• Korean Journal of Fisheries and Aquatic Sciences
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• v.53 no.4
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• pp.650-655
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• 2020

Chilsan-do Island, South Korea, has previously been identified as one of the biggest spawning sites of the small yellow croaker Larimichthys polyactis in the Yellow Sea. To determine whether Chilsan-do still serves as a spawning site for L. polyactis, three to five stations around Chilsan-do Island were surveyed for eggs from April to June (the main spawning season of L. polyactis) in 2019, using an RN80 net. For the first time, three L. polyactis eggs were identified at two stations, located just in front of Chilsan-do Island and between Chilsan-do and the coastline, only in May. The diameter of L. polyactis eggs (1.26-1.34 mm) was very similar to those of Collichthys niveatus (1.30-1.37 mm) and Setipinna tenuifilis (1.34-1.35 mm). During the survey period, the sea surface salinity remained constant (32.0-32.1 psu), but the sea surface temperature (SST) rapidly rose from 13.6-13.7℃ in April to 22.1℃ in May. Our findings suggest that L. polyactis still spawns near Chilsan-do Island today, but on a very small scale, and that changes in SST promote spawning of L. polyactis.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.47 no.4
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• pp.419-423
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• 2014

We consider changes in the fishing ground of the small yellow croaker Larimichthys polyactis and discuss their utility in predicting fishing conditions for this species. The fishing ground, which having been formed around Jeju Island since the 1970s, is dominated by the Yellow Sea Bottom Cold Water (YSBCW), and variation in its southward expansion from the Yellow Sea is the single most key environmental factor affecting the L. polyactis catch. When the YSBCW showed strong expansion and the fishing ground shifted to the west and southwest of Jeju Island, as occurred in the late 1980s, late 1990s, and early 2000s, the L. polyactis catch was low; conversely, when expansion was weak, as in the early 1990s and late 2000s, the L. polyactis catch was high. This relationship was statistically significant and should be useful in predicting fishing conditions for L. polyactis.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.56 no.3
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• pp.324-330
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• 2023

We investigated the relative growth and squamation of larvae and juveniles of cultured Larimichthys polyactis. Analysis of the relative growth of larvae and juveniles showed that their preanal length, head length, eye diameter, body depth, and snout length increased with growth. There was no significant chage in the relative growth. The ratio of preanus length to standard length (SL) increased rapidly until SL was approximately 12 mm, and then increased gradually. Cycloid scales first appeared on the lateral line, progressed to the abdominal cavity at 15.13 mm SL, and expanded to the occipital region, base of pectoral fin, and ventral region of the eye at 17.82 mm SL. At 18.03 mm SL, scales formed on the cheek, and those at the base of pectoral fin and in the abdominal cavity were connected to each other. At 19.06 mm SL, major part of the head was covered by scales, except near the lower jaw. Cycloid scales on the lateral line changed to ctenoid scales at the range of 31.71-32.24 mm SL, and those on the nape changed at the range of 69.02-70.84 mm SL. Our results may help to establish conservation and management strategy for Larimichthys polyactis aquaculture.

• Animal cells and systems
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• v.16 no.4
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• pp.313-320
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• 2012

Genetic variation was surveyed at four microsatellite loci and 1416 base pairs (bp) of the mitochondrial DNA (mtDNA) cytochrome c oxidase I gene (COI) to clarify the genetic structure of the small yellow croaker, Larimichthys polyactis, in the Yellow and East China Seas, especially regarding four provisional populations, (one Korean and three Chinese populations). Based on microsatellite DNA variations, the estimated expected heterozygosity ($H_E$) in each population ranged from 0.776 to 0.947. The microsatellite pairwise $F_{ST}$ estimates showed no significant genetic differentiation between the populations. MtDNA variations also indicated no genetic structure in L. polyactis, but very high variability. The absence of genetic differentiation among and within populations of L. polyactis may either result from the random migration of the adult or the passive dispersal of the eggs and larvae.

• Fisheries and Aquatic Sciences
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• v.13 no.4
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• pp.350-353
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• 2010

This study demonstrated that cryopreserved semen from dead fish can be used for seedling production. Yellow croakers, Larimichthys polyactis, were killed and stored at temperatures of $20^{\circ}C$ or $0^{\circ}C$ for 6 hours. At 2 hour intervals, semen from these fish was collected using abdominal pressure and evaluated for spermatozoa motility and semen cryopreservation. Semen collected after 6 hours from dead fish stored at $0^{\circ}C$ could be cryopreserved and attained fertilization and hatching rates of $15.0{\pm}1.2%$ and $14.8{\pm}1.6%$, respectively. This study suggests that germ cells such as the semen of dead fish can be cryopreserved and utilized in the restoration of a species.

• Journal of fish pathology
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• v.35 no.1
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• pp.135-140
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• 2022

In this study, we determined the cause of a disease outbreak in small yellow croaker(Larimichthys polyactis) in Jeju island. The major external signs in the dead fish were hemorrhage of the skin. Vibrio harveyi were isolated from a few fishes and viruses were not detected from the diseased fish. However, flukes were confirmed on the skin and we conducted molecular identification and phylogenetic analysis of the isolated parasites. The obtained 28S rRNA sequence of our specimen(Accession No. OM333244) showed the highest homology with Neobenedenia girellae, while the COI sequence of our specimen showed the highest homology with N. melleni. Further sequence analysis with other genes and morphological observation are necessary for accurate identification.

• Korean Journal of Environmental Biology
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• v.38 no.4
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• pp.507-517
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• 2020

Several methods including morphometric analysis were used to distinguish small yellow croaker (Larimichthys polyactis) from yellow croaker (Larimichthys crocea), which have very similar external shapes. Morphometric analysis showed four considerable differences (p<0.05) among the total 48 morphometric dimensions, but no differences were seen in the classical dimensions (p>0.05). Rather, significant differences were seen in two truss dimensions: Insertion of dorsal fin base - origin of pectoral fin base and origin of anal fin base - origin of pectoral fin base, and two head part dimension: most anterior extension of the head - above of eye and above of eye - posterior aspect of operculum(p<0.05). However, the yellow croaker had higher values than the small yellow croaker in the other three morphometric dimensions except for the head part dimension of above of eye - posterior aspect of operculum of the four morphometric dimensions (p<0.05). The X-ray photographs indicated that the small yellow croaker (45.1±2.34°) had 8.4% more curved vertebral column than the yellow croaker(38.4±1.82°). A diamond-shaped cranium was found when the skin was peeled off from both fish but the commonly held fact that only the small yellow croaker has a diamond-shaped cranium is not accurate. Our results confirmed that the two fish could be definitely distinguished by their external body shape.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.56 no.2
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• pp.228-242
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• 2023

We examined the osteological development of the cranium, visceral skeleton, pectoral girdle, vertebral column, fins, and pterygiophore of small yellow croaker Larimichthys polyactis cultured at the Jeju Fisheries Research Institute. At 5.89 mm NL (notochord length), the larvae already had ossified frontal and basioccipital bones, parasphenoids, and vomer in the cranium. All elements of the visceral skeleton except the metapterygoid were ossified at 5.89 mm NL. Preorbital bone was ossified at 8.11 mm SL (standard length), and suborbital bones were ossified at 12.90 mm SL. In the vertebral column, ossification proceeded from the first to last centrum. The urostyle ossified at 7.41 mm SL. The caudal skeleton ossified at 6.78 mm NL, along with three hypural bones. In the pectoral girdle, the cleithrum, supracleithrum, postcleithrum, and post-temporal bones ossified at 5.89 mm NL. Caudal fin ossification began at 6.19 mm SL and was complete at 7.16 mm SL. Dorsal and anal fin ossification began at 7.16 mm SL and was complete at 8.62 mm and 8.11 mm SL, respectively. Anal and dorsal pterygiophore bone ossification was complete at 9.86 mm and 11.54 mm SL, respectively, and that of the supraneural bones was complete at 9.60 mm SL.

• Journal of the Korean Society of Fisheries and Ocean Technology
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• v.48 no.1
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• pp.10-19
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• 2012

The mesh selectivity of a drift net for yellow croaker (Larimichthys polyactis) was examined in field experiments with six different net mesh size (40, 45, 50, 55, 60 and 65mm) from April to December, 2008 in the coastal areas of Jeollanam-do in Korea. The total catch of 6,748 consisted of yellow croaker (n=6,310; 89.1% of total catch), common mackerel (n=158; 5.6%) and other species (n=280; 9.6%). The selectivity curve for yellow croaker was fit by the models of selectivity curve in SELECT method. The optimal mesh size for 50% retention for minimum landing size (191mm) of yellow croaker was estimated as 49.6mm-51mm by selectivity curves. And the bi-normal model for the selectivity curve was found to fit the data best.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.42 no.5
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• pp.518-522
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• 2009

The mesh selectivity of drift gill net for yellow croaker (Larimichthys polyactis) was examined in field experiments with six different net mesh size (40, 45, 50, 55, 60 and 65 mm) from April to December, 2008 in the northwestern coastal waters of Gageo-do, Korea. The total catch of 8,091 consisted of yellow croaker (n=7,574; 89.5% of total catch), common mackerel (n=162; 4.8%) and other species (n=355; 5.8%). The selectivity curve for the small size yellow croaker was fit by Kitahara's method to the polynomial equation S(R)=exp{($-0.552R^3$+$4.927R^2$-11.591R+9.320)-6.717}. The optimal mesh size for 50% retention for minimum landing size(191mm) of yellow croaker was estimated as 51.1 mm. This is very similar to the current drift net mesh size used in Gageo-do.