6 research outputs found

    The role of invertebrates in the diet, growth and survival of red grouse (Lagopus lagopus scoticus) chicks

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    The role of diet on the growth, survival and movement of red grouse chicks was examined. We compared two areas of moorland in Scotland; a dry heath with a low density of red grouse and poor chick survival and a wetter heath/bog with relatively higher red grouse numbers and higher rates of chick survival. There were no differences in clutch size, or the proportion of eggs hatching between the two moors but brood survival was significantly lower on the dry heath. Radiotagged hens with broods were monitored during the first 12 days following hatching, the chicks captured, weighed and faecal samples collected. Invertebrate samples were collected within brood feeding ranges. Analysis of chick faeces was used to identify dietary components. Heather comprised the major dietary component on both moors. Invertebrates formed a higher component of diet on the wet moor, and this was positively correlated with growth rates, which in turn were positively correlated with chick survival. We present data from an experiment carried out in 1982, in which chicks showed higher growth rates with increasing insect availability. We also show that broods in which all the chicks survived (4-10 days) had smaller home range areas than broods in which some of the chicks died during this period. We suggest that the differences in chick survival between the two populations was due to variations in the abundance of invertebrates, particularly Tipulids. The protein provided by a high invertebrate component in the diet is, therefore, an important determinant of young red grouse chick growth and survival in some areas

    Movements of Wolves at the Northern Extreme of the Species' Range, Including during Four Months of Darkness

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    Information about wolf (Canis lupus) movements anywhere near the northern extreme of the species' range in the High Arctic (>75°N latitude) are lacking. There, wolves prey primarily on muskoxen (Ovibos moschatus) and must survive 4 months of 24 hr/day winter darkness and temperatures reaching −53 C. The extent to which wolves remain active and prey on muskoxen during the dark period are unknown, for the closest area where information is available about winter wolf movements is >2,250 km south. We studied a pack of ≥20 wolves on Ellesmere Island, Nunavut, Canada (80°N latitude) from July 2009 through mid-April 2010 by collaring a lead wolf with a Global Positioning System (GPS)/Argos radio collar. The collar recorded the wolf's precise locations at 6:00 a.m. and 6:00 p.m. daily and transmitted the locations by satellite to our email. Straight-line distances between consecutive 12-hr locations varied between 0 and 76 km. Mean (SE) linear distance between consecutive locations (n = 554) was 11 (0.5) km. Total minimum distance traveled was 5,979 km, and total area covered was 6,640 km2, the largest wolf range reported. The wolf and presumably his pack once made a 263-km (straight-line distance) foray to the southeast during 19–28 January 2010, returning 29 January to 1 February at an average of 41 km/day straight-line distances between 12-hr locations. This study produced the first detailed movement information about any large mammal in the High Arctic, and the average movements during the dark period did not differ from those afterwards. Wolf movements during the dark period in the highest latitudes match those of the other seasons and generally those of wolves in lower latitudes, and, at least with the gross movements measurable by our methods, the 4-month period without direct sunlight produced little change in movements
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