20-Hz pulses and other vocalizations of fin whales, Balaenoptera physalus, in the Gulf of California, Mexico.

Low-frequency vocalizations were recorded from fin whales, Balaenoptera physalus, in the Gulf of California, Mexico, during three cruises. In March 1985, recorded 20-Hz pulses were in sequences of regular 9-s interpulse intervals. In August 1987, nearly all were in sequences of doublets with alternating 5- and 18-s interpulse intervals. No 20-Hz pulse sequences of any kind were detected in February 1987. The typical pulse modulated from 42 to 20 Hz and its median duration was 0.7 s (1985 data). Most other fin whale sounds were also short tonal pulses averaging 82, 56, and 68 Hz, respectively, for the three cruises; 89% were modulated in frequency, mostly downward. Compared to Atlantic and Pacific Ocean regions, Gulf of California 20-Hz pulses were unique in terms of frequency modulation, interpulse sound levels, and temporal patterns. Fin whales in the Gulf may represent a regional stock revealed by their sound characteristics, a phenomenon previously shown for humpback whales, birds, and fish. Regional differences in fin whale sounds were found in comparisons of Atlantic and Pacific locations.     

Characteristics of biosonar signals from the northern bottlenose whale, Hyperoodon ampullatus

The biosonar pulses from free-ranging northern bottlenose whales (Hyperoodon ampullatus) were recorded with a linear hydrophone array. Signals fulfilling criteria for being recorded close to the acoustic axis of the animal (a total of 10 clicks) had a frequency upsweep from 20 to 55 kHz and durations of 207 to 377 μs (measured as the time interval containing 95% of the signal energy). The source level of these signals, denoted pulses, was 175-202 dB re 1 μPa rms at 1 m. The pulses had a directionality index of at least 18 dB. Interpulse intervals ranged from 73 to 949 ms (N?=?856). Signals of higher repetition rates had interclick intervals of 5.8-13.1 ms (two sequences, made up of 59 and 410 clicks, respectively). These signals, denoted clicks, had a shorter duration (43-200 μs) and did not have the frequency upsweep characterizing the pulses of low repetition rates. The data show that the northern bottlenose whale emits signals similar to three other species of beaked whale. These signals are distinct from the three other types of biosonar signals of toothed whales. It remains unclear why the signals show this grouping, and what consequences it has on echolocation performance.     

The acoustic calls of blue whales off California with gender data

The acoustic calls of blue whales off California are described with visual observations of behavior and with acoustic tracking. Acoustic call data with corresponding position tracks are analyzed for five calling blue whales during one 100-min time period. Three of the five animals produced type A-B calls while two produced another call type which we refer to as type D. One of the animals producing the A-B call type was identified as male. Pauses in call production corresponded to visually observed breathing intervals. There was no apparent coordination between the calling whales. The average call source level was calculated to be 186 dB re: 1 muPa at 1 m over the 10-110-Hz band for the type B calls. On two separate days, female blue whales were observed to be silent during respective monitoring periods of 20 min and 1 h.     

Blue whale (Balaenoptera musculus) sounds from the North Atlantic

Sounds of blue whales were recorded from U.S. Navy hydrophone arrays in the North Atlantic. The most common signals were long, patterned sequences of very-low-frequency sounds in the 15-20 Hz band. Sounds within a sequence were hierarchically organized into phrases consisting of one or two different sound types. Sequences were typically composed of two-part phrases repeated every 73 s: a constant-frequency tonal "A" part lasting approximately 8 s, followed 5 s later by a frequency-modulated "B" part lasting approximately 11 s. A common sequence variant consisted only of repetitions of part A. Sequences were separated by silent periods averaging just over four minutes. Two other sound types are described: a 2-5 s tone at 9 Hz, and a 5-7 s inflected tone that swept up in frequency to ca. 70 Hz and then rapidly down to 25 Hz. The general characteristics of repeated sequences of simple combinations of long-duration, very-low-frequency sound units repeated every 1-2 min are typical of blue whale sounds recorded in other parts of the world. However, the specific frequency, duration, and repetition interval features of these North Atlantic sounds are different than those reported from other regions, lending further support to the notion that geographically separate blue whale populations have distinctive acoustic displays.     

Stimulus parameters governing confusion effects in forward masking

In forward masking, performance may be affected by confusion, that is, by the difficulty of discriminating a suprathreshold signal from the preceding masker. This study investigated confusion effects for forward maskers composed of repeated bursts of a 100-Hz sinusoid followed by sinusoidal signals; such "pulsing" maskers produce confusion when the properties of the signal are identical to those of an individual masker "pulse." The level, frequency, and duration of the signal relative to an individual masker pulse, as well as offset-onset delay, were varied to determine the minimum change necessary to eliminate confusion. For maskers composed of 20-ms pulses, confusion was eliminated by changes in signal level of 5 dB or changes in signal frequency of 30 to 40 Hz. For maskers composed of 10-, 20-, or 40-ms pulses, confusion was eliminated by signal delays of 8 to 16 ms or by signal durations less than half or greater than twice the masker-pulse duration. Results with adaptive procedures designed to measure confusion-free or confusion-determined thresholds suggest that confusion effects can be minimized or avoided by extensive listener training with a procedure in which the signal and masker are not presented at similar intensities.     

Sounds and source levels from bowhead whales off Pt. Barrow, Alaska

Sounds were recorded from bowhead whales migrating past Pt. Barrow, AK, to the Canadian Beaufort Sea. They mainly consisted of various low-frequency (25- to 900-Hz) moans and well-defined sound sequences organized into "song" (20-5000 Hz) recorded with our 2.46-km hydrophone array suspended from the ice. Songs were composed of up to 20 repeated phrases (mean, 10) which lasted up to 146 s (mean, 66.3). Several bowhead whales often were within acoustic range of the array at once, but usually only one sang at a time. Vocalizations exhibited diurnal peaks of occurrence (0600-0800, 1600-1800 h). Sounds which were located in the horizontal plane had peak source spectrum levels as follows--44 moans: 129-178 dB re: 1 microPa, 1 m (median, 159); 3 garglelike utterances: 152, 155, and 169 dB; 33 songs: 158-189 dB (median, 177), all presumably from different whales. Based on ambient noise levels, measured total propagation loss, and whale sound source levels, our detection of whale sounds was theoretically noise-limited beyond 2.5 km (moans) and beyond 10.7 km (songs), a model supported by actual localizations. This study showed that over much of the shallow Arctic and sub-Arctic waters, underwater communications of the bowhead whale would be limited to much shorter ranges than for other large whales in lower latitude, deep-water regions.     

Communicative pulsed signals of beluga whales in the reproductive gathering off Solovetskii Island in the White Sea

Results of the perceptive and acoustic analysis of communicative pulsed signals recorded in a reproductive gathering of beluga whales off Solovetskii Island in the white sea are presented. The mean signal duration varies from 0.04 to 1.52 s for various signal types, the pulse repetition rate on the average ranges from 13 to 1300 (possibly, 2700) impulses per second, and the mean peak frequency falls within 0.2 to 11.3 kHz. A high degree of similarity between the communicative pulsed signals produced by beluga whales from different populations is revealed.     

Off-axis effects on the multipulse structure of sperm whale usual clicks with implications for sound production

Sperm whales (Physeter macrocephalus) produce multipulsed clicks with their hypertrophied nasal complex. The currently accepted view of the sound generation process is based on the click structure measured directly in front of, or behind, the whale where regular interpulse intervals (IPIs) are found between successive pulses in the click. Most sperm whales, however, are recorded with the whale in an unknown orientation with respect to the hydrophone where the multipulse structure and the IPI do not conform to a regular pulse pattern. By combining far-field recordings of usual clicks with acoustic and orientation information measured by a tag on the clicking whale, we analyzed clicks from known aspects to the whale. We show that a geometric model based on the bent horn theory for sound production can explain the varying off-axis multipulse structure. Some of the sound energy that is reflected off the frontal sac radiates directly into the water creating an intermediate pulse p1/2 seen in off-axis recordings. The powerful p1 sonar pulse exits the front of the junk as predicted by the bent-horn model, showing that the junk of the sperm whale nasal complex is both anatomically and functionally homologous to the melon of smaller toothed whales.     

Multiple Nonlinear Stimulated Echoes

Three-pulse sequences in the presence of magnetic field gradients at high magnetic fields produce multiple nonlinear stimulated echoes (NOSE) at timesnτ₁after the third pulse, wherenis an integer and τ₁the interval between the first two pulses. These phenomena are due to the demagnetizing field produced by the spatial modulation of the nuclear magnetization arising in the sample after the first two pulses. The theory is presented and compared with experiments. The dependence of the NOSE amplitudes on the flip angles and on the pulse intervals is described. Implications for multidimensional NMR experiments based on sequences of three or more pulses in the presence of field gradients are discussed.     

Measuring the off-axis angle and the rotational movements of phonating sperm whales using a single hydrophone

The common use of the bent-horn model of the sperm whale sound generator describes sperm whale clicks as the pulse series {p0, p1, p2, p3,...}. Clicks, however, deviate from this standard when recorded using off-axis hydrophones. The existence of additional pulses within the {p0, p1, p2, p3, ...} series can be explained still using the bent-horn model. Multiple reflections on the whale's frontal and distal sacs of the p0 pulse lead to additional sets of pulses detectable using a farfield, off-axis hydrophone. The travel times of some of these additional pulses depend on the whale's orientation. The authors propose a method to estimate the off-axis angle of sperm whale clicks. They also propose a method to determine the nature of the movement (if it is pitch, yaw, or roll) of phonating sperm whales. The application of both methods requires the measurement of the travel time differences between pulses composing a sperm whale click. They lead, using a simple apparatus consisting of a single hydrophone at an unknown depth, to new measurements of the underwater movements of sperm whales. Using these methods shows that sperm whales would methodically scan seawater while searching for prey, by making periodic pitch and yaw movements in sync with their acoustic activity.     

Sounds, source levels, and associated behavior of humpback whales, southeast Alaska

Humpback whales in Southeast Alaskan waters produced five categories of sounds: moans, grunts, pulse trains, blowhole-associated sounds, and surface impacts. Frequencies (Hz) of moans and grunts were 20-1900. Major energy in low-frequency pulse trains was in a band of 25-80 Hz with pulse duration of 300-400 ms. Blowhole-associated sounds, recorded as transiting whales encountered one another, were of two types: shrieks, 555-2000 Hz, and trumpetlike horn blasts with fundamental at 414 Hz (median). Pulses and spread spectrum noise were associated with gas bubble formation and explosive bursts, respectively, in connection with spiral feeding maneuvers. Surface impacts resulted from fluke or flipper slaps in sequences of 3-21 sounds. Source levels ranged from 162 (low-frequency pulse trains) to 192 dB (surface impacts), re: 1 microPa, 1 m. Songs, commonly heard on winter breeding grounds, were absent from our recordings. Feeding and perhaps certain other whale activities can be monitored based on sound production.     

Intraband effects on ultrafast pulse propagation in semiconductor optical amplifier

High bit-rate (>10 Gb/s) signals are composed of very short pulses and propagation of such pulses through a semiconductor optical amplifier (SOA) requires consideration of intraband phenomena. Due to the intraband effects, the propagating pulse sees a fast recovering nonlinear gain which introduces less distortion in the pulse shape and spectrum of the output pulse but introduces a positive chirping at the trailing edge of the pulse.     

Low-frequency whale and seismic airgun sounds recorded in the mid-Atlantic Ocean

Beginning in February 1999, an array of six autonomous hydrophones was moored near the Mid-Atlantic Ridge (35 degrees N-15 degrees N, 50 degrees W-33 degrees W). Two years of data were reviewed for whale vocalizations by visually examining spectrograms. Four distinct sounds were detected that are believed to be of biological origin: (1) a two-part low-frequency moan at roughly 18 Hz lasting 25 s which has previously been attributed to blue whales (Balaenoptera musculus); (2) series of short pulses approximately 18 s apart centered at 22 Hz, which are likely produced by fin whales (B. physalus); (3) series of short, pulsive sounds at 30 Hz and above and approximately 1 s apart that resemble sounds attributed to minke whales (B. acutorostrata); and (4) downswept, pulsive sounds above 30 Hz that are likely from baleen whales. Vocalizations were detected most often in the winter, and blue- and fin whale sounds were detected most often on the northern hydrophones. Sounds from seismic airguns were recorded frequently, particularly during summer, from locations over 3000 km from this array. Whales were detected by these hydrophones despite its location in a very remote part of the Atlantic Ocean that has traditionally been difficult to survey.     

Efficiency of Spurious Signal Cancellation under the NQR Detection of Some Explosives by the SLIME-Type Pulse Sequences

Two versions of the spin-lock inversion mid-echo pulse sequence used for the prompt nuclear quadrupole resonance detection of explosives have been studied experimentally. These sequences are modifications of the conventional multiple pulse spin-locking sequence and differ from it by additional groups of pulses which invert echo signals. It was found that spurious signals produced by some magnetic objects are suppressed by one of these sequences much stronger than by the other. The attenuation of echo signals due to their inversion by the group of the inverting pulses is measured. The number of pulses is optimized in both the sequences to obtain maximum signal-to-noise ratio, taking into account some loss in the magnitude of inverted echoes.     

Specific features of vowel-like signals of white whales

The set of acoustic signals of White-Sea white whales comprises about 70 types of signals. Six of them occur most often and constitute 75% of the total number of signals produced by these animals. According to behavioral reactions, white whales distinguish each other by acoustic signals, which is also typical of other animal species and humans. To investigate this phenomenon, signals perceived as vowel-like sounds of speech, including sounds perceived as a “bleat,” were chosen A sample of 480 signals recorded in June and July, 2000, in the White Sea within a reproductive assemblage of white whales near the Large Solovetskii Island was studied. Signals were recorded on a digital data carrier (a SONY minidisk) in the frequency range of 0.06–20 kHz. The purpose of the study was to reveal the perceptive and acoustic features specific to individual animals. The study was carried out using the methods of structural analysis of vocal speech that are employed in lingual criminalistics to identify a speaking person. It was demonstrated that this approach allows one to group the signals by coincident perceptive and acoustic parameters with assigning individual attributes to single parameters. This provided an opportunity to separate conditionally about 40 different sources of acoustic signals according to the totality of coincidences, which corresponded to the number of white whales observed visually. Thus, the application of this method proves to be very promising for the acoustic identification of white whales and other marine mammals, this possibility being very important for biology.     

Magnetic resonance imaging of cortical bone with ultrashort TE pulse sequences

PurposeNormal adult cortical bone has a very short T₂ and characteristically produces no signal with pulse sequence echo times (TEs) routinely used in clinical practice. We wished to determine whether it was possible to use ultrashort TE (UTE) pulse sequences to detect signal from cortical bone in human subjects and use this signal to characterise this tissue.Subjects and MethodsSeven volunteers and 10 patients were examined using ultrashort TE pulse sequences (TE=0.07 or 0.08 ms). Short and long inversion as well as fat suppression pulses were used as preparation pulses. Later echo images were also obtained as well as difference images produced by subtracting a later echo image from a first echo image. Saturation pulses were used for T₁ measurement and sequences with progressively increasing TEs for T₂* measurement. Intravenous gadodiamide was administered to four subjects.ResultsSignal in cortical bone was detected with UTE sequences in children, normal adults and patients. This signal was usually made more obvious by subtracting a later echo image from the first provided that the signal-to-noise ratio was sufficiently high.Normal mean adult T₁s ranged from 140 to 260 ms, and mean T₂*s ranged from 0.42 to 0.50 ms. T₁ increased significantly with age (P<.01).Increased signal was observed after contrast enhancement in the normal volunteer and the three patients to whom it was administered.Reduction in signal from short T₂ components was seen in acute fractures, and increase in signal in these components was seen with new bone formation after fracture malunion. In a case of osteoporosis, bone cross-sectional area and signal level appeared reduced.ConclusionSignal can be detected from normal and abnormal cortical bone with UTE pulse sequences, and this can be used to measure its T₁ and T₂* as well as observe contrast enhancement. Difference images are of value in increasing the conspicuity of cortical bone and observing abnormalities in disease.     

The transient processes in multi-pulse nitrogen-14 NQR

It has been demonstrated that transient processes, observed in a single crystal of NaNO₂ acted upon by pulse sequences MW-2 and MW-4 and their modifications with 180° flip angle of the pulses (Solid State Nucl. Magn. Resonance 10 (1997) 63; Sov. Phys.—JETP 88(5) (1999) 1580), which manifest themselves in the oscillating form of the NQR signals envelope, can be explained in the frames of a two-particle model. It has been proved that the nature of echo signals in the effective field of multi-pulse sequences received by the inversion of the phase of the sequence pulses or by introducing an additional 180° pulse is connected with re-focusing of accumulated digressions of the flip angle from the ideal 180° pulse. Experimental results of observing single and multiple echoes in a number of powdered nitrogenated substances in the effective field of various sequences at room temperature have been presented.     

Modeling acoustic propagation of airgun array pulses recorded on tagged sperm whales (Physeter macrocephalus)

In 2002 and 2003, tagged sperm whales (Physeter macrocephalus) were experimentally exposed to airgun pulses in the Gulf of Mexico, with the tags providing acoustic recordings at measured ranges and depths. Ray trace and parabolic equation (PE) models provided information about sound propagation paths and accurately predicted time of arrival differences between multipath arrivals. With adequate environmental information, a broadband acoustic PE model predicted the relative levels of multipath arrivals recorded on the tagged whales. However, lack of array source signature data limited modeling of absolute received levels. Airguns produce energy primarily below 250 Hz, with spectrum levels about 20-40 dB lower at 1 kHz. Some arrivals recorded near the surface in 2002 had energy predominantly above 500 Hz; a surface duct in the 2002 sound speed profile helps explain this effect, and the beampattern of the source array also indicates an increased proportion of high-frequency sound at near-horizontal launch angles. These findings indicate that airguns sometimes expose animals to measurable sound energy above 250 Hz, and demonstrate the influences of source and environmental parameters on characteristics of received airgun pulses. The study also illustrates that on-axis source levels and simple geometric spreading inadequately describe airgun pulse propagation and the extent of exposure zones.     

Solvent Suppression in High-Resolution 1H NMR Spectroscopy Using Conventional and Phase Alternated Continuous Wave Free Precession

Solvent suppression is frequently mandatory in ¹H high-resolution nuclear magnetic resonance (NMR), especially for those experiments designed for non-deuterated solvent, normally used in protein and in vivo analysis, and also in liquid chromatography-NMR. Here, simple pulse sequences, which are based on continuous wave free precession (CWFP), consisting of a train of pulses separated by a time interval $ T_{\text{p}} \ll T_{2}^{*} $ , is applied to suppress one or more solvent signals in ¹H high-resolution NMR experiments, because of its dependency on the offset frequency. The conventional CWFP pulse sequence, that uses pulses with the same phase and duration, introduces some phase anomaly in the Fourier-transformed spectrum. This problem is minimized when the pulses are applied with phase alternation by π/2 in relation to the preceding pulse. Some problems with signal intensity can also be minimized using a shorter pulse width. Both CWFP and phase alternated CWFP can be easily used to suppress two solvent signals simultaneously, just using the correct T _p value, that must be equal to the inverse of frequency difference (?ν) between both signals to be suppressed. After modifications, we could introduce the CWFP train into 2D routine pulse sequences.