Feeding behavior of the ctenophore Thalassocalyce inconstans: revision of anatomy of the order Thalassocalycida
- 794 Downloads
Behavioral observations using a remotely operated vehicle (ROV) in the Gulf of California in March, 2003, provided insights into the vertical distribution, feeding and anatomy of the rare and delicate ctenophore Thalassocalyce inconstans. Additional archived ROV video records from the Monterey Bay Aquarium Research Institute of 288 sightings of T. inconstans and 2,437 individual observations of euphausiids in the Gulf of California and Monterey Canyon between 1989 and 2005 were examined to determine ctenophore and euphausiid prey depth distributions with respect to temperature and dissolved oxygen concentration [dO]. In the Gulf of California most ctenophores (96.9%) were above 350 m, the top of the oxygen minimum layer. In Monterey Canyon the ctenophores were more widely distributed throughout the water column, including the hypoxic zone, to depths as great as 3,500 m. Computer-aided behavioral analysis of two video records of the capture of euphausiids by T. inconstans showed that the ctenophore contracted its bell almost instantly (0.5 s), transforming its flattened, hemispherical resting shape into a closed bi-lobed globe in which seawater and prey were engulfed. Euphausiids entrapped within the globe displayed a previously undescribed escape response for krill (‘probing behavior’), in which they hovered and gently probed the inner surfaces of the globe with antennae without stimulating further contraction by the ctenophore. Such rapid bell contraction could be effected only by a peripheral sphincter muscle even though the presence of circumferential ring musculature was unknown for the Phylum Ctenophora. Thereafter, several live T. inconstans were collected by hand off Barbados and microscopic observations confirmed that assumption.
KeywordsVideo Sequence Escape Response Remotely Operate Vehicle Ring Muscle Generic Escape
The authors thank MBARI for the use of its archives and video software. The help of George Matsumoto, Tony Moss, and Jack Costello, who read early versions of this manuscript, and Mike Dawson, who assisted with later drafts, is greatly appreciated. George Matsumoto and Kevin Raskoff were invaluable in assisting with questions about MBARI archives and data. We thank the pilots of MBARI’s ROVs, Tiburon and Ventana, and the crews of the support ships R/V Western Flyer and R/V Point Lobos. Supported by the David and Lucile Packard Foundation and NOAA Grant #NA06OAR4600091.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
- Brinton E, Fleminger A, Seigel-Causy D (1986) The temperate and tropical planktonic biotas of the Gulf of California. Calif Coop Ocean Fish Invest Rep 27:228–266Google Scholar
- Hamner WM (1985) The importance of ethology for investigations of marine zooplankton. Bull Mar Sci 37:414–424Google Scholar
- Hamner WM, Dunn DF (1980) Tropical Corallimorpharia (Coelenterata: Anthozoa): feeding by envelopment. Micronesica 16:37–41Google Scholar
- Hunt JC (1999) Laboratory observations of the feeding behavior of the cirrate octopod, Grimpoteuthis sp.: one use of cirri. Veliger 42:152–156Google Scholar
- Hurst A (1968) The feeding mechanism and behavior of the opisthobranch Melibe leonine. Symp Zool Soc Lond 22:151–166Google Scholar
- Jimenez-Perez JC, Lara-Lara JR (1988) Zooplankton biomass and copepod community structure in the Gulf of California during the 1982–1983 El Niño event. Calif Coop Ocean Fish Invest Rep 29:122–128Google Scholar
- Kils Ü (1979) Swimming speed and escape capacity of Antarctic krill, Euphausia superba. Meeresforsch 27:264–266Google Scholar
- Madin LP (1990) Overview: being there—the role of in situ science in oceanography. Mar Technol Soc J 24:19–21Google Scholar
- Madin LP, Harbison GR (1978) Thalassocalyce inconstans, new genus and species, an enigmatic ctenophore representing a new family and order. Bull Mar Sci 28:680–687Google Scholar
- Robison BH (1992) Midwater research methods with MBARI’s ROV. Mar Technol Soc J 26:32–39Google Scholar
- Thuesen EV, Rutherford LD Jr, Brommer PL (2005b) The role of aerobic metabolism and intragel oxygen in hypoxia tolerance of three ctenophores: Pleurobranchia bachei, Bolinopsis infundibulum and Mnemiopsis leidyi. J Mar Biol Assoc UK 85:627–633. doi: https://doi.org/10.1017/S0025315405011550 CrossRefGoogle Scholar
- Vinogradov GM, Vinogradov ME, Musaeva EI (2004) New zooplankton studies in the Guaymas Basin (Gulf of California). Oceanology 44:679–689 (Transl from Okeanologiva 44:723–733)Google Scholar
Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License (https://creativecommons.org/licenses/by-nc/2.0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.