Effects of temperature and salinity on the development of embryos and larvae of the veined rapa whelk Rapana venosa (Valenciennes, 1846)

Shaojun Ban; Tao Zhang; Hengqian Pan; Yang Pan; Pingchuan Wang; Dongxiu Xue

doi:10.1007/s00343-014-3264-6

Your Location：

Home >

Browse articles >

Effects of temperature and salinity on the development of embryos and larvae of the veined rapa whelk Rapana venosa (Valenciennes, 1846)

Updated：2023-05-16

- Effects of temperature and salinity on the development of embryos and larvae of the veined rapa whelk Rapana venosa (Valenciennes, 1846)
- Journal of Oceanology and Limnology Vol. 32, Issue 4, Pages: 773-782(2014)
- Affiliations：
  
  1. Institute of Oceanology Chinese Academy of Sciences
  2. University of Chinese Academy of Sciences
  3. Ocean University of China
  4. Qingdao Agricultural University
- Author bio：
- Funds：
- DOI：10.1007/s00343-014-3264-6
  CLC：
- Online First：11 July 2014，
  
  Published：2014
- Accepted：
Scan QR Code
Ban, S., Zhang, T., Pan, H. et al. Effects of temperature and salinity on the development of embryos and larvae of the veined rapa whelk Rapana venosa (Valenciennes, 1846)., Chin. J. Ocean. Limnol. 32, 773–782 (2014). https://doi.org/10.1007/s00343-014-3264-6
DOI：

Ban, S., Zhang, T., Pan, H. et al. Effects of temperature and salinity on the development of embryos and larvae of the veined rapa whelk Rapana venosa (Valenciennes, 1846)., Chin. J. Ocean. Limnol. 32, 773–782 (2014). https://doi.org/10.1007/s00343-014-3264-6 DOI：

摘要

Abstract

The major population of the veined rapa whelk Rapana venosa (Valenciennes

1846)

which is an important fishery resource

is facing a large decline in China. We studied the effects of incubation temperature (16–34°C at salinity 30) and salinity (5–45 at 25°C) on the incubation period and subsequent larval development. In the temperature experiment

the shortest incubation period was 12 days at 34°C

the lower temperature limit was 16°C

the longest mean shell length (1 193±17 μm) occurred at 25°C and the highest survival rate 72.28%±5.62% was observed at 28°C. In the salinity experiment

the shortest incubation period was 15 days at 25. The salinity tolerance range was 15–40

the longest mean shell length (855±9 μm) and the highest survival rate 72.93%±4.85% were both observed at 35. This study demonstrated that

during the egg-mass stage

temperature and salinity regimes influence later growth and survival of larvae. These observations deepen our understanding of the ecology and conservation of natural populations of Rapana venosa.

关键词

Keywords

references

Ahn H, Yamada Y, Okamura A, Horie N, Mikawa N, Tanaka S Tsukamoto K. 2012. Effect of water temperature on embryonic development and incubation period of the Japanese eel Anguilla japonica. Aquaculture, 330–333: 100–105.

Bao Y B, You Z J. 2004. Influences of several environmental factors on growth in marine shellfish larvae. Fish. Sci., 23(12): 39–41.

Brenko M H, Calabrese. 1969. The combined effects of salinity and temperature on larvae of the mussel Mytilus edulis. Mar. Biol., 4(3): 224–226.

Cain T D. 1973. The combined effects of temperature and salinity on embryos and larvae of the clam Rangia cuneata. Mar. Biol., 21: 1–6.

Calabrese A. 1969. Individual and combined effects of salinity and temperature on embryos and larvae of the coot clam, Mulinia lateralis (Say). Biol. Bull., 137(3): 417–428.

Camus P. 2001. Un bien discret et redoutable préadateur de coquillages, l’exotique globe-trotter: Rapana venosa. La Vigie, 26: 3–9.

Davis H C, Calabrese. 1964. Combined effects of temperature and salinity on development of eggs and growth of larvae of M. mercenaria and C. virginica. Fishery Bulletin of the Fish and Wildlife Service, 63: 643–655.

Doroudi M S, Southgate P C, Mayer R J. 1999. The combined effects of temperature and salinity on embryos and larvae of the black-lip pearl oyster, Pinctada margaritifera (L.). Aquac. Res., 30(4): 271–277.

Drapkin E. 1963. Effect of Rapana bezoar Linne (Mollusca, Muricidae) on the Black Sea fauna. Doklady Akademii Nauk SRR, 151: 700–703.

Giberto D A, Bremec C S, Schejter L et al. 2006. The invasive Rapa Whelk Rapana venosa (Valenciennes 1846): status and potential ecological impacts in the Río de la Plata estuary, Argentina-Uruguay. J. Shellfish Res., 25(3): 919–924.

Harding J M, Mann R, Kilduff C W. 2008. Influence of environmental factors and female size on reproductive output in an invasive temperate marine gastropod Rapana venosa (Muricidae). Mar. Biol., 155(6): 571–581.

Harding J M, Mann R. 1999. Observations on the biology of the veined rapa whelk, Rapana venosa (Valenciennes, 1846) in the Chesapeake Bay. J. Shellfish Res., 18(1): 9–17.

Harding J M, Mann R. 2005. Veined rapa whelk (Rapana venosa) range extensions in the Virginia waters of Chesapeake Bay, USA. J. Shellfish Res., 24(2): 381–385.

Harding J M. 2006. Growth and development of veined rapa whelk Rapana venosa veligers. J. Shellfish Res., 25(3): 941–946.

Kinne O, Kinne E M. 1962. Rates of development in embryos of a cyprinodont fish exposed to different temperaturesalinity-oxygen combinations. Can. J. Zoology, 40(2): 231–253.

Kool S. 1993. Phylogenetic analysis of the Rapaninae (Neogastropoda: Muricidae). Malacologia, 35(2): 155–259.

Lee J Y. 1959. Reproduction and embryonic development of Rapana pecheliensis crabau and king. Periodical of Ocean University of China, 1: 92–130. (in Chinese with English abstract)

Lough R G, Gonor J J. 1973. A response surface approach to the combined effects of temperature and salinity on the larval development of Adula californiensis (Pelecypoda: Mytilidae). II. Long-term larval survival and growth in relation to respiration. Mar. Biol., 22: 295–305.

Mann R, Harding J M. 2003. Salinity tolerance of larval Rapana venosa: implications for dispersal and establishment of an invading predatory gastropod on the North American Atlantic coast. Biol. Bull., 204(1): 96–103.

Mann R, Harding J. 2002. Production. In: Veined rapa whelk (Rapana venosa) R esearch in North America: Summary of Research Through February 2002. Virginia Institute of Marine Science, College of William and May, Gloucester Point, Virginia. 26p.

Mann R, Occhipinti A, Harding J M. 2004. Alien species alert: Rapana venosa (veined whelk). ICES, 264: 1–14.

Nieweg D C, Post J N J, Vink R J. 2005. Rapana venosa (Gastropoda: Muricidae): a new invasive species in the north sea. Deinsea, 11: 169–174.

Pechenik J A. 1993. Egg capsules of Nucella lapillus (L.) protect against low-salinity stress. J. Exp. Mar. Biol. Ecol., 71(2): 165–179.

Pechenik J A. 1986. The encapsulation of eggs and embryos by molluscs: an overview. Am. Malacal. Bull., 4(2): 165–172.

Robert R, His E, Dinet A. 1988. Combined effects of temperature and salinity on fed and starved larvae of the European flat oyster Ostrea edulis. Mar. Biol., 97(1): 95–100.

Scheltema R S. 1967. The relationship of temperature to the larval development of Nassarius obsoletus (Gastropoda). Biol. Bull., 132(2): 253–265.

Spight T M. 1975. Factors extending gastropod embryonic development and their selective cost. Oecologia, 21(1): 1–16.

Tang B J, Yin F, Gui C S, Chen X Z, Liu B Z. 2012. Hatching, growth and hatchling dietary preference in Hemifusus ternatanus (Gmelin, 1791). Aquaculture, 326–329: 141–147.

Tettelbach S T, Rhodes E W. 1981. Combined effects of temperature and salinity on embryos and larvae of the Northern Bay scallop Argopecten irradians irradians. Mar. Biol., 63: 249–256.

Thorson G. 1950. Reproductive and larval ecology of marine bottom invertebrates. Biol. Rev., 25(1): 1–45.

Wang H, Zhu X W, Wang Y N, Luo M M, Liu Z G. 2012. Determination of optimum temperature and salinity for fertilization and hatching in the Chinese pearl oyster Pinctada martensii (Dunker). Aquaculture, 358–359: 292–297.

Wang J, Wang Z S, Dong Y, Li D C, Liu Z Y. 2003. Effect of salinity on incubation of fertilized Rapana venosa eggs and survival and growth of its larvae. Fish. Sci., 22(5): 9–11.

Wei L P, Qiu S Y, Wang B G, Sun X F, Wang X D. 1999. Studies on the reproductive biology of Rapana Venosa. Journal of Fisheries of China, 23: 150–155. (in Chinese with English abstract)

Yang J, Li Q, Kong L, Zheng X, Wang R. 2008. Genetic structure of the veined rapa whelk (Rapana venosa) popolations along the coast of China. Biochem. Genet., 46: 539–548.

Zolotarev V. 1996. The Black Sea ecosystem changes related to the introduction of new mollusc species. Mar. Ecol., 17: 227–236.

Views

Downloads

CSCD

Alert me when the article has been cited

Submit

Tools

Publicity Resources

Sound speed profiles in high spatiotemporal resolution using multigrid three-dimensional variational method: a coastal experiment off northern Shandong Peninsula

Upper ocean response to typhoon Kujira (2015) in the South China Sea by multiple means of observation

Effects of temperature and salinity on the asexual reproduction of Aurelia coerulea polyps

Impact assessment of modified clay on embryo-larval stages of turbot Scophthalmus maximus L.

Effect of temperature, salinity, and body length on the energy budget of Daphniopsis tibetana Sars (Cladocera: Daphniidae)

Related Author

Guangchao HOU

Jingsheng ZHAI

Qi SHAO

Yanling ZHAO

Wei LI

Guijun HAN

Kangzhuang LIANG

GUO Jie

Related Institution

School of Marine Science and Technology, Tianjin University

Tianjin Key Laboratory for Oceanic Meteorology

The PLA 31010 Units

Key Laboratory of Coastal Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research (YIC), Chinese Academy of Sciences (CAS)

Shandong Key Laboratory of Coastal Environmental Processes, YICCAS

Address：Editorial Office of JOL, 88 Haijun Rd. Qingdao, 266000, China
Tel：+86-532-82898754 Email：jol@qdio.ac.cn
Technical support is provided by Beijing Founder electronics co., LTD 京ICP备09064830号-19 京公网安备11010802024621
It is recommended to read the content of this site in Chrome&IE9+. Please switch to extreme mode in browser 360.
Cookies We use cookies to help provide and enhance our service and tailor content. By continuing, you agree to the use of cookies.

⁰