneath the floating Pine Island Glacier ice shelf, and constrain the date at which the g
160 ano, based on ice-core records from Illimani glacier in Bolivia, providing the first complete history
161 n cryoconite and proglacial sediments from a glacier in British Columbia, Canada, and compare values
163 e concentrations in rivers draining Leverett Glacier in southwest Greenland and Kiattuut Sermiat in s
165 solution ice-core Hg record from the Belukha glacier in the Siberian Altai, covering the time period
166 at the remnant eastern ice shelf of Thwaites Glacier in West Antarctica had thinned between 10 and 33
167 present thinning and retreat of Pine Island Glacier in West Antarctica is part of a climatically for
168 el of Thwaites Glacier, a marine-terminating glacier in West Antarctica that is thought to be unstabl
174 UFG), Wyoming, is one of the few continental glaciers in the contiguous United States known to preser
175 ed at other locations around the world, some glaciers in the High Mountains of Asia appear to have ga
179 rate increases of up to 6.3% (7 cm a(-1)) on glaciers in three different mountain environments in Kyr
180 accelerated ice-mass loss from large outlet glaciers in W and SE Greenland has been linked to warmin
181 unding zones of the Pine Island and Thwaites glaciers in West Antarctica need to retreat only short d
182 ayment are among the fastest changing outlet glaciers in West Antarctica with large consequences for
184 .e.a(-1)) mass balances for lake-terminating glaciers, in comparison to land-terminating glaciers, wi
185 Our results show that both L. tumana and Z. glacier inhabit an extremely narrow distribution, restri
187 ate time-varying elevations near the melange-glacier interface, generating a factor of three or more
191 alayas has gradually spawned more than 5,000 glacier lakes that are dammed by potentially unstable mo
192 tion experiments in a wild population of the glacier lily (Erythronium grandiflorum, Liliaceae) from
193 ogy and morphology caused by climate-induced glacier loss are projected to be the greatest of any hyd
197 pact of riverine organic matter subsidies to glacier-marine habitats by developing a multi-trophic le
200 of surface debris cover and glacial lakes on glacier mass loss across the Himalaya since the 1970s.
202 t projections forced by RCP8.5 underestimate glacier mass loss which could exceed this worst-case sce
207 ascribed to the delivery of dense and turbid glacier meltwaters mixing PFAS throughout the Lake Hazen
208 iodiversity and functional roles of mountain glacier microbiota; describe the ecological implications
212 glacier change (ca. 1850-2015) datasets for Glacier National Park, USA, to test the prediction that
213 , we report the recent, rapid retreat of the glaciers near Puncak Jaya by quantifying the loss of ice
215 Rapid changes observed today in mountain glaciers need to be put into a longer-term context to un
216 the terminal moraine complex of the Ngozumpa Glacier, Nepal, to aid assessment of future terminus sta
217 riverine organic matter assimilation by the glacier-nesting seabirds Kittlitz's murrelet (Brachyramp
219 theast Greenland, hosts three of the largest glaciers of the Greenland Ice Sheet; these have been maj
220 ge of surface meltwater to the bed of outlet glaciers on the Antarctic Peninsula occurs and triggers
221 he mass loss of debris-covered and clean-ice glaciers over our study period, but substantially more n
222 s that potentially accelerate the retreat of glaciers over the Himalayas and Tibetan Plateau (HTP).
225 te representing a minor portion of the total glacier population (~10%), the recession of lake-termina
226 sections of cold, alpine streams often below glaciers predicted to disappear over the next two decade
227 ronosequences at the forefront of retreating glaciers provide information about colonization rates of
231 ates points to factors capable of amplifying glacier recession in addition to climatic change along t
234 esert (SD) and greening of the Arctic tundra-glacier region (ArcTG) have been hot subjects under exte
238 poraneous ocean-forced change and of ongoing glacier response to an earlier perturbation in driving i
242 ble estimate of blue carbon change caused by glacier retreat along Antarctic fjords and thus to estab
246 This observation constrains maximum Holocene glacier retreat here to less than 6 km from present-day
247 We started by multiplying ~40 year mean glacier retreat rates by the number of retreating WAP fj
248 ional Park, USA, to test the prediction that glacier retreat reduces biodiversity in mountain ecosyst
250 l in Antarctica, 2) after re-exposure due to glacier retreat, instead of dying (due to high rates of
251 er year; P < 0.03) and also suggest that the glaciers' retreat is augmented by El Nino-Southern Oscil
252 8,000 years before present [YBP]); after the glacier retreated, ice patches remained on the island un
253 f Alaska originates from landscapes draining glacier runoff, but the influence of the influx of river
255 tive, the contribution from India to the HTP glaciers shows a rapid increasing trend while the contri
256 Here, we synthesize current evidence of how glacier shrinkage will alter hydrological regimes, sedim
259 on rate is usually modelled as a function of glacier sliding velocity, but the empirical basis for th
260 nly associated with glacier area proportion, glacier source proportion, total nitrogen, dissolved org
261 e meltwater stonefly (Lednia tumana) and the glacier stonefly (Zapada glacier) - were recently propos
263 ment produced the highest recorded Karakoram glacier surface flow rate using feature tracking (~18 +/
265 re samples from the high-alpine Fiescherhorn glacier (Swiss Alps), and used high-performance liquid c
266 of the January 2009 collapse of the Nathorst Glacier System (NGS) in Svalbard, we show that an underl
268 and sediment dynamics: a shoal forms at the glacier terminus, reducing ice discharge and causing adv
270 future warming could trigger advance even in glaciers that are steady or retreating, complicating int
271 search, with less attention paid to mountain glaciers that overlap environmentally and ecologically w
274 Climate plays a paradoxical role as cold glacier thinning and retreat promote basal freezing whic
275 imperils the persistence of L. tumana and Z. glacier throughout their ranges, highlighting the role o
276 By contrast, in front of the retreating Pia Glacier (Tierra del Fuego, Chile), a Nothofagus forest i
277 We show a rare fully instrumented coupled glacier/till record of contrasting summer and winter sti
279 ertain response of marine terminating outlet glaciers to climate change at time scales beyond short-t
280 ia was extensive, and the sensitivity of its glaciers to climate variability during the last terminat
281 rence lies in the susceptibility of mountain glaciers to the near-term threat of climate change, as t
282 data from an Icelandic soft-bedded temperate glacier, to show that there are two distinct seasonal st
283 beneath an East Antarctic ice shelf, Shirase Glacier Tongue, driven by southward-flowing warm water g
285 ter can reduce till strength under tidewater glacier tongues to orchestrate a temporal clustering of
288 erization of samples collected from within a glacier using a melt probe, and the only Antarctic subgl
292 nia tumana) and the glacier stonefly (Zapada glacier) - were recently proposed for listing under the
294 on), dammed the proglacial river of Muchuhar Glacier, which formed an ice-dammed lake and generated a
295 iated with melting permafrost and retreating glaciers, while lowest burial rates occurred during the
297 Yet, assessing how much and how fast both glaciers will weaken if these changes continue remains a
298 most rapid erosion is achieved at temperate glaciers with high mean annual precipitation, which serv
300 glaciers, in comparison to land-terminating glaciers, with the largest differences occurring after 2