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1.
Environ Toxicol Chem ; 31(4): 899-908, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22328269

RESUMO

A flow-through system was developed to investigate the effects of time-variable exposure of pesticides on algae. A recently developed algae population model was used for simulations supported and verified by laboratory experiments. Flow-through studies with Desmodesmus subspicatus and Pseudokirchneriella subcapitata under time-variable exposure to isoproturon were performed, in which the exposure patterns were based on the results of FOrum for Co-ordination of pesticide fate models and their USe (FOCUS) model calculations for typical exposure situations via runoff or drain flow. Different types of pulsed exposure events were realized, including a whole range of repeated pulsed and steep peaks as well as periods of constant exposure. Both species recovered quickly in terms of growth from short-term exposure and according to substance dissipation from the system. Even at a peak 10 times the maximum predicted environmental concentration of isoproturon, only transient effects occurred on algae populations. No modified sensitivity or reduced growth was observed after repeated exposure. Model predictions of algal growth in the flow-through tests agreed well with the experimental data. The experimental boundary conditions and the physiological properties of the algae were used as the only model input. No calibration or parameter fitting was necessary. The combination of the flow-through experiments with the algae population model was revealed to be a powerful tool for the assessment of pulsed exposure on algae. It allowed investigating the growth reduction and recovery potential of algae after complex exposure, which is not possible with standard laboratory experiments alone. The results of the combined approach confirm the beneficial use of population models as supporting tools in higher-tier risk assessments of pesticides.


Assuntos
Clorófitas/efeitos dos fármacos , Modelos Teóricos , Praguicidas/farmacologia , Compostos de Fenilureia/farmacologia , Clorófitas/crescimento & desenvolvimento , Ecologia/métodos , Exposição Ambiental/efeitos adversos , Luz , Fósforo/metabolismo , Dinâmica Populacional , Temperatura
2.
Comp Biochem Physiol C Toxicol Pharmacol ; 155(2): 407-15, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22115822

RESUMO

Results are presented from a validation (with 5 laboratories) of the Fish Sexual Development Test (FSDT) developed to detect endocrine disrupters (EDs) and included in the OECD (Organisation for Economic Co-operation and Development) working program. The aromatase-inhibiting fungicide prochloraz was tested in zebrafish (Danio rerio) and fathead minnow (Pimephales promelas). The fish were exposed during sexual differentiation and development from 0 to 60 days post hatch (dph). After exposure, the vitellogenin (VTG) concentrations were quantified in head/tail homogenate and the sex ratio was determined (defined as female, male, intersex or undifferentiated). NOEC/LOEC and EC(x) designs were compared to optimize the test approach. Results show that both species are highly sensitive to prochloraz during sexual development. They respond by skewing of the sex ratio towards male phenotype and by a VTG decline in females. The NOEC/LOEC approach is preferred because sex ratio is difficult to analyze with a regression model. The mean NOEC/LOEC for prochloraz on the sex ratio was 43.3/134 µg/L and 101/293 µg/L for zebrafish and fathead minnow, respectively. The mean NOEC/LOEC on the decline in female VTG concentration was 65/110 µg/L and ~30/68 µg/L respectively. In conclusion, zebrafish and fathead minnow are suitable species in the FSDT and their sexual differentiation is equally labile to EDs.


Assuntos
Cyprinidae/fisiologia , Imidazóis/toxicidade , Maturidade Sexual/efeitos dos fármacos , Peixe-Zebra/fisiologia , Animais , Cyprinidae/metabolismo , Feminino , Fungicidas Industriais/toxicidade , Masculino , Nível de Efeito Adverso não Observado , Análise de Regressão , Razão de Masculinidade , Especificidade da Espécie , Testes de Toxicidade/métodos , Vitelogeninas/metabolismo , Peixe-Zebra/metabolismo
3.
Ecotoxicology ; 16(1): 221-30, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17268839

RESUMO

Selecting an appropriate invertebrate assay has been a primary goal of national and international testing programs for endocrine disrupting chemicals. The available information on the endocrine system, its hormones and their modes of action in controlling physiological processes in invertebrates is limited and the selection of appropriate test species still presents a challenge. This paper outlines the development of a higher-tier full life cycle (FLC) test for pesticides with the non-biting midge Chironomus riparius (Insecta, Diptera, Chironomidae). As an insect, C. riparius represents the species' richest and ecologically one of the most important groups of invertebrates. In addition, the endocrine system of insects is one of the best studied among the invertebrates. Acute and chronic tests with Chironomus spp. are commonly used for testing and risk assessment of agrochemicals. A chironomid FLC test protocol has been developed and its suitability investigated in an inter-laboratory comparison. The protocol used is based on existing OECD and US-EPA test methods. To verify the suitability of the test to generate endpoints that encompass adverse effects on the arthropod endocrine system, a juvenile hormone analog was selected as positive control substance. Results have demonstrated that the proposed chironomid FLC can be performed in separate laboratories and that the selected arthropod juvenile hormone mimic causes effects. However, the observed toxicity is not proof of an endocrine disruptive mechanism and could equally be evoked by other compounds. Contrary to a screening assay, which aims at revealing a substance's mode-of-action, the FLC test generates robust, population-relevant endpoints that can be used in the risk assessment of agrochemicals. Since the initial results presented in this paper are encouraging we propose to complete the validation of this assay under OECD with high priority.


Assuntos
Chironomidae/efeitos dos fármacos , Disruptores Endócrinos/toxicidade , Modelos Animais , Praguicidas/toxicidade , Testes de Toxicidade Crônica/métodos , Animais , Chironomidae/fisiologia , Clorofenóis/toxicidade , Feminino , Estágios do Ciclo de Vida/efeitos dos fármacos , Masculino , Nível de Efeito Adverso não Observado , Reprodutibilidade dos Testes , Medição de Risco
4.
Ecotoxicol Environ Saf ; 67(3): 399-405, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17289144

RESUMO

Acute and reproductive toxicity tests were conducted on seven strains of Daphnia magna from six laboratories in five countries. 3,4-Dichloroaniline (DCA) and fenoxycarb were used as test chemicals. Acute toxicity tests revealed that estimated EC(50) (50% effective concentration) values for DCA varied by a factor of 2.1 among strains (310-640 microg/L), whereas the EC(50) values for fenoxycarb varied by a factor of 4 (210-860 microg/L). EC(50) values for reproductive toxicity tests with DCA ranged from 5.9 to 38 microg/L among strains. Fenoxycarb exposure induced the production of male neonates in all the strains used in the present study. Estimated EC(50) values for the induction of male offspring were highly variable among strains: sensitivity to fenoxycarb differed by a factor of approximately 23 overall (0.45-10 microg/L). The present pre-validation tests suggest that induction of male sex in neonates by a juvenile hormone analog is universal among genetically different strains. Decreased total numbers of neonates at increased concentrations of fenoxycarb as well as other juvenoids may, however, obscure the incidence of male neonates production in the 21-day reproduction tests due to the low statistical power.


Assuntos
Compostos de Anilina/toxicidade , Daphnia/efeitos dos fármacos , Fenilcarbamatos/toxicidade , Reprodução/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Animais , Daphnia/genética , Relação Dose-Resposta a Droga , Feminino , Masculino , Reprodução/genética , Razão de Masculinidade , Especificidade da Espécie , Testes de Toxicidade
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