Hostname: page-component-78c5997874-v9fdk Total loading time: 0 Render date: 2024-11-18T12:16:45.993Z Has data issue: false hasContentIssue false

Cannibalism in Naticidae from the La Meseta Formation (Eocene, Antarctica)

Published online by Cambridge University Press:  04 February 2016

S.S. Brezina*
Affiliation:
Instituto de Investigación en Paleobiología y Geología, Universidad Nacional de Río Negro, Belgrano 516, R8332FDJ, General Roca, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Rivadavia 1917, C1033AAJ, Ciudad Autónoma de Buenos Aires, Argentina
N. Cech
Affiliation:
Instituto de Investigación en Paleobiología y Geología, Universidad Nacional de Río Negro, Belgrano 516, R8332FDJ, General Roca, Argentina
D. Martín Serralta
Affiliation:
Facultad de Ciencias Exactas y Naturales, Universidad Nacional de La Pampa, Uruguay 151, L6300CLN, Santa Rosa, Argentina
S. Casadío
Affiliation:
Instituto de Investigación en Paleobiología y Geología, Universidad Nacional de Río Negro, Belgrano 516, R8332FDJ, General Roca, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Rivadavia 1917, C1033AAJ, Ciudad Autónoma de Buenos Aires, Argentina

Abstract

Polinices marambioensis is a naticid gastropod which is the most common constituent in fossil accumulations in the upper section of the Cucullaea I Allomember (Middle Eocene) of the La Meseta Formation in James Ross Basin, Antarctic Peninsula. This species was an important predator of infaunal bivalves and gastropods, including other naticids. The aim of this work was to assess the pattern of predation and cannibalistic behaviour of P. marambioensis. A total of 2648 specimens of P. marambioensis were examined for drill holes, which were assigned to Oichnus paraboloides. Drilling frequency data were measured as a proxy for predation intensity and statistical analyses were performed. Further, the site of each drill hole was established according to the morphological features of the shell on each specimen to assess possible preference of predators for the site of perforation. Results suggest that P. marambioensis is an efficient cannibalistic predator for a specific size range of prey (8–22 mm), and drill holes are distributed preferentially in two specific sectors of their shells. This selective cannibalistic prey behaviour in P. marambioensis affected not only the dynamics of their populations but the ecological structure of the community in which they lived.

Type
Earth Sciences
Copyright
© Antarctic Science Ltd 2016 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Allmon, W.D., Nieh, J.C. & Norris, R.D. 1990. Drilling and peeling of turritelline gastropods since the Late Cretaceous. Palaeontology, 33, 595611.Google Scholar
Askin, R.A. 1997. Eocene-¿earliest Oligocene terrestrial palynology of Seymour Island. In Ricci, C.A., ed. The Antarctic Region: geological evolution and processes. Siena: Terra Antarctica Publications, 993996.Google Scholar
Carriker, M.R. & Gruber, G.L. 1999. Uniqueness of the gastropod accessory boring organ (ABO): comparative biology, an update. Journal of Shellfish Research, 18, 579595.Google Scholar
Chattopadhyay, D. & Dutta, S. 2013. Prey selection by drilling predators: a case study from Miocene of Kutch, India. Palaeogeography, Palaeoclimatology, Palaeoecology, 374, 187196.CrossRefGoogle Scholar
Chattopadhyay, D., Rathie, A., Miller, D.J. & Baumiller, T.K. 2013. Hydrodynamic effects of drill holes on post-mortem transportation of bivalve shells and its taphonomic implications. Palaios, 28, 875884.Google Scholar
Chattopadhyay, D., Sarkar, D., Dutta, S. & Prasanjit, S.R. 2014. What controls cannibalism in drilling gastropods? A case study on Natica tigrina. Palaeogeography, Palaeoclimatology, Palaeoecology, 410, 126133.Google Scholar
Das, A., Mondal, S. & Bardhan, S. 2013. A note on exceptionally high confamilial naticid drilling frequency on Natica gualteriana from the Indian subcontinent. Historical Biology, 26, 758764.CrossRefGoogle Scholar
Dietl, G.P. & Alexander, R.R. 2000. Post-Miocene shift in stereotypic naticid predation on confamilial prey from the Mid-Atlantic shelf: coevolution with dangerous prey. Palaios, 15, 414429.Google Scholar
Dutton, A.L., Lohmann, K.C. & Zinsmeister, W.J. 2002. Stable isotope and minor element proxies for Eocene climate of Seymour Island, Antarctica. Paleoceanography, 17, 10.1029/2000PA000593.Google Scholar
Feldmann, R.M. & Woodburne, M.O. eds. 1988. Geology and paleontology of Seymour Island, Antarctic Peninsula. Geological Society of America Memoir 169, 556 pp.Google Scholar
Goin, F.J., Case, J.A., Woodburne, M.O., Vizcaíno, S.F. & Reguero, M.A. 1999. New discoveries of “opposum-like” marsupials from Antarctica (Seymour Island, medial Eocene). Journal of Mammalian Evolution, 6, 335365.Google Scholar
Hara, U. 2001. Bryozoans from the Eocene of Seymour Island, Antarctic Peninsula. Palaeontologica Polonica, 60, 33100.Google Scholar
Herbert, G.S. & Dietl, G.P. 2002. Tests of the escalation hypothesis: the role of multiple predators. Geological Society of America Abstracts with Programs, 34, 538539.Google Scholar
Huntley, J.W. & Kowalewski, M. 2007. Strong coupling of predation intensity and diversity in the Phanerozoic fossil record. Proceedings of the National Academy of Sciences of United States of America, 104, 15 00615 010.Google Scholar
Hutchings, J.A. & Herbert, G.S. 2013. No honor among snails: conspecific competition leads to incomplete drill holes by a naticid gastropod. Palaeogeography, Palaeoclimatology, Palaeoecology, 379, 3238.Google Scholar
Ivany, L.C., Lohmann, K.C., Hasiuk, F., Blake, D.B., Glass, A., Aronson, R.B. & Moody, R.M. 2008. Eocene climate record of a high southern latitude continental shelf: Seymour Island, Antarctica. Geological Society of America Bulletin, 120, 659678.Google Scholar
Kelley, P.H. 1988. Predation by Miocene gastropods of the Chesapeake Group stereotyped and predictable. Palaios, 3, 436448.Google Scholar
Kelley, P.H. 1991. Apparent cannibalism by Chesapeake Group naticid gastropods: a predictable result of selective predation. Journal of Paleontology, 65, 7579.Google Scholar
Kelley, P.H. & Hansen, T.A. 1993. Evolution of the naticid gastropod predator–prey system: an evaluation of the hypothesis of escalation. Palaios, 8, 358375.CrossRefGoogle Scholar
Kelley, P.H. & Hansen, T.A. 2003. The fossil record of drilling predation on bivalves and gastropods. In Kelley, P.H., Kowalewski, M. & Hansen, T.A., eds. Predator–prey interactions in the fossil record: topics in geobiology, series 20. New York, NY: Plenum Press/Kluwer, 113133.Google Scholar
Kelley, P.H. & Hansen, T.A. 2007. A case for cannibalism: confamilial and conspecific predation by naticid gastropods, Cretaceous through Pleistocene of the United States Coastal Plain. In Elewa, A.M.T., ed. Predation in organisms. Berlin: Springer, 151170.Google Scholar
Kelley, P.H., Thomann, C.D., Hansen, T.A., Aronson, R.B. & Blake, D.B. 1997. A world apart but not so different: predation by naticid gastropods in Antarctica and the US Gulf Coast during the Eocene. Geological Society of America Abstract with Programs, 29, 107.Google Scholar
Kitchell, J.A., Boggs, C.H., Rice, J.A., Kitchell, J.F., Hoffman, A. & Martinell, J. 1986. Anomalies in naticid predatory behavior: a critique and experimental observations. Malacologia, 27, 291298.Google Scholar
Kowalewski, M. 2002. The fossil record of predation: an overview of analytical methods. In Kowalewski, M. & Kelley, P.H., eds. The fossil record of predation. Paleontological Society Special Papers, No. 8, 3–42.Google Scholar
Marenssi, S.A. 2006. Eustatically controlled sedimentation recorded by Eocene strata of the James Ross Basin, Antarctica. In Francis, J.E., Pirrie, D. & Crame, J.A., eds. Cretaceous-Tertiary high-latitude palaeoenvironments, James Ross Basin, Antarctica. Special Publication of the Geological Society of London, No. 258, 125–133.Google Scholar
Marenssi, S., Santillana, S.N. & Rinaldi, C.A. 1998. Paleoambientes sedimentarios de la Aloformación La Meseta (Eoceno), Isla Marambio (Seymour), Antártida. Instituto Antártico Argentino, Contribución 464, 1–51.Google Scholar
Martinell, J., Domenech, R., Aymar, J. & Kowalewski, M. 2010. Confamilial predation in Pliocene naticid gastropods from Southern France: utility of preexisting collections in quantitative paleoecology. Palaios, 25, 221228.CrossRefGoogle Scholar
Nagel-Myers, J., Dietl, G. & Aronson, R.B. 2014. The cost of drilling in the cold: climate change and cannibalism in naticid gastropods from the La Meseta Formation at Seymour Island, Antarctica. Geological Society of America Abstract with Programs, 46, 630.Google Scholar
Pastorino, G. & Ivanov, V. 1996. Marcas de predación en bivalvos del Cuaternario marino de la costa de la provincia de Buenos Aires, Argentina. Iberus, 14, 93101.Google Scholar
Roy, K., Miller, D.J. & Labarbera, M. 1994. Taphonomic bias in analysis of drilling predation: effects of gastropod drill holes on bivalve shell strength. Palaios, 9, 413421.Google Scholar
Signorelli, J.H., Pastorino, G. & Griffin, M. 2006. Naticid boreholes on a tertiary cylichnid gastropod from southern Patagonia. Malacologia, 48, 299304.Google Scholar
Stafford, E.S. & Leighton, L.R. 2011. Vermeij crushing analysis: a new old technique for estimating crushing predation in gastropod assemblages. Palaeogeography, Palaeoclimatology, Palaeoecology, 305, 123137.Google Scholar
Stanton, R.J. & Nelson, P.C. 1980. Reconstruction of the trophic web in paleontology: community structure in the Stone City Formation (Middle Eocene, Texas). Journal of Paleontology, 54, 118135.Google Scholar
Stilwell, J.D. & Zinsmeister, W.J. 1992. Molluscan systematics and biostratigraphy: Lower Tertiary La Meseta Formation, Seymour Island, Antarctic Peninsula. Antarctic Research Series, 55, 1192.Google Scholar
Taylor, J.D. 1970. Feeding habits of predatory gastropods in a Tertiary (Eocene) molluscan assemblage from the Paris basin. Palaeontology, 13, 254260.Google Scholar
Taylor, P.D., Casadío, S. & Gordon, D.P. 2008. A rare form of frontal shield development in the new cheilostome bryozoan genus Uharella from the Eocene of Antarctica. Paläontologische Zeitschrift, 82, 262268.Google Scholar
Vermeij, G.J. 1987. Evolution and escalation. An ecological history of life. Princeton, NJ: Princeton University Press, 527 pp.CrossRefGoogle Scholar
Visaggi, C.C., Dietl, G.P. & Kelley, P.H. 2013. Testing the influence of sediment depth on drilling behaviour of Neverita duplicata (gastropoda: naticidae), with a review of alternative modes of predation by naticids. Journal of Molluscan Studies, 79, 310322.Google Scholar
Zinsmeister, W.J. & Camacho, H.H. 1982. Late Eocene (to possibly earliest Oligocene) molluscan fauna of the La Meseta Formation of Seymour Island, Antarctic Peninsula. In Craddock, C., ed. Antarctic geoscience. Madison, WI: University of Wisconsin Press, 299304.Google Scholar