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(1929)
Modes and mechanisms of speciation in microalgae generally remain obscure. T o date sexual isolation has been reported to occur within single nomenspecies in Astrephomene
Functional geometry of seaweeds : ecological consequences of thallus layering and shape in contrasting light environments
J. Ramus (1978)
SEAWEED ANATOMY AND PHOTOSYNTHETIC PERFORMANCE: THE ECOLOGICAL SIGNIFICANCE OF LIGHT GUIGES, HETEROGENEOUS ABSORPTION AND MULTIPLE SCATTER 1 2Journal of Phycology, 14
W. Litaker, C. Duke, B. Kenney, J. Ramus (1987)
Short-term environmental variability and phytoplankton abundance in a shallow tidal estuaryMarine Biology, 96
B. Lapointe, K. Tenore (1981)
Experimental outdoor studies with Ulva fasciata Delile. I. Interaction of light and nitrogen on nutrient uptake, growth, and biochemical compositionJournal of Experimental Marine Biology and Ecology, 53
G. Rosenberg, J. Ramus (1984)
Uptake of inorganic nitrogen and seaweed surface area: Volume ratiosAquatic Botany, 19
G. Rosenberg, J. Ramus (1981)
Ecological Growth Strategies in the Seaweeds Gracilaria foliifera (Rhodophyceae) and Ulva sp. (Chlorophyceae): The Rate and Timing of Growth, 24
J. Ramus (1983)
A PHYSIOLOGICAL TEST OF THE THEORY OF COMPLEMENTARY CHROMATIC ADAPTATION. II. BROWN, GREEN AND RED SEAWEEDS 1Journal of Phycology, 19
M. Hanisak, M. Harlin (1978)
UPTAKE OF INORGANIC NITROGEN BY CODIUM FRAGILE SUBSP. TOMENTOSOIDES (CHLOROPHYTA) 1Journal of Phycology, 14
(1985)
Temporal scales of nitrogen availability and seaweed physiological response
M. Littler, D. Littler (1980)
The Evolution of Thallus Form and Survival Strategies in Benthic Marine Macroalgae: Field and Laboratory Tests of a Functional Form ModelThe American Naturalist, 116
(1980)
T h e evolution of thallus
J. Carlton, J. Scanlon (1985)
Progression and Dispersal of an Introduced Alga: Codium fragile ssp. tomentosoides (Chlorophyta) on the Atlantic Coast of North America, 28
ABSTRACT The growth rates of two chlorophyte macroalgae, Codium fragile and Ulva curvata, are compared in response to varied, but non‐random, NH4+ enrichments (pulses). The species were chosen to contrast radically different morphologies. Pulse frequency and pulse duration were varied independently; however, an equivalent mass of NH4+ was added in each treatment. The growth rate of Codium varied neither as a function of pulse frequency nor duration; the growth rate of Ulva varied with pulse frequency, but not pulse duration. These data are combined with life form and physiological characters, and are discussed in the context of the “function form” hypothesis. From the evidence we argue that by virtue of its life form, Ulva is capable of utilizing transiently high NH4+ concentrations and is capable of high growth rates, attributes contributing to its role as a ruderal species. In contrast, Codium's life form does not allow utilization of transiently high NH4+ concentrations or high growth rates, thereby contributing to its role as a persistent species.
Journal of Phycology – Wiley
Published: Dec 1, 1987
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