Effects of Atrazine and Nicosulfuron on Phytoplankton in Systems of
Increasing Complexity
F. Seguin,
1
C. Leboulanger,
2
F. Rimet,
3
J. C. Druart,
2
A. Bérard
2
1
INRA, Ecobiologie et Qualité des Hydrosystèmes Continentaux, 65 rue de St Brieuc, 35042 Rennes, France
2
INRA, Station d’Hydrobiologie Lacustre, BP 511, 74203 Thonon les Bains Cedex, France
3
CRP-Gabriel Lippmann, CREBS, 162a av. de la Faiencerie, 1511 Luxembourg
Received: 30 March 2000/Accepted: 28 August 2000
Abstract. We have tested the sensitivity of phytoplankton to
the herbicides atrazine and nicosulfuron in experiments con-
duced in increasingly complex systems, from single strain
phytoplankton cultures (microplates) to mesocosms mimicking
whole ecosystems. The endpoints used to assess sensitivity to
atrazine and nicosulfuron were total biomass increase, photo-
synthetic efficiency, and community diversity, depending on
the system considered. Nicosulfuron appeared to be very much
less toxic to phytoplankton than atrazine, in accord with the
planned changes in agricultural practices to reduce the effects
of surface water contamination on aquatic biota. Nevertheless,
nicosulfuron had significant effects in some systems (princi-
pally microcosms), whereas the single monocultures were al-
most insensitive to it. This points out the inaccuracy of stan-
dardized toxicity test on phytoplanktonic algae alone for
predicting the effects of xenobiotics on natural communities
and the need for tests in microcosms and mesocosms to obtain
reliable evidence about the toxicity of a given chemical on
freshwater aquatic ecosystems.
Intensive crop production has used more and more herbicides
over the past several decades. Increased production crops, such
as cereals, involves massive herbicide consumption that leads
to the significant contamination of surface water. Some uses of
atrazine can result in triazine content of such water exceeding
10 g/L (Caux and Kent 1995; Solomon et al. 1996). As
atrazine (chloro-2 ethylamino-4 isopropylamino-6 triazine-
1,3,5) inhibits the photosystem II, it may damage nontarget
aquatic primary producers (phytoplankton, periphyton, and
macrophytes). Microalgae are potential targets of herbicides in
aquatic ecosystems. Herbicides can alter the ecophysiology and
algal population dynamics, so that the most sensitive species
are killed, allowing more tolerant species to develop; contam-
ination may thus cause a shift in community structure (Kasai et
al. 1993). Atrazine may indirectly influence the whole trophic
food web of aquatic ecosystems, with damage to phytoplank-
ton, periphyton, and macrophytes that may reduce the capacity
of the aquatic habitat to sustain invertebrates and fish (Solomon
et al. 1996).
An agrienvironmental program was launched in France in
1993. This program promoted environmentally friendly agri-
cultural practices (Dabène and Larguier 1994). One of these
measures involves replacing atrazine with nicosulfuron [2-(4,6-
dimethoxypyrimidin-2-ylcarbamoylsulphanoyl)-N,N-dimethyl
nicotinamide], which is considered to be less harmful. This
sulfonylurea herbicide prevents the synthesis of ILE, LEU, and
VAL by inhibiting the enzyme ALS (Simpson et al. 1995).
Unfortunately, there are few published data on the ecotoxico-
logical effects of this compound. It is thus necessary to detect
and compare the effects of atrazine and nicosulfuron on the
aquatic biota in order to assess the contamination risk produced
by changes in agricultural practices. This can be done in
several ways. The most widely used experiments are monospe-
cific toxicity tests because of their low cost, satisfactory repro-
ducibility, and ease of execution. They are often standardized
(e.g., AFNOR 1998; EPA 1989). Though they are essential for
understanding how toxic compounds act, they cannot yield
reliable risk assessment (Pratt et al. 1988; Bérard and Pelte
1999). The most complex experiments involve aquatic meso-
cosms that have structural and functional characteristics similar
to the ecosystems they are intended to model. The bioavail-
ability and toxicity of pesticides can be assessed using a rep-
resentative set of natural aquatic ecosystems (Crossland 1994;
Touart 1994), and environmental realism is the main reason for
using mesocosm instead of less complex experiments
(Kraufvelin 1998). However, increased ecological realism of-
ten implies less accurate measurements and statistical analyses
(Giesy and Allred 1985). This method is also costly and hard to
implement. Indoor and outdoor microcosms, in which natural
communities are isolated from the whole ecosystem, are inter-
mediate between monospecific tests and a holistic approach
(mesocosm). Toxicity can be assessed in a multispecies com-
munity, but not necessarily on an entire trophic web. These
three experimental systems are thus complementary, and using
them all provides a better understanding of the effects of toxic
chemicals on aquatic species and their environment. Correspondence to: C. Leboulanger; email: leboulan@thonon.intra.fr
Arch. Environ. Contam. Toxicol. 40, 198 –208 (2001)
DOI: 10.1007/s002440010164
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