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Bat Echolocation Researc h - Bat Conservation International

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The sensitivity of the microphone used, and its relative<br />

position to the bat emitting the echolocation calls, may<br />

mean that the calls are not sufficiently loud enough to<br />

elicit a response from the microphone. Recording techniques<br />

and situations can also affect the quality of signal<br />

recorded, and therefore our ability to identify the<br />

species emitting a particular call (Parsons and Obrist<br />

2003; Parsons et al. 2000; Pye 1993).<br />

<strong>Bat</strong>s exhibit flexibility in the design of echolocation<br />

calls. Call structure varies with degree of acoustic clutter<br />

(e.g., Jensen and Miller 1999; Kalko and Schnitzler<br />

1989, 1993; Rydell 1990; Simmons and Stein 1980), and<br />

at different stages in a bat’s approach to objects such as<br />

prey items and roosts (Kalko 1995; Masters et al. 1991;<br />

Parsons et al. 1997; Simmons et al. 1979). Age also has<br />

an effect on the echolocation calls of bats, independent<br />

of morphology (Jones and Kokurewicz 1994; Jones et al.<br />

1992; Masters et al. 1995). Morphology also influences<br />

call design and can cause convergence in call design<br />

between morphologically similar species (Bogdanowicz<br />

et al. 1999; Jones 1996, 1999).<br />

Species identification systems must be able to cope<br />

with substantial intra- and interspecific variation in call<br />

design. They must also be able to separate species that<br />

produce seemingly identical calls. This is an enormously<br />

difficult task. Central to the development of such a system<br />

is the identification of call parameters that best separate<br />

species. Once identified, these parameters must be<br />

measured in a repeatable, quantitative manner to ensure<br />

the reliability of the results.<br />

To classify calls to species level using a single analysis,<br />

given the number of species in this study and the<br />

number of variables measured per call, is not a trivial<br />

task, especially given the highly variable nature of the<br />

data. We hypothesized that the use of a hierarchical<br />

classification system, in which calls were classified to<br />

genus and species level by separate functions or networks,<br />

would improve the ability of the automated neural<br />

networks to correctly classify species by spreading<br />

the complexity of the task over several analyses. Ultimately,<br />

the success of such an approach is reflected in<br />

increased correct identification rates at the species level.<br />

At every level, (all species together, genus only, within<br />

genera containing multiple species) the automated neural<br />

networks outperformed their equivalent discriminant<br />

function analysis. Analysis uses a series of functions that<br />

best separate the groups and then classifies each data<br />

point in turn. However, the neural network we<br />

employed in this study used an error back-propagation<br />

algorithm (Rumelhart et al. 1986) based on the errorcorrection<br />

learning rule. Error back-propagation learning<br />

consists of two passes through the different layers of<br />

the network: a forward pass and a backward pass. In the<br />

forward pass, inputs are presented to the network and a<br />

signal passes through the various layers resulting in a set<br />

of actual response from the network. During the forward<br />

pass, the synaptic weights of the neurons in the network<br />

are fixed. During the backward pass, these synaptic<br />

weights are adjusted to make the actual response of the<br />

network match the desired response. The use of a network<br />

with hidden neurons i.e., neurons not part of the<br />

input or output layers, means that the network can learn<br />

complex tasks by extracting progressively more meaningful<br />

features from the input data. Therefore, given the<br />

complexity of species identification, it is not surprising<br />

that the artificial neural networks outperformed discriminant<br />

function analysis.<br />

CONCLUSIONS<br />

The accuracy and success of a species-identification<br />

system relies on the quality of the data presented to it<br />

and the conditions under which the recording was made<br />

(e.g., equipment used, degree of acoustic clutter).<br />

Parameters measured from calls must be chosen for low<br />

intraspecific and high interspecific variability. If possible,<br />

the entire echolocation repertoire of the bats should<br />

also be recorded. Using appropriate signal-processing<br />

techniques, parameters can be measured in a quantitative<br />

and repeatable manner. Classification systems must be<br />

flexible but also able to make subtle decisions when separating<br />

calls from different species. Artificial neural networks,<br />

because of the error-minimization routines, outperform<br />

traditional statistical methods.<br />

LITERATURE CITED<br />

Fig. 5—Correct identification rates for the artificial neural networks<br />

trained to identify calls to genus level.<br />

Section 3: Ultrasound Species Identification<br />

BOGDANOWICZ, W., M. B. FENTON, and K. DALESZCZYK. 1999.<br />

The relationship between echolocation calls, morphology<br />

and diet in insectivorous bats. Journal of<br />

Zoology 247:381-393.<br />

HAYKIN, S. 1999. Neural Networks. Prentice-Hall, New Jersey.<br />

JENSEN, M. E., and L. A. MILLER. 1999. <strong>Echolocation</strong> signals of<br />

the bat Eptesicus serotinus recorded using a vertical<br />

microphone array: effect of flight altitude on searching<br />

signals. Behavioral Ecology and Sociobiology<br />

47:60-69.<br />

JONES, G. 1996. Does echolocation constrain the evolution of<br />

body size in bats? Symposia of the Zoological Soci-<br />

119

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