EURASIP Journal on Advances in Signal Processing
Volume 2008 (2008), Article ID 245936, 10 pages
doi:10.1155/2008/245936
Research Article

Segmentation of Killer Whale Vocalizations Using the Hilbert-Huang Transform

Laboratorie d'Images, Signaux et Systemes Intelligents (LiSSi - iSnS), Université de Paris 12, 61 avenue de Gaulle, 94010 Creteil Cedex, France

Received 1 September 2007; Revised 3 March 2008; Accepted 14 April 2008

Academic Editor: Daniel Bentil

Copyright © 2008 Olivier Adam. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

The study of cetacean vocalizations is usually based on spectrogram analysis. The feature extraction is obtained from 2D methods like the edge detection algorithm. Difficulties appear when signal-to-noise ratios are weak or when more than one vocalization is simultaneously emitted. This is the case for acoustic observations in a natural environment and especially for the killer whales which swim in groups. To resolve this problem, we propose the use of the Hilbert-Huang transform. First, we illustrate how few modes (5) are satisfactory for the analysis of these calls. Then, we detail our approach which consists of combining the modes for extracting the time-varying frequencies of the vocalizations. This combination takes advantage of one of the empirical mode decomposition properties which is that the successive IMFs represent the original data broken down into frequency components from highest to lowest frequency. To evaluate the performance, our method is first applied on the simulated chirp signals. This approach allows us to link one chirp to one mode. Then we apply it on real signals emitted by killer whales. The results confirm that this method is a favorable alternative for the automatic extraction of killer whale vocalizations.

1. Introduction

Marine mammals show a vast diversity of vocalizations from one species to another and from one individual to another within a species. This can be problematic in analyzing vocalizations. The Fourier spectrogram remains today the classical time-frequency tool used by cetologists [13]—and sometimes the only one proposed—for use with typical software dedicated to bioacoustic sound analysis, such as MobySoft Ishmael, RainbowClick, Raven, Avisoft, and XBat, respectively, developed by [48].

In general, when analyzing bioacoustic sounds, posttreatment consists of binarizing the spectrogram by comparing the frequency energy to a manually fixed threshold [4, 9]. Then, feature extraction of the detected vocalizations is carried out using 2D methods specific to image processing. These algorithms, like the edge detection algorithm, are applied on the time-frequency representations [4, 5, 10].

Though the Fourier transform provides satisfactory results as far as cetologists are concerned, all hypotheses are not consistently verified. This is particularly true for the analysis of continuous recordings when signals and noises are varying in time and frequency [11]. Moreover, these time-frequency representations have interference structures, especially for the type 1 Cohen’s class (e.g., as the Wigner-Ville distribution) [12]. In addition, the uniform time-frequency resolution of the spectrogram has drawbacks for nonstationary signal analysis [13].

To overcome these difficulties, the following approaches have been recently proposed: parametric linear models such as autoregressive filters, Schur algorithm, and wavelet transform [1417]. A comparative study of these approaches can be found in [16]. All of these methods are based on specific functions for providing the decomposition of the original signals. These functions can present a bias in the results proving a disadvantage in analyzing a large set of different signals, such as killer whale vocalizations. Also, concerning the wavelet transform, it should be noted that, in general, bioacoustic signals are never decomposed using the same wavelet family. For example, in analyzing the sperm whale regular clicks, authors have presented the Mexican hat wavelet, the wavelet package, and the Daubechies wavelet, and so forth [15, 16, 1820]. It seems that the choice to use one specific wavelet family is influenced less by the shape of the sperm whale click than by the global performance on the complete dataset used by the authors in their application.

Introduced as the generalization of the wavelet transform [21], the chirplet transform appears a possible solution in our application because of the specific shape of certain killer whale vocalizations (e.g., chirps). However, this method has some disadvantages. First, it requires the presegmentation of the signals (unnecessary in our method). Second, it is known that the computation time of the chirplet transform is lengthy and the proposed method to compensate for this drawback limits the analysis to one single chirp per presegment [21, 22]. This is not feasible for our approach because more than one vocalization is likely to be simultaneously present in the recordings.

This paper endeavors to adapt the Hilbert-Huang transform (HHT) to the killer whale vocalization detection and analysis. We introduce the HHT because it is well suited for nonlinear nonstationary signals analysis [12]. This transform is used as a reliable alternative to the wavelet transform for many applications [23, 24], including underwater acoustic sounds [25, 26]. The detailed advantages are promising for detecting underwater biological signals even if they have a wide diversity, as mentioned above. In our previous work, we have confirmed positive results for the analysis of sperm whale clicks using the HHT [27, 28].

In these articles, we demonstrated how to detect these transient signals emitted by sperm whales. The modes obtained from the HHT were used for extracting and characterizing sperm whale clicks, as detailed in [29]. We compared results from different approaches to obtain the best time resolution. First, this allowed us to characterize the shape of the emitted sounds (evaluation of the size of the sperm whale head with precision). Second, we optimized the computation of time delays for arrivals of the same sound on different hydrophones to minimize the error margin on the sperm whale localization. In conclusion, the HHT was presented as the alternative to the spectrograms.

Also, in these articles, we did not discuss the role of each mode obtained from the HHT and we did not present the method based on the combined modes as we do in this article. Considering that our current work is not only aimed at illustrating a new application of the HHT but also, through our application dedicated to killer whale vocalizations, we introduce an original method based on the combined modes detailed in the following section.

2. Method

Proposed by Huang et al. in 1998 [12], the Hilbert-Huang transform is based on the following two consecutive steps: (1) the empirical mode decomposition (EMD) extracts modes from the original signal. These modes are also referred to as intrinsic mode functions (IMFs), and (2) by applying the Hilbert transform on each mode, it is possible to provide time-frequency representation of the original signal. It is important to note that (1) the EMD is not defined by mathematical formalism; the algorithm can be found in [12], and (2) the second step is optional. Some authors limit their application solely to the use of the EMD [30, 31].

The use of these modes can be compared to a filter bank [32]. At time k, the decreasing frequencies are placed in successive modes, from first to last. Our method takes advantage of this characteristic. Our contribution is an original process for the segmentation/combination of these modes. The objective is to link a single killer whale vocalization to a single mode.

2.1. Brief Theory of the HHT

The EMD is applied on the original signal. This decomposition is one of the advantages of this method because no a priori functions are required: no function has to be chosen, and consequently, no bias results from this.

The EMD is based on the extraction of the upper and lower envelopes of the original signal (by extrema interpolation). The mode is extracted when (1) the number of the extrema and the number of zero crossings are equal to or differ at most by one, and (2) the mean of these two envelopes is equal to zero.

The original sampled signal is (1)with where is the length of the signal s. M is the number of modes extracted from the signal using EMD. is the ith IMF and the residue. and are 1-dimension signals with T samples.

We note that the EMD could be applied on any nonzero-mean signal. However, each mode is a zero-mean signal. It is important to note that all the modes are monocomponent time-variant signals. The algorithm is shown in Figure 1.

Figure 1: Algorithm for the IMF extraction from the original signal s.

The time-frequency representation is provided after computation of the Hilbert transform on each mode,(2)where is the convolution.

From the analytic mode , also written , we define the instantaneous amplitude response and the instantaneous phase. For each mode, the instantaneous frequency is obtained by(3)Lastly, the time variations of the instantaneous frequencies of each mode correspond to the time-frequency representation.

2.2. Segmentation and Combination of the Modes

For cetologists, the acoustic observations of a specific marine zone consist of detecting sounds emitted by marine mammals. Once achieved, a feature extraction is carried out to identify the species.

It is possible to use the HHT in performing the emitted sound detection. We assume that the original zero-mean real signal has not been previously segmented by means of another technique. The EMD provides a limited number of modes (IMFs) resulting from this original signal. Note that each mode is the same length as the original signal (same number of samples). In any application, the challenge in using the HHT is in interpreting the contents of each mode as all signal components are divided between all the IMFs according to their instantaneous frequency [12]. For this reason, we propose the segmentation of the modes in order to link a part of this information to one single mode. Our method allows for segmentation to be based on the strong variations of the mode frequencies: these variations can be used to distinguish the presence of different chirps (cf. the example detailed in Section 3.1) or different vocalizations (cf. Section 3.2). Our segmentation is based on the three following rules: (1) all the modes are composed by the same number of segments, (2) the jth segments of all the modes have the same length, and (3) different segments of one single mode could be different lengths. To perform this segmentation, we could have used a criterion based on the discontinuities of the instantaneous amplitude. But vocalizations show a continuous fundamental frequency (signal with a constant or time-varying frequency) in their complete duration (time between two silences like that which the human ear can hear). Also, for our purposes, we have chosen to work with variations of the frequencies because we want to track killer whale vocalizations. Moreover, tracking the frequency variations for extracting the killer whale vocalizations is possible because these frequencies are much higher in pitch than the underwater ambient noise.

The detection of the frequency variations helps us identify the exact beginning and end of each vocalization. For the detection approach, our criterion is based on the derivative of the instantaneous frequency. But it is important to keep in mind that the phase is a local parameter. To avoid fluctuations due mainly to ambient noise, Cexus et al. have recently proposed the use of the Teager-Kaiser operator [33]. But this seemingly promising operator has not been evaluated for our application. Up to now, we calculate the derivative of the mean instantaneous frequency for establishing the limits of all segments for one mode,(4)where is the mean of the successive instantaneous frequencies. This step is added for attenuating the variations of these instantaneous frequencies. is the median of :(5)The length of the time window for providing this mean depends on the application. In this paper, the value is empirically established from the study of our dataset.

The idea of our detection approach is to track the signal via analysis of the functions . These functions correspond to the frequency variations of each monocomponent IMF. Strong variations in these IMFs which indicate the presence of signal information (start or end of one vocalization) provoke notable changes in the functions , hypothesis Otherwise, these functions are nearly constant, hypothesis The functions are given by (6)where denotes the comparison threshold. For our application, this value is constant (), but it could be made adaptive.

When a new vocalization appears in the recordings, the function calculated from the first mode is suddenly varying. The value of the detection criterion is superior to the threshold .

Moreover, this function will have a positive maximum and a negative maximum, respectively, for the start and the end of one single vocalization as the vocalization frequencies are currently higher than the low ambient noise frequencies.

Moreover, because two vocalizations have two different main frequencies, will present discontinuities, which are used for the vocalization segmentation.

Our criterion is successively applied on the first mode, then the second mode, and so on. At the end of this process, we obtain all the segments and we can determine their length.

The ith IMF is (7)with being the jth segment of defined by(8)where and are the time of the last sample of segments and respectively. Note that and .

In our approach, we validate either the decreasing shift or the permutation of the jth segments between two modes and These combinations allow us to link specific information to one single IMF. Our objective is to track the fundamental frequency and the harmonics of the killer whale vocalizations (see Section 3). Each vocalization will be linked to one mode.

The new mode m is the result of the combined previous IMF,(9)The combination depends on the positive or negative maximum of when .

(i) . This means that the instantaneous frequency of the end of segment is less than the instantenous frequency of the start of the next segment . Concerning segment , the vocalization could continue on segment . So, our process consists of switching this segment to the new and putting zeros in the new ,(10)We repeat this process on the segment of each following mode: with Whereas segment is the start of a new vocalization. Our process does not modify this segment or those that follow.

(ii) . The instantaneous frequency of the end of segment is higher than the instantenous frequency of the start of the next segment . This means that segment marks the end of the vocalization. This segment is not modified. All the following segments (lj +1) of this mode are switched to the next mode (k +1): and we replace the current segments with zeros .

This process is summarized in Table 1.

Table 1: Combination of segments; case 1: ; case 2: (the dotted line is the separation of 2 successive segments).

This process of combining is done from the first to the last IMF. Because the number of modes and the number of segments are finite, the process ends on its own.

The new obtained signal is 1-dimensional with T samples and is given by(11)The following step is optional. We use a weighted factor () on each segment,(12)We diminish the role of each segment by using low values of the weighted factors; we can even delete certain segments by using . Consequently, this step allows us to am- plify or attenuate one or more segments of the combined IMF. The value of these weighted coefficients must be chosen based on the objective of the application. In many cases, it could be appropriate to fix a value dependent on the signal frequencies. In our application, we amplify the highest frequencies and attenuate the lowest frequencies in relation to the killer whale vocalizations and the ambient noise, respectively—we use our process like a filter. In other applications, the objective could be to use a criterion based on the signal energy, for example, to reduce high-energy segments and amplify low-energy segments.

Equation (12) demonstrates the possibility of using the new IMF for the selection of certain parts of the original signal.

3. Results

Our research team is involved in a scientific project based on the detection and localization of marine mammals using passive acoustics. We have already used the HHT for different kinds of bioacoustic transient signals, particularly sperm whale clicks [27]. Now, we are applying the method on harmonic signals. In this section, we show the results obtained on simulated chirps, then we illustrate its performance on killer whale vocalizations.

3.1. Analysis of the Simulated Three Chirps Signal

To present our method in detail, we have generated a simulated signal composed of the three chirps with varying frequencies (linear, convex, or concave) (Figure 2(A)).

Figure 2

The normalized frequencies of the first chirp vary from 0.062 to 0.022. is the second chirp having a concave variation of the normalized frequency from 0.016 to 0.08. is the third chirp containing the linear variation of the normalized frequency from 0.008 to 0.012.

In this example, we use normalized frequency as it is important to know the frequencies of the chirps rather than the value of the sampling frequency.

The spectrogram is provided in Figure 2(B).

The first step of our approach involves performing the EMD (Figure 2(C)). We note that the three first modes present all the frequency variations of the three chirps.

Providing the time-frequency representation of all these modes will reveal the frequencies of each chirp. With the EMD, these frequencies are hierarchically allocated to each mode, meaning that at each moment, the first mode has the highest frequency and the last mode, the lowest frequency.

Figure 2(D) shows that the IMFs have frequencies originating from all three chirps. Therefore, IMF 1 successively contains the frequencies from chirp , then from , then from , and then from again. Similarly, IMF 2 is composed of frequencies from , then , and again. Finally, IMF 3 contains only a short part of the frequency of .

Feature extraction from the time-frequency representation (Figure 2(B)) requires 2D algorithms, such as the edge detection algorithm, for example. Our goal allows us to avoid using these algorithms so common in image processing.

In our simulated signal analysis, the work results in linking one complete chirp to one single IMF. The point of using the new combined IMF is that the new IMF 1 receives its frequency solely from chirp . New IMF 2 and IMF 3 will, respectively, receive frequencies solely from and (6).

To segment these IMFs, we monitor the variations of the parameter (Figure 2(E)). In our example, the five segments are obtained from this parameter (Figure 2(F)). Note that to avoid the side effects resulting from the segmentation process, we force the segments to start and end at zero by applying the Tukey window [34].

Then, the IMFs are combined (see (6) and Figure 2(G)). We provide the time-frequency representation. The Hilbert transform is applied on these new combined IMFs. Thus, the obtained figure confirms that the new IMFs have the frequencies of the original chirps.

If one of these chirps is considered a source of noise, we could discard this chirp by using the weighted coefficients equal to zero. For example, we can delete by applying .

The advantage is that we can use a 1D algorithm to extract the frequency from each new IMF (in our case, the interpolation could be done by using a simple 1-order or 2-order polynomial regression). We do not have to employ 2D algorithms.

In conclusion, we have linked one chirp to one single new IMF. We have shown too that it is possible to filter the signal through this method.

3.2. Analysis of Killer Whale Vocalizations

Killer whales emit vocalizations with various time and frequency characteristics (short, long, with or without harmonics, etc.). Killer whales live and evolve in social groups, so it is very rare to have recordings from only one individual, unless we consider the animals in the aquarium. Therefore, in these recordings, it is current to find more than one vocalization at the same time. This complicates the detection of these vocalizations. Another challenge is to find one complete vocalization. At times, a single complete vocalization is segmented into many components. This depends on the method used to provide the time-frequency representation. When the signal-to-noise ratio is weak, it is common that the binarized spectrogram separately extracts different parts of one single vocalization. To prevent this, other methods have been proposed like the chirplet transform and the wavelet transform [16, 21, 25].

In our dataset, the vocalizations have been recorded from a group of killer whales in their natural environment. Vocalization segmentation is commonly accomplished by applying the spectrogram. The analysis of this time-frequency representation is executed with the aid of a threshold to binarize the spectrogram, or of an edge detector [4, 5]. The performance depends on (1) the signal-to-noise ratio which is varying during all the recordings, and (2) the simultaneous presence of more than one vocalization. Our method was introduced as a solution to overcome these two obstacles. First, the ambient noise has lower frequencies than the vocalizations. So it is coded by the last IMFs. Second, each vocalization is linked to a single combined IMF. This facilitates feature extraction (duration of the vocalization, start and end frequencies, and shape).

In our application, we do not take into account the last IMFs. In our previous work [27], we defined a performance/complexity criterion based on the contribution of each mode for obtaining the complete original signal. Applied on this dataset, this criterion shows that only the first five IMFs are sufficient for extracting killer whale vocalizations. This low number of IMFs is coherent with the results obtained by Wang et al. [25]. Considering only the first five IMFs contributes to minimize the execution time of this approach.

In the second step of the process, the modes are com- bined following our algorithm to link one vocalization to one mode.

We have compared the detection performance of the three methods: the spectrogram, the chirplet transform, and our approach based on the combined IMFs. Results appear in Table 2. We consider our detection to be accurate when the vocalization is determined in its full length. The segmented vocalization is considered to be falsely detected.

Table 2: Detection of vocalizations; % of detection of complete vocalizations, % of detection of simultaneous vocalizations.

When using the spectrogram, detection quality depends mainly on the threshold value. In this application, we have used a fixed threshold for the complete dataset in spite of the presence of the varying ambient noise. The consequence is that 25% of the vocalizations are segmented. Thus, the spectrogram detector extracts many successive vocalizations that are in fact all components of the same vocalization. These results could be slightly improved by using an adaptive threshold.

With the chirplet transform, the results decrease significantly in the presence of simultaneous vocalizations. In these cases, it seems that the algorithm extracts the vocalization containing the greatest energy. Our method is more robust because these different vocalizations are linked to different combined modes. The detection process is done on each mode.

Another advantage of our approach concerns vocalizations with harmonics. The presence of these harmonics helps biologists characterize and classify sounds emitted by animals. Our method equally enables linking one harmonic to a single mode (as seen in Figure 3). Unlike in the previous case, the vocalizations with harmonics are distinguishible from simultanous vocalizations because all the harmonic components have the same shape.

Figure 3: Decomposition of two harmonic killer whale vocalizations; (a) original signal, (b) EMD, (c) Hilbert transform of each new IMF.

Another advantage of our method is that it allows us to easily characterize each vocalization by applying the Hilbert transform on each combined mode (duration, start and end frequency, and shape). We employ a simple 1D function to model the vocalizations. This is illustrated on a sample of our dataset (Figure 4); we have extracted the start and the end of the vocalization and the shape by applying a 3-order polynomial regression.

Figure 4: Extraction of the vocalization features; (a) original signal, (b) Hilbert transform, (c) characterization of the vocalization.

4. Conclusion

After achieving promising results obtained on sperm whale clicks (transient signals), our objective is to evaluate the Hilbert-Huang transform on harmonic killer whale vocalizations. To this end, we propose a new method based on an original combination of the intrinsic mode functions obtained by the empirical mode decomposition. The advantages of our method are (1) we filter the signal from the new combined modes; (2) we link one vocalization (or one harmonic) to one single mode; (3) we use a 1D algorithm to characterize the vocalizations.

Acknowledgment

This work was supported by Association DIRAC (France).

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