Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings
Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abunda...
Ausführliche Beschreibung
Autor*in: |
Jones, Joshua M. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2022 |
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Anmerkung: |
© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 |
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Übergeordnetes Werk: |
Enthalten in: Polar biology - Berlin : Springer, 1982, 45(2022), 3 vom: 21. Jan., Seite 449-463 |
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Übergeordnetes Werk: |
volume:45 ; year:2022 ; number:3 ; day:21 ; month:01 ; pages:449-463 |
Links: |
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DOI / URN: |
10.1007/s00300-022-03008-5 |
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Katalog-ID: |
SPR046429999 |
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520 | |a Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. | ||
650 | 4 | |a Passive acoustic monitoring |7 (dpeaa)DE-He213 | |
650 | 4 | |a Echolocation |7 (dpeaa)DE-He213 | |
650 | 4 | |a Classification |7 (dpeaa)DE-He213 | |
650 | 4 | |a Beluga |7 (dpeaa)DE-He213 | |
650 | 4 | |a Narwhal |7 (dpeaa)DE-He213 | |
700 | 1 | |a Frasier, Kaitlin E. |4 aut | |
700 | 1 | |a Westdal, Kristin H. |4 aut | |
700 | 1 | |a Ootoowak, Alex J. |4 aut | |
700 | 1 | |a Wiggins, Sean M. |4 aut | |
700 | 1 | |a Hildebrand, John A. |4 aut | |
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10.1007/s00300-022-03008-5 doi (DE-627)SPR046429999 (SPR)s00300-022-03008-5-e DE-627 ger DE-627 rakwb eng Jones, Joshua M. verfasserin (orcid)0000-0002-1033-5563 aut Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. Passive acoustic monitoring (dpeaa)DE-He213 Echolocation (dpeaa)DE-He213 Classification (dpeaa)DE-He213 Beluga (dpeaa)DE-He213 Narwhal (dpeaa)DE-He213 Frasier, Kaitlin E. aut Westdal, Kristin H. aut Ootoowak, Alex J. aut Wiggins, Sean M. aut Hildebrand, John A. aut Enthalten in Polar biology Berlin : Springer, 1982 45(2022), 3 vom: 21. Jan., Seite 449-463 (DE-627)271175427 (DE-600)1478942-5 1432-2056 nnns volume:45 year:2022 number:3 day:21 month:01 pages:449-463 https://dx.doi.org/10.1007/s00300-022-03008-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 45 2022 3 21 01 449-463 |
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10.1007/s00300-022-03008-5 doi (DE-627)SPR046429999 (SPR)s00300-022-03008-5-e DE-627 ger DE-627 rakwb eng Jones, Joshua M. verfasserin (orcid)0000-0002-1033-5563 aut Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. Passive acoustic monitoring (dpeaa)DE-He213 Echolocation (dpeaa)DE-He213 Classification (dpeaa)DE-He213 Beluga (dpeaa)DE-He213 Narwhal (dpeaa)DE-He213 Frasier, Kaitlin E. aut Westdal, Kristin H. aut Ootoowak, Alex J. aut Wiggins, Sean M. aut Hildebrand, John A. aut Enthalten in Polar biology Berlin : Springer, 1982 45(2022), 3 vom: 21. Jan., Seite 449-463 (DE-627)271175427 (DE-600)1478942-5 1432-2056 nnns volume:45 year:2022 number:3 day:21 month:01 pages:449-463 https://dx.doi.org/10.1007/s00300-022-03008-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 45 2022 3 21 01 449-463 |
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10.1007/s00300-022-03008-5 doi (DE-627)SPR046429999 (SPR)s00300-022-03008-5-e DE-627 ger DE-627 rakwb eng Jones, Joshua M. verfasserin (orcid)0000-0002-1033-5563 aut Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. Passive acoustic monitoring (dpeaa)DE-He213 Echolocation (dpeaa)DE-He213 Classification (dpeaa)DE-He213 Beluga (dpeaa)DE-He213 Narwhal (dpeaa)DE-He213 Frasier, Kaitlin E. aut Westdal, Kristin H. aut Ootoowak, Alex J. aut Wiggins, Sean M. aut Hildebrand, John A. aut Enthalten in Polar biology Berlin : Springer, 1982 45(2022), 3 vom: 21. Jan., Seite 449-463 (DE-627)271175427 (DE-600)1478942-5 1432-2056 nnns volume:45 year:2022 number:3 day:21 month:01 pages:449-463 https://dx.doi.org/10.1007/s00300-022-03008-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 45 2022 3 21 01 449-463 |
allfieldsGer |
10.1007/s00300-022-03008-5 doi (DE-627)SPR046429999 (SPR)s00300-022-03008-5-e DE-627 ger DE-627 rakwb eng Jones, Joshua M. verfasserin (orcid)0000-0002-1033-5563 aut Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. Passive acoustic monitoring (dpeaa)DE-He213 Echolocation (dpeaa)DE-He213 Classification (dpeaa)DE-He213 Beluga (dpeaa)DE-He213 Narwhal (dpeaa)DE-He213 Frasier, Kaitlin E. aut Westdal, Kristin H. aut Ootoowak, Alex J. aut Wiggins, Sean M. aut Hildebrand, John A. aut Enthalten in Polar biology Berlin : Springer, 1982 45(2022), 3 vom: 21. Jan., Seite 449-463 (DE-627)271175427 (DE-600)1478942-5 1432-2056 nnns volume:45 year:2022 number:3 day:21 month:01 pages:449-463 https://dx.doi.org/10.1007/s00300-022-03008-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 45 2022 3 21 01 449-463 |
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10.1007/s00300-022-03008-5 doi (DE-627)SPR046429999 (SPR)s00300-022-03008-5-e DE-627 ger DE-627 rakwb eng Jones, Joshua M. verfasserin (orcid)0000-0002-1033-5563 aut Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. Passive acoustic monitoring (dpeaa)DE-He213 Echolocation (dpeaa)DE-He213 Classification (dpeaa)DE-He213 Beluga (dpeaa)DE-He213 Narwhal (dpeaa)DE-He213 Frasier, Kaitlin E. aut Westdal, Kristin H. aut Ootoowak, Alex J. aut Wiggins, Sean M. aut Hildebrand, John A. aut Enthalten in Polar biology Berlin : Springer, 1982 45(2022), 3 vom: 21. Jan., Seite 449-463 (DE-627)271175427 (DE-600)1478942-5 1432-2056 nnns volume:45 year:2022 number:3 day:21 month:01 pages:449-463 https://dx.doi.org/10.1007/s00300-022-03008-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 45 2022 3 21 01 449-463 |
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Enthalten in Polar biology 45(2022), 3 vom: 21. Jan., Seite 449-463 volume:45 year:2022 number:3 day:21 month:01 pages:449-463 |
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Enthalten in Polar biology 45(2022), 3 vom: 21. Jan., Seite 449-463 volume:45 year:2022 number:3 day:21 month:01 pages:449-463 |
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Passive acoustic monitoring Echolocation Classification Beluga Narwhal |
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Jones, Joshua M. @@aut@@ Frasier, Kaitlin E. @@aut@@ Westdal, Kristin H. @@aut@@ Ootoowak, Alex J. @@aut@@ Wiggins, Sean M. @@aut@@ Hildebrand, John A. @@aut@@ |
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Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. 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author |
Jones, Joshua M. |
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Jones, Joshua M. misc Passive acoustic monitoring misc Echolocation misc Classification misc Beluga misc Narwhal Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings |
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Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings Passive acoustic monitoring (dpeaa)DE-He213 Echolocation (dpeaa)DE-He213 Classification (dpeaa)DE-He213 Beluga (dpeaa)DE-He213 Narwhal (dpeaa)DE-He213 |
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misc Passive acoustic monitoring misc Echolocation misc Classification misc Beluga misc Narwhal |
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misc Passive acoustic monitoring misc Echolocation misc Classification misc Beluga misc Narwhal |
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Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings |
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Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings |
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Jones, Joshua M. |
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Jones, Joshua M. Frasier, Kaitlin E. Westdal, Kristin H. Ootoowak, Alex J. Wiggins, Sean M. Hildebrand, John A. |
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beluga (delphinapterus leucas) and narwhal (monodon monoceros) echolocation click detection and differentiation from long-term arctic acoustic recordings |
title_auth |
Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings |
abstract |
Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 |
abstractGer |
Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 |
abstract_unstemmed |
Abstract Beluga (Delphinapterus leucas) and narwhal (Mondon monoceros) echolocation signals have been described in numerous acoustic studies but reported characteristics of their clicks vary across studies. Here, a year of acoustic recordings was collected in the Chukchi Sea where belugas are abundant, and narwhals are not present. A second year was recorded in Eclipse Sound, Nunavut, where beluga sightings are rare and narwhals abundant. The same calibrated hydrophone was used at both locations to facilitate data comparison. Click detection and signal parameter measurements were carried out using a single analysis method. Peak frequency of detected clicks decreased with peak-to-peak received sound pressure level (RL) for both species. High RL beluga clicks (n = 23,946) and narwhal clicks (n = 25,433) had a modal peak frequency of 56 kHz. Lower RL modal peak frequency of beluga clicks (n = 688,601) was 53 kHz and for narwhal clicks (n = 616,536) was 22.5 kHz. Modal inter-click interval (ICI) for beluga clicks (n = 872,336) was 49 ms. Narwhal ICI distribution (n = 791,905) was bimodal and right skewed with modal values of 4 and 144 ms. Clicks of belugas and narwhals are distinguishable by frequency spectra and ICI distribution. These parameters provide a reliable way to discriminate between the monodontid species in large acoustic datasets. Received sound levels substantially influence measured frequency spectra and must be carefully accounted for in acoustic identification of monodontid echolocation. Frequency-dependent acoustic absorption of seawater results in longer propagation and detection distance predictions for narwhal clicks that show greater energy below 30 kHz than found in beluga click spectra. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 |
collection_details |
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container_issue |
3 |
title_short |
Beluga (Delphinapterus leucas) and narwhal (Monodon monoceros) echolocation click detection and differentiation from long-term Arctic acoustic recordings |
url |
https://dx.doi.org/10.1007/s00300-022-03008-5 |
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Frasier, Kaitlin E. Westdal, Kristin H. Ootoowak, Alex J. Wiggins, Sean M. Hildebrand, John A. |
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Frasier, Kaitlin E. Westdal, Kristin H. Ootoowak, Alex J. Wiggins, Sean M. Hildebrand, John A. |
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doi_str |
10.1007/s00300-022-03008-5 |
up_date |
2024-07-03T22:28:51.127Z |
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score |
7.4016027 |