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1

Kwon, Oh-Seok, Donghwa Kim, Chang-Kwon Kim, et al. "Cytotoxic Scalarane Sesterterpenes from the Sponge Hyrtios erectus." Marine Drugs 18, no. 5 (2020): 253. http://dx.doi.org/10.3390/md18050253.

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Twelve new sesterterpenes along with eight known sesterterpenes were isolated from the marine sponge Hyrtios erectus collected off the coast of Chuuk Island, the Federated State of Micronesia. Based upon a combination of spectroscopic and computational analyses, these compounds were determined to be eight glycine-bearing scalaranes (1–8), a 3-keto scalarane (9), two oxidized-furan-bearing scalaranes (10 and 11), and a salmahyrtisane (12). Several of these compounds exhibited weak antiproliferation against diverse cancer cell lines as well as moderate anti-angiogenesis activities. The antiproli
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2

Kaweetripob, Wirongrong, Chulabhorn Mahidol, Pittaya Tuntiwachwuttikul, Somsak Ruchirawat, and Hunsa Prawat. "Cytotoxic Sesterterpenes from Thai Marine Sponge Hyrtios erectus." Marine Drugs 16, no. 12 (2018): 474. http://dx.doi.org/10.3390/md16120474.

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Four sesterterpenes, erectusolides B, C, D, and seco-manoalide-25-methyl ether, two 2-furanone derivatives, erectusfuranones A and B, together with thirteen known sesterterpenes, (6Z)-neomanoalide-24-acetate, two diastereomers of 24-O-methylmanoalide, luffariolide B, manoalide, (6E)- and (6Z)-neomanoalide, seco-manoalide, scalarafuran, 12-acetylscalarolide, 12-epi-O-deacetyl-19-deoxyscalarin, 12-epi-scalarin, and 12-O-deacetyl-12-epi-scalarin, three indole alkaloids, 5-hydroxy-1H-indole-3-carbaldehyde, hyrtiosine A, and variabine B, and one norterpene, cavernosine were isolated from the marine
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3

Ashour, Mohamed A., Ehab S. Elkhayat, Rainer Ebel, RuAngelie Edrada, and Peter Proksch. "Indole alkaloid from the Red Sea sponge Hyrtios erectus." Arkivoc 2007, no. 15 (2007): 225–31. http://dx.doi.org/10.3998/ark.5550190.0008.f22.

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4

Faten A. S. Alsulaimany, Salma A.O. Saleh, Mahmoud A. Elfaky, and Sameh S. Elhady. "Anti-Helicobacter pylori Activity of Red Sea Hyrtios erectus sponge and micro-organisms Extracts." International Journal of Research in Pharmaceutical Sciences 11, no. 3 (2020): 4963–76. http://dx.doi.org/10.26452/ijrps.v11i3.2816.

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Helicobacter pylori were considered one of the most bacterial infections in the world. Recently, the resistance of antibiotic against H. pylori is increasing and hence, it is necessary to find new and natural effective agents. Marine organisms and microorganism produce complex secondary metabolites and some of these compounds are antimicrobials agents. This study aimed to provide preliminary data to determine if marine Hyrtios erectus sponge, actinomycetes, and fungi extracts can inhibit the growth of H. pylori. In this study, the methanol extracts of the three samples of Hyrtios erectus spong
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5

S. Elhady, Sameh, Alaa A. Bagalagel, Hanin A. Bogari, Safwat A. Ahmed, and Reem M. Diri. "New Bromoindole Alkaloid Isolated from the Marine Sponge Hyrtios erectus." HETEROCYCLES 96, no. 4 (2018): 749. http://dx.doi.org/10.3987/com-18-13869.

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6

Kaweetripob, Wirongrong, Chulabhorn Mahidol, Siriporn Wongbundit, Pittaya Tuntiwachwuttikul, Somsak Ruchirawat, and Hunsa Prawat. "Sesterterpenes and phenolic alkenes from the Thai sponge Hyrtios erectus." Tetrahedron 74, no. 2 (2018): 316–23. http://dx.doi.org/10.1016/j.tet.2017.11.073.

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7

Iguchi, Kazuo, Yoshie Shimada, and Yasuji Yamada. "Hyrtiosal, a new sesterterpenoid with a novel carbon skeleton from the Okinawan marine sponge Hyrtios erectus." Journal of Organic Chemistry 57, no. 2 (1992): 522–24. http://dx.doi.org/10.1021/jo00028a023.

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8

Elhady, Sameh, Ahmed Al-Abd, Ali El-Halawany, Abdulrahman Alahdal, Hashim Hassanean, and Safwat Ahmed. "Antiproliferative Scalarane-Based Metabolites from the Red Sea Sponge Hyrtios erectus." Marine Drugs 14, no. 7 (2016): 130. http://dx.doi.org/10.3390/md14070130.

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9

Alarif, Walied M., Sultan S. Al-Lihaibi, Mohamed A. Ghandourah, Mohamed I. Orif, Salim A. Basaif, and Seif-Eldin N. Ayyad. "Cytotoxic scalarane-type sesterterpenes from the Saudi Red Sea sponge Hyrtios erectus." Journal of Asian Natural Products Research 18, no. 6 (2015): 611–17. http://dx.doi.org/10.1080/10286020.2015.1115019.

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10

Elhady, Sameh, Ali El-Halawany, Abdulrahman Alahdal, Hashim Hassanean, and Safwat Ahmed. "A New Bioactive Metabolite Isolated from the Red Sea Marine Sponge Hyrtios erectus." Molecules 21, no. 1 (2016): 82. http://dx.doi.org/10.3390/molecules21010082.

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11

Ju, Eunsin, Abdul Latif, Chang-Suk Kong, et al. "Antimalarial activity of the isolates from the marine sponge Hyrtios erectus against the chloroquine-resistant Dd2 strain of Plasmodium falciparum." Zeitschrift für Naturforschung C 73, no. 9-10 (2018): 397–400. http://dx.doi.org/10.1515/znc-2018-0025.

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Abstract This work reports the isolation of the three known compounds, smenotronic acid (1), ilimaquinone (2), and pelorol (3), from the 85% methanol (MeOH)-soluble fraction of the sponge Hyrtios erectus. The structures of the isolated compounds were determined with the help of modern spectroscopic techniques, and the resulting compounds were then subjected to in vitro screening to determine their antimalarial potential against the chloroquine-resistant Dd2 strain of Plasmodium falciparum. Amongst the three compounds, pelorol (3) showed significant activity against P. falciparum with an IC50 v
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12

Shreadah, Mohamed A., Nehad M. A. El Moneam, Samy A. El-Assar, and Asmaa Nabil-Adam. "Metabolomics and Pharmacological Screening of Aspergillus versicolor Isolated from Hyrtios erectus Red Sea Sponge; Egypt." Current Bioactive Compounds 16, no. 7 (2020): 1083–102. http://dx.doi.org/10.2174/1573407215666191111122711.

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Background: Aspergillus Versicolor is a marine-derived fungus isolated from Hyrtios Erectus Red Sea sponge. Methods: The aim of this study was to carry out a pharmacological screening and investigation for the in vitro biological activity (antioxidant, cholinergic, antidiabetic and anticancer) of Aspergillus Versicolor crude extract’s active compounds by using different qualitative and quantitative methods. Results: The present study results showed that Aspergillus Versicolor crude extracts contain 0.6 mg total phenolic/mg crude extract. Aspergillus Versicolor also showed a potent antioxidativ
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13

De, ArunKumar, Ramachandran Muthiyan, Nilkamal Mahanta, Balwin Nambikkairaj, and Titus Immanuel. "Antioxidant and anti-inflammatory effects of a methanol extract from the marine sponge Hyrtios erectus." Pharmacognosy Magazine 14, no. 58 (2018): 534. http://dx.doi.org/10.4103/pm.pm_133_17.

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14

Alahdal, Abdulrahman, Hani Asfour, Safwat Ahmed, et al. "Anti-Helicobacter, Antitubercular and Cytotoxic Activities of Scalaranes from the Red Sea Sponge Hyrtios erectus." Molecules 23, no. 4 (2018): 978. http://dx.doi.org/10.3390/molecules23040978.

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15

Hawas, Usama W., Lamia T. Abou El-Kassem, Mohamed S. Abdelfattah, et al. "Cytotoxic activity of alkyl benzoate and fatty acids from the red sea sponge Hyrtios erectus." Natural Product Research 32, no. 12 (2017): 1369–74. http://dx.doi.org/10.1080/14786419.2017.1344662.

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16

El-Gendy, Mervat Morsy Abbas Ahmed, Shaymaa M. M. Yahya, Ahmed R. Hamed, Maha M. Soltan, and Ahmed Mohamed Ahmed El-Bondkly. "Phylogenetic Analysis and Biological Evaluation of Marine Endophytic Fungi Derived from Red Sea Sponge Hyrtios erectus." Applied Biochemistry and Biotechnology 185, no. 3 (2018): 755–77. http://dx.doi.org/10.1007/s12010-017-2679-x.

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17

De, ArunKumar, Ramachandran Muthiyan, Balwin Nambikkairaj, et al. "Antiproliferative and proapoptotic activities of marine sponge Hyrtios erectus extract on breast carcinoma cell line (MCF-7)." Pharmacognosy Magazine 13, no. 49 (2017): 41. http://dx.doi.org/10.4103/0973-1296.203983.

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18

Chakraborty, Kajal, and Prima Francis. "Apoptotic effect of chromanone derivative, hyrtiosone A from marine demosponge Hyrtios erectus in hepatocellular carcinoma HepG2 cells." Bioorganic Chemistry 114 (September 2021): 105119. http://dx.doi.org/10.1016/j.bioorg.2021.105119.

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19

El-Moneam, Nehad, Samy El-Assar, Mohamed Shreadah, and Asmaa Adam. "Isolation, Identification And Molecular Screening of Pseudomonas sp. Metabolic Pathways NRPs and PKS associated with the Red sea Sponge, Hyrtios aff. Erectus, Egypt." Journal of Pure and Applied Microbiology 11, no. 3 (2017): 1299–311. http://dx.doi.org/10.22207/jpam.11.3.10.

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20

Elhady, Sameh S., Reda F. A. Abdelhameed, Rania T. Malatani, et al. "Molecular Docking and Dynamics Simulation Study of Hyrtios erectus Isolated Scalarane Sesterterpenes as Potential SARS-CoV-2 Dual Target Inhibitors." Biology 10, no. 5 (2021): 389. http://dx.doi.org/10.3390/biology10050389.

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Presently, the world is under the toll of pandemic coronavirus disease-2019 (COVID-19) outbreak caused by SARS-CoV-2. Lack of effective and safe therapeutics has stressed the scientific community for developing novel therapeutics capable of alleviating and stopping this pandemic. Within the presented study, molecular docking, ADME properties and all-atom molecular dynamic (MD) simulation, along with two standard antiviral agents (lopinavir and benzopurpurin-4B), were applied to investigate 15 scalaranes sesterterpenes natural compounds, purified from the Red Sea marine sponge Hyrtios erectus,
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21

De, Arun Kumar, Ramachandran Muthiyan, Samiran Mondal, et al. "A Natural Quinazoline Derivative from Marine Sponge Hyrtios erectus Induces Apoptosis of Breast Cancer Cells via ROS Production and Intrinsic or Extrinsic Apoptosis Pathways." Marine Drugs 17, no. 12 (2019): 658. http://dx.doi.org/10.3390/md17120658.

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Here, we report the therapeutic potential of a natural quinazoline derivative (2-chloro-6-phenyl-8H-quinazolino[4,3-b]quinazolin-8-one) isolated from marine sponge Hyrtios erectus against human breast cancer. The cytotoxicity of the compound was investigated on a human breast carcinoma cell line (MCF-7). Antiproliferative activity of the compound was estimated by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. MTT assay showed significant inhibition of MCF-7 cells viability with the IC50 value of 13.04 ± 1.03 µg/mL after 48 h. The compound induced down-regulation of a
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22

Francis, Prima, and Kajal Chakraborty. "Anti-inflammatory scalarane-type sesterterpenes, erectascalaranes A–B, from the marine sponge Hyrtios erectus attenuate pro-inflammatory cyclooxygenase-2 and 5-lipoxygenase." Medicinal Chemistry Research 30, no. 4 (2021): 886–96. http://dx.doi.org/10.1007/s00044-020-02682-6.

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23

NABIL-ADAM, Asmaa, Mohamed A. SHREADAH, Nehad M. Abd EL MONEAM, and Samy A. EL-ASSAR. "Various In Vitro Bioactivities of Secondary Metabolites Isolated from the Sponge Hyrtios aff. Erectus from the Red Sea Coast of Egypt." Turkish Journal of Pharmaceutical Sciences 17, no. 2 (2020): 127–35. http://dx.doi.org/10.4274/tjps.galenos.2018.72677.

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24

Fristiohady, Adryan, and Lidya Agriningsih Haruna. "Review Jurnal: Potensi Spons Laut Sebagai Anti Kanker Payudara." Jurnal Mandala Pharmacon Indonesia 6, no. 01 (2020): 30–52. http://dx.doi.org/10.35311/jmpi.v6i01.56.

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Angka kejadian dan kematian pada penderita kanker payudara terus mengalami peningkatan di setiap tahunnya. Prevalensi kejadian 8-9% wanita mengalami kanker payudara. Menurut data World Health Organization (WHO) tahun 2018 menyebutkan angka kejadian kanker payudara di Indonesia sebesar 42,1 per 100.000 penduduk dengan rata-rata angka kematian 17 per 100.000 penduduk. Kanker payudara adalah kanker invasif paling sering terjadi pada wanita di seluruh dunia dan penyebab kematian kanker tertinggi kedua, setelah kanker paru-paru. Kebanyakan wanita dengan kanker payudara akan menjalani beberapa jenis
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25

Abd El-Moneam, Nehad M., Mohamed A. Shreadah, Samy A. El-Assar, and Asmaa Nabil-Adam. "Protective role of antioxidants capacity of Hyrtios aff. Erectus sponge extract against mixture of persistent organic pollutants (POPs)-induced hepatic toxicity in mice liver: biomarkers and ultrastructural study." Environmental Science and Pollution Research 24, no. 27 (2017): 22061–72. http://dx.doi.org/10.1007/s11356-017-9805-8.

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26

Bergman, Jan, Tomasz Janosik, and Ann-Louise Johnsson. "Synthesis of Hyrtiosin B, a Bis-indole Alkaloid from the Okinawan Marine Sponge Hyrtios erecta." Synthesis 1999, no. 04 (1999): 580–82. http://dx.doi.org/10.1055/s-1999-3439.

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27

SWANTARA, I. MADE DIRA, WIWIK SUSANAH RITA, and ANISA HERNINDYA. "Identifikasi Isolat Antikanker Spons Hyrtios Erecta." Indonesian Journal of Cancer 10, no. 4 (2017): 123. http://dx.doi.org/10.33371/ijoc.v10i4.456.

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ABSTRACTIsolation, anticancer activity test, and identification of the toxic isolate from ethanol extract of the sponge Hyrtios erecta taken from Pari Island beach (Jakarta) has conducted. Extraction of the sponges was carried out by 70% ethanol at room temperature. Partition and purification of the compounds were done by column chromatography with the stationary phase of silica gel and the mobile phase of n-hexane-chloroform (2:8). Toxicity screening test was done based on BhrineShrimp Lethality Test (BSLT). In vitro anticancer activity test of the isolate was carried out using HeLa cell line
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Bergman, Jan, Tomasz Janosik, and Ann-Louise Johnsson. "ChemInform Abstract: Synthesis of Hyrtiosin B, a Bis-indole Alkaloid from the Okinawan Marine Sponge Hyrtios erecta." ChemInform 30, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199931250.

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Swantara, I. Made Dira, Wiwik Susanah Rita, and Rr Anisa Hernindy. "ISOLATION AND PHYTOCHEMICAL TEST OF ANTICANCER ISOLATE OF SPONGE Hyrtios erecta." Journal of Health Sciences and Medicine 1, no. 1 (2017): 16. http://dx.doi.org/10.24843/jhsm.2017.v01.i01.p05.

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AbstractThis research aims to isolate and phytochemically test of the toxic isolate from ethanol extract of the sponge Hyrtios
 erecta taken from the waters of Pari Island beach, Thousand Islands (Jakarta). Extraction of the sponges was carried out by
 70% ethanol at room temperature. Partition and purification of the compounds were done by column chromatography with the
 stationary phase of silica gel and the mobile phase of n-hexane-chloroform (2:8). Toxicity screening test was done based on
 Bhrine Shrimp Lethality Test (BSLT). The compounds of the active isolate were pe
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30

Crews, Phillip, and Pedro Bescansa. "Sesterterpenes from a Common Marine Sponge, Hyrtios erecta." Journal of Natural Products 49, no. 6 (1986): 1041–52. http://dx.doi.org/10.1021/np50048a012.

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31

Pettit, George R., Zbigniew A. Cichacz, Rui Tan, et al. "Antineoplastic Agents 385. The Isolation and Structure of a Scalarane-Type Sesterterpene from the Indian Ocean Porifera Hyrtios erecta." Collection of Czechoslovak Chemical Communications 63, no. 10 (1998): 1671–77. http://dx.doi.org/10.1135/cccc19981671.

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Bioassay-guided separation techniques were employed to isolate (3.3·10-7% yield) a new murine P388 lymphocytic leukemia cell line inhibitor (ED50 2.9 μg/ml) 12-O-deacetyl-19-deoxyscalarin from extracts of the Republic of Maldives marine sponge Hyrtios erecta. The structure was deduced using high field 2D NMR and high resolution mass spectral methods and confirmed by X-ray crystal structure determination.
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32

He, Wen-Fei, Duo-Qing Xue, Li-Gong Yao, Jing-Ya Li, Jia Li, and Yue-Wei Guo. "Hainanerectamines A–C, Alkaloids from the Hainan Sponge Hyrtios erecta." Marine Drugs 12, no. 7 (2014): 3982–93. http://dx.doi.org/10.3390/md12073982.

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33

Pettit, Robin K., Shane C. McAllister, George R. Pettit, Cherry L. Herald, J. Morris Johnson, and Zbigniew A. Cichacz. "A broad-spectrum antifungal from the marine sponge Hyrtios erecta." International Journal of Antimicrobial Agents 9, no. 3 (1998): 147–52. http://dx.doi.org/10.1016/s0924-8579(97)00044-7.

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34

Bourguet-Kondracki, M. L., M. T. Martin, C. Debitus, and M. Guyot. "12-epi-heteronemin : New sesterterpene from the marine sponge Hyrtios erecta." Tetrahedron Letters 35, no. 1 (1994): 109–10. http://dx.doi.org/10.1016/0040-4039(94)88175-8.

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35

Bourguet-Kondracki, M. L., M. T. Martin та M. Guyot. "A new β-carboline alkaloid isolated from the marine sponge Hyrtios erecta". Tetrahedron Letters 37, № 20 (1996): 3457–60. http://dx.doi.org/10.1016/0040-4039(96)00573-4.

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36

Kobayashi, Jun'ichi, Tetsuya Murayama, Masami Ishibashi, et al. "Hyrtiosins A and B, new indole alkaloids from the Okinawan marine sponge Hyrtios erecta." Tetrahedron 46, no. 23 (1990): 7699–702. http://dx.doi.org/10.1016/s0040-4020(01)90065-1.

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37

BOURGUET-KONDRACKI, M. L., M. T. MARTIN та M. GUYOT. "ChemInform Abstract: A New β-Carboline Alkaloid Isolated from the Marine Sponge Hyrtios erecta." ChemInform 27, № 34 (2010): no. http://dx.doi.org/10.1002/chin.199634239.

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38

AOKI, Shunji, Ying YE, Kouichi HIGUCHI, et al. "Novel Neuronal Nitric Oxide Synthase (nNOS) Selective Inhibitor, Aplysinopsin-Type Indole Alkaloid, from Marine Sponge Hyrtios erecta." CHEMICAL & PHARMACEUTICAL BULLETIN 49, no. 10 (2001): 1372–74. http://dx.doi.org/10.1248/cpb.49.1372.

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39

Pettit, George R., Rui Tan, Noeleen Melody, et al. "Antineoplastic agents 397: Isolation and structure of sesterstatins 4 and 5 from hyrtios erecta (the republic of maldives)." Bioorganic & Medicinal Chemistry Letters 8, no. 16 (1998): 2093–98. http://dx.doi.org/10.1016/s0960-894x(98)00373-4.

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KOBAYASHI, J., T. MURAYAMA, M. ISHIBASHI, et al. "ChemInform Abstract: Hyrtiosins A (I) and B (II), New Indole Alkaloids from the Okinawan Marine Sponge Hyrtios erecta." ChemInform 22, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199108318.

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Aoki, Shunji, Ying Ye, Kouichi Higuchi, et al. "ChemInform Abstract: Novel Neuronal Nitric Oxide Synthase (nNOS) Selective Inhibitor, Aplysinopsin-Type Indole Alkaloid, from Marine Sponge Hyrtios erecta." ChemInform 33, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.200212248.

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Du, Li, Liangliang Shen, Zhiguo Yu, et al. "Hyrtiosal, from the Marine SpongeHyrtios erectus, Inhibits HIV-1 Integrase Binding to Viral DNA by a New Inhibitor Binding Site." ChemMedChem 3, no. 1 (2008): 173–80. http://dx.doi.org/10.1002/cmdc.200700223.

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PETTIT, G. R., R. TAN, N. MELODY, et al. "ChemInform Abstract: Antineoplastic Agents 397: Isolation and Structure of Sesterstatins 4 (Ia) and 5 (Ib) from Hyrtios erecta (the Republic of Maldives)." ChemInform 29, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.199851224.

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KOBAYASHI, Motomasa, Takumi OKAMOTO, Kozo HAYASHI, Norio YOKOYAMA, Takuma SASAKI, and Isao KITAGAWA. "Marine Natural Products. XXXII. Absolute Configurations of C-4 of the Manoalide Family, Biologically Active Sestertepenes from the Marine Sponge Hyrtios erecta." CHEMICAL & PHARMACEUTICAL BULLETIN 42, no. 2 (1994): 265–70. http://dx.doi.org/10.1248/cpb.42.265.

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45

Duckworth, Alan R., and Carsten W. Wolff. "Patterns of abundance and size of Dictyoceratid sponges among neighbouring islands in central Torres Strait, Australia." Marine and Freshwater Research 58, no. 2 (2007): 204. http://dx.doi.org/10.1071/mf06104.

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Distribution and size frequency patterns of sessile organisms such as sponges may vary among and within neighbouring reefs. In the present study, we examined small-scale variation of dictyoceratid sponges (class Demospongiae), commonly found on coral reefs, by surveying six neighbouring islands in central Torres Strait. Each island had four study sites, at least 1 km apart, with each site consisting of three shallow (4 to 6 m) and three deep (10 to 15 m) 20 m2 transects. For each transect, we recorded the number of each species and measured the size of the more common dictyoceratid sponges. Se
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Sun, Tao, Qi Wang, Zhiguo Yu та ін. "Hyrtiosal, a PTP1B Inhibitor from the Marine SpongeHyrtios erectus, Shows Extensive Cellular Effects on PI3K/AKT Activation, Glucose Transport, and TGFβ/Smad2 Signaling". ChemBioChem 8, № 2 (2007): 187–93. http://dx.doi.org/10.1002/cbic.200600349.

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47

Enders, Dieter, and Thomas Schuesseler. "First Highly Efficient Asymmetric Synthesis of the Hyrtios erectus Diketotriterpenoid." ChemInform 34, no. 11 (2003). http://dx.doi.org/10.1002/chin.200311185.

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48

MARZUKI, ISMAIL, MUDYAWATI KAMARUDDIN, and Rasheed Ahmad. "Identification of marine sponges-symbiotic bacteria and their application in degrading polycyclic aromatic hydrocarbons." Biodiversitas Journal of Biological Diversity 22, no. 3 (2021). http://dx.doi.org/10.13057/biodiv/d220352.

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Abstract. Marzuki I, Kamaruddin M, Ahmad R. 2021. Identification of marine sponges-symbiotic bacteria and their application in degrading polycyclic aromatic hydrocarbons. Biodiversitas 22: 1481-1488. Diverse and abundant microbial species that occupy marine sponges may make important contributions to host metabolism. Sponges are filter feeders and devour microorganisms from the seawater around them. Each microbe that endures the sponges’ digestive and immune responses are related symbiotically. Marine sponges symbiont bacteria can comprise as much as 40% of sponge tissue volume, and these are
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49

Chakraborty, Kajal, and Prima Francis. "Hyrtioscalaranes A and B, two new scalarane-type sesterterpenes from Hyrtios erectus with anti-inflammatory and antioxidant effects." Natural Product Research, July 27, 2020, 1–12. http://dx.doi.org/10.1080/14786419.2020.1795854.

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Cleary, DFR, ARM Polónia, YM Huang, S. Putchakarn, NCM Gomes, and NJ de Voogd. "A comparison of prokaryote communities inhabiting sponges, bacterial mats, sediment and seawater in Southeast Asian coral reefs." FEMS Microbiology Ecology, October 21, 2019. http://dx.doi.org/10.1093/femsec/fiz169.

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Abstract:
Abstract In the present study, we used Illumina sequencing to explore the prokaryote communities of 17 demosponge species and how they compare with bacterial mat, sediment and seawater samples (all sampled from coral reef habitat in Taiwan and Thailand). The studied sponge species formed three clusters. OTU richness and evenness were by far highest in the sediment and bacterial mat biotopes. There were pronounced differences in OTU richness and evenness among clusters and also considerable variation among certain host species within clusters. Additionally, the relative abundance of some prokar
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