DOI QR코드

DOI QR Code

Reproductive Phenology of Four Korean Seagrasses, Zostera caespitosa, Z. caulescens, Z. japonica and Z. marina

한국산 해초 포기거머리말, 수거머리말, 애기거머리말과 거머리말의 생물계절학

  • Lee, Sung-Mi (Department of Environmental Marine Science, College of Science and Technology Hanyang University) ;
  • Lee, Sang-Yong (Department of Environmental Marine Science, College of Science and Technology Hanyang University) ;
  • Choi, Chung-Il (Department of Environmental Marine Science, College of Science and Technology Hanyang University)
  • 이성미 (한양대학교 과학기술대학 해양환경과학과) ;
  • 이상룡 (한양대학교 과학기술대학 해양환경과학과) ;
  • 최청일 (한양대학교 과학기술대학 해양환경과학과)
  • Published : 2005.06.30

Abstract

This study described the phonology and reproductive potential of four species of Korean seagrasses, Zostera caespitosa, Z. caulescem, Z. Japonica and Z. marina. Z. caespitosa and Z. caulescens sampled from a mixed stand at the subtidal area of Yulpo Bay, Geojedo of the South Sea of Korea in November 2002 and August 2003. Z japonica and Z. marina occurred at the depth between the middle intertidal and shallow subtidal (<1m below mean sea level) of Seungbongdo (in Yellow Sea) samples collected in February and October 2003. The sexual reproductive phase of the four Zostera species was apparently different in timing of flowering, reproductive period, fruiting and seed maturing. Z. caespitosa flowered from February to early May $(10-16^{\circ}C)$, and its seed production completed in early May. The reproductive shoots of Z. caulescens began to appear in January $(9^{\circ}C)$, and its flowering followed from February to June $(10-19^{\circ}C)$. The flowers of Z. japonica were observed from July to September $(18-22^{\circ}C)$, and its seeds matured from August to September. The most commonly I marina flowered from April to August $(7-21^{\circ}C)$ and developed into seeds in July. Z. caulescens, the largest plant, had the highest number of seeds per shoot and longest spadix length. Z. marina, which was intermediate In size, recorded the highest reproductive potential. The study indicates that the reproductive phase and potential of the four species of seagrass from Korea are highly related to water temperature, and the populations of these species show a perennial lifespan with a low sexual reproductive input.

한반도 연안에 자생하는 거머리말속(Zostera) 해초 4종인 포기거머리말(Z caespitosa), 수거머리말(Z. caulescens), 애기거머리말(Z. japonica), 그리고 거머리말(Z. marina)에 대한 생물계절학과 생식지 특징을 조사하였다. 율포만의 조하대에 혼재하는 포기거머리말과 수거머리말은 2002년 11월부터 2003년 8월까지 조사하였다. 승봉도의 애기거머리말은 조간대 중부에서 하부까지 분포하였으며, 식물체는 2002년 11월부터 2003년 10월까지 채집하였다. 거머리말은 승봉도의 조간대 하부에서부터 간조시 수심 1m 내외의 조하대까지 패치로 분포하였으며, 생물계절학적 특징은 2003년 2월부터 2003년 10월까지 조사하였다. 거머리말속 종들의 유성생식 단계는 개화, 열매, 종자 출현시기와 생식기간이 명확하게 구분되어 나타났다. 포기거머리말의 개화는 2월에서 5월초$(10{\sim}16^{\circ}C)$까지 출현하였지만, 최대 종자는 5월초에 나타났다. 수거리말의 생식지는 1월$(9^{\circ}C)$에 출현하였으며, 개화는 2월부터 6월$(10{\sim}19^{\circ}C)$까지 출현하였다. 애기거머리말의 개화는 7월에서 9월$(18{\sim}22^{\circ}C)$까지 출현하였으며, 종자는 8월부터 9월까지 성숙하였다. 거머리말의 개화는 4월에서 8월$(7{\sim}21^{\circ}C)$까지 출현하였으며, 7월에 종자가 나타났다. 수거머리말의 생식지와 육수화서는 가장 길게 신장하였으며, 개체당 종자 수도 가장 높았다. 거머리말의 생식지는 중간 크기이며, 생식능력이 가장 높게 나타났다. 거머리말속 4종에 대한 생식지의 생식 단계와 생식 능력은 증가하는 수온과 관련된 것으로 판단되었다. 본 연구지역에서 거머리말속 개체군의 생식 전략은 유성 생식 능력이 낮은 다년생의 특징을 보였다.

Keywords

References

  1. 국립수산과학원. 2003. 해양조사연보. Vol. 51.
  2. 국립수산과학원. 2004. 해양조사연보. Vol. 52.
  3. de Cock, A.W.A.M. 1981. Development of the flowering shoot of Zostera marina L. under controlled conditions in comparison to the development in two different natural habitats in the Netherlands. Aquat. Bot., 10, 99-113. https://doi.org/10.1016/0304-3770(81)90013-9
  4. den Hartog, C. 1970. The Sea-Grasses of the World. North-Holland Publication Co. 275 p.
  5. Huong, T.T.L., J.E. Vermaat, J. Terrados, N.V. Tien, C.M. Duarte, J. Borum, and N.H. Tfi. 2003. Seasonality and depth zonation of intertidal Halophila ovalis and Zostera japonica in Ha Long Bay (northern Vietnam). Aquat. Bot., 75, 147-157. https://doi.org/10.1016/S0304-3770(02)00172-9
  6. Jacobs, R.P.W.M. and E.S. Pierson. 1981. Phenology of reproductive shoots of eelgrass, Zostera marina L., at Roscoff (France). Aquat. Bot., 10, 45-60. https://doi.org/10.1016/0304-3770(81)90004-8
  7. Keddy, C.J. 1987. Reproduction of annual eelgrass variation among habitats and comparison with perennial eelgrass (Zostera marina L.). Aquat. Bot., 27, 243-256. https://doi.org/10.1016/0304-3770(87)90044-1
  8. Keddy, C.J. and D.G. Patriquin. 1978. An annual form of eelgrass in Nova Scotia. Aquat. Bot., 5, 163-170. https://doi.org/10.1016/0304-3770(78)90059-1
  9. Lee, S.Y. 1997. Annual cycle of biomass of a threatened population of intertidal seagrass Zostera japonica in Hong Kong. Mar. Biol., 129, 183-193. https://doi.org/10.1007/s002270050159
  10. Lee, S.Y. 2001. A study on the ecological and taxonomical characteristics of Zostera (Zosteraceae) in Korea. Ph. D. Thesis, Hanyang Univ. 167 p.
  11. Lee, S.Y., S.M. Lee, and C.I. Choi. 2002a. Phenology and morphometrics change of Zostera caespitosa Miki populations at the Duksan Port in the eastern coast of Korea. Kor. J. Environ. Biol., 20, 339-346.
  12. Lee, S.Y., S.M. Lee, J.H. Kim, and C.I. Choi. 2003. Phenology and morphometrics change of Zostera marina L. population at Duksan Port in the Eastern Coast of Korea. J. Kor. Soc. Oceanogr. The Sea, 8, 70-77.
  13. Lee, S.Y., Y. Suh, S. Kim, and C.I. Choi. 2002b. Ecological and morphological characteristics of Zostera caulescens Miki (Zosteraceae) in Korea. Ocean & Polar Res., 24, 345-357. https://doi.org/10.4217/OPR.2002.24.4.345
  14. Meling-Lopez, A.E. and S.E. Ibarra-Obando. 1999. Annual life cycles of two Zostera marina L. populations in the Gulf of California: contrasts in seasonality and reproductive effort. Aquat. Bot., 65, 59-69. https://doi.org/10.1016/S0304-3770(99)00031-5
  15. Miki, S. 1932. On seagrass new to Japan. Bot. Mag., 46, 774-788. https://doi.org/10.15281/jplantres1887.46.774
  16. Nakaoka, M., N. Kouchi, and K. Aioi. 2003. Seasonal dynamics of Zostera caulescens: relative importance of flowering shoots to net production. Aquat. Bot., 77, 277-293. https://doi.org/10.1016/j.aquabot.2003.08.002
  17. Olesen, B. 1999. Reproduction in Danish eelgrass (Zostera marina L.) stands: size-dependence and biomass partitioning. Aquat. Bot., 65, 209-219. https://doi.org/10.1016/S0304-3770(99)00041-8
  18. Omori, Y. 1994. Seasonal changes of the reproductive shoot of Zostera caulescens (Zosteraceae) in Sagami Bay, central Japan. Sci. Rep. Yokosuka City Mus., 42, 65-69.
  19. Orth, R.J. and K.A. Moore. 1986. Seasonal and year-to-year variations in growth of Zostera marina L. (eelgrass) in the lower Chesapeake Bay. Aquat. Bot., 24, 335-341. https://doi.org/10.1016/0304-3770(86)90100-2
  20. Orth, R.J., M. Luckenbach, and K.A. Moore. 1994. Seed dispersal in a marine macrophyte: implications for colonization and restoration. Ecology, 75, 1927-1939. https://doi.org/10.2307/1941597
  21. Phillips, R.C. and T. Backman. 1983. Phenology and reproductive biology of eelgrass (Zostera marina L.) at Bahia Kino, Sea of Cortez, Mexico. Aquat. Bot., 17, 85-90. https://doi.org/10.1016/0304-3770(83)90020-7
  22. Phillips, R.C., C. McMillan, and K.W. Bridges. 1983. Phenology of eelgrass, Zostera marina L., along latitudinal gradients in North America. Aquat. Bot., 15, 145-156. https://doi.org/10.1016/0304-3770(83)90025-6
  23. Robertson, A.I. and K.H. Mann. 1984. Disturbance by ice and life-history adaptations of eelgrass Zostera marina. Mar. Biol., 80, 131-141. https://doi.org/10.1007/BF02180180
  24. Santamaria-Gallegos, N.A., J.L. Sanchez-Lizaso, and E.F. Felix-Pico. 2000. Phenology and growth cycle of annual subtidal eelgrass in a subtropical locality. Aquat. Bot., 66, 329-339. https://doi.org/10.1016/S0304-3770(99)00082-0
  25. Shin, H. and H.K. Choi. 1998. Taxonomy and distribution of Zostera (Zosteraceae) in eastern Asia, with special reference to Korea. Aquat. Bot., 60, 49-66. https://doi.org/10.1016/S0304-3770(97)00066-1
  26. Tomlinson, P.B. 1974. Vegetative morphology and meristem dependence the foundation of productivity in seagrasses. Aquaculture, 4, 107-130. https://doi.org/10.1016/0044-8486(74)90027-1
  27. Van Lent, F. and J.M. Verschuure. 1994. Intraspecific variability of Zostera marina L. (eelgrass) in the estuaries and lagoons of the southwestern Netherlands. II. Relation with environmental factors. Aquat. Bot., 48, 59-75. https://doi.org/10.1016/0304-3770(94)90073-6
  28. Vermaat, J.E., N.S.R. Agawin, C.M. Duarte, M.D. Fortes, N. Marba, and J. Uri. 1995. Meadow maintenance, growth and productivity of a mixed Phillippine seagrass bed. Mar. Ecol. Prog. Ser., 124, 215-225. https://doi.org/10.3354/meps124215
  29. Walker D.I., B. Olesen, and R.C. Phillips. 2001. Reproduction and phenology in seagrasses. p. 59-78. In: Global Seagrass Research Methods. ed. by F.T. Short and R.G. Coles. Elesevier. Amsterdam.

Cited by

  1. Seasonal Changes of Community Structure of Phytoplankton in Three Korean Seagrass Beds vol.28, pp.2, 2006, https://doi.org/10.4217/OPR.2006.28.2.095
  2. Population analysis of eelgrass, Zostera marina L. in Geojedo, Gaedo, and Jedo on the southern coastal water of Korea using RAPD-PCR vol.17, pp.4, 2007, https://doi.org/10.5352/JLS.2007.17.4.455
  3. Estimating Spatial and Vertical Distribution of Seagrass Habitats Using Hydroacoustic System vol.28, pp.3, 2006, https://doi.org/10.4217/OPR.2006.28.3.225
  4. Antioxidant Activity of the Seagrass Zostera japonica vol.29, pp.4, 2014, https://doi.org/10.7841/ksbbj.2014.29.4.271
  5. Cytotoxic Effect of Zostera asiatica on Growth of Human Cancer Cells vol.27, pp.4, 2012, https://doi.org/10.7841/ksbbj.2012.27.4.227
  6. Inhibitory Effect of Zostera japonica on Growth of Human Cancer Cells vol.34, pp.4, 2012, https://doi.org/10.4217/OPR.2012.34.4.385
  7. First report on the occurrence of the comb pen shell, Atrina pectinata (Linnaeus, 1767) (Bivalvia: Pinnidae) in Ulleungdo Island in the East Sea: Ecology and molecular identification of the species using COI gene sequence vol.50, pp.4, 2015, https://doi.org/10.1007/s12601-015-0059-4