Long-term patterns of muskox (Ovibos moschatus) demographics in high arctic Greenland

Polar Biology ◽  
2015 ◽  
Vol 38 (10) ◽  
pp. 1667-1675 ◽  
Author(s):  
Niels Martin Schmidt ◽  
Stine Højlund Pedersen ◽  
Jesper Bruun Mosbacher ◽  
Lars Holst Hansen
Keyword(s):  
Rangifer ◽  
2003 ◽  
Vol 23 (5) ◽  
pp. 213 ◽  
Author(s):  
Frank L. Miller ◽  
Anne Gunn

The Peary caribou (Rangifer tarandus pearyi) was recognized as 'Threatened' by the Committee on the Status of Endangered Wildlife in Canada in 1979 and 'Endangered' in 1991. It is the only member of the deer family (Cervidae) found on the Queen Elizabeth Islands (QEI) of the Canadian High Arctic. The Peary caribou is a significant part of the region's biodiversity and a socially important and economically valuable part of Arctic Canada's natural heritage. Recent microsatellite DNA findings indicate that Peary caribou on the QEI are distinct from caribou on the other Arctic Islands beyond the QEI, including Banks Island. This fact must be kept in mind if any translocation of caribou to the QEI is proposed. The subspecies is too gross a level at which to recognize the considerable diversity that exists between Peary caribou on the QEI and divergent caribou on other Canadian Arctic Islands. The Committee on the Status of Endangered Wildlife in Canada should take this considerable diversity among these caribou at below the subspecies classification to mind when assigning conservation divisions (units) to caribou on the Canadian Arctic Islands. In summer 1961, the first and only nearly range-wide aerial survey of Peary caribou yielded a population estimate on the QEI of 25 845, including about 20% calves. There was a strong preference for range on the western QEI (WEQI), where 94% (24 363) of the estimated caribou occurred on only 24% (ca. 97 000 km2) of the collective island-landmass. By summer 1973, the overall number of Peary caribou on the QEI had decreased markedly and was estimated at about 7000 animals. The following winter and spring (1973-74), the Peary caribou population declined 49% on the WQEI. The estimated number dropping to <3000, with no calves seen by us in summer 1974. Based on estimates from several aerial surveys conducted on the WQEI from 1985 to 1987, the number of Peary caribou on the QEI as a whole was judged to be 3300-3600 or only about 13-14% of the 1961 estimate. After a partial recovery in the late 1980s and early 1990s, Peary caribou on the WQEI declined drastically between 1994 and 1997 and were estimated at an all-time known low of about 1100 animals by summer 1997. The number of Peary caribou on the QEI in summer 1997 was likely no more than 2000-2400 or only 8-9% of the 1961 estimate. The four known major die-offs of Peary caribou on the WQEI between 1973 and 1997 occurred during winter and spring periods (1 Sep-21 Jun) with significantly greater (P<0.005) total snowfall, when compared to the long-term mean obtained from 55 caribou-years (1 Jul-30 Jun), 1947/48-2001/02, of weather records from Resolute Airport on Cornwallis Island. Of ecological significance is that the die-offs occurred when the caribou were at low mean overall densities and involved similar high annual rates of loss among muskoxen (Ovibos moschatus). All of the available evidence indicates that Peary caribou (and muskoxen) on the QEI experienced die-offs from prolonged, under-nutrition (starvation) caused by relative unavailability of forage-the forage was there but it was inaccessible to the caribou due to snow and/or ice cover. We cannot control the severe weather that greatly restricts the forage supply but we should try to reduce the losses of Peary caribou from other sources-humans, predators and competitors.


2016 ◽  
Vol 121 (5) ◽  
pp. 1236-1248 ◽  
Author(s):  
Philipp R. Semenchuk ◽  
Casper T. Christiansen ◽  
Paul Grogan ◽  
Bo Elberling ◽  
Elisabeth J. Cooper

2017 ◽  
Vol 11 (1) ◽  
pp. 191-215 ◽  
Author(s):  
Torbjørn Ims Østby ◽  
Thomas Vikhamar Schuler ◽  
Jon Ove Hagen ◽  
Regine Hock ◽  
Jack Kohler ◽  
...  

Abstract. Estimating the long-term mass balance of the high-Arctic Svalbard archipelago is difficult due to the incomplete geodetic and direct glaciological measurements, both in space and time. To close these gaps, we use a coupled surface energy balance and snow pack model to analyse the mass changes of all Svalbard glaciers for the period 1957–2014. The model is forced by ERA-40 and ERA-Interim reanalysis data, downscaled to 1 km resolution. The model is validated using snow/firn temperature and density measurements, mass balance from stakes and ice cores, meteorological measurements, snow depths from radar profiles and remotely sensed surface albedo and skin temperatures. Overall model performance is good, but it varies regionally. Over the entire period the model yields a climatic mass balance of 8.2 cm w. e.  yr−1, which corresponds to a mass input of 175 Gt. Climatic mass balance has a linear trend of −1.4 ± 0.4 cm w. e.  yr−2 with a shift from a positive to a negative regime around 1980. Modelled mass balance exhibits large interannual variability, which is controlled by summer temperatures and further amplified by the albedo feedback. For the recent period 2004–2013 climatic mass balance was −21 cm w. e.  yr−1, and accounting for frontal ablation estimated by Błaszczyk et al.(2009) yields a total Svalbard mass balance of −39 cm w. e.  yr−1 for this 10-year period. In terms of eustatic sea level, this corresponds to a rise of 0.037 mm yr−1. Refreezing of water in snow and firn is substantial at 22 cm w. e.  yr−1 or 26 % of total annual accumulation. However, as warming leads to reduced firn area over the period, refreezing decreases both absolutely and relative to the total accumulation. Negative mass balance and elevated equilibrium line altitudes (ELAs) resulted in massive reduction of the thick (>  2 m) firn extent and an increase in the superimposed ice, thin (<  2 m) firn and bare ice extents. Atmospheric warming also leads to a marked change in the thermal regime, with cooling of the glacier mid-elevation and warming in the ablation zone and upper firn areas. On the long-term, by removing the thermal barrier, this warming has implications for the vertical transfer of surface meltwater through the glacier and down to the base, influencing basal hydrology, sliding and thereby overall glacier motion.


2011 ◽  
Vol 17 (10) ◽  
pp. 3187-3194 ◽  
Author(s):  
ERIC G. LAMB ◽  
SUKKYUN HAN ◽  
BRIAN D. LANOIL ◽  
GREG H. R. HENRY ◽  
MARTIN E. BRUMMELL ◽  
...  

2004 ◽  
Vol 10 (12) ◽  
pp. 1981-1995 ◽  
Author(s):  
Jeffrey M. Welker ◽  
Jace T. Fahnestock ◽  
Greg H. R. Henry ◽  
Kevin W. O'Dea ◽  
Rodney A. Chimner

1997 ◽  
Vol 75 (10) ◽  
pp. 1628-1635 ◽  
Author(s):  
Steeve D. Côté ◽  
James A. Schaefer ◽  
François Messier

Synchrony of activities and time budgets of age–sex classes of muskoxen (Ovibos moschatus) was studied on Victoria Island in the Canadian High Arctic during late winter (April – late May), spring (late May – early June) and summer (mid-June – July). As revealed by the kappa (κ) coefficient of agreement, herd members exhibited significant synchrony in 79 of 82 groups. The degree of synchrony was not related to group size in mixed herds but decreased with group size in bachelor herds. Diversity in age–sex classes, group type (mixed versus bachelor), and season did not affect synchrony. However, synchrony was less among adult males than among other age–sex classes. Muskoxen were more synchronised at the start of activity bouts than at the end. As revealed by principal components analysis, calves tended to spend more time lying and standing and less time feeding than other age–sex classes. In addition, males in bachelor groups tended to feed more and rest less than males in mixed herds. Duration of active and lying bouts was not affected by age–sex class. Length of active bouts did not change with season, but lying bouts decreased in length significantly from late winter to spring and from spring to summer. We suggest that synchrony of activities maintains group cohesion but constrains the time budget of some group members, especially adult males.


2016 ◽  
Vol 5 (5) ◽  
pp. 856-869 ◽  
Author(s):  
Sunil Mundra ◽  
Rune Halvorsen ◽  
Håvard Kauserud ◽  
Mohammad Bahram ◽  
Leho Tedersoo ◽  
...  

2019 ◽  
Vol 646 ◽  
pp. 158-167 ◽  
Author(s):  
Philipp R. Semenchuk ◽  
Eveline J. Krab ◽  
Mattias Hedenström ◽  
Carly A. Phillips ◽  
Francisco J. Ancin-Murguzur ◽  
...  

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