- Open Access
Automated detection of elephants in wildlife video
© Zeppelzauer; licensee Springer. 2013
Received: 30 January 2013
Accepted: 31 July 2013
Published: 12 August 2013
Biologists often have to investigate large amounts of video in behavioral studies of animals. These videos are usually not sufficiently indexed which makes the finding of objects of interest a time-consuming task. We propose a fully automated method for the detection and tracking of elephants in wildlife video which has been collected by biologists in the field. The method dynamically learns a color model of elephants from a few training images. Based on the color model, we localize elephants in video sequences with different backgrounds and lighting conditions. We exploit temporal clues from the video to improve the robustness of the approach and to obtain spatial and temporal consistent detections. The proposed method detects elephants (and groups of elephants) of different sizes and poses performing different activities. The method is robust to occlusions (e.g., by vegetation) and correctly handles camera motion and different lighting conditions. Experiments show that both near- and far-distant elephants can be detected and tracked reliably. The proposed method enables biologists efficient and direct access to their video collections which facilitates further behavioral and ecological studies. The method does not make hard constraints on the species of elephants themselves and is thus easily adaptable to other animal species.
Many biologists study the behavior of free-ranging animals in the field. For this purpose they collect large video corpora which include monitoring video, videos from field trips, and personally recorded wildlife video footage . The result of this data collection is the large amounts of video which sometimes span several hundreds of hours. Unfortunately, the access to the videos is limited because objects (e.g., the presence of a particular animal) and events of interest (e.g., particular animal behaviors) are not indexed. In many cases only (handwritten) field notes exist from the recording sessions. For manual indexing biologists have to browse linearly through the videos to find and describe objects and events of interest. This is a time-consuming and tedious task for large amounts of videos . Since indexing should preferably be performed by domain experts, it quickly becomes an expensive task. Visual analysis methods have the ability to significantly accelerate the process of video indexing and enable novel ways to efficiently access and search large video collections.
Wildlife recordings captured in the field represent a challenging real-life scenario for automated visual analysis. While a lot of research has been performed on the visual analysis of human beings and human-related events, the automated analysis of animals has been widely neglected in the past. Existing approaches on animal analysis frequently operate in highly controlled environments, for example, with a fixed camera, in a well-defined location, with static background, and without interfering environmental factors, such as occlusions, different lighting conditions, and interfering objects [3, 4]. A typical example for a controlled setting is the monitoring applications where the camera is usually fixed and the background is mostly static . In such a scenario we can easily learn a background model and identify objects of interest by detecting changes to the background. The video material we investigate in this work does not provide such a well-defined setting.
We are provided with a large collection of wildlife videos captured by biologists in the field. The videos have been captured during different field trips and serve as a basis for the investigation of the behavior and communication of African elephants. The videos show a large number of different locations, elephants and elephant groups of different sizes, poses, and distances to the camera. In many sequences elephants are partly or completely absent. Assumptions and constraints of specialized approaches (derived from controlled environments) do not hold for such unconstrained video footage. The question arises as to which degree visual analysis methods can facilitate the access to such video collections.
We develop a method for the automated detection and tracking of elephants in wildlife video. The method does not make any assumptions about the environment and the recording setting. In a first step we learn a color model of the elephants from a small set of annotated training images. Learning the model does not include domain knowledge and explicitly specified constraints about elephants and their environment. The trained model is applied to individual frames of wildlife video sequences to identify candidate detections. Next, we track the candidate detections over time and join temporally coherent detections in consecutive frames. As a result we obtain spatiotemporally consistent detections which provide additional (stronger) clues for the detection of elephants. At the same time we obtain all information necessary to track the elephants in space and time.
Experiments show that the proposed method yields high performance on wildlife video. We are able to detect and track elephants of different sizes, poses, and distances to the camera. The method is robust to occlusions, camera motion, different backgrounds, and lighting conditions. Most elephants can be detected and tracked successfully (above 90%), while the number of false detections is small (below 5%).
The paper is organized as follows. In Section 2 we survey the related work on the automated visual analysis of animals. Section 3 describes the proposed method for elephant detection, and Section 4 presents the employed wildlife video collection and the experimental setup for our evaluation. We show qualitative and quantitative results of elephant detection in Section 5. Finally, we draw conclusions and summarize our main findings in Section 6.
2 Related work
The analysis of animals and animal behavior that is a complex task for computer vision has been rarely addressed so far . Recently, methods related to the analysis of animals have been introduced for different tasks such as species classification , gait recognition , individual animal recognition , and the detection of animal-related events . The basis for most tasks is the detection of animals in an image or video stream. In the following discussion, we provide an overview of the different approaches for the detection of animals whereby we follow a path from highly restricted approaches (e.g., semiautomatic approaches) to less-constrained methods (e.g., methods building upon unsupervised learning).
Many approaches on automated animal analysis require human interaction for the detection of animals. For example in  the authors present a method for the identification of salamanders by dorsal skin patterns. The method requires that key points along the skeleton of the animal are labeled manually by the user. Similar user input is required in  for the identification of elephants from their ear profile. Authors in [13, 14] rely on user-defined regions of interest as a basis for the identification of animals.
Other approaches restrict the recording setting or the video material to reduce the complexity of animal detection. Authors in  classifies animals using a highly constrained setup with a static camera mounted at one side of a corridor. This setup makes the detection of animals passing the corridor trivial. Alternatively, some methods require that animals take a specific pose towards the camera and then apply, for example, face detection  or the detection of other characteristic body parts .
A popular clue for the detection of animals is motion. Methods that exploit motion often set hard constraints on the recording setting and the environment. In  the underlying assumption is that the background is static and can easily be subtracted. All blobs that remain after background subtraction are treated as candidate detections. While this works well in restricted domains, e.g., for underwater video , such assumptions do not hold in more general settings. A method applicable to moving backgrounds (e.g., due to camera motion) is presented in  and . The authors track sparse feature points over time and apply RANSAC to separate foreground and background motion. Thereby, the background motion is assumed to be the dominant motion in the scene. The remaining motion is assumed to belong to a single object which is the animal of interest. Other moving objects would disturb the approach and may be falsely detected as animals. Authors in  propose a method for animal species detection and make similar constraints concerning the foreground objects in the video: While the camera is static in the investigated setting, the detector requires that the foreground objects are in motion. If several moving foreground objects are detected, the one with the largest motion component is considered to be the animal of interest and all other objects are rejected. This assumption is highly specific to the particular setting and not valid in the context of wildlife video where several animals may be present at the same time.
In real-life settings with unconstrained video material, the detection of animals by specialized detectors becomes unsuitable and does not work reliably due to the large number of unpredictable environmental influences, like occlusions, lighting variations, and background motion. Only a limited number of approaches has been introduced that faces the challenges of unconstrained wildlife video. A method for the detection and tracking of animals in wildlife video is proposed by Burghardt and Ćalić . The authors apply the face detector by Viola and Jones  trained for a particular animal species. Once an animal face is detected, the authors try to track it over time. Similar to our work, a tracking scheme is proposed that allows gaps in tracking. Gaps in the context of  occur, for example, when an animal turns its head away from the camera. The approach can be applied to different animal species by using adequately trained detectors. However, the face detector of Viola and Jones requires a large training set to learn the dominant face characteristics of a given species. For the detection of lion faces in , a training set of 680 positive and 1,000 negative images is employed. Our approach requires only a minimal training set of 10 to 20 images. This significantly reduces the efforts of building a training set, makes the approach more convenient for the actual users (e.g., biologists), and increases the applicability of our approach to new video footage. An advantage of using a well-trained face detector is that the confidence of the resulting detections is relatively high since faces represent particularly distinctive patterns. However, face detection requires the animals to look into the direction of the camera which is, in general, not given in wildlife video.
The authors of  present a method for the detection of hunt scenes in wildlife footage. Since hunt scenes are characterized by a significant amount of motion, detection relies on the classification of moving regions. First, color and texture features are extracted for each pixel. Next, each pixel is classified by an artificial neural network to either belong to the animal class or not. A moving region is classified as an animal if the majority of pixels in the region are assigned to the animal class. Operating on individual pixels is computationally expensive and introduces noise. We apply image segmentation as a preprocessing step and perform detection at the segment level. The segmentation improves the robustness of detection and obviates the need for a postprocessing of noisy pixel-based detections. Furthermore, our approach does not rely on motion clues, which additionally enables the detection of animals which are resting or moving slowly.
An interesting approach for the detection and tracking of animals is proposed in . The authors build models of animals in an unsupervised manner from candidate segments detected consistently over successive frames. The candidate segments are obtained from a rectangle detector which uses Haar-like templates at different scales and orientations. For each segment a feature vector is constructed which consists of a color histogram and the rectangle’s width and height. The authors cluster the segments and identify temporally consistent and visually similar rectangles within each cluster. For the detection of animals, the authors extract a texture descriptor from the temporally consistent segments based on SIFT and match it against a precomputed library of animal textures. The authors of  report satisfactory results for animals with textured skin, such as zebras, tigers, and giraffes. The authors state that the detection of animals such as elephants and rhinoceroses is hard because their hides are homogeneous and they do not exhibit a distinct texture. The authors further state that their approach is only applicable to videos with single animals and with little background clutter. Both conditions are not met in wildlife video.
We observe an explicit trend towards highly textured animals from computer vision literature which focuses on animals. The ‘favorite’ species are apparently zebras, giraffes, and tigers; see for example [7, 9, 13, 14]. One reason for this bias is that animals with a distinct texture are easier to discriminate from the background. The visual detection of animals without a distinctive texture is hard because only weak visual clues, such as color, exist that can be exploited for detection (a more detailed discussion of visual clues is provided in the following section).
There is rarely work on the visual analysis of species with poorly textured skin such as elephants. The species of elephants is addressed only marginally, e.g., for image classification in . To our knowledge no work on the automated visual detection of elephants in wildlife video has been performed so far. In this article we present a novel approach for the detection of elephants in their natural habitat. The approach enables a more efficient access to wildlife video collections and thus bears the potential to support biologists in behavioral studies.
Knowledge about the environment and the recording setup is an important factor for designing automated visual detectors because it enables the derivation of constraints and visual clues that facilitate detection. In an uncontrolled environment like wildlife video, as investigated in this work, the identification of robust constraints and clues is difficult. The video material we investigate has been captured by different people with a hand camera. Recordings were partly made in an ad hoc fashion. This means that we cannot make assumptions about the environment and the camera operation. As a consequence, we have to rely on the very basic visual cues such as shape, texture, motion, and color for the detection of elephants. Prior to the design of our method, we have investigated the suitability of the different visual cues.
A straightforward clue for the detection of elephants is their shape. Elephants have a characteristic shape, especially due to their trunk. In practice however shape is not applicable for the detection of elephants in the field because elephants in different poses and viewed from different directions may have diverse shapes. Additionally in most cases, parts of the animals are occluded and only certain body parts are visible which results in arbitrary shapes, as shown in the introductory examples in Figure 1. Similar conclusions are also drawn in  for animal detection.
Texture may be another useful clue, since elephant skin has numerous fine wrinkles. However, the resulting texture has such a fine granularity that it is not detectable in practice from a reasonable distance to the camera. While texture is not directly applicable to the detection of elephants, we show in Section 3.5 how texture information can be exploited to make the detection of elephants more robust.
Motion is another important visual clue for automated detectors . Even if we compensate for camera motion, the remaining object motion of elephants provides only weak clues since elephants move slowly and often remain stationary for a long time. This is especially a problem when the animals are far away from the camera. In such cases motion can hardly be exploited.
A more promising visual clue is color. The skin color of elephants covers different shades of brown and gray. Additionally, the skin color is highly influenced by lighting (highlights and backlight) resulting in shades of very light and dark gray, respectively. However, color represents only a weak and ambiguous clue since many objects in the environment (e.g., different grounds and rocks) have similar colors to elephants and easily provoke false-positive detections. In our investigations we observe that color is well-suited as an initial visual clue for the detection of elephants. However, additional clues are necessary to make the detection more robust.
Since we work with video, temporal clues are another important source of information. Elephants do not appear and vanish abruptly in the course of time. We exploit temporal relationships between detections in subsequent frames to improve the robustness of detection.
The goal of preprocessing is to reduce the amount of data for processing and to obtain a more abstract representation of the input image sequence. We first downscale the input images (full HD resolution) by a factor of 0.25 to speed up subsequent operations. Next, we perform color segmentation of the images by mean-shift clustering . Prior to segmentation we transform the images to the LUV color space. The LUV color space is a perceptually uniform space. It better approximates color similarity perception than the RGB space and allows similarity judgments using Euclidean distance . After segmentation for each segment, the mean color of all covered pixels is computed and stored as a representative color for each segment.
3.2 Model generation
We learn a discriminative color model of elephant skin from a small set of labeled training images. The model represents foreground colors representing elephants as well as background colors from the surrounding environment. The training images represent different environments and differently shaded elephants in varying lighting situations.
We generate a discriminative color model by training a support vector machine (SVM) with a radial basis function (RBF) kernel from the foreground and background colors. Due to the asymmetry between the two sets of color, we assign the foreground class higher misclassification costs than the background class. This reduces the risk that the SVM misses a true elephant detection and at the same time, it increases the chance of false detections. The preferential treatment of the foreground class is intended at this stage of processing to keep the detection rate high. We handle false detections at a later stage of processing (see Section 3.6).
We observe that the RBF kernel separates both classes well. We set parameter gamma of the RBF kernel in a way that the number of support vectors is minimized. This assures a low complex decision boundary which increases the generalization ability of the classifier. The training error (estimated by fivefold cross-validation) is 92.83%. Experiments on test images show that the classifier detects segments that correspond to elephants with high accuracy. At the same time the number of false-positive detections is moderate. More results on the test data are presented in Section 5.1.
From the two sets of colors (see Figure 5), we observe that both sets occasionally contain very dark (near-black) and very bright (near-white) colors. For such colors a reasonable decision cannot be made by the classifier resulting in unreliable predictions. We apply a luminance filter to avoid these cases. Colors with near-black and near-white luminance are removed from the list of foreground colors. This assures that segments with colors near white or near black are rejected in elephant detection. We investigate the effect of luminance filtering in Section 5.4.
The color model presented in this section is completely adaptive to the provided training images. It does not make any assumptions about the underlying video material and is generally applicable to different objects of interest.
3.3 Color classification
The goal of color classification is to detect segments in the images of a sequence that are likely to belong to an elephant according to the trained color model. The emphasis of the color detector (as mentioned in Section 3.2) is primarily to maintain a high detection rate (no elephants should be missed), while a few false-positive detections are tolerated.
Each input image sequence is first preprocessed (resized and segmented) as described in Section 3.1. Next, we take the color (in LUV space) of each segment and classify the segments with the color model (without luminance filtering). We reject all segments that are predicted to belong to the background class and keep only segments predicted to be members of the foreground class. We refer to this approach as one-stage classification since classification is performed in one step.
To compensate for this limitation, we propose a more fine-grained two-stage classification that operates on the individual pixels of a segment. First, we classify each pixel by the classifier used in one-stage classification. In a second step we apply a voting to the individual predictions. If the percentage of positively classified pixels is above two thirds, we classify the segment as positively detected; otherwise, we reject the entire segment. Results show that the two-stage classification is more robust in false detections while it detects elephants equally well. See Figures 6d,e and 7d,e for an illustration.
The result of color classification is a set of segments (candidate detections) that are likely to represent elephants in the scene. At this processing stage temporal relationships between the individual detections are not available. Another important clue for detection is temporal continuity. In the next step, we track the detected segments over time in order to temporally connect corresponding detections in different frames.
3.4.1 Segment tracing
3.4.2 Trace intersection
The traces are the basis for the establishment of temporal relationships between segments. For each frame in the temporal window of size w, we intersect the corresponding traced segment with the positively detected segments in the frame. For each segment we compute the area of intersection with the traced segment. The amount of intersection serves as a confidence measure for the establishment of temporal relationships. The confidence is computed as c = |T ∩ S | / |T ∪ S|, where T is the set containing all pixels covered by the traced segment and S is the set containing all pixels covered by the segment. The confidence corresponds to the portion of overlap between the trace and the segment. If the confidence between a segment and the trace is above a threshold C, we establish a temporal relationship (a link) between the intersecting segment and the source segment of the trace.
Tracking segments by the intersections of their traces has several advantages: (a) it implicitly handles cases where segments split and merge; (b) when temporal window sizes of w > 1 are used, temporal relationships over several frames (maximum w) can be established (in each direction). This enables the tracking of a segment even when it is missed for a few frames and then reappears; (c) from the temporal relationships established by trace intersection, we can derive spatial relationships between segments in the same frame (see Section 3.4.4).
3.4.3 Connectivity graph construction
Trace intersection is performed for all segments detected by color classification. The temporal relationships generated by trace intersection can be considered as a graph. Nodes in the graph are segments which are associated with a particular frame, and the edges in the graph are temporal relationships (links) between segments. The graph is directed since tracing generates forward- and backward-directed links. However, for the subsequent processing the direction of the edges is not important and thus we neglect their orientation. Due to splitting and merging of segments the graph may contain cycles. The density of the graph is dependent on the threshold C used in trace intersection (see Section 3.4.2). A higher (more stricter) threshold C impedes the creation of links and increases the sparsity of the graph, while a lower value of C facilitates the establishment of temporal relationships and increases the density of the graph.
3.4.4 Subgraph extraction
The graph constructed in the previous section is sparse and consists of a number of disjoint subgraphs. The graph shown, for example, in Figure 11 consists of four disjoint subgraphs. Each subgraph represents the spatiotemporal track of a group of segments which are assumed to represent the same object.
We extract all subgraphs from the graph by a recursive procedure. For a given starting node (this can be an arbitrary node of the graph), we recursively traverse the entire graph and search for all nodes which are connected to this node. The resulting subgraph is removed from the original graph and the recursive search for the next subgraph in the remaining graph is performed. The procedure terminates when the remaining graph becomes empty.
The subgraph provides useful information for detection and tracking. From the temporal relationships provided by the subgraph, we can infer spatial coherences between segments in the same frame. If for two segments from the same frame a connection exists somewhere in the subgraph (e.g., because the two segments are merged in a neighboring frame), this is a strong indicator that these two segments belong together and describe the same object.
3.5 Spatiotemporal feature extraction
In Section 3.3 we point out that color is only a weak clue for the detection of elephants and that many false-positive detections are generated during color classification. The spatiotemporal segments obtained from tracking are spatially more meaningful than the original segments and additionally contain temporal information. They provide spatiotemporal clues which were not available during color classification and thus bear the potential to improve the quality of detection.
Each spatiotemporal segment represents a separate detection in the video sequence. The task is to decide whether a spatiotemporal segment is a false-positive detection or a true-positive detection. We extract spatiotemporal features from the segments to support this decision. We extract three different types of features: consistency, shape, and texture.
3.5.1 Consistency features
Consistency features measure how long and how reliable a detection can be tracked. We extract two features: (a) the temporal duration (lifetime) of a spatiotemporal segment (the number of frames the segment can be tracked) and (b) the instability which is the portion of frames where a detection cannot be tracked during its lifetime (the portion of gaps that occur during tracking). The consistency features help to remove unreliable detections (with numerous gaps and short lifetimes) which often represent false positives.
3.5.2 Shape features
The shape of elephants does usually not change abruptly. Slow changes in shape indicate correctly detected elephants while abrupt and fast changes rather suggest a false-positive detection. We design a feature that represents the variation of shape over time (shape change). First, we compute the area of a spatiotemporal segment at each frame which results in a series of areas a=a 1,a 2,a 3,...,a n , where n is the number of frames spanned by a spatiotemporal segment. Next, we compute the difference between the maximum and the minimum of the areas and normalize this value by the maximum area: f sc = (max(a)− min(a))/ max(a). The result is a value between 0 and 1, where 0 means that the area remains constant over time and higher values indicate strong temporal variations of the area.
3.5.3 Texture features
The sum over an individual edge histogram corresponds to the portion of pixels in a segment that represent edges. Edge density represents the mean portion of pixels that represent edges over the entire spatiotemporal segment. The higher the edge density, the more textured is the corresponding spatiotemporal segment.
First, the value range for each single bin of the histograms is computed. The mean over all bins provides an aggregated estimate of the temporal variation which is representative for the entire spatiotemporal segment.
3.6 Candidate validation
The goal of candidate validation is the improvement of detector robustness by the confirmation of correct detections and the rejection of false detections. This decision is based on the spatiotemporal features which allow for a temporal consistency analysis of the candidate detections. Note, that this consistency analysis does not require that the elephants actually move. The consistency analysis is applied to both, moving and static objects.
Each spatiotemporal segment represents one candidate detection. A spatiotemporal segment is either confirmed in its entirety or rejected in its entirety. Deciding over entire spatiotemporal segments exploits temporal information and thus is more robust than validating single (temporally disconnected) detections in a frame-wise manner. Candidate validation is based on the spatiotemporal features introduced in the previous section. First, individual decisions are made by thresholding each feature. Next, the individual decisions are combined into an overall decision for a candidate detection.
The determination of thresholds for automated analysis methods is a problematic issue for two reasons: First, thresholds increase the dependency on the input data and thus increase the risk of overfitting. Second, thresholds often depend on each other, e.g., when the decision by one threshold is the basis for a decision by a second threshold. Robust values for dependent thresholds cannot be determined separately from each other which in turn impedes model fitting and the evaluation of the method.
For a given candidate detection, each feature is compared to its threshold. The resulting decisions are then combined using logical AND. This means that a spatiotemporal segment is confirmed as a positive detection if it passes all validations; otherwise, it is rejected. The logical AND combination assures that thresholds remain independent from each other and we do not have to investigate any interdependencies. The features capture different visual aspects (e.g., texture and shape) and thus complement each other for the rejection of false positives. The principle is illustrated in Figure 14. In Figure 14a three false detections (circles) pass the validation using f 1 and threshold t 1. Adding a second feature f 2, as shown in Figure 14b, enables the correct rejection of an additional false detection due to the synergy of the two features.
The proposed validation scheme has several advantages: (a) each threshold value can be estimated separately, (b) the estimation of the thresholds using safe values is straightforward and reduces the dependency from the data, and (c) the logical AND combination of the single decisions exploits the complementary nature of the features.
In addition to the proposed validation scheme, we apply an SVM to the spatiotemporal features to reject false detections. The SVM is trained on a subset of video sequences using a cross-validation protocol. The trained classifier is then applied in the validation step instead of the proposed scheme. Since the required complexity of the decision boundary is not known during the design phase, we evaluate different kernels.
4 Experimental setup
In this section we introduce the video collection for the evaluation, the employed performance measures for quantitative evaluation, and the setup of the experiments.
The analyzed data set is a corpus of videos captured by biologists during different field trips. The videos have been recorded during numerous field sessions in the Addo Elephant National Park (South Africa) in 2011 and 2012. During the recording sessions only handwritten field notes have been made which provide notes on selected events of interest and important observations. The generation of additional (more complete and systematic) descriptions during field sessions is out of scope due to temporal constraints. Consequently, the video data which are inputs to our method is temporally and spatially not indexed. It is unknown if and where elephants can be observed.
The videos are captured in high-definition format (1,920 × 1,080 pixels) at a rate of 25 frames per second. The entire data set contains about 150 GB of video files which corresponds to approximately 22 h of video and 2 million frames. For the evaluation of the approach we select a subset of the video collection. The main reason not to evaluate on the entire data set is that no ground truth is available for the data and the manual ground truth generation is extremely time-consuming.
We manually select a heterogeneous data set for evaluation that consists of 26 video sequences. The selected subset is representative for the data collection which in turn enables an objective evaluation of the approach. During selection we reject sequences which are too similar to the already selected ones to increase the heterogeneity in the data set. Figure 1 in Section 1 shows frames from selected sequences in the data set. The sequences contain elephants (groups and individual elephants) of different sizes (from far distance and intermediate distance to near distance). Elephants are visible in arbitrary poses and ages performing different activities, such as eating, drinking, running, and different bonding behaviors. The sequences show different locations, such as elephants at a water hole, elephants passing a trail, and highly occluded elephants in bushes. Sequences have been captured at different times of the day, in different lighting and weather conditions. Recording settings vary across the sequences from almost static camera (mounted on a tripod) to shaking handheld camera with pans and zooms. Additionally, there are sequences which contain no elephants at all and sequences where elephants enter and leave the scene.
The ground truth data are not only used for evaluation but also for training the color model introduced in Section 3.2. We exclude 16 randomly chosen images from the data set (this corresponds to 2% of the entire data set) and use them to train the color model. From the training images only individual pixel colors are used for training. Higher-level information such as spatial information is not used. This minimizes the dependency of the evaluation from the training data. Naturally, the training images for the color model are not used in the evaluation of the proposed method.
4.2 Evaluation measures
We evaluate the performance of the proposed approach for the detection of elephants. Note that this is different from evaluating the performance for the segmentation of elephants which is not the focus of our investigation. For elephant detection an elephant does not necessarily have to be segmented correctly to be successfully detected. We evaluate the detection performance spatially and temporally using the ground truth labels. We declare a detection to be successful if it coincides with a labeled ground truth region and thus with an image region covered by one or several (spatially overlapping) elephants. For performance estimation we compute the detection rate and the false-positive rate over the entire data set.
We systematically investigate the different components of the proposed approach. While we have presented intermediate qualitative results already in Section 3, a quantitative investigation of the components’ performance is necessary for an objective and comprehensive evaluation.
First, we investigate the performance of the approach using color classification only in Section 5.1. For this purpose we neglect temporal analysis and detect elephants using the color model introduced in Section 3.2. We investigate the discriminatory capabilities of the color model and compare the robustness of one-stage and two-stage classifications (see Section 3.3). For two-stage classification we further investigate the influence of different decision thresholds. The comparison of both classification schemes allows us to evaluate whether or not the additional processing costs of the two-stage classification are justified.
Second, we investigate how the robustness of the detector can be improved by temporal analysis in Section 5.2. We apply motion tracking and candidate validation by spatiotemporal features. We evaluate different combinations of spatiotemporal features to demonstrate the beneficial effect of their complementary nature. Additionally, we apply an SVM for candidate validation. The SVM is trained on the spatiotemporal features by using different kernels to discriminate positive and false-positive candidate detections. We perform cross-validation to evaluate the performance independently from the selection of the training data. Finally, we report the mean detection rate and mean false-positive rate over all cross-validation sets.
Third, we investigate the overall performance of the approach using different classifiers in Section 5.3. For this purpose, we apply SVMs with different kernels and compare the SVMs with nearest neighbor (NN), k-nearest neighbor (KNN), and linear discriminant analysis (LDA). We show that the ability of the classifiers to build robust color models varies significantly.
Fourth, the influence of different luminance filters (see Section 3.2) on the overall performance is evaluated in Section 5.4. We expect that luminance filtering improves the robustness of the approach, since it removes colors with particularly low and high luminance components which are often unreliably classified.
After systematic evaluation we present results for two different use cases which are provided by biologists. In both use cases automated elephant detection forms the basis for further investigations by the biologists. The first use case addresses the detection of elephants to assist biologists in detailed behavioral studies. Objects of interest in this use case are elephants at intermediate and near distance to the camera. Elephants far apart from the camera are not of interest since the individuals are too small for a detailed investigation of their behavior.
The second use case focuses on the detection of distant elephants in wide open areas. Biologists are interested in the presence of (groups of) elephants over wide surveyed areas. The detection of far-distant elephants should support biologists in the investigation of elephant groups, their sizes, and their migration routes. The objects of interest in this use case are significantly smaller than in the first use case which makes this task especially hard.
We present evaluation results for different components of the proposed approach. Performance is measured in terms of detection rate (D) and false-positive rate (FP). We first present results for pure color classification. Next, we add temporal information and demonstrate the influence on performance. Additionally, we provide the overall performance using different classifiers and luminance filters. Finally, we present results for the investigated use cases (case 1 and case 2) presented in Section 4.3.
5.1 Pure color classification
Performance of different color classification schemes (one-stage classification vs. two-stage classification with different decision rules)
From the results in Table 1, we observe that the false-positive rate is generally high. For the proposed two-stage classification, approximately each third detection is a false detection. This shows that color alone is a weak clue for elephant detection. Similar to  we observe that it is hard to build robust detectors from low-level information. An additional clue for detection is temporal continuity. In the following discussion, we investigate the potential of temporal analysis for automated detection.
5.2 Incorporation of temporal information
The effect of temporal information on the overall performance
Consistency + shape
Consistency + shape + texture
The results in Table 2 show that the spatiotemporal features significantly increase the robustness of the detector. The false-positive rate is reduced in total by 25.4% to only 6.6%, while the detection rate remains relatively stable (96.4% versus 93.0%). Especially, the texture features are remarkable since they keep the detection rate constant and at the same time significantly reduce the false-positive rate. From Table 2 we further observe that the combination of different spatiotemporal features is highly beneficial for detector performance. The features are sensitive to different types of false detections since they represent complementary information.
We compare the proposed validation scheme with an alternative method based on an SVM as described in Section 4.3. We evaluate different kernels (linear, RBF, and polynomial) and optimize the respective hyperparameters using model selection. Additionally, we evaluate different subsets of the spatiotemporal features.
Results show that a linear SVM clearly outperforms the other kernels. The linear SVM yields a detection rate of 93% at a false-positive rate of 23%. The best result for the RBF kernel is obtained with a gamma of 1. The detection rate is 58% and the false-positive rate is 22%. The SVM with polynomial kernel performs suboptimal as well and yields a detection rate of 85% at a false-positive rate of 36%. In sum, the SVM-based method produces similar detection rates as the proposed validation scheme, however, the false-positive rate is significantly higher (22% versus 6.6%). Additionally, we evaluate different selections of spatiotemporal features. We observe that removing one or more features from the selection leads to a decreased performance. Optimal results are only obtained when all features are employed.
5.3 Robustness of classifiers
The effect of different classifiers on detection performance
The nearest neighbor classifier obtains a comparable detection rate as the SVM with RBF kernel. Unfortunately, the false-positive rate is higher (by 3.8%). Nevertheless, the result is impressive regarding the fact that the nearest neighbor classifier (in contrast to SVM) actually does not abstract from the training data. The KNN (with K=5) performs similar to the linear SVM. The two versions of LDA perform suboptimally compared to SVM with RBF kernel. Similar to the linear SVM, the linear and quadratic boundaries of LDA are not able to model the complex boundary between the classes.
5.4 Filtering luminance
The potential of luminance filtering
5.5 Case 1: detection of elephants at intermediate and near distances
Figure 18b shows two elephants walking on a sandy trail. The elephants do not set themselves apart from the background well (especially from the trail). While the color model produces false-positive detections on the trail, we are able to reject the entire trail during the candidate validation. The two elephants can be tracked reliably through the sequence. Note that we consider both elephants as one object to detect since they cover overlapping image regions.
Figure 18c,d shows frames from sequences where the elephants are relatively near to the camera. The proposed method robustly detects and tracks the animals over time. Figure 18c shows that the approach is able to detect elephants even if they are partly occluded: The calf in the lower left quarter of the image is widely occluded by grass and vegetation but can be detected and tracked successfully. Figure 18d shows a backlight scene where the elephant skin exhibits particularly low contrast. While the elephants are detected remarkably well, no false detections are made in similar dark background regions (labeled by arrows). The grass in the foreground of Figure 18d is likely to produce false detections because the color resembles that of sunlit elephant skin. This becomes evident when we compare the colors surrounding label ‘A’ in Figure 18c,d. False detections in such areas cannot be distinguished by color. However, additional texture and shape clues enable the rejection of false positives in this area.
Figure 18e shows a group of elephants which has previously been shown in Figure 7 in Section 3.3. From Figure 7d,e we observe numerous false detections of color classification in the background. Figure 18e shows the result after temporal analysis. The false detections in the background are temporally not stable and are removed by consistency constraints, while the detection of the elephant group remains stable.
Figure 18f shows an image with a false detection in the background (yellow). The false detection originates from the earthy area around the detection (labeled with arrows) and cannot be removed during candidate validation. The three elephants in the sequence are tracked consistently through the sequence.
5.6 Case 2: detection of elephants at far distances
The detection of far-distant elephants is challenging for two reasons. First, due to the small size of the elephants, the image must be segmented at a finer scale during preprocessing to assure that each elephant is represented by at least one segment. However, due to this fine-grained segmentation, the number of segments grows significantly. At the same time the portion of segments related to elephants decreases drastically due to the small size of the elephants. Thus, detecting elephants becomes significantly harder and the probability of false detections increases. Second, small image segments are less expressive and exhibit less distinctive features then larger segments which impedes the automated detection.
For the detection of distant elephants, we decrease the minimum size of an image segment to 20 pixels during segmentation. Note that for experiments on intermediate and near-distant elephants, a minimum size of 150 pixels is adequate (at the employed video resolution). In quantitative experiments we obtain a detection rate of 88% at a false-positive rate of 39%. While the detection rate is satisfactory, the false-positive rate is high compared to previous experiments. This is a result of the finer segmentation which significantly increases the complexity of the task.
Figure 20b shows a small group of elephants in the field. All regions covered by elephants are detected correctly. Note that no false positives are generated in regions (labeled with arrows) which have nearly the same color as the elephants.
In Figure 20c, a scene with large occlusions is shown. The depicted scene demonstrates well that shape is not a valid cue for the detection of elephants. Although the elephants are mostly occluded (especially the right one, labeled with an arrow), we are able to robustly detect and track them through the sequence.
An example where the detector generates inaccurate results is provided in Figure 20d. Additionally, to correct elephant detections, a number of false-positive detections are returned. One false-positive detection is located in a darker area in the grassland. The other false positives are located in the upper right corner which is covered by the windshield of a microphone that extends into the view of the camera. In the detection process the fine-grained segmentation splits the area covered by the windshield into numerous small segments. The small segments exhibit only weak texture clues. As a consequence, they are not rejected during candidate validation.
The presented results demonstrate both the capabilities and the limitations of the proposed approach. We are able to robustly detect elephants with high accuracy, which shows that the approach is well-suited to support biologists in their investigations. We yield a low false-positive rate for the detection of elephants at intermediate and near distances. The detection of far-distant elephants demonstrates the limitations of the approach. Due to the fine granularity of the analysis, the number of false positives increases. However, most false positives are reasonable and occur in areas where they would be expected. Aside from false positives, we are able to detect and track most elephants even if they are occluded or represented only by a small image area.
The contribution of this work is a reliable method for the detection and tracking of elephants applicable to unconstrained wildlife video. Unlike related approaches, we do not make strong assumptions about the video material and the environment, such as the number of animals present, their poses to the camera, the amount of background clutter, and the camera operation. As a consequence, we are able to detect and track elephants of different sizes and poses in their natural habitat. The approach robustly handles occlusions and detects elephants even if most of their bodies are hidden, e.g., behind vegetation. Experiments show that robust and accurate detection is possible in heterogeneous scenarios at a remarkable small false-positive rate of only 2.5%. We reach the limits of the approach by the detection of far-distant elephants. While the detection rate in this case is still high, the sensitivity to false positives grows. We conclude that this use case requires the integration of additional constraints related to the shape and size of far-distant elephants.
The major benefit of this work is a novel approach that enables the automated indexing of unconstrained wildlife video. As an additional information, our approach provides the spatial location and complete tracking information for each detection. This makes the approach a sound basis for higher-level analysis tasks, from the automated estimation of group sizes, to the identification of animals, and to the automated recognition of different activities and behaviors.
We would like to thank Angela Stöger-Horwath for providing wildlife video material and her expertise and Annette Mossel and Christian Breiteneder for helpful discussions and comments on the paper. Furthermore, we thank the Addo Elephant National Park for their support and efforts. This work received financial support from the Austrian Science Fund (FWF) under grant number P23099.
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