20 Ago 2019

La concentración de sargazo en las playas caribeñas de México en años recientes se ha convertido en un problema no solo ambiental sino también económico, y desde luego en tema de estudios científicos para solventar o mitigar los efectos.

Con el fin de apoyar en el sustento de proyectos de investigación en ECOSUR en torno a este hecho, se presenta esta bibliografía extraída de los índices de calidad de la producción científica Web of Science y Scopus,

En ambos índices se utilizaron los términos “Pelagic Sargassum”, “Sargassum natans”, “Sargassum fluitans“, y las zonas geográficas Atlantic y Caribbean. El resultado fueron 78 referencias, de las cuales, como se observa, hay una gran cantidad de publicaciones en 2019 por ser tema emergente.

Esta bibliografía será actualizada mensualmente, de acuerdo con las alertas que generen los respectivos sistemas de Web of Science y Scopus.

2019

Wang, M., Hu, C., Barnes, B. B., Mitchum, G., Lapointe, B., & Montoya, J. P. (2019). The great Atlantic Sargassum belt. Science, 364(6448), 83–87. https://doi.org/10.1126/science.aaw7912

Oviatt, C. A., Huizenga, K., Rogers, C. S., & Miller, W. J. (2019). What nutrient sources support anomalous growth and the recent sargassum mass stranding on Caribbean beaches? A review. Marine Pollution Bulletin, 145, 517–525. https://doi.org/10.1016/j.marpolbul.2019.06.049

Rodríguez-Martínez, R. E., Medina-Valmaseda, A. E., Blanchon, P., Monroy-Velázquez, L. V, Almazán-Becerril, A., Delgado-Pech, B., García-Rivas, M. C. (2019). Faunal mortality associated with massive beaching and decomposition of pelagic Sargassum. Marine Pollution Bulletin, 146, 201–205. https://doi.org/10.1016/j.marpolbul.2019.06.015

Boisnoir, A., Pascal, P.-Y., Cordonnier, S., & Lemée, R. (2019). Spatio-temporal dynamics and biotic substrate preferences of benthic dinoflagellates in the Lesser Antilles, Caribbean sea. Harmful Algae, 81, 18–29. https://doi.org/10.1016/j.hal.2018.11.012

Mohammed, C., Mahabir, S., Mohammed, K., John, N., Lee, K.-Y., & Ward, K. (2019). Calcium Alginate Thin Films Derived from Sargassum natans for the Selective Adsorption of Cd 2+ , Cu 2+ , and Pb 2+ Ions. Industrial and Engineering Chemistry Research, 58(3), 1417–1425. https://doi.org/10.1021/acs.iecr.8b03691

Brooks, M. T., Coles, V. J., & Coles, W. C. (2019). Inertia Influences Pelagic Sargassum Advection and Distribution. Geophysical Research Letters, 46(5), 2610–2618. https://doi.org/10.1029/2018GL081489

Arellano-Verdejo, J., Lazcano-Hernandez, H. E., & Cabanillas-Terán, N. (2019). ERISNet: deep neural network for Sargassumdetection along the coastline of the Mexican Caribbean. PeerJ, 7, e6842. https://doi.org/10.7717/peerj.6842

Mohammed, A., Bissoon, R., Bajnath, E., Mohammed, K., Lee, T., Bissram, M., … Ward, K. (2018). Multistage extraction and purification of waste Sargassum natans to produce sodium alginate: An optimization approach. Carbohydrate Polymers, 198, 109–118. https://doi.org/10.1016/j.carbpol.2018.06.067

Quintal-Novelo, C., Rangel-Méndez, J., Ortiz-Tello, Á., Graniel-Sabido, M., Vaca, R. P.-C. D., & Moo-Puc, R. (2018). A Sargassum fluitans Borgesen Ethanol Extract Exhibits a Hepatoprotective Effect in Vivo in Acute and Chronic Liver Damage Models. BioMed Research International, 2018. https://doi.org/10.1155/2018/6921845

Sembera, J. A., Meier, E. J., & Waliczek, T. M. (2018). Composting as an alternative management strategy for sargassum drifts on coastlines. HortTechnology, 28(1), 80–84. https://doi.org/10.21273/HORTTECH03836-17

Baker, P., Minzlaff, U., Schoenle, A., Schwabe, E., Hohlfeld, M., Jeuck, A., … Arndt, H. (2018). Potential contribution of surface-dwelling Sargassum algae to deep-sea ecosystems in the southern North Atlantic. Deep-Sea Research Part II: Topical Studies in Oceanography, 148, 21–34. https://doi.org/10.1016/j.dsr2.2017.10.002

Sanchez-Rubio, G., Perry, H., Franks, J. S., & Johnson, D. R. (2018). Occurrence of pelagic Sargassum in waters of the US Gulf of Mexico in response to weather-related hydrographic regimes associated with decadal and interannual variability in global climate. Fishery Bulletin, 116(1), 93–106. https://doi.org/10.7755/FB.116.1.10

Cuevas, E., Uribe-Martínez, A., & Liceaga-Correa, M. D. L. Á. (2018). A satellite remote-sensing multi-index approach to discriminate pelagic Sargassum in the waters of the Yucatan Peninsula, Mexico. International Journal of Remote Sensing, 39(11), 3608–3627. https://doi.org/10.1080/01431161.2018.1447162

Brooks, M. T., Coles, V. J., Hood, R. R., & Gower, J. F. R. (2018). Factors controlling the seasonal distribution of pelagic Sargassum. Marine Ecology Progress Series, 599, 1–18. https://doi.org/10.3354/meps12646

2018

Wang, M., & Hu, C. (2018). On the continuity of quantifying floating algae of the central west atlantic between modis and viirs. International Journal of Remote Sensing, 39(12), 3852–3869. https://doi.org/10.1080/01431161.2018.1447161

Putman, N. F., Goni, G. J., Gramer, L. J., Hu, C., Johns, E. M., Trinanes, J., & Wang, M. (2018). Simulating transport pathways of pelagic Sargassum from the Equatorial Atlantic into the Caribbean Sea. Progress in Oceanography, 165, 205–214. https://doi.org/10.1016/j.pocean.2018.06.009

Wang, M., Hu, C., Cannizzaro, J., English, D., Han, X., Naar, D., … Hernandez, F. (2018). Remote Sensing of Sargassum Biomass, Nutrients, and Pigments. Geophysical Research Letters, 45(22), 12,312-359,367. https://doi.org/10.1029/2018GL078858

Barros-Alves, S. de P., Alves, D. F. R., & Cobo, V. J. (2018). Brachyuran crab (Crustacea, Decapoda) assemblage associated with Sargassum cymosum in southeastern Brazil. Marine Biodiversity, 48(4), 2043–2055. https://doi.org/10.1007/s12526-017-0730-3

Russell, B. J., & Dierssen, H. M. (2018). Color change in the Sargassum crab, Portunus sayi: response to diel illumination cycle and background albedo. Marine Biology, 165(2), 28. https://doi.org/10.1007/s00227-018-3287-1

West, L. E., & Randy Brooks, W. (2018). Host location and selection by the symbiotic sargassum crab Portunus sayi: the role of chemical, visual and tactile cues. Symbiosis, 76(2), 177–185. https://doi.org/10.1007/s13199-018-0561-4

2017

Maréchal, J.-P., Hellio, C., & Hu, C. (2017). A simple, fast, and reliable method to predict Sargassum washing ashore in the Lesser Antilles. Remote Sensing Applications: Society and Environment, 5, 54–63. https://doi.org/10.1016/j.rsase.2017.01.001

van Tussenbroek, B. I., Hernández Arana, H. A., Rodríguez-Martínez, R. E., Espinoza-Avalos, J., Canizales-Flores, H. M., González-Godoy, C. E., … Collado-Vides, L. (2017). Severe impacts of brown tides caused by Sargassum spp. on near-shore Caribbean seagrass communities. Marine Pollution Bulletin, 122(1–2), 272–281. https://doi.org/10.1016/j.marpolbul.2017.06.057

Molodtsova, T. N., Galkin, S. V, Kobyliansky, S. G., Simakova, U. V, Vedenin, A. A., Dobretsova, I. G., & Gebruk, A. V. (2017). First data on benthic and fish communities from the Mid-Atlantic Ridge, 16°40′− 17°14′N. Deep-Sea Research Part II: Topical Studies in Oceanography, 137, 69–77. https://doi.org/10.1016/j.dsr2.2016.10.006

Amaral-Zettler, L. A., Dragone, N. B., Schell, J., Slikas, B., Murphy, L. G., Morrall, C. E., & Zettler, E. R. (2017). Comparative mitochondrial and chloroplast genomics of a genetically distinct form of Sargassum contributing to recent “Golden Tides” in the Western Atlantic. Ecology and Evolution, 7(2), 516–525. https://doi.org/10.1002/ece3.2630

Sissini, M. N., De Barros Barreto, M. B. B., Szećhy, M. T. M., De Lucena, M. B., Oliveira, M. C., Gower, J., … Horta, P. A. (2017). The floating Sargassum (Phaeophyceae) of the South Atlantic Ocean – Likely scenarios. Phycologia, 56(3), 321–328. https://doi.org/10.2216/16-92.1

McDonald, T. L., Schroeder, B. A., Stacy, B. A., Wallace, B. P., Starcevich, L. A., Gorham, J., … Witherington, B. E. (2017). Density and exposure of surface-pelagic juvenile sea turtles to Deepwater Horizon oil. Endangered Species Research, 33(1), 69–82. https://doi.org/10.3354/esr00771

Wang, M., & Hu, C. (2017). Predicting Sargassum blooms in the Caribbean Sea from MODIS observations. Geophysical Research Letters, 44(7), 3265–3273. https://doi.org/10.1002/2017GL072932

2016

Milledge, J. J., & Harvey, P. J. (2016). Golden Tides: Problem or golden opportunity? The valorisation of Sargassum from beach inundations. Journal of Marine Science and Engineering, 4(3). https://doi.org/10.3390/jmse4030060

Ayala, D., Riemann, L., & Munk, P. (2016). Species composition and diversity of fish larvae in the Subtropical Convergence Zone of the Sargasso Sea from morphology and DNA barcoding. Fisheries Oceanography, 25(1), 85–104. https://doi.org/10.1111/fog.12136

Wang, M., & Hu, C. (2016). Mapping and quantifying Sargassum distribution and coverage in the Central West Atlantic using MODIS observations. Remote Sensing of Environment, 183, 350–367. https://doi.org/10.1016/j.rse.2016.04.019

Hu, C., Hardy, R., Ruder, E., Geggel, A., Feng, L., Powers, S., … McDonald, T. (2016). Sargassum coverage in the northeastern Gulf of Mexico during 2010 from Landsat and airborne observations: Implications for the Deepwater Horizon oil spill impact assessment. Marine Pollution Bulletin, 107(1), 15–21. https://doi.org/10.1016/j.marpolbul.2016.04.045

2015

Gavio, B., Rincón-Díaz, M. N., & Santos-Martínez, A. (2015). Massive quantities of pelagic Sargassum on the shores of San Andres Island, southwestern Caribbean [Cantidades masivas de Sargassum pelágicos en las costas de San Andrés Isla, Caribe suroccidental]. Acta Biologica Colombiana, 20(1), 239–241. https://doi.org/10.15446/abc.v20n1.46109

Mancera-Rodríguez, N. J., & Castro-Hernández, J. J. (2015). Feeding ecology of the planehead filefish Stephanolepis hispidus (Pisces: Monacanthidae), in the Canary Islands area. Revista de biología marina y oceanografía, 50(2), 221–234. https://doi.org/10.4067/S0718-19572015000300002

Russell, B. J., & Dierssen, H. M. (2015). Use of Hyperspectral Imagery to Assess Cryptic Color Matching in Sargassum Associated Crabs. PLOS ONE, 10(9), e0136260. https://doi.org/10.1371/journal.pone.0136260

Cruz-Rivera, E., Flores-Díaz, M., & Hawkins, A. (2015). A fish kill coincident with dense Sargassum accumulation in a tropical ba. Bulletin of Marine Science, 91(4), 455–456. https://doi.org/10.5343/bms.2015.1048

2014

Cottrell, B. A., Gonsior, M., Timko, S. A., Simpson, A. J., Cooper, W. J., & van der Veer, W. (2014). Photochemistry of marine and fresh waters: A role for copper-dissolved organic matter ligands. Marine Chemistry, 162, 77–88. https://doi.org/10.1016/j.marchem.2014.03.005

Huffard, C. L., von Thun, S., Sherman, A. D., Sealey, K., & Smith K.L., J. (2014). Pelagic Sargassum community change over a 40-year period: temporal and spatial variability. Marine Biology, 161(12), 2735–2751. https://doi.org/10.1007/s00227-014-2539-y

Lapointe, B. E., West, L. E., Sutton, T. T., & Hu, C. (2014). Ryther revisited: Nutrient excretions by fishes enhance productivity of pelagic Sargassum in the western North Atlantic Ocean. Journal of Experimental Marine Biology and Ecology, 458, 46–56. https://doi.org/10.1016/j.jembe.2014.05.002

Gavio, B., Rincón-Díaz, M. N., & Santos-Martínez, A. (2014). Massive quantities of pelagic sargassum on the shores of San Andres Island, Southwestern Caribbean. Acta Biológica Colombiana, 20(1), 239–241. https://doi.org/10.15446/abc.v20n1.46109

Tansel, B., Lee, M., Berbakov, J., Tansel, D. Z., & Koklonis, U. (2014). Dispersion of Louisiana crude oil in salt water environment by Corexit 9500A in the presence of natural coastal materials. Estuarine, Coastal and Shelf Science, 143, 58–64. https://doi.org/10.1016/j.ecss.2014.03.022

Farrell, E. R., Boustany, A. M., Halpin, P. N., & Hammond, D. L. (2014). Dolphinfish (Coryphaena hippurus) distribution in relation to biophysical ocean conditions in the northwest Atlantic. Fisheries Research, 151, 177–190. https://doi.org/10.1016/j.fishres.2013.11.014

Sehein, T., Siuda, A. N. S., Shank, T. M., & Govindarajan, A. F. (2014). Connectivity in the slender Sargassum shrimp (Latreutes fucorum): implications for a Sargasso Sea protected area. Journal of Plankton Research, 36(6), 1408–1412. https://doi.org/10.1093/plankt/fbu081

2013

Fleury, A. G., & Drazen, J. C. (2013). Abyssal Scavenging Communities attracted to Sargassum and fish in the Sargasso Sea. Deep Sea Research Part I: Oceanographic Research Papers, 72, 141–147. https://doi.org/10.1016/j.dsr.2012.11.004

2012

de Széchy, M. T. M., Guedes, P. M., Baeta-Neves, M. H., & Oliveira, E. N. (2012). Verification of Sargassum natans (Linnaeus) Gaillon (Heterokontophyta: Phaeophyceae) from the Sargasso Sea off the coast of Brazil, western Atlantic Ocean. Check List, 8(4), 638–641.

Witherington, B., Hirama, S., & Hardy, R. (2012). Young sea turtles of the pelagic Sargassum-dominated drift community: Habitat use, population density, and threats. Marine Ecology Progress Series, 463, 1–22. https://doi.org/10.3354/meps09970

Moser, M. L., & Lee, D. S. (2012). Foraging over Sargassum by Western North Atlantic Seabirds. The Wilson Journal of Ornithology, 124(1), 66–72. https://doi.org/10.1676/11-067.1

2011

Van Ginneken, V. J. T., Helsper, J. P. F. G., De Visser, W., Van Keulen, H., & Brandenburg, W. A. (2011). Polyunsaturated fatty acids in various macroalgal species from north Atlantic and tropical seas. Lipids in Health and Disease, 10. https://doi.org/10.1186/1476-511X-10-104

Gower, J. F. R., & King, S. A. (2011). Distribution of floating Sargassum in the Gulf of Mexico and the Atlantic Ocean mapped using MERIS. International Journal of Remote Sensing, 32(7), 1917–1929. https://doi.org/10.1080/01431161003639660

De Oliveira, O. M. P., & Marques, A. C. (2011). Global and local patterns in the use of macrophytes as substrata by hydroids (Hydrozoa: Anthoathecata and Leptothecata). Marine Biology Research, 7(8), 786–795. https://doi.org/10.1080/17451000.2011.578647

2010

Shank, G. C., Lee, R., Vähätalo, A., Zepp, R. G., & Bartels, E. (2010). Production of chromophoric dissolved organic matter from mangrove leaf litter and floating Sargassum colonies. Marine Chemistry, 119(1–4), 172–181. https://doi.org/10.1016/j.marchem.2010.02.002

Rudershausen, P. J., Buckel, J. A., Edwards, J., Gannon, D. P., Butler, C. M., & Averett, T. W. (2010). Feeding Ecology of Blue Marlins, Dolphinfish, Yellowfin Tuna, and Wahoos from the North Atlantic Ocean and Comparisons with other Oceans. Transactions of the American Fisheries Society, 139(5), 1335–1359. https://doi.org/10.1577/T09-105.1

2009

Wells, R. J. D., & Rooker, J. R. (2009). Feeding ecology of pelagic fish larvae and juveniles in slope waters of the Gulf of Mexico. Journal of Fish Biology, 75(7), 1719–1732. https://doi.org/10.1111/j.1095-8649.2009.02424.x

Jobe, C. F., & Randy Brooks, W. (2009). Habitat selection and host location by symbiotic shrimps associated with Sargassum communities: The role of chemical and visual cues. Symbiosis, 49(2), 77–85. https://doi.org/10.1007/s13199-009-0017-y

2008

Krimsky, L. S., & Epifanio, C. E. (2008). Multiple cues from multiple habitats: Effect on metamorphosis of the Florida stone crab, Menippe mercenaria. Journal of Experimental Marine Biology and Ecology, 358(2), 178–184. https://doi.org/10.1016/j.jembe.2008.02.010

Casazza, T. L., & Ross, S. W. (2008). Fishes associated with pelagic Sargassum and open water lacking Sargassum in the Gulf Stream off North Carolina. Fishery Bulletin, 106(4), 348–363.

2007

Vandendriessche, S., Messiaen, M., O’Flynn, S., Vincx, M., & Degraer, S. (2007). Hiding and feeding in floating seaweed: Floating seaweed clumps as possible refuges or feeding grounds for fishes. Estuarine, Coastal and Shelf Science, 71(3–4), 691–703. https://doi.org/10.1016/j.ecss.2006.09.017

2006

Rooker, J. R., Turner, J. P., & Holt, S. A. (2006). Trophic ecology of Sargassum-associated fishes in the Gulf of Mexico determined from stable isotopes and fatty acids. Marine Ecology Progress Series, 313, 249–259. https://doi.org/10.3354/meps313249

Vandendriessche, S., De Keersmaecker, G., Vincx, M., & Degraer, S. (2006). Food and habitat choice in floating seaweed clumps: the obligate opportunistic nature of the associated macrofauna. Marine Biology, 149(6), 1499–1507. https://doi.org/10.1007/s00227-006-0292-6

Vandendriessche, S., Vincx, M., & Degraer, S. (2006). Floating seaweed in the neustonic environment: A case study from Belgian coastal waters. Journal of Sea Research, 55(2), 103–112. https://doi.org/10.1016/j.seares.2005.09.002

Turner, J. P., & Rooker, J. R. (2006). Fatty acid composition of flora and fauna associated with Sargassum mats in the Gulf of Mexico. Marine Biology, 149(5), 1025–1036. https://doi.org/10.1007/s00227-006-0269-5

2004

Davis, T. A., Ali, F. E., Giannitti, E., Volesky, B., & Mucci, A. (2004). Cadmium biosorption by S-fluitans: Treatment, resilience and uptake relative to other Sargassum spp. and brown algae. Water Quality Research Journal of Canada, 39(3), 183–189.

Wells, R. J. D., & Rooker, J. R. (2004). Spatial and temporal patterns of habitat use by fishes associated with Sargassum mats in the northwestern Gulf of Mexico. Bulletin of Marine Science, 74(1), 81–99.

Wells, R. J. D., & Rooker, J. R. (2004). Distribution, age, and growth of young-of-the-year greater amberjack (Seriola dumerili) associated with pelagic Sargassum. Fishery Bulletin, 102(3), 545–554.

2000

Knap, A. H., Connelly, D. P., & Butler, J. N. (2000). The Sargasso Sea and Bermuda. Elsevier Science Inc.

1997 – 1970

Stachowicz, J. J., & Lindquist, N. (1997). Chemical defense among hydroids on pelagic Sargassum: Predator deterrence and absorption of solar UV radiation by secondary metabolites. Marine Ecology Progress Series, 155, 115–126. https://doi.org/10.3354/meps155115

Snelgrov, P. V. R., Grassle, J. F., & Petrecca, R. F. (1996). Experimental evidence for aging food patches as a factor contributing to high deep-sea macrofaunal diversity. Limnology and Oceanography, 41(4), 605–614. https://doi.org/10.4319/lo.1996.41.4.0605

Calder, D. R. (1995). Hydroid assemblages on holopelagic Sargassum from the Sargasso Sea at Bermuda. Bulletin of Marine Science, 56(2), 537–546.

Lapointe, B. E. (1995). A comparison of nutrient‐limited productivity in Sargassum natans from neritic vs. oceanic waters of the western North Atlantic Ocean. Limnology and Oceanography, 40(3), 625–633. https://doi.org/10.4319/lo.1995.40.3.0625

Woodcock, A. H. (1993). Winds subsurface pelagic Sargassum and Langmuir circulations. Journal of Experimental Marine Biology and Ecology, 170(1), 117–125. https://doi.org/10.1016/0022-0981(93)90132-8

Hacker, S. D., & Madin, L. P. (1991). Why habitat architecture and color are important to shrimps living in pelagic Sargassum: use of camouflage and plant-part mimicry. Marine Ecology Progress Series, 70(2), 143–155. https://doi.org/10.3354/meps070143

Calder, D. R. (1991). Associations between hydroid species assemblages and substrate types in the mangal at Twin Cays, Belize. Canadian Journal of Zoology, 69(8), 2067–2074. https://doi.org/10.1139/z91-288

Lapointe, B. E. (1986). Phosphorus-limited photosynthesis and growth of Sargassum natans and Sargassum fluitans (Phaeophyceae) in the western North Atlantic. Deep Sea Research Part A, Oceanographic Research Papers, 33(3), 391–399. https://doi.org/10.1016/0198-0149(86)90099-3

Haney, J. (1986). Seabird Patchiness in Tropical Oceanic Waters – the Influence of Sargassum Reefs. Auk, 103(1), 141–151.

Niermann, U. (1986). Distribution ofSargassum natans and some of its epibionts in the Sargasso Sea. Helgoländer Meeresuntersuchungen, 40(4), 343–353. https://doi.org/10.1007/BF01983817

Stoner, A. W., & Greening, H. S. (1984). Geographic variation in the macrofaunal associates of pelagic Sargassum and some biogeographic implications. Marine Ecology Progress Series, 20, 185–192. https://doi.org/10.3354/meps020185

Stoner, A. W. (1983). Pelagic Sargassum: Evidence for a major decrease in biomass. Deep Sea Research Part A, Oceanographic Research Papers, 30(4), 469–474. https://doi.org/10.1016/0198-0149(83)90079-1

Winston, J. E. (1982). Drift plastic-An expanding niche for a marine invertebrate? Marine Pollution Bulletin, 13(10), 348–351. https://doi.org/10.1016/0025-326X(82)90038-8

Fine, M. L. (1970). Faunal variation on pelagic Sargassum. Marine Biology, 7(2), 112–122. https://doi.org/10.1007/BF00354914