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Journal articles on the topic 'Cymodocea nodosa'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Monterroso, Oscar, Rodrigo Riera, and Jorge Núñez. "Subtidal soft-bottom macroinvertebrate communities of the Canary Islands. An ecological approach." Brazilian Journal of Oceanography 60, no. 1 (March 2012): 1–9. http://dx.doi.org/10.1590/s1679-87592012000100001.

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The Canarian archipelago is characterized by a mosaic of soft-bottoms such as Cymodocea nodosa meadows, Caulerpa spp. meadows, mäerl bottoms, sabellid fields and bare sandy seabeds, including various macroinfaunal communities. Vegetated habitats (e.g. Cymodocea and Caulerpa) maintain more diverse communities than the non-vegetated seabeds. The results indicated that Caulerpa meadows and, to a lesser extent, Cymodocea nodosa and sabellid fields are the richest and most diverse ecosystems in the study area. Moreover, biodiversity differences among islands could be detected with maximum values on the eastern islands (Lanzarote and Gran Canaria) and lowest values on the western ones (La Palma).

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2

Tsioli, Soultana, Sotiris Orfanidis, Vasillis Papathanasiou, Christos Katsaros, and Athanasios Exadactylos. "Effects of salinity and temperature on the performance of Cymodocea nodosa and Ruppia cirrhosa: a medium-term laboratory study." Botanica Marina 62, no. 2 (April 24, 2019): 97–108. http://dx.doi.org/10.1515/bot-2017-0125.

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Abstract The effects of salinity and temperature on the photosynthetic and growth performance of the seagrasses Cymodocea nodosa and Ruppia cirrhosa were studied to understand their local seasonality and distribution. Cymodocea nodosa shoots were collected from Cape Vrasidas, and R. cirrhosa shoots from the coastal lagoon Fanari, all from the Eastern Macedonian and Thrace Region, Greece. Effective quantum yield (ΔF/Fm′), leaf chlorophyll-a content (mg g−1 wet mass) and growth (% of maximum) were tested at different temperatures (10–40°C) and salinities (5–60). The results showed that: (a) R. cirrhosa was more euryhaline (5–55/60) than C. nodosa (10–50), (b) the upper thermal tolerance of C. nodosa (34–35°C) was higher than that of R. cirrhosa (32–34°C), (c) C. nodosa could not tolerate 10°C, whereas R. cirrhosa could, and (d) the growth optimum of C. nodosa was 30°C and that of R. cirrhosa 20–30°C. The thermal optima and tolerances of growth and photosynthesis confirm the seasonal patterns of R. cirrhosa but not of C. nodosa. However, the sensitivity of C. nodosa to low salinities and temperatures may explain its absence from shallow coastal lagoons. Ruppia cirrhosa could be vulnerable to future climate change.

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3

Marián, Fernando D., Pilar Garcia-Jimenez, and Rafael R. Robaina. "Polyamine levels in the seagrass Cymodocea nodosa." Aquatic Botany 68, no. 2 (October 2000): 179–84. http://dx.doi.org/10.1016/s0304-3770(00)00111-x.

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4

Sánchez, A. "Biosorption of copper and zinc by Cymodocea nodosa." FEMS Microbiology Reviews 23, no. 5 (October 1999): 527–36. http://dx.doi.org/10.1016/s0168-6445(99)00019-4.

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5

Jiménez‐Ramos, Rocío, Luis G. Egea, Juan J. Vergara, and Fernando G. Brun. "Factors modulating herbivory patterns in Cymodocea nodosa meadows." Limnology and Oceanography 66, no. 6 (May 19, 2021): 2218–33. http://dx.doi.org/10.1002/lno.11749.

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6

Alexandre, A., and R. Santos. "Competition for nitrogen between the seaweed Caulerpa prolifera and the seagrass Cymodocea nodosa." Marine Ecology Progress Series 648 (August 27, 2020): 125–34. http://dx.doi.org/10.3354/meps13429.

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The rhizophytic seaweed Caulerpa prolifera has been expanding rapidly in the Ria Formosa lagoon, southern Portugal, taking over deeper unvegetated areas and mixing with the native seagrass Cymodocea nodosa in shallower areas. In the Ria Formosa lagoon, belowground ammonium uptake from the sediment represents the main source of nitrogen for the 2 macrophytes, except during the ammonium pulses from the sediment to the water column that are incorporated through aboveground plant parts. We examined the competition for inorganic and organic nitrogen between C. prolifera and C. nodosa through a series of 15N-ammonium and 15N-amino acid surge uptake experiments combining single-species and mixed incubations at a range of nutrient concentrations. Our results showed that C. prolifera is generally faster than C. nodosa in the acquisition of ammonium and amino acids by both above- and belowground parts, and that the uptake rates of ammonium and amino acids of one species were not affected by the presence of the other species. The exception was the amino acid uptake through the rhizoids of C. prolifera, which was slightly enhanced in the presence of C. nodosa. In this situation, the aboveground ammonium uptake becomes the main contributor to the nitrogen budget of C. nodosa but not to that of C. prolifera. When ammonium pulses are considered, C. nodosa is more competitive for nitrogen than C. prolifera. In this case, the leaf uptake of ammonium is the largest contributor to the total nitrogen (ammonium plus amino acids) budget of the seagrass. Our results showed that the different nutritional strategies of the 2 macrophytes allow their coexistence in the Ria Formosa lagoon.

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7

Buia, Maria Cristina, Gianluigi Cancemi, and Lucia Mazzella. "Structure and growth dynamics of Cymodocea nodosa meadows." Scientia Marina 66, no. 4 (December 30, 2002): 365–73. http://dx.doi.org/10.3989/scimar.2002.66n4365.

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8

RUGGIERO, M. V., T. B. H. REUSCH, and G. PROCACCINI. "Polymorphic microsatellite loci for the marine angiosperm Cymodocea nodosa." Molecular Ecology Notes 4, no. 3 (September 2004): 512–14. http://dx.doi.org/10.1111/j.1471-8286.2004.00709.x.

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9

Despalatović, Marija, Boris Antolić, Ivana Grubelić, and Ante Žuljević. "First record of the Indo-Pacific gastropod Melibe fimbriata in the Adriatic Sea." Journal of the Marine Biological Association of the United Kingdom 82, no. 5 (October 2002): 923–24. http://dx.doi.org/10.1017/s0025315402006380.

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The specimens of Melibe fimbriata were found during October 2001 in Stari Grad Bay (Island of Hvar, Croatia) in Cymodocea nodosa and Posidonia oceanica beds on sandy and sandy–muddy bottoms at depths of 2 to 15 m. Presently, this is the northernmost record of this lessepsian immigrant in the Mediterranean basin.

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10

Moreno, Diego, and José Guirado. "Nuevos datos sobre la distribución de las fanerkamas marinas en las provincias de Almería y Granada (SE España)." Acta Botanica Malacitana 28 (January 1, 2003): 105–20. http://dx.doi.org/10.24310/abm.v28i0.7270.

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RESUMEN. Nuevos datos sobre la distribución de las fanerkamas marinas en las provincias de Almería y Granada (SE España). Se estudia la distribución de las distintas especies de fanerógamas marinas en el litoral de las provincias de Almería y Granada. Se detallan las áreas cubiertas por praderas de Posidonia oceanica (L.) Delile en la provincia de Almería y las localidades donde todavía se encuentran manchas de esta especie en la provincia de Granada. Se aportan datos sobre la distribución en la zona de Cymodocea nodosa (Ucria)Ascherson, así como nuevos y numerosos datos sobre la presencia en el área de estudio de Zostera marina L. y Zostera noltii Hornemann. Se relaciona la distribución de las distintas especies de faner6gamas con el frente Almería-Orán, como límite biogeográfico difícil de franquear en la distribución de la mayoría de ellas, y se revisa el estado de conservación de las praderas dentro de los espacios naturales protegidos que existen en la zona.Palabras clave. Distribución, fanerógamas marinas, SE España, Posidonia, Cymodocea, Zostera.ABSTRACT. New data on the seagrasses distribution in Almería and Granada (SE Spain). The distribution of the four species of seagrasses in Almería and Granada is studied. The meadows of Posidonia oceanica (L.) Delile in Almería province and the few localities where it is present in Granada province are detailed. The distribution of Cymodocea nodosa (Ucria)Ascherson in this area and new data on the presence of Zostera marina L. and Zostera noltii Hornemann are included. The Almería-Oran front as a biogeographical boundary is related with the four seagrasses species. The conservation status of seagrasses meadows in the Marine Protected Arcas along the studied coast is revised.Key words. Distribution, seagrasses, SE Spain, Posidonia, Cymodocea, Zostera.

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11

Sanmartí, N., L. Saiz, I. Llagostera, M. Pérez, and J. Romero. "Tolerance responses to simulated herbivory in the seagrass Cymodocea nodosa." Marine Ecology Progress Series 517 (December 15, 2014): 159–69. http://dx.doi.org/10.3354/meps11084.

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12

Marbà, N., and CM Duarte. "Growth and sediment space occupation by seagrass Cymodocea nodosa roots." Marine Ecology Progress Series 224 (2001): 291–98. http://dx.doi.org/10.3354/meps224291.

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13

Terrados, J., CM Duarte, and WJ Kenworthy. "Experimental evidence for apical dominance in the seagrass Cymodocea nodosa." Marine Ecology Progress Series 148 (1997): 263–68. http://dx.doi.org/10.3354/meps148263.

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14

Infantes, Eduardo, Alejandro Orfila, Tjeerd J. Bouma, Gonzalo Simarro, and Jorge Terrados. "Posidonia oceanica and Cymodocea nodosa seedling tolerance to wave exposure." Limnology and Oceanography 56, no. 6 (October 22, 2011): 2223–32. http://dx.doi.org/10.4319/lo.2011.56.6.2223.

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15

Duarte, CM, and K. Sand-Jensen. "Seagrass colonization: patch formation and patch growth in Cymodocea nodosa." Marine Ecology Progress Series 65 (1990): 193–200. http://dx.doi.org/10.3354/meps065193.

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16

Siljeström, P., A. Moreno, R. Carbó, J. Rey, and J. Cara. "Selectivity in the acoustic response of Cymodocea nodosa (Ucria) Ascherson." International Journal of Remote Sensing 23, no. 14 (January 2002): 2869–76. http://dx.doi.org/10.1080/01431160110075875.

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17

Caye, G., and A. Meinesz. "Experimental study of seed germination in the seagrass Cymodocea nodosa." Aquatic Botany 26 (January 1986): 79–87. http://dx.doi.org/10.1016/0304-3770(86)90006-9.

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18

Png-Gonzalez, Lydia, Maite Vázquez-Luis, and Fernando Tuya. "Comparison of epifaunal assemblages between Cymodocea nodosa and Caulerpa prolifera meadows in Gran Canaria (eastern Atlantic)." Journal of the Marine Biological Association of the United Kingdom 94, no. 2 (November 22, 2013): 241–53. http://dx.doi.org/10.1017/s0025315413001513.

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Epifaunal invertebrates are sensitive to changes in the identity of the dominant host plant, so assessing differences in the structure of epifaunal assemblages is particularly pertinent in areas where seagrasses have been replaced by alternative vegetation (e.g. green seaweeds). In this study, we aimed to compare the diversity, abundance and structure of epifaunal assemblages, particularly amphipods, between meadows dominated by the seagrass Cymodocea nodosa and the green rhizophytic algae Caulerpa prolifera on shallow soft bottoms of Gran Canaria Island, determining whether patterns were temporally consistent between two times. The epifaunal assemblage structure (abundance and composition) consistently differed between both plants, those assemblages associated with C. prolifera-dominated beds being more diverse and abundant relative to C. nodosa meadows. Amphipods constituted ~70% of total crustaceans for the overall study, including 37 species belonging to 16 families. The amphipod abundance was ~3 times larger in C. prolifera-dominated beds than in C. nodosa meadows. We detected species-specific affinities; for example, Microdeutopus stationis, Dexamine spinosa, Aora spinicornis, Ischyrocerus inexpectatus and Apherusa bispinosa were more abundant in C. prolifera-dominated beds; while the caprellid Mantacaprella macaronensis dominated in C. nodosa meadows. However, some species, such as Pseudoprotella phasma and Ampithoe ramondi, were found in both habitats with varying abundances between times.

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19

Costa, Monya M., João Silva, Isabel Barrote, and Rui Santos. "Heatwave Effects on the Photosynthesis and Antioxidant Activity of the Seagrass Cymodocea nodosa under Contrasting Light Regimes." Oceans 2, no. 3 (June 25, 2021): 448–60. http://dx.doi.org/10.3390/oceans2030025.

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Global climate change, specifically the intensification of marine heatwaves, affect seagrasses. In the Ria Formosa, saturating light intensities may aggravate heatwave effects on seagrasses, particularly during low spring tides. However, the photophysiological and antioxidant responses of seagrasses to such extreme events are poorly known. Here, we evaluated the responses of Cymodocea nodosa exposed at 20 °C and 40 °C and 150 and 450 μmol quanta m−2 s−1. After four-days, we analyzed (a) photosynthetic responses to irradiance, maximum photochemical efficiency (Fv/Fm), the effective quantum yield of photosystem II (ɸPSII); (b) soluble sugars and starch; (c) photosynthetic pigments; (d) antioxidant responses (ascorbate peroxidase, APX; oxygen radical absorbance capacity, ORAC, and antioxidant capacity, TEAC); (d) oxidative damage (malondialdehyde, MDA). After four days at 40 °C, C. nodosa showed relevant changes in photosynthetic pigments, independent of light intensity. Increased TEAC and APX indicated an “investment” in the control of reactive oxygen species levels. Dark respiration and starch concentration increased, but soluble sugar concentrations were not affected, suggesting higher CO2 assimilation. Our results show that C. nodosa adjusts its photophysiological processes to successfully handle thermal stress, even under saturating light, and draws a promising perspective for C. nodosa resilience under climate change scenarios.

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20

Tsioli, Soultana, Vasillis Papathanasiou, Anastasia Rizouli, Maria Kosmidou, Christos Katsaros, Eva Papastergiadou, Frithjof C. Küpper, and Sotiris Orfanidis. "Diversity and composition of algal epiphytes on the Mediterranean seagrass Cymodocea nodosa: a scale-based study." Botanica Marina 64, no. 2 (March 15, 2021): 101–18. http://dx.doi.org/10.1515/bot-2020-0057.

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Abstract Cymodocea nodosa, a typical marine angiosperm species in the Mediterranean Sea, hosts a range of epiphytic algae. Epiphyte abundance varies at different spatial scales, yet epiphyte diversity and community composition are poorly understood. This study explores the epiphytes on C. nodosa from two reference meadows (Thasos, Vrasidas) and one anthropogenically stressed meadow (Nea Karvali) in the northern Aegean Sea (Kavala Gulf, Greece). A nested destructive sampling design at three spatial scales (metres, hundreds of metres, kilometres) and stereoscopic/microscopic observations were used. Light microscopy revealed a total of 19 taxa of macroalgae populating the leaves of C. nodosa. The most commonly encountered taxa with highest cover (%) were Hydrolithon cruciatum and Feldmannia mitchelliae. DNA sequencing (18S rDNA) confirms the presence of a number of dinoflagellate and red algal epiphytes, and this represents the first application of DNA metabarcoding to study the diversity of seagrass epiphytes. Epiphytic communities studied at species/taxon and functional (Ecological Status Groups) levels separated the reference low-stressed meadows from the degraded one, with the functional approach having higher success. The ecological evaluation index classified the studied meadows into different Ecological Status Classes according to anthropogenic stress.

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21

Najdek, Mirjana, Marino Korlević, Paolo Paliaga, Marsej Markovski, Ingrid Ivančić, Ljiljana Iveša, Igor Felja, and Gerhard J. Herndl. "Dynamics of environmental conditions during the decline of a <i>Cymodocea nodosa</i> meadow." Biogeosciences 17, no. 12 (June 30, 2020): 3299–315. http://dx.doi.org/10.5194/bg-17-3299-2020.

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Abstract. The dynamics of the physicochemical and biological parameters were followed during the decline of a Cymodocea nodosa meadow in the northern Adriatic Sea from July 2017 to October 2018. During the regular growth of C. nodosa from July 2017 to March 2018, the species successfully adapted to the changes in environmental conditions and prevented H2S accumulation by its reoxidation, supplying the sediment with O2 from the water column and/or leaf photosynthesis. The C. nodosa decline was most likely triggered in April 2018 when light availability to the plant was drastically reduced due to increased seawater turbidity that resulted from increased terrigenous input, indicated by a decrease in salinity accompanied with a substantial increase in particulate matter concentration, combined with resuspension of sediment and elevated autotrophic biomass. Light reduction impaired photosynthesis of C. nodosa and the oxidation capability of belowground tissue. Simultaneously, a depletion of oxygen due to intense oxidation of H2S occurred in the sediment, thus creating anoxic conditions in most of the rooted areas. These linked negative effects on the plant performance caused an accumulation of H2S in the sediments of the C. nodosa meadow. During the decay of aboveground and belowground tissues, culminating in August 2018, high concentrations of H2S were reached and accumulated in the sediment as well as in bottom waters. The influx of oxygenated waters in September 2018 led to the re-establishment of H2S oxidation in the sediment and remainder of the belowground tissue. Our results indicate that if disturbances of environmental conditions, particularly those compromising the light availability, take place during the recruitment phase of plant growth when metabolic needs are at a maximum and stored reserves minimal, a sudden and drastic decline of the seagrass meadow occurs.

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22

Marba, Nuria, and Carlos M. Duarte. "Coupling of Seagrass (Cymodocea Nodosa) Patch Dynamics to Subaqueous dune Migration." Journal of Ecology 83, no. 3 (June 1995): 381. http://dx.doi.org/10.2307/2261592.

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23

Terrados, J., CM Duarte, and WJ Kenworthy. "Is the apical growth of Cymodocea nodosa dependent on clonal integration?" Marine Ecology Progress Series 158 (1997): 103–10. http://dx.doi.org/10.3354/meps158103.

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24

Agostini, Sylvia, Gérard Pergent, and Bernard Marchand. "Growth and primary production of Cymodocea nodosa in a coastal lagoon." Aquatic Botany 76, no. 3 (July 2003): 185–93. http://dx.doi.org/10.1016/s0304-3770(03)00049-4.

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25

Kontiza, Ioanna, Michael Stavri, Mire Zloh, Constantinos Vagias, Simon Gibbons, and Vassilios Roussis. "New metabolites with antibacterial activity from the marine angiosperm Cymodocea nodosa." Tetrahedron 64, no. 8 (February 2008): 1696–702. http://dx.doi.org/10.1016/j.tet.2007.12.007.

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26

Duarte, CM, and K. Sand-Jensen. "Seagrass colonization: biomass development and shoot demography in Cymodocea nodosa patches." Marine Ecology Progress Series 67 (1990): 97–103. http://dx.doi.org/10.3354/meps067097.

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27

Espino, F., A. Brito, R. Haroun, and F. Tuya. "Macroecological analysis of the fish fauna inhabiting Cymodocea nodosa seagrass meadows." Journal of Fish Biology 87, no. 4 (October 2015): 1000–1018. http://dx.doi.org/10.1111/jfb.12771.

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28

Moawad, Madelyn N., Abeer A. M. El-Sayed, and Naglaa A. El-Naggar. "Biosorption of cadmium and nickel ions using marine macrophyte, Cymodocea nodosa." Chemistry and Ecology 36, no. 5 (April 16, 2020): 458–74. http://dx.doi.org/10.1080/02757540.2020.1752199.

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29

Kolsi, Rihab Ben Abdallah, Jawhar Fakhfakh, Fatma Krichen, Imed Jribi, Antonia Chiarore, Francesco Paolo Patti, Christophe Blecker, Noureddine Allouche, Hafedh Belghith, and Karima Belghith. "Structural characterization and functional properties of antihypertensive Cymodocea nodosa sulfated polysaccharide." Carbohydrate Polymers 151 (October 2016): 511–22. http://dx.doi.org/10.1016/j.carbpol.2016.05.098.

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30

Caye, G., C. Bulard, A. Meinesz, and F. Loquès. "Dominant role of seawater osmotic pressure on germination in Cymodocea nodosa." Aquatic Botany 42, no. 2 (January 1992): 187–93. http://dx.doi.org/10.1016/0304-3770(92)90007-6.

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31

Perez, Marta, Carlos M. Duarte, Javier Romero, Kaj Sand-Jensen, and Teresa Alcoverro. "Growth plasticity in Cymodocea nodosa stands: the importance of nutrient supply." Aquatic Botany 47, no. 3-4 (March 1994): 249–64. http://dx.doi.org/10.1016/0304-3770(94)90056-6.

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32

Binzer, Thomas, Jens Borum, and Ole Pedersen. "Flow velocity affects internal oxygen conditions in the seagrass Cymodocea nodosa." Aquatic Botany 83, no. 3 (November 2005): 239–47. http://dx.doi.org/10.1016/j.aquabot.2005.07.001.

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Curiel, Daniele, Sandra Kraljević Pavelić, Agata Kovačev, Chiara Miotti, and Andrea Rismondo. "Marine Seagrasses Transplantation in Confined and Coastal Adriatic Environments: Methods and Results." Water 13, no. 16 (August 21, 2021): 2289. http://dx.doi.org/10.3390/w13162289.

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The anthropogenic pressures of the twentieth century have seriously endangered the Mediterranean coastal zone; as a consequence, marine seagrass habitats have strongly retreated, mostly those of Posidonia oceanica. For this reason, over time, restoration programs have been put in place through transplantation activities, with different success. These actions have also been conducted with other Mediterranean marine seagrasses. The results of numerous transplanting operations conducted in the Northern Adriatic Sea and lagoons with Cymodocea nodosa, Zostera marina and Z. noltei and in the Central and Southern Adriatic Sea with P. oceanica (only within the project Interreg SASPAS), are herein presented and compared, taking also into account the presence of extensive meadows of C. nodosa, Z. marina and Z. noltei, along the North Adriatic coasts and lagoons.

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34

Smadi, Abla, Maria Ciavatta, Fatma Bitam, Marianna Carbone, Guido Villani, and Margherita Gavagnin. "Prenylated Flavonoids and Phenolic Compounds from the Rhizomes of Marine Phanerogam Cymodocea nodosa." Planta Medica 84, no. 09/10 (November 23, 2017): 704–9. http://dx.doi.org/10.1055/s-0043-122747.

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AbstractChemical investigation of the rhizomes of the marine phanerogam Cymodocea nodosa resulted in the isolation of two new prenylated flavon-di-O-glycosides, cymodioside A (1) and B (2), along with known phenolic compounds 3–7, some of which never reported from seagrasses to date. The structures of compounds 1 and 2 were established by extensive nuclear magnetic resonance analysis. In addition, the absolute configuration of 4-(2,5-dihydroxyhexyl) benzene-1,2-diol (7), which was not previously reported in the literature, has been now determined.

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35

Marbà, N., and CM Duarte. "Growth response of the seagrass Cymodocea nodosa to experimental burial and erosion." Marine Ecology Progress Series 107 (1994): 307–11. http://dx.doi.org/10.3354/meps107307.

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36

Kontiza, Ioanna, Dennis Abatis, Katerina Malakate, Constantinos Vagias, and Vassilios Roussis. "3-Keto steroids from the marine organisms Dendrophyllia cornigera and Cymodocea nodosa." Steroids 71, no. 2 (February 2006): 177–81. http://dx.doi.org/10.1016/j.steroids.2005.09.004.

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37

Silva, João, Isabel Barrote, Monya M. Costa, Sílvia Albano, and Rui Santos. "Physiological Responses of Zostera marina and Cymodocea nodosa to Light-Limitation Stress." PLoS ONE 8, no. 11 (November 28, 2013): e81058. http://dx.doi.org/10.1371/journal.pone.0081058.

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38

Kontiza, Ioanna, Constantinos Vagias, Jasmin Jakupovic, Dimitri Moreau, Christos Roussakis, and Vassilios Roussis. "Cymodienol and cymodiene: new cytotoxic diarylheptanoids from the sea grass Cymodocea nodosa." Tetrahedron Letters 46, no. 16 (April 2005): 2845–47. http://dx.doi.org/10.1016/j.tetlet.2005.02.123.

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39

Pagès, Jordi F., Marta Pérez, and Javier Romero. "Sensitivity of the seagrass Cymodocea nodosa to hypersaline conditions: A microcosm approach." Journal of Experimental Marine Biology and Ecology 386, no. 1-2 (April 2010): 34–38. http://dx.doi.org/10.1016/j.jembe.2010.02.017.

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40

Jiménez-Ramos, Rocío, Monique Mancilla, Beatriz Villazán, Luis G. Egea, Vanessa González-Ortiz, Juan José Vergara, José Lucas Pérez-Lloréns, and Fernando G. Brun. "Resistance to nutrient enrichment varies among components in the Cymodocea nodosa community." Journal of Experimental Marine Biology and Ecology 497 (December 2017): 41–49. http://dx.doi.org/10.1016/j.jembe.2017.09.008.

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41

Malta, Erik-Jan, Fernando G. Brun, Juan J. Vergara, Ignacio Hernández, and J. Lucas Pérez-Lloréns. "Recovery of Cymodocea nodosa (Ucria) Ascherson photosynthesis after a four-month dark period." Scientia Marina 70, no. 3 (September 30, 2006): 413–22. http://dx.doi.org/10.3989/scimar.2006.70n3413.

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Garciadeblás, Blanca, Rosario Haro, and Begoña Benito. "Cloning of two SOS1 transporters from the seagrass Cymodocea nodosa. SOS1 transporters from Cymodocea and Arabidopsis mediate potassium uptake in bacteria." Plant Molecular Biology 63, no. 4 (November 12, 2006): 479–90. http://dx.doi.org/10.1007/s11103-006-9102-2.

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Balestri, Elena, and Francesco Cinelli. "Isolation and cell wall regeneration of protoplasts from Posidonia oceanica and Cymodocea nodosa." Aquatic Botany 70, no. 3 (July 2001): 237–42. http://dx.doi.org/10.1016/s0304-3770(01)00157-7.

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Rismondo, Andrea, Daniele Curiel, Mara Marzocchi, and Mario Scattolin. "Seasonal pattern of Cymodocea nodosa biomass and production in the lagoon of Venice." Aquatic Botany 58, no. 1 (July 1997): 55–64. http://dx.doi.org/10.1016/s0304-3770(96)01116-3.

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Egea, L. G., R. Jiménez-Ramos, J. J. Vergara, I. Hernández, and F. G. Brun. "Interactive effect of temperature, acidification and ammonium enrichment on the seagrass Cymodocea nodosa." Marine Pollution Bulletin 134 (September 2018): 14–26. http://dx.doi.org/10.1016/j.marpolbul.2018.02.029.

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Barrón, Cristina, Nùria Marbé, Jorge Terrados, Hilary Kennedy, and Carlos M. Duarte. "Community metabolism and carbon budget along a gradient of seagrass (Cymodocea nodosa ) colonization." Limnology and Oceanography 49, no. 5 (September 2004): 1642–51. http://dx.doi.org/10.4319/lo.2004.49.5.1642.

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Cebrián, Just, Carlos M. Duarte, and Núria Marbà. "Herbivory on the seagrass Cymodocea nodosa (Ucria) Ascherson in contrasting Spanish Mediterranean habitats." Journal of Experimental Marine Biology and Ecology 204, no. 1-2 (October 1996): 103–11. http://dx.doi.org/10.1016/0022-0981(96)02574-9.

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Marbà, Núria, Just Cebrián, Susana Enríquez, and Carlos M. Duarte. "Migration of large-scale subaqueous bedforms measured with seagrasses (Cymodocea nodosa ) as tracers." Limnology and Oceanography 39, no. 1 (January 1994): 126–33. http://dx.doi.org/10.4319/lo.1994.39.1.0126.

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Papathanasiou, Vasillis, Sotiris Orfanidis, and Murray T. Brown. "Intra-specific responses of Cymodocea nodosa to macro-nutrient, irradiance and copper exposure." Journal of Experimental Marine Biology and Ecology 469 (August 2015): 113–22. http://dx.doi.org/10.1016/j.jembe.2015.04.022.

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Llagostera, I., M. Pérez, and J. Romero. "Trace metal content in the seagrass Cymodocea nodosa: Differential accumulation in plant organs." Aquatic Botany 95, no. 2 (August 2011): 124–28. http://dx.doi.org/10.1016/j.aquabot.2011.04.005.

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