Wolves on the Katmai coast hunt sea otters and harbor seals

IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY
Ecology Pub Date : 2023-10-03 DOI:10.1002/ecy.4185
Kelsey R. Griffin, Gretchen H. Roffler, Ellen M. Dymit
{"title":"Wolves on the Katmai coast hunt sea otters and harbor seals","authors":"Kelsey R. Griffin,&nbsp;Gretchen H. Roffler,&nbsp;Ellen M. Dymit","doi":"10.1002/ecy.4185","DOIUrl":null,"url":null,"abstract":"<p>Although considered to be primarily ungulate predators, gray wolves (<i>Canis lupus</i>) display a high degree of dietary plasticity and consume a variety of alternate prey including marine life (Newsome et al., <span>2016</span>). Wolf consumption of marine mammals including seals (<i>Phoca</i> spp.), Steller sea lions (<i>Eumetopias jubatus</i>), humpback whales (<i>Megaptera novaeangliae</i>), walrus (<i>Odobenus rosmarus divergens</i>), and sea otters (<i>Enhydra lutris</i>) has been documented in diet studies using stable isotope ratios or by identification of prey remains within dried scats (Collins et al., <span>2019</span>; Lewis &amp; Lafferty, <span>2014</span>; Watts et al., <span>2010</span>). In some areas, marine mammals constitute a large proportion of wolf diets (Collins et al., <span>2019</span>; Meiklejohn, <span>1994</span>; Roffler et al., <span>2023</span>). Wolves have been observed consuming sea otter carcasses, but the method by which wolves obtain these and the frequency of scavenging versus hunting marine prey is largely unknown. On the Alaska Peninsula, evidence suggests that coastal wolves may rely more heavily on nearshore species such as sea otters, harbor seals (<i>Phoca vitulina</i>), and seasonal salmon (<i>Oncorhynchus</i> spp.) runs, particularly when ungulate prey (i.e., moose [<i>Alces alces</i>] and caribou [<i>Rangifer tarandus</i>]) are scarce or absent (Stanek et al., <span>2017</span>; Watts &amp; Newsome, <span>2017</span>). Because so few investigations have been conducted in these systems, the predator–prey dynamics between wolves and marine mammals are not well characterized.</p><p>Harbor seals are common along the Katmai coast and can be seen hauling out on rocky islands and sandbars or swimming near shore and in-stream outlets to hunt salmon and other fish. On 22 July 2016, while conducting fieldwork in Hallo Bay in Katmai National Park, we witnessed a male wolf hunt and kill a harbor seal (Figure 1a,b; Video S1; Video S1 Legend). The wolf was positioned near the mouth of an intertidal creek and at ~10:30 he charged into the water, grabbing the tail of a harbor seal that was swimming out of the creek toward the bay with an outgoing tide. The wolf tore a wound in the seal's tail with its teeth and maintained a hold on the seal dragging it into shallower water while the seal resisted by continuously arching its back and attempting to bite the wolf. During this struggle, the wolf occasionally released its hold and circled the seal. Briefly, the seal moved a short distance into deeper water; however, the wolf was able to regain hold of its tail. The wolf continued to tear into the flesh of the seal's tail and after a ~30-min struggle, the seal appeared to tire, straining to lift its head above water. The wolf dragged the seal onto the exposed sandbar and began to tear into the existing wound and consume the tail. The wolf then noticed our presence and after a few minutes left the carcass and crossed into the meadow. We began walking slowly down the beach away from the harbor seal, and after several minutes we observed the male wolf and a second wolf travel across the beach berm to the carcass and begin feeding.</p><p>On 23 May 2016, we observed a wolf carrying a young sea otter carcass at Swikshak Bay (Figure 1b,c) followed by additional observations of wolves carrying sea otter carcasses on 23 June 2018 (Figure 1d) and on an offshore island at Hallo Bay on 8 July 2019. The sea otter population on the Katmai coast was decimated during the industrial fur trade. Although sea otters were protected from the fur harvest in 1911, their population slowly increased through most of the century. However, by 2012, sea otters on the Katmai coast had made a robust recovery with numbers reaching suspected carrying capacity (~8600 animals) and population growth limited by food availability (Coletti et al., <span>2016</span>). Now, sea otters are seen frequently along the Katmai coast including on nearshore haul-outs. With more numerous sea otters and their need to haul out to thermoregulate and conserve energy (Bodkin, <span>2001</span>), it is not known if wolves feeding on them is a rare event or a more frequent occurrence.</p><p>To further investigate how wolves were preying on or scavenging sea otters, we bolted a timelapse camera tripod into beach cast logs at Swikshak in August 2019 (Figure 1e). The camera pointed at a large rocky island, ~530 m offshore, where wolves were suspected of obtaining the sea otters. Photographs were taken with a Reconyx Ultrafire XP9 every 2 min with varying photograph periods to exclude nighttime photographs and maximize capturing an animal transiting from the island. Both this island and a nearby smaller island (730 m from shore) are exposed during negative tide cycles and entirely submerged by very high tides. On 29 September 2019, we captured photographs of a wolf carrying a sea otter carcass from the larger island at 10:00 during a low tide (Figure 1f, Table 1, Griffin, <span>2023</span>). We did not obtain any additional photographs of sea otter consumption, but wolves and bears were recorded frequenting the islands. All wolf observations from photographs were of single wolves except for one photograph event of two wolves. Almost all wolves in photographs on or near the island (<i>n</i> = 9) during the camera deployment period were detected during a low tide (Table 1, Griffin, <span>2023</span>). Six out of seven wolf visits to the island lasted from 20 to 170 min, suggesting that wolves were searching for prey (Table 1, Griffin, <span>2023</span>). Bear activity on the island also coincided with low tide and was observed in photographs on 4 days in 2019, 5 days in 2020, and two in 2021 with a bear visiting the island ~1 h after the wolf in 2019 was seen leaving with a sea otter. Animals on or near the large island appeared very small and grainy in photographs due to the distance of the island, so it is likely that some animals went undetected.</p><p>On 25 June 2021 we watched wolves hunt and consume an adult sea otter on a rocky island at Swikshak Bay during a negative tide cycle (Figure 2). We arrived at the site on 21 June at low tide and immediately observed a single lactating female wolf walking along the island's intertidal zone, occasionally slowing her pace and crouching. The following day (22 June) we observed sea otters hauled out on shallow rocks near the larger island. On 25 June, we saw the lactating female wolf visit the large island at 07:40. She seemed alert and focused, stopping frequently and appearing to “scan” the island before she moved to the small island where she eventually disappeared over the rocks out of sight. Two male wolves (including a large breeding male) walked across the intertidal zone toward the islands. Both male wolves headed to the large island while the single female wolf on the small island remained out of sight. The two male wolves soon approached the small island from different angles on either side of where the female disappeared. All wolves disappeared from view for ~1 min, then reappeared carrying a limp sea otter over the rocks to the top of the island. At 08:45 the wolves began working together to tear the sea otter apart, eventually ripping pieces off. The large male took a piece that appeared to be the head and lay down to eat while the other wolves continued to tear at the carcass. The three wolves fed on the carcass for ~60 min. The smaller male departed the island carrying a piece of sea otter pelt in his mouth (Figure 2a) followed by the female's departure. The large male moved slowly away from the island down the beach, stopping briefly to drink sea water. We immediately examined the kill site and found an area of concentrated blood where the sea otter was likely killed while resting on a fairly steep rocky area within 3–4 m of the water (Figure 2b). The presence of blood indicates the sea otter had been alive when ambushed by the wolves, as opposed to a scavenged carcass that would not produce fresh blood pooling (Cristescu et al., <span>2022</span>). A visible blood trail across the exposed rocks led from the blood pool to the location where we observed the wolves tearing apart and consuming the sea otter. Here the only sea otter parts remaining were scattered rib bones stripped of the muscle tissue, the mandible in two pieces, and the liver (Figure 2c,d). The size of the mandible and tooth wear indicated it was likely an adult female sea otter (J. L. Bodkin, personal communication, March 31, 2022). The liver tissue was tested at the University of Alaska Fairbanks for mercury and contained a concentration of 48.8 total Hg ppb wet weight (liver collected under United States Fish and Wildlife Service MMPA permit no. 067925). Although this level of mercury is not markedly high, the liver was tested at the Alaska State Environmental Health Laboratory for paralytic shellfish toxins and contained a high concentration (140 μg/100 g) compared with the Federal Drug Administration's regulatory health hazard safety limit of 80 μg/100 g. In addition, we discovered in further tests of trace element concentrations (performed at the University of Alaska Anchorage) high levels of rubidium (μg/kg = 4,000,000; SD = 710,000), which can indicate liver toxicity in rats at that level (Usuda et al., <span>2014</span>). The elevated concentration of paralytic shellfish toxins and rubidium supports our suspicion that the wolves did not consume the liver as a conditioned response to avoid ingesting toxins.</p><p>Wolf hunting behavior has been comprehensively described through detailed observations of ungulate hunting, in groups or singly, that generally involve cursorial behavior to chase prey (Peterson &amp; Ciucci, <span>2003</span>). Although wolves are known to hunt seals, first-hand accounts of successful predation have not been well documented (Mech et al., <span>2015</span>). Some observations of wolves hunting prey such as beavers indicate that wolves can incorporate intentional processes such as planning and foresight of future events to position themselves for a successful ambush (Gable et al., <span>2018</span>; Mech et al., <span>2015</span>). Our observations of wolves ambushing marine mammals on the Katmai coast suggest that they may focus their hunting efforts at sites where prey presence is most predictable; for example, tidal streams or rocky island haul-outs. We have also detected temporal patterns in wolf prey-searching activities in the nearshore coinciding with low tide cycles indicating that they are aware of periods of greater access to haul-out sites. Solitary or partial pack hunting of marine mammals may be an efficient strategy to maximize prey intake. Our observations indicate that solitary wolves may successfully ambush seals and sea otters on the Katmai coast and may have developed unique hunting and foraging strategies compared with their interior counterparts. With the Katmai sea otter population peaking in 2012 at an estimated 8600 animals (Coletti et al., <span>2016</span>), there may be more frequent opportunities for wolves to obtain sea otters than previously thought. Sea otters could be an important contribution to wolf diets, with implications for terrestrial predator–prey dynamics.</p><p>The authors declare no conflicts of interest.</p>","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"104 12","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2023-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://esajournals.onlinelibrary.wiley.com/doi/epdf/10.1002/ecy.4185","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ecology","FirstCategoryId":"93","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ecy.4185","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Although considered to be primarily ungulate predators, gray wolves (Canis lupus) display a high degree of dietary plasticity and consume a variety of alternate prey including marine life (Newsome et al., 2016). Wolf consumption of marine mammals including seals (Phoca spp.), Steller sea lions (Eumetopias jubatus), humpback whales (Megaptera novaeangliae), walrus (Odobenus rosmarus divergens), and sea otters (Enhydra lutris) has been documented in diet studies using stable isotope ratios or by identification of prey remains within dried scats (Collins et al., 2019; Lewis & Lafferty, 2014; Watts et al., 2010). In some areas, marine mammals constitute a large proportion of wolf diets (Collins et al., 2019; Meiklejohn, 1994; Roffler et al., 2023). Wolves have been observed consuming sea otter carcasses, but the method by which wolves obtain these and the frequency of scavenging versus hunting marine prey is largely unknown. On the Alaska Peninsula, evidence suggests that coastal wolves may rely more heavily on nearshore species such as sea otters, harbor seals (Phoca vitulina), and seasonal salmon (Oncorhynchus spp.) runs, particularly when ungulate prey (i.e., moose [Alces alces] and caribou [Rangifer tarandus]) are scarce or absent (Stanek et al., 2017; Watts & Newsome, 2017). Because so few investigations have been conducted in these systems, the predator–prey dynamics between wolves and marine mammals are not well characterized.

Harbor seals are common along the Katmai coast and can be seen hauling out on rocky islands and sandbars or swimming near shore and in-stream outlets to hunt salmon and other fish. On 22 July 2016, while conducting fieldwork in Hallo Bay in Katmai National Park, we witnessed a male wolf hunt and kill a harbor seal (Figure 1a,b; Video S1; Video S1 Legend). The wolf was positioned near the mouth of an intertidal creek and at ~10:30 he charged into the water, grabbing the tail of a harbor seal that was swimming out of the creek toward the bay with an outgoing tide. The wolf tore a wound in the seal's tail with its teeth and maintained a hold on the seal dragging it into shallower water while the seal resisted by continuously arching its back and attempting to bite the wolf. During this struggle, the wolf occasionally released its hold and circled the seal. Briefly, the seal moved a short distance into deeper water; however, the wolf was able to regain hold of its tail. The wolf continued to tear into the flesh of the seal's tail and after a ~30-min struggle, the seal appeared to tire, straining to lift its head above water. The wolf dragged the seal onto the exposed sandbar and began to tear into the existing wound and consume the tail. The wolf then noticed our presence and after a few minutes left the carcass and crossed into the meadow. We began walking slowly down the beach away from the harbor seal, and after several minutes we observed the male wolf and a second wolf travel across the beach berm to the carcass and begin feeding.

On 23 May 2016, we observed a wolf carrying a young sea otter carcass at Swikshak Bay (Figure 1b,c) followed by additional observations of wolves carrying sea otter carcasses on 23 June 2018 (Figure 1d) and on an offshore island at Hallo Bay on 8 July 2019. The sea otter population on the Katmai coast was decimated during the industrial fur trade. Although sea otters were protected from the fur harvest in 1911, their population slowly increased through most of the century. However, by 2012, sea otters on the Katmai coast had made a robust recovery with numbers reaching suspected carrying capacity (~8600 animals) and population growth limited by food availability (Coletti et al., 2016). Now, sea otters are seen frequently along the Katmai coast including on nearshore haul-outs. With more numerous sea otters and their need to haul out to thermoregulate and conserve energy (Bodkin, 2001), it is not known if wolves feeding on them is a rare event or a more frequent occurrence.

To further investigate how wolves were preying on or scavenging sea otters, we bolted a timelapse camera tripod into beach cast logs at Swikshak in August 2019 (Figure 1e). The camera pointed at a large rocky island, ~530 m offshore, where wolves were suspected of obtaining the sea otters. Photographs were taken with a Reconyx Ultrafire XP9 every 2 min with varying photograph periods to exclude nighttime photographs and maximize capturing an animal transiting from the island. Both this island and a nearby smaller island (730 m from shore) are exposed during negative tide cycles and entirely submerged by very high tides. On 29 September 2019, we captured photographs of a wolf carrying a sea otter carcass from the larger island at 10:00 during a low tide (Figure 1f, Table 1, Griffin, 2023). We did not obtain any additional photographs of sea otter consumption, but wolves and bears were recorded frequenting the islands. All wolf observations from photographs were of single wolves except for one photograph event of two wolves. Almost all wolves in photographs on or near the island (n = 9) during the camera deployment period were detected during a low tide (Table 1, Griffin, 2023). Six out of seven wolf visits to the island lasted from 20 to 170 min, suggesting that wolves were searching for prey (Table 1, Griffin, 2023). Bear activity on the island also coincided with low tide and was observed in photographs on 4 days in 2019, 5 days in 2020, and two in 2021 with a bear visiting the island ~1 h after the wolf in 2019 was seen leaving with a sea otter. Animals on or near the large island appeared very small and grainy in photographs due to the distance of the island, so it is likely that some animals went undetected.

On 25 June 2021 we watched wolves hunt and consume an adult sea otter on a rocky island at Swikshak Bay during a negative tide cycle (Figure 2). We arrived at the site on 21 June at low tide and immediately observed a single lactating female wolf walking along the island's intertidal zone, occasionally slowing her pace and crouching. The following day (22 June) we observed sea otters hauled out on shallow rocks near the larger island. On 25 June, we saw the lactating female wolf visit the large island at 07:40. She seemed alert and focused, stopping frequently and appearing to “scan” the island before she moved to the small island where she eventually disappeared over the rocks out of sight. Two male wolves (including a large breeding male) walked across the intertidal zone toward the islands. Both male wolves headed to the large island while the single female wolf on the small island remained out of sight. The two male wolves soon approached the small island from different angles on either side of where the female disappeared. All wolves disappeared from view for ~1 min, then reappeared carrying a limp sea otter over the rocks to the top of the island. At 08:45 the wolves began working together to tear the sea otter apart, eventually ripping pieces off. The large male took a piece that appeared to be the head and lay down to eat while the other wolves continued to tear at the carcass. The three wolves fed on the carcass for ~60 min. The smaller male departed the island carrying a piece of sea otter pelt in his mouth (Figure 2a) followed by the female's departure. The large male moved slowly away from the island down the beach, stopping briefly to drink sea water. We immediately examined the kill site and found an area of concentrated blood where the sea otter was likely killed while resting on a fairly steep rocky area within 3–4 m of the water (Figure 2b). The presence of blood indicates the sea otter had been alive when ambushed by the wolves, as opposed to a scavenged carcass that would not produce fresh blood pooling (Cristescu et al., 2022). A visible blood trail across the exposed rocks led from the blood pool to the location where we observed the wolves tearing apart and consuming the sea otter. Here the only sea otter parts remaining were scattered rib bones stripped of the muscle tissue, the mandible in two pieces, and the liver (Figure 2c,d). The size of the mandible and tooth wear indicated it was likely an adult female sea otter (J. L. Bodkin, personal communication, March 31, 2022). The liver tissue was tested at the University of Alaska Fairbanks for mercury and contained a concentration of 48.8 total Hg ppb wet weight (liver collected under United States Fish and Wildlife Service MMPA permit no. 067925). Although this level of mercury is not markedly high, the liver was tested at the Alaska State Environmental Health Laboratory for paralytic shellfish toxins and contained a high concentration (140 μg/100 g) compared with the Federal Drug Administration's regulatory health hazard safety limit of 80 μg/100 g. In addition, we discovered in further tests of trace element concentrations (performed at the University of Alaska Anchorage) high levels of rubidium (μg/kg = 4,000,000; SD = 710,000), which can indicate liver toxicity in rats at that level (Usuda et al., 2014). The elevated concentration of paralytic shellfish toxins and rubidium supports our suspicion that the wolves did not consume the liver as a conditioned response to avoid ingesting toxins.

Wolf hunting behavior has been comprehensively described through detailed observations of ungulate hunting, in groups or singly, that generally involve cursorial behavior to chase prey (Peterson & Ciucci, 2003). Although wolves are known to hunt seals, first-hand accounts of successful predation have not been well documented (Mech et al., 2015). Some observations of wolves hunting prey such as beavers indicate that wolves can incorporate intentional processes such as planning and foresight of future events to position themselves for a successful ambush (Gable et al., 2018; Mech et al., 2015). Our observations of wolves ambushing marine mammals on the Katmai coast suggest that they may focus their hunting efforts at sites where prey presence is most predictable; for example, tidal streams or rocky island haul-outs. We have also detected temporal patterns in wolf prey-searching activities in the nearshore coinciding with low tide cycles indicating that they are aware of periods of greater access to haul-out sites. Solitary or partial pack hunting of marine mammals may be an efficient strategy to maximize prey intake. Our observations indicate that solitary wolves may successfully ambush seals and sea otters on the Katmai coast and may have developed unique hunting and foraging strategies compared with their interior counterparts. With the Katmai sea otter population peaking in 2012 at an estimated 8600 animals (Coletti et al., 2016), there may be more frequent opportunities for wolves to obtain sea otters than previously thought. Sea otters could be an important contribution to wolf diets, with implications for terrestrial predator–prey dynamics.

The authors declare no conflicts of interest.

Abstract Image

卡特迈海岸的狼捕食海獭和海豹。
虽然灰狼(Canis lupus)被认为是主要的有蹄类捕食者,但灰狼(Canis lupus)表现出高度的饮食可塑性,并消耗各种替代猎物,包括海洋生物(Newsome et al., 2016)。狼食用海洋哺乳动物,包括海豹(Phoca spp.)、虎耳海狮(Eumetopias jubatus)、座头鲸(Megaptera novaeangliae)、海象(Odobenus rosmarus divergens)和海獭(Enhydra lutris),这些都在饮食研究中得到了记录,研究使用稳定的同位素比率或通过识别干粪便中的猎物遗骸(Collins等人,2019;路易斯,拉弗蒂,2014;Watts et al., 2010)。在某些地区,海洋哺乳动物在狼的饮食中占很大比例(Collins等人,2019;Meiklejohn, 1994;Roffler et al., 2023)。人们曾观察到狼吃海獭的尸体,但狼吃海獭尸体的方法和食腐与捕猎海洋猎物的频率在很大程度上是未知的。在阿拉斯加半岛,有证据表明,沿海狼可能更依赖于近岸物种,如海獭、斑海豹(Phoca vitulina)和季节性鲑鱼(Oncorhynchus spp.),特别是当有蹄类猎物(即驼鹿[Alces Alces]和驯鹿[Rangifer tarandus])稀缺或缺失时(Stanek等人,2017;瓦,Newsome, 2017)。由于在这些系统中进行的调查很少,狼和海洋哺乳动物之间的捕食者-猎物动态并没有很好地表征。在卡特迈海岸,海豹很常见,可以看到它们在岩石岛屿和沙洲上拖着船,或者在岸边和水流出口附近游泳,捕食鲑鱼和其他鱼类。2016年7月22日,在卡特迈国家公园的哈罗湾进行实地考察时,我们目睹了一只公狼猎杀海豹(图1a,b;视频S1;视频S1图例)。这只狼被安置在一条潮间带溪口附近,10点半左右,它冲进水里,抓住一只海豹的尾巴,那只海豹正随着退潮从溪口游向海湾。狼用牙齿撕破海豹尾巴上的一个伤口,咬住海豹,把它拖到较浅的水域,而海豹则不断拱起背,试图咬狼。在这场搏斗中,狼偶尔会松开手,绕着海豹转一圈。短暂地,海豹向较深的水域移动了一小段距离;然而,狼还是抓住了自己的尾巴。狼继续撕咬海豹的尾巴,经过大约30分钟的挣扎,海豹似乎累了,努力把头抬起水面。狼把海豹拖到暴露在外的沙洲上,开始撕裂海豹的伤口,吃掉它的尾巴。狼注意到了我们的存在,几分钟后离开了尸体,走进了草地。我们开始慢慢地沿着海滩走,远离海豹,几分钟后,我们看到公狼和另一只狼穿过海滩的护堤,走向海豹的尸体,开始进食。2016年5月23日,我们在Swikshak湾观察到一只携带海獭幼崽尸体的狼(图1b,c),随后在2018年6月23日(图1d)和2019年7月8日在Hallo湾的一个离岸岛屿观察到携带海獭尸体的狼。在工业毛皮贸易期间,卡特迈海岸的海獭数量大幅减少。虽然海獭在1911年受到保护,不受皮毛收获的影响,但在20世纪的大部分时间里,它们的数量缓慢增长。然而,到2012年,Katmai海岸的海獭已经强劲恢复,数量达到了可疑的承载能力(约8600只),种群增长受到食物供应的限制(Coletti et al., 2016)。现在,在卡特迈海岸经常可以看到海獭,包括近岸拖出。由于海獭的数量越来越多,它们需要拖到外面来调节体温和保存能量(Bodkin, 2001),目前尚不清楚狼以它们为食是罕见事件还是更频繁发生。为了进一步研究狼是如何捕食或清除海獭的,我们于2019年8月在Swikshak将延时相机三脚架固定在海滩投下的原木上(图1e)。摄像机指向离岸约530米的一个巨大的岩石岛,狼群被怀疑在那里捕获了海獭。用Reconyx Ultrafire XP9每2分钟拍摄一次不同的照片周期,以排除夜间照片,并最大限度地捕捉从岛上过境的动物。这个岛和附近的一个小岛(距离海岸730米)在负潮周期中暴露在外,完全被非常高的潮汐淹没。2019年9月29日,我们在退潮期间10:00从大岛拍摄了一只狼携带海獭尸体的照片(图1f,表1,Griffin, 2023)。我们没有获得海獭消费的任何其他照片,但有狼和熊经常出没于这些岛屿的记录。 从照片中观察到的所有狼都是单狼,除了一张照片事件是两只狼。在相机部署期间,几乎所有在岛上或附近拍摄的狼(n = 9)都是在退潮期间被发现的(表1,Griffin, 2023)。7只狼中有6只造访该岛的时间从20到170分钟不等,这表明狼是在寻找猎物(表1,Griffin, 2023)。熊在岛上的活动也恰逢退潮,在2019年的4天、2020年的5天和2021年的2天的照片中观察到,在2019年看到狼和海獭离开1小时后,一只熊访问了该岛。由于距离较远,大岛上或附近的动物在照片中显得非常小,而且颗粒状,因此很可能有些动物没有被发现。2021年6月25日,在负潮周期期间,我们观察到狼在Swikshak湾的一个岩石岛上猎杀并吃掉了一只成年海獭(图2)。6月21日,我们在退潮时到达现场,立即观察到一只哺乳的母狼沿着岛上的潮间带行走,偶尔放慢脚步并蹲伏。第二天(6月22日),我们观察到海獭被拖到大岛附近的浅滩上。6月25日,我们在07:40看到哺乳的母狼来到大岛。她看起来机警而专注,经常停下来,似乎在“扫视”这个岛,然后才搬到小岛上,最终消失在岩石上,消失在人们的视线之外。两只公狼(包括一只大型繁殖的公狼)穿过潮间带向岛屿走去。两只公狼都向大岛走去,而小岛上的那只母狼却一直躲在那里。两只公狼很快就从母狼消失的两侧的不同角度接近了小岛。所有的狼消失了大约1分钟,然后又出现了,拖着一只软弱无力的海獭越过岩石来到了岛的顶部。8点45分,狼开始一起把海獭撕成碎片,最终把它撕成了碎片。那只大公狼拿了一块看起来像是头的东西,躺下来吃,而其他狼继续撕扯尸体。三只狼吃了大约60分钟的尸体。较小的雄性带着一块海獭皮离开了岛屿(图2a),紧随其后的是雌性。这只大雄鲸慢慢地离开了小岛,沿着海滩走下去,短暂地停下来喝了一口海水。我们立即检查了死亡地点,发现了一个血液集中的区域,海獭可能是在离水3-4米的相当陡峭的岩石上休息时被杀死的(图2b)。血液的存在表明海獭在被狼伏击时还活着,而不是被清理过的尸体,不会产生新鲜的血液池(Cristescu et al., 2022)。在裸露的岩石上有一条明显的血迹,从血池一直延伸到我们观察到狼群撕裂并吃掉海獭的地方。这里仅存的海獭部分是分散的肋骨,肌肉组织被剥离,下颌骨分成两部分,以及肝脏(图2c,d)。下颌骨的大小和牙齿磨损表明它可能是一只成年雌性海獭(J. L. Bodkin, personal communication, March 31, 2022)。肝组织在阿拉斯加费尔班克斯大学进行了汞含量测试,其湿重浓度为48.8汞ppb(根据美国鱼类和野生动物管理局MMPA许可号收集的肝脏)。067925)。虽然这一汞含量并不明显高,但阿拉斯加州环境卫生实验室对肝脏进行了麻痹性贝类毒素测试,与联邦药物管理局规定的80 μg/100 g的健康危害监管安全限值相比,肝脏的汞含量很高(140 μg/100 g)。此外,我们在对微量元素浓度的进一步测试(在阿拉斯加安克雷奇大学进行)中发现了高水平的铷(μg/kg = 4,000,000;SD = 710,000),这可以表明在该水平下大鼠的肝脏毒性(Usuda et al., 2014)。麻痹性贝类毒素和铷浓度的升高支持了我们的怀疑,即狼并不是为了避免摄入毒素而消耗肝脏的条件反应。通过对有蹄类动物狩猎的详细观察,狼的狩猎行为已经得到了全面的描述,无论是群体狩猎还是单独狩猎,通常都涉及到追逐猎物的游猎行为(Peterson &Ciucci, 2003)。虽然狼捕食海豹是已知的,但成功捕食海豹的第一手资料并没有得到很好的记录(Mech et al., 2015)。对狼捕猎猎物(如海狸)的一些观察表明,狼可以将有意的过程(如对未来事件的规划和预见)纳入其中,为成功的伏击做好准备(Gable等人,2018;Mech et al., 2015)。 我们对狼在卡特迈海岸伏击海洋哺乳动物的观察表明,它们可能会在最容易预测猎物存在的地方集中捕猎;例如,潮汐流或岩石岛拖出。我们还发现了近岸狼捕食活动的时间模式,与低潮周期相吻合,表明它们意识到更容易进入拖运地点的时期。海洋哺乳动物的单独或部分群体狩猎可能是最大限度地获取猎物的有效策略。我们的观察表明,孤狼可能成功地伏击了Katmai海岸的海豹和海獭,并且与内陆的同类相比,可能已经形成了独特的狩猎和觅食策略。2012年Katmai海獭数量达到峰值,估计为8600只(Coletti et al., 2016),狼获得海獭的机会可能比以前想象的要频繁。海獭可能对狼的饮食有重要贡献,对陆地捕食者-猎物动态有影响。作者声明无利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ecology
Ecology 环境科学-生态学
CiteScore
8.30
自引率
2.10%
发文量
332
审稿时长
3 months
期刊介绍: Ecology publishes articles that report on the basic elements of ecological research. Emphasis is placed on concise, clear articles documenting important ecological phenomena. The journal publishes a broad array of research that includes a rapidly expanding envelope of subject matter, techniques, approaches, and concepts: paleoecology through present-day phenomena; evolutionary, population, physiological, community, and ecosystem ecology, as well as biogeochemistry; inclusive of descriptive, comparative, experimental, mathematical, statistical, and interdisciplinary approaches.
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