784 research outputs found

    Whistles as potential indicators of stress in bottlenose dolphins (Tursiops truncatus)

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    Stress has been defined as an environmental effect on an individual that overtaxes its functional abilities. The diversity of stress responses among marine mammals makes it difficult to develop a comprehensive diagnostic protocol to evaluate stress. The development of a relatively non-invasive tool with which to evaluate stress in bottlenose dolphins (Tursiops truncatus) could allow for assessments of animals that may be at risk, and assessment of free-ranging animals without capture-release. The goal of this study was to evaluate whether vocalizations, specifically signature whistles, could serve as possible indicators of acute (or short-term) stress in bottlenose dolphins. Recordings made during brief capture-release events and during focal follows of undisturbed animals in Sarasota Bay, FL, were used to address this question. Although there is no evidence that capture-release events have any long or short term adverse impacts on members of the Sarasota dolphin community, it is likely that they are a source of short-term stress to the dolphins. I asked the following questions: Will whistle rates and number of loops (repetitive elements in whistles) be greater: (1) during capture-release than during undisturbed focal follows? (2) at the beginning of a capture-release session than at the end of a session? (3) during an individual’s first capture-release session than during later sessions? (4) when a mother is caught and released with a dependent calf than without a dependent calf? I also examined whether the duration of loops and/or inter-loop intervals, and maximum and minimum frequency of whistles change in any of the above contexts. Loop number was significantly higher during capture-release than during focal follows, and decreased significantly from the beginning to the end of an individual’s capture-release session. Loop duration was significantly shorter at the beginning than at the end of an individual session. Whistle rate was also significantly higher during capture-release than during focal follows, and during a dolphin’s first capture-release than during subsequent sessions. Females caught with a dependent calf produced whistles with significantly higher maximum frequencies and shorter inter-loop intervals than when caught and released without a dependent calf. Based on the results of this study, further research would be warranted on assessing the utility of signature whistle rate and loop number as behavioral indicators of short-term stress in bottlenose dolphins. These measures could potentially be utilized independently, or in conjunction with physiological indicators, in assessments of the impact of potentially stressful human activities on bottlenose dolphins

    Low frequency vocalizations attributed to sei whales (Balaenoptera borealis)

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    Author Posting. © Acoustical Society of America, 2008. This article is posted here by permission of Acoustical Society of America for personal use, not for redistribution. The definitive version was published in Journal of the Acoustical Society of America 124 (2008): 1339-1349, doi:10.1121/1.2945155.Low frequency (<100 Hz) downsweep vocalizations were repeatedly recorded from ocean gliders east of Cape Cod, MA in May 2005. To identify the species responsible for this call, arrays of acoustic recorders were deployed in this same area during 2006 and 2007. 70 h of collocated visual observations at the center of each array were used to compare the localized occurrence of this call to the occurrence of three baleen whale species: right, humpback, and sei whales. The low frequency call was significantly associated only with the occurrence of sei whales. On average, the call swept from 82 to 34 Hz over 1.4 s and was most often produced as a single call, although pairs and (more rarely) triplets were occasionally detected. Individual calls comprising the pairs were localized to within tens of meters of one another and were more similar to one another than to contemporaneous calls by other whales, suggesting that paired calls may be produced by the same animal. A synthetic kernel was developed to facilitate automatic detection of this call using spectrogram-correlation methods. The optimal kernel missed 14% of calls, and of all the calls that were automatically detected, 15% were false positives.Funding was provided by the NOAA National Marine Fisheries Service and the WHOI Ocean Life Institute

    Evidence of a North Atlantic right whale calf (Eubalaena glacialis) born in northeastern U.S. waters

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    Author Posting. © The Author(s), 2008. This is the author's version of the work. It is posted here by permission of John Wiley & Sons for personal use, not for redistribution. The definitive version was published in Marine Mammal Science 25 (2009): 462-477, doi:10.1111/j.1748-7692.2008.00261.x.The general temporal and geographical patterns of North Atlantic right whale (Eubalaena glacialis) calving events have been clarified during the last quarter century of research (Kraus and Rolland 2007). Right whales give birth to a single calf every three to five years after a twelve- to thirteen-month gestation period (Best 1994; Kraus and Hatch 2001). Most calves are born between December and March in the coastal waters of the southeastern U.S., the only known calving ground for this species (Kraus et al. 2007; Winn et al. 1986). Although historical whaling records suggest that there were once two winter calving grounds, one off the southeastern U.S. and the other off northwestern Africa, it appears that only the former is still used today (Notarbartolo di Sciara et al. 1998; Reeves and Mitchell 1986; 1988). In the late winter, right whales leave the calving grounds and migrate to their foraging grounds off the northeastern U.S. and Canadian Maritimes. North Atlantic right whales can be found in Cape Cod and Massachusetts Bays throughout the late winter and early spring (Hamilton and Mayo 1990; Mayo and Marx 1990; Schevill et al. 1986), in the Great South Channel during mid-spring to early summer (Kenney et al. 1995), and in the Bay of Fundy (Kraus et al. 1982) and on the Scotian Shelf (Mitchell et al. 1986; Stone et al. 1988) during the summer and fall. Some individuals (mostly pregnant females and juveniles) return to the calving grounds off the southeastern U.S. in December and January, but the location of the rest of the population during those months is currently unknown (although recent evidence suggests that right whales are present in the Gulf of Maine and on the Scotian Shelf throughout the winter (Mellinger et al. 2007; T. Cole pers comm. ; S. Van Parijs pers comm. )

    Whistles as potential indicators of stress in bottlenose dolphins (Tursiops truncatus

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    We examined the possibility that parameters of bottlenose dolphin signature whistles may serve as indicators of stress. Bottlenose dolphins (Tursiops truncatus) in Sarasota Bay, Florida, were recorded during brief capturerelease events, which are potentially a source of short-term stress to these dolphins, although no effects of chronic or long-term stress have been observed over the 37+-year duration of the research. Whistles recorded during both brief capture-release and undisturbed, free-ranging conditions were examined to determine whether whistle parameters differ during capture-release versus undisturbed conditions; at the beginning of a capturerelease session versus at the end of a session; during an individual&apos;s 1st capture-release session versus later capture-release sessions; and when a mother is caught and released with a dependent calf versus without a dependent calf (i.e., she has no dependent calf at the time of capture-release). We examined a variety of acoustic parameters, including whistle rate, number of loops (repetitive elements), maximum and minimum frequency, and loop, interloop, and whistle duration. We found that whistle rate and number of loops were greater during brief capture-release events than during undisturbed conditions; number of loops decreased and loop duration increased over the duration of a capture-release session; whistle rates decreased with number of capture-release sessions; and females caught and released with dependent calves produced whistles with higher maximum frequencies and shorter interloop intervals than when they did not have dependent calves. Thus, whistles appear to have potential as noninvasive indicators of stress in bottlenose dolphins. Further research is warranted in this area, for example by correlating physiological indices to whistle rates under varying levels of stress. Reliable, noninvasive correlates of stress could be used to monitor dolphins in a variety of circumstances, such as during exposure to anthropogenic noise

    Search for squarks and gluinos in events with isolated leptons, jets and missing transverse momentum at s√=8 TeV with the ATLAS detector

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    The results of a search for supersymmetry in final states containing at least one isolated lepton (electron or muon), jets and large missing transverse momentum with the ATLAS detector at the Large Hadron Collider are reported. The search is based on proton-proton collision data at a centre-of-mass energy s√=8 TeV collected in 2012, corresponding to an integrated luminosity of 20 fb−1. No significant excess above the Standard Model expectation is observed. Limits are set on supersymmetric particle masses for various supersymmetric models. Depending on the model, the search excludes gluino masses up to 1.32 TeV and squark masses up to 840 GeV. Limits are also set on the parameters of a minimal universal extra dimension model, excluding a compactification radius of 1/R c = 950 GeV for a cut-off scale times radius (ΛR c) of approximately 30

    Measurements of fiducial and differential cross sections for Higgs boson production in the diphoton decay channel at s√=8 TeV with ATLAS

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    Measurements of fiducial and differential cross sections are presented for Higgs boson production in proton-proton collisions at a centre-of-mass energy of s√=8 TeV. The analysis is performed in the H → γγ decay channel using 20.3 fb−1 of data recorded by the ATLAS experiment at the CERN Large Hadron Collider. The signal is extracted using a fit to the diphoton invariant mass spectrum assuming that the width of the resonance is much smaller than the experimental resolution. The signal yields are corrected for the effects of detector inefficiency and resolution. The pp → H → γγ fiducial cross section is measured to be 43.2 ±9.4(stat.) − 2.9 + 3.2 (syst.) ±1.2(lumi)fb for a Higgs boson of mass 125.4GeV decaying to two isolated photons that have transverse momentum greater than 35% and 25% of the diphoton invariant mass and each with absolute pseudorapidity less than 2.37. Four additional fiducial cross sections and two cross-section limits are presented in phase space regions that test the theoretical modelling of different Higgs boson production mechanisms, or are sensitive to physics beyond the Standard Model. Differential cross sections are also presented, as a function of variables related to the diphoton kinematics and the jet activity produced in the Higgs boson events. The observed spectra are statistically limited but broadly in line with the theoretical expectations

    Evidence for the Higgs-boson Yukawa coupling to tau leptons with the ATLAS detector

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    Results of a search for H → τ τ decays are presented, based on the full set of proton-proton collision data recorded by the ATLAS experiment at the LHC during 2011 and 2012. The data correspond to integrated luminosities of 4.5 fb−1 and 20.3 fb−1 at centre-of-mass energies of √s = 7 TeV and √s = 8 TeV respectively. All combinations of leptonic (τ → `νν¯ with ` = e, µ) and hadronic (τ → hadrons ν) tau decays are considered. An excess of events over the expected background from other Standard Model processes is found with an observed (expected) significance of 4.5 (3.4) standard deviations. This excess provides evidence for the direct coupling of the recently discovered Higgs boson to fermions. The measured signal strength, normalised to the Standard Model expectation, of µ = 1.43 +0.43 −0.37 is consistent with the predicted Yukawa coupling strength in the Standard Model

    Measurement of the production of a W boson in association with a charm quark in pp collisions at √s = 7 TeV with the ATLAS detector

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    The production of a W boson in association with a single charm quark is studied using 4.6 fb−1 of pp collision data at s√ = 7 TeV collected with the ATLAS detector at the Large Hadron Collider. In events in which a W boson decays to an electron or muon, the charm quark is tagged either by its semileptonic decay to a muon or by the presence of a charmed meson. The integrated and differential cross sections as a function of the pseudorapidity of the lepton from the W-boson decay are measured. Results are compared to the predictions of next-to-leading-order QCD calculations obtained from various parton distribution function parameterisations. The ratio of the strange-to-down sea-quark distributions is determined to be 0.96+0.26−0.30 at Q 2 = 1.9 GeV2, which supports the hypothesis of an SU(3)-symmetric composition of the light-quark sea. Additionally, the cross-section ratio σ(W + +c¯¯)/σ(W − + c) is compared to the predictions obtained using parton distribution function parameterisations with different assumptions about the s−s¯¯¯ quark asymmetry

    Measurement of the top pair production cross section in 8 TeV proton-proton collisions using kinematic information in the lepton plus jets final state with ATLAS

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    A measurement is presented of the ttˉt\bar{t} inclusive production cross-section in pppp collisions at a center-of-mass energy of s=8\sqrt{s}=8 TeV using data collected by the ATLAS detector at the CERN Large Hadron Collider. The measurement was performed in the lepton+jets final state using a data set corresponding to an integrated luminosity of 20.3 fb1^{-1}. The cross-section was obtained using a likelihood discriminant fit and bb-jet identification was used to improve the signal-to-background ratio. The inclusive ttˉt\bar{t} production cross-section was measured to be 260±1(stat.)23+22(syst.)±8(lumi.)±4(beam)260\pm 1{\textrm{(stat.)}} ^{+22}_{-23} {\textrm{(syst.)}}\pm 8{\textrm{(lumi.)}}\pm 4{\mathrm{(beam)}} pb assuming a top-quark mass of 172.5 GeV, in good agreement with the theoretical prediction of 25315+13253^{+13}_{-15} pb. The ttˉ(e,μ)+jetst\bar{t}\to (e,\mu)+{\mathrm{jets}} production cross-section in the fiducial region determined by the detector acceptance is also reported.Comment: Published version, 19 pages plus author list (35 pages total), 3 figures, 2 tables, all figures including auxiliary figures are available at http://atlas.web.cern.ch/Atlas/GROUPS/PHYSICS/PAPERS/TOPQ-2013-06
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