Marc Ruiz-Sagalés, Asunción Borrell, Sverrir D. Halldórsson, Valerie Chosson, Guðjón M. Sigurðsson, Alex Aguilar
Baleen plates have been widely used to investigate the life cycle of mysticetes using a variety of chemical markers. Among these, stable isotope analysis (SIA) has been consistently applied to investigate their migratory movements and shifts in diet. However, the location of the baleen segment reflecting the most recently incorporated stable isotopes, corresponding to the whale's most contemporary habitat and diet composition, remains unclear and hampers the correct interpretation of the results. In this study, we analyzed δ15N, δ13C, and δ34S values along the baleen plate of a pregnant fin whale (Balaenoptera physalus) and its fetus to identify the baleen segment/s that were simultaneously deposited in both individuals. Our approach was based on the premise that the fetal baleen had been synthesized soon before sampling and therefore reflected contemporary habitat and diet signals of the pregnant whale. To allow comparison, the results were corrected for fetal–mother discrimination (F-MD) factors (i.e., the isotopic differences between fetal and maternal tissues). Fetal δ15N and δ13C values aligned most closely with maternal baleen segments located 2–4 cm below the gingiva line, indicating that they had likely been deposited simultaneously with fetal baleen formation and therefore reflect the pregnant whale's most recent diet and habitat use. Conversely, fetal δ34S values did not consistently align with any maternal baleen segments, probably due to dissimilar incorporation rates and/or differences in tissue discrimination factors. Our results highlight the importance of extracting baleen from its base, below the gingival line, to correctly assign the timing of deposition of the various baleen segments and ensure accurate interpretation in chronological studies using intrinsic markers on baleen plates.
{"title":"Multielement Stable Isotope Ratios in the Baleen of Maternal and Fetal Fin Whales Provide Evidence for the Most Recently Formed Segment of Balaenopterid Baleen","authors":"Marc Ruiz-Sagalés, Asunción Borrell, Sverrir D. Halldórsson, Valerie Chosson, Guðjón M. Sigurðsson, Alex Aguilar","doi":"10.1111/mms.70105","DOIUrl":"https://doi.org/10.1111/mms.70105","url":null,"abstract":"<p>Baleen plates have been widely used to investigate the life cycle of mysticetes using a variety of chemical markers. Among these, stable isotope analysis (SIA) has been consistently applied to investigate their migratory movements and shifts in diet. However, the location of the baleen segment reflecting the most recently incorporated stable isotopes, corresponding to the whale's most contemporary habitat and diet composition, remains unclear and hampers the correct interpretation of the results. In this study, we analyzed <i>δ</i><sup>15</sup>N, <i>δ</i><sup>13</sup>C, and <i>δ</i><sup>34</sup>S values along the baleen plate of a pregnant fin whale (<i>Balaenoptera physalus</i>) and its fetus to identify the baleen segment/s that were simultaneously deposited in both individuals. Our approach was based on the premise that the fetal baleen had been synthesized soon before sampling and therefore reflected contemporary habitat and diet signals of the pregnant whale. To allow comparison, the results were corrected for fetal–mother discrimination (F-MD) factors (i.e., the isotopic differences between fetal and maternal tissues). Fetal <i>δ</i><sup>15</sup>N and <i>δ</i><sup>13</sup>C values aligned most closely with maternal baleen segments located 2–4 cm below the gingiva line, indicating that they had likely been deposited simultaneously with fetal baleen formation and therefore reflect the pregnant whale's most recent diet and habitat use. Conversely, fetal <i>δ</i><sup>34</sup>S values did not consistently align with any maternal baleen segments, probably due to dissimilar incorporation rates and/or differences in tissue discrimination factors. Our results highlight the importance of extracting baleen from its base, below the gingival line, to correctly assign the timing of deposition of the various baleen segments and ensure accurate interpretation in chronological studies using intrinsic markers on baleen plates.</p>","PeriodicalId":18725,"journal":{"name":"Marine Mammal Science","volume":"42 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mms.70105","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145739452","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alessandra Cani, Massimiliano Drago, Meica Valdivia, Enrique M. González, Luis Cardona
<p>South American fur seals (<i>Arctocephalus australis</i>) are land-breeding eared pinnipeds found exclusively within the southern regions of South America, along the Southwestern Atlantic and Southeastern Pacific Oceans (Figure 1). On the Atlantic side, the northernmost breeding colonies are in the islands near Cabo Polonio in Uruguay, where the population has steadily increased since the cessation of sealing (Figure 1; Cárdenas-Alayza <span>2018</span>; Drago et al. <span>2017</span>).</p><p>The Uruguayan fur seal population was intensively exploited between 1873 and 1949, when hunting was restricted by the Uruguayan Government to only males and finally banned in 1991 (Arbiza et al. <span>2012</span>; Franco-Trecu et al. <span>2021</span>; de Ponce León <span>2000</span>). Despite the significant reduction of this population throughout the 19th and 20th centuries, the species has shown a steady increase in abundance in the last decades (Franco-Trecu, Drago, et al. <span>2019</span>) and seems to be recovering better than other sympatric species that were also exploited, such as the South American sea lion <i>Otaria byronia</i> (Franco-Trecu et al. <span>2021</span>).</p><p>The diet of South American fur seals includes small pelagic species such as anchovies (<i>Engraulis anchoita and Anchoa marinii</i>) as well as larger benthic and bentho-pelagic species such as striped weakfish (<i>Cynoscion guatucupa</i>), cutlassfish (<i>Trichiurus lepturus</i>), <i>and cephalopods (</i>Arbiza et al. <span>2012</span>; Naya et al. <span>2002</span>), but it can vary with prey availability and individual foraging behaviors (Cárdenas-Alayza <span>2018</span>). The marked sexual dimorphism observed in South American fur seals is one of the main determinants of individual diet variability. Adult males are considerably larger than adult females, reaching up to 2 m long and 200 kg, whereas females rarely exceed 1.5 m long and 60 kg (Cárdenas-Alayza <span>2018</span>). This allows males to perform deeper dives and reach more distant areas. Furthermore, the foraging grounds of nursing females are closer to their rookeries since they must return periodically to feed their pups, whereas males often travel longer distances during the non-reproductive periods (Cárdenas-Alayza <span>2018</span>). Consequently, differences between males and females for the southwestern Atlantic fur seal population have been reported in terms of trophic ecology and temporal variations of their isotopic niche (Cani et al. <span>2023</span>; Drago et al. <span>2017</span>, <span>2018</span>; de Lima et al. <span>2021</span>).</p><p>One of the most commonly used techniques to study the trophic ecology of marine mammals is stable isotope analysis, which often uses tissues collected from stranded individuals (Rubenstein and Hobson <span>2004</span>). For instance, the carbon stable isotope ratio (δ<sup>13</sup>C) informs about the primary source of C fueling the food web, and is frequently u
南美海狗(Arctocephalus australis)是一种陆地繁殖的有耳鳍足类动物,仅在南美洲南部地区,沿西南大西洋和东南太平洋发现(图1)。在大西洋一侧,最北端的繁殖种群位于乌拉圭卡波洛尼奥附近的岛屿上,自停止封海豹以来,那里的种群数量稳步增加(图1;Cárdenas-Alayza 2018; Drago et al. 2017)。乌拉圭海狗种群在1873年至1949年期间被集中开发,当时乌拉圭政府将狩猎限制为仅限雄性,并于1991年最终被禁止(Arbiza et al. 2012; franco - treu et al. 2021; de Ponce León 2000)。尽管在整个19世纪和20世纪,该种群数量显著减少,但在过去几十年里,该物种的丰度稳步增加(Franco-Trecu, Drago, et al. 2019),并且似乎比其他同样被开发的同域物种恢复得更好,例如南美海狮Otaria byronia (Franco-Trecu et al. 2021)。南美海狗的饮食包括小型远洋物种,如凤尾鱼(Engraulis anchoita和marinii凤尾鱼),以及大型底栖和底栖远洋物种,如条纹弱鱼(Cynoscion guatucupa)、弯鱼(Trichiurus lepturus)和头足类动物(Arbiza等人,2012;Naya等人,2002),但它会随着猎物的可用性和个体觅食行为而变化(Cárdenas-Alayza 2018)。在南美海狗中观察到的明显的两性二态性是个体饮食差异的主要决定因素之一。成年雄性比成年雌性大得多,可达2米长,200公斤重,而雌性很少超过1.5米长,60公斤重(Cárdenas-Alayza 2018)。这使得雄性可以潜得更深,到达更远的地方。此外,哺乳期雌性的觅食地更靠近它们的巢穴,因为它们必须定期返回喂养它们的幼崽,而雄性在非繁殖期通常会走更远的距离(Cárdenas-Alayza 2018)。因此,西南大西洋海狗种群的雄性和雌性在营养生态学和同位素生态位的时间变化方面存在差异(Cani et al. 2023; Drago et al. 2017,2018; de Lima et al. 2021)。研究海洋哺乳动物营养生态学最常用的技术之一是稳定同位素分析,它通常使用从搁浅个体收集的组织(Rubenstein和Hobson 2004)。例如,碳稳定同位素比值(δ13C)告诉我们食物网中碳的主要来源,经常被用来区分底栖和远洋食物网,以及近海和近海来源。同样,氮的稳定同位素比率(δ15N)表明了个体的营养地位,因为沿着食物网积累了较重的分子,也称为营养富集(Newsome et al. 2010; Rubenstein and Hobson 2004)。对乌拉圭国家自然历史博物馆收藏的南美海狗骨骼材料的δ13C和δ15N值的分析揭示了1971-1983年至1991-2012年期间的主要饮食变化(Drago etal . 2017)。这些变化在雄性中更为明显,并被解释为在更高营养水平的底栖猎物消费的增加,可能是条纹弱鱼,这可能是两个非互斥过程的结果。首先,继1950年乌拉圭设定的狩猎限制和随后1991年封印结束后,南美毛海豹数量呈指数增长(Drago et al. 2017; de Ponce León 2000),这可能增加了种内竞争。其次,自20世纪90年代以来,由于该地区工业底拖网捕捞的增加,底栖鱼类的平均尺寸减少(Drago et al. 2017; de Miranda and Haimovici 2007)。然而,由于捕食者的δ13C和δ15N值受到其食物组成和觅食地同位素基线的影响(Newsome et al. 2010),因此目前尚不清楚Río de la Plata河口沿岸南美海狗觅食地的位置是否也同时发生了变化。因此,添加其他主要受环境条件影响的栖息地示踪剂,如硫(δ34S)和氧(δ18O)的稳定同位素比值,可以提供更详细的喂养区变化信息(Connolly et al. 2004; Gat 1996)。Río de la Plata是南美洲最大的河口之一;它位于约35°S和55°W(图1),具有强烈的垂直和水平盐度分层(Guerrero et al. 1997)和浊度锋的存在,该浊度锋决定了浮游植物生长的光可用性和沿河流羽流的植物碎屑分布(Acha et al. 2008; Cani et al.)。 2023年;carcarto et al. 2008;Miloslavich et al. 2011)。在这种环境下,根据河口沿岸的觅食地,海洋哺乳动物的δ34S和δ18O值是不同的(Cani et al. 2023)。这是因为δ34S反映了初级生物生长的氧化还原条件(Peterson et al. 1985),其中陆生和海生底栖植物利用缺氧沉积物中的还原性硫化物作为S源,与利用水柱硫酸盐的浮游植物和海洋大型藻类相比,在34S中被高度耗尽(Connolly et al. 2004; Peterson et al. 1985)。同样,δ18O与水文循环密切相关,与海水相比,河流输入的淡水在18O中高度枯竭,因此河口的δ18O值随盐度线性增加(Gat 1996; Hoefs 2018)。南美洲海狗在该地区的主要栖息地位于Río de la Plata河口外部的Cabo Polonio附近的岛屿(Cárdenas-Alayza 2018)。已知来自该栖息地的海狗会在河口和邻近沿海地区的不同地点觅食(Dassis et al. 2012; Franco-Trecu et al. 2021),但这些觅食地的相对贡献可能会随着时间的推移而改变。从上述环境梯度来看,取食近岸和靠近河口的海狗的δ34S和δ18O值比取食近海和河羽外的海狗的δ34S和δ18O值要低,这分别反映了来自河流输入和海洋/远洋食物网的同位素值。因此,为了更好地了解和表征各性别的栖息地利用、营养生态和同位素生态位随时间的变化,本研究对1971-1983年(以下简称“1970年代”)和2006-2012年(以下简称“2010年代”)南美海狗雌性(n = 23)和雄性(n = 27)的骨骼样本进行了δ34S和δ18O两个互补的栖息地示踪值分析。由于其相对较慢的周转率,骨组织整合了每个个体在几年内使用栖息地的信息(Hobson et al. 2010; Fahy et al. 2017)。所有样本均来自乌拉圭海岸沿岸的死搁浅个体,之前由Drago等人(2017)分析了δ13C和δ15N。此外,20世纪70年代的个体对应于乌拉圭海岸封禁和工业底拖网渔船开始之前的时期,而2010年代的个体对应于封禁结束后的十年,该地区已经开展了大规模的底拖网捕捞业(Arbiza et al. 2012; franco - treu et al. 2021; de Ponce León 2000)。每个样本由鼻腔鼻甲骨的一小块碎片组成,可在国家自然历史博物馆(MNHN)和乌拉圭蒙得维的亚共和国大学科学学院的科学收藏中获得。性别由外部形态决定,并通过颅骨的第二性征来确认,只有性成熟的成年
{"title":"Shifts in the Isotopic Niche of Contemporary Male South American Fur Seals May Reflect Significant Environmental Changes in the Western South Atlantic","authors":"Alessandra Cani, Massimiliano Drago, Meica Valdivia, Enrique M. González, Luis Cardona","doi":"10.1111/mms.70106","DOIUrl":"https://doi.org/10.1111/mms.70106","url":null,"abstract":"<p>South American fur seals (<i>Arctocephalus australis</i>) are land-breeding eared pinnipeds found exclusively within the southern regions of South America, along the Southwestern Atlantic and Southeastern Pacific Oceans (Figure 1). On the Atlantic side, the northernmost breeding colonies are in the islands near Cabo Polonio in Uruguay, where the population has steadily increased since the cessation of sealing (Figure 1; Cárdenas-Alayza <span>2018</span>; Drago et al. <span>2017</span>).</p><p>The Uruguayan fur seal population was intensively exploited between 1873 and 1949, when hunting was restricted by the Uruguayan Government to only males and finally banned in 1991 (Arbiza et al. <span>2012</span>; Franco-Trecu et al. <span>2021</span>; de Ponce León <span>2000</span>). Despite the significant reduction of this population throughout the 19th and 20th centuries, the species has shown a steady increase in abundance in the last decades (Franco-Trecu, Drago, et al. <span>2019</span>) and seems to be recovering better than other sympatric species that were also exploited, such as the South American sea lion <i>Otaria byronia</i> (Franco-Trecu et al. <span>2021</span>).</p><p>The diet of South American fur seals includes small pelagic species such as anchovies (<i>Engraulis anchoita and Anchoa marinii</i>) as well as larger benthic and bentho-pelagic species such as striped weakfish (<i>Cynoscion guatucupa</i>), cutlassfish (<i>Trichiurus lepturus</i>), <i>and cephalopods (</i>Arbiza et al. <span>2012</span>; Naya et al. <span>2002</span>), but it can vary with prey availability and individual foraging behaviors (Cárdenas-Alayza <span>2018</span>). The marked sexual dimorphism observed in South American fur seals is one of the main determinants of individual diet variability. Adult males are considerably larger than adult females, reaching up to 2 m long and 200 kg, whereas females rarely exceed 1.5 m long and 60 kg (Cárdenas-Alayza <span>2018</span>). This allows males to perform deeper dives and reach more distant areas. Furthermore, the foraging grounds of nursing females are closer to their rookeries since they must return periodically to feed their pups, whereas males often travel longer distances during the non-reproductive periods (Cárdenas-Alayza <span>2018</span>). Consequently, differences between males and females for the southwestern Atlantic fur seal population have been reported in terms of trophic ecology and temporal variations of their isotopic niche (Cani et al. <span>2023</span>; Drago et al. <span>2017</span>, <span>2018</span>; de Lima et al. <span>2021</span>).</p><p>One of the most commonly used techniques to study the trophic ecology of marine mammals is stable isotope analysis, which often uses tissues collected from stranded individuals (Rubenstein and Hobson <span>2004</span>). For instance, the carbon stable isotope ratio (δ<sup>13</sup>C) informs about the primary source of C fueling the food web, and is frequently u","PeriodicalId":18725,"journal":{"name":"Marine Mammal Science","volume":"42 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mms.70106","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145750699","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kira A. Telford, John Calambokidis, Kiirsten R. Flynn, Jasmine Witt, Alie Perez, John W. Durban, Holly Fearnbach, Erin L. Meyer-Gutbrod
Although the eastern North Pacific gray whale (Eschrichtius robustus) population has recovered from population declines associated with whaling, they are closely monitored, especially in association with Unusual Mortality Events. Metrics to improve assessment of the health of individual animals, when averaged, are valuable to inform monitoring and management. We used 30 years of photographic data of a unique gray whale feeding aggregation to develop and test a new methodology for assessing body condition. This group of individuals (20 as of 2021, but 11 in the study group), known as the Sounders, regularly enter Puget Sound, Washington, USA, to forage on ghost shrimp in the spring and early summer. Almost 35,000 images were examined and 729 were selected as being suitable to assess individual body condition. Geometric measuring tools in open-source image analysis software were used to measure a novel body condition angle, °BC, as a proxy for changes in blubber thickness. This °BC varied significantly with the day of the year, with increases in blubber thickness observed as individuals progressed through the feeding season. Other metrics, such as year and surfacing interval, were not found to have a significant effect on °BC within this dataset. This novel index of body condition illustrates the opportunity to develop new methods to quantitatively assess change in individuals at both seasonal and annual scales. Expansion of this method to the larger eastern North Pacific gray whale population may allow for a more detailed examination of fluctuations in body condition to better understand both environmental and anthropogenic impacts. There is also potential for adaptation of the method to apply to historic photo catalogs of other baleen whale species, creating opportunities for enhanced data-driven management plans.
{"title":"How Robust is Eschrichtius robustus? A Novel Photographic Index of Body Condition From Boat-Based Photographs of Gray Whales","authors":"Kira A. Telford, John Calambokidis, Kiirsten R. Flynn, Jasmine Witt, Alie Perez, John W. Durban, Holly Fearnbach, Erin L. Meyer-Gutbrod","doi":"10.1111/mms.70091","DOIUrl":"https://doi.org/10.1111/mms.70091","url":null,"abstract":"<p>Although the eastern North Pacific gray whale (<i>Eschrichtius robustus</i>) population has recovered from population declines associated with whaling, they are closely monitored, especially in association with Unusual Mortality Events. Metrics to improve assessment of the health of individual animals, when averaged, are valuable to inform monitoring and management. We used 30 years of photographic data of a unique gray whale feeding aggregation to develop and test a new methodology for assessing body condition. This group of individuals (20 as of 2021, but 11 in the study group), known as the Sounders, regularly enter Puget Sound, Washington, USA, to forage on ghost shrimp in the spring and early summer. Almost 35,000 images were examined and 729 were selected as being suitable to assess individual body condition. Geometric measuring tools in open-source image analysis software were used to measure a novel body condition angle, <i>°BC</i>, as a proxy for changes in blubber thickness. This <i>°BC</i> varied significantly with the day of the year, with increases in blubber thickness observed as individuals progressed through the feeding season. Other metrics, such as year and surfacing interval, were not found to have a significant effect on <i>°BC</i> within this dataset. This novel index of body condition illustrates the opportunity to develop new methods to quantitatively assess change in individuals at both seasonal and annual scales. Expansion of this method to the larger eastern North Pacific gray whale population may allow for a more detailed examination of fluctuations in body condition to better understand both environmental and anthropogenic impacts. There is also potential for adaptation of the method to apply to historic photo catalogs of other baleen whale species, creating opportunities for enhanced data-driven management plans.</p>","PeriodicalId":18725,"journal":{"name":"Marine Mammal Science","volume":"42 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mms.70091","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145686501","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jessalyn J. Taylor, Chloé Huetz, Isabelle Charrier, Rachael B. Gray, Rebecca R. McIntosh
Marine vessel traffic is a significant contributor to anthropogenic noise pollution and a source of disturbance for many marine species. It is important to assess the impact of vessel visitation and the number of potential disturbance events at sensitive marine sites to ensure management strategies are adequate. This study integrated passive acoustic monitoring (PAM), direct visual observation, and vessel traffic data to monitor vessel visitation at Seal Rocks, the largest Australian fur seal (Arctocephalus pusillus doriferus) breeding colony and site with the least stringent vessel approach limits. Vessel visitation was compared between the assumed low (off-peak) and high (peak) visitation seasons. Visual observations were also used to map visitation around the colony and determine breaches of approach regulations. Vessel visitation and the associated noise were significantly higher in the peak season and direct visual observations showed that breaches of approach regulations were common (32%), highlighting the need for improved education and enforcement of compliance at the site. This study provides important context for assessing the impact of vessel noise and visitation at Seal Rocks and can be applied to conservation and management strategies at this and other sensitive marine sites.
{"title":"Passive Acoustic Monitoring and Mapping of Vessel Visitation at an Australian Fur Seal Breeding Colony","authors":"Jessalyn J. Taylor, Chloé Huetz, Isabelle Charrier, Rachael B. Gray, Rebecca R. McIntosh","doi":"10.1111/mms.70100","DOIUrl":"https://doi.org/10.1111/mms.70100","url":null,"abstract":"<p>Marine vessel traffic is a significant contributor to anthropogenic noise pollution and a source of disturbance for many marine species. It is important to assess the impact of vessel visitation and the number of potential disturbance events at sensitive marine sites to ensure management strategies are adequate. This study integrated passive acoustic monitoring (PAM), direct visual observation, and vessel traffic data to monitor vessel visitation at Seal Rocks, the largest Australian fur seal (<i>Arctocephalus pusillus doriferus</i>) breeding colony and site with the least stringent vessel approach limits. Vessel visitation was compared between the assumed low (off-peak) and high (peak) visitation seasons. Visual observations were also used to map visitation around the colony and determine breaches of approach regulations. Vessel visitation and the associated noise were significantly higher in the peak season and direct visual observations showed that breaches of approach regulations were common (32%), highlighting the need for improved education and enforcement of compliance at the site. This study provides important context for assessing the impact of vessel noise and visitation at Seal Rocks and can be applied to conservation and management strategies at this and other sensitive marine sites.</p>","PeriodicalId":18725,"journal":{"name":"Marine Mammal Science","volume":"42 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mms.70100","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145619356","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Laura J. May-Collado, Maia Austin, Lucas Bernier, Jeffrey Bernus, Beth Brady, Lauren Viegas, Eric A. Ramos
Fraser's dolphin (Lagenodelphis hosei) remains poorly studied due to its elusive behavior, rarity, and preference for deep offshore habitats. While dolphins use frequency-modulated whistles for communication, detailed acoustic descriptions exist for only a few species. This study provides the first comprehensive characterization of Fraser's dolphin whistle acoustic structure and repertoire, based on recordings from eight groups (15–300 individuals) collected during boat-based surveys at three sites in the Lesser Antilles. A total of 2999 whistles were analyzed for acoustic structure, with 1802 contours and a subsample of 728 whistles (weighted by group size) categorized using Beluga and ARTwarp to estimate repertoire size and composition. Whistles exhibited a broader frequency range (1.12–31.40 kHz) than previously reported. Acoustic overlap across sites supports the hypothesis of a proposed single population in the region. The repertoire was comprised of 298 whistle types, predominantly upsweeps and sine contours. Whistle type richness (q = 0) did not plateau, indicating incomplete sampling of rare types, whereas Shannon (q = 1) and Simpson (q = 2) diversity did plateau, suggesting that the most produced whistle types were well represented in this study. These findings offer a detailed baseline of Fraser's dolphin whistle repertoire and contribute to the development of species-specific detectors for passive acoustic monitoring, as well as future research on geographic variation, social communication, and responses to environmental and anthropogenic changes.
{"title":"A Detailed Characterization of the Whistle Repertoire of Fraser's Dolphins (Lagenodelphis hosei) From the Lesser Antilles","authors":"Laura J. May-Collado, Maia Austin, Lucas Bernier, Jeffrey Bernus, Beth Brady, Lauren Viegas, Eric A. Ramos","doi":"10.1111/mms.70101","DOIUrl":"https://doi.org/10.1111/mms.70101","url":null,"abstract":"<p>Fraser's dolphin (<i>Lagenodelphis hosei</i>) remains poorly studied due to its elusive behavior, rarity, and preference for deep offshore habitats. While dolphins use frequency-modulated whistles for communication, detailed acoustic descriptions exist for only a few species. This study provides the first comprehensive characterization of Fraser's dolphin whistle acoustic structure and repertoire, based on recordings from eight groups (15–300 individuals) collected during boat-based surveys at three sites in the Lesser Antilles. A total of 2999 whistles were analyzed for acoustic structure, with 1802 contours and a subsample of 728 whistles (weighted by group size) categorized using Beluga and ARTwarp to estimate repertoire size and composition. Whistles exhibited a broader frequency range (1.12–31.40 kHz) than previously reported. Acoustic overlap across sites supports the hypothesis of a proposed single population in the region. The repertoire was comprised of 298 whistle types, predominantly upsweeps and sine contours. Whistle type richness (<i>q</i> = 0) did not plateau, indicating incomplete sampling of rare types, whereas Shannon (<i>q</i> = 1) and Simpson (<i>q</i> = 2) diversity did plateau, suggesting that the most produced whistle types were well represented in this study. These findings offer a detailed baseline of Fraser's dolphin whistle repertoire and contribute to the development of species-specific detectors for passive acoustic monitoring, as well as future research on geographic variation, social communication, and responses to environmental and anthropogenic changes.</p>","PeriodicalId":18725,"journal":{"name":"Marine Mammal Science","volume":"42 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mms.70101","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145626848","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cortney A. Watt, Joanne Whitehead, Ashley Elliott, Lisa Loseto, Justine Hudson, Julia L. MacIsaac, Kristy Dever, Robert T. Brooke, Milda Milčiūtė, Juozas Gordevicius, Michael S. Kobor
Age is an important parameter to understand species life-history characteristics. Recently, DNA methylation methods have emerged as innovative tools to estimate the age of marine mammals. Narwhal (Monodon monoceros) epigenetic age estimates were computed using beluga (Delphinapterus leucas), killer whale (Orcinus orca), bowhead (Balaena mysticetus), odontocete, cetacean, and mammalian epigenetic clocks and were compared with age estimates from counting growth layer groups in tusks (n = 7) and/or aspartic acid racemization of eye lenses (n = 25). Pearson's correlation coefficients (R) ranged 0.68–0.87 for the clocks, but the absolute accuracy of age estimates was quite low, with median absolute error (MAE) between epigenetic and reference age ranging 7–37.5 years. To address this lack of accuracy, we more broadly investigated DNA methylation levels at cytosine-guanine sites (CpGs) for this same set of aged narwhals to develop a narwhal-specific epigenetic clock. Using a penalized regression model on 1009 CpG sites, ten CpGs (plus intercept) were selected, resulting in a model with a R = 0.70 and MAE of 8.6 years. This is the first study to age narwhals using DNA methylation patterns and to develop a narwhal-specific epigenetic aging clock, which will assist with understanding important life-history characteristics for sustainable conservation management.
{"title":"Estimating Narwhal (Monodon monoceros) Age Using Epigenetic Analysis of Skin","authors":"Cortney A. Watt, Joanne Whitehead, Ashley Elliott, Lisa Loseto, Justine Hudson, Julia L. MacIsaac, Kristy Dever, Robert T. Brooke, Milda Milčiūtė, Juozas Gordevicius, Michael S. Kobor","doi":"10.1111/mms.70102","DOIUrl":"https://doi.org/10.1111/mms.70102","url":null,"abstract":"<p>Age is an important parameter to understand species life-history characteristics. Recently, DNA methylation methods have emerged as innovative tools to estimate the age of marine mammals. Narwhal (<i>Monodon monoceros</i>) epigenetic age estimates were computed using beluga (<i>Delphinapterus leucas</i>), killer whale (<i>Orcinus orca</i>), bowhead (<i>Balaena mysticetus</i>), odontocete, cetacean, and mammalian epigenetic clocks and were compared with age estimates from counting growth layer groups in tusks (<i>n</i> = 7) and/or aspartic acid racemization of eye lenses (<i>n</i> = 25). Pearson's correlation coefficients (<i>R</i>) ranged 0.68–0.87 for the clocks, but the absolute accuracy of age estimates was quite low, with median absolute error (MAE) between epigenetic and reference age ranging 7–37.5 years. To address this lack of accuracy, we more broadly investigated DNA methylation levels at cytosine-guanine sites (CpGs) for this same set of aged narwhals to develop a narwhal-specific epigenetic clock. Using a penalized regression model on 1009 CpG sites, ten CpGs (plus intercept) were selected, resulting in a model with a <i>R</i> = 0.70 and MAE of 8.6 years. This is the first study to age narwhals using DNA methylation patterns and to develop a narwhal-specific epigenetic aging clock, which will assist with understanding important life-history characteristics for sustainable conservation management.</p>","PeriodicalId":18725,"journal":{"name":"Marine Mammal Science","volume":"42 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mms.70102","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145618966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jason D. Baker, Thea C. Johanos, Hope Ronco, Tracy A. Mercer, Brenda L. Becker
<p>Plastic pollution is a recognized threat to global oceans (National Academies of Sciences, Engineering, and Medicine <span>2022</span>; United Nations Environment Programme <span>2021</span>; United Nations Environment Programme <span>2023</span>). Hawaiian monk seals <i>(Neomonachus schauinslandi)</i>, listed as endangered under the US Endangered Species Act and currently numbering approximately 1600 individuals (Carretta et al. <span>2024</span>), have been the subject of long-term demographic study and conservation action. Since the early 1980s, when regular monitoring of the species began, entanglement of monk seals in marine debris has been recognized as a serious threat, and efforts to disentangle seals and remove debris from their habitat have been major conservation activities (Donohue et al. <span>2001</span>; Henderson <span>2001</span>). Baker et al. (<span>2024</span>) showed that large-scale marine debris removal efforts have effectively reduced this threat to monk seals in some locations.</p><p>Henderson (<span>2001</span>) analyzed monk seal entanglements observed during 17 years (1982–1998) and reported that pup and juvenile monk seals were more likely to become entangled than older seals, and the relative frequency of entangling debris types (i.e., nets versus lines) varied with seal age class. Here, we analyze more than 40 years of entanglement and population monitoring data collected by the US National Oceanic and Atmospheric Administration (NOAA), revealing new information about the relative entanglement risk faced by different demographic groups. We also summarize the number of documented entanglements, their outcomes, and the types of entangling material involved.</p><p>The Hawaiian monk seal metapopulation comprises nine geographically defined subpopulations spanning the Archipelago (Figure 1). Eight subpopulations are in the Northwestern Hawaiian Islands (NWHI). The ninth subpopulation in the main Hawaiian Islands (MHI), consists of eight primary islands (Figure 1), where seals were rarely seen until the late 20th century, but now number approximately 400 individuals (Baker and Johanos <span>2004</span>; Carretta et al. <span>2024</span>).</p><p>In the early 1980s, monk seal population monitoring was established in the NWHI by NOAA and has since been conducted nearly annually during seasonal field camps deployed at the six subpopulation locations from Kure Atoll to French Frigate Shoals (Figure 1). Regular monitoring at Midway Atoll was initiated in the mid-1990s when that seal subpopulation began to repopulate. Pups are weaned at roughly 5–7 weeks of age and subsequently marked with plastic flipper tags and implanted Passive Integrated Transponder (PIT) tags (Henderson and Johanos <span>1988</span>; Johanos et al. <span>1994</span>). During field seasons each year, standardized beach surveys were conducted regularly during which seals were resighted and identified using tags, temporary pelage bleach marks, and photogra
塑料污染是对全球海洋的公认威胁(美国国家科学院、工程院和医学院2022年;联合国环境规划署2021年;联合国环境规划署2023年)。夏威夷僧海豹(Neomonachus schauinslandi)被美国濒危物种法案列为濒危物种,目前约有1600只(Carretta et al. 2024),一直是长期人口统计研究和保护行动的主题。自20世纪80年代初开始对该物种进行定期监测以来,僧海豹被海洋垃圾缠住已被认为是一个严重的威胁,努力解开海豹并从其栖息地清除碎片已成为主要的保护活动(Donohue et al. 2001; Henderson 2001)。Baker等人(2024)表明,在某些地区,大规模的海洋垃圾清除工作有效地减少了对僧海豹的威胁。亨德森(2001)分析了17年间(1982-1998)观察到的僧海豹缠结情况,报告说幼海豹和幼海豹比年长海豹更容易被缠结,而且缠结碎片类型(即网和线)的相对频率随海豹年龄的不同而不同。在此,我们分析了美国国家海洋和大气管理局(NOAA)收集的40多年缠结和种群监测数据,揭示了不同人口群体面临的相对缠结风险的新信息。我们还总结了记录的缠结的数量,它们的结果,以及所涉及的缠结材料的类型。夏威夷僧海豹的超种群包括横跨群岛的九个地理上确定的亚种群(图1)。8个亚群分布在夏威夷群岛西北部。第9个亚群位于夏威夷主岛(MHI),由8个主要岛屿组成(图1),在那里直到20世纪末才见到海豹,但现在数量约为400只(Baker and Johanos 2004; Carretta et al. 2024)。在20世纪80年代早期,美国国家海洋和大气管理局(NOAA)在NWHI建立了僧海豹种群监测,此后几乎每年都在从Kure Atoll到French Frigate Shoals的六个亚种群地点部署季节性野外营地进行监测(图1)。在20世纪90年代中期,当海豹亚群开始重新繁殖时,对中途岛环礁的定期监测开始了。幼犬在大约5-7周龄断奶,随后用塑料鳍标签和植入的被动集成应答器(PIT)标签进行标记(Henderson and Johanos 1988; Johanos et al. 1994)。在每年的野外季节,定期进行标准化的海滩调查,在此期间使用标签,临时漂白剂标记和照片识别来重新观察和识别海豹(Harting et al. 2004)。记录每名视力正常的女性复视后每年的生殖状况。由于夏威夷僧海豹的分娩是不同步的,全年都有发生,高峰在3月至8月,一些繁殖事件没有被检测到,因为监测通常只在3月至8月的一部分时间进行(Harting et al. 2007; Johanos et al. 1994)。对海豹个体的年度调查和终生接触历史得出了关键的人口统计信息,如丰度、特定年龄的生存和繁殖能力、年龄-性别结构以及亚种群之间的迁移(Baker和Thompson 2007; Baker等人2016;Harting等人2007;Johanos等人2014)。由于它们的生态敏感性和难以接近性,Necker和Nihoa群岛(图1)通常每年只调查几天,因此缺乏这些亚种群的详细僧海豹人口统计数据。在从考阿伊岛到夏威夷伊岛的MHI地区,自21世纪初以来,主要通过志愿者的目击网络、公众报告和政府合作伙伴对僧海豹进行全年监测(Baker et al. 2011)。自2013年以来,在私人拥有的尼伊豪岛和附近的乐华岩,通过美国政府和尼伊豪岛居民的合作,每年进行1至2天的空中、船只和地面调查。在上述人口监测期间以及1974年至2022年期间,夏威夷僧海豹纠缠被记录下来。针对缠结的监测方案包括收集日期、位置、碎片类型、海豹身份、大小类别和性别等信息。还注意到缠结造成的伤害和死亡。缠住是由于活跃的渔具,碎片,或未知。在可能的程度上,当非noaa观测者报告缠结时获得了相同的数据。在某些情况下,缠结碎片并没有直接在海豹身上观察到,但最近的缠结是从已知个体的特征伤口或疤痕中推断出来的。 在这种情况下,无法确定碎片的类型。我们还记录了海豹是否被人类手工解开,它们的碎片是在没有人为干预的情况下脱落的,纠缠导致死亡,或者在最后一次观察时海豹仍然纠缠在一起。先前纠缠在一起的海豹被认为是在没有任何帮助的情况下,在没有任何人为干预的情况下,将碎片清理干净。虽然有可能,但除了NOAA及其合作伙伴之外,其他人不太可能进行未报告的解开缠结。当海豹目击记录时,根据视觉评估的大小和形态特征来分配海豹的大小等级(Stone 1984)。大小类别包括哺乳幼崽,断奶幼崽,幼崽(通常为1或2岁),亚成年(通常为3-4岁)和成年(通常为5岁及以上)。幼崽从第一天看到没有成年雌性看护的幼崽开始被认定为断奶,直到它们出生那年的12月31日。印章的身份被归类为永久的,如果它们有足够的标记(通常是标签或自然标记),允许每年重新识别。相比之下,临时身份表明海豹只有在目前的野外季节才能识别,通常是用临时的皮毛漂白剂标记。缠绕碎片类型记录为线、网、带、环、其他或未知(图2)。这些分类很宽泛,通常不能确定碎片的来源。例如,“线”包括从粗绳到单丝钓鱼线的所有类型。“网”包括所有类型的渔网,如拖网、围网和单丝刺网。“皮带”主要包括塑料包装带,但也可能包括其他可弯曲的圆形物体。“环”表示相对刚性的圆形物体。“其他”被分配给一组不属于上述类别的对象。在某些情况下,实地记录有助于更详细地澄清碎片类型,但这些记录没有足够的规律,也被认为不够可靠,例如无法区分拖网和围网。然而,“环”或“其他”碎片类别的一个亚型被分离为自己的类型,名为“鳗鱼锥”。这些是非常独特的圆锥形物体,是用来捕捉鳗鱼和盲鳗的陷阱装置的一部分。通常情况下,只有断奶的僧海豹幼崽被发现在它们的嘴上贴着鳗鱼锥。有时只涉及鳗鱼锥体基部环而不涉及圆锥形部分。所有NWHI渔具的缠结都被认为涉及废弃、丢失或以其他方式丢弃的渔具(ALDFG),而不是有效的渔具,因为自2009年以来,NWHI没有任何渔业活动。在此之前,三个NWHI渔业(金枪鱼和长嘴鱼的延绳钓,底栖鱼的手绳钓和龙虾陷阱渔业)偶尔会与僧海豹互动(Nitta和Henderson 1993)。然而,除了1986年一只僧海豹在被龙虾捕笼的主线和笼头缠住后淹死的案例(Nitta和Henderson 1993)外,没有记录到在这些国家卫生组织渔业中使用的有效渔具类型被缠住的案例。在MHI,僧海豹纠缠发生在活跃渔具和ALDFG。13起MHI缠结事件显然涉及主动捕捞的刺网或单丝线。这些在我们的分析中被省略,因为本研究的重点是碎片纠缠而不是直接的渔业相互作用。其余的MHI缠结事件被归类为不涉及活动渔具,或者在无法确定时归类为未知情况。一些MHI案件被确定不涉及活跃的渔具,因为缠绕物品要么不是渔具,要么是在夏威夷岛不使用的渔具类型(例如拖网或围网)。在其他情况下,当材料被严重风化时,就排除了活跃的渔具,这表明它很久以前就丢失或丢弃了。我们在现有人口统计数据的背景下评估了观察到的纠缠模式。例如,我们比较了观察到的大小类别和性别的纠缠比例,以及在相同类别中确定的海豹在多年和亚种群中所占的相对比例。我们之所以使用这种方法,是因为通常无法通过大小类别和性别来估计丰度。野外努力、
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Simon H. Elwen, Rebecca Hannén, Steve Benjamin, Claudio Velasquez Rojas, Rachel Probert, Tess Gridley
Large “super-groups” of feeding humpback whales (Megaptera novaeangliae) have occurred regularly off the West Coast of South Africa since ca. 2011, but little is known about their feeding behavior. We used opportunistic underwater video footage to investigate near-surface lunge feeding behavior, group coordination, and the use of pectoral fins in feeding. We analyzed 113 min of underwater video footage collected over 6 days. Whales passed through the frame on 623 occasions and were seen actively lunging on 182 occasions. No lateralization or coordinated foraging was observed. Gape cycles were short (mean mouth opening phase: 2.38 s and mouth closing: 1.69 s) with buccal pouch draining lasting the longest (15.61 s) and being a mostly passive action. The whales often surfaced while the pouch still contained water. Lunges and draining took place in all directions but mostly at ascending and even near vertical angles. Active flipper movements were observed during 81% of feeding lunges, providing further evidence that these uniquely large appendages are used hydrodynamically when feeding and may also play a role in prey herding. Disruption of feeding by diver presence was low. This study provides novel insight into the feeding behavior of Southern Hemisphere humpback whale super-groups, and potential human-whale interactions.
{"title":"Underwater Behavior of Southern Hemisphere Humpback Whales (Megaptera novaeangliae) Feeding in Super-Groups, From Video Footage","authors":"Simon H. Elwen, Rebecca Hannén, Steve Benjamin, Claudio Velasquez Rojas, Rachel Probert, Tess Gridley","doi":"10.1111/mms.70096","DOIUrl":"https://doi.org/10.1111/mms.70096","url":null,"abstract":"<p>Large “super-groups” of feeding humpback whales (<i>Megaptera novaeangliae</i>) have occurred regularly off the West Coast of South Africa since ca. 2011, but little is known about their feeding behavior. We used opportunistic underwater video footage to investigate near-surface lunge feeding behavior, group coordination, and the use of pectoral fins in feeding. We analyzed 113 min of underwater video footage collected over 6 days. Whales passed through the frame on 623 occasions and were seen actively lunging on 182 occasions. No lateralization or coordinated foraging was observed. Gape cycles were short (mean mouth opening phase: 2.38 s and mouth closing: 1.69 s) with buccal pouch draining lasting the longest (15.61 s) and being a mostly passive action. The whales often surfaced while the pouch still contained water. Lunges and draining took place in all directions but mostly at ascending and even near vertical angles. Active flipper movements were observed during 81% of feeding lunges, providing further evidence that these uniquely large appendages are used hydrodynamically when feeding and may also play a role in prey herding. Disruption of feeding by diver presence was low. This study provides novel insight into the feeding behavior of Southern Hemisphere humpback whale super-groups, and potential human-whale interactions.</p>","PeriodicalId":18725,"journal":{"name":"Marine Mammal Science","volume":"42 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mms.70096","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145581134","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}