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At least 73 records · Page 4Linked to original sources
USGS2018

Spring temperature, migration chronology, and nutrient allocation to eggs in three species of arctic‐nesting geese: Implications for resilience to climate warming

The macronutrients that Arctic herbivores invest in their offspring are derived from endogenous reserves of fat and protein (capital) that females build prior to the period of investment or from foods they consume concurrently with investment (income). The relative contribution from each source can be influenced by temporal and environmental constraints on a female's ability to forage on Arctic breeding areas. Warming temperatures and advancing Arctic phenology may alter those constraints. From 2011–2014, we examined relationships among spring temperature, timing of migration and reproduction, and the sources of nutrients females deposited in eggs for three sympatric species of geese that nested in northern Alaska. Compared to lesser snow geese ( Anser caerulescens caerulescens ) and greater white‐fronted geese ( Anser albifrons frontalis ), black brant ( Branta bernicla nigricans ) were more likely to initiate follicle development during migration, resulting in fewer days between their arrival in the Arctic and the onset of incubation, and requiring a relatively greater capital investment in eggs. Delaying follicle development until after their arrival in the Arctic provided snow geese and white‐fronted geese an opportunity to forage near their nesting area and to deposit exogenous nutrients in eggs. With warmer spring temperatures brant invested more capital in eggs but snow geese invested less capital. Brant likely used capital to meet costs associated with earlier onset of follicle development when phenology was advanced, whereas snow geese used capital to compensate for poor foraging conditions during colder Arctic springs. Global warming is likely to reduce the quality of lower‐latitude marine habitats where brant acquire endogenous reserves, and advancing Arctic phenology may increase their reliance on those reserves during reproduction. Near‐term warming in northern Alaska may improve foraging conditions and favor the reproductive strategies of some herbivores such as snow geese and white‐fronted geese that mainly invest Arctic nutrients in their offspring.

Global Change Biology↗
USGS2005

The Circumpolar Arctic vegetation map

Question: What are the major vegetation units in the Arctic, what is their composition, and how are they distributed among major bioclimate subzones and countries? Location: The Arctic tundra region, north of the tree line. Methods: A photo-interpretive approach was used to delineate the vegetation onto an Advanced Very High Resolution Radiometer (AVHRR) base image. Mapping experts within nine Arctic regions prepared draft maps using geographic information technology (ArcInfo) of their portion of the Arctic, and these were later synthesized to make the final map. Area analysis of the map was done according to bioclimate subzones, and country. The integrated mapping procedures resulted in other maps of vegetation, topography, soils, landscapes, lake cover, substrate pH, and above-ground biomass. Results: The final map was published at 1:7 500 000 scale map. Within the Arctic (total area = 7.11 x 106 km 2), about 5.05 ?? 106 km2 is vegetated. The remainder is ice covered. The map legend generally portrays the zonal vegetation within each map polygon. About 26% of the vegetated area is erect shrublands, 18% peaty graminoid tundras, 13% mountain complexes, 12% barrens, 11% mineral graminoid tundras, 11% prostrate-shrub tundras, and 7% wetlands. Canada has by far the most terrain in the High Arctic mostly associated with abundant barren types and prostrate dwarf-shrub tundra, whereas Russia has the largest area in the Low Arctic, predominantly low-shrub tundra. Conclusions: The CAVM is the first vegetation map of an entire global biome at a comparable resolution. The consistent treatment of the vegetation across the circumpolar Arctic, abundant ancillary material, and digital database should promote the application to numerous land-use, and climate-change applications and will make updating the map relatively easy. ?? IAVS; Opulus Press.

Journal of Vegetation Science↗
USGS1966

Magnetic data on the structure of the central Arctic Region

A study of 23,000 miles of total intensity aeromagnetic profiles in the central Arctic has been made by the U. S. Geological Survey and the U. S. Coast and Geodetic Survey. The profiles were flown at 20,000 feet above sea level and cover approximately 1,350,000 square miles of the Arctic Ocean between the North Pole and the North American continent. When the profiles are smoothed to remove crustal anomalies, the resulting contoured values differ from the U. S. Hydrographic Office Chart 1703 N for 1955 corrected to 1951 by as much as 2000 gammas in the northern part of the Arctic Archipelago. A nondipole regional focus east of Greenland has decreased in amplitude but has changed very little in position since 1907.5. There is a profound difference in the magnetic characteristics of the rocks on either side of the underwater Lomonosov Ridge across the Arctic Ocean. In the Eurasian Basin the high-altitude profiles are relatively smooth or show only minor anomalies, but on the North American side of the ridge there is a large area of closely spaced, high-amplitude anomalies which has been designated the Central Magnetic Zone. Although the anomaly trends parallel the Alpha Rise, this zone is far more extensive, including nearly half of the Canadian Basin on one side and probably all the Central Arctic Basin on the other side of the rise. The Lomonosov Ridge is marked by a persistent anomaly of moderate size that indicates the presence of magnetic material in the ridge. Probable block-fault structures along the flanks of the Alpha Rise are associated with blocklike magnetic anomalies of comparable widths. A characteristic magnetic pattern occurs over an area of jagged bottom topography in the Eurasian Basin. A similar magnetic pattern over part of the Lena Trough may indicate another area of jagged topography. The belt of epicenters associated with the Mid-Atlantic Ridge continues through this rugged part of the Eurasian Basin, but the absence of the typical high magnetic anomaly makes it doubtful that the mid-oceanic ridge extends through this part of the Arctic . Magnetic data indicate that the thick sections of sedimentary rocks in the Paleozoic geosynclinal belts of northern Ellesmere Island and northern Greenland continue out under the adjacent continental shelves north of Greenland, west of the Arctic Archipelago, north of the part of Alaska east of Barrow, and under part of the Chukchi Shelf, and that they make up the bulk of the Nansen Swell off Spitsbergen. Thick sedimentary fill is indicated in the magnetically flat areas of the Eurasian Basin next to the Lomonosov Ridge and in the southern part of the Canadian Basin. The magnetic profiles on the Eurasian side of the Lomonosov Ridge closely resemble typical magnetic profiles over both Atlantic and Pacific oceans, where as the profiles of the Central Magnetic Zone on the North American side of the Lomonosov Ridge are completely unlike the oceanic data and show a striking similarity to typical profiles over the Precambrian rocks of the Canadian Shield and its buried equivalent under the Central Stable Region of the United States. Therefore, it is concluded that the Arctic region consists of a probable oceanic area on the Eurasian side and a basin formed by downdropped continental rocks, presumably a Precambrian complex similar to that of the Canadian Shield, on the North American side of the ridge.

Geological Society of America Bulletin↗
USGS2001

The effect of depuration on transmission of Aeromonas salmonicida between the freshwater bivalve Amblema plicata Arctic char

A model system was used to study bacterial fish pathogen transmission between the freshwater bivalve Amblema plicata and two strains (Nauyuk and Labrador) of Arctic char Salvelinus alpinus. Aeromonas salmonicida , the cause of fish furunculosis, was readily transmitted from Arctic char to A. plicata and vice versa via simple cohabitation. Clinical furunculosis was artificially established in Nauyuk Arctic char via horizontal exposure to Labrador Arctic char that received intraperitoneal injections of A. salmonicida. After the Nauyuk Arctic char began to die, A. plicata were placed in the tank with the fish. After 33 d of cohabitation, a group of 10 A. plicata was cultured, and A. salmonicida was isolated from all 10. The remaining A. plicata were transferred to other tanks being supplied with specific-pathogen-free water. At 1, 5, 15, and 30 d after transfer, 60 uninfected Labrador Arctic char were cohabitated with the A. plicata. Transmission of A. salmonicida from A. plicata to the Arctic char was evaluated via fish mortality and bacterial culture after 3–4 weeks of exposure. Mortality to A. salmonicida occurred in groups exposed to A. plicata after 1 and 5 d of depuration but not in groups exposed after 15 and 30 d. The bacterium was not isolated from either the A. plicata or the Arctic char in the 15- and 30-d groups. Results indicate that the current minimum 30-d quarantine of freshwater bivalves destined for relocation to prevent spread of zebra mussels Dreissena polymorpha is sufficient to allow depuration of a fish pathogen and, thus, to prevent the spread of disease.

West Virginia↗
USGS2013

Trajectory of the arctic as an integrated system

Although much remains to be learned about the Arctic and its component processes, many of the most urgent scientific, engineering, and social questions can only be approached through a broader system perspective. Here, we address interactions between components of the Arctic System and assess feedbacks and the extent to which feedbacks (1) are now underway in the Arctic; and (2) will shape the future trajectory of the Arctic system. We examine interdependent connections among atmospheric processes, oceanic processes, sea-ice dynamics, marine and terrestrial ecosystems, land surface stocks of carbon and water, glaciers and ice caps, and the Greenland ice sheet. Our emphasis on the interactions between components, both historical and anticipated, is targeted on the feedbacks, pathways, and processes that link these different components of the Arctic system. We present evidence that the physical components of the Arctic climate system are currently in extreme states, and that there is no indication that the system will deviate from this anomalous trajectory in the foreseeable future. The feedback for which the evidence of ongoing changes is most compelling is the surface albedo-temperature feedback, which is amplifying temperature changes over land (primarily in spring) and ocean (primarily in autumn-winter). Other feedbacks likely to emerge are those in which key processes include surface fluxes of trace gases, changes in the distribution of vegetation, changes in surface soil moisture, changes in atmospheric water vapor arising from higher temperatures and greater areas of open ocean, impacts of Arctic freshwater fluxes on the meridional overturning circulation of the ocean, and changes in Arctic clouds resulting from changes in water vapor content.

Ecological Applications↗
USGS2012

Moderate-resolution sea surface temperature data and seasonal pattern analysis for the Arctic Ocean ecoregions

Sea surface temperature (SST) is an important environmental characteristic in determining the suitability and sustainability of habitats for marine organisms. In particular, the fate of the Arctic Ocean, which provides critical habitat to commercially important fish, is in question. This poses an intriguing problem for future research of Arctic environments - one that will require examination of long-term SST records. This publication describes and provides access to an easy-to-use Arctic SST dataset for ecologists, biogeographers, oceanographers, and other scientists conducting research on habitats and/or processes in the Arctic Ocean. The data cover the Arctic ecoregions as defined by the "Marine Ecoregions of the World" (MEOW) biogeographic schema developed by The Nature Conservancy as well as the region to the north from approximately 46°N to about 88°N (constrained by the season and data coverage). The data span a 29-year period from September 1981 to December 2009. These SST data were derived from Advanced Very High Resolution Radiometer (AVHRR) instrument measurements that had been compiled into monthly means at 4-kilometer grid cell spatial resolution. The processed data files are available in ArcGIS geospatial datasets (raster and point shapefiles) and also are provided in text (.csv) format. All data except the raster files include attributes identifying latitude/longitude coordinates, and realm, province, and ecoregion as defined by the MEOW classification schema. A seasonal analysis of these Arctic ecoregions reveals a wide range of SSTs experienced throughout the Arctic, both over the course of an annual cycle and within each month of that cycle. Sea ice distribution plays a major role in SST regulation in all Arctic ecoregions.

Open-File Report↗
USGS2020

Evaluation of Arctic warming in mid-Pliocene climate simulations

Palaeoclimate simulations improve our understanding of the climate, inform us about the performance of climate models in a different climate scenario, and help to identify robust features of the climate system. Here, we analyse Arctic warming in an ensemble of 16 simulations of the mid-Pliocene Warm Period (mPWP), derived from the Pliocene Model Intercomparison Project Phase 2 (PlioMIP2). The PlioMIP2 ensemble simulates Arctic (60–90 ∘ N) annual mean surface air temperature (SAT) increases of 3.7 to 11.6 ∘ C compared to the pre-industrial period, with a multi-model mean (MMM) increase of 7.2 ∘ C. The Arctic warming amplification ratio relative to global SAT anomalies in the ensemble ranges from 1.8 to 3.1 (MMM is 2.3). Sea ice extent anomalies range from −3.0 to - 10.4 × 10 6 "> − 10.4 × 10 6 km 2 , with a MMM anomaly of - 5.6 × 10 6 "> − 5.6 × 10 6 km 2 , which constitutes a decrease of 53 % compared to the pre-industrial period. The majority (11 out of 16) of models simulate summer sea-ice-free conditions ( ≤ 1 × 10 6 "> ≤ 1 × 10 6 km 2 ) in their mPWP simulation. The ensemble tends to underestimate SAT in the Arctic when compared to available reconstructions, although the degree of underestimation varies strongly between the simulations. The simulations with the highest Arctic SAT anomalies tend to match the proxy dataset in its current form better. The ensemble shows some agreement with reconstructions of sea ice, particularly with regard to seasonal sea ice. Large uncertainties limit the confidence that can be placed in the findings and the compatibility of the different proxy datasets. We show that while reducing uncertainties in the reconstructions could decrease the SAT data–model discord substantially, further improvements are likely to be found in enhanced boundary conditions or model physics. Lastly, we compare the Arctic warming in the mPWP to projections of future Arctic warming and find that the PlioMIP2 ensemble simulates greater Arctic amplification than CMIP5 future climate simulations and an increase instead of a decrease in Atlantic Meridional Overturning Circulation (AMOC) strength compared to pre-industrial period. The results highlight the importance of slow feedbacks in equilibrium climate simulations, and that caution must be taken when using simulations of the mPWP as an analogue for future climate change.

Climate of the Past↗
USGS2018

Mineral constraints on arctic caribou (Rangifer tarandus): a spatial and phenological perspective

Arctic caribou ( Rangifer tarandus ) have the longest terrestrial migration of any ungulate but little is known about the spatial and seasonal variation of minerals in summer forages and the potential impacts of mineral nutrition on the foraging behavior and nutritional condition of arctic caribou. We investigated the phenology, availability, and mechanistic relationships of calcium, phosphorus, magnesium, sodium, potassium, iron, manganese, copper, and zinc in three species of woody browse, three species of graminoids, and one forb preferred by caribou over two transects bisecting the ranges of the Central Arctic (CAH) and Western Arctic (WAH) caribou herds in Alaska. Transects traversed three ecoregions (Coastal Plain, Arctic Foothills and Brooks Range) along known migration paths in the summer ranges of both herds. Concentrations of mineral in forages were compared to estimated dietary requirements of lactating female caribou. Spatial distribution of the abundance of minerals in caribou forage was associated with interactions of soil pH and mineral content, while temporal variation was related to plant maturity, and thus nitrogen and fiber content of forages. Concentrations of sodium were below caribou requirements in all forage species for most of the summer and adequate only on the Coastal Plain during the second half of summer. Phosphorus declined in plants from emergence to senescence and was below requirements in all forages by mid‐summer, while concentrations of copper declined to marginal concentrations at plant senescence. Interactions of sodium with potassium, calcium with phosphorus, and copper with zinc in forages likely exacerbate the constraints of low concentrations sodium, phosphorus, and copper. Forages on the WAH contained significantly more phosphorus and copper than forages collected on the CAH transect. We suspect that migrations of caribou to the Arctic Coastal Plain may allow parturient females to replenish sodium stores depleted by foraging inland through the long arctic winters, while also extending the availability of adequate phosphorus, if animals are able to selectively track emerging waves of forage.

Alaska↗
USGS2020

Trophic structure of apex fish communities in closed versus leaky lakes of arctic Alaska

Despite low species diversity and primary production, trophic structure (e.g., top predator species, predator size) is surprisingly variable among Arctic lakes. We investigated trophic structure in lakes of arctic Alaska containing arctic char Salvelinus alpinus using stomach contents and stable isotope ratios in two geographically-close but hydrologically-distinct lake clusters to investigate how these fish may interact and compete for limited food resources. Aside from different lake connectivity patterns (‘leaky’ versus ‘closed’), differing fish communities (up to five versus only two species) between lake clusters allowed us to test trophic hypotheses including: (1) arctic char are more piscivorous, and thereby grow larger and obtain higher trophic positions, in the presence of other fish species; and, (2) between arctic char size classes, resource polymorphism is more prominent, and thereby trophic niches are narrower and overlap less, in the absence of other predators. Regardless of lake cluster, we observed little direct evidence of arctic char consuming other fishes, but char were larger (mean TL = 468 vs 264 mm) and trophic position was higher (mean TP = 4.0 vs 3.8 for large char) in lakes with other fishes. Further, char demonstrated less intraspecific overlap when other predators were present whereas niche overlap was up to 100% in closed, char only lakes. As hydrologic characteristics (e.g., lake connectivity, water temperatures) will change across the Arctic owing to climate change, our results provide insight regarding potential concomitant changes to fish interactions and increase our understanding of lake trophic structure to guide management and conservation goals.

Alaska↗
USGS2023

Rivers of Arctic North America

This chapter describes the geomorphology, hydrology, chemistry, biodiversity, and ecology of rivers in the North American Arctic. The history, physiography, climate, and land use of the Arctic regions are also described. The chapter includes details on the Kobuk and Colville rivers in Alaska, the Thelon and Kazan rivers in the central Canadian Arctic, Koroc River and Nakvak Brook in the eastern Canadian low Arctic, Thomsen River on Banks Island in the western Canadian Arctic Archipelago, and Ruggles River on Ellesmere Island in the Canadian high Arctic. The rivers are characteristic of the major ecoregions of the North American Arctic, covering a range of geomorphological and physiographic conditions. The history of use of the rivers by Inuit and Dene First Nations Peoples of the north provides the foundation to understand the social, cultural, and economic importance of the river systems, and potential threats to the rivers from climate change are outlined.

Book chapter↗
USGS2004

Contrasting glacial/interglacial regimes in the western Arctic Ocean as exemplified by a sedimentary record from the Mendeleev Ridge

Distinct cyclicity in lithology and microfaunal distribution in sediment cores from the Mendeleev Ridge in the western Arctic Ocean (water depths ca. 1. 5 km) reflects contrasting glacial/interglacial sedimentary patterns. We conclude that during major glaciations extremely thick pack ice or ice shelves covered the western Arctic Ocean and its circulation was restricted in comparison with interglacial, modern-type conditions. Glacier collapse events are marked in sediment cores by increased contents of ice-rafted debris, notably by spikes of detrital carbonates and iron oxide grains from the Canadian Arctic Archipelago. Composition of foraminiferal calcite ?? 18O and ??13C also shows strong cyclicity indicating changes in freshwater balance and/or ventilation rates of the Arctic Ocean. Light stable isotopic spikes characterize deglacial events such as the last deglaciation at ca. 12 14C kyr BP. The prolonged period with low ??18O and ??13C values and elevated contents of iron oxide grains from the Canadian Archipelago in the lower part of the Mendeleev Ridge record is interpreted to signify the pooling of freshwater in the Amerasia Basin, possibly in relation to an extended glaciation in arctic North America. Unique benthic foraminiferal events provide a means for an independent stratigraphic correlation of sedimentary records from the Mendeleev Ridge and other mid-depth locations throughout the Arctic Ocean such as the Northwind and Lomonosov Ridges. This correlation demonstrates the disparity of existing age models and underscores the need to establish a definitive chronostratigraphy for Arctic Ocean sediments. ?? 2003 Elsevier B.V. All rights reserved.

Palaeogeography, Palaeoclimatology, Palaeoecology↗
USGS2010

Microfaunal evidence for elevated Pliocene temperatures in the Arctic Ocean

The migration of thermophilic marine Ostracoda into the Arctic Ocean during the Pliocene indicates that winter and summer ocean temperatures around Arctic margins were ≥ 0 °C and > 3 °C, respectively, and that ice-free conditions existed for most or all of the Arctic. By at least 3.5–3.0 Ma, probably earlier, the opening of the Bering Strait allowed marine organisms to migrate through the Arctic Ocean, mostly from the Pacific Ocean. Migrant taxa such as Cythere, Hemicythere, and Neomonoceratina are known from Pliocene deposits of Alaska and Canada as well as Neogene deposits of the North Pacific and Atlantic oceans. On the basis of ecological and Zoogeographic information on ostracode species from more than 800 modern “core top” samples for the North Atlantic, North Pacific, and Arctic Oceans, we determined winter and summer temperature tolerances for migrant taxa to be at or above about 0 °C and 3 °C. This suggests ice-free summers, and probably, a perennially ice-free Arctic Ocean in some regions. Elevated water temperatures in the Arctic Ocean between 3.5 and 2.0 Ma is supported by evidence for late Pliocene increased meridional heat transport in the North Atlantic Ocean.

Paleoceanography and Paleoclimatology↗
USGS2006

Episodic fresh surface waters in the Eocene Arctic Ocean

It has been suggested, on the basis of modern hydrology and fully coupled palaeoclimate simulations, that the warm greenhouse conditions that characterized the early Palaeogene period (55-45 Myr ago) probably induced an intensified hydrological cycle with precipitation exceeding evaporation at high latitudes. Little field evidence, however, has been available to constrain oceanic conditions in the Arctic during this period. Here we analyse Palaeogene sediments obtained during the Arctic Coring Expedition, showing that large quantities of the free-floating fern Azolla grew and reproduced in the Arctic Ocean by the onset of the middle Eocene epoch (???50 Myr ago). The Azolla and accompanying abundant freshwater organic and siliceous microfossils indicate an episodic freshening of Arctic surface waters during an ???800,000-year interval. The abundant remains of Azolla that characterize basal middle Eocene marine deposits of all Nordic seas probably represent transported assemblages resulting from freshwater spills from the Arctic Ocean that reached as far south as the North Sea. The termination of the Azolla phase in the Arctic coincides with a local sea surface temperature rise from ???10??C to 13??C, pointing to simultaneous increases in salt and heat supply owing to the influx of waters from adjacent oceans. We suggest that onset and termination of the Azolla phase depended on the degree of oceanic exchange between Arctic Ocean and adjacent seas. ?? 2006 Nature Publishing Group.

Nature↗
USGS2013

The impact of lower sea-ice extent on Arctic greenhouse-gas exchange

In September 2012, Arctic sea-ice extent plummeted to a new record low: two times lower than the 1979–2000 average. Often, record lows in sea-ice cover are hailed as an example of climate change impacts in the Arctic. Less apparent, however, are the implications of reduced sea-ice cover in the Arctic Ocean for marine–atmosphere CO 2 exchange. Sea-ice decline has been connected to increasing air temperatures at high latitudes. Temperature is a key controlling factor in the terrestrial exchange of CO 2 and methane, and therefore the greenhouse-gas balance of the Arctic. Despite the large potential for feedbacks, many studies do not connect the diminishing sea-ice extent with changes in the interaction of the marine and terrestrial Arctic with the atmosphere. In this Review, we assess how current understanding of the Arctic Ocean and high-latitude ecosystems can be used to predict the impact of a lower sea-ice cover on Arctic greenhouse-gas exchange.

Nature Climate Change↗
USGS2018

Global and Arctic climate sensitivity enhanced by changes in North Pacific heat flux

Arctic amplification is a consequence of surface albedo, cloud, and temperature feedbacks, as well as poleward oceanic and atmospheric heat transport. However, the relative impact of changes in sea surface temperature (SST) patterns and ocean heat flux sourced from different regions on Arctic temperatures are not well constrained. We modify ocean-to-atmosphere heat fluxes in the North Pacific and North Atlantic in a climate model to determine the sensitivity of Arctic temperatures to zonal heterogeneities in northern hemisphere SST patterns. Both positive and negative ocean heat flux perturbations from the North Pacific result in greater global and Arctic surface air temperature anomalies than equivalent magnitude perturbations from the North Atlantic; a response we primarily attribute to greater moisture flux from the subpolar extratropics to Arctic. Enhanced poleward latent heat and moisture transport drive sea-ice retreat and low-cloud formation in the Arctic, amplifying Arctic surface warming through the ice-albedo feedback and infrared warming effect of low clouds. Our results imply that global climate sensitivity may be dependent on patterns of ocean heat flux in the northern hemisphere.

Nature Communications↗
USGS2022

Drivers, dynamics and impacts of changing Arctic coasts

Arctic coasts are vulnerable to the effects of climate change, including rising sea levels and the loss of permafrost, sea ice and glaciers. Assessing the influence of anthropogenic warming on Arctic coastal dynamics, however, is challenged by the limited availability of observational, oceanographic and environmental data. Yet, with the majority of permafrost coasts being erosive, coupled with projected intensification of erosion and flooding, understanding these changes is critical. In this Review, we describe the morphological diversity of Arctic coasts, discuss important drivers of coastal change, explain the specific sensitivity of Arctic coasts to climate change and provide an overview of pan-Arctic shoreline change and its multifaceted impacts. Arctic coastal changes impact the human environment by threatening coastal settlements, infrastructure, cultural sites and archaeological remains. Changing sediment fluxes also impact the natural environment through carbon, nutrient and pollutant release on a magnitude that remains difficult to predict. Increasing transdisciplinary and interdisciplinary collaboration efforts will build the foundation for identifying sustainable solutions and adaptation strategies to reduce future risks for those living on, working at and visiting the rapidly changing Arctic coast.

Alaska↗
USGS2018

Global sea-level contribution from Arctic land ice: 1971 to 2017

The Arctic Monitoring and Assessment Program (AMAP) (AMAP, 2017) identifies the Arctic as the largest regional source of land ice to global sea-level rise in the 2003 to 2014 period. Yet, this contextualization ignores the longer perspective from in-situ records of glacier mass balance. Here, using 18 (> 55 °N latitude) glacier and ice cap mass balance series in the 1971 to 2017 period, we develop a semi-empirical estimate of annual sealevel contribution from seven Arctic regions by scaling the in-situ records to GRACE averages. We contend that our estimate represents the most accurate mass balance assessment so far available before the 1992 start of satellite altimetry. We estimate the 1971 to 2017 eustatic sea-level contribution from land ice north of ~55° N to be 23.0±12.3 mm sea-level equivalent (SLE). In all regions, the cumulative sealevel rise curves exhibit an acceleration, especially after 1988. Greenland is the source of 46% of the Arctic sea-level rise contribution (10.6±7.3 mm), followed by Alaska (5.7±2.2 mm), Arctic Canada (3.2±0.7 mm) and the Russian High Arctic (1.5±0.4 mm). Our annual results exhibit co-variability over a 43 year overlap (1971 to 2013) with the alternative dataset of Marzeion et al (2015) (M15). However, we find a 1.36x lower sea-level contribution, in agreement with satellite gravimetry. The IPCC Fifth Assessment report identified constraining the pre-satellite era sealevel budget as a topic of low scientific understanding that we address and specify sealevel contributions coinciding with IPCC Special Report on the Ocean and Cryosphere in a Changing Climate (SROCC) “present day” (2005-2015) and “recent past” (1986-2005) reference periods. We assess an Arctic land ice loss of 8.3 mm SLE during the recent past and 12.4 mm SLE during the present day.

Environmental Research Letters↗
USGS2022

Marine mammal hotspots across the circumpolar Arctic

Aim Identify hotspots and areas of high species richness for Arctic marine mammals. Location Circumpolar Arctic. Methods A total of 2115 biologging devices were deployed on marine mammals from 13 species in the Arctic from 2005 to 2019. Getis-Ord G i * hotspots were calculated based on the number of individuals in grid cells for each species and for phylogenetic groups (nine pinnipeds, three cetaceans, all species) and areas with high species richness were identified for summer (Jun-Nov), winter (Dec-May) and the entire year. Seasonal habitat differences among species’ hotspots were investigated using Principal Component Analysis. Results Hotspots and areas with high species richness occurred within the Arctic continental-shelf seas and within the marginal ice zone, particularly in the “Arctic gateways” of the north Atlantic and Pacific oceans. Summer hotspots were generally found further north than winter hotspots, but there were exceptions to this pattern, including bowhead whales in the Greenland-Barents Seas and species with coastal distributions in Svalbard, Norway and East Greenland. Areas with high species richness generally overlapped high-density hotspots. Large regional and seasonal differences in habitat features of hotspots were found among species but also within species from different regions. Gap analysis (discrepancy between hotspots and IUCN ranges) identified species and regions where more research is required. Main conclusions This study identified important areas (and habitat types) for Arctic marine mammals using available biotelemetry data. The results herein serve as a benchmark to measure future distributional shifts. Expanded monitoring and telemetry studies are needed on Arctic species to understand the impacts of climate change and concomitant ecosystem changes (synergistic effects of multiple stressors). While efforts should be made to fill knowledge gaps, including regional gaps and more complete sex and age coverage, hotspots identified herein can inform management efforts to mitigate the impacts of human activities and ecological changes, including creation of protected areas.

Diversity and Distributions↗