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Journal articles on the topic 'Bangiales'

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1

DUMILAG, RICHARD V., ZAE-ZAE A. AGUINALDO, CYNTHIA B. MINTU, MYRNA P. QUINTO, EVELYN C. AME, ROLANDO C. ANDRES, WILBERTO D. MONOTILLA, et al. "A review of the current taxonomic status of foliose Bangiales (Rhodophyta) in the Philippines." Phytotaxa 312, no. 1 (July 4, 2017): 47. http://dx.doi.org/10.11646/phytotaxa.312.1.3.

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Causes of taxonomic confusion are lamentably well known in foliose Bangiales. A magnitude of these uncertainties stems from the paucity of available taxonomic traits in morphologically homoplastic species. At present, the taxonomic identity and systematics of many of the Philippine foliose Bangiales are in a state of flux. A critical examination of published literature on Philippine records of 10 species of foliose Bangiales has rendered the need for re-confirmation of the presence of Porphyra atropurpurea, Porphyra marcosii, Pyropia denticulata, and Pyropia suborbiculata while records of Porphyra umbilicalis, Pyropia vietnamensis, Wildemania variegata, and the invalid name Porphyra crispata have been omitted from the list. Currently, there are only two confirmed species of foliose Bangiales in the Philippines, which are Pyropia acanthophora and Pyropia tanegashimensis. Thus, this review exhorts a re-examination of collected Philippine foliose Bangiales materials using both morphological and molecular analysis.
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DUMILAG, RICHARD V., ZAE-ZAE A. AGUINALDO, CYNTHIA B. MINTU, MYRNA P. QUINTO, EVELYN C. AME, ROLANDO C. ANDRES, WILBERTO D. MONOTILLA, and SANDRA L. YAP. "Morphological and molecular confirmation of the occurrence of Pyropia tanegashimensis (Bangiales, Rhodophyta) from Palaui Is., Sta. Ana, Cagayan, Philippines." Phytotaxa 255, no. 1 (April 5, 2016): 83. http://dx.doi.org/10.11646/phytotaxa.255.1.8.

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The known morphological features in identifying common species of foliose Bangiales (e.g., members of Pyropia and Porphyra), which are very few and often overlapping, are recently resolved using comparative analysis of DNA sequences and statistics. Records of foliose Bangiales in the Philippines were historically identified based on morphology. Considering the recent radical changes in the taxonomy among these rhodophytes and problems posed by morphology-based identification, taxonomic re-appraisal of Philippine foliose Bangiales based on critical morphological and molecular studies is needed. This study used plastid rbcL and mitochondrial COI-5P gene sequences to investigate the identity of foliose Bangiales collected in Palaui Is., Sta. Ana, Cagayan, Philippines. Observation of key phenotypes revealed the identity of the collected materials as Py. tanegashimensis. Resulting phylogenetic trees showed placement of our collected specimens into a highly supported Py. tanegashimensis clade from Japan and Brazil. Our molecular analysis also suggested that the Philippine Py. tanegashimensis includes endemic populations distinct from the introduced strain originally reported from Brazil.
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3

Dumilag, Richard V., and Sandra L. Yap. "Pyropia lunae sp. nov. and Pyropia islae sp. nov. (Bangiales, Rhodophyta) from the Philippines." Botanica Marina 61, no. 5 (September 25, 2018): 467–80. http://dx.doi.org/10.1515/bot-2018-0024.

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AbstractChallenges in morphology come to bear when assigning specific names in foliose Bangiales. Recent studies suggest that the integration of molecular and phenotypic data is essential, particularly in setting species boundaries and revealing the true species diversity of a given area. In an attempt to further elucidate the diversity of foliose Bangiales in the Philippines, two new species,Pyropia lunaesp. nov. andPyropia islaesp. nov. are described. Each species differs from other closely related taxa by a combination of morphological and anatomical characters, and nucleotide sequences. Phylogenetic reconstruction based onrbcL gene sequences supports the sister relationship ofP. lunaeandPyropia acanthophora, whereasP. islaeis recovered as a species allied toPyropia tanegashimensisandPyropia denticulata. These two previously undescribed species increase the number of confirmed PhilippinePyropiaspecies to four. So far,P. lunaeandP. islaeare found only from the Batanes Islands whileP. acanthophoraandP. tanegashimensisare known to extend their native distributions across into the Indo-Pacific waters. Questions remain, however, with regard to the true species diversity of foliose Bangiales in the Philippines. A wider sampling effort and the application of molecular methods will make it possible to resolve the remaining gaps in the taxonomy of Philippine foliose Bangiales.
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4

Kumar, C. Anil, and M. V. N. Panikkar. "Indian species ofPorphyra (Rhodophyceae, Bangiales)." Feddes Repertorium 108, no. 5-6 (August 1997): 419–23. http://dx.doi.org/10.1002/fedr.4921080516.

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Kumar, C. Anil, and M. V. N. Panikkar. "Indian species of Porphyra (Rhodophyceae, Bangiales)." Feddes Repertorium 108, no. 5-6 (April 18, 2008): 419–23. http://dx.doi.org/10.1002/fedr.19971080516.

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6

Kornmann, P., and P. H. Sahling. "ThePorphyra species of Helgoland (Bangiales, Rhodophyta)." Helgoländer Meeresuntersuchungen 45, no. 1-2 (March 1991): 1–38. http://dx.doi.org/10.1007/bf02365634.

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7

Koizumi, Jiro, Naoki Takatani, Noritoki Kobayashi, Koji Mikami, Kazuo Miyashita, Yumiko Yamano, Akimori Wada, Takashi Maoka, and Masashi Hosokawa. "Carotenoid Profiling of a Red Seaweed Pyropia yezoensis: Insights into Biosynthetic Pathways in the Order Bangiales." Marine Drugs 16, no. 11 (November 1, 2018): 426. http://dx.doi.org/10.3390/md16110426.

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Carotenoids are natural pigments that contribute to light harvesting and photo-protection in photosynthetic organisms. In this study, we analyzed the carotenoid profiles, including mono-hydroxy and epoxy-carotenoids, in the economically valuable red seaweed Pyropia yezoensis, to clarify the detailed biosynthetic and metabolic pathways in the order Bangiales. P. yezoensis contained lutein, zeaxanthin, α-carotene, and β-carotene, as major carotenoids in both the thallus and conchocelis stages. Monohydroxy intermediate carotenoids for the synthesis of lutein with an ε-ring from α-carotene, α-cryptoxanthin (β,ε-caroten-3’-ol), and zeinoxanthin (β,ε-caroten-3-ol) were identified. In addition, β-cryptoxanthin, an intermediate in zeaxanthin synthesis from β-carotene, was also detected. We also identified lutein-5,6-epoxide and antheraxanthin, which are metabolic products of epoxy conversion from lutein and zeaxanthin, respectively, by LC-MS and 1H-NMR. This is the first report of monohydroxy-carotenoids with an ε-ring and 5,6-epoxy-carotenoids in Bangiales. These results provide new insights into the biosynthetic and metabolic pathways of carotenoids in red seaweeds.
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8

Zou, Dinghui, and Kunshan Gao. "Photosynthetic bicarbonate utilization inPorphyra haitanensis (Bangiales, Rhodophyta)." Chinese Science Bulletin 47, no. 19 (October 2002): 1629–33. http://dx.doi.org/10.1007/bf03184112.

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9

Lindstrom, Sandra C., Mandy R. Lindeberg, and Daniel A. Guthrie. "Marine macroalgae of the Aleutian Islands: I. Bangiales." ALGAE 30, no. 4 (December 15, 2015): 247–63. http://dx.doi.org/10.4490/algae.2015.30.4.247.

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10

Kikuchi, Norio, Shogo Arai, Goro Yoshida, Jong-Ahm Shin, Judy E. Broom, Wendy A. Nelson, and Masahiko Miyata. "Porphyra migitae sp. nov. (Bangiales, Rhodophyta) from Japan." Phycologia 49, no. 4 (July 2010): 345–54. http://dx.doi.org/10.2216/09-82.1.

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11

Fujita, Yuji, and Munehisa Saito. "Protoplast isolation and fusion in Porphyra (Bangiales, Rhodophyta)." Hydrobiologia 204-205, no. 1 (September 1990): 161–66. http://dx.doi.org/10.1007/bf00040228.

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12

Xiao-rong, Tang, and Fei Xiu-geng. "Development of suspended conchocelis ofPorphyra haitanensis (Bangiales, Rhodophyta)." Chinese Journal of Oceanology and Limnology 16, no. 4 (December 1998): 339–45. http://dx.doi.org/10.1007/bf02844931.

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13

West, Andrew L., Arthur C. Mathieson, Anita S. Klein, Christopher D. Neefus, and Troy L. Bray. "Molecular ecological studies of New England species of Porphyra (Rhodophyta, Bangiales)." Nova Hedwigia 80, no. 1-2 (February 1, 2005): 1–24. http://dx.doi.org/10.1127/0029-5035/2005/0080-0001.

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14

Nelson, W. A., and J. E. S. Broom. "The identity of Porphyra columbina (Bangiales, Rhodophyta) originally described from the New Zealand subantarctic islands." Australian Systematic Botany 23, no. 1 (2010): 16. http://dx.doi.org/10.1071/sb09032.

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Porphyra columbina Mont. (Bangiales, Rhodophyta) was collected in 1840 from the Auckland Islands in the New Zealand subantarctic region. This name has been applied to bladed Bangiales exhibiting a wide range of morphological forms, and found throughout the New Zealand region and in much of the southern hemisphere, particularly in Australia and Chile. By using morphological and anatomical characters as well as nSSU and rbcL sequence data, Montagne’s description of P. columbina is re-examined in the light of recent collections from the New Zealand region and the Southern Ocean. We conclude that P. columbina is primarily distributed in cold temperate conditions, including the Auckland, Campbell, Antipodes, Chatham and Falkland Islands, and is only rarely present on mainland New Zealand. Specimens from the type locality and other subantarctic locations have a rosette to ovate growth form and are typically less than 5 cm in height/width, with specimens from more northern locations including some ribbon-like growth forms. Thalli are purple to grey, bleaching golden green. Mature specimens have a distinctly spotted appearance, with conspicuous large, purple–red clusters of phyllospores and golden marginal areas of spermatangia. Five unique rbcL haplotypes, differing by 1–6 substitutions, were obtained from 26 specimens, with the most common haplotype found in specimens from the Auckland, Campbell and the Falkland Islands.
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15

Niwa, Kyosuke, and Atsushi Kobiyama. "Speciation in the marine crop Pyropia yezoensis (Bangiales, Rhodophyta)." Journal of Phycology 50, no. 5 (September 3, 2014): 897–900. http://dx.doi.org/10.1111/jpy.12220.

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16

ZOU, Dinghui. "Photosynthetic bicarbonate utilization in Porphyra haitanen-sis (Bangiales, Rhodophyta)." Chinese Science Bulletin 47, no. 19 (2002): 1629. http://dx.doi.org/10.1360/02tb9358.

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17

Choi, Sung-Je, Yonguk Kim, Jawon Shin, Dong-Wook Kim, Hak-Sung Lee, and Chulyung Choi. "Complete chloroplast genome sequences of Pyropia dentata (Bangiales, Rhodophyta)." Mitochondrial DNA Part B 5, no. 2 (April 2, 2020): 1785–86. http://dx.doi.org/10.1080/23802359.2020.1749164.

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18

Wang, Jinfeng, Pu Xu, Jianyi Zhu, Wei Zhou, Jianrong Xu, Xiugeng Fei, and Xuecheng Zhang. "The characterization of color mutations in Bangiaceae (Bangiales, Rhodophyta)." Journal of Applied Phycology 20, no. 5 (November 20, 2007): 499–504. http://dx.doi.org/10.1007/s10811-007-9278-0.

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19

Dumilag, Richard V., and Wilberto D. Monotilla. "Molecular diversity and biogeography of Philippine foliose Bangiales (Rhodophyta)." Journal of Applied Phycology 30, no. 1 (July 1, 2017): 173–86. http://dx.doi.org/10.1007/s10811-017-1201-8.

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20

Lin-sheng, Song, Duan De-lin, Li Xiao-hong, and Li Chen-xi. "Use of rapd for detecting and identifyingPorphyra (Bangiales, Rhodophyta)." Chinese Journal of Oceanology and Limnology 16, no. 3 (September 1998): 237–42. http://dx.doi.org/10.1007/bf02848729.

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21

Cao, Min, Kuipeng Xu, Xinzi Yu, Guiqi Bi, Yang Liu, Fanna Kong, Peipei Sun, et al. "A chromosome‐level genome assembly of Pyropia haitanensis (Bangiales, Rhodophyta)." Molecular Ecology Resources 20, no. 1 (November 12, 2019): 216–27. http://dx.doi.org/10.1111/1755-0998.13102.

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22

Reed, Robert H. "Osmoacclimation inBangia atropurpurea(Rhodophyta, Bangiales): the osmotic role of floridoside." British Phycological Journal 20, no. 3 (September 1985): 211–18. http://dx.doi.org/10.1080/00071618500650221.

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23

Yamazaki, Ayano, Koichi Nakanishi, and Naotsune Saga. "AXENIC TISSUE CULTURE AND MORPHOGENESIS IN PORPHYRA YEZOENSIS (BANGIALES, RHODOPHYTA)." Journal of Phycology 34, no. 6 (December 1998): 1082–87. http://dx.doi.org/10.1046/j.1529-8817.1998.341082.x.

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24

Zhang, Yuan, Xing-hong Yan, and Yusho Aruga. "The Sex and Sex Determination in Pyropia haitanensis (Bangiales, Rhodophyta)." PLoS ONE 8, no. 8 (August 26, 2013): e73414. http://dx.doi.org/10.1371/journal.pone.0073414.

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25

Lee, Hak-Jyung, and Jong-il Choi. "Enhancing temperature tolerance of Pyropia tenera (Bangiales) by inducing mutation." Phycologia 58, no. 5 (September 3, 2019): 496–503. http://dx.doi.org/10.1080/00318884.2019.1623547.

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26

Ohme, Masaru, and Akio Miura. "Tetrad analysis in conchospore germlings of Porphyra yezoensis (Rhodophyta, Bangiales)." Plant Science 57, no. 2 (January 1988): 135–40. http://dx.doi.org/10.1016/0168-9452(88)90079-9.

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27

Wang, Wen Jun, Zong Gen Shen, Xiu Tao Sun, Fu Li Liu, Zhou Rui Liang, Fei Jiu Wang, and Jian Yi Zhu. "Photosynthetic response of Bangia fuscopurpurea (Bangiales, Rhodophyta) towards dehydration and hyposalinity." Biologia 73, no. 4 (April 2018): 333–37. http://dx.doi.org/10.2478/s11756-018-0040-7.

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28

Hwang, Mi-Suk, and In-Gyu Lee. "CHARACTER ANALYSIS AND NUMERICAL TAXONOMY OF PORPHYRA (BANGIALES, RHODOPHYTA) FROM KOREA." ALGAE 17, no. 4 (December 31, 2002): 217–33. http://dx.doi.org/10.4490/algae.2002.17.4.217.

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29

Sin, Jong Am. "Yield Improvement Using Recombinant Wild-Type in Porphyra yezoensis (Bangiales, Rhodophyta)." ALGAE 18, no. 1 (March 31, 2003): 89–94. http://dx.doi.org/10.4490/algae.2003.18.1.089.

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30

Jo, Young-Hyun, Sung-Pil Kang, Tae-Ho Seo, Sung-Je Choi, Kang-Hee Kho, Kazuyoshi Kuwano, Naotsune Saga, Min-Yong Kim, and Jong-Ahm Shin. "Cryopreservation of Sporothalli of the Genus Porphyra (Bangiales, Rhodophyta) from Korea." ALGAE 18, no. 4 (December 31, 2003): 321–31. http://dx.doi.org/10.4490/algae.2003.18.4.321.

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31

Hwang, Mi Sook, Jin Koo Kim, Doo Saing Sim, Yoon Sik Oh, and Han Gu Choi. "Growth and Reproduction of Porphyra Kuniedae Kurogi (Bangiales, Rhodophyta) from Korea." Key Engineering Materials 277-279 (January 2005): 569–76. http://dx.doi.org/10.4028/www.scientific.net/kem.277-279.569.

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Growth and reproduction of Porphyra kuniedae from the southern coast of Korea were investigated. Biomass, plant size and occurrence of reproductive structures were monitored every other week from November 2001 to March 2002. Release of zygotospores and monospores from the plants was induced and the number of spores was counted in the laboratory culture every month. Biomass and plant size were found to be inversely correlated with water temperature. The maximum values in biomass and plant size were observed in mid-January with the lowest water temperature, and the values decreased with the increase of water temperature. Based on the cohort analysis, three cohorts started in late November, one to two cohorts were added every other week, and the maximum was eight in mid-January. The percentage of matured plants in the field was the highest in January. In the laboratory culture test, zygotospores were released more than monospores from large plants in late December while monospores were released much more than zygotospores since late January.
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32

Nelson, Wendy A. "Bangiadulcis gen. nov.: a new genus for freshwater filamentous Bangiales (Rhodophyta)." TAXON 56, no. 3 (August 2007): 883–86. http://dx.doi.org/10.2307/25065869.

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33

Silva, Mayra Y., and Jeffery R. Hughey. "Complete mitochondrial genome of the holotype specimen ofWildemania schizophylla(Bangiales: Rhodophyta)." Mitochondrial DNA 27, no. 2 (June 18, 2014): 1001–2. http://dx.doi.org/10.3109/19401736.2014.926524.

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34

Niwa, Kyosuke, and Takashi Sakamoto. "ALLOPOLYPLOIDY IN NATURAL AND CULTIVATED POPULATIONS OF PORPHYRA (BANGIALES, RHODOPHYTA)1." Journal of Phycology 46, no. 6 (September 27, 2010): 1097–105. http://dx.doi.org/10.1111/j.1529-8817.2010.00897.x.

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35

Jia, Zhaojun, Jianfeng Niu, Li Huan, Xiaojie Wu, Guangce Wang, and Zhaojun Hou. "Cyclophilin Participates in Responding to Stress Situations inPorphyra haitanensis(Bangiales, Rhodophyta)." Journal of Phycology 49, no. 1 (December 12, 2012): 194–201. http://dx.doi.org/10.1111/j.1529-8817.2012.01234.x.

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36

Hwang, Mi Sook, Seung-Oh Kim, Dong-Soo Ha, Jee Eun Lee, and Sang-Rae Lee. "Complete mitochondrial genome sequence of Pyropia yezoensis (Bangiales, Rhodophyta) from Korea." Plant Biotechnology Reports 8, no. 2 (January 9, 2014): 221–27. http://dx.doi.org/10.1007/s11816-013-0314-z.

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37

López-Vivas, Juan Manuel, Raquel Muñiz-Salazar, Rafael Riosmena-Rodríguez, Isaí Pacheco-Ruíz, and Charles Yarish. "Endemic Pyropia species (Bangiales, Rhodophyta) from the Gulf of California, Mexico." Journal of Applied Phycology 27, no. 2 (August 20, 2014): 1029–41. http://dx.doi.org/10.1007/s10811-014-0366-7.

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38

Kavale, Monica Gajanan, Mudassar Anisoddin Kazi, and Juliet Brodie. "Phycocalidia species (Bangiales, Rhodophyta), from the warm West Coast of India." European Journal of Phycology 56, no. 3 (January 18, 2021): 337–47. http://dx.doi.org/10.1080/09670262.2020.1829714.

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39

Boedeker, Christian, Tracy J. Farr, and Wendy A. Nelson. "Unusual Rhizoidal Development in Bangia (Bangiales, Rhodophyta) -Another Form of Vegetative Reproduction?" ALGAE 22, no. 1 (March 1, 2007): 31–36. http://dx.doi.org/10.4490/algae.2007.22.1.031.

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40

Diehl, Nora, Gwang Hoon Kim, and Giuseppe C. Zuccarello. "A pathogen of New Zealand Pyropia plicata (Bangiales, Rhodophyta), Pythium porphyrae (Oomycota)." ALGAE 32, no. 1 (March 15, 2017): 29–39. http://dx.doi.org/10.4490/algae.2017.32.2.25.

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41

Nelson, Wendy A., Tracy J. Farr, and Judy E. S. Broom. "Phylogenetic relationships and generic concepts in the red order Bangiales: challenges ahead." Phycologia 45, no. 3 (May 2006): 249–59. http://dx.doi.org/10.2216/05-26.1.

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42

Contreras-Porcia, L., D. Thomas, V. Flores, and J. A. Correa. "Tolerance to oxidative stress induced by desiccation in Porphyra columbina (Bangiales, Rhodophyta)." Journal of Experimental Botany 62, no. 6 (December 31, 2010): 1815–29. http://dx.doi.org/10.1093/jxb/erq364.

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43

Nelson, W. A., J. E. Broom, and T. J. Farr. "CONFUSING CONVERGENT MORPHOLOGIES: DIVERSITY AND DIFFICULTIES IN NEW ZEALAND ERYTHROPELTIDALES AND BANGIALES." Journal of Phycology 36, s3 (December 2000): 51. http://dx.doi.org/10.1046/j.1529-8817.1999.00001-152.x.

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44

Nakajima, Maiko, Yukihiro Kitade, Osamu Iitsuka, Satoru Fukuda, and Naotsune Saga. "Rapid extraction of high-quality genomic DNA from Porphyra yezoensis (Bangiales, Rhodophyta)." Phycological Research 48, no. 1 (March 2000): 15–17. http://dx.doi.org/10.1111/j.1440-1835.2000.tb00125.x.

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45

Yan, Xing-Hong, and Yusho Aruga. "Genetic analysis of artificial pigmentation mutants in Porphyra yezoensis Ueda (Bangiales, Rhodophyta)." Phycological Research 48, no. 3 (September 2000): 177–87. http://dx.doi.org/10.1111/j.1440-1835.2000.tb00214.x.

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46

Coll, Javier, and Eurico C. Oliveira. "Porphyra drewiana, a new species of red algae (Bangiales, Rhodophyta) from Brazil." Phycological Research 49, no. 1 (March 2001): 67–72. http://dx.doi.org/10.1111/j.1440-1835.2001.tb00234.x.

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47

Shin, Jong-ahm, and Akio Miura. "Estimation of the degree of self-fertilization in Porphyra yezoensis (Bangiales, Rhodophyta)." Hydrobiologia 204-205, no. 1 (September 1990): 397–400. http://dx.doi.org/10.1007/bf00040262.

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48

Pueschel, Curt M., and Kathleen M. Cole. "ULTRASTRUCTURE OF GERMINATING CARPOSPORES OF PORPHYRA VARIEGATA (KJELLM.) HUS (BANGIALES, RHODOPHYTA)1." Journal of Phycology 21, no. 1 (October 29, 2004): 146–54. http://dx.doi.org/10.1111/j.0022-3646.1985.00146.x.

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49

Gargiulo, Gaetano M., Flora Masi, and Giacomo Tripodi. "KARYOLOGY OF BANGIA ATROPURPUREA (RHODOPHYTA, BANGIALES) FROM MEDITERRANEAN AND NORTHEASTERN ATLANTIC POPULATIONS1." Journal of Phycology 27, no. 2 (April 1991): 306–9. http://dx.doi.org/10.1111/j.0022-3646.1991.00306.x.

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50

Niu, Jian-Feng, Guang-Ce Wang, Bai-Cheng Zhou, Xiang-Zhi Lin, and Chang-Sheng Chen. "Purification of R-phycoerythrin fromPorphyra haitanensis(Bangiales, Rhodophyta) using expanded-bed absorption1." Journal of Phycology 43, no. 6 (December 2007): 1339–47. http://dx.doi.org/10.1111/j.1529-8817.2007.00401.x.

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