Retrospective analysis of the marine flora of Vostok Bay, Sea of Japan

Kozhenkova, S. I.

doi:10.1134/s1063074009040014

Cited by 17 publications

(8 citation statements)

References 5 publications

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“…It is now known to have a distribution in the eastern North Pacific from the Kodiak Archipelago, Alaska, to Baja California, Mexico (Abbott and Hollenberg 1976, Hawkes et al 1978, Scagel et al 1989, Lindeberg and Lindstrom 2010, Riosmena-Rodríguez et al 2011. The known distribution for D. serrulata is from northern Japan (Okamura 1908), Korea (Lee and Kang 1986), and eastern Russia (Perestenko 1996, Kozhenkova 2009). The Delesseria serrulata depicted from Australia by Harvey (1858, Pl.…”

Section: Discussionmentioning

confidence: 99%

Taxonomic assessment of North American species of the genera Cumathamnion, Delesseria, Membranoptera and Pantoneura (Delesseriaceae, Rhodophyta) using molecular data

Wynne¹,

Saunders²

2012

ALGAE

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Evidence from molecular data supports the close taxonomic relationship of the two North Pacific species Delesseria decipiens and D. serrulata with Cumathamnion, up to now a monotypic genus known only from northern California, rather than with D. sanguinea, the type of the genus Delesseria and known only from the northeastern North Atlantic. The transfers of D. decipiens and D. serrulata into Cumathamnion are effected. Molecular data also reveal that what has passed as Membranoptera alata in the northwestern North Atlantic is distinct at the species level from northeastern North Atlantic (European) material; M. alata has a type locality in England. Multiple collections of Membranoptera and Pantoneura fabriciana on the North American coast of the North Atlantic prove to be identical for the three markers that have been sequenced, and the name Membranoptera fabriciana (Lyngbye) comb. nov. is proposed for them. Many collections of Membranoptera from the northeastern North Pacific (predominantly British Columbia), although representing the morphologies of several species that have been previously recognized, are genetically assignable to a single group for which the oldest name applicable is M. platyphylla.Key Words: Cumathamnion; Delesseria; Delesseriaceae; Membranoptera; molecular markers; Pantoneura; Rhodophyta; taxonomy INTRODUCTIONThe generitype of Delesseria J. V. Lamour. is D. sanguinea (Huds.) J. V. Lamour., a species occurring in the colder waters of the northeastern Atlantic Ocean, ranging from Arctic Norway and Iceland to Spain (South and Tittley 1986), as well as a reduced form extending into the Baltic Sea (Levring 1940, Nellen 1966, Lüning 1990. Its handsome image depicted by Oeder in Flora danica (1766, Pl. 349, as Fucus sanguineus) and reproduced in Wynne (2006) was based on a specimen collected in Iceland by Johann Gerhard König, a student of Linnaeus, in 1764-1765 and initially illustrated in the field by Helt, a young illustrator who accompanied König to Iceland. Helt's preliminary sketch was later refined in Copenhagen by Rösler (information from Peter Wagner, communicated by Ruth Nielsen, Copenhagen). Being a genus described so early (Lamouroux 1813), Delesseria has had numerous species assigned to it over the years. For example, J. Agardh (1872) assigned 48 species to his broadly defined Delesseria. Fifteen species are currently recognized in the genus (Guiry and Guiry 2012). This list of taxa now placed in DelesseriaReceived May 11, 2012, Accepted August 12, 2012 *Corresponding Author E-mail: mwynne@umich.edu Tel: This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. 156(Hudson) Stackhouse, the generitype, has been recognized on both sides of the North Atlantic (Rosenvinge 1923-1924, Taylor 1962, Bird and McLachlan 1992, Maggs and Hommersand...

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Section: Discussionmentioning

confidence: 99%

Taxonomic assessment of North American species of the genera Cumathamnion, Delesseria, Membranoptera and Pantoneura (Delesseriaceae, Rhodophyta) using molecular data

Wynne¹,

Saunders²

2012

ALGAE

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“…Boo & Brawley and Fucus sp., reported by Zaks (1927), were not found in the present study. The disappearance of fucoids was earlier reported for other parts of Peter the Great Bay (Kozhenkova, 2008) and interpreted as being linked to both climatic changes and anthropogenic pressure. In the previous study on the species composition and biomass of subtidal macrophytes in Sobol Bay by Zaks (1927), three typical assemblages were reported in the spring-summer period: a Phyllospadix iwatensis assemblage; a Sargassum spp., Coccophora langsdorfii and Cystoseira crassipes dominated assemblage with numerous accompanying species; and an assemblage of Desmarestia viridis.…”

Section: Species Groupsmentioning

confidence: 85%

“…According to Perestenko (1980), in Peter the Great Bay, the monodominant assemblages with a high number of accompanying species prevailed. Polydominant assemblages are more characteristic of the southern parts of the Sea of Japan (Kim et al , 1998; Yoo 2003a, b; Chavanich et al , 2006) and shallow bays of Peter the Great Bay (Kozhenkova, 2008). Secondly, among dominant species, algae of warm water affinity ( Undaria pinnatifida , Codium fragile , Ulva lactuca and Coccophora langsdorfii ) are represented.…”

Section: Discussionmentioning

confidence: 99%

“…Perestenko, 1980; Kafanov & Zhukov, 1993; Kashenko, 1999, 2002; Gusarova, 2003, 2008; Yoo 2003a, b; Yatsuya et al , 2007; Kang et al , 2008; Kozhenkova, 2008; Shin et al , 2008), only limited information is available on the dynamics of macrophytes communities. Some publications have described long-term and seasonal changes in macroalgal assemblages along the Russian coast of the Sea of Japan (Kafanov & Zhukov, 1993; Gusarova, 2003, 2008; Kozhenkova, 2008; Levenets & Skriptsova, 2008a) or the eastern coast of Korea (Kim et al , 1998; Kang et al , 2008; Shin et al , 2008), and only a few studies have analysed temporal variations of macrophytes communities in the eastern part of the Sea of Japan (Yatsuya et al , 2007). Studies of seasonal variations of macrophyte assemblages based on quantitative and qualitative estimates of species occurrence showed that both the species diversity and total biomass of the algal community in Peter the Great Bay (Russian coast of the Sea of Japan) were highest from April to July (Kafanov & Zhukov, 1993; Gusarova, 2003).…”

Section: Introductionmentioning

confidence: 99%

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Seasonal dynamics of subtidal macrophyte assemblages in Sobol Bay (Peter the Great Bay, Sea of Japan) in relation to depth

Скрипцова

Levenets

2011

J. Mar. Biol. Ass.

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Seasonal dynamics of subtidal macrophyte assemblages in Sobol Bay (Peter the Great Bay, Sea of Japan) in relation to depth anna v. skriptsova and irina r. levenets A.V. Zhirmunsky Institute of Marine Biology, Far-Eastern Branch of the Russian Academy of Sciences, Vladivostok, 690041, Russia This paper describes the species composition, vertical distribution, and the seasonal changes in the biomass of subtidal macrophytes in Sobol Bay (Peter the Great Bay, Sea of Japan). The samples were collected in the depth-range from 0.5 to 4 m. A total of 65 macrophyte species were identified, among which were 10 species of Chlorophyta, 17 of Phaeophyceae, 37 of Rhodophyta and 1 of Magnoliophyta. Multivariate analyses were performed to detect spatial and temporal variations. Maximum species richness was registered in June, with a particularly dramatic biomass increase of brown algae. Both the number of species and the biomass of macrophytes decreased with increasing depth. Depth clearly affected the patterns of seasonal fluctuations of the species composition and biomass. In the study area, the species composition of the shallow-water algal assemblages was more stable throughout the year compared to that of the algal assemblages found in deeper waters. In total, four macrophyte assemblages were identified in the bay. A Phyllospadix iwatensis and Coccophora langsdorfii dominated assemblage occupied muddy-gravel bottoms in depths from 0.5 to 2 m throughout the year. An assemblage, co-dominated by annual brown algae Desmarestia viridis and Costaria costata, occurred at depths more than 3 m at late spring. Two other assemblages occurred on the rock and boulder bottom at 0.5 -2 m depths, but they were temporally separated. An assemblage co-dominated by annual laminarian algae (Undaria pinnatifida and Costaria costata) developed at late spring and was succeeded in the autumn and winter by a Tichocarpus crinitus, Ulva lactuca, Sargassum pallidum and Codium fragile co-dominated assemblage. A comparison between the data obtained in the present study and the results of a previous study conducted in 1927 shows that the macrophytes assemblages in Sobol Bay underwent little change.

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“…The red alga Gelidium vagum Okamura commonly occurs in Korea, Japan, China and far eastern Russia (Kang 1966, Zhang and Xia 1988, Yoshida 1998, Kozhenkova 2009. The species was first described on the basis of intertidal specimens from western coast of Hokkaido to Iwaki Province (Okamura 1934).…”

Section: Introductionmentioning

confidence: 99%

Mitochondrial cox1 and cob sequence diversities in Gelidium vagum (Gelidiales, Rhodophyta) in Korea

Yoon¹,

Kim²,

Boo³

et al. 2014

ALGAE

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The number of species of non-native and invasive marine algae is growing, with concomitant public concern about native ecosystems and coastlines. Gelidium vagum, recently introduced from northeast Asia to Europe and North America, commonly occurs from the intertidal to subtidal zones in Korea, China, and Japan. To investigate the level of genetic diversity of native populations, we analyzed mitochondrial cox1 and cob from 108 specimens of G. vagum from Korea, China, eastern Russia, including from the Netherlands and USA. The haplotype network of individual and cox1 + cob datasets revealed no genetic structure in local populations, suggesting genetic flow between Korean populations. Our results corroborate a typical pattern of genetic diversity for introduced species, with low levels in introduced populations and high levels in native populations. All haplotypes were shared between the Netherlands and USA, but not between Korea and the Netherlands / USA except cox1. Additional sampling will identify donor populations in native northeast Asian waters. This is the first report of the utility of the mitochondrial coding cob sequences in red algae.

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Retrospective analysis of the marine flora of Vostok Bay, Sea of Japan

Cited by 17 publications

References 5 publications

Taxonomic assessment of North American species of the genera Cumathamnion, Delesseria, Membranoptera and Pantoneura (Delesseriaceae, Rhodophyta) using molecular data

Taxonomic assessment of North American species of the genera Cumathamnion, Delesseria, Membranoptera and Pantoneura (Delesseriaceae, Rhodophyta) using molecular data

Seasonal dynamics of subtidal macrophyte assemblages in Sobol Bay (Peter the Great Bay, Sea of Japan) in relation to depth

Mitochondrial cox1 and cob sequence diversities in Gelidium vagum (Gelidiales, Rhodophyta) in Korea

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