Skip to main content

Advertisement

Log in

Assessment of negative phototaxis in long-term fasted Glyptocidaris crenularis: a new insight into measuring stress responses of sea urchins in aquaculture

  • Biology
  • Published:
Chinese Journal of Oceanology and Limnology Aims and scope Submit manuscript

Abstract

A cost-effective method was designed to measure the behavioral response of negative phototaxis to high-intensity illumination in the sea urchin Glyptocidaris crenularis. Ninety sea urchins were randomly and equally divided into two aquaculture environment groups: a fasted group, which was starved during the experiment, and a fed group. After 10 months, the total mortality of each group was recorded. Then, 15 sea urchins were randomly selected from each group and behavioral responses to high-intensity illumination were investigated for each sea urchin. After the behavioral experiment, body measurements of the trial sea urchins were taken. The results reveal that food deprivation significantly affected test diameter (P<0.01), body weight (P<0.01), gonad weight (P<0.01), and gut weight (P<0.01). Furthermore, food deprivation also affected negative phototaxis behaviors of time to rapid spine movement (P<0.01), time to the 1 cm position (P<0.05), and walking distance in 300 s (P<0.01), but not time to body reaction (P>0.05). The mortality rates of fasted and fed urchins were 6.7% and 0%, respectively. The present study provides evidence that food deprivation has a significant effect on phenotypic traits and behavioral responses to high-intensity illumination in the sea urchin G. crenularis. With this method, environmental stressors can be easily detected by measuring proper optional indicators. This study provides a new insight into measuring stress responses of sea urchins in aquaculture. However, further studies should be carried out to understand more environmental factors and to compare this potential behavioral method with immune, physiological, and epidemiological approaches.

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.

Similar content being viewed by others

References

  • Bayne B L. 1985. Responses to environmental stress: tolerance, resistance and adaptation. In: Bayne B L ed. Marine Biology of Polar Regions and Effects of Stress on Marine Organisms. Wiley, London.

    Google Scholar 

  • Bayne C J, Gerwick L. 2001. The acute phase response and innate immunity of fish. Dev. Comp. Immuno., 25(8): 725–743.

    Article  Google Scholar 

  • Boyd C E, Schmittou H R. 1999. Achievement of sustainable aquaculture through environmental management. Aquac. Econ. Manag., 3(1): 59–69.

    Article  Google Scholar 

  • Branco P C, Borges J C S, Santos M F et al. 2013. The impact of rising sea temperature on innate immune parameters in the tropical subtidal sea urchin Lytechinus variegatus and the intertidal sea urchin Echinometra lucunter. Mar. E nviron. Res., 92: 95–101.

    Article  Google Scholar 

  • Branco P C, Pressinotti L N, Borges J C S et al. 2012. Cellular biomarkers to elucidate global warming effects on Antarctic sea urchin Sterechinus neumayeri. Polar Biol., 35(2): 221–229.

    Article  Google Scholar 

  • Cenni F, Parisi G, Scapini F, Gherardi F. 2010. Sheltering behavior of the abalone, Haliotis tuberculata L. in artificial and natural seawater: the role of calcium. Aquaculture, 299: 67–72.

    Article  Google Scholar 

  • Chang Y, Ding J, Song J, Yang W. 2004. Biology and Aquaculture of Sea Cucumbers and Sea Urchins. Ocean Press, Beijing, China. p.27–217. (in Chinese)

    Google Scholar 

  • Constable A J. 1993. The role of sutures in shrinking of the test in Heliocidaris erythrogramma (Echinoidea: Echinometridae). Mar. Biol., 117: 423–430.

    Google Scholar 

  • Downs C A, Fauth J E, Woodley C M. 2001. Assessing the health of grass shrimp (Palaeomonetes pugio) exposed to natural and anthropogenic stressors: a molecular biomarker system. Mar. Biotechnol., 3(4): 380–397.

    Article  Google Scholar 

  • Dubois P, Chen C P. 1989. Calcification in echinoderms. Echinoderm. Stud., 3: 109–178.

    Google Scholar 

  • Ebert T A. 1967. Negative growth and longevity in the purple sea urchin Stongylocentrotus purpuratus (Stimpson). Science, 157: 557–558.

    Article  Google Scholar 

  • Ebert T A. 1968. Growth rates of the sea urchin Strongylocentrotus purpuratus related to food availability and spine abrasion. Ecology, 49: 1 075–1 091.

    Article  Google Scholar 

  • Filosto S, Roccheri M C, Bonaventura R et al. 2008. Environmentally relevant cadmium concentrations affect development and induce apoptosis of Paracentrotus lividus larvae cultured in vitro. Cell Biol. Toxicol., 24(6): 603–610.

    Article  Google Scholar 

  • Hoegh-Guldberg O, Bruno J F. 2010. The impact of climate change on the world’s marine ecosystems. Science, 328(5985): 1 523–1 528.

    Article  Google Scholar 

  • Kienle C, Köhler H R, Filser J, Gerhardt A. 2008. Effects of nickel chloride and oxygen depletion on behaviour and vitality of zebrafish (Danio rerio, Hamilton, 1822) (Pisces, Cypriniformes) embryos and larvae. Environ. Pollut., 152: 612–620.

    Article  Google Scholar 

  • Lares M T, Pomory C M. 1998. Use of body components during starvation in Lytechinus variegatus (Lamarck) (Echinodermata: Echinoidea). J. Exp. Marine Biol. Ecol., 225(1): 99–106.

    Article  Google Scholar 

  • Lehtonen H. 1996. Potential effects of global warming on northern European freshwater fish and fisheries. Fish. Manag. Ecol., 3(1): 59–71.

    Article  Google Scholar 

  • Lesser M P, Carleton K L, Böttger S A, Barry T M, Walker C W. 2011. Sea urchin tube feet are photosensory organs that express a rhabdomeric-like opsin and PAX6. Proc. R. Soc. B., 278: 3 371–3 379.

    Article  Google Scholar 

  • Levitan D R. 1988. Density-dependent size regulation and negative growth in the sea urchin Diadema antillarum Philippi. Oecologia, 76: 627–629.

    Article  Google Scholar 

  • Levitan D R. 1991. Skeletal changes in the test and jaws of the sea urchin Diadema antillarum in response to food limitation. Mar. Biol., 111: 431–435.

    Article  Google Scholar 

  • Luo S, Tian X, Zhao C, Zhou H, Zhang W, Feng W, Chang Y. 2014. Phenotypic correlations of somatic and gonad traits of sea urchins Glyptocidaris crenularis in two sampled periods: first insight into its breeding and aquaculture. Chin. J. O ceanol. Limn., 32(2): 1–5.

    Google Scholar 

  • McCarron E, Burnell G, Mouzakitis G. 2009. Growth assessment on three size classes of the purple sea urchin Paracentrotus lividus using continuous and intermittent feeding regimes. Aquaculture, 288: 83–91.

    Article  Google Scholar 

  • Noga E J, Ullal A J, Corrales J, Femandes J M O. 2011. Application of antimicrobial polypeptide host defenses to aquaculture: exploitation of downregulation and upregulation responses. C omp. Biochem. Phys. D., 6(1): 44–54.

    Google Scholar 

  • Pearse J S. 2006. Ecological role of purple sea urchins. Science, 314: 940–941.

    Article  Google Scholar 

  • Pinsino A, Della Torre C, Sammarini V et al. 2008. Sea urchin coelomocytes as a novel cellular biosensor of environmental stress: a field study in the Tremiti Island Marine Protected Area, Southern Adriatic Sea, Italy. Cell B iol. T oxicol., 24(6): 541–552.

    Google Scholar 

  • Robinson N, Smith B, Cooke I, Strugnell J. 2013. A snail’s pace: a preliminary analysis of the effects of stress and genetics on movement of Haliotis. Aquaculture, 25(35): 376–379.

    Google Scholar 

  • Robohm R A, Draxler A F J, Wieczorek D, Kapareiko D, Pitchford S. 2005. Effects of environmental stressors on disease susceptibility in American lobsters: a controlled laboratory study. J. Shellfish. Res., 24(3): 773–779.

    Article  Google Scholar 

  • Ryan R M, Frederick C. 1997. On energy, personality, and health: subjective vitality as a dynamic reflection of wellbeing. J. Per. Soci. Psycho., 530–561.

    Google Scholar 

  • Schreck C B, Lorz H W. 1978. Stress response of coho salmon (Oncorhynchus kisutch) elicited by cadmium and copper and potential use of cortisol as an indicator of stress. J. Fish. Board. Can., 35(8): 1 124–1 129.

    Article  Google Scholar 

  • Tian D, Li N, Huang H, Fu Z, Zhang X. 2009. A decision support system for evaluating quality safety risk contaminated by water pollution in aquaculture pond. Computer and Computing Technologies in Aquaculture II, 293: 643–652.

    Google Scholar 

  • Tseng C K, Wu C Y, Ren K Z. 1962. The influence of temperature on the growth and development of Haidai (Laminaria japonica) gametophytes. Oceanol. et Limnol. Sinica., 4(1–2): 22–28.

    Google Scholar 

  • Viarengo A, Canesi L. 1991. Mussels as biological indicators of pollution. Aquaculture, 94(2): 225–243.

    Article  Google Scholar 

  • Yoshida M. 1957. Positive phototaxis in Psammechinus microtuberculatus (Blainville). Publ. Staz. Zool. Napoli., 30: 260–262.

    Google Scholar 

  • Yoshida M. 1962. The effect of light on the shadow reaction of the sea urchin, Diadema setosum (Leske). J. Exp. Biol., 39(4): 589–602.

    Google Scholar 

  • Yoshimura K, Motokawa T. 2010. Bilaterality in the regular sea urchin Anthocidaris crassispina is related to efficient defense not to efficient locomotion. Mar. Biol. Res., 11(157): 2 475–2 488.

    Article  Google Scholar 

  • Zhang W, Zhao C, Luo S, Chang Y, Song J. 2011. Design of a cost-effective facility for family breeding programs of marine organisms. Aquacult. Engine., 45: 146–147.

    Article  Google Scholar 

  • Zhao C, Li X, Luo S, Chang Y. 2011. Assessments of lysosomal membrane responses to stresses with neutral red retention assay and its potential application in the improvement of bivalve aquaculture. Afr. J. Biotechnol., 10(64): 13 968–13 973.

    Google Scholar 

  • Zhao C, Zhang W, Chang Y, Zhou H, Song J, Luo S. 2013. Effects of continuous and diel intermittent feeding regimes on food consumption, growth and gonad production of the sea urchin Strongylocentrotus intermedius of different size classes. Aquacult. Int., 21: 699–708.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yaqing Chang  (常亚青).

Additional information

Supported by the National High Technology Research and Development Program of China (863 Program) (No. 2012AA10A412)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tian, X., Wei, J., Zhao, C. et al. Assessment of negative phototaxis in long-term fasted Glyptocidaris crenularis: a new insight into measuring stress responses of sea urchins in aquaculture. Chin. J. Ocean. Limnol. 33, 37–44 (2015). https://doi.org/10.1007/s00343-015-3323-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00343-015-3323-7

Keyword