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Journal articles on the topic 'Raphidophyceans'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Band-Schmidt, Christine J., Lourdes Morquecho, David U. Hernández-Becerril, Amada Reyes-Salinas, and Ernesto Bravo-Sierra. "Raphidophyceans on the coasts of Mexico." Hydrobiologia 515, no. 1-3 (2004): 79–89. http://dx.doi.org/10.1023/b:hydr.0000027320.00977.8b.

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2

Pérez-Morales, A., and C. J. Band-Schmidt. "BREVETOXINAS EN LAS COSTAS DE MÉXICO: EFECTOS POTENCIALES EN LA SALUD PÚBLICA." CICIMAR Oceánides 26, no. 2 (2011): 59. http://dx.doi.org/10.37543/oceanides.v26i2.103.

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Las brevetoxinas provocan la intoxicación neurotóxica por mariscos. Las rutas principales son por ingesta e inhalación con efectos adversos en la salud. A nivel celular las brevetoxinas activan los canales de sodio sensibles al voltaje, permitiendo la entrada de iones de sodio y despolarizando la membrana nerviosa. Diversas especies de microalgas producen estas toxinas, principalmente dinoflagelados del género Karenia, así como rafidofíceas de los géneros Chattonella, Fibrocapsa y Heterosigma. El objetivo de este manuscrito es describir las brevetoxinas, los organismos que las producen, sus me

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3

Moreira, González Angel Ramón. "Nuevos registros de flagelados causantes de mareas rojas en la bahía de Cienfuegos, Cuba." Revista de Investigaciones Marinas 44, no. 2 (2024): e-10324. https://doi.org/10.5281/zenodo.14047654.

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Nuevos registros de flagelados marinos causantes de discoloraciones del agua fueron documentados para la bahía de Cienfuegos, centro-sur de Cuba. Estas floraciones fueron ocasionadas por la rafidofita <em>Chattonella subsalsa</em>, y los dinoflagelados <em>Akashiwo sanguinea</em> y <em>Prorocentrum gracile</em>. <em>Akashiwo sanguinea</em> presentó la mayor densidad celular en la floración, mientras que <em>Chattonella subsalsa</em> presentó la menor. Se brinda información acerca de la morfología, distribución y potencial nocividad de estas micr

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4

Servienė, Elena, Irena Kemežienė, Jūratė Kasperovičienė, Brigita Čapukoitienė, Vida Rančelienė, and Judita Koreivienė. "Optimization of DNA isolation and PCR parameters for RAPD analysis of Gonyostomum semen (Raphidophyceae)." Botanica Lithuanica 18, no. 1 (2012): 40–45. http://dx.doi.org/10.2478/v10279-012-0006-6.

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Abstract Servienė E., Kemežienė I., Kasperovičienė J., čapukoitienė B., Rančelienė V., Koreivienė J., 2012: Optimization of DNA isolation and PCR parameters for RAPD analysis of Gonyostomum semen (Raphidophyceae) [DNR izoliavimas ir PGR parametrų optimizavimas Gonyostomum semen (Raphidophyceae) dumblių RAPD analizei]. - Bot. Lith., 18(1): 40-45. The genomic DNA purification method for Gonyostomum semen algae was optimized by applying different DNA purification techniques and rational modifications. This method allowed to obtain high quality DNA preparations suitable for the phylogenetic analys

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5

Fani, F., C. Nuccio, L. Lazzara, L. Massi, C. Battocchi, and A. Penna Abstract. "Fibrocapsa japonica (Raphidophyceae) occurrence and ecological features within the phytoplankton assemblage of a cyclonic eddy, offshore the Eastern Alboran Sea." Mediterranean Marine Science 15, no. 2 (2014): 250–62. https://doi.org/10.12681/mms.398.

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Fani, F., Nuccio, C., Lazzara, L., Massi, L., Battocchi, C., Abstract, A. Penna (2014): Fibrocapsa japonica (Raphidophyceae) occurrence and ecological features within the phytoplankton assemblage of a cyclonic eddy, offshore the Eastern Alboran Sea. Mediterranean Marine Science 15 (2): 250-262, DOI: 10.12681/mms.398, URL: http://dx.doi.org/10.12681/mms.398

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6

Lee, Juyun, Man Chang, and Myung-Soo Han. "Effect of Salinity and Micronutrients on the Growth Rate of Bloom from Heterosigma akashiwo (Raphidophyceae)." Korean Journal of Environmental Biology 32, no. 2 (2014): 129–37. http://dx.doi.org/10.11626/kjeb.2014.32.2.129.

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7

Cronberg, Gertrud. "The life cycle ofGonyostomum semen(Raphidophyceae)." Phycologia 44, no. 3 (2005): 285–93. http://dx.doi.org/10.2216/0031-8884(2005)44[285:tlcogs]2.0.co;2.

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8

Oda, Tatsuya, Atsushi Nakamura, Midori Shikayama, Ienobu Kawano, Atsushi Ishimatsu, and Tsuyoshi Muramatsu. "Generation of Reactive Oxygen Species by Raphidophycean Phytoplankton." Bioscience, Biotechnology, and Biochemistry 61, no. 10 (1997): 1658–62. http://dx.doi.org/10.1271/bbb.61.1658.

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9

Romanov, R. E., and A. A. Gontcharov. "New algae species records (Chlorophyta, Cryptophyta, Ochrophyta) for the southern regions of West-Siberian Plain and Far East." Проблемы ботаники южной сибири и монголии 20, no. 1 (2021): 379–82. http://dx.doi.org/10.14258/pbssm.2021076.

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The new records of genera and species of algae (Chlorodendrophyceae, Chlorophyceae, Cryptophyceae,Mesostigmatophyceae, Raphidophyceae, Xanthophyceae) for the West-Siberian Plain and the Far East, including AltaiKrai, Novosibirsk Oblast and Primorskii Krai, were revealed. All species listed are new ones for the regions, 3 genera and14 species are new for West-Siberian Plain and the Far East, including 1 genus new for Siberia and 1 genus new for the FarEast. The localities and regional distribution are reported for each species.

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10

Hara, Yoshiaki, and Mitsuo Chihara. "Morphology, ultrastructure and taxonomy of the raphidophycean algaHeterosigma akashiwo." Botanical Magazine Tokyo 100, no. 2 (1987): 151–63. http://dx.doi.org/10.1007/bf02488320.

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11

Vesk, M., and �. Moestrup. "The flagellar root system inHeterosigma akashiwo (Raphidophyceae)." Protoplasma 137, no. 1 (1987): 15–28. http://dx.doi.org/10.1007/bf01281173.

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12

Kim, Joo-Hwan, Bum Soo Park, Pengbin Wang, Jin Ho Kim, Seok Hyun Youn, and Myung-Soo Han. "Cyst morphology and germination in Heterosigma akashiwo (Raphidophyceae)." Phycologia 54, no. 5 (2015): 435–39. http://dx.doi.org/10.2216/15-26.1.

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13

Hara, Yoshiaki, and Mitsuo Chihara. "Ultrastructure and taxonomy of Fibrocapsa japonica (class raphidophyceae)." Archiv für Protistenkunde 130, no. 1-2 (1985): 133–41. http://dx.doi.org/10.1016/s0003-9365(85)80038-5.

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14

Khan, Saleha, Osamu Arakawa, and Yoshio Onoue. "Neurotoxin Production by a Chloromonad Fibrocapsa japonica (Raphidophyceae)." Journal of the World Aquaculture Society 27, no. 3 (1996): 254–63. http://dx.doi.org/10.1111/j.1749-7345.1996.tb00607.x.

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15

Throndsen, Jahn. "Note on the taxonomy of Heterosigma akashiwo (Raphidophyceae)." Phycologia 35, no. 4 (1996): 367. http://dx.doi.org/10.2216/i0031-8884-35-4-367.1.

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16

de Boer, M. Karin, Monika R. Tyl, Meng Fu, et al. "Haemolytic activity within the species Fibrocapsa japonica (Raphidophyceae)." Harmful Algae 8, no. 5 (2009): 699–705. http://dx.doi.org/10.1016/j.hal.2009.02.001.

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17

Noh, Il-Hyeon, Seok-Jin Oh, Jong-Sick Park, Hyeon-Ho Shin, and Yang-Ho Yoon. "Growth Kinetics on the Nutrient of the Harmful Algae Chattonella marina and C. ovata (Raphidophyceae) Isolated from the South Sea of Korea." Korean Journal of Fisheries and Aquatic Sciences 42, no. 6 (2009): 674–82. http://dx.doi.org/10.5657/kfas.2009.42.6.674.

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18

Hagman, Camilla Hedlund Corneliussen, Thomas Rohrlack, Silvio Uhlig, and Vladyslava Hostyeva. "Heteroxanthin as a pigment biomarker for Gonyostomum semen (Raphidophyceae)." PLOS ONE 14, no. 12 (2019): e0226650. http://dx.doi.org/10.1371/journal.pone.0226650.

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19

Shikata, Tomoyuki, Souta Yoshikawa, Tadashi Matsubara, et al. "Growth dynamics ofHeterosigma akashiwo(Raphidophyceae) in Hakata Bay, Japan." European Journal of Phycology 43, no. 4 (2008): 395–411. http://dx.doi.org/10.1080/09670260801979295.

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20

Leborans, Gregorio Fernandez, and A. Novillo. "Toxicity and bioaccumulation of cadmium in Olisthodiscus luteus (Raphidophyceae)." Water Research 30, no. 1 (1996): 57–62. http://dx.doi.org/10.1016/0043-1354(95)00084-x.

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21

Kai, A. K. L., Y. K. Cheung, P. K. K. Yeung, and J. T. Y. Wong. "Development of single-cell PCR methods for the Raphidophyceae." Harmful Algae 5, no. 6 (2006): 649–57. http://dx.doi.org/10.1016/j.hal.2006.01.002.

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22

Kato, Junichi, Junya Amie, Yoshinori Murata, Akio Kuroda, Atsushi Mitsutani, and Hisao Ohtake. "Development of a Genetic Transformation System for an Alga-Lysing Bacterium." Applied and Environmental Microbiology 64, no. 6 (1998): 2061–64. http://dx.doi.org/10.1128/aem.64.6.2061-2064.1998.

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ABSTRACT Four marine bacteria, Alteromonas sp. strains A27, A28, A29, and A30, that lyse the diatom Skeletonema costatumNIES-324 were isolated from coastal seawater samples. They were also able to lyse the diatoms Thalassiosira sp. andEucampia zodiacs and the raphidophycean flagellateChattonella antiqua. Cryptic indigenous plasmids, designated pAS28 and pAS29, were detected in Alteromonassp. strains A28 and A29, respectively. These plasmids appeared to be similar based on size and restriction site analysis. A shuttle vector that replicates in Escherichia coli andAlteromonas sp. strain A28 was

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23

OKAMOTO, Tarou, Daekyung KIM, Tatsuya ODA, Kazumi MATSUOKA, Atsushi ISHIMATSU, and Tsuyoshi MURAMATSU. "Concanavalin A-Induced Discharge of Glycocalyx of Raphidophycean Flagellates,Chattonella marinaandHeterosigma akashiwo." Bioscience, Biotechnology, and Biochemistry 64, no. 8 (2000): 1767–70. http://dx.doi.org/10.1271/bbb.64.1767.

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24

Tarutani, K., K. Nagasaki, and M. Yamaguchi. "Virus adsorption process determines virus susceptibility in Heterosigma akashiwo (Raphidophyceae)." Aquatic Microbial Ecology 42 (2006): 209–13. http://dx.doi.org/10.3354/ame042209.

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25

TAKEMOTO, Youichi, Katsuhiro FURUMOTO, and Akihide TADA. "DIEL VERTICAL MIGRATION OF Gonyostomum semen (Raphidophyceae) IN KAWAHARA LAKE." PROCEEDINGS OF HYDRAULIC ENGINEERING 46 (2002): 1061–66. http://dx.doi.org/10.2208/prohe.46.1061.

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26

Itakura, Shigeru, Keizo Nagasaki, Mineo Yamaguchi, and Ichiro Imai. "Cyst formation in the red tide flagellate Heterosigma akashiwo (Raphidophyceae)." Journal of Plankton Research 18, no. 10 (1996): 1975–79. http://dx.doi.org/10.1093/plankt/18.10.1975.

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27

Kahn, S., O. Arakawa &, and Y. Onoue. "Physiological investigations of a neurotoxin-producing phytoflagellate, Chattonella marina (Raphidophyceae)." Aquaculture Research 29, no. 1 (1998): 9–17. http://dx.doi.org/10.1111/j.1365-2109.1998.tb01096.x.

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28

Khan, Saleha, Osamu Arakawa, and Yoshio Onoue. "Growth Characteristics of a Neurotoxin-Producing Chloromonad Fibrocapsa japonica (Raphidophyceae)." Journal of the World Aquaculture Society 27, no. 3 (1996): 247–53. http://dx.doi.org/10.1111/j.1749-7345.1996.tb00606.x.

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29

Khan, S., O. Arakawa, and Y. Onoue. "A toxicological study of the marine phytoflagellate, Chattonella antiqua (Raphidophyceae)." Phycologia 35, no. 3 (1996): 239–44. http://dx.doi.org/10.2216/i0031-8884-35-3-239.1.

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30

Patterson, Glenn W., and Shirley D. Valkenburg. "STEROLS OF DICTYOCHA FIBULA (CHRYSOPHYCEAE) AND OLISTHODISCUS LUTEUS (RAPHIDOPHYCEAE)1." Journal of Phycology 26, no. 3 (1990): 484–89. http://dx.doi.org/10.1111/j.0022-3646.1990.00484.x.

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31

Mangahas, Jeff L., Rose Ann Cattolico, and Ann E. Reynolds. "ANALYSIS OF HETEROSIGMA CARTERAE1 (CHROMOPHYTA, RAPHIDOPHYCEAE) CHLOROPLAST rpoB GENE SEQUENCE2." Journal of Phycology 31, no. 5 (1995): 808–12. http://dx.doi.org/10.1111/j.0022-3646.1995.00808.x.

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32

Figueroa, Rosa Isabel, and Karin Rengefors. "LIFE CYLE AND SEXUALITY OF THE FRESHWATER RAPHIDOPHYTEGONYOSTOMUM SEMEN(RAPHIDOPHYCEAE)." Journal of Phycology 42, no. 4 (2006): 859–71. http://dx.doi.org/10.1111/j.1529-8817.2006.00240.x.

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33

Dingman, Jennifer E., and Janice E. Lawrence. "Heat-stress-induced programmed cell death in Heterosigma akashiwo (Raphidophyceae)." Harmful Algae 16 (April 2012): 108–16. http://dx.doi.org/10.1016/j.hal.2012.02.003.

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34

Branco, S., M. Menezes, C. Alves-de-Souza, P. Domingos, MA Schramm, and LAO Proença. "Recurrent blooms of Heterosigma akashiwo (Raphidophyceae) in the Piraquê Channel, Rodrigo de Freitas Lagoon, southeast Brazil." Brazilian Journal of Biology 74, no. 3 (2014): 529–37. http://dx.doi.org/10.1590/bjb.2014.0074.

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Six blooms of Heterosigma akashiwo(Raphidophyceae) were observed from March 2007 through March 2008 in the Rodrigo de Freitas Lagoon, a semi-confined eutrophic system located in Rio de Janeiro state, southeast Brazil. Vegetative cells of H. akashiwo analysed by optical and electron microscopy showed morphology as described in the literature. The blooms (2.8 × 104 to 4 × 108 cell.L–1) were restricted to the middle section of the Piraquê Channel, which is situated in the northeastern part of the lagoon and receives freshwater inflow. The salinity of subsurface water and the channel depth showed

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35

Barría, Camila, Piera Vásquez-Calderón, Catalina Lizama, et al. "Spatial Temporal Expansion of Harmful Algal Blooms in Chile: A Review of 65 Years Records." Journal of Marine Science and Engineering 10, no. 12 (2022): 1868. http://dx.doi.org/10.3390/jmse10121868.

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Harmful Algal Blooms (HABs) have been classified depending on the causative organism and its impacts: non-toxic HAB (microalgae capable of affecting tourism and causing oxygen deficiency, which generates mortality of marine organisms), toxic HAB (microalgae capable of transferring toxins to the food chain), and ichthyotoxic HAB (microalgae capable of generating mechanical damage in fish). HABs represent a worldwide problem and have apparently increased in frequency, intensity, and geographic distribution at different latitudes. This review details the occurrence of HAB events in the Southeast

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36

Menezes, Mariângela, and Carlos Eduardo de Mattos Bicudo. "Freshwater Raphidophyceae from the State of Rio de Janeiro, Southeast Brazil." Biota Neotropica 10, no. 3 (2010): 323–31. http://dx.doi.org/10.1590/s1676-06032010000300030.

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This paper presents a floristic survey of Raphidophyceae (Heterokontophyta) found in three freshwater environments in the municipality of Rio de Janeiro, based on samples collected bimonthly from September 1988 to August 1991. A total of 117 samples were collected, and eight of these contained cells of raphidophytes. Altogether five raphidophyte species, representing the genera Gonyostomum (2), Merotrichia (1), and Vacuolaria (2) were identified. Four species are new records for the State of Rio de Janeiro (G. semen, G. depressum, M. bacillata, V. virescens var. virescens), and one is reported

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37

NISHIBORI, Naoyoshi, and Shinsuke FUJIHARA. "Changes in intracellular polyamine concentration during growth of Heterosigma akashiwo (Raphidophyceae)." Fisheries Science 72, no. 2 (2006): 350–55. http://dx.doi.org/10.1111/j.1444-2906.2006.01156.x.

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38

Branco, Suema, Lidiane L. Almeida, Catharina Alves‐de‐Souza, Mair M. M. Oliveira, Luis A. O. Proença, and Mariângela Menezes. "Morphological and genetic characterization of bloom‐forming Raphidophyceae from Brazilian coast." Phycological Research 67, no. 4 (2019): 279–90. http://dx.doi.org/10.1111/pre.12377.

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39

Eloranta, Pertti, and Marjo Järvinen. "Growth of Gonyostomum semen (Ehr.) Diesing (Raphidophyceae): Results from culture experiments." SIL Proceedings, 1922-2010 24, no. 4 (1991): 2657–59. http://dx.doi.org/10.1080/03680770.1989.11900047.

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40

Billard, Chantal. "Fibrocapsa japonica (Raphidophyceae), algue planctonique nouvelle pour les côtes de France." Cryptogamie. Algologie 13, no. 3 (1992): 225–31. http://dx.doi.org/10.5962/p.309351.

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41

Veluppillai, J. M., M. A. Jacobs, M. R. Duplessis, L. Choi, and R. A. Cattolico. "165 The Chloroplast Genome of the Toxic Stramenopile Heterosigma Akashiwo (Raphidophyceae)." Journal of Phycology 39, s1 (2003): 57. http://dx.doi.org/10.1111/j.0022-3646.2003.03906001_165.x.

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42

Demura, Mikihide, Takuro Nakayama, Fumie Kasai, and Masanobu Kawachi. "Genetic structure of JapaneseChattonella marina(Raphidophyceae) populations revealed using microsatellite markers." Phycological Research 62, no. 2 (2014): 102–8. http://dx.doi.org/10.1111/pre.12047.

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43

Garg, Shikha, Andrew L. Rose, Aurélie Godrant, and T. David Waite. "Iron uptake by the ichthyotoxicChattonella marina(Raphidophyceae): impact of superoxide generation1." Journal of Phycology 43, no. 5 (2007): 978–91. http://dx.doi.org/10.1111/j.1529-8817.2007.00394.x.

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44

Heywood, Peter. "Binucleate cells and bimitosis occur in cultures of the raphidophycean alga Vacuolaria virescens and are inducible by caffeine." Nova Hedwigia 119, no. 3-4 (2024): 251–60. https://doi.org/10.1127/nova_hedwigia/2024/1043.

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45

Karol, Kenneth G., Michael A. Jacobs, Yang Zhou, Elizabeth H. Sims, Will D. Gillett, and Rose Ann Cattolico. "Comparative analysis of complete mitochondrial genome sequences from two geographically distinct Heterosigma akashiwo (Raphidophyceae) strains." Nova Hedwigia, Beihefte 136 (June 24, 2010): 261–82. http://dx.doi.org/10.1127/1438-9134/2010/0136-0261.

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46

Passarinho, Kathrin Nere, Maria Rosélia Marques Lopes, and Sueli Train. "Diel responses of phytoplankton of an Amazon floodplain lake at the two main hydrological phases." Acta Limnologica Brasiliensia 25, no. 4 (2013): 361–74. http://dx.doi.org/10.1590/s2179-975x2013000400002.

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AIM: This study examines the short-term changes of phytoplankton in an oxbow lake on the floodplain of the Acre River, Amazonia, Brazil. METHODS: Samples were taken with a Van Dorn bottle, at three depths (surface, middle and bottom), in two periods (low waters and high waters), for seven consecutive days in two schedules, night and morning. RESULTS: Phytoplankton was represented by 198 taxa and the Class Euglenophyceae, with 62 taxa, was the best-represented group in both periods. There were abrupt changes in the community during the high waters (potamophase). During this period, in condition

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47

Merino-Virgilio, Fany Del Carmen, Yuri B. Okolodkov, Ana C. Aguilar-Trujillo, and Jorge A. Herrera- Silveira. "Phytoplankton of the northern coastal and shelf waters of the Yucatan Peninsula, southeastern Gulf of Mexico, Mexico." Check List 9, no. 4 (2013): 771. http://dx.doi.org/10.15560/9.4.771.

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Based on long-term monitoring (2001-2012) and four oceanographic cruises (2010-2012) in the coastal and shelf waters of the Yucatan Peninsula, SE Gulf of Mexico, a list of 306 strictly phytoplanktonic and tychoplanktonic species from 131 genera is presented: centric diatoms (83 species), raphid diatoms (47), araphid diatoms (22), Dinoflagellata (124), Cyanoprokaryota (18), Ebriacea (2), Chlorophyceae (3), Dictyochophyceae (2), Euglenophyceae (2), Cryptophyceae (1), Prymnesiophyceae (1), and Raphidophyceae (1). Diatoms also dominated the number of genera (80) followed by dinoflagellates (39) an

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48

Dochin, Kostadin. "Phytoplankton species composition in seven fish ponds with a grass carp polyculture (2018-2019)." Annual of Sofia University "St. Kliment Ohridski", Faculty of Biology, Book 2 – Botany 104 (2020): 58–74. http://dx.doi.org/10.60066/gsu.biofac.bot.104.58-74.

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The present article is an attempt to analyze the seasonal changes in the structure and the biomass of phytoplankton in fish ponds with a polyculture with two-year-old grass carp as a mean of biological control of unwanted aquatic vegetation. During a two-year study (2018-2019), 259 planktonic algae were identified with considerably higher number of species during the first year (216) in comparison with the second year (150), when the grass carp stocking densities were twice less. This decrease in the biodiversity was accompanied by a significant change in the dominant structure: in 2018, the m

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49

Merino-Virgilio, Fany, Yuri Okolodkov, Ana Aguilar-Trujillo, and Silveira Jorge Herrera-. "Phytoplankton of the northern coastal and shelf waters of the Yucatan Peninsula, southeastern Gulf of Mexico, Mexico." Check List 9, no. (4) (2013): 771–79. https://doi.org/10.15560/9.4.771.

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Based on long-term monitoring (2001-2012) and four oceanographic cruises (2010-2012) in the coastal and shelf waters of the Yucatan Peninsula, SE Gulf of Mexico, a list of 306 strictly phytoplanktonic and tychoplanktonic species from 131 genera is presented: centric diatoms (83 species), raphid diatoms (47), araphid diatoms (22), Dinoflagellata (124), Cyanoprokaryota (18), Ebriacea (2), Chlorophyceae (3), Dictyochophyceae (2), Euglenophyceae (2), Cryptophyceae (1), Prymnesiophyceae (1), and Raphidophyceae (1). Diatoms also dominated the number of genera (80) followed by dinoflagellates (39) an

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50

Münzner, Karla, Raphael Gollnisch, Karin Rengefors, Judita Koreiviene, and Eva S. Lindström. "High Iron Requirements for Growth in the Nuisance Alga Gonyostomum semen (Raphidophyceae)." Journal of Phycology 57, no. 4 (2021): 1309–22. http://dx.doi.org/10.1111/jpy.13170.

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