Results 171 to 180 of about 898,912 (212)

Need for Mechanisms to Monitor Ocean Circulation-Driven Seagrass Population Expansions. [PDF]

Ecol Evol
Wang Z, Zhou B, Yan W.
europepmc   +1 more source

An updated checklist of vascular plants of Myanmar. [PDF]

PhytoKeys
Aung YL, Aung MH, Tan Y, Jin X.
europepmc   +1 more source

The population ecology of the seagrass, Zostera muelleri, in south-eastern Australia: dispersal, recruitment, growth andconnectivity of a marine angiosperm

, 2016
Richard Stafford-Bell
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Back to the Seabed: The Unique Photosystem I Architecture of the Seagrass Posidonia oceanica

Bassi R, Amelii A, Capaldi S, Russo M, Guardini Z, Sanità G, Esposito E, Olivé I, Maiuri M, Dall'Osto L, Cerullo G, Procaccini G.   +11 more
europepmc   +1 more source

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Chemical Ecology of Marine Angiosperms: Opportunities at the Interface of Marine and Terrestrial Systems

Journal of Chemical Ecology, 2013
This review examines the state of the field for chemically mediated interactions involving marine angiosperms (seagrasses, mangroves, and salt marsh angiosperms). Small-scale interactions among these plants and their herbivores, pathogens, fouling organisms, and competitors are explored, as are community-level effects of plant secondary metabolites. At
R. D. Sieg, J. Kubanek
semanticscholar   +3 more sources

Photosynthesis and photorespiration of marine angiosperms

Aquatic Botany, 1989
Abstract The marine angiosperms, or seagrasses, constitute a small but important plant group, common to many coastal habitats. In spite of their high productivity within near-shore ecosystems, the photosynthetic mechanisms of these plants have received relatively little investigation.
S. Beer
semanticscholar   +2 more sources

Nitrogen fixation in the rhizosphere of marine angiosperms

Marine Biology, 1972
High rates of acetylene reduction were observed in systems containing excised rhizomes of the Caribbean marine angiosperms Thalassia testudinum, Syringodium filiforme and Diplanthera wrightii, and the temperate marine angiosperm Zostera marina. For 4 plant and plant-sediment systems the ratio of acetylene reduced/N2 fixed varied from 2.6 to 4.6. For T.
D. Patriquin, R. Knowles
semanticscholar   +2 more sources

Discrete subcellular localization of membrane-bound ATPase activity in marine angiosperms and marine algae

Planta, 2004
The subcellular distribution of membrane-bound ATPases was compared among terrestrial plants, seagrasses and marine algae by cytochemical techniques. High ATPase activity was detected in the copiously invaginated plsma membrane that was characteristic of transfer cells but not in the tonoplast of epidermal cells in mature leaves of seagrasses ...
Jun-yong Pak, Toshiyuki Fukuhara, Takeshi Nitta   +2 more
semanticscholar   +3 more sources

Mating System and Clonal Architecture: A Comparative Study in Two Marine Angiosperms

Evolutionary Ecology, 2005
In the present study, we compared the clonal architecture between two seagrass species, the dioecious Cymodocea nodosa and the hermaphroditic, self-compatible Zostera noltii, in order to verify the hypothesis that clonal growth strategies and resulting genet architecture are associated with mating system in clonal plants.
Maria Valeria Ruggiero, Stefano Capone, Patrizia Pirozzi, T. Reusch, G. Procaccini   +4 more
semanticscholar   +3 more sources

Chromosome numbers and their systematic implications in Australian marine angiosperms: ThePosidoniaceae

Plant Systematics and Evolution, 1990
Somatic chromosome numbers of 2n = 20 are reported for all eight species of AustralianPosidonia: P. angustifolia, P. australis, P. coriacea, P. denhartogii, P. kirkmanii, P. ostenfeldii, P. robertsonae, andP. sinuosa. All species apparently have five larger and five smaller pairs of chromosomes.
J. Kuo, S. H. James, H. Kirkman, C. Hartog   +3 more
semanticscholar   +2 more sources