DOI QR코드

DOI QR Code

Reproductive characteristics, egg and larval development of short ninespine stickleback, Pungitius kaibarae

  • Hwang, In Joon (Inland Fisheries Research Institute, National Institute of Fisheries Science) ;
  • Lee, Si Woo (Southeast Sea Fisheries Research Institute, National Institute of Fisheries Science) ;
  • Han, Young Sim (Inland Fisheries Research Institute, National Institute of Fisheries Science) ;
  • Kim, Kyeong Hwan (Inland Fisheries Research Institute, National Institute of Fisheries Science)
  • Received : 2021.07.30
  • Accepted : 2021.10.06
  • Published : 2021.11.30

Abstract

In this study, the reproductive behavior and embryonic and larval development of the short ninespine stickleback Pungitius kaibarae was described and illustrated based on observations during spawning, hatching, and larval rearing trials. Adult P. kaibarae were collected downstream in Jinhae during the reproductive season (April-May). Males had nuptial coloration on their entire black bodies, with blue dorsal spines and yellow eyes, whereas females had a brown spotted pattern on their bodies. Males built nests on the stems of water weeds and attracted females. Fertilization occurred in the nest immediately after spawning, and males guarded the eggs until hatching. The fertilized eggs of P. kaibarae were spherical, demersal, adhesive, and transparent, and each egg measured 1.43 ± 0.07 mm in diameter. The morula, blastula, and gastrula stages, as well as hatching began at 5, 18.5, 21.5, and 96 post fertilization (HPF), respectively, at 20.0 ± 0.5℃. The newly hatched larvae had a total length (TL) of 5.67 ± 0.50 mm, with a yolk volume of 0.583 ± 0.059 mm3. Their mouths and anuses had not yet opened. At 2 days posthatching (days post hatching, DPH), the yolk was completely absorbed and the larvae began to feed exogenously. Pigmentation was observed in freshly hatched larvae 4 h after hatching, with the presence of eight areas with a dotted pattern on the dorsal surface of the larvae and dispersed spots on the head and yolk sac. At 30 DPH, the TL of the juveniles was 21.34 ± 1.70 mm. The nest area and number of eggs were 259.56 ± 101.39 mm2 (75.18-506.04) and 155.33 ± 114.12 (0-437), respectively.

Keywords

Acknowledgement

This study was supported by a grant from National Institute of Fisheries Science, Korea (R2021040).

References

  1. Bae HG, Suk HY. Population genetic structure and colonization history of short ninespine sticklebacks (Pungitius kaibarae). Ecol Evol. 2015;5:3075-89. https://doi.org/10.1002/ece3.1594
  2. Bae HG, Lee YJ, Jeon HB, Kim DY, Won H, Park S, et al. The complete mitochondrial genomes of three geographical lineages in short ninespine stickleback (Pungitius kaibarae) complex and their phylogenetic implication. Mitochondrial DNA B Resour. 2017;2:500-1. https://doi.org/10.1080/23802359.2017.1361362
  3. Barber I, Nairn D, Huntingford FA. Nests as ornaments: revealing construction by male sticklebacks. Behav Ecol. 2001;12:390-6. https://doi.org/10.1093/beheco/12.4.390
  4. Blaxter JHS. The early life history of fish. Berlin: Springer Verlag; 1974.
  5. Chae BS, Yang HJ. Spawning and growth of eightspine stickleback, Pungitius sinensis kaibarae (Tanaka) (Gasterosteidae, Pisces), in the Chayang stream, a tributary of Kumho river, Korea. Korean J Zool. 1993;36:181-92.
  6. Coste P. Nidification des epinoches et des epinochettes. Mem Pres Div Savants Acad Sci Inst Natl Fr. 1848;10:574-88.
  7. Cunningham JT. IV.-The eggs and larvae of teleosteans. Earth Environ Sci Trans R Soc Edinb. 1887;33:97-136. https://doi.org/10.1017/S0080456800025485
  8. FitzGerald GJ. The reproductive behavior of the stickleback. Sci Am. 1993;268:80-5. https://doi.org/10.1038/scientificamerican0493-80
  9. Fraipont M, FitzGerald GJ, Guderley H. Age-related differences in reproductive tactics in the three-spined stickleback, Gasterosteus aculeatus. Anim Behav. 1993;46:961-8. https://doi.org/10.1006/anbe.1993.1277
  10. Hahlbeck E, Katsiadaki I, Mayer I, Adolfsson-Erici M, James J, Bengtsson BE. The juvenile three-spined stickleback (Gasterosteus aculeatus L.) as a model organism for endocrine disruption II-kidney hypertrophy, vitellogenin and spiggin induction. Aquat Toxicol. 2004;70:311-26. https://doi.org/10.1016/j.aquatox.2004.10.004
  11. Hancock A. Observations on the nidification of Gasterosteus aculeatus and Gasterosteus spinachia. Ann Mag Nat Hist 1852;10:241-8. https://doi.org/10.1080/03745485609495690
  12. Heins DC, Johnson JM, Baker JA. Rerpdoductive ecology of the nine-spined stickleback from south-central Alaska. J Fish Biol. 2003;63:1131-43. https://doi.org/10.1046/j.1095-8649.2003.00232.x
  13. Hwang DS, Song HB, Lee JS. Complete mitochondrial genome of the Amur stickleback Pungitius kaibarae (Gasterosteiformes, Gasterosteidae). Mitochondrial DNA. 2012;23:313-4. https://doi.org/10.3109/19401736.2012.683183
  14. Ishikawa A, Kitano J. Diversity in reproductive seasonality in the three-spined stickleback, Gasterosteus aculeatus. J Exp Biol. 2020;223:jeb208975. https://doi.org/10.1242/jeb.208975
  15. Jang MH, Yoon JD, Chae BS, Joo GJ. Molecular phylogeny of Pungitius kaibarae from mitochondrial DNA sequences in selected streams flowing into the East Sea. Korean J Ecol Environ. 2006;39:265-70.
  16. Kim IS. Illustrated encyclopedia of fauna and flora of Korea. Vol. 37. Freshwater fishes. Yeongi: Ministry of Education of Korea; 1997.
  17. Kim IS, Yoon CH, Lee JH. Morphological variation and karyotype of the Korean species of sticklebacks, (Pisces, Gasterosteidae) in Korea. Korean J Syst Zool. 1989;5:107-19.
  18. Kim S, Zhang CI. Fish ecology. Seoul: Seoul Press; 1994.
  19. McKenzie JA, Keenleyside MHA. Reproductive behavior of ninespine sticklebacks (Pungitius pungitius (L.)) in South Bay, Manitoulin Island, Ontario. J Fish Res Board Can. 1970;48:55-61.
  20. Ministry of Environment of Korea. Conservation and management laws of wildlife. Law No. 10977 (2016).
  21. Morris D. The reproductive behaviour of the ten-spined stickleback (Pygosteus pungiyius L.). Behav Suppl. 1958;6:1-154.
  22. Park SR, Lee JH. Territorial behavior of eightspine stickleback, Pungitius sinensis kaibarae in Korea. Korean J Ecol. 1999;22:163-7.
  23. Park SR, Lee JH, Cheong S. Comparison of reproductive behaviors between two species of Eghtspine sticlebacks (genus: Pungitius). Korean J Biol Sci. 2001;5:127-32. https://doi.org/10.1080/12265071.2001.9647593
  24. Pianka ER. Evolutionary ecology. 3rd ed. New York: Harper & Row; 1983.
  25. Seo WI, Han KH, Yoon SM, Kim CC, Hwang SY, Lee SH, et al. Early life history of the Liobagrus obesus (Pisces, Amblycipitidae). Dev Reprod. 2006;10:41-5.
  26. Sokolowska E, Kulczykowska E. Annual reproductive cycle in two free living populations of three-spined stickleback (Gasterosteus aculeatus L.): patterns of ovarian and testicular development. Oceanologia. 2006;48:103-24.
  27. Swarup H. Stages in the development of the stickleback Gasterosteus aculeatus (L.). J Embryol Exp Morphol. 1958;6:373-83.