The effect of desiccation on the emission of volatile bromocarbons from two common temperate macroalgae

Biogeosciences

Volumn 12, Issue 2, 2015, Pages 387-398

  Leedham Elvidge, E C ^a   Phang, S M ^b,c   Sturges, W T ^a   Malin, G ^a  

^a UNIVERSITY OF EAST ANGLIA   (United Kingdom)

^b UNIVERSITY OF MALAYA   (Malaysia)

^c UNIVERSITY OF MALAYA   (Malaysia)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIOXIDANT; BIOGENIC EMISSION; BROWN ALGA; DESICCATION; GREEN ALGA; HALOCARBON; INTERTIDAL COMMUNITY; IODIDE; IODINE; MACROALGA; PHOTOSYNTHESIS; VOLATILE ORGANIC COMPOUND;

ALGAE; FUCUS VESICULOSUS; ULVA INTESTINALIS;

EID: 84921500753     PISSN: 17264170     EISSN: 17264189     Source Type: Journal    
DOI: 10.5194/bg-12-387-2015     Document Type: Article

References (46)

1. Ball, S. M., Hollingsworth, A. M., Humbles, J., Leblanc, C., Potin, P., and McFiggans, G.: Spectroscopic studies of molecular iodine emitted into the gas phase by seaweed, Atmos. Chem. Phys., 10, 6237-6254, doi:10.5194/acp-10-6237-2010, 2010.
2. Bravo-Linares, C. M., Mudge, S. M., and Loyola-Sepulveda, R. H.: Production of volatile organic compounds (VOCs) by temperate macroalgae: The use of Solid Phase Microextraction (SPME) coupled to GC-MS as method of analysis, J. Chilean Chem. Soc., 55, 227-232, doi:10.4067/S0717-97072010000200018, 2010.
3. Burritt, D. J., Larkindale, J., and Hurd, C. L.: Antioxidant metabolism in the intertidal red seaweed Stictosiphonia arbuscula following desiccation, Planta, 215, 829-838, doi:10.1007/s00425-002-0805-6, 2002.
4. Cainey, J. M., Keywood, M., Bigg, E. K., Grose, M. R., Gillett, R. W., and Meyey, M.: Flux chamber study of particle formation from Durvillaea potatorum, Environ. Chem., 4, 151-154, doi:10.1071/EN07006, 2007.
5. Carpenter, L. J. and Liss, P.: On temperate sources of bromoform and other reactive organic bromine gases, J. Geophys. Res., 105, 20539-20547, doi:10.1029/2000JD900242, 2000.
6. Carpenter, L. J., Sturges, W. T., Penkett, S. A., Liss, P. S., Alicke, B., Hebestreit, K., and Platt, U.: Short-lived alkyl iodides and bromides at Mace Head, Ireland: Links to biogenic sources and halogen oxide production, J. Geophys. Res., 104, 1679-1689, doi:10.1029/98JD02746, 1999.
7. Collén, J. and Davison, I. R.: Stress tolerance and reactive oxygen metabolism in the intertidal red seaweeds Mastocarpus stellatus and Chondrus crispus, Plant. Cell Environ., 22, 1143-1151, doi:10.1046/j.1365-3040.1999.00477.x, 1999.
8. Collén, J., Ekdahl, A., Abrahamsson, K., and Pedersén, M.: The involvement of hydrogen peroxide in the production of volatile halogenated compounds by Meristiella gelidium, Phytochemistry, 36, 1197-1202, doi:10.1016/S0031-9422(00)89637-5, 1994.
9. Davison, I. R. and Pearson, G. A.: Stress tolerance in intertidal seaweeds, J. Phycol., 32, 197-211, doi:10.1111/j.0022-3646.1996.00197.x, 1996.
10. Edwards, D. M., Reed, R. H., and Stewart, W. D. P.: Osmoacclimation in Enteromorpha intestinalis: Long-term effects of osmotic stress on organic solute accumulation, Mar. Biol., 98, 467-476, doi:10.1007/BF00391537, 1988.
11. Goodwin, K. D., North, W. J., and Lidstrom, M. E.: Production of bromoform and dibromomethane by Giant Kelp: Factors affecting release and comparison to anthropogenic bromine sources, Limnol. Oceanogr., 42, 1725-1734, doi:10.4319/lo.1997.42.8.1725, 1997.
12. Gschwend, P. M., MacFarlane, J. K., and Newman, K. A.: Volatile halogenated organic compounds released to seawater from temperate marine macroalgae, Science, 227, 1033-1035, doi:10.1126/science.227.4690.1033, 1984.
13. Hughes, C., Chuck, A. L., Rossetti, H., Mann, P. J., Turner, S. M., Clarke, A., Chance, R., and Liss, P. S.: Seasonal cycle of seawater bromoform and dibromomethane concentrations in a coastal bay on the western Antarctic Peninsula, Global Biogeochem. Cy., 23, GB2024, doi:10.1029/2008GB003268, 2009.
14. Hughes, C., Johnson, M., von Glasow, R., Chance, R., Atkinson, H., Souster, T., Lee, G. A., Clarke, A., Meredith, M., Venables, H. J., Turner, S. M., Malin, G., and Liss, P. S.: Climateinduced change in biogenic bromine emissions from the Antarctic marine biosphere, Global Biogeochem. Cy., 26, GB3019, doi:10.1029/2012GB004295, 2012.
15. Ji, Y. and Tanaka, J.: Effect of desiccation on the photosynthesis of seaweeds from the intertidal zone in Honshu, Japan. Phycol. Res., 50, 145-153, doi:10.1046/j.1440-1835.2002.00268.x, 2002.
16. Jones, C. E., Hornsby, K. E., Dunk, R. M., Leigh, R. J., and Carpenter, L. J.: Coastal measurements of short-lived reactive iodocarbons and bromocarbons at Roscoff, Brittany during the RHaMBLe campaign, Atmos. Chem. Phys., 9, 8757-8769, doi:10.5194/acp-9-8757-2009, 2009.
17. Keng, F. S.-L., Phang, S.-M., Rahman, N. A., Leedham, E. C., Hughes, C., Robinson, A. D., Harris, N. R. P., Pyle, J. A., and Sturges, W. T.: Volatile halocarbon emissions by three tropical brown seaweeds under different irradiances, J. Appl. Phycol., 25, 1377-1386, doi:10.1007/s10811-013-9990-x, 2013.
18. Klick, S.: The release of volatile halocarbons to seawater by untreated and heavy metal exposed samples of the brown seaweed Fucus vesiculosus, Mar. Chem., 42, 211-221, doi:10.1016/0304-4203(93)90013-E, 1993.
19. Kumar, M., Gupta, V., Trivedi, N., Kumari, P., Bijo, A. J., Reddy, C. R. K., and Jha, B.: Desiccation induced oxidative stress and its biochemical responses in intertidal red alga Gracilaria corticata (Gracilariales, Rhodophyta), Environ. Exp. Bot., 72, 194-201, doi:10.1016/j.envexpbot.2011.03.007, 2011.
20. Küpper, F. C., Kloareg, B., Guern, J., and Potin, P.: Oligoguluronates elicit an oxidative burst in the brown algal kelp Laminaria digitata, Plant Physiol., 125, 278-291, doi:10.1104/pp.125.1.278, 2001.
21. Küpper, 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., Kronek, P. M. H., Meyer-Klaucke, W., and Feiters, M. C.: Iodine accumulation provides kelp with an inorganic antioxidant impacting atmospheric chemistry, P. Natl. Acad. Sci. USA, 105, 6954-6958, doi:10.1073/pnas.0709959105, 2008.
22. Küpper, F. C., Carpenter, L. J., Leblanc, C., Toyama, C., Uchida, Y., Maskrey, B. H., Robinson, J., Vergaeghe, E. F., Malin, G., Luther III, G. W., Kroneck, P. M. H., Kloareg, B., Meyer-Klaucke, W., Muramatsu, Y., Megson, I. L., Potin, P., and Feiters, M. C.: In vivo speciation studies and antioxidant properties of bromine in Laminaria digitata reinforce the significance of iodine accumulation for kelps, J. Exp. Bot., 64, 2653-2664, doi:10.1093/jxb/ert110, 2013.
23. Leedham, E. C., Hughes, C., Keng, F. S. L., Phang, S.-M., Malin, G., and Sturges, W. T.: Emission of atmospherically significant halocarbons by naturally occurring and farmed tropical macroalgae, Biogeosciences, 10, 3615-3633, doi:10.5194/bg-10-3615-2013, 2013.
24. 2, inferred from CARIBIC air samples collected 1998-2012, Atmos. Chem. Phys. Discuss., 14, 20721-20765, doi:10.5194/acpd-14-20721-2014, 2014.
25. Lesser, M. P.: Oxidative stress in marine environments: Biochemistry and physiological ecology, Annu. Rev. Physiol., 68, 253-278, doi:10.1146/annurev.physiol.68.040104.110001, 2006.
26. Lewis, S., Donkin, M. E., and Depledge, M. H.: Hsp70 expression in Enteromorpha intestinalis (Chlorophyta) exposed to environmental stressors, Aquat. Toxicol., 51, 277-291, doi:10.1016/S0166-445X(00)00119-3, 2001.
27. Lobban, C. S., Harrison, P. J., and Duncan, M. J.: Seashore Communities. The Physiological Ecology of Seaweed, Cambridge University Press, New York, 154-188, 1985.
28. Lüning, K.: Seaweeds, Their environment, biogeography and ecophysiology, John Wiley & Sons, Inc., New York, 1990.
29. m used to improve productivity estimates in macroalgae, Mar. Biol., 130, 203-208, doi:10.1007/s002270050239, 1997.
30. Mäkelä, J. M., Hoffmann, T., Holzke, C., Väkevä, M., Suni, T., Mattila, T., Aalto, P. P., Tapper, U., Kauppinen, E. I., and O'Dowd, C. D.: Biogenic iodine emissions and identification of end-products in coastal ultrafine particles during nucleation bursts, J. Geophys. Res., 107, 8110, doi:10.1029/2001JD000580, 2002.
31. Manley, S.: Phytogenesis of halomethanes: A product of selection or a metabolic accident?, Biogeochemistry, 60, 163-180, 2002.
32. Markes International: Thermal Desorption Technical Support Note 5: Advice on sorbent selection, tube conditioning, tube storage and air sampling, Markes; UK, 2008.
33. Markes International: Thermal Desorption Technical Note 20: Confirming sorbent tube retention volumes and checking for analyte breakthrough, Markes; UK, 2012.
34. McFiggans, G., Coe, H., Burgess, R., Allan, J., Cubison, M., Alfarra, M. R., Saunders, R., Saiz-Lopez, A., Plane, J. M. C., Wevill, D., Carpenter, L., Rickard, A. R., and Monks, P. S.: Direct evidence for coastal iodine particles from Laminaria macroalgae - linkage to emissions of molecular iodine, Atmos. Chem. Phys., 4, 701-713, doi:10.5194/acp-4-701-2004, 2004.
35. Montzka, S. A., Reimann, S., et al.: Chapter 1, Ozone-Depleting Substances (ODSs) and Related Chemicals, in: Scientific Assessment of Ozone Depletion: 2010, Global Ozone Research and Monitoring Project Report No. 52, World Meteorological Organisation; Geneva, 2010.
36. Nightingale, P. D., Malin, G., and Liss, P. S.: Production of chloroform and other low molecular-weight halocarbons by some species of macroalgae, Limnol. Oceanogr., 40, 680-689, doi:10.4319/lo.1995.40.4.0680, 1995.
37. Nitschke, U., Ruth, A. A., Dixneuf, S., and Stengel, D. B.: Molecular iodine emission rates and photosynthetic performance of different thallus parts of Laminaria digitata (Phaeophyceae) during emersion, Planta, 233, 737-748, doi:10.1007/s00425-010-1334-3, 2011.
38. Palmer, C. J., Anders, T. L., Carpenter, L. J., Küpper, F. C., and McFiggans, G. B.: Iodine and halocarbon response of Laminaria digitata to oxidative stress and links to atmospheric new particle production, Environ. Chem., 2, 282-290, doi:10.1071/EN05078, 2005.
39. Pearson, G., Kautsky, L., and Serrão, E.: Recent evolution in Baltic Fucus vesiculosus: Reduced tolerance to emersion stresses compared to intertidal (North Sea) populations, Mar. Ecol. Prog. Ser., 202, 67-79, doi:10.3354/meps202067, 2000.
40. Pedersén, M., Collén, J., Abrahamsson, K., and Ekdahl, A.: Production of halocarbons from seaweeds an oxidative stress reaction?, Scientia Marina 60, 257-263, 1996.
41. Pena, E. J., Zingmark, R., and Nietch, C.: Comparative photosynthesis of two species of intertidal epiphytic macroalgae on mangrove roots during submersion and emersion, J. Phycol., 35, 1206-1214, doi:10.1046/j.1529-8817.1999.3561206.x, 1999.
42. Saenko, G. N., Kravtsova, Y. Y., Ivanenko, V. V., and Sheludko, S. I.: Concentration of iodine and bromine by plants in the Seas of Japan and Okhotsk, Mar. Biol., 47, 243-250, doi:10.1007.BF00541002, 1978.
43. Sampath-Wiley, P., Neefus, C. D., and Jahnke, L. S.: Seasonal effects of sun exposure and emersion on intertidal seaweed physiology: Fluctuations in antioxidant contents, photosynthetic pigments and photosynthetic efficiency in the red alga Porphyra umbilicalis Kützing (Rhodophyta, Bangiales), J. Exp. Mar. Biol. Ecol., 361, 83-91, doi:10.1016/j.jembe.2008.05.001, 2008.
44. Schlarb-Ridley, B. and Parker, B.: A UK roadmap for algal technologies. Report for the National Environmental Research Council (NERC) Technology Strategy Board (TSB) Algal Bioenergy-Special Interest Group (AB-SIG), 2013.
45. Walz GmBH: Underwater fluorometer Diving-PAM Submersible Photosynthesis Yield Analyzer - Handbook of Operation, Walz; Germany, 1998.
46. Williams, S. L. and Dethier, M. N.: High and dry: Variation in net photosynthesis of the intertidal seaweed Fucus gardneri, Ecology, 86, 2373-2379, doi:10.1890/04-1569, 2005.