Skip to main content

Advertisement

Log in

A new quantitative analysis of ovarian development in echinoderms: the maturity stage index

  • Original Paper
  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

This study developed an objective quantitative method for detecting small-scale temporal or spatial differences in gametogenesis in echinoderms. The method was applied to conventional monthly samples of the planktotrophic brittle star, Ophiopholis aculeata, collected at a single site in Newfoundland (eastern Canada) at 10–15 m depth. The samples were analysed to determine gonad index, oocyte size and gonadal stage using histology. The maturity stage index (MSI) was developed to integrate a measure of brittle star size (disc diameter), oocyte size and oocyte density. The MSIs ranged from 0 to 800 and had significantly different means among the four gametogenic stages (early growth, growth, mature and spent). The MSI was more sensitive in revealing significant differences between consecutive stages than any of its individual constituents. The MSI was also applied to gametogenic data from the lecithotrophic holothuroid, Mesothuria lactea, again revealing significant differences between successive oogenic stages. This method is expected to be useful in field and experimental studies of gametogenesis in echinoderms (and possibly other taxa), where it is important to detect not just the timing of annual peaks in reproduction but small differences in reproductive status among individuals or populations (e.g. from different habitats or feeding regimes).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+
from $39.99 /Month
  • Starting from 10 chapters or articles per month
  • Access and download chapters and articles from more than 300k books and 2,500 journals
  • Cancel anytime
View plans

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

References

  • Baillon S, Hamel J-F, Mercier A (2011) Comparative study of reproductive synchrony at various scales in deep-sea echinoderms. Deep-Sea Res Part I 58:260–272

    Article  Google Scholar 

  • Bayne BL, Holland DL, Moore MN, Lowe DM, Widdows J (1978) Further studies on the effects of stress in the adult on the eggs of Mytilus edulis. J Mar Biol Assoc UK 58:825–842

    Article  Google Scholar 

  • Blake SEJ (1978) The reproductive cycle of Ophiopholis aculeata (Echinodermata: Ophiuroidea) in the Northwestern Atlantic. Ph.D. dissertation, University of Maine, Orono

  • Boolootian RA (1966) Reproductive physiology. In: Boolootian RA (ed) Physiology of Echinodermata. Interscience, New York, pp 561–613

  • Bowmer T (1982) Reproduction in Amphiura filiformis (Echinodermata: Ophiuroidea): seasonality in gonad development. Mar Biol 69:281–290

    Article  Google Scholar 

  • Buchanan S (2001) Measuring reproductive condition in the Greenshell™ mussel Perna canaliculus. NZ J Mar Freshw Res 35:859–870

    Article  Google Scholar 

  • Devlaming V, Grossman G, Chapman F (1982) On the use of the gonosomatic index. Comp Biochem Phys A 73:31–39

    Article  Google Scholar 

  • Doyle G (2011) Effect of spatial and environmental factors on the reproductive cycle of the brittle star, Ophiopholis aculeata, based on a new maturity stage index. M.Sc. dissertation, Memorial University, St. John’s

  • Ebert TA, Hernandez JC, Russell MP (2011) Problems of the gonad index and what can be done: analysis of the purple sea urchin Strongylocentrotus purpuratus. Mar Biol 158:47–58

    Article  Google Scholar 

  • Enríquez-Díaz M, Pouvreau S, Chávez-Villalba J, Le Pennec M (2009) Gametogenesis, reproductive investment, and spawning behavior of the Pacific giant oyster Crassostrea gigas: evidence of an environment-dependent strategy. Aquac Int 17:491–506

    Article  Google Scholar 

  • Falk-Petersen IB (1982) Breeding season and egg morphology of echinoderms in Balsfjorden, Northern Norway. Sarsia 67:215–221

    Google Scholar 

  • Falkner I, Byrne M (2003) Reproduction of Ophiactis resiliens (Echinodermata: Ophiuroidea) in New South Wales with observations on recruitment. Mar Biol 143:459–466

    Article  Google Scholar 

  • Fenaux L (1970) Maturation of the gonads and seasonal cycle of the planktonic larvae of the ophiuroid Amphiura chiajei Forbes. Biol Bull 138:262–271

    Article  Google Scholar 

  • Fuji A (1960) Studies on the biology of the sea urchin. I. Superficial and histological gonadal changes in gametogenic process of two sea urchins, Strongylocentrotus nudus and Strongylocentrotus intermedius. Bull Fac Fish Hokkaido Univ 11:1–14

    Google Scholar 

  • Giese AC, Pearse JS (1974) Introduction: general principles. In: Giese AC, Pearse JS (eds) Reproduction of marine invertebrates. Academic Press, New York, pp 1–49

    Google Scholar 

  • Gómez-Robles E, Rodríguez-Jaramillo C, Saucedo PE (2005) Digital image analysis of lipid and protein histochemical markers for measuring oocyte development and quality in pearl oyster Pinctada mazatlantica (Hanley, 1856). J Shellfish Res 24:1197–1202

    Google Scholar 

  • Gosner KL (1978) Atlantic Seashore. Houghton Mifflin, Boston

  • Grant A (1986) The biometry of asteroid oogenesis: some observations. Int J Invert Rep Dev 10:113–116

    Google Scholar 

  • Grant A, Tyler PA (1986) An analysis of the reproductive pattern in the sea star Astropecten irregularis (Pennant) from the Bristol Channel. Int J Invert Rep Dev 9:345–361

    Google Scholar 

  • Hamel J-F, Mercier A (1996) Evidence of chemical communication during the gametogenesis of holothuroids. Ecology 77:1600–1616

    Article  Google Scholar 

  • Hendler G (1991) Chapter 6: Echinodermata: Ophiuroidea. In: Giese AC, Pearse JS, Pearse VB (eds) Reproduction of marine invertebrates. The Boxwood Press, Pacific Grove, pp 355–511

    Google Scholar 

  • Himmelman JH, Dumont CP, Gaymer CF, Vallières C, Drolet D (2008) Spawning synchrony and aggregative behaviour of cold-water echinoderms during multi-species mass spawnings. Mar Ecol Prog Ser 361:161–168

    Google Scholar 

  • Hughes AD, Kelly MS, Barnes DKA, Catarino AI, Black KD (2006) The dual functions of sea urchin gonads are reflected in the temporal variations of their biochemistry. Mar Biol 148:789–798

    Article  Google Scholar 

  • Junqueira LC, Carneiro J, Long JA (1986) Basic histology. Appleton-Century-Crofts, Norwalk

    Google Scholar 

  • Lowe DM, Moore MN, Bayne BL (1982) Aspects of gametogenesis in the marine mussel Mytilus edulis (L.). J Mar Biol Assoc UK 62:133–145

    Article  Google Scholar 

  • MacDonald BA, Thompson RJ (1986) Influence of temperature and food availability on the ecological energetics of the giant scallop Placopecten magellanicus. Mar Biol 93:37–48

    Article  Google Scholar 

  • Mercier A, Hamel JF (2009) Endogenous and exogenous control of gametogenesis and spawning in echinoderms. Adv Mar Biol 55:1–302

    Article  Google Scholar 

  • Newell RIE, Hilbish TJ, Koehn RK, Newell CJ (1982) Temporal variation in the reproductive cycle of Mytilus edulis (Bivalvia, Mytilidae) from localities on the east coast of the United States. Biol Bull 162:299–310

    Article  Google Scholar 

  • Osada M, Nakamura S, Kijima A (2007) Quantitative analysis of pattern of gonial proliferation during sexual maturation in Japanese scallop Patinopecten yessoensis. Fish Sci 73:1318–1324

    CAS  Google Scholar 

  • Patent DH (1969) The reproductive cycle of Gorgonocephalus caryi (Echinodermata: Ophiuroidea). Biol Bull 136:241–252

    Article  CAS  Google Scholar 

  • Schoenmakers HJN, Goedhart MJ, Voogt PA (1984) Biometrical and histological aspects of the reproductive cycle of the ovaries of Asterias rubens (Echinodermata). Biol Bull 166:328–348

    Article  Google Scholar 

  • Singh R, MacDonald BA, Lawton P, Thomas MLH (2001) The reproductive biology of the dendrochirote sea cucumber Cucumaria frondosa (Echinodermata: Holothuroidea) using new quantitative methods. Invertebr Reprod Dev 40:125–141

    Article  Google Scholar 

  • Toro JE, Thompson RJ, Innes DJ (2002) Reproductive isolation and reproductive output in two sympatric mussel species (Mytilus edulis, M. trossulus) and their hybrids from Newfoundland. Mar Biol 141:897–909

    Article  Google Scholar 

  • Tyler PA (1977) Seasonal variation and ecology of gametogenesis in the genus Ophiura (Ophiuroidea: Echinodermata) from the Bristol Channel. J Exp Mar Biol Ecol 30:185–197

    Article  Google Scholar 

  • Urrutia MB, Ibarrola I, Iglesias JIP, Navarro E (1999) Energetics of growth and reproduction in a high-tidal population of the clam Ruditapes decussatus from Urdaibai Estuary (Basque Country, N. Spain). J Sea Res 42:35–48

    Article  Google Scholar 

  • Yoshida M (1952) Some observations on the maturation of the sea-urchin, Diadema setosum. Annot Zool Jpn 25:265–271

    Google Scholar 

Download references

Acknowledgments

Special thanks to P. Gagnon for logistic support, guidance and valued help in the field, and to S. Caines, W. Coffey, R. Guest, R. Hooper, K. Matheson, R. O’Donnell, P. Sargent, and C. Vickers for assistance with field work and sample collection. Many thanks as well to OSC Laboratory Services, the MI Centre for Aquaculture and Development, J. Foote, N. Laite, C. Short, J. So and Z. Sun for technical and moral support and to S. Baillon for her work on M. lactea. This study was financially supported by grants from the Natural Sciences and Engineering Research Council of Canada (NSERC) and the Canada Foundation for Innovation (CFI) to A. Mercier. It was conducted in partial fulfilment of the MSc degree of G. Doyle, who wishes to thank examiners for helping to improve earlier versions of this manuscript. We also thank two anonymous reviewers for constructive comments.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Annie Mercier.

Additional information

Communicated by J. P. Grassle.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 136 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Doyle, G.M., Hamel, JF. & Mercier, A. A new quantitative analysis of ovarian development in echinoderms: the maturity stage index. Mar Biol 159, 455–465 (2012). https://doi.org/10.1007/s00227-011-1823-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00227-011-1823-3

Keywords