Botanica Marina 55 (2012): 253–259 © 2012 by Walter de Gruyter • Berlin • Boston. DOI 10.1515/bot-2011-0074
Effects of temperature, salinity, irradiance, and nutrients
on the development of carposporelings and tetrasporophytes
in Gracilaria domingensis (Kütz.) Sonder ex Dickie
(Rhodophyta, Gracilariales)
Fernanda Ramlov
1,
*, Jonatas M.C. de Souza
1
,
André Farias
1
, Marcelo Maraschin
2
, Paulo A. Horta
3
and Nair S. Yokoya
1
1
Núcleo de Pesquisa em Ficologia, Instituto de Botânica,
CP 3005, 01061-970, São Paulo, SP, Brazil,
e-mail: fe_biotec@yahoo.com.br
2
Laboratório de Morfogênese e Bioquímica Vegetal,
Núcleo de Produtos Naturais, Universidade Federal de
Santa Catarina, CP 476, 88049-900, Florianópolis, SC,
Brazil
3
Laboratório de Ficologia, Departamento de Botânica,
Universidade Federal de Santa Catarina, CP 476,
88049-900, Florianópolis, SC, Brazil
* Corresponding author
Abstract
Different environmental factors play important roles in the
growth, reproduction, and distribution of marine macroalgae.
We investigated the effects of temperature, salinity, irradi-
ance, and nutrients on the growth of carposporelings and
tetrasporophytes of Gracilaria domingensis. Carposporelings
grew at temperatures of 25 °C and 30 °C, but they did not
survive at 15 °C and 20 °C. In contrast, tetrasporophytes grew
over a wide range of temperatures (15–30 °C) with optimum
growth between 20 °C and 25 °C. Both carposporelings and
tetrasporophytes tolerated a wide range of salinity (25–60 and
10–50, respectively), but carposporelings were more sensi-
tive to lower salinities (10–20), while tetrasporophytes were
more sensitive to higher salinities (60). The highest growth
rates in basal discs of carposporelings occurred when they
were grown in 25% strength von Stosch enriched medium
(VSES) with an illumination of 150 μmol photons m
-2
s
-1
;
erect fronds grew best in 25% and 50% strength VSES
with illumination of 100 μmol photons m
-2
s
-1
. The VSES
strength did not influence the growth of tetrasporophytes of
G. domingensis. Highest growth rates of tetrasporophytes
occurred at 100 μmol photons m
-2
s
-1
. These results demon-
strate very different physiological responses between carpo-
sporelings and tetrasporophytes of G. domingensis and, as
such, they offer guidelines for the selection of potential areas
for the cultivation of the species.
Keywords: Gracilaria domingensis; irradiance; nutrients;
salinity; temperature.
Introduction
Recommendations for the cultivation of colloid-producing
red algae are commonplace in the literature because there is
a growing demand for biomass from the seaweed industries,
while natural seaweed beds are limited (Yokoya and Oliveira
1992a). However, it is not simple to attain commercial cul-
tivation of colloid-producing algae in Brazil because a clear
understanding will require better knowledge of the physiol-
ogy and ecology of the selected species.
Gracilaria, which is harvested or cultivated worldwide,
is a genus of red alga utilized for the commercial produc-
tion of agar, combining a rapid growth rate and tolerance
to cultivation conditions (Kain and Destombe 1995). At
the same time, the increased demand for agar has brought
about a depletion of natural seaweed beds along the north-
eastern Brazilian coast (Oliveira and Miranda 1998). In
order to provide rational support for mariculture, basic
information about the biology of suitable species is under
investigation.
Environmental factors, including temperature, salinity,
light, and nutrients, play important roles in the growth,
reproduction, and distribution of marine macroalgae (Kirst
1989, Lobban and Harrison 1994). Temperature plays a sig-
nificant role in the survival and growth of sporelings and
adult plants of Gracilaria species (Yokoya and Oliveira
1992a, 1993, Wilson and Critchley 1997, Orduña-Rojas
and Robledo 1999, Choi et al. 2006, Kakita and Kamishima
2006). Extreme salinity is another factor that interferes with
biological processes and affects the concentration of ions
and osmoregulation. Thus, this parameter has a significant
role in the distribution of macroalgae in different environ-
ments. Species of Gracilaria are generally considered to
be euryhaline (Yokoya and Oliveira 1992b, 1993, Wilson
and Critchley 1997, Raikar et al. 2001, Choi et al. 2006).
A wide range of optimal irradiance levels for growth have
been reported for Gracilaria spp. (Wilson and Critchley
1997, Kakita and Kamishima 2006). Nutrient levels may
also limit the growth of seaweeds (Hanisak 1990), and
some studies have shown that the growth of Gracilaria
spp. is favored at low concentration of nutrients (Ursi 2005,
Ferreira et al. 2006, Ferreira 2008).
In this context, cultivation of seaweeds in the laboratory
becomes an important tool, as the factors mentioned above
can be manipulated and controlled, allowing an evaluation of
their effects on vegetative and reproductive performance and,
in turn, allowing us to look toward mariculture technologies
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