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Relevant bibliographies by topics / Baleen whales Baleen whales Baleen whales

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Academic literature on the topic 'Baleen whales Baleen whales Baleen whales'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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Journal articles on the topic "Baleen whales Baleen whales Baleen whales"

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Lubetkin, S. C., J. E. Zeh, C. Rosa, and J. C. George. "Age estimation for young bowhead whales (Balaena mysticetus) using annual baleen growth increments." Canadian Journal of Zoology 86, no. 6 (2008): 525–38. http://dx.doi.org/10.1139/z08-028.

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We compiled age estimates and baleen plate δ13C data from 86 bowhead whales ( Balaena mysticetus L., 1758). We used previous whale age estimates based on aspartic acid racemization (AAR) and corpora counts to extend the use of δ13C data for age determination from cycle counting to a modified exponential model using annual baleen growth increments. Our approach used the growth increment data from individual whales in a nonlinear mixed effects model to assess both population-level and whale-specific growth parameters. Although age estimates from baleen-based models become less precise as the whales age, and baleen growth and length near steady state, the growth increment model shows promise in estimating ages of bowhead whales 10–13.5 m long with baleen lengths <250 cm, where other techniques are less precise or the data are scarce. Ages estimated using the growth increment data from such whales ranged from 6.4 to 19.8 years.

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Lubetkin, S. C., J. E. Zeh, and J. C. George. "Statistical modeling of baleen and body length at age in bowhead whales (Balaena mysticetus)." Canadian Journal of Zoology 90, no. 8 (2012): 915–31. http://dx.doi.org/10.1139/z2012-057.

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We used baleen lengths and age estimates from 175 whales and body lengths and age estimates from 205 whales to test which of several single- and multi-stage growth models best characterized age-specific baleen and body lengths for bowhead whales ( Balaena mysticetus L., 1758) with the goal of determining which would be best for predicting whale age based on baleen or body length. Previous age estimates were compiled from several techniques, each of which is valid over a relatively limited set of physical characteristics. The best fitting single-stage growth model was a variation of the von Bertalanffy growth model for both baleen and body length data. Based on Bayesian information criterion, the two- and three-stage versions of the von Bertalanffy model fit the data better than did the single-stage models for both baleen and body length. The best baleen length models can be used to estimate expected ages for bowhead whales with up to 300–325 cm baleen, depending on sex, which correspond to age estimates approaching 60 years. The best body length models can be used to estimate expected ages for male bowhead whales up to 14 m, and female bowheads up to 15.5 m or ages up to approximately 40 years.

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Moore, Sue E. "Is it ‘boom times’ for baleen whales in the Pacific Arctic region?" Biology Letters 12, no. 9 (2016): 20160251. http://dx.doi.org/10.1098/rsbl.2016.0251.

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The marine ecosystem in the Pacific Arctic region has experienced dramatic transformation, most obvious by the loss of sea ice volume (75%), late-summer areal extent (50%) and change in phenology (four to six weeks longer open-water period). This alteration has resulted in an opening of habitat for subarctic species of baleen whales, many of which are recovering in number from severe depletions from commercial whaling in the nineteenth and twentieth centuries. Specifically, humpback, fin and minke whales ( Megaptera novaeangliae , Balaenoptera physalus and Balaenoptera acutorostrata ) are now regularly reported during summer and autumn in the southern Chukchi Sea. These predators of zooplankton and forage fishes join the seasonally resident grey whale ( Eschrichtius robustus ) and the arctic-endemic bowhead whale ( Balaena mysticetus ) in the expanding open-ocean habitat of the Pacific Arctic. Questions arising include: (i) what changes in whale-prey production and delivery mechanisms have accompanied the loss of sea ice, and (ii) how are these five baleen whale species partitioning the expanding ice-free habitat? While there has been no programme of research specifically focused on these questions, an examination of seasonal occurrence, foraging plasticity and (for bowhead whales) body condition suggests that the current state of Pacific Arctic marine ecosystem may be ‘boom times’ for baleen whales. These favourable conditions may be moderated, however, by future shifts in ecosystem structure and/or negative impacts to cetaceans related to increased commercial activities in the region.

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Volkenandt, Mareike, Ian O’Connor, Jean-Marc Guarini, Simon Berrow, and Ciaran O’Donnell. "Fine-scale spatial association between baleen whales and forage fish in the Celtic Sea." Canadian Journal of Fisheries and Aquatic Sciences 73, no. 2 (2016): 197–204. http://dx.doi.org/10.1139/cjfas-2015-0073.

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Baleen whales can be regularly observed in the Celtic Sea; however, little is known about their local foraging behaviour. The study objective was to determine whether or not baleen whales selectively prey upon particular forage fish species or, on the contrary, is predation on the Celtic Sea plateau driven by random encounters between prey and predator? Concurrent sighting surveys for fin (Balaenoptera physalus), minke (Balaenoptera acutorostrata), and humpback (Megaptera novaeangliae) whales were carried out simultaneously from 2007 to 2013 during dedicated fisheries acoustic surveys assessing the abundance and distribution of forage fish. Probabilities of spatial overlap between baleen whales and forage fish were analysed and compared with the probability of a random encounter. For estimations of foraging threshold and prey selectivity, mean fish biomass and fish length were calculated when baleen whales and forage fish co-occurred. Whales were dominantly observed in areas with herring (Clupea harengus) and sprat (Sprattus sprattus), while areas with mackerel (Scomber scombrus) were not targeted. A prey detection range of up to 8 km was found, which enables baleen whales to track their prey to minimize search effort. Fish densities within the defined foraging distance ranged from 0.001 to 3 kg·m−2 and were correlated to total fish abundance. No prey size selectivity according to fish length was found. By linking baleen whale distribution to high-density herring and sprat areas, it was possible to identify the Celtic Sea as a prey hot spot for baleen whales during autumn.

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Belikov, Stanislav E., and Andrei N. Boltunov. "Distribution and migrations of cetaceans in the Russian Arctic according to observations from aerial ice reconnaissance." NAMMCO Scientific Publications 4 (July 21, 2002): 69. http://dx.doi.org/10.7557/3.2838.

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This paper is based on 748 observations of belugas (Delphinapterus leucas) and 382 observations of baleen whales in the Russian Arctic, the majority of the data provided by aerial reconnaissance of sea ice (ARSI). Although the data are not suitable for the estimation of the number and density of the animals, they represent a multi-year (1958-1995) range of observations to update our knowledge on the seasonal distribution and migrations of the species. Belugas inhabit not only shelf waters but also the zone of the shelf slope and the abyssal zone of the Arctic Ocean, where the animals appear mostly in summer. In winter belugas were observed only in the Barents Sea. In June-August, the frequency of beluga observations was highest in the Laptev Sea, which has previously been believed to have considerably lower numbers of beluga than the Kara and Barents seas. Patterns of seasonal distribution and ice cover suggest the existence of a natural border preventing or reducing population exchange between belugas inhabiting the western and eastern parts of the Russian Arctic. A brief review of available data on distribution of the narwhal (Monodon monoceros) in the Russian Arctic is also given. Two species of baleen whales were frequently seen in the Russian Arctic: the bowhead whale (Balaena mysticetus), and the grey whale (Eschrichtius robustus). The majority of such observations were made in the southeastern part of the East-Siberian Sea and the southern part of the Chukchi Sea. In the Bering Sea baleen whales were usually seen near the Chukotka Peninsula, in Anadyr Bay and southeast of it. Whales were usually seen in ice-free water: observations of whales among rarefied ice and near the ice edge were rare. There were considerable annual and seasonal variations in distribution and migrations of baleen whales in the region, probably caused mainly by the dynamics of ice conditions.

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Werth, Alexander J., Robert W. Harriss, Michael V. Rosario, J. Craig George, and Todd L. Sformo. "Hydration affects the physical and mechanical properties of baleen tissue." Royal Society Open Science 3, no. 10 (2016): 160591. http://dx.doi.org/10.1098/rsos.160591.

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Baleen, an anisotropic oral filtering tissue found only in the mouth of mysticete whales and made solely of alpha-keratin, exhibits markedly differing physical and mechanical properties between dried or (as in life) hydrated states. On average baleen is 32.35% water by weight in North Atlantic right whales ( Eubalaena glacialis ) and 34.37% in bowhead whales ( Balaena mysticetus ). Baleen's wettability measured by water droplet contact angles shows that dried baleen is hydrophobic whereas hydrated baleen is highly hydrophilic. Three-point flexural bending tests of mechanical strength reveal that baleen is strong yet ductile. Dried baleen is brittle and shatters at about 20–30 N mm −2 but hydrated baleen is less stiff; it bends with little force and absorbed water is squeezed out when force is applied. Maximum recorded stress was 4× higher in dried (mean 14.29 N mm −2 ) versus hydrated (mean 3.69 N mm −2 ) baleen, and the flexural stiffness was >10× higher in dried (mean 633N mm −2 ) versus hydrated (mean 58 N mm −2 ) baleen. In addition to documenting hydration's powerful effects on baleen, this study indicates that baleen is far more pliant and malleable than commonly supposed, with implications for studies of baleen's structure and function as well as its susceptibility to oil or other hydrophobic pollutants.

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Werth, Alexander J., Shemar M. Blakeney, and Adrian I. Cothren. "Oil adsorption does not structurally or functionally alter whale baleen." Royal Society Open Science 6, no. 5 (2019): 182194. http://dx.doi.org/10.1098/rsos.182194.

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Mysticete whales filter small prey from seawater using baleen, a unique keratinous oral tissue that grows from the palate, from which it hangs in hundreds of serial plates. Laboratory experiments testing effects of oils on material strength and flexibility, particle capture and tissue architecture of baleen from four mysticete species (bowhead, Balaena mysticetus ; North Atlantic right, Eubalaena glacialis ; fin, Balaenoptera physalus ; humpback, Megaptera novaeangliae ) indicate that baleen is hydrophilic and oleophobic, shedding rather than adsorbing oil. Oils of different weights and viscosities were tested, including six petroleum-based oils and two fish or plankton oils of common whale prey. No notable differences were found by oil type or whale species. Baleen did not adsorb oil; oil was readily rinsed from baleen by flowing water, especially from moving fringes. Microscopic examination shows minimal wrinkling or peeling of baleen's cortical keratin layers, probably due to oil repelling infiltrated water. Combined results cast doubt on fears of baleen fouling by oil; filter porosity is not appreciably affected, but oil ingestion risks remain. Particle capture studies suggest potentially greater danger to mysticetes from plastic pollution than oil.

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Leaper, Rebecca, and Cara Miller. "Management of Antarctic baleen whales amid past exploitation, current threats and complex marine ecosystems." Antarctic Science 23, no. 6 (2011): 503–29. http://dx.doi.org/10.1017/s0954102011000708.

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AbstractAs baleen whales recover from severe exploitation, they are probably subject to a wide variety of threats within the Antarctic marine ecosystem, including directed take. Here we review both the management and current status of Antarctic baleen whales and consider those threats likely to impact on them. Threats range from global problems - marine pollution and climate change - to localized issues including shipping, habitat disturbance, unregulated wildlife tourism and fishery activities. We identify the most pressing anthropogenic threats to baleen whales including scientific whaling and climate change. It is unclear whether current management approaches will be able to effectively encompass all these threats while also accounting both for the differing levels of scientific understanding and for the differing recovery rates of the whale species. For management we recommend the following: 1) incorporation of both ecosystem considerations and the suite of identified threats not limited to direct take, 2) identification of measurable indicators of changes in whales that allow more certainty in monitoring of populations and the environment, and 3) recognition of significant relationships between baleen whales and habitat features to provide information on distribution and use.

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Stimpert, Alison K., David N. Wiley, Whitlow W. L. Au, Mark P. Johnson, and Roland Arsenault. "‘Megapclicks’: acoustic click trains and buzzes produced during night-time foraging of humpback whales ( Megaptera novaeangliae )." Biology Letters 3, no. 5 (2007): 467–70. http://dx.doi.org/10.1098/rsbl.2007.0281.

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Humpback whales ( Megaptera novaeangliae ) exhibit a variety of foraging behaviours, but neither they nor any baleen whale are known to produce broadband clicks in association with feeding, as do many odontocetes. We recorded underwater behaviour of humpback whales in a northwest Atlantic feeding area using suction-cup attached, multi-sensor, acoustic tags (DTAGs). Here we describe the first recordings of click production associated with underwater lunges from baleen whales. Recordings of over 34 000 ‘megapclicks’ from two whales indicated relatively low received levels at the tag (between 143 and 154 dB re 1 μPa pp), most energy below 2 kHz, and interclick intervals often decreasing towards the end of click trains to form a buzz. All clicks were recorded during night-time hours. Sharp body rolls also occurred at the end of click bouts containing buzzes, suggesting feeding events. This acoustic behaviour seems to form part of a night-time feeding tactic for humpbacks and also expands the known acoustic repertoire of baleen whales in general.

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Werth, Alexander J. "Hydrodynamic and Sensory Factors Governing Response of Copepods to Simulated Predation by Balaenid Whales." International Journal of Ecology 2012 (2012): 1–13. http://dx.doi.org/10.1155/2012/208913.

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Predator/prey interactions between copepods and balaenid (bowhead and right) whales were studied with controlled lab experiments using moving baleen in still water and motionless baleen in flowing water to simulate zooplankton passage toward, into, and through the balaenid oral cavity. Copepods showed a lesser escape response to baleen and to a model head simulating balaenid oral hydrodynamics than to other objects. Copepod escape response increased as water flow and body size increased and was greatest at distances ≥10 cm from baleen and at copepod density = 10,000 m−3. Data from light/dark experiments suggest that escape is based on mechanoreception, not vision. The model head captured 88% of copepods. Results support previous research showing hydrodynamic effects within a whale’s oral cavity create slight suction pressures to draw in prey or at least preclude formation of an anterior compressive bow wave that could scatter or alert prey to the presence of the approaching whale.

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Dissertations / Theses on the topic "Baleen whales Baleen whales Baleen whales"

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Winn, Jeremy Paul. "Modeling Large Whale Entanglement Injuries: An Experimental Analysis of the Influence of Tissue Compliance, Line Tension, and Draw-Length on Epidermal Abrasion Resistance." Fogler Library, University of Maine, 2006. http://www.library.umaine.edu/theses/pdf/WinnJP2006.pdf.

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Pinto, Sheldon James Dominick. "On the filtration mechanisms and oral anatomy of lunge-feeding baleen whales." Thesis, University of British Columbia, 2011. http://hdl.handle.net/2429/37849.

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Here we endeavoured to quantify the filtration mechanics of rorquals and the material properties of baleen “gums” (termed zwischensubstanz) by examining and testing the baleen of a fin whale (Balaenoptera physalus). It was hypothesized that fin whales use cross-flow filtration to filter krill from engulfed seawater such that krill and other debris do not become entangled in the baleen fringes. Cross-flow filtration was proposed as an alternate mechanism to dead-end sieving since it would create a highly concentrated suspension of krill inside the mouth (potentially at the oesophageal opening) and would also not require krill to contact the baleen, eliminating clogging and filtering efficiency losses. We tested filtration mechanisms by placing a sixty-two centimetre section of baleen from a fin whale in a circular water tank and imitating the whale’s environment through various flow scenarios and setups. It was not conclusively determined whether cross-flow filtration is the mechanism used by fin whales, but a new mechanism was proposed called centripetal filtration in which two slugs of water spiral anteriorly on the left and right side of the whale’s oral cavity. Further examination of this proposed mechanism is required. The material properties of the zwischensubstanz that holds baleen plates together and the development of baleen plates through this zwischensubstanz were also examined. Zwischensubstanz exhibits isotropic properties similar to soft rubber in compression with an average Young’s modulus of 2.56 ± 0.60 MPa and 44.4 ± 2.4% hysteresis when compressed at 0.5 Hz, as it appears to space the baleen plates and absorb stresses translated from the plates. Through this rubbery zwischensubstanz, the baleen plates develop from conical papillae to hard, keratinized plates. The zwischensubstanz forms a matrix around the papillae and is calcified and keratinized before exiting the zwischensubstanz as a fully developed plate. The discoveries made here with regard to centripetal filtration and the properties of zwischensubstanz are preliminary attempts at quantifying baleen whale filtration and its associated feeding structures. Such work has been rare in the literature and there are many questions left to be answered by eager scientists with regard to the greatest biomechanical event in the world.

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Lysiak, Nadine Stewart J. "Investigating the migration and foraging ecology of North Atlantic right whales with stable isotope geochemistry of baleen and zooplankton." Restricted access (UM), 2008. http://libraries.maine.edu/gateway/oroauth.asp?file=orono/etheses/37803141.pdf.

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Risch, Denise [Verfasser]. "Baleen whale acoustic ecology with focus on minke whales (Balaenoptera acutorostrata) and reference to anthropogenic noise / Denise Risch." Kiel : Universitätsbibliothek Kiel, 2014. http://d-nb.info/1062535995/34.

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Marques, Fernanda F. C. "Baleen whale distributional patterns and the potential influence of biological and physical processes." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1996. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/MQ36151.pdf.

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Woodward, Becky. "Locomotory Strategies, Dive Dynamics, and Functional Morphology of the Mysticetes: Using Morphometrics, Osteology, and DTAG Data to Compare Swim Performance in Four Species of Baleen Whales." Fogler Library, University of Maine, 2006. http://www.library.umaine.edu/theses/pdf/WoodwardBX2006.pdf.

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Pangerc, Tanja. "Baleen whale acoustic presence around South Georgia." Thesis, University of East Anglia, 2010. https://ueaeprints.uea.ac.uk/19109/.

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Punt, A. E. "Management procedures for Cape hake and baleen whale resources: Part 1." Thesis, University of Cape Town, 1991. http://hdl.handle.net/11427/23366.

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Drake, Summer Elizabeth. "Sensory hairs in the bowhead whale (Cetacea, Mammalia)." Kent State University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=kent1406300822.

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Saloma, Anjara. "Humpback whales (Megaptera novaeangliae) mother-calf interactions." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS138.

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Chez les baleines à bosse (Megaptera novaeangliae), le maintien des liens sociaux entre les femelles et leurs nouveau-nés implique différentes modalités sensorielles telles que l'ouïe, le toucher et la vision. Si la communication acoustique chez les mâles chanteurs de cette espèce a été largement étudiée, les sons sociaux, en particulier ceux produits par les femelles et leurs nouveau-nés, ont été peu reportés. Cette étude décrit les sons sociaux présents dans les enregistrements acoustiques axés sur les groupes mère-baleineau et discute des vocalisations produites par les femelles et les baleineaux dans les interactions mère-jeune. En considérant les sons les plus fréquents de ce répertoire vocal, une analyse centrée sur la détermination de la source des sons de bass fréquence produits par la mère a été effectuée et des analyses ont été réalisées pour mettre en évidence l'individualité de certaines vocalisations appartenant à la mère et à son petit. Une description du contexte comportemental de leur production vocale a été réalisée et parallèlement, les profils de plongée des mères et de leurs nouveau-nés ont été décrits. En outre, les femelles et leurs petits passent beaucoup de temps à la surface de l'eau. Les mères sont souvent statiques à la surface tandis que les baleineaux évoluent autour d'elles. Cette étude est également consacrée à la compréhension de leurs comportements de surface, en tenant compte des comportements initiés par les baleineaux. Des séries d’analyses ont été réalisées pour déterminer si les baleineaux présentaient des comportements de latéralisation par rapport à leur mère. Enfin, en utilisant la méthode de photogrammétrie, les tailles des femelles et des nouveau-nés ont été mesurées, ainsi que l'espace utilisée par les baleineaux autour de leur mère<br>In humpback whales (Megaptera novaeangliae), maintaining social bonds between females and their newborns involves different sensory modalities such as hearing, touching and vision. While acoustic communication in male singers of this species has been extensively studied, social sounds, especially those produced by the females and their newborns have been poorly documented. This study describes the social sounds present in acoustic recordings focused on mother-calf groups and discusses the vocalizations used by females and calves in mother-offspring interactions. By considering the most frequent sounds from their vocal repertoire, an analysis focused on the determination of the source of the low-frequency sounds produced by the mother have been carried out and analyses were performed to investigate the individuality of some vocalizations belonging to the mothers and the calves. A description of the behavioural context of their vocal production was performed and the diving profiles of mother-calf pairs were described. Moreover, females with their calves spend a lot of time on the water surface. Mothers are often static at the surface while calves move around them. This study is also dedicated to the understanding of their surface behaviours, considering the behaviours initiated by calves. A series of analyses were carried out to determine whether calves exhibited lateralization behaviours in relation to their mothers. Finally, by using photogrammetry method, mother-calf lengths were measured, and calves spatial range around their mothers was investigated

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Books on the topic "Baleen whales Baleen whales Baleen whales"

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Baleen whales. Rourke, 1996.

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Johnson, Christina. Blue whales and other baleen whales. World Book, Inc., 2006.

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Ridgway, Sam H., and Richard John Harrison. The sirenians and baleen whales. Academic, 1985.

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Ridgway, Sam H. The sirenians and baleen whales. Academic, 1985.

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Kerrod, Robin. Mammals: Primates, insect-eaters and Baleen whales. Facts on File, 1988.

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A, Arsenʹev V., and Geptner V. G. 1901-1975, eds. Usatye kity. "Nauka", 1994.

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Sokolov, Vladimir Evgenʹevich. Mammals of Russia and adjacent regions. Smithsonian Institution Libraries, 2005.

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Parks, Susan Elizabeth. Acoustic communication in the North Atlantic right whale (Eubalaena glacialis). Massachusetts Institute of Technology, 2003.

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Kerrod, Robin. Mammals. Facts on File, 1988.

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Greenlanders, whales, and whaling: Sustainability and self-determination in the Arctic. University Press of New England, 1997.

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Book chapters on the topic "Baleen whales Baleen whales Baleen whales"

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Leaper, Rebecca, and Simon Childerhouse. "Present and Future Conservation Management of Antarctic Baleen Whales." In Antarctic Futures. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6582-5_4.

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Bernasconi, Matteo, Ruben Patel, and Leif Nøttestad. "Behavioral Observations of Baleen Whales in Proximity of a Modern Fishing Vessel." In Advances in Experimental Medicine and Biology. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-7311-5_75.

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Schell, D. M., S. M. Saupe, and N. Haubenstock. "Natural Isotope Abundances in Bowhead Whale (Balaena mysticetus) Baleen: Markers of Aging and Habitat Usage." In Stable Isotopes in Ecological Research. Springer New York, 1989. http://dx.doi.org/10.1007/978-1-4612-3498-2_15.

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Raftery, Adrian E., and Judith E. Zeh. "Estimation of Bowhead Whale, Balaena mysticetus, Population Size." In Case Studies in Bayesian Statistics. Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4612-2714-4_4.

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Higdon, J. W., and S. H. Ferguson. "Past, Present, and Future for Bowhead Whales (Balaena mysticetus) in Northwest Hudson Bay." In A Little Less Arctic. Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-90-481-9121-5_8.

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Bannister, J. L. "Baleen Whales." In Encyclopedia of Ocean Sciences. Elsevier, 2001. http://dx.doi.org/10.1016/b978-012374473-9.00429-x.

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Bannister, J. L. "Baleen Whales." In Encyclopedia of Ocean Sciences. Elsevier, 2001. http://dx.doi.org/10.1006/rwos.2001.0429.

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Bannister, John L., and Stephanie K. Adamczak. "Baleen Whales." In Encyclopedia of Ocean Sciences. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-409548-9.11396-x.

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"VLADIMIR GEORGIEVICH HEPTNER." In Baleen Whales. Science Publishers, 2006. http://dx.doi.org/10.1201/b10993-2.

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"ORDER OF CETACEANS." In Baleen Whales. Science Publishers, 2006. http://dx.doi.org/10.1201/b10993-3.

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Conference papers on the topic "Baleen whales Baleen whales Baleen whales"

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Patris, Julie, Dimitri Komatitsch, Maritza Sepulveda, et al. "Mono-hydrophone localization of baleen whales: a study of propagation using a spectral element method applied in Northern Chile." In OCEANS 2019 - Marseille. IEEE, 2019. http://dx.doi.org/10.1109/oceanse.2019.8867333.

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Reports on the topic "Baleen whales Baleen whales Baleen whales"

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Baumgartner, Mark. Environmental Influences on Diel Calling Behavior in Baleen Whales. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada598564.

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Baumgartner, Mark, and David M. Fratantoni. Environmental Influences on Diel Calling Behavior in Baleen Whales. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada573311.

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Hunt, Kathleen E., Rosalind M. Rolland, and Scott D. Kraus. Development of Novel Noninvasive Methods of Stress Assessment in Baleen Whales. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada617502.

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Teilmann, Jonas. Acquisition of Oceanographic Measurements from Baleen Whales and Acquisition of Oceanographic Measurements from Baleen Whales: Field Deployments of Tags Developed Under Grant ONR (N00014-13-1-0854). Defense Technical Information Center, 2015. http://dx.doi.org/10.21236/ad1014311.

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Calambokidis, John. Behavioral and Physiological Response of Baleen Whales to Ships and Ship Noise. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada617027.

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Calambokidis, John. Behavioral and Physiological Response of Baleen Whales to Ships and Ship Noise. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada604988.

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Stokes, M. D. The Effects of Ambient Noise Field on the Behavior of Baleen Whales - Pilot Program. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada425285.

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Friedlaender, Ari S., and Elliott L. Hazen. Interactions Among Behavioral Responses of Baleen Whales to Acoustic Stimuli, Oceanographic Features, and Prey Availability. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada573481.

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Friedlaender, Ari S., Brandon L. Southall, and Elliott L. Hazen. Interactions Among Behavioral Responses of Baleen Whales to Acoustic Stimuli, Oceanographic Features, and Prey Availability. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada616546.

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Friedlaender, Ari S., Brandon L. Southall, and Elliott L. Hazen. Interactions Among Behavioral Responses of Baleen Whales to Acoustic Stimuli, Oceanographic Features, and Prey Availability. Defense Technical Information Center, 2015. http://dx.doi.org/10.21236/ada619114.

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