Cynthia Moss

Prof. Cynthia Moss

Department of Psychological and Brain Sciences, John Hopkins University, Baltimore, MD 21287, USA
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Research Focus & Metrics

Academic Career Length

44Years (1983-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2003 in Trends in Ecology & Evolution
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HSHans-Ulrich Schnitzler
Hans-Ulrich Schnitzler
Cynthia MossCynthia Moss
Cynthia Moss
ADAnnette Denzinger
Annette Denzinger

1 November 2000 in The Journal of the Acoustical Society of America
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ASAnnemarie Surlykke
Annemarie Surlykke
Cynthia MossCynthia Moss
Cynthia Moss
Echolocation signals were recorded from big brown bats, Eptesicus fuscus, flying in the field and the laboratory. In open field areas the interpulse intervals (IPI) of search signals were either around 134 ms or twice that value, 270 ms. At long IPI’s the signals were of long duration (14 to 18–20 ms), narrow bandwidth, and low frequency, sweeping down to a minimum frequency (Fmin) of 22–25 kHz. At short IPI’s the signals were shorter (6–13 ms), of higher frequency, and broader bandwidth. In wooded areas only short (6–11 ms) relatively broadband search signals were emitted at a higher rate (avg. IPI=122 ms) with higher Fmin (27–30 kHz). In the laboratory the IPI was even shorter (88 ms), the duration was 3–5 ms, and the Fmin 30–35 kHz, resembling approach phase signals of field recordings. Excluding terminal phase signals, all signals from all areas showed a negative correlation between signal duration and Fmin, i.e., the shorter the signal, the higher was Fmin. This correlation was reversed in the terminal phase of insect capture sequences, where Fmin decreased with decreasing signal duration. Overall, the signals recorded in the field were longer, with longer IPI’s and greater variability in bandwidth than signals recorded in the laboratory.

7 January 2007 in Nature Neuroscience
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NUNachum Ulanovsky
Nachum Ulanovsky
Cynthia MossCynthia Moss
Cynthia Moss

18 April 2006 in PLOS Biology
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KGKaushik Ghose
Kaushik Ghose
THTimothy K Horiuchi
Timothy K Horiuchi
PKP. S Krishnaprasad
P. S Krishnaprasad
Cynthia MossCynthia Moss
Cynthia Moss
Acquisition of food in many animal species depends on the pursuit and capture of moving prey. Among modern humans, the pursuit and interception of moving targets plays a central role in a variety of sports, such as tennis, football, Frisbee, and baseball. Studies of target pursuit in animals, ranging from dragonflies to fish and dogs to humans, have suggested that they all use a constant bearing (CB) strategy to pursue prey or other moving targets. CB is best known as the interception strategy employed by baseball outfielders to catch ballistic fly balls. CB is a time-optimal solution to catch targets moving along a straight line, or in a predictable fashion—such as a ballistic baseball, or a piece of food sinking in water. Many animals, however, have to capture prey that may make evasive and unpredictable maneuvers. Is CB an optimum solution to pursuing erratically moving targets? Do animals faced with such erratic prey also use CB? In this paper, we address these questions by studying prey capture in an insectivorous echolocating bat. Echolocating bats rely on sonar to pursue and capture flying insects. The bat's prey may emerge from foliage for a brief time, fly in erratic three-dimensional paths before returning to cover. Bats typically take less than one second to detect, localize and capture such insects. We used high speed stereo infra-red videography to study the three dimensional flight paths of the big brown bat, Eptesicus fuscus, as it chased erratically moving insects in a dark laboratory flight room. We quantified the bat's complex pursuit trajectories using a simple delay differential equation. Our analysis of the pursuit trajectories suggests that bats use a constant absolute target direction strategy during pursuit. We show mathematically that, unlike CB, this approach minimizes the time it takes for a pursuer to intercept an unpredictably moving target. Interestingly, the bat's behavior is similar to the interception strategy implemented in some guided missiles. We suggest that the time-optimal strategy adopted by the bat is in response to the evolutionary pressures of having to capture erratic and fast moving insects.

1 October 2001 in The Journal of the Acoustical Society of America
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Cynthia MossCynthia Moss
Cynthia Moss
ASAnnemarie Surlykke
Annemarie Surlykke
Echolocating bats transmit ultrasonic vocalizations and use information contained in the reflected sounds to analyze the auditory scene. Auditory scene analysis, a phenomenon that applies broadly to all hearing vertebrates, involves the grouping and segregation of sounds to perceptually organize information about auditory objects. The perceptual organization of sound is influenced by the spectral and temporal characteristics of acoustic signals. In the case of the echolocating bat, its active control over the timing, duration, intensity, and bandwidth of sonar transmissions directly impacts its perception of the auditory objects that comprise the scene. Here, data are presented from perceptual experiments, laboratory insect capture studies, and field recordings of sonar behavior of different bat species, to illustrate principles of importance to auditory scene analysis by echolocation in bats. In the perceptual experiments, FM bats (Eptesicus fuscus) learned to discriminate between systematic and random delay sequences in echo playback sets. The results of these experiments demonstrate that the FM bat can assemble information about echo delay changes over time, a requirement for the analysis of a dynamic auditory scene. Laboratory insect capture experiments examined the vocal production patterns of flying E. fuscus taking tethered insects in a large room. In each trial, the bats consistently produced echolocation signal groups with a relatively stable repetition rate (within 5%). Similar temporal patterning of sonar vocalizations was also observed in the field recordings from E. fuscus, thus suggesting the importance of temporal control of vocal production for perceptually guided behavior. It is hypothesized that a stable sonar signal production rate facilitates the perceptual organization of echoes arriving from objects at different directions and distances as the bat flies through a dynamic auditory scene. Field recordings of E. fuscus, Noctilio albiventris, N. leporinus, Pippistrellus pippistrellus, and Cormura brevirostris revealed that spectral adjustments in sonar signals may also be important to permit tracking of echoes in a complex auditory scene.

3 March 1995 in Science
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PKPaul L. Koch
Paul L. Koch
JHJennifer Heisinger
Jennifer Heisinger
Cynthia MossCynthia Moss
Cynthia Moss
RCRichard W. Carlson
Richard W. Carlson
MFMarilyn L. Fogel
Marilyn L. Fogel
ABAnna K. Behrensmeyer
Anna K. Behrensmeyer
The carbon, nitrogen, and strontium isotope compositions of elephants in Amboseli Park, Kenya, were measured to examine changes in diet and habitat use since the 1960s. Carbon isotope ratios, which reflect the photosynthetic pathway of food plants, record a shift in diet from trees and shrubs to grass. Strontium isotope ratios, which reflect the geologic age of bedrock, document the concentration of elephants within the park. The high isotopic variability produced by behavioral and ecological shifts, if it is representative of other East African elephant populations, may complicate the use of isotopes as indicators of the source region of ivory.