Published October 31, 2021 | Version v1

Halocarbon emissions by selected tropical seaweeds exposed to different temperatures

  • 1. * & Institute of Ocean and Earth Sciences (IOES), University of Malaya, 50603, Kuala Lumpur, Malaysia & Institute for Advanced Studies, University of Malaya, 50603, Kuala Lumpur, Malaysia

Description

Keng, Fiona Seh-Lin, Phang, Siew-Moi, Rahman, Noorsaadah Abd, Yeong, Hui-Yin, Malin, Gill, Elvidge, Emma Leedham, Sturges, William (2021): Halocarbon emissions by selected tropical seaweeds exposed to different temperatures. Phytochemistry (112869) 190: 1-10, DOI: 10.1016/j.phytochem.2021.112869, URL: http://dx.doi.org/10.1016/j.phytochem.2021.112869

Files

Restricted

The record is publicly accessible, but files are restricted. Log in to check if you have access.

Linked records

Additional details

Identifiers

LSID
urn:lsid:plazi.org:pub:FF8ADF47FF88FF9AFF98FFA2FFC9FFE4

References

  • Abrahamsson, K., Choo, K.S., Pedersen, M., Johansson, G., Snoeijs, P., 2003. Effects of temperature on the production of hydrogen peroxide and volatile halocarbons by brackish water algae. Phytochemistry 6, 725-734. https://doi.org/10.1016/s0031- 9422(03)00419-9.
  • Allakhverdiev, S.I., Kreslavski, V.D., Klimov, V.V., Los, D.A., Carpentier, R., Mohanty, P., 2008. Heat stress: an overview of molecular responses in photosynthesis. Photosynth. Res. 98, 541-550. https://doi.org/10.1007/s11120-008-9331-0.
  • Almeida, M., Filipe, S., Humanes, M., Maia, M.F., Melo, R., Severino, N., da Silva, J.A., Frausto da Silva, J.J., Wever, R., 2001. Vanadium haloperoxidases from brown algae of the Laminariaceae family. Phytochemistry 57, 633-642. https://doi.org/10.1016/ s0031-9422(01)00094-2.
  • Baharum, H., Chu, W.-C., Teo, S.-S., Ng, K.-Y., Abdul Rahim, R., Ho, C.-L., 2013. Molecular cloning, homology modeling and site-directed mutagenesis of vanadiumdependent bromoperoxidase (GcVBPO1) from Gracilaria changii (Rhodophyta). Phytochemistry 92, 49-59. https://doi.org/10.1016/j.phytochem.2013.04.014.
  • Bartsch, I., Wiencke, C., Laepple, T., 2012. Global seaweed biogeography under a changing climate, the prospected effects of temperature. In: Wiencke, C., Bischof, K. (Eds.), Seaweed Biology: Ecological Studies (Analysis and Synthesis), vol. 219. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-28451-9_18.
  • Bindoff, N.L., Cheung, W.W.L., Kairo, J.G., Aristegui, J., Guinder, V.A., Hallberg, R., Hilmi, N., Jiao, N., Karim, M.S., Levin, L., O' Donoghue, S., Purca Cuicapusa, S.R., Rinkevich, B., Suga, T., Tagliabue, A., Williamson, P., 2019. Changing ocean, marine ecosystems, and dependent communities. In: P¨ortner, H.O., Roberts, D.C., Masson- Delmotte, V., Zhai, P., Tignor, M., Poloczanska, E., Mintenbeck, K., Alegria, A., Nicolai, M., Okem, A., Petzold, P., Rama, B., Weyer, N.M. (Eds.), IPCC Special Report on the Ocean and Cryosphere in a Changing Climate accessed 13 January 2021. htt ps://www.ipcc.ch/site/assets/uploads/sites/3/2019/11/09_SROCC_Ch05_FINAL. pdf.
  • Borlongan, I.A.G., Gerung, G.S., Nishihara, G.N., Terada, R., 2016. Light and temperature effects on photosynthetic activity of Eucheuma denticulatum and Kappaphycus alvarezii (brown and green color morphotypes) from Sulawesi Utara, Indonesia. Phycol. Res. 65 (1), 69-79. https://doi.org/10.1111/pre.12155.
  • Boyd, P.W., Collins, S., Dupont, S., Fabricius, K., Gattuso, J.P., Havenhand, J., Hutchins, D.A., Riebesell, U., Rintoul, M.S., Vichi, M., 2018. Experimental strategies to assess the biological ramifications of multiple drivers of global ocean change-a review. Global Change Biol. 24 (6), 2239-2261. https://doi.org/10.1111/ gcb.14102.
  • Brodie, J., Williamson, C.J., Smale, D.A., Kamenos, N.A., Mieszkowska, N., Santos, R., Cunliffe, M., Steinke, M., Yesson, C., Anderson, K.M., Asnaghi, V., Brownlee, C., Burdett, H., Burrows, M.T., Collins, S., Donohue, P.J.C., Harvey, B., Foggo, A., Noisette, F., Nunes, J., Ragazzola, F., Raven, J.A., Schmidt, D.N., Suggett, D., Teichberg, M., Hall-Spencer, J.M., 2014. The future of the northeast Atlantic benthic flora in a high CO2 world. Ecol. Evol. 4 (13), 2787-2798. https://doi.org/10.1002/ ece3.1105.
  • Carpenter, L., MacDonald, S.M., Shaw, M.D., Kumar, R., Saunders, R.W., Parthipan, R., Wilson, J., Plane, J.M., 2013. Atmospheric iodine levels influenced by sea surface emissions of inorganic iodine. Nat. Geosci. 6 (2), 108-111. https://doi.org/10.1038/ NGEO1687.
  • Carpenter, L.J., Malin, G., Liss, P.S., 2000. Novel biogenic iodine-containing trihalomethanes and other short-lived halocarbons in the coastal East Atlantic. Global Biogeochem. Cycles 14 (4), 1191-1204. https://doi.org/10.1029/ 2000GB001257.
  • Colvard, N.B., Carrington, E., Helmuth, B., 2014. Temperature-dependent photosynthesis in the intertidal alga Fucus gardneri and sensitivity to ongoing climate change. J. Exp. Mar. Biol. Ecol. 458, 6-12. https://doi.org/10.1016/j.jembe.2014.05.001.
  • de Silva, H.C.C., Asaeda, T., 2017. Effects of heat stress on growth, photosynthetic pigments, oxidative damage and competitive capacity of three submerged macrophytes. J. Plant Interact. 12 (1), 228-236. https://doi.org/10.1080/ 17429145.2017.1322153.
  • FAO, 2020. The State of World Fisheries and Aquaculture 2020. Sustainability in Action. Rome. https://doi.org/10.4060/ca9229en.
  • Gill, S.S., Tuteja, N., 2010. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem. 48, 909-930. https://doi. org/10.1016/j.plaphy.2010.08.016.
  • Hamzah, A., Kipli, S.H., Ismail, S.R., Una, R., Sarmani, S., 2011. Microbiological study in coastal water of Port Dickson, Malaysia. Sains Malays. 46 (2), 93-99.
  • Hopkins, F.E., Suntharalingam, P., Gehlen, M., Andrews, O., Archer, S.A., Bopp, L., Buitenhuis, E., Dadou, I., Duce, R., Goris, N., Jickells, T., Johnson, M., Keng, F., Law, C.S., Lee, K., Liss, P.S., Lizotte, M., Malin, G., Murrell, J.C., Naik, H., Rees, A.P., Schwinger, J., Williamson, P., 2020. The impacts of ocean acidification on marine trace gases and the implications for atmospheric chemistry and climate. Proc. R. Soc. A 476, 20190769. https://doi.org/10.1098/rspa.2019.0769.
  • Hossaini, R., Patra, P.K., Leeson, A.A., Krysztofiak, G., Abraham, N.L., Andrews, S.J., Archibald, A.T., Aschmann, J., Atlas, E.L., Belikov, D.A., B¨onisch, H., Carpenter, L.J., Dhomse, S., Dorf, M., Engel, A., Feng, W., Fuhlbrugge, S., Griffiths, P.T., Harris, N.R. P., Hommel, R., Keber, T., Kruger, K., Lennartz, S.T., Maksyutov, S., Mantle, H., Mills, G.P., Miller, B., Montzka, S.A., Moore, F., Navarro, M.A., Oram, D.E., Pfeilsticker, K., Pyle, J.A., Quack, B., Robinson, A.D., Saikawa, E., Saiz-Lopez, A., Sala, S., Sinnhuber, B.-M., Taguchi, S., Tegtmeier, S., Lid- ster, R.T., Wilson, C., Ziska, F., 2016. A multi-model intercom-parison of halogenated very short-lived substances (TransCom- VSLS): linking oceanic emissions and tropospheric transport for a reconciled estimate of the stratospheric source gas injection of bromine. Atmos. Chem. Phys. 16, 9163-9187. https://doi.org/10.5194/acp-16-9163-2016.
  • Ismail, M.M., Osman, M.E.H., 2016. Seasonal fluctuation of photosynthetic pigments of most common red seaweed species collected from Abu Qir, Alexandria, Egypt. Rev. Biol. Mar. Oceanogr. 51 (3), 515-525. https://doi.org/10.4067/S0718- 19572016000300004.
  • Keng, F.S.-L., Phang, S.-M., Abd Rahman, N., Leedham, E.C., Hughes, C., Robinson, A.D., Harris, N.R.P., Pyle, J.A., Sturges, W.T., 2013. Volatile halocarbon emissions by three tropical brown seaweeds under different irradiances. J. Appl. Phycol. 25 (5), 1377-1386. https://doi.org/10.1007/s10811-013-9990-x.
  • Keng, F.S.-L., Phang, S.-M., Abd Rahman, N., Leedham Elvidge, E.C., Malin, G., Sturges, W.T., 2020. The emission of volatile halocarbons by seaweeds and their response towards environmental changes. J. Appl. Phycol. 32, 1377-1394. https:// doi.org/10.1007/s10811-019-02026-x.
  • Kongkiattikajorn, J., Ruenwongsa, P., 2006. Isolation and characterisation of vanadium bromoperoxidases from Thai red alga Gracilaria tenuistipitata. Sci. Asia 32 (1), 31-35. https://doi.org/10.2306/scienceasia1513-1874.2006.32(s1).031.
  • Kumar, Y.N., Poong, S.-W., Gachon, C., Brodie, J., Sade, A., Lim, P.E., 2020. Impact of elevated temperature on the physiological and biochemical responses of Kappaphycus alvarezii (Rhodophyta). PloS One 15 (9), e0239097. https://doi.org/ 10.1371/journal.pone.0239097.
  • Kupper, F.C., Carpenter, L.J., McFiggans, G.B., Palmer, C.J., Waite, T.J., Boneberg, E.-M., Woitsch, S., Weiller, M., Abela, R., Grolimund, D., Potin, P., Butler, A., Luther III, G. W., Kroneck, P.M.H., Meyer-Klaucke, W., Feiter, M.C., 2008. Iodide accumulation provides kelp with an inorganic antioxidant impacting atmospheric chemistry. Proc. Natl. Acad. Sci. U. S. A. 105, 6954-6958. https://doi.org/10.1073/ pnas.0709959105.
  • Laturnus, F., Giese, B., Wiencke, C., Adams, F.C., 2000. Low-molecular-weight organoiodine and organobromine compounds released by polar macroalgae-The influence of abiotic factors. Fresenius' J. Anal. Chem. 368, 297-302. https://doi.org/ 10.1007/s002160000491.
  • Leedham, E.C., Hughes, C., Keng, F.S.L., Phang, S.-M., Malin, G., Sturges, W.T., 2013. Emission of atmospherically significant halocarbons by naturally occurring and farmed tropical macroalgae. Biogeosciences 10 (6), 3615-3633. https://doi.org/ 10.5194/bg-10-3615-2013.