Abstract

Detecting when and where animals feed is key to understanding their ecophysiology, but our ability to collect these data in marine mammals remains limited. Here, we test a tag-based accelerometry method to detect prey capture in California sea lions. From synchronized underwater video and acceleration data of two trained sea lions, we isolated a combined acceleration and Jerk pattern that reliably indicated prey capture in training datasets. We observed a stereotyped feeding motion in underwater video that included (1) mouth opening while approaching prey; (2) head deceleration to allow initial suction or prey engulfment, and (3) jaw closure. This motion (1–3) was repeated if a prey item was not initially engulfed. This stereotyped feeding motion informed a signal pattern phrase that accurately detected feeding in a training dataset. This phrase required (1) an initial heave-axis Jerk signal surpassing a threshold based on sampling rate; (2) an estimated dynamic surge-axis deceleration signal surpassing −0.7 g beginning within 0.2 s of the initial Jerk signal; and (3) an estimated dynamic surge-axis acceleration signal surpassing 1.0 g within 0.5 s of the beginning of the prior deceleration signal. We built an automated detector in MATLAB to identify and quantify these patterns. Blind tests of this detector on non-training datasets found high true-positive detection rates (91%–100%) with acceleration sampled at 50–333 Hz and low false-positive detection rates (0%–4.8%) at all sampling rates (16–333 Hz). At 32 Hz and below, true-positive detection rates decreased due to attenuation of signal detail. A detector optimized for an adult female was also accurate at 32–100 Hz when tested on an adult male’s data, suggesting the potential future use of a generalized detector in wild subjects. When tested on the same data, a published triaxial Jerk method produced high true-positive detection rates (91–100%) and low-to-moderate false-positive detection rates (15–43%) at ≥ 32 Hz. Using our detector, larger prey elicited longer prey capture duration in both animals at almost all sampling rates 32 Hz or faster. We conclude that this method can accurately detect feeding and estimate relative prey length in California sea lions.

Highlights

  • Quantitative feeding observations are key in determining an animal’s foraging efficiency, ecophysiology, and ecological impact (e.g., [5, 8, 39]), but our ability to collect these data in many marine mammals remains limited

  • A slight dip in True positive (TP) detection rates at 333 Hz relative to 100 and 200 Hz is due to the need for a relatively stricter heave axis Jerk threshold to help filter out nonfeeding signals

  • The analysis introduced and validated in this study accurately detected feeding by California sea lions in a controlled setting, using strict detection requirements to help minimize false-positive detections

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Summary

Introduction

Quantitative feeding observations are key in determining an animal’s foraging efficiency, ecophysiology, and ecological impact (e.g., [5, 8, 39]), but our ability to collect these data in many marine mammals remains limited. Animal-borne video cameras can directly observe feeding and estimate prey size and species [2, 4, 26], but are limited by restrictive battery life and may potentially bias results if a light source is used at depth. Cole et al Anim Biotelemetry (2021) 9:44 following collection will limit the extent of deployments and may render the use of video cameras impractical or unviable for many studies. Mandibular gape-angle sensors (IMASEN) can detect jaw opening in pinnipeds [19, 27, 38], but feeding on small prey is often missed, and cabling may fail or affect the tagged animal over long durations

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