Nitrogen fixation on a coral reef

Acetylene reduction was used to assess nitrogen fixation on all major substrates at all major areas over a period of 1 to 6 yr (1980–1986) at One Tree Reef (southern Great Barrier Reef). Experiments using ¹⁵N₂ gave a ratio of 3.45:1.0 for C₂H₂ reduced:N₂ fixed. Acetylene reduction was largely light-dependent, saturated at 0.15 ml C₂H₂ per ml seawater, and linear over 6 h. High fixation was associated with two emergent cyanophyte associations, Calothrix crustacea and Scytonema hofmannii, of limited distribution. Subtidally, the major contribution to nitrogen fixation came from well-grazed limestone substrates with an epilithic algal community in the reef flat and patch reefs (3 to 15 nmol C₂H₄ cm^-2 h^-1). Similar substrates from the outer reef slope showed lower rates. Nitrogen fixation on beach rock, intertidal coral rubble, reef crest and lagoon sand was relatively small (0.3 to 1.0 nmol C₂H₄ cm^-2 h^-1). Seasonal changes in light-saturated rates were small, with slight reduction only in winter. Rates are also reported for experimental coral blocks (13 to 39 nmol cm^-2 h^-1) and for branching coral inside and outside territories of gardening damselfish (3 to 28 nmol cm^-2 h^-1). This work supports the hypothesis that the high nitrogen fixation on the reef flat and patch reefs of the lagoon (34 to 68 kg N ha^-1 yr^-1) is because these subtidal areas support highly disturbed communities with the greatest abundance of nitrogen-fixing cyanophyte algae. It is calculated from a budget of all areas that One Tree Reef has an annual nitrogen fixation rate of 8 to 16 kg N ha^-1 yr^-1.     

Synthesis and antifungal property of N,N′-bis(trans-cinnamaldehyde)-1,2-diiminoethane and its derivatives

N,N′-bis(trans-cinnamaldehyde)-1,2-diiminoethane and its derivatives were designed and synthesized. Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (¹H-NMR) techniques were applied to characterize chemical structures, and the filter paper disk method was used to test for antifungal effect of the products against Aspergillus niger, Paecilomyces variotii, and Paecilomyces lilacinus. Chemical structure charaterization showed that the products are target compounds. Antimicrobial experiment results indicated that N,N′-bis(trans-cinnamaldehyde)-1,2-diiminoethane displayed reliable antifungal effects against three fungi, and its antifungal effect is close to that of cinnamaldehyde. N,N′-bis(p-methoxy cinnamaldehyde)-1,2-diiminoethane and N,N′-bis(p-chlorocinnamaldehyde)-1,2-diiminoethane also showed antifungal effects at a low concentration. Of the two, N,N′-bis(p-methoxy cinnamaldehyde)-1,2-diiminoethane appeared to be more suitable as it was more effective at higher concentrations against Paecilomyces.     

Copper (II) adsorption studies using models of synthetic humic acids

A polymer with characteristics similar to those of humic acids was obtained by synthesis reactions from oxidative polymerization in an alkaline medium using para-benzoquinone, hydroquinone and 4-aminobenzoic acid as precursors. Samples of natural and synthetic humic acid were used to examine the adsorption behavior of Cu²⁺ ions on these substrates. The mathematical models described by Langmuir and Freundlich equations were applied, yielding the maximum adsorption intensity values K′ (Langmuir), maximum adsorption capacity, b (Langmuir) and the adsorbent adsorption capacity, m (Freundlich). Based on solubility studies, pH 3 was selected for the development of the adsorption experiment. The Cu²⁺ ion presented a favorable adsorption, with RL (equilibrium parameter) responses in Langmuir isotherms falling within the desirable ranges.     

Detoxification of pyrrolizidine alkaloids by the harvestman <Emphasis Type="Italic">Mitopus morio</Emphasis> (Phalangidae) a predator of alkaloid defended leaf beetles

Summary. The harvestman Mitopus morio (Phalangidae) is a generalist predator. It is known to prey on larvae of the chrysomelid leaf beetle Oreina cacaliae defended by plant acquired pyrrolizidine alkaloids (PAs). Tracer feeding experiments were performed to determine how harvestmen tolerate protoxic PAs. Minced meat containing either [¹⁴C]senecionine or [¹⁴C]senecionine N-oxide was fed to M. morio and subsequently feces and bodies were analyzed. Labeled alkaloid N-oxide remained stable and was eliminated almost unaltered with the feces; only 10% was recovered as tertiary PA. In contrast, approximately 80% of labeled tertiary alkaloid (senecionine) ingested with the diet was N-oxidized and eliminated; the remaining 20% consisted of unchanged senecionine and a polar metabolite of unknown structure. Harvestmen process their diet by excreting digestive juice, indicated by bleaching of the meat color. Analysis of the processed diet revealed some N-oxidation of [¹⁴C]senecionine, suggesting the gut as the site of Noxidation. Analysis of the bodies of harvestmen 80 hours after the tracer feeding pulse revealed only trace amounts of the polar metabolite. Neither senecionine nor its N-oxide could be detected in the body extracts. The results are discussed in relation to the strategies of PA adapted insects to avoid accumulation of tertiary PAs in living tissues.     

Nitrogen fixation (acetylene reduction) in the phyllosphere of Thalassia testudinum

N₂ fixation (C₂H₂ reduction) associated with the leaves of the sea grass Thalassia testudinum was investigated at 5 sites in South Florida (Biscayne Bay) and one site in the Bahamas (Bimini Harbor). Significant activities were correlated with the occurrence of a heterocystous blue-green alga (Calothrix sp.) on the leaves. C₂H₂ reduction was not stimulated by organic compounds, either aerobically or anaerobically in the light or dark. Therefore, other physiological types of microbes were not important in N₂ fixation. Diurnal and seasonal variations in N₂ fixation occurred, with maximal rates during the daytime and in the late spring and early summer. N₂ fixation was negligible at four stations in Biscayne Bay. At the fifth station, near Fowey Rock, about 5 kg N ha^-1 year^-1 was fixed. In the summer, the N₂ fixed per day (4–5 mg N m^-2) could provide 4 to 23% of the foliar productivity demands of T. testudinum at this site and the station in Bimini Harbor. N₂ fixation at the periphery of a sea-grass patch, near Fowey Rock, could provide 8 to 38% of the daily nitrogen requirement for leaf production, and thereby might compensate for a less effective trapping and recycling of nitrogen from dead leaves in such regions.     

Quantitative analysis and sorption of cadmium in environmental samples with a functionalized synthetic polymer

Quantitative analysis of cadmium in environmental samples was achieved with a polymeric sorbent synthesized by copolymerization of N,N-dimethylacrylamide and allyl glycidyl ether/iminodiacetic acid as chelating monomers with N,N′-methylenebisacrylamide as cross-linker. The polymer was characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, and scanning electron microscopy. The sorption capacity of the functionalized sorbent was 70 mg g^?1. The equilibrium sorption data of Cd(II) on polymeric sorbent were analyzed using Langmuir, Freundlich, Temkin, and Redlich–Peterson models. Based on equilibrium adsorption data, the constants at pH 4.2 and 20 °C were determined for the first three as 0.33 (L mg^?1), 17.5 (mg g^?1) (L mg^?1)^1/n, and 12.9 (J mol^?1). Recovery of 94% of the metal ion was obtained with 0.5 mol L^?1 nitric acid as an eluting agent.     

Daily rhythm of O2-evolution in the cyanobacterium Trichodesmium thiebautii under natural and constant conditions

The rate of oxygen evolution by the tropical marine cyanobacterium Trichodesmium thiebautii was recorded at different times during the day in samples collected in 1992 from the Bahama Islands and the NE Caribbean Sea. This cyanobacterium is unique in that it is the only non-heterocystous diazotroph capable of N₂-fixation in daylight. Oxygen evolution was measured under conditions of natural day/night (LD, N=50), constant light (LL, N=14), and constant dark (DD, N=2×14). Photosynthesis vs intensity (P-I) relationships were calculated at various times of day, and the following parameters were used for further evaluation: photosynthesic capacity (P _max, 66 to 91 mg O₂ mg chl a ^-1 h^-1), initial slope of the P-I curve (, 0.23 to 0.27), dark respiration (R, 12 to 27 mg O₂ mg chl a ^-1 h^-1), and the intensity at which O₂ consumption is compensated by O₂ production (I _c, 78 to 160 Em^-2 s^-1). All means showed large standard deviations (for some parameters more than 200%). In some cases, these variations could be explained with a sinusoidal 24-h time course, but only the compensation point showed a significant daily variation (p0.001) in both LD and DD. The fact that the time course of I _c typical for natural conditions remains rhythmic under constant dark conditions strongly suggests a circadian regulation. Few circadian rhythms have been observed in prokaryotes, and this appears to be the first observation of such a rhythm in a cyanobacterium which fixes N₂ in daytime.     

Synthesis of some novel (2-oxo-3-(arylimino) indolin-1-yl)-N-aryl acetamides and evaluation as antimicrobial agents

A series of sixteen 2-oxo-3-(arylimino) indolin-1-yl)-N-aryl acetamide derivatives were synthesized, characterized by physical and spectral data (IR, ¹H nuclear magnetic resonance (NMR), and mass spectrometry), and evaluated for their antibacterial and antifungal activities against various pathogenic microorganisms. Some of the synthesized compounds showed promising antibacterial and antifungal activities, the best being 2-(3-(4-chlorophenylimino)-2-oxoindolin-1-yl)-N-(3-methoxyphenyl) acetamide.     

Biodegradation of phenylurea herbicide diuron by microorganisms from long-term-treated sugarcane-cultivated soils in Kenya

The phenylurea herbicide diuron [N-(3,4-dichlorophenyl)-N,N-dimethylurea] is widely used alone or in a broad range of herbicide formulations. Its degradation in sugarcane-cultivated soils which have been impacted by the herbicide through repeated applications was studied. Liquid culture experiments with diuron as the only carbon source led to the isolation of different bacterial strains capable of degrading diuron. The bacterial species belonging to the genera Bacillus, Vagococcus, and Burkholderia, identified through biochemical and molecular characterization, degraded diuron to different extents. The isolated Bacillus cereus, Vagococcus fluvialis, Burkholderia ambifaria, and Bacillus spp1 degraded diuron by 21%, 25%, 22%, and 19% of the initially applied concentration of 40?mg?L^?1, respectively, after 35 days of incubation in liquid culture media. Small amounts of 3,4-dichloroaniline and the de-methylated metabolite N-(3,4-dichlorophenyl)-N-methylurea were detected in liquid culture media. The combination of V. fluvialis and B. ambifaria showed an enhanced degradation of up to 30% of the initially applied concentration of 40?mg?L^?1. Degradation by pure isolates was low (18–25%) compared to the capacities of diuron degradation shown by the bacterial communities (58–74%). This study showed the presence of diuron degraders in sugarcane-cultivated soils impacted by diuron due to repeated applications.     

Nitrogen accretion,and the nature and possible significance of N2 fixation (Acetylene reduction) in a Nova Scotian Spartina alterniflora stand

Total aboveground nitrogen accretion through the 1975 growing season at a short Spartina alterniflora stand was estimated as 78 kg N ha^-1, compared to estimated N₂ fixation on the mud surface of 22 kg N ha^-1 and subsurface N₂ fixation of 93 kg N ha^-1. Subsurface N accretion was estimated to be of the order of 77 kg N ha^-1. Mudsurface ARA (acetylene-reducing activity) exhibited a pronounced mid-season maximum, while subsurface ARA exhibited a general trend of increase from May to September, and then a decline as a function of falling temperature. Various experiments suggested that mud-surface ARA was associated largely with non-heterocystous blue-green algae and photosynthetic bacteria, while subsurface ARA was associated mainly with vital activity of S. alterniflora. Counts of various groups of bacteria indicated an enrichment of anaerobic (glucose-utilizing) and microaerophilic (malateutilizing) N₂-fixing bacteria in the rhizosphere in comparison to non-rhizosphere soil. Treatment of roots with chloramine-t for 2 h reduced total numbers (plate count), anaerobic N₂ fixers, and microaerophilic N₂ fixers by factors of 357, 172, and 22, respectively, suggesting a relative enrichment of microaerophiles in the interior or endorhizosphere of the roots. ARA of excised roots was correlated with ¹⁴C-activity for roots from a plant previously exposed to ¹⁴CO₂, and with branching and age of the roots.     

Nitrogen fixation (acetylene reduction) associated with macroalgae in a coral-reef community in the Bahamas

N₂ fixation (C₂H₂ reduction) was associated with several species of macroalgae on a coral reef near Grand Bahama Island. The highest rates were associated with Microdictyon sp. (Chlorophyceae) and Dictyota sp. (Phaeophyceae). Extensive mats of filamentous blue-green algae, not heterotrophic bacteria, were the N₂ fixing agents: in experiments with samples of Microdictyon sp., the activity was lightdependent and not stimulated by organic compounds under either aerobic or anaerobic conditions. Assays in situ, at 20 m depth, and on shipboard, gave similar rates of N₂ fixation; the cyanophytes presumably have pigment adaptations to function in blue light. The maximum rate of N₂ fixation, associated with Microdictyon sp., was 3.8 g N fixed g dry weight^-1 h^-1. Coral-reef communities flourish in nutrientimpoverished waters, and therefore any input of nitrogen is probably important in stabilizing such ecosystems.     

Photoelectrochemical treatment of ammonium using seawater as a natural supporting electrolyte

In the present study, a photoelectrochemical process containing seawater as a natural low-cost supporting electrolyte was used to remove ammonium from wastewater in a continuous flow mode. Based on central composite design (CCD), response surface methodology (RSM) was employed to evaluate the performance of the process in ammonia removal. The effect of four main independent parameters, including initial ammonium concentration, hydraulic retention time (HRT), current intensity and initial pH on the removal of ammonia was evaluated by the model. The optimal initial ammonium concentration, HRT, current intensity and initial pH were 917 mg NH ₄? N;·L ^?1, 108 min, 1.8 A and 8.4, respectively. The high coefficients (R ²=0.97 and adjusted R ²=0.94) obtained by the analysis of variance (ANOVA) demonstrated close correlation between predicted and experimental values. Also, treating the reject water from the sludge dewatering unit as an ammonium-rich wastewater showed the effectiveness of the process for treating real wastewaters (86% ammonium removal). The results revealed that the present process can be an efficient method for ammonium removal from polluted effluents in coastal areas based on the availability of seawater as a cost-efficient supporting electrolyte.     

A fast and reliable method for quantitative determination of total mercury in vegetables

A cloud-point extraction (CPE) process using the nonionic surfactant, polyethylene glycol tert octylphenyl ether (Triton X-114) was employed for determination of Hg(II) ions in aqueous solutions. The method is based on the ion-pairing reaction of Hg(II) with Pyronin B (PyrB⁺) in the presence of excess iodide at pH 6.0 and extraction of the complex formed. The chemical variables affecting CPE efficiency were studied, and the analytical characteristics of the method were obtained. The calibration curves were linear in the range of 1–40 μg L^?1 with the detection limits of 0.35 and 0.30 μg L^?1 at 556 and 521 nm. Selectivity was also tested. The coefficients of variation of the method are 2.4% and 5.2% for five replicate measurements of mercury at levels of 10 and 25 μg L^?1, respectively. The results obtained for two certified reference samples were in a good agreement with the certified values. The method was applied to the determination of total mercury in vegetable samples.     

Nitrogen fixation by blue-green algae associated with the siphonous green seaweed Codium decorticatum: effects on ammonium uptake

Nitrogen fixation (acetylene reduction) at rates of up to 1.2 g N₂ g dry wt^-1 h^-1 was measured for the siphonous green seaweed Codium decorticatum. No nitrogenase activity was detected in C. isthmocladum. The nitrogenase activity was light sensitive and was inhibited by the addition of DCMU and triphenyl tetrazolium chloride. Additions of glucose did not stimulate nitrogen fixation. Blue-green algae (Calothrix sp., Anabaena sp., and Phormidium sp.) were implicated as the organisms responsible for the nitrogenase activity. They occurred in a reduced microzone within the C. decorticatum thallus where nitrogen fixation was optimized. Nitrogen fixation did not affect the kinetic constants for ammonium uptake in C. decorticatum (K_s=12.0 M, V_max=13.4 mol NH₃ g dry wt^-1 h^-1) determined using the perturbation method. Nevertheless, C. decorticatum thalli which fixed nitrogen had internal dissolved nitrogen concentrations which were over 1.4 times higher than in non-fixing thalli. This suggests that if C. decorticatum does derive part of its nitrogen requirement from the blue-green algae which it harbors, the transfer does not involve competition between this process and the uptake of ambient ammonium.     

三唑醇杀菌剂在雄性丽斑麻蜥体内的对映选择性降解、蓄积和肝毒性研究

三唑醇(triadimenol, TN)是一种广泛使用的手性三唑类杀菌剂,它含有2个手性中心,4个手性对映体,包括对映体A(A1(R,S)和A2(S,R))以及对映体B(B1(R,R)和B2(S,S))。为了研究三唑醇在爬行动物体内的对映选择性行为和潜在的肝毒性,将雄性丽斑麻蜥分别一次经口暴露和28 d长期暴露于三唑醇(100 mg·kg~(-1) body weight),一次经口暴露结果显示,三唑醇进入大脑和肾中的浓度低于肝、性腺、皮肤和尾,B2(S,S)和B1(R,R)对映体具有相似的代谢速率。代谢过程中A1(R,S)的浓度明显高于A2(S,R),并且在暴露后12 h出现二次上升,这可能是A2(S,R)在体内手性转换为A1(R,S)导致。丽斑麻蜥长期(28 d)暴露于三唑醇后,性腺和肾中无明显蓄积现象,皮和尾中浓度显著高于其他组织,各个组织中三唑醇趋向于保持外消旋状态。三唑醇暴露后肝中主要的代谢基因cyp1a1c、yp3a4c、yp2b1和cyp2d3的表达量都出现明显上升,组织病理学分析进一步显示,三唑醇暴露后的肝组织出现组织空泡、血窦阻塞的症状,说明三唑醇对肝组织具有一定的毒性作用。上述结果为手性农药对爬行动物的生态毒理学评价提供了重要依据。     

N-acyl homoserine lactone production by bacteria within the sponge Suberites domuncula (Olivi, 1792) (Porifera, Demospongiae)

Many bacteria live in close association with sponges. Within these consortia, molecules of communication such as quorum-sensing and hormone-like molecules may occur in order to regulate the partnership. Of particular interest, bacterial N-acyl-l-homoserine lactones (AHLs) were screened in supernatants from Suberites domuncula-associated bacteria using an E. coli bioluminescent reporter system. These sponge-associated bacteria were beforehand isolated on several media supplemented or not with a sponge extract to attempt to isolate sponge-specific bacteria. Out of 81 AHL-producing bacteria, three strains requiring sponge extract to grow were selected for AHL characterization. The in vitro produced AHLs, that is, in bacterial culture supernatants, were identified as N-(3-butanoyl)-l-homoserine lactone and N-(3-oxododecanoyl)-l-homoserine lactone and quantified using LC–ESI–MS/MS. The in vivo production of AHLs by sponge-associated bacteria has also been demonstrated in a healthy host for the first time: N-(3-oxododecanoyl)-l-homoserine lactone, N-(3-hexanoyl)-l-homoserine lactone, and N-(3-heptanoyl)-l-homoserine lactone. This AHL production in sponges may suggest a potential role of these molecules between sponge-associated bacteria and/or between sponge-associated bacteria and the sponge.     

Binding of trinitrotoluene (TNT) to water extractable humus

Solid-state ¹⁵N NMR was applied to the aqueous extracts of a ¹³C-enriched plant slurry (Lolium perenne), anaerobically incubated with ¹⁵N₃-trinitrotoluene (TNT). Almost all ¹⁵N₃-TNT transformation products became covalently bound to the plant-derived organic material extractable with water. DCPMAS ¹⁵N ¹³C NMR revealed a three-step reaction scheme. After reduction of TNT, the aryl amines are acetylated. Subsequent alkylation of the resulting amides strengthens the incorporation of TNT-transformation products into humic material. Comparable results have been recently obtained under aerobic conditions, which indicates that this pathway is a common process during biological TNT transformation.     

The use of metabolic ratios for determining the catabolic substrates of a solitary ascidian

In a previous study, Hatcher (1989: Mar. Biol. 102: 445–452) found that variations in CO₂ and O₂ respiration rates in individual marine invertebrates led to RQ (respiratory quotient) values which were variable and often outside theoretical limits. The present study was designed to examine the variability in several excretionbased metabolic ratios which are often used as alternatives for the RQ in qualitative predictions of catabolic substrates. The experimental organism was a solitary ascidian,Herdmania momus (Savigny), collected near Perth, Western Australia, between January and July 1984. Respiration and excretion rates ofH. momus were examined as a function of a progressive nutritional stress, and covariation was examined. Nutritional stress accounted for more of the variation over time in respiration rates (40 to 50%) than in NH ₄ ⁺ excretion rates (20%). Significant net exchanges of dissolved organic compounds were measured. Qualitative predictions of catabolic substrates were based on a comparison of metabolic ratios with theoretical limits. The O:PO ₄ ^3- ratios were lower than the theoretical limits. The values of the O:NH ₄ ⁺ and NH ₄ ⁺ :PO ₄ ^3- ratios were not influenced by nutritional conditions but changed as a function of reproductive condition of the ascidians. Based on the results of this study, it was concluded that metabolic ratios measured on individual ascidians cannot be reliable predictors of catabolic substrates.     

Zooxanthellae providing assimilatory power for the incorporation of exogenous acetate in Heteroxenia fuscescens (Cnidaria: Alcyonaria)

The soft coral Heteroxenia fuscescens (Ehrb.) and its isolated zooxanthellae (endosymbiotic dinoflagellates) were investigated with particular regard to uptake and utilization of exogenously supplied ¹⁴C-acetate in the light and in the dark. The incorporation of ¹⁴C from ¹⁴C-acetate into the host tissue and into the zooxanthellae was consistently much higher in the light than in the dark. The incorporated ¹⁴C-acetate was rapidly metabolized by the host and algae and was recovered from different assimilate fractions. The major proportion of radiocarbon from metabolized ¹⁴C-acetate was located in host tissue. The CHCl₃-soluble fraction composed of diverse lipids showed the strongest ¹⁴C-labelling. Zooxanthellae isolated prior to incubation accounted for about 80% of the acetate incorporation recorded for zooxanthellae in situ (in vivo). It is concluded from a comparison of acetate incorporation and conversion under light and dark conditions that most of the lipid reserve of the host tissue originates from fatty acids, which are synthesized within the algal symbionts and are then translocated to the heterotrophic partner via extrusion. The acetate units needed for lipid synthesis are obtained by absorption of free acetate from dissolved organic matter (DOM) in the seawater as well as by photosynthetic assimilation of inorganic carbon. Thus, in H. fuscescens, lipogenesis is operated as a light-driven process to which the zooxanthellae considerably contribute assimilatory power by performing fatty acid synthesis and translocation of lipid compounds to their intracellular environment (host cell). A metabolic scheme is proposed to account for the different pathways of carbon conversion observed in H. fuscescens. The incubations took place in August 1980 and the analytical part from October 1980 to January 1984.     

Spatial variations in the N2O emissions and denitrification potential of riparian buffer strips in a contaminated urban river

Spatial variations in the N₂O emissions and denitrification potential of riparian buffer strips (RBS) in a polluted river were examined. The river received large pollutant inputs from urban runoff and wastewater discharge, resulting in impaired water quality in the river and downstream reservoir. The potential for nitrogen removal by RBS was evaluated by measuring in situ N₂O emission fluxes in static closed chambers and sediment denitrification potentials with acetylene inhibition techniques. The results showed that N₂O emission fluxes decreased from the upstream (16.39 μg/(m²·h)) to downstream (0.30 μg/(m²·h)) sites and from the water body to upland sites. The trend in decreasing N₂O emission fluxes in the downstream direction was mainly associated with sediment/soil textures (clay loam→sandy soil) and sediment/soil water contents and was also related to the vegetation along the RBS and nutrients in the sediments/soils. The correlation coefficient was highest (r=0.769) between the N₂O emission flux and sediment/soil water content. Sediment/soil denitrification potentials under N-amended and ambient conditions were higher (highest 32.86 mg/(kg·h)) for the upstream sites, which were consistent with in situ N₂O flux rates.