Proposal for selective differentiating of nerve agent G and V type with utilisation of modified Ellman’s method

We studied issues of organophosphorus agents’ analysis. Immobilised enzyme–inhibitors complexes (e.g. acetylcholinesterase-organophosphate nerve agent) were studied with modified Ellman’s biochemical method utilised for assessment of acetylcholinesterase activity. Biochemical reactions are widespread and they are the most frequent used analytical methods for determination of nerve agents. This modified method is based on the nucleophilic reactions of mono- and bispyridinium aldoximes of a type 2-PAM, MMB-4 and HI-6, their homologues and isomers with enzyme–inhibitor complexes. The procedure for a gradual analysis of G and V type, Sarin, Cyclohexylsarin, Soman, Tabun, agent VX and R-33 was proposed in terms of studied nucleophilic substitution reactions quantification results. This method enables selective determination of these chemical warfare agents. A gradual analysis was evaluated by statistic method of probabilistic calculus. This type of analysis can be used for assessment of acetylcholinesterase inhibitors in very low concentrations close to hygienic limits.     

Changes in cardiac rhythm and calcium levels in guinea pigs treated chronically with fenitrothion

Fenitrothion, an acetylcholinesterase inhibitor, causes bradycardia following long‐term exposure. To analyse the mechanism underlying these cardiac changes, ginea pigs were exposed to fenitrothion 5 and 10 mg/kg for 30 consecutive days. Electrocardiogram (ECG) showed increase in PR and RR intervals. These changes were more prominent in the animals receiving 10 mg/kg fenitrothion which occasionally showed extrasystoles. In isolated atria preparation heart rate was decreased at higher dose. Amplitude of cardiac rhythm decreased with respect to increased ACh concentration. Hypocalcemia was recorded in fenitrothion‐treated animals. The residual content of fenitrothion was increased in both groups of animals following a pattern: brain> spleen> heart> liver> kidney.     

Relative susceptibility of some common mosquito vector larvae to synthetic insecticidal compounds in north-western Rajasthan

Relative susceptibility of three important mosquito vector larvae viz., Anopheles stephensi, Aedes aegypti and Culex quinquefasciatus, prevalent in the arid region was determined against four organophosphates (malathion, fenitrothion, fenthion, temephos) and three synthetic pyrethroid (alphamethrin, deltamethrin and fanvalerate) compounds. Studies were carried out on late 3rd or early 4th instar larvae of these species using standard WHO technique. Based on concentration mortality data LC50 and LC90 values along with their fiducial limits, regression equation, chi-square (chi2)/heterogeneity of the response have been determined by log probit regression analysis. LC50 values as observed for the above seven insecticides were 0.8097, 0.0398. 0.0432, 0.0035, 0.0025, 0.0092, 0.1006; 1.2370, 0.0531, 0.0655, 0.0076, 0.00004, 0.00004, 0.0046 and 1.4980, 0.0719, 0.0817, 0.0056, 0.00021, 0.00073, 0.0112 mg/l for the above three mosquito species respectively Among the four organophosphates tested temephos was the most effective followed by fenitrothion, fenthion and malathion. In general, Anopheles was found more susceptible as compared to the other two culicines to the above four compounds. The results also showed that larvae of Ae. aegypti were most susceptible followed by Cx. quinquefasciatus and An. stephensi to all the three pyrethroids tested. Among the three compounds tested alphamethrin was found to be the most toxic followed by deltamethrin while fanvalerate was the least toxic. The study would be of great importance while planning use of these insecticides for the control of different vector species in this area.     

Effects of two root-secreted phenolic compounds from a subalpine coniferous species on soil enzyme activity and microbial biomass

In order to evaluate the ecological consequences and potential mechanisms of specific C compounds on soil microbial processes under climate warming, we injected solutions of two modelled root exudates, 2,6-di-tert-butyl-4-methylphenol (BHT) and 1,2-benzenedicarboxylic acid, dibutyl ester (DBP), respectively, into soil at two concentrations (20 and 1000?µg?g^?1 soil). For all treatments, soils amended with the two phenolic compounds were incubated at two temperatures (20°C and 30°C) for 30 days. The responses of soil enzyme activity and microbial property to modelled root exudates to some extent depended on temperature regime, exudation component, and addition concentration. For example, the addition of BHT tended to decrease the soil enzyme activities. However, DBP addition generally increased the two metabolic enzyme activities at 30°C, and tended to decrease the two enzyme activities at 20°C, but a significant reduction was observed only at a high concentration at 20°C. The microbial biomass and enzyme activity were generally lower at 30°C compared to those at 20°C, when averaged across all treatment combinations. Taken together, our results indicated that the amounts and quality of liable root-derived C can differentially affect microbial processes, and various environmental changes will greatly complicate root–microbe–soil interactions in forests.     

Carbofuran-induced effects on acetylcholinesterase (AChE) in erythrocytes and liver of Cyprinus carpio

A study was conducted to determine the effects of long-term exposure to carbofuran on erythrocyte and liver acetylcholinesterase (AChE) activity in Cyprinus carpio, and assess which tissue was more sensitive to pesticide exposure examining this enzyme. Fish were allowed to accilimatize in toxicant-free water for 24 days after 60-day exposure. AChE activity was determined with a spectrophotometer using acetylthiocholine iodide as a substrate in erythrocytes and liver. Enzymic activity of erythrocytes and liver decreased over time. A higher degree of enzyme inhibition was observed in erythrocyte compared to liver. The degree of enzyme inhibition was positively correlated with exposure time. When exposed fish were transferred to clean water, recovery was greater in erythrocytes than liver. Erythrocyte AChE activity recovered after 18 days, while it required 21 days in liver. The findings of this study indicate that erythrocyte AChE is more sensitive to carbofuran than liver. The greater sensitivity of erythrocyte AChE suggests that it may be more useful as a biomarker for monitoring status of pollution in freshwater bodies.     

Influence of temperature and pH on the effects of zinc and copper on proteolytic activities of the intestinal mucosa of planktivorous and benthophagous fishes and their potential preys

Influences of temperature (0 and 20°C) and pH (3.0, 5.0, and 7.4) on the effect of zinc (Zn) and copper (Cu) on proteolytic activities of intestinal mucosa in planktivorous (blue bream, bleak), bentophagous (bream, roach) fishes and their potential preys (pond snail Limnaea stagnalis, planorbid Planorbarius purpura, dreissena Dreissena polymorpha, midge larvae Chironomus sp., water flea Daphnia longispina and total zooplankton) are revealed in this article. Cu decreases the caseinolytic and hemoglobinolytic activities in both fish and their preys more than Zn at temperature 20°C and pH 7.4. Low temperature intensifies the negative effect of the metals on the protease activity in fish (in the case of Zn 5–10 times, in the case of Cu 5–30 times). In fish prey species, the negative effect of the metals on the proteinase activity may be more significant. The influence of pH on Zn and Cu effects is less pronounced than that of low temperature. Maximum reduction of enzyme activities is observed for the combined action of low temperature and pH as well as of the studied metals.     

Toxicological attributes of plant chemicals and their biochemical impacts on cholinesterase and protein levels in relation with conventional insecticides against mosquito larvae of Karachi city

In order to control mosquito, different chemicals were applied against the larvae of Culex fatigans (Diptera Culicidae). The tested chemicals were Lambda cyhalothrin, chlorpyrifos, Azadirachta indica (Spindales meliaceae) neem extract, and Sueda monoica extract. All chemicals were found to have significant efficacy against Culex fatigans mosquito larvae. In terms of efficacy, the biochemical effects after treatment with such chemicals were found to vary. Total protein levels and acetylcholinesterase (AChE) activity were the parameters examined. Chlorpyrifos, Lambda cyhalothrin, and neem elevated AChE activity levels whereas the plant extract S. monoica decreased enzymic activity. Total protein levels were decreased by Lambda cyhalothrin and chlorpyrifos whereas protein was increased by neem extract and S. monoica.     

Two herbivore-deterrent iridoid glycosides reduce the in-vitro growth of a specialist but not of a generalist pathogenic fungus of Plantago lanceolata L

Summary. Many secondary plant compounds are involved in defense against both insect herbivores and pathogens. Two secondary plant compounds of Plantago lanceolata, the iridoid glycosides catalpol and its precursor aucubin, are well known for their deterrent effects on generalist and non-adapted specialist insect herbivores. We tested the effects of these compounds on the in-vitro growth of a specialist and generalist fungal pathogen of this host species. Two chemical forms of these iridoids were tested. The glycosides and their aglycones, the products of enzymatic conversion by specific $/Beta$-glucosidase enzymes. The glycosides enhanced growth of both the specialist fungus Diaporthe adunca and the generalist fungus Fusarium moniliforme var. subglutinans. The positive effect of these glycosides on the generalist fungus is in sharp contrast with the generally negative effects of these glysosides on generalist insect herbivores. The aglycones of aucubin and catalpol reduced the growth of the specialist fungus D. adunca, but, contrary to expectation, enhanced the growth of the generalist fungus F. moniliforme var. subglutinans. Effects of aucubin on D. adunca were stronger than effects of catalpol. This was true both for the growth stimulating effects of the glycosides and for the fungitoxic effects of the aglycones. We therefore expect that the effects of these iridoids in P. lanceolata on the specialist fungus will strongly depend on the ratio between catalpol and its precursor aucubin and the chemical form (glycoside or aglycone) in which these compounds are encountered by the fungus during growth. Our results suggest that iridoid glycosides in P. lanceolata can be used as defense against both herbivores and pathogens, but that their effects are highly specific with respect to the natural enemy species that is encountered. Received 11 April 2002; accepted 9 August 2002     

Effects to perfluorooctane sulfonate (PFOS) on the mollusk Unio ravoisieri under laboratory exposure

To understand acute toxicity and oxidative stress of perfluorinated compounds in the freshwater ecosystems, we exposed freshwater mussels (Unio ravoisieri) to perfluorooctane sulfonate (PFOS), over a range of concentrations from 10 to 100?mg/L, in a laboratory experiment. Lethal concentration (LC50) was of about 65.9?mg/L after 96?h of exposure. The oxidative stress was assessed in gill and digestive gland of the freshwater mussels after 7 days of exposure to different nominal PFOS concentrations (C1=?2?mg/L, C2?=?6?mg/L and C3=?10?mg/L). C1 and C2 increased significantly (p?<?.05) the superoxide dismutase activity in both tissues compared, while the highest C3 decreased the enzyme activity. This implements an unfavourable response that highlights the excess of reactive oxygen species produced after contamination. The Catalase activity was also increased by about 40.05% and 66.63%, respectively, in gill and digestive gland after exposure to C3. The Malondialdehyde (MDA) level was increased in both gill and digestive gland in a concentration-dependent pattern. In contrast, the contamination of U. ravoisieri by PFOS did not affect the acetylcholinesterase activity in both organs (p?>?.005). These results provided information on potential biomarkers that could be effectively applied for the monitoring of freshwater ecosystem using indicator species such as U. ravoisieri.     

Functional diversity loss and change in nocturnal behavior of mammals under anthropogenic disturbance

In the Anthropocene, understanding the impacts of anthropogenic influence on biodiversity and behavior of vulnerable wildlife communities is increasingly relevant to effective conservation. However, comparative studies aimed at disentangling the concurrent effect of different types of human disturbance on multifaceted biodiversity and on activity patterns of mammals are surprisingly rare. We applied a multiregion community model to separately estimate the effects of cumulative human modification (e.g., settlement, agriculture, and transportation) and human presence (aggregated presence of dogs, people, and livestock) on species richness and functional composition of medium- and large-bodied mammals based on camera trap data collected across 45 subtropical montane forests. We divided the detected mammal species into three trophic guilds–carnivores, herbivores, and omnivores–and assessed the nocturnal shifts of each guild in response to anthropogenic activities. Overall, species richness tended to increase (β coefficient = 0.954) as human modification increased but richness decreased as human presence increased (β = –1.054). Human modification was associated with significantly lower functional diversity (mean nearest taxon distance [MNTD], β = –0.134; standardized effect sizes of MNTD, β = –0.397), community average body mass (β = –0.240), and proportion of carnivores (β = –0.580). Human presence was associated with a strongly reduced proportion of herbivores (β = –0.522), whereas proportion of omnivores significantly increased as human presence (β = 0.378) and habitat modification (β = 0.419) increased. In terms of activity patterns, omnivores (β = 12.103) and carnivores (β = 9.368) became more nocturnal in response to human modification. Our results suggest that human modification and human presence have differing effects on mammals and demonstrate that anthropogenic disturbances can lead to drastic loss of functional diversity and result in a shift to nocturnal behavior of mammals. Conservation planning should consider concurrent effects of different types of human disturbance on species richness, functional diversity, and behavior of wildlife communities.     

Hydrolytic enzymes in the two North Sea ctenophores Pleurobrachia pileus and Beroe gracilis

Hydrolytic enzyme activities were determined in tissue extracts of the two North Sea ctenophores Pleurobrachia pileus and Beroe gracilis. The following activities were measured in field samples and characterized according to their mean specific activities and their pH optima: protease, aminopeptidase, amylase, N-acetylglucosaminidase, -glucosidase, chitinase, carboxylesterase, phosphatase. Many of the enzyme activities are correlated, indicating their control by the same factors (i.e. nutritional conditions). Differences found between the phosphatase activities and the apparent lack of the chitinolytic system in B. gracilis reflect the differences in body composition and food specialization in both ctenophores, respectively. The low amylase and -glucosidase activities in both ctenophores agree with the low carbohydrate content of their prey. In spite of high carboxylesterase activities, no lipolytic activity was detected in either of the ctenophores. In a laboratory feeding experiment with P. pileus, the enzyme activities increased but did not reach the activities found in the field samples. In B. gracilis, seasonal variations of some enzyme activities are discussed in relation to the seasonal abundance of its prey, P. pileus.     

Comparison of 1-(2-naphthyloxymethylcarbonyl) pyrrolidine,PP-20/DPJ,newly synthesized compound with the nootropic drug piracetam in normal and aluminum-induced neurotoxic state

Nootropic drugs like piracetam, oxiracetam, and nifiracetam are used as memory enhancers. They are thought to directly influence the energetic processes in the brain and produce elevated acetylcholine levels, but they lack protecting therapeutic potentials. Thus, there is a continuing effort directed towards developing a new cognition-enhancing agent, which would be more effective than the currently available drugs, and 2-Naphthyloxy derivatives (PP-20/DPJ) were consequently developed. This in vivo study was designed to compare the memory enhancing potential of PP-20/DPJ with the known nootropic agent, piracetam, in aluminum (Al)-induced neurotoxic model. Results indicated that PP-20/DPJ improved the short-term memory and cognitive behaviors similar to piracetam. Further, both the compounds were equally effective in elevating the acetylcholinesterase and Mg⁺-ATPase enzyme activity in both the brain regions after Al treatment. Thus the current study suggests, that PP-20/DPJ acts as both a cognition-enhancing agent and as a metabolic enhancer.     

Effects of different management strategies on long-term trends of Australian threatened and near-threatened mammals

Monitoring is critical to assess management effectiveness, but broadscale systematic assessments of monitoring to evaluate and improve recovery efforts are lacking. We compiled 1808 time series from 71 threatened and near-threatened terrestrial and volant mammal species and subspecies in Australia (48% of all threatened mammal taxa) to compare relative trends of populations subject to different management strategies. We adapted the Living Planet Index to develop the Threatened Species Index for Australian Mammals and track aggregate trends for all sampled threatened mammal populations and for small (<35 g), medium (35–5500 g), and large mammals (>5500 g) from 2000 to 2017. Unmanaged populations (42 taxa) declined by 63% on average; unmanaged small mammals exhibited the greatest declines (96%). Populations of 17 taxa in havens (islands and fenced areas that excluded or eliminated introduced red foxes [Vulpes vulpes] and domestic cats [Felis catus]) increased by 680%. Outside havens, populations undergoing sustained predator baiting initially declined by 75% but subsequently increased to 47% of their abundance in 2000. At sites where predators were not excluded or baited but other actions (e.g., fire management, introduced herbivore control) occurred, populations of small and medium mammals declined faster, but large mammals declined more slowly, than unmanaged populations. Only 13% of taxa had data for both unmanaged and managed populations; index comparisons for this subset showed that taxa with populations increasing inside havens declined outside havens but taxa with populations subject to predator baiting outside havens declined more slowly than populations with no management and then increased, whereas unmanaged populations continued to decline. More comprehensive and improved monitoring (particularly encompassing poorly represented management actions and taxonomic groups like bats and small mammals) is required to understand whether and where management has worked. Improved implementation of management for threats other than predation is critical to recover Australia's threatened mammals.     

Genotoxicity,antifungal and antibacterial activity of newly synthesized N-(3-phthalidyl)amines and o-benzoyl benzamide derivatives

A number of newly synthesized phthalidylamines and o-benzoylbenzamide derivatives were evaluated for some biological activities. Synthesis was established by condensation of 3-acetoxyphthalide 1 with morpholine, piperidine, N,N-diisobutyl-N,N-dibenzylamines and piperazine, which afforded N-(3-phthalidyl)amines 3a–d, and 4 respectively, while with N,N-diisopropylamine, o-formyl-N,N-diisopropyl benzamide 5a is formed exclusively. On the other hand, the reaction of 3-acetoxy-3-phenylphthalide 2 with secondary amines afforded o-benzoylbenzamide derivatives 5b–c, 6 in a high yield. The structure of the reaction products was established from their spectral data. These products were screened for antifungal, antibacterial and genotoxic effect. It was found that all tested compounds have antifungal activity. Compounds 1, 2, 3d and 5b were found to be active against Escherichia coli, Bacillus subtilis and Staphylococcus aureus. Genotoxic effects using Ames test showed that Compounds 1 and 2 have a weak base-pair substitution mutagenicity while a clear base-pair substitution mutagenic activity was shown by 3a using TA100-strain of Salmonella typhimurium. Compound 4 showed a frameshift mutgenicity while a weak oxidative mutagenic action was revealed by 6. No change on the mutagenicity of the tested chemicals was observed after using the S9 metabolic activation system.     

Studies on the nutrition of marine flatfish. The effect of oral administration of diethylstilboestrol and cyproheptadine on the growth of Pleuronectes platessa

Two organic compounds, diethylstilboestrol a synthetic oestrogen substitute, and cyproheptadine which acts as an appetite stimulant in some mammals, were added separately at 3 different concentrations to diets fed to plaice (Pleuronectes platessa), and their effect on growth examined. Over a 10 week period, low orally-administered diethylstilboestrol (600 g/kg moist diet) gave rise to increased weight gain, food consumption and food conversion. Higher dietary concentrations of diethylstilboestrol (up to 2400 g/kg diet) were without effect on these parameters. Cyproheptadine did not stimulate appetite, weight gain or food conversion at any of the levels tested.With an Appendix on Statistics by J. A. Pope and A. M. Shanks     

Toxicological effects of N,N,N′,N′-tetramethylethylenediamine on electric eel (Electrophorus electricus) acetylcholinesterase and human serum butyrylcholinesterase

This study examined the adverse effects of N,N,N′,N′-tetramethylethylenediamine (TEMED) on electric eel (Electrophorus electricus) acetylcholinesterase (AChE) and human serum butyrylcholinesterase (BChE). Data show that TEMED inhibited AChE in electric eel as well as human serum BChE. Kinetic studies indicated that the inhibition produced by TEMED in both sources was of mixed type, i.e. K_m increased and V _max decreased in a concentration-dependent manner. K_I (constant of ChE–substrate–TEMED complex into ChE–substrate complex and TEMED) was estimated to be 0.674 mM for electric eel and 0.024 mM for human serum BChE. The γK_m (dissociation constant of ChE–substrate–TEMED complex into ChE–TEMED complex and substrate) was 0.083 and 0.2 mM for electric eel AChE and human serum BChE, respectively. The IC₅₀ for electric eel and for human serum ChE was 1.57 and 0.043 mM, respectively. The present results suggest that TEMED produced adverse effects on electric eel and human serum via inhibition of ChE.     

马拉硫磷及其水解产物对圆瘤浮萍的生长抑制及氧化损伤作用

为了探讨马拉硫磷和主要水解产物对圆瘤浮萍的生长抑制作用及可能的氧化损伤机制,采用静态培养法,研究不同浓度的马拉硫磷及其水解产物二甲基二硫代磷酸酯(DMDTP)、二甲基硫代磷酸酯(DMTP)、二甲基磷酸酯(DMP)对圆瘤浮萍生长、叶绿素含量、叶绿体活性、超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活性及丙二醛(MDA)含量的影响。结果表明,暴露7 d后,浓度为100 mg a.i.·L-1处理下的浮萍叶状体生长量与空白对照组无显著性差异;DMDTP、DMTP和DMP对圆瘤浮萍叶状体生长量的半数抑制浓度(7 d-IC50)分别为52.9、45.5和98.0 mg a.i.·L-1。随着试验液中DMDTP、DMTP和DMP浓度的升高,圆瘤浮萍叶绿素含量均明显降低,叶绿体活性则分别表现为诱导-抑制、抑制和抑制效应。在DMDTP、DMTP和DMP胁迫下,脂质过氧化产物丙二醛(MDA)含量明显增加;圆瘤浮萍体内的抗氧化酶系统均受到影响。总体表现为随着DMDTP浓度的增加,SOD活性先降低后升高;DMTP和DMP胁迫下,SOD活性呈现先降后升再降的趋势;POD和CAT活性则随3种水解产物浓度的增加呈现先升后降趋势;这表明抗氧化酶系统对外部胁迫的应答很复杂。马拉硫磷对圆瘤浮萍的毒性较小,其水解产物DMDTP、DMTP和DMP均对圆瘤浮萍的生长产生一定的毒性作用。在实际生产中,应多加关注马拉硫磷水解产物对环境生物的风险评估。     

In vitro evaluation of human liver cancer cells and the potential cytotoxicity of Tecoma stans (Bignoniaceae) and Brickellia cavanillesi (Asteraceae) both single and in combination

Medicinal herbs are steadily increasing in complementary use for chronic and alterative therapies. The health risks associated with herbal supplements have therefore been identified as a top research priority. Tecoma stans (Tronadora), a Bignoniaceae plant, is a herbal drug traditionally consumed as tea in South America for the control of diabetes. It contains the alkaloids of tecomine and tecostanine which were shown as functional compounds responsible for hypoglycemic activity. However, the side effects of aqueous extracts of this herbal tea have not been reported. In this study, studies sought to evaluate the cytotoxicity of water extracts from T. stans in human hepatoblastoma (HepG2). Toxic effects of T. stans were concentration- and time-dependent in the presence and absence of fetal bovine serum (FBS). Cells were incubated for up to 72-h with varying concentrations of herbal extracts (60–100%), cytotoxicity was determined spectrophotometrically by MTT and reported in terms of % cell viability. For IC₅₀ assay (24 h exposure), cytotoxicity was found at concentration of 60–100%. Evaluation of the effects of T. stans and Brickellia cavanillesi (Asteraceae) in combination revealed that extracts of both herbal extracts' nontoxic levels of T. stans significantly reduced cell viability in a time-dependent manner. Further studies are needed regarding the identification, toxicity, and molecular mechanism of action of active compounds, as well as their cytotoxicity to other cell lines following exposure to both single and combined herbal extracts of these plants with anti-diabetic properties.     

The polymorphism of the human serum paraoxonase †

The activity of paraoxonase, the enzyme which hydrolyses paraoxon, 0,0‐diethyl‐0–4‐nitrophenylphosphate, in human serum shows a genetically determined polymorphism with strong interethnic differences. The serum paraoxonase genotype has a significant influence on the paraoxon clearance. Individuals with high serum paraoxonase activity may be better protected against the toxic effects of parathion (0,0‐diethyl‐0–4‐nitrophenylthiophosphate).

In Caucasians the polymorphism is governed by two alleles. The first allele has a gene frequency p _low of 0.67 to 0.78, and is manifested in both the form of a first homozygotic group with low activities and a second heterozygotic group with medium activities. About 50% of all Europeans belong to the low activity group. The second allele with a gene frequency q _high of 0.22 to 0.33 is manifested in the second heterozygotic and a third homozygotic group with medium resp. high activities. The Hardy‐Weinberg rule for a two allele model is valid for the distribution.

The percentage of the low activity group decreases as one moves from Europe to Africa and Asia. In most of the Mongoloids and Negroids only 5 to 20% of the population can be included in the low activity group, which is not even demonstrable in Aborigines, Maoris, Tonga and some African and Indian (Central America) tribes. The validity of the Hardy‐Weinberg rule for a two‐ or three‐allele model must be rejected in non‐Caucasians.     

Seaweed secondary metabolites as antifoulants: effects of Dictyota spp. diterpenes on survivorship, settlement, and development of marine invertebrate larvae

Summary. A recent investigation showed that the brown seaweed Dictyota menstrualis was unfouled relative to co-occurring seaweeds, and that larvae of fouling invertebrates avoided settling on D. menstrualis due to chemicals on its surface. The secondary metabolites dictyol E and pachydictyol A are among the compounds found on this alga's surface. In the present study, we tested the effects of specific diterpenes from Dictyota on the survivorship, growth, and development of invertebrate larvae and developing juveniles that could foul seaweeds. Exposure to dictyol E, dictyol B acetate, pachydictyol A, and dictyodial from Dictyota menstrualis and D. ciliolata caused significant larval mortality, abnormal development, and reduce growth rates for three species of co-occurring invertebrates when their larvae were forced into contact with these metabolites. Larvae were damaged at metabolite concentrations as low as 5% of maximum possible surface concentrations of these compounds for the populations of Dictyota we studied. The negative effects of these secondary metabolites on potential foulers, in conjunction with data demonstrating larval avoidance of dictyol-covered surfaces, suggest that these compounds could function as chemical defenses against fouling, and could select for larvae that avoid hosts producing these metabolites. Received 25 May 1998; accepted 22 June 1998.