Application of a fluorescence in situ hybridization (FISH) method to study green tides in the Yellow Sea

被引:13
|
作者
Zhang, Qing-Chun [1 ]
Liu, Qing [1 ,2 ]
Yu, Ren-Cheng [1 ]
Kang, Zhen-Jun [1 ,2 ]
Guo, Wei [1 ,2 ]
Ding, Yue-Min [1 ,2 ]
Chen, Jian-Hua [1 ,2 ]
Wang, Yun-Feng [1 ]
Li, Yan [3 ]
Yan, Tian [1 ]
Zhou, Ming-Jiang [1 ]
机构
[1] Chinese Acad Sci, Inst Oceanol, Key Lab Marine Ecol & Environm Sci, Qingdao 266071, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] State Ocean Adm, Key Lab Sci & Engn Marine Ecol & Environm, Qingdao 266061, Peoples R China
基金
中国国家自然科学基金;
关键词
green tide; Ulva prolifera; fluorescence in situ hybridization (FISH); Yellow Sea; ENTEROMORPHA-PROLIFERA; SEAWEED AQUACULTURE; ULVA-PROLIFERA; CHLOROPHYTA; GROWTH; ALGAE; ULVOPHYCEAE; MACROALGAE; DIVERSITY; EXPANSION;
D O I
10.1016/j.ecss.2014.09.005
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Massive green tides of Ulva prolifera have been recorded consecutively since 2007 in the Yellow Sea (YS). It has been proposed that the floating green algae in the YS are originally from the culture rafts of Porphyra yezoensis in the Subei Shoal. However, there is still much debate about this, mainly due to the difficulty in rapid and accurate identification of U. prolifera. In this study, a developed fluorescence in situ hybridization (FISH) method was adopted to identify U. prolifera and assess its relative abundance in the green algal community. Using this method, several processes related to the formation of green tides were studied, including: (1) variation of the relative abundance of U. prolifera in the green algal community attached to Porphyra rafts in the Subei Shoal; (2) contribution of the microscopic propagules in seawater to the U. prolifera population attached to the rafts; and (3) variation of the proportion of U. prolifera in the floating green algae in the YS. U. prolifera were detected in the green algae attached to Porphyra rafts from March to May 2012, where its relative abundance increased rapidly from 10% at the end of April to 40 -60% in mid-May. Microscopic propagules of U. prolifera, which could be detected from seawater and sediment, contributed significantly to the dramatic increase of the attached U. prolifera on the Porphyra rafts. After the attached green algae were removed from the rafts, U. prolifera rapidly demonstrated dominance in the floating green algal community, and the proportion of U. prolifera increased gradually from south to north. Our conceptual model is that the germination of U. prolifera microscopic propagules on Porphyra rafts promotes the proliferation of attached U. prolifera on the rafts, which release more microscopic propagules into seawater and sediments after they became mature. This positive feedback enhances the dominance of U. prolifera in the attached green algal community in late May, which leads to the formation of green tides after the attached plants are removed from the rafts during Porphyra harvest. The proportion of U. prolifera then increases rapidly in the resuspended and floating green algal community due to its unique structure, making it the most dominant species of floating green algae. The application of the FISH method clearly depicted the early development of green tides in the Subei Shoal and greatly helped to solidify the proposed linkage between Porphyra culture rafts and the formation of green tides in the YS. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:112 / 119
页数:8
相关论文
共 50 条
  • [31] Distribution characteristics of green tides and its impact on environment in the Yellow Sea
    Wang, Sheng
    Zhao, Liang
    Wang, Yuheng
    Zhang, Haiyan
    Li, Fei
    Zhang, Yijie
    [J]. MARINE ENVIRONMENTAL RESEARCH, 2022, 181
  • [32] A Fluorescence In Situ Hybridization (FISH) Test for Diagnosing Babesiosis
    Shah, Jyotsna S.
    Mark, Olivia
    Caoili, Eddie
    Poruri, Akhila
    Horowitz, Richard I.
    Ashbaugh, Alan D.
    Ramasamy, Ranjan
    [J]. DIAGNOSTICS, 2020, 10 (06)
  • [33] A fluorescence in situ hybridization (FISH) protocol for stickleback tissue
    James, Noelle
    Liu, Xiaochen
    Bell, Alison
    [J]. EVOLUTIONARY ECOLOGY RESEARCH, 2016, 17 (04) : 603 - 617
  • [34] Fluorescence in situ hybridization (FISH) for the rapid diagnosis of melioidosis
    Hagen, R. M.
    Frickmann, H.
    Elschner, M.
    Melzer, F.
    Neubauer, H.
    Racz, P.
    Poppert, S.
    [J]. TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2011, 16 : 262 - 262
  • [35] Oncogene amplification detection by fluorescence in situ hybridization (FISH)
    Ooi, A
    [J]. ACTA HISTOCHEMICA ET CYTOCHEMICA, 2001, 34 (06) : 391 - 397
  • [36] Fluorescence in situ hybridization (FISH) for direct visualization of microorganisms
    Moter, A
    Göbel, UB
    [J]. JOURNAL OF MICROBIOLOGICAL METHODS, 2000, 41 (02) : 85 - 112
  • [37] Fluorescence in Situ Hybridization (FISH) assay in melanoma prognostication
    Dyduch, G.
    Sinczak-Kuta, A.
    Szpor, J.
    Bialas, M.
    Demczuk, S.
    Okon, K.
    [J]. VIRCHOWS ARCHIV, 2013, 463 (02) : 127 - 127
  • [38] Fluorescence in situ hybridization (FISH):: Overview and medical applications
    Anguiano, A
    [J]. JOURNAL OF CLINICAL LIGAND ASSAY, 2000, 23 (01): : 33 - 42
  • [39] Fluorescence in situ hybridization (FISH) in pigmented neoplasm diagnostics
    Frank, G.
    Ryazantseva, A.
    Zavalishina, L.
    Andreeva, Y.
    [J]. VIRCHOWS ARCHIV, 2009, 455 : 274 - 274
  • [40] Fluorescence in situ hybridization(FISH) in the diagnosis of urine samples
    Colom, H
    Lowery-Nordberg, M
    Herrera, GA
    Turbat-Herrera, EA
    [J]. MODERN PATHOLOGY, 2001, 14 (01) : 50A - 50A