Selective predation by brown bears (Ursus arctos) foraging on spawning sockeye salmon (Oncorhynchus nerka)

2000 ◽  
Vol 78 (6) ◽  
pp. 974-981 ◽  
Author(s):  
Gregory T Ruggerone ◽  
Renn Hanson ◽  
Donald E Rogers

Selective predation by and predation rates of brown bears (Ursus arctos) foraging on spawning sockeye salmon (Oncorhynchus nerka) in a small shallow creek in the Wood River lake system near Bristol Bay, Alaska, were quantified during 1986 and 1990–1992. Bears killed a high proportion of spawning salmon when few salmon entered the creek (92% of 505 fish) and a much smaller proportion when the spawning population reached a historical high (16% of 15 631 fish). Selective predation on salmon that differed in length, sex, and spawning condition was measured by tagging salmon at the mouth of the creek immediately prior to upstream migration and then recovering dead tagged fish during daily surveys of the entire creek. The relative frequencies of large, medium-sized, and small salmon killed by bears indicated that the risk of predation was more than 150% greater for large than for small salmon. A higher proportion of the male salmon population was killed and a greater proportion of male bodies were consumed than female salmon. Selectivity for male salmon increased as the spawning season progressed, possibly because male salmon weakened earlier and lived longer in a weakened state than female salmon. Male salmon were attacked mostly along the dorsal hump area, whereas female salmon tended to be attacked along the abdomen, where eggs could be exposed. Bears selectively killed female salmon prior to spawning during 1 of the 3 years, but only 6.1–7.8% of the female spawning populations were killed prior to spawning. These data support the hypothesis that selective predation by bears may influence the body morphology of spawning salmon.

2003 ◽  
Vol 60 (5) ◽  
pp. 553-562 ◽  
Author(s):  
T P Quinn ◽  
S M Gende ◽  
G T Ruggerone ◽  
D E Rogers

The number of sockeye salmon (Oncorhynchus nerka) killed by brown bears (Ursus arctos) in 13 streams over more than a decade in southwestern Alaska was best explained by an asymptotic increase to about 3000 salmon killed per stream per year as salmon density increased to 10 000 fish·ha–1 of stream. Divergence from this pattern at some streams probably reflected variation in the number of bears using the stream (which we did not determine) and variation in salmon biomass consumed per fish killed. Daily surveys at one creek over 11 years revealed about 100–130 salmon killed per day, ranging from a few to over 600. Higher proportions of the available salmon were killed early and late in the season, when densities were low. Thus the number of salmon killed within and among years increased with salmon abundance but at a declining rate, and the proportion killed generally decreased. Our previous work indicated that the average proportion of salmon killed among streams was controlled mostly by stream size, affecting the ability of bears to catch salmon. These findings are important for understanding the effects of bears on salmon population dynamics and their role in the transport of nutrients from salmon carcasses.


2020 ◽  
pp. 9-17 ◽  
Author(s):  
A.E. Lincoln ◽  
A.J. Wirsing ◽  
T.P. Quinn

Scavenging, an underappreciated mechanism of prey consumption for many predators, can contribute substantially to nutritional intake. Facultative scavengers such as brown bears (Ursus arctos Linnaeus, 1758) may both kill and scavenge Pacific salmon (genus Oncorhynchus Suckley, 1861), though the extent of scavenging and factors affecting this behavior are unclear. We tagged 899 sockeye salmon (Oncorhynchus nerka (Walbaum in Artedi, 1792)) carcasses and placed them on streambanks over 5 years at multiple sites in southwestern Alaska (USA) where brown bears annually prey on spawning sockeye salmon. Examination of carcasses revealed overall scavenging rates of 15% after 1 day and 54% after 3 days. Scavenging rate varied by site and year and increased throughout the salmon run. Contrary to predictions, scavenging was more frequent in senescent or bear-killed carcasses than ripe carcasses. Carcass consumption ranged from minimal to almost complete; body and brain tissues were most frequently consumed after 3 days (68% and 63% of carcasses, respectively). We also documented secondary scavenging (i.e., tissue consumption on two separate events) and delayed scavenging (i.e., scavenging observed after 3 days but not 1 day). Taken together, the results indicated that scavenging in these streams contributes significantly to total consumption of salmon by bears, with ramifications for other components of these salmon-dependent ecosystems.


2014 ◽  
Vol 92 (10) ◽  
pp. 893-903 ◽  
Author(s):  
Thomas P. Quinn ◽  
Aaron J. Wirsing ◽  
Brendan Smith ◽  
Curry J. Cunningham ◽  
Jason Ching

The seasonal and diel movements of predators to take advantage of shifts in prey availability are fundamental elements of their foraging ecology, and also have consequences for the prey populations. In this study, we used complementary noninvasive techniques (motion-activated cameras and hair snares) to investigate seasonal and diel activity of brown bears (Ursus arctos L., 1758) along six proximate streams supporting spawning populations of sockeye salmon (Oncorhynchus nerka (Walbaum in Artedi, 1792)) in southwestern Alaska. Camera records over 3 years showed a rapid increase in bear activity around the time salmon arrived in the streams, with differences among streams corresponding to differences in salmon phenology. Bears were active throughout the day and night, but there were clear crepuscular peaks when camera data were pooled. When wire snares (to collect hair samples) were paired with cameras, the data showed similar seasonal patterns, but each technique detected bears missed by the other. Roughly equal numbers of bears left hair but no camera image, and images but no hair, at paired sites. Taken together, the results indicated a close correspondence between bear activity and salmon timing, differences in diel timing among streams, and the complementarity of data obtained by motion-activated cameras and hair snares.


2011 ◽  
Vol 68 (5) ◽  
pp. 758-767 ◽  
Author(s):  
Douglas C. Braun ◽  
John D. Reynolds

We examine the importance of stream habitat characteristics in governing variation in spawning densities of sockeye salmon ( Oncorhynchus nerka ) across 32 streams in the Fraser River Basin, British Columbia, Canada. We used mixed-effects models to examine four competing hypotheses for the influence of abiotic stream characteristics acting on either adult salmon or embryo mortality. All models that received support using Akaike’s information criterion included stream characteristics that are associated with cover. These included the percent area of pools, percentage of the banks that were undercut, and large woody debris (in that order). These results suggest the importance of stream characteristics, which reduce risk of predation on adults, in determining spawning sockeye salmon densities. Thus, identification of a small number of physical characteristics of streams provides insight into ecological processes that determine population densities. This information can be used to quantify habitat quality, which can guide habitat prioritization for conservation.


2018 ◽  
Vol 195 ◽  
pp. 128-139
Author(s):  
V. F. Bugaev

Two groups of juvenile sockeye salmon are feeding in Lake Azabachye. They belong to the 2nd order stock of the lake (stock A) and to other 2nd order stocks of middle and down stream tributaries of the Kamchatka River which underyearlings migrate into the lake for feeding and wintering (group E). The main part of the stock A leaves the lake to the sea at the age 2+ (mainly 2.3) and the youngsters of the group E migrate to the sea at the age 1+ (mainly 1.3). The body length and weight parameters of the stock A smolts at the age 2+ and the group E smolts at the age 1+ could be similar or dissimilar in particular years. The maximal difference between the smots of these stocks is observed in the years with higher body length and weight for the stock A. Mean for 1979–2016 length and weight of smolts at abovementioned ages are evaluated as 98.42/87.46 mm and 10.40/7.38 g for the A/E stocks. For the stock A, statistically signifcant positive correlation is noted between size-weight parameters of smolts in the years of emigration and their abundance in the years of mass return. However, the regression has a shift between the periods of emigration/return of 1979–2000/1982–2003 and 2003–2013/2006–2016. The correlation is higher for the frst period (r = 0.820; P < 0.001 for body weight and r = 0.797; P < 0.001 for body length, n = 16) than for the second one with higher abundance (r = 0.669; P < 0.05 for body weight and r = 0.711; P < 0.05 for body length, n = 11). On opposite, the returns of the group E depend weakly on size-weight parameters of its smolts for the period of emigration/return of 1979–1997/1982–2000 (no data for return in 1999) and the dependence is insignifcant for the period of 2000–2013/2003–2016.


2018 ◽  
Vol 193 ◽  
pp. 78-87
Author(s):  
V. F. Bugaev ◽  
I. V. Tiller

Runs and escapements of sockeye salmon to the Zhupanova River have increased since 1985 with the run of 10.63 . 103 ind. instead of 1.45 . 103 ind. in 1960–1984, on average. The increasing was reasoned by change of the pink salmon odd year-classes domination in West Kamchatka to domination of even year-classes after the extremely high escapement in 1983. In 2005–2006, the sockeye salmon stock in the Zhupanova River became even more higher that continues till nowadays (runs of 68.20 . 103 ind. in 2005–2017, on average). This growth corresponds with general increasing of the pacific salmons abundance in the Russian Far East as the result of favorable environmental and feeding conditions in the North Pacific. General biological indices (age, body length and weight, maturity, fecundity) of mature sockeye salmon originated from the Zhupanova River are presented on the data of commercial catches in the sea in 1999–2017. The sockeye salmon population from this river has 11 age groups. The age group 1.3 is the most abundant and associated with the age groups 1.2 and 1.4. Majority of sockeye in the catches from the Zhupanova has the age 1.3 (on average 66.2 % in 1999–2017). Besides, returns of underyearlings with age 0.2, 0.3, and 0.4, and the fish with age 2.2, 2.3, 2.4, 3.2, and 3.3 are detected. The body length and weight are similar for all age groups of sockeye salmon: for males/females the mean length is 57.56/57.70 cm, mean weight is 2.69/2.62 kg. The mean males:females ratio is 44.7 : 55.3. The mean absolute fecundity is 4121 eggs. In opposite of sockeye salmon in some rivers of East Kamchatka, the population of the Zhupanova has no negative year-to-year trend of the body length or weight.


PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e9982
Author(s):  
Yuri Shirane ◽  
Fumihiko Mori ◽  
Masami Yamanaka ◽  
Masanao Nakanishi ◽  
Tsuyoshi Ishinazaka ◽  
...  

Body condition is an important determinant of health, and its evaluation has practical applications for the conservation and management of mammals. We developed a noninvasive method that uses photographs to assess the body condition of free-ranging brown bears (Ursus arctos) in the Shiretoko Peninsula, Hokkaido, Japan. First, we weighed and measured 476 bears captured during 1998–2017 and calculated their body condition index (BCI) based on residuals from the regression of body mass against body length. BCI showed seasonal changes and was lower in spring and summer than in autumn. The torso height:body length ratio was strongly correlated with BCI, which suggests that it can be used as an indicator of body condition. Second, we examined the precision of photograph-based measurements using an identifiable bear in the Rusha area, a special wildlife protection area on the peninsula. A total of 220 lateral photographs of this bear were taken September 24–26, 2017, and classified according to bear posture. The torso height:body/torso length ratio was calculated with four measurement methods and compared among bear postures in the photographs. The results showed torso height:horizontal torso length (TH:HTL) to be the indicator that could be applied to photographs of the most diverse postures, and its coefficient of variation for measurements was <5%. In addition, when analyzing photographs of this bear taken from June to October during 2016–2018, TH:HTL was significantly higher in autumn than in spring/summer, which indicates that this ratio reflects seasonal changes in body condition in wild bears. Third, we calculated BCI from actual measurements of seven females captured in the Rusha area and TH:HTL from photographs of the same individuals. We found a significant positive relationship between TH:HTL and BCI, which suggests that the body condition of brown bears can be estimated with high accuracy based on photographs. Our simple and accurate method is useful for monitoring bear body condition repeatedly over the years and contributes to further investigation of the relationships among body condition, food habits, and reproductive success.


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