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Journal articles on the topic 'Palaemon serratus'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Nakagawa, Heisuke, and Hubert J. Ceccaldi. "Circadian variations of haemolymph lipoprotein of Palaemon serratus." Biochemical Systematics and Ecology 13, no. 3 (1985): 345–48. http://dx.doi.org/10.1016/0305-1978(85)90047-x.

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2

Perina, Alejandra, Ana M. González-Tizón, Iago F. Meilán, and Andrés Martínez-Lage. "De novo transcriptome assembly of shrimp Palaemon serratus." Genomics Data 11 (March 2017): 89–91. http://dx.doi.org/10.1016/j.gdata.2016.12.009.

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3

Lovell, J. M., M. M. Findlay, R. M. Moate, and H. Y. Yan. "The hearing abilities of the prawn Palaemon serratus." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 140, no. 1 (January 2005): 89–100. http://dx.doi.org/10.1016/j.cbpb.2004.11.003.

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4

González-Tizón, Ana M., Andrés Martínez-Lage, Verónica Rojo, Zeltia Torrecilla, and Elisabetta Menini. "Karyological analysis of the shrimp Palaemon serratus (Decapoda: Palaemonidae)." Journal of Crustacean Biology 33, no. 6 (January 1, 2013): 843–48. http://dx.doi.org/10.1163/1937240x-00002185.

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5

Lozano, Gonzalo, Elena Herraiz, Arturo Hardisson, Angel J. Gutiérrez, Dailos González-Weller, and Carmen Rubio. "Heavy and trace metal concentrations in three rockpool shrimp species (Palaemon elegans, Palaemon adspersus and Palaemon serratus) from Tenerife (Canary Islands)." Environmental Monitoring and Assessment 168, no. 1-4 (August 15, 2009): 451–60. http://dx.doi.org/10.1007/s10661-009-1126-z.

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6

Alexander, C. G. "Tegumental glands in the paragnaths of Palaemon serratus (Crustacea: Natantia)." Journal of the Marine Biological Association of the United Kingdom 69, no. 1 (February 1989): 53–63. http://dx.doi.org/10.1017/s0025315400049109.

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The three lobed paragnath of Palaemon serratus (Pennant) contains numerous rosette-type tegumental glands often arranged in clusters of up to ten glands. Each gland is made up of around ten cells most of which stain deeply with toluidine blue and whose contents have a reticulate appearance in electron micrographs. One, or occasionally two, cells stain faintly and have a fine granular appearance in electron micrographs. The central region of each gland contains the main drainage duct together with feeder canals from the vesicular storage areas. The actively secreting region of each cell is peripheral and typified by abundant rough endoplasmic reticulum and Golgi apparatus. There are nerves adjacent to the glands and their contents are probably discharged in response to a food stimulus. The structure and possible function of the glands are discussed in relation to those of other species The secretions could act as a lubricant and as a binding agent to aid in the ingestion of particulate food. There is no evidence for any direct digestive function.

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7

Guerao, G., and C. Ribera. "Locomotor Activity Patterns and Feeding Habits in the Prawn Palaemon Serratus (Pennant, 1777) (Decapoda, Palaemonidae) in the Alfacs Bay, Ebro Delta, Spain." Crustaceana 69, no. 1 (1996): 101–12. http://dx.doi.org/10.1163/156854096x00132.

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AbstractDiel activity rhythms of the prawn Palaemon serratus from Alfacs Bay, Ebro Delta, Spain, were studied under laboratory conditions by time-lapse video recording. The activity pattern showed endogenous rhythmicity of a circadian period with maximum activity at night. The feeding habits of P. serratus were studied using the frequency-of-occurrence method and the points method. The food of this species mainly consists of molluscs and crustaceans, and the remains of gastropods, amphipods, isopods, bivalves, mysids, copepods, and decapods were identified. The remaining items consisted of cnidarians, polychaetes, ophiuroids, plant material, sand, and unidentified organic debris. Results indicate that P. serratus is a predator of benthic invertebrates rather than a scavenger or detritus feeder. Diet composition changes with the size of the prawn.

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8

MEYRAND, PIERRE, and MAURICE MOULINS. "Phylogenetic Plasticity of Crustacean Stomatogastric Circuits: I. Pyloric Patterns and Pyloric Circuit of the Shrimp Palaemon Serratus." Journal of Experimental Biology 138, no. 1 (September 1, 1988): 107–32. http://dx.doi.org/10.1242/jeb.138.1.107.

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Recordings from the muscles of the pyloric chamber of the shrimp Palaemon display a rhythmic pattern which is either monophasic or biphasic, and is different from the triphasic pyloric pattern of large decapods. Identification of the pyloric neurones in the stomatogastric ganglion and study of their synaptic relationships indicate that the pyloric circuit of Palaemon is very similar to the pyloric circuit of large decapods. It is concluded that homologous neuronal circuits in related species, although similar in terms of their ‘wiring diagram’, are able to produce significantly different patterned outputs.

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9

Madeira, Diana, Vanessa Mendonça, Marta Dias, Joana Roma, Pedro M. Costa, Miguel Larguinho, Catarina Vinagre, and Mário S. Diniz. "Physiological, cellular and biochemical thermal stress response of intertidal shrimps with different vertical distributions: Palaemon elegans and Palaemon serratus." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 183 (May 2015): 107–15. http://dx.doi.org/10.1016/j.cbpa.2014.12.039.

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10

Roustiau, Sylvie, Yves Batrel, Annie Bernicard-Peron, and Yves Le Gal. "Effect of thermal acclimation on subunit cooperativity in Palaemon serratus glutamate dehydrogenase." Biochemical Systematics and Ecology 13, no. 1 (January 1985): 45–50. http://dx.doi.org/10.1016/0305-1978(85)90012-2.

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11

Oliveira, Cristiana, Joana R. Almeida, Lúcia Guilhermino, Amadeu M. V. M. Soares, and Carlos Gravato. "Swimming velocity, avoidance behavior and biomarkers in Palaemon serratus exposed to fenitrothion." Chemosphere 90, no. 3 (January 2013): 936–44. http://dx.doi.org/10.1016/j.chemosphere.2012.06.036.

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12

E. Abdelme, Nabila, Hassan E. Awad, Ahmed M. Ibrahim, and Nabiha A. Yousef. "Ultrastructural Changes in Hepatopancreas of Palaemon serratus, Following Treatment with Petroleum Carcinogenic Compounds." Pakistan Journal of Nutrition 8, no. 6 (May 15, 2009): 770–81. http://dx.doi.org/10.3923/pjn.2009.770.781.

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13

Thébault, M. T., J. P. Raffin, and R. Pichon. "The Effect of the Stimulation Regime on Palaemon serratus Tail Muscle Energy Metabolism." Comparative Biochemistry and Physiology Part A: Physiology 116, no. 4 (April 1997): 337–40. http://dx.doi.org/10.1016/s0300-9629(96)00216-2.

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14

Thébault, Marie T., Anna Biegniewska, Jean P. Raffin, and Edward F. Skorkowski. "Short term cadmium intoxication of the shrimp Palaemon serratus: Effect on adenylate metabolism." Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology 113, no. 3 (March 1996): 345–48. http://dx.doi.org/10.1016/0742-8413(95)02044-6.

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15

MEYRAND, PIERRE, and MAURICE MOULINS. "Phylogenetic Plasticity of Crustacean Stomatogastric Circuits: II. Extrinsic Inputs to the Pyloric Circuit of the Shrimp Palaemon Serratus." Journal of Experimental Biology 138, no. 1 (September 1, 1988): 133–53. http://dx.doi.org/10.1242/jeb.138.1.133.

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The rhythmic motor patterns produced by the pyloric circuit of the shrimp Palaemon are substantially different from those of large decapods, although the homologous neuronal circuits are very similar (Meyrand & Moulins, 1988). The extrinsic inputs received by the Palaemon pyloric circuit were similar, at least qualitatively, to the extrinsic inputs known to impinge upon the pyloric circuit of large decapods. These include: rhythmic inputs that descend from another oscillator (the commissural pyloric oscillator, CPO) which appears to impose its own rhythm on neurones of the pyloric circuit; and inputs that have long-lasting effects and control the expression of endogenous burst-generating properties of individual neurones within the circuit via modulatory mechanisms. The AB—PD neurones were not observed to oscillate, and so do not appear to act as pacemakers for the pyloric circuit as they do in large decapods, probably because of differences in the organization of the modulatory extrinsic inputs. It is our conclusion that differences in the control of expression of intrinsic properties of neurones of homologous (and structurally similar) circuits belonging to related species can explain how such circuits produce widely different patterned motor outputs.

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16

Guerao, Guillermo, and Carles Ribera. "POPULATION CHARACTERISTICS OF THE PRAWN PALAEMON SERRATUS (DECAPODA, PALAEMONIDAE) IN A SHALLOW MEDITERRANEAN BAY." Crustaceana 73, no. 4 (2000): 459–68. http://dx.doi.org/10.1163/156854000504543.

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17

Raffin, J. P., and M. T. Thebault. "Purification and partial characterization of an AMP deaminase from the marine invertebrate Palaemon serratus." Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 88, no. 4 (January 1987): 1071–76. http://dx.doi.org/10.1016/0305-0491(87)90007-1.

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18

Rollin, Marc, Romain Coulaud, Béatrice Rocher, Aurélie Duflot, Agnes Poret, Frank Le Foll, and Benoit Xuereb. "N-acetyl-β-d-glucosaminidase activity in Palaemon serratus - Methodological optimisation and intrinsic variability." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 256 (June 2021): 110932. http://dx.doi.org/10.1016/j.cbpa.2021.110932.

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19

Weiss, Ronja, Zeltia Torrecilla, Enrique González-Ortegón, Ana M. González-Tizón, Andrés Martínez-Lage, and Christoph D. Schubart. "Genetic differentiation between Mediterranean and Atlantic populations of the common prawn Palaemon serratus (Crustacea: Palaemonidae) reveals uncommon phylogeographic break." Journal of the Marine Biological Association of the United Kingdom 98, no. 6 (June 8, 2017): 1425–34. http://dx.doi.org/10.1017/s0025315417000492.

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The Atlantic–Mediterranean transition zone between the Alborán Sea and the Gulf of Cádiz constitutes the most prominent marine geographic barrier in European waters and includes known phylogeographic breaks such as the Strait of Gibraltar and the Almería-Oran Front. A genetic shift in this area has been previously documented for the European littoral shrimp Palaemon elegans. Here we carried out a phylogeographic analysis with the congeneric and sympatric species Palaemon serratus to test for similar intraspecific genetic differentiation and geographic structure. This littoral prawn is distributed in the Northeastern Atlantic Ocean, the Mediterranean Sea and the Black Sea. We compared DNA sequences from the mitochondrial genes Cox1 and to a lesser extent from 16S rRNA of several Atlantic and Mediterranean populations. Furthermore, sequences from the nuclear gene Enolase were included for corroborating differences between Mediterranean and Atlantic individuals. A pronounced genetic differentiation was detected between the Mediterranean and Atlantic populations, amounting to 10.14% in Cox1 and 2.0% in 16S, indicating the occurrence of two independent evolutionary lineages. Interestingly, specimens from the Atlantic Gulf of Cadiz cluster together with the Mediterranean individuals, indicating that a biogeographic barrier appears to be located west of the Strait of Gibraltar.

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20

Frasco, Manuela F., Didier Fournier, Félix Carvalho, and Lúcia Guilhermino. "Does mercury interact with the inhibitory effect of dichlorvos on Palaemon serratus (Crustacea: Decapoda) cholinesterase?" Science of The Total Environment 404, no. 1 (October 2008): 88–93. http://dx.doi.org/10.1016/j.scitotenv.2008.06.012.

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21

Vincent, Michel. "Influence of water temperature on carotenoids and carotenoid metabolism in Palaemon serratus (Pennant) (Crustacea: Decapoda)." Biochemical Systematics and Ecology 17, no. 4 (July 1989): 319–22. http://dx.doi.org/10.1016/0305-1978(89)90011-2.

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22

Frasco, Manuela F., Ida Eržen, Jure Stojan, and Lúcia Guilhermino. "Localization and Properties of Cholinesterases in the Common Prawn (Palaemon serratus): a Kinetic-Histochemical Study." Biological Bulletin 218, no. 1 (February 2010): 1–5. http://dx.doi.org/10.1086/bblv218n1p1.

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23

Spindler, K. D., A. van Wormhoudt, D. Sellos, and M. Spindler-Barth. "Ecdysteroid levels during embryogenesis in the shrimp, Palaemon serratus (Crustacea decapoda): Quantitative and qualitative changes." General and Comparative Endocrinology 66, no. 1 (April 1987): 116–22. http://dx.doi.org/10.1016/0016-6480(87)90356-x.

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24

Oliveira, Cristiana, Joana Almeida, Lúcia Guilhermino, Amadeu M. V. M. Soares, and Carlos Gravato. "Acute effects of deltamethrin on swimming velocity and biomarkers of the common prawn Palaemon serratus." Aquatic Toxicology 124-125 (November 2012): 209–16. http://dx.doi.org/10.1016/j.aquatox.2012.08.010.

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25

Sánchez-Marín, Paula, and Ricardo Beiras. "Subcellular distribution and trophic transfer of Pb from bivalves to the common prawn Palaemon serratus." Ecotoxicology and Environmental Safety 138 (April 2017): 253–59. http://dx.doi.org/10.1016/j.ecoenv.2017.01.003.

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26

Kelly, Eoghan, Oliver Tully, and Ronan Browne. "Effects of temperature and salinity on the survival and development of larval and juvenile Palaemon serratus (Decapoda: Palaemonidae) from Irish waters." Journal of the Marine Biological Association of the United Kingdom 92, no. 1 (April 20, 2011): 151–61. http://dx.doi.org/10.1017/s0025315411000415.

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The combined effects of temperature and salinity on the survival and development of larval and juvenile Palaemon serratus from the west coast of Ireland were investigated. Survival over time was measured at thirty combinations of temperature and salinity ranging from 10–19°C and 9–34‰ in a fully factorial design. Salinity had a stronger influence than temperature on survival at all larval stages except stage V. For juveniles the main effect changed from temperature between 100 and 200 degree days to salinity between 200 and 600 degree days and temperature between 600 and 800 degree days. Estimates of time taken to 50% mortality showed that juveniles tolerated lower salinities for longer periods and exhibited optimal salinity values which were 3‰ lower than larvae, at temperatures between 10 and 15°C. Larval stage durations were found to be influenced by temperature but not salinity. Comparison with published data suggests that populations of P. serratus have adapted to local conditions of temperature and salinity. The results presented here have practical implications for fisheries assessment and management, as the incorporation of environmental effects into stock–recruitment models can improve their predictive capacity.

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27

Erraud, Alexandre, Marc Bonnard, Olivier Geffard, Romain Coulaud, Agnès Poret, Aurélie Duflot, Joëlle Forget-Leray, Alain Geffard, and Benoit Xuereb. "Signification of DNA integrity in sperm of Palaemon serratus (Pennant 1777): Kinetic responses and reproduction impairment." Marine Environmental Research 144 (February 2019): 130–40. http://dx.doi.org/10.1016/j.marenvres.2019.01.005.

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28

González-Ortegón, Enrique, Luis Giménez, Julian Blasco, and Lewis Le Vay. "Effects of food limitation and pharmaceutical compounds on the larval development and morphology of Palaemon serratus." Science of The Total Environment 503-504 (January 2015): 171–78. http://dx.doi.org/10.1016/j.scitotenv.2014.08.118.

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29

Azevedo, C., L. Corral, and CP Vivarès. "Ultrastructure of the microsporidian Inodosporus octospora (Thelohaniidae), a parasite of the shrimp Palaemon serratus (Crustacea, Decapoda)." Diseases of Aquatic Organisms 41 (2000): 151–58. http://dx.doi.org/10.3354/dao041151.

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30

Lovell, J. M. "The relationship between body size and evoked potentials from the statocysts of the prawn Palaemon serratus." Journal of Experimental Biology 209, no. 13 (July 1, 2006): 2480–85. http://dx.doi.org/10.1242/jeb.02211.

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31

Hussein, Rim, Khalid Al-Ghanim, Magda Abd-El-Atty, and Laila Mohamed. "Contamination of Red Sea Shrimp (Palaemon serratus) with Polycyclic Aromatic Hydrocarbons: a Health Risk Assessment Study." Polish Journal of Environmental Studies 25, no. 2 (2016): 615–20. http://dx.doi.org/10.15244/pjoes/60767.

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32

Favrel, P., A. Van-Wormhoudt, J. M. Studler, and C. Bellon. "Immunochemical and biochemical characterization of gastrin/cholecystokinin-like peptides in Palaemon serratus (Crustacea decapoda): Intermolt variations." General and Comparative Endocrinology 65, no. 3 (March 1987): 363–72. http://dx.doi.org/10.1016/0016-6480(87)90121-3.

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33

Yúfera, M., and A. Rodríguez. "Effect of prey density on feeding rates during larval rearing of Palaemon serratus Pennant (Crustacea: Palaemonidae)." Aquaculture 50, no. 1-2 (November 1985): 31–38. http://dx.doi.org/10.1016/0044-8486(85)90150-4.

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34

Lamharzi, N., Y. Arlot-Bonnemains, G. Milhaud, and M. Fouchereau-peron. "Calcitonin and calcitonin gene-related peptide in the shrimp, Palaemon serratus: Variations during the molt cycle." Comparative Biochemistry and Physiology Part A: Physiology 102, no. 4 (August 1992): 679–82. http://dx.doi.org/10.1016/0300-9629(92)90722-3.

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35

Gravato, Carlos, Joana R. Almeida, Carlos Silva, Cristiana Oliveira, and Amadeu M. V. M. Soares. "Using a multibiomarker approach and behavioural responses to assess the effects of anthracene in Palaemon serratus." Aquatic Toxicology 149 (April 2014): 94–102. http://dx.doi.org/10.1016/j.aquatox.2014.01.024.

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36

Goudeau, Henri, and Marie Goudeau. "External Mg2+ is required for hyperpolarization to occur in ovulated oocytes of the prawn Palaemon serratus." Developmental Biology 118, no. 2 (December 1986): 371–78. http://dx.doi.org/10.1016/0012-1606(86)90006-0.

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37

Thebault, MT, JP Raffin, R. Pichon, and A. Smine. "31P NMR studies of the metabolic changes in the prawns Palaemon serratus and P. elegans during exercise." Marine Ecology Progress Series 111 (1994): 73–78. http://dx.doi.org/10.3354/meps111073.

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38

Franchet, Cécile. "Mercury chloride induces changes in the Mg2+-stimulated membrane currents in oocytes of the prawn Palaemon serratus." Aquatic Toxicology 47, no. 1 (October 1999): 1–8. http://dx.doi.org/10.1016/s0166-445x(99)00017-x.

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39

Thebault, MT, and JP Raffin. "Seasonal variations in Palaemon serratus abdominal muscle metabolism and performance during exercise, as studied by 31P NMR." Marine Ecology Progress Series 74 (1991): 175–83. http://dx.doi.org/10.3354/meps074175.

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40

Thebault, MT, and JP Raffin. "Seasonal variations in Palaemon serratus abdominal muscle metabolism and performance during exercise, as studied by 31P NMR." Marine Ecology Progress Series 75 (1991): 175–83. http://dx.doi.org/10.3354/meps075175.

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41

Goudeau, H., and M. Goudeau. "Voltage dependence of the [Ca2+]ioscillations system, in the Mg2+-stimulated oocyte of the prawn Palaemon serratus." Cell Calcium 29, no. 2 (February 2001): 97–109. http://dx.doi.org/10.1054/ceca.2000.0174.

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42

Taylor, A. C., and J. I. Spicer. "Metabolic responses of the prawns Palaemon elegans and P. serratus (Crustacea: Decapoda) to acute hypoxia and anoxia." Marine Biology 95, no. 4 (September 1987): 521–30. http://dx.doi.org/10.1007/bf00393095.

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43

Frasco, Manuela F., Didier Fournier, Félix Carvalho, and Lúcia Guilhermino. "Cholinesterase from the common prawn (Palaemon serratus) eyes: Catalytic properties and sensitivity to organophosphate and carbamate compounds." Aquatic Toxicology 77, no. 4 (May 2006): 412–21. http://dx.doi.org/10.1016/j.aquatox.2006.01.011.

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44

Papathanassiou, E., and PE King. "Ultrastructural changes in hepatopancreatic cells of the prawn Palaemon serratus induced by exposure to acutely toxic cadmium concentrations." Diseases of Aquatic Organisms 2 (1986): 39–47. http://dx.doi.org/10.3354/dao002039.

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45

C. Mariño-Balsa, E. Poza, E, J. "Comparative Toxicity of Dissolved Metals to Early Larval Stages of Palaemon serratus , Maja squinado , and Homarus gammarus (Crustacea:Decapoda)." Archives of Environmental Contamination and Toxicology 39, no. 3 (September 1, 2000): 345–51. http://dx.doi.org/10.1007/s002440010114.

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46

Webster, S. G. "The Effect of Eyestalk Removal, Wounding and Limb Loss Upon Moulting and Proecdysis in the Prawn Palaemon Elegans (Rathke)." Journal of the Marine Biological Association of the United Kingdom 65, no. 2 (May 1985): 279–92. http://dx.doi.org/10.1017/s0025315400050402.

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Most current literature concerning moult control in crustaceans concludes that initiation of premoult is controlled by changes in the level of moult-inhibiting hormone (MIH) produced by the eyestalk neurosecretory organs. MIH is thought to act by repressing the secretory activity of the Y-organs, preventing increases in circulating ecdysteriod levels, necessary for moulting (see Kleinholz & Keller, 1979). This hypothesis is based upon the observation that eyestalk removal, by removing the source of MIH, leads to accelerated moulting (see Passano, 1960; Vernet-Cornubert, 1961; Sochasky, 1973, for reviews), and it survives despite many contrary reports indicating that moulting is unaffected by eyestalk removal (Sochasky, 1973). Perhaps the best known of the most contradictory data of this nature have been reported for Palaemon serratus for which Drach (1944, 1947), Panouse (1946, 1947) have shown that eyestalk removal generally accelerates moulting in this species. In contrast, Scheer & Scheer (1954) and Carlisle (1953) demonstrated no moult inhibition in this species following eyestalk removal.

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47

Kurun, A., H. Balkıs, and N. Balkıs. "Accumulations of total metal in dominant shrimp species (Palaemon adspersus, Palaemon serratus, Parapenaeus longirostris) and bottom surface sediments obtained from the Northern Inner Shelf of the Sea of Marmara." Environmental Monitoring and Assessment 135, no. 1-3 (April 4, 2007): 353–67. http://dx.doi.org/10.1007/s10661-007-9655-9.

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48

Lynch, Sharon A., Rachel Breslin, Babette Bookelaar, Tawut Rudtanatip, Kanokpan Wongprasert, and Sarah C. Culloty. "Immunomodulatory and Antiviral Effects of Macroalgae Sulphated Polysaccharides: Case Studies Extend Knowledge on Their Importance in Enhancing Shellfish Health, and the Control of a Global Viral Pathogen Ostreid Herpesvirus-1 microVar." Polysaccharides 2, no. 2 (April 1, 2021): 202–17. http://dx.doi.org/10.3390/polysaccharides2020014.

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Macroalgae are the primary source of non-animal sulphated polysaccharides (SPs) in the marine environment with fucoidans derived from brown algae (Phaeophyta) and carrageenans from red algae (Rhodophyta). Much research has been carried out on SP effects on Asian shrimp species (genera Penaeus and Metapenaeus) but their effect on commercially important bivalve mollusc species is limited and in Pacific oyster Crassostrea gigas is unknown. Knowledge of their impact on bivalve pathogens and Palaemon shrimp is unknown. The objectives of this study were to assess the effects of Fucus vesiculosus (Phaeophyta), Mastocarpus stellatus (Rhodophyta) and algal derivatives (fucoidan and κ-carrageenan) on C. gigas performance, and on ostreid herpesvirus-1 microvar (OsHV-1 μVar) and bacteria Vibrio spp. development. Both pathogens have been associated with significant oyster mortalities and economic losses globally. The effects of sulphated galactan from Gracilaria fisheri (Rhodophyta) on European common prawn Palaemon serratus, an important fishery species, was also assessed. Findings indicate a rapid and prolonged increase in total blood cell count, lysozyme (enzyme that destroys pathogens), and a difference in the ratio of blood cell types in treated individuals compared to their control counterparts. A significantly lower OsHV-1 μVar prevalence was observed in treated oysters and κ-carrageenan was found to suppress viral replication (loads), while OsHV-1 μVar was not detected in the fucoidan treated oysters from Day 8 of the 26-day trial. No antibacterial effect was observed however, the oysters did not succumb to vibriosis. These findings contribute further knowledge to macroalgae sulphated polysaccharide biotherapeutic properties, their twofold effect on animal health and viral suppression.

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Narciso, L., and S. Morais. "FATTY ACID PROFILE OF PALAEMON SERRATUS (PALAEMONIDAE) EGGS AND LARVAE DURING EMBRYONIC AND LARVAL DEVELOPMENT USING DIFFERENT LIVE DIETS." Journal of Crustacean Biology 21, no. 3 (August 2001): 566–74. http://dx.doi.org/10.1651/0278-0372(2001)021[0566:fapops]2.0.co;2.

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Narciso, L., and S. Morais. "Fatty Acid Profile of Palaemon Serratus (Palaemonidae) Eggs and Larvae During Embryonic and Larval Development Using Different Live Diets." Journal of Crustacean Biology 21, no. 3 (January 1, 2001): 566–74. http://dx.doi.org/10.1163/20021975-99990158.

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