Hostname: page-component-586b7cd67f-tf8b9 Total loading time: 0 Render date: 2024-11-20T06:52:04.520Z Has data issue: false hasContentIssue false

Structure of novel exocrine glands in Calanus species with notes on their possible function

Published online by Cambridge University Press:  01 September 2010

Shuhei Nishida*
Affiliation:
Ocean Research Institute, University of Tokyo, 1-15-1 Minamidai, Nakano, Tokyo 164–8639, Japan
Takumi Nonomura
Affiliation:
Ocean Research Institute, University of Tokyo, 1-15-1 Minamidai, Nakano, Tokyo 164–8639, Japan Tottori Prefectural Fisheries Station, 1166 Ishiwaki, Yunashihama, Touhaku 689-0602, Japan
*
Correspondence should be addressed to: S. Nishida, Atmosphere and Ocean Research Institute, University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa 277-8564, Japan email: [email protected]

Abstract

The structure of hitherto-unknown exocrine glands in the caudal rami of the pelagic copepods of the genus Calanus was investigated, together with the vertical, diel and seasonal variations in the occurrence of granules secreted from the glands. Zooplankton samples were collected in Sagami Bay by vertical tows of a net from 4 discrete layers at 250-m intervals in the upper 1000 m both day and night, with an additional seasonal sampling in the upper 200 m. The samples contained copepodids of Calanus sinicus (stages IV–VI), C. jashnovi (stages IV–V), and unidentified Calanus (stages I–III), which possessed the glands regardless of the developmental stage and sex. Each caudal ramus has an inner- and an outer gland each of which opens in a pore at the ventral base of a caudal seta. According to light microscopy the cavities of only the inner glands contained many transparent granules, some of which appeared to have been discharged to the environment. The granules were present regardless of day/night, depth, and season, with the maximum number of 52/copepod. The cells surrounding the inner cavity contained well-developed rough endoplasmic reticulum, mitochondria, Golgi-bodies, and secretory granules; the outer cavity contained granules of much lower density than those in the inner cavity. These observations rule out the possible functions of the glands for egg and sex pheromone production, and suggest most likely function is predator avoidance. However, neither has mechanical disturbance excited luminescence, nor has ultraviolet emission excited fluorescence, suggesting the secretion is non-luminescent. Alternative possible functions include secretion of defensive substances or substances that might enhance swarm formation. A survey of preserved copepod collections indicated presence of similar glands in Calanus helgolandicus, C. pacificus, Cosmocalanus darwinii, Mesocalanus tenuicornis, and Nannocalanus minor, suggesting evolution of the glands in the common ancestor of these species that comprise a monophyletic group within the Calanidae.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

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

REFERENCES

Bannister, N.J. and Herring, P.J. (1989) Distribution and structure of luminous cells in four marine copepods. Journal of the Marine Biological Association of the United Kingdom 69, 523533.CrossRefGoogle Scholar
Boxshall, G.A. (1992) Copepoda. In Harrison, F.W. (ed.) Microscopic anatomy of invertebrates, Volume 9. Crustacea. New York: Wiley-Liss Inc., pp. 347384.Google Scholar
Bucklin, A. and Wiebe, P.H. (1998) Low mitochondrial diversity and small effective population sizes of the copepods Calanus finmarchicus and Nannocalanus minor: possible impact of climatic variation during recent glaciation. Journal of Heredity 89, 383392.CrossRefGoogle ScholarPubMed
Bucklin, A., Frost, B.W., Bradford-Grieve, J., Allen, L.D. and Copley, N.J. (2003) Molecular systematic and phylogenetic assessment of 34 calanoid copepod species of the Calanidae and Clausocalanidae. Marine Biology 142, 333343.Google Scholar
Chiba, T. (1953) Some observations on the morphological characteristics especially on the reproductive organ of Copepoda, Calanus darwinii. Journal of Shimonoseki College of Fisheries 3, 235238.Google Scholar
Conover, R.J. (1988) Comparative life histories in the genera Calanus and Neocalanus in high-latitude of the northern hemisphere. Hydrobiologia 167, 127142.Google Scholar
Davis, A.D., Weatherby, T.M., Hartline, D.K. and Lenz, P.H. (1999) Myelin-like sheaths in copepod axons. Nature 398, 571.Google Scholar
Herring, P.J. (1988) Copepod luminescence. Hydrobiologia 167/168, 183195.CrossRefGoogle Scholar
Lenz, P.H., Hower, A.E. and Hartline, D.K. (2004) Force production during pereiopod power strokes in Calanus finmarchicus. Journal of Marine Systems 49, 133144.Google Scholar
Lowe, E. (1935) On the anatomy of a marine copepod Calanus finmarchicus (Gunnerus). Transactions of the Royal Society of Edinburgh 58, 561603.Google Scholar
Marshall, S.M. and Orr, A.P. (1955) The biology of a marine copepod Calanus finmarchicus (Gunnerus). Edinburgh and London: Oliver & Boyd.Google Scholar
Mauchline, J. (1998) The biology of calanoid copepods. Advances in Marine Biology 33, 1710.Google Scholar
Motoda, S. (1959a) North pacific standard plankton net. Information Bulletin on Planktology in Japan 4, 1315.Google Scholar
Motoda, S. (1959b) Devices of simple plankton apparatus. Memoirs of Faculty of Fisheries, Hokkaido University 7, 7494.Google Scholar
Nishida, S. (1989) Distribution, structure and importance of the cephalic dorsal hump, a new sensory organ in calanoid copepods. Marine Biology 101, 173185.Google Scholar
Nonomura, T., Machida, R.J. and Nishida, S. (2008) Stage-V copepodites of Calanus sinicus and C. jashnovi (Copepoda: Calanoida) in mesopelagic zone of Sagami Bay as identified with genetic markers, with special reference to their vertical distribution. Progress in Oceanograhy 77, 4555.CrossRefGoogle Scholar
Terazaki, M. and Tomatsu, C. (1997) A vertical multiple opening and closing plankton sampler. Journal of Advanced Marine Science and Technology Society 3, 127–32.Google Scholar