Growth and nutrient uptake of green alga, Scenedesmus dimorphus, under a wide range of nitrogen/phosphorus ratio—I. Experimental study

In order to elucidate the relation between algal growth and nutrients such as nitrogen and phosphorus, a chemostat culture experiment using Scenedesmus dimorphus was performed under the conditions of T-N/T-P ratio of 2–50 mg N mg⁻¹ P and dilution rate of 1–4 day⁻¹. It was ensured from the results that nitrogen and/or phosphorus is the limiting nutrient for the growth of this alga under these conditions. The optimum T-N/T-P ratio for its growth was observed to change from 20 to 5 mg N mg⁻¹ P as the dilution rate varied from 1 to 4 day⁻¹ and, in most of the range of T-N/T-P ratio and dilution rate, its growth rate was not regulated by only one of the available nitrogen and phosphorus concentrations in the medium and algal nitrogen and phosphorus contents. Based on these facts, the multiplicative effect rather than the threshold effect of these two nutrients on its growth was considered to exist. It has been suggested, however, that algal nitrogen and phosphorus contents, especially nitrogen content, are the most important factors regulating its growth. Nitrogen uptake rate of this alga increased at a given concentration of available nitrogen in the medium as T-N/T-P ratio decreased down to 2 or 5 mg N mg⁻¹ P. It is also suggested that a multiplicative effect of nitrogen and phosphorus on uptake of these nutrients by S. dimorphus may exist.     

The acute toxicity of dissolved elemental phosphorus to cod (Gadus morhua)

The acute toxicity of dissolved elemental phosphorus to cod (Gadus morhua) has been investigated in the absence of colloidal phosphorus. The 48 h lc₅₀ for dissolved elemental phosphorus is 14·4 μg l⁻¹, and evidence is presented that the incipient lethal level is ca. 1–2 μg l⁻¹. Elemental phosphorus was rapidly assimilated into the body tissues of the test animals. The distribution of phosphorus was homogeneous in the muscle tissue with levels ca. 10–30 times the exposure level, highest concentrations were measured in the liver.Preliminary data are reported which indicate that the biological half life of accumulated elemental phosphorus is very short when exposure is ended.     

Accumulation of zinc, cadmium and lead by field populations of Lemanea

A study has been made of the concentrations of zinc, cadmium and lead in populations of the red alga Lemanea growing in fast-flowing rivers in Britain, France. Germany, Ireland and Sardinia (Italy). The sites were selected to provide a wide range of aqueous concentrations of these metals. Many of the sites are influenced by past or present mining activities and Lemanea was found at aqueous concentrations of zinc up to 1.16 mg 1⁻¹. In contrast to previous studies with filamentous green algae, no evidence could be found to support the hypothesis that populations differ genetically in their ability to tolerate these heavy metals. Samples of alga consisted of pooled 2 cm long terminal tips of filaments detached from approx. 1 cm² rock surface. Significant positive correlations were found between the logarithm of the mean concentration of zinc, cadmium and lead in four such samples collected from within 10 m reaches at 59 sites and the logarithm of the concentration of each metal in both unfiltered and filtered water. The enrichment ratios for each metal decreased with increasing aqueous metal concentrations. Although the aqueous concentrations of the three metals were strongly intercorrelated, differences in the ratio of metal concentrations were reflected in the composition of Lemanea filaments. The results suggest that high levels of calcium (and/or magnesium) result in decreased uptake of zinc. Intensive sampling from a single population showed that part of the zinc content of filaments is sensitive to short-term fluctuations in concentrations in the surrounding water. In the particular population studied this was about 20%; a similar percentage could be eluted in the laboratory with EDTA. Transplants of Lemanea were made between reaches with different aqueous concentrations of zinc and in all cases the zinc concentration in filament tips increased or decreased to stabilise at a concentration similar to that in filaments native to the reach. It is suggested that chemical analyses of natural or transplanted populations of Lemanea could provide a valuable aid in monitoring contamination of rivers by zinc, cadmium or lead.     

Internal phosphorus loading in a shallow eutrophic lake

Internal loading of phosphorus has been implicated as a major eutrophicating factor in Long Lake, Washington (Kitsap County). As a result of such loading, summer total phosphorus concentrations approach or exceed 100 μgP l⁻¹. Most of the summer loading of phosphorus is thought to have been released directly from the rich, flocculent sediment in the mid and northern part of the lake as a result of high pH (up to 10) related to phytoplankton photosynthesis. The lake also supports a dense submersed macrophyte crop (areal weighted mean dry weight of about 220 g m⁻²) composed primarily of Elodea densa. Although excretion of phosphorus from healthy E. densa was found to be minimal, the potential contribution of P indirectly from sediment via macrophyte uptake and subsequent decomposition in the winter was on the order of 200–400 kg yr⁻¹ or about 25–50% of the external loading. Nevertheless, loading of phosphorus during predrawdown summers is thought to have originated largely as a direct release from sediment due to high pH. Estimates of sediment phosphorus release determined from laboratory experiments, mass balance and core analyses ranged from 2.2 to 5.6 mg m⁻² day⁻¹.As a component of the restoration program, the lake (mean depth of 2 m) was drawn down nearly 2 m for 4 months during the summer and fall of 1979. The lake's trophic status was expected to improve due to sediment consolidation and/or macrophyte reduction. The drawdown resulted in an 84% reduction in macrophyte biomass in 1980 but minimal sediment consolidation (0.1 m). Winter decomposition of the much smaller macrophyte crop, apparently provided insufficient phosphorus in the spring to stimulate phytoplankton and to enrich midlake sediments, which has probably occurred in previous years. Low water column pH during the postdrawndown summer of 1980 resulted from relatively low rates of plankton photosynthesis. During the summer of 1980 internal loading of phosphorus was reduced and total phosphorus remained below 50 μg l⁻¹.     

Anaerobic treatment of wastes containing methanol and higher alcohols

Experiments have been performed to ascertain the feasibility of anaerobic digestion for the treatment of an alcoholic waste (i.e. fusel oil), consisting of approx. 50% methanol and 50% higher alcohols. Batch experiments as well as continuous experiments have been conducted. The continuous experiments have been carried out using the “Upflow Anaerobic Sludge Blanket” (UASB-) process. As inoculum a sugar beet waste grown and highly settleable and active anaerobic sludge (SBA-sludge) has been used. The SBA-sludge was shown to be superior to digested sewage sludge as seed material for an anaerobic treatment process, because—although it in fact is adapted to the fermentation of volatile fatty acids (VFA)—it does not have any significant difficulty with respect to the methanogenesis of the alcohols present in the fusel oil waste. The breakdown of higher alcohols starts immediately and that of methanol within a few days, depending on the initial load applied. In the UASB-experiments sludge loads up to 0.6 kg COD·kg VSS⁻¹·day⁻¹ could already be well accommodated within 1 week, so that within this period a space load could be handled as high as 20 kg COD·m⁻³·day⁻¹, simply by supplying the reactor with approx. 30 kg SBA-VSS·m⁻³ averaged over the total reactor volume.Contrary to recent findings of Smith & Mah (Appl. envir. Microbial. 36, 870–879, 1978), which were obtained with a pure culture of Methanosarcina barkeri, the sludge is capable of fermenting VFA and methanol rapidly and simultaneously, provided the conditions for VFA and methanol fermentation are favourable. However, as in previous experiments with aqueous solutions of methanol (Lettinga et al., Water Res. 13, 725–737, 1979), we observed that the digestion process can easily become upset, especially with respect to the degradation of VFA. Once again indications have been obtained that one or more trace elements are of eminent importance with respect to the stability of the process. At present the operation of a stable anaerobic treatment process for methanolic wastes cannot be guaranteed.     

Use of large submerged chambers to measure sediment-water interactions

Submerged chambers were designed and constructed primarily to study in situ sediment phosphorus release in Shagawa Lake, Minnesota. Initial experiments indicated anoxic phosphorus release rates of 7 mg m⁻² day⁻¹. Oxygen consumption rates within the chambers were also measured; an average consumption rate of 0.17 g m⁻² day⁻¹ was obtained.     

Effects of lignin and chlorolignin in pulp mill effluents on the binding and bioavailability of hydrophobic organic pollutants

The partition coefficients (K_p) of benzo(a)pyrene (BaP), 3,3′,4,4′-tetrachlorobiphenyl (TCB) and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) to dissolved kraft lignin (Indulin AT), chlorolignin isolated from a bleached kraft mill effluent (BKME) and dissolved organic matter (DOM) in a lake receiving BKME were measured by equilibrium dialysis. The K_p values of kraft lignin were 28.2 × 10⁵, 6.5 × 10⁵ and 15.9 × 10⁵ and those of chlorolignin were 8.3 × 10⁵, 2.9 × 10⁵ and 2.2 × 10⁵ for BaP, TCB and TCDD, respectively. In addition, DOM in a series of lake water samples collected from the southern part of Lake Saimaa, SE Finland, receiving BKME revealed higher binding capacities to all of the three model compounds than natural DOM in water upstream from the pulp mill. An important phenomenon related to the environmental transport and fate of xenobiotics was almost the full reversibility of the binding between chlorolignin and model compounds. The obtained K_p values of chlorolignin after a 4 day dissociation period were 12.6 × 10⁵ and 4.6 × 10⁵ for BaP and TCDD, respectively.In short-term (24 h) accumulation experiments with Daphnia magna the effects of kraft lignin and chlorolignin on the bioavailability of three model compounds was very clear. The bioconcentration factors of the xenobiotics in the chlorolignin containing water (DOC = 10 mg C/l) were 20–30 and 25–35% of those organic-free control and upstream reference waters (DOC = 7.2 mg C/l), respectively. The effect of chlorolignin of BKME on the bioavailability of model compounds was also seen in the lake water series of Lake Saimaa.     

Utilization of organic phosphates by selected bacteria and algae

Studies showed that synthetic phosphates of a surface active nature may become a source of carbon and energy for the Bacillus licheniformis. Bacillus mycoides, Bacillus cougulans and Azotobacter agilis bacteria in spite of the fact they are hardly oxidizable. In addition, it was found that these compounds may also become a source of phosphorus for the Scenedesmus obliquus alga which proves that these algae contain suitable phosphatases permitting utilization of a specific organic compound.     

Rate constants of reactions of ozone with organic and inorganic compounds in water—II: Dissociating organic compounds

Rate constants of reactions of ozone with non-ionized solutes, such as aliphatic alcohols, olefins, chlorosubstituted ethylenes, substituted benzenes and carbohydrates, have been determined from the absolute rates with which ozone reacts in the presence of various concentrations of these compounds in water. They have been tested by comparison with the relative rates by which pairs of these solutes are transformed by ozone. Different experimental methods have been developed to determine such rate constants in the range from 10⁻² to 10⁵ M⁻¹ s⁻¹. Interferences between the direct reactions of ozone and reactions due to its preliminary decomposition to secondary oxidants could be eliminated. The kinetics of all the reactions studied are first order with respect to ozone and solute concentration. The rate constants of many types of organic compounds in water are of the same order of magnitude as in organic solvents. Substituted benzenes, however, react in water about 100 times faster. They obey a linear free energy relationship with p = −3.1 when based on δ_p⁺ values. Comparisons of rate constants with chemical structures of the reacting groups show that all reactions of ozone are highly selective and electrophilic. The kinetic data allow explanation of the chemical effects of ozone observed in water treatment practice.     

Modelling phosphorus transport in soils and groundwater with two-consecutive reactions

A model is presented for one-dimensional transport of phosphorus (P) in soils and groundwater. Convective transport, hydrodynamic dispersion and time-dependent phosphorus sorption are accounted for in the model formulation. Time-dependent sorption of soil-P is considered to follow the two consecutive reaction model of Barrow and Shaw (J. Soil Sci.30, 67–76, 1979) which has been extensively tested against experimental data and can be described by S = k · Cⁿt^m. The assumed sorption model allows parameters to be obtained by independent batch and column experiments. A numerical technique is used to solve the solute transport equation incorporating a correction to numerical dispersion to improve the numerical solution. An analytical solution for a simplified case is also presented to test the numerical technique. Parameter sensitivity analysis shows that influent concentration and the parameter k strongly affect the initial breakthrough time of solute, with m and n affecting the shape of the breakthrough curve. Preliminary investigations show that the applicability of the model to describe column experimental breakthrough curves is promising.     

Effects of fungal species,cultivation time,growth substrate,and air exposure velocity on the fluorescence properties of airborne fungal spores

Real‐time bioaerosol monitoring is possible with fluorescence based instruments. This study provides information on major factors that can affect the fluorescence properties of airborne fungal spores. Two fluorescence‐based bioaerosol detectors, BioScout, and ultraviolet aerodynamic particle sizer (UVAPS), were used to study fluorescent particle fractions (FPFs) of released spores of three fungal species (Aspergillus versicolor, Cladosporium cladosporioides, and Penicillium brevicompactum). Two culture media (agar and gypsum board), three ages of the culture (one week, one month, and four months), and three aerosolization air velocities (5, 15, and 27 m/s) were tested. The results showed that the FPF values for spores released from gypsum were typically lower than for those released from agar indicating that poor nutrient substrate produces spores with lower amounts of fluorescent compounds. The results also showed higher FPF values with lower air velocities in aerosolization. This indicates that easily released fully developed spores have more fluorescent compounds compared to forcibly extracted non‐matured spores. The FPFs typically were lower with older samples. The FPF results between the two instruments were similar, except with four‐month‐old samples. The results can be utilized in field measurements of fungal spores to estimate actual concentrations and compare different instruments with fluorescence‐based devices as well as in instrument calibration and testing in laboratory conditions.     

Identification of nitrogen as a growth-limiting nutrient in wastewaters and coastal marine waters through continuous culture algal assays

Two series of continuous culture algal assays conducted in 1973 and 1974, totalling 63 experiments, were performed on mixtures of seawater and wastewater—both treated and untreated— from five locations along the coasts of MA and RI. The results conclusively show that nitrogen was the growth-limiting nutrient in these wastewaters and in coastal marine environments receiving such wastes. There was a linear relationship between total inorganic nitrogen (ΣN) in the influent and particulate nitrogen (PN) representing algal biomass up to a ΣN concentration of about 10 mg1⁻¹. In addition, the N:P ratios in the test alga. Phaeodactylum tricornutum, varied between 10 and 20 (by atoms), whereas the N:P ratios in the wastewater-seawater mixtures were between 4 and 12, thus providing additional evidence that nitrogen was limiting. Enrichment with nitrogen and/or phosphorus to span a range of N:P ratios from 3.9 to 20 resulted in a linear response in PN concentration to ΣN additions. Additions of P had no effect on algal growth. Removal of detergent-P in communities practicing marine waste disposal will hence have little impact on the control of eutrophication in coastal waters.     

The impact of barley straw conditioning on the inhibition of Scenedesmus using chemostats

The current paper investigates the role of barley straw conditioning on inhibiting the alga Scenedesmus. Fresh, pre-rotted and white rot fungi (WRF) augmented straw was tested in a series of chemostat experiments over 15 weeks. All three systems were effective at inhibiting the alga with differences observed in the lag time before inhibition occurred and the rate of alga decline. Lag times of 8, 4 and 1 week(s) were recorded for the fresh, rotted and fungi-treated straws, respectively, with a maximum inhibition rate of >7 × 10⁴ cells week⁻¹ observed for the fungi pre-treated system. Overall, the results indicate that pre-treatment is a viable method to enable barley straw to be used in a more reactive manner. Explanation is postulated that during pre-treatment no alternative sources of nitrogen are available, thereby leading to greater bacterial decomposition of straw lignin to release inhibitory substances. The principle of utilising an engineered pre-treatment by inoculating barley straw with WRF to enhance the impact of the straw on algal inhibition has been clearly demonstrated. Further work is required to understand how the straw pre-treatment stage can be reduced to minimise its duration while maximising the inhibitory effect of adding barley straw.     

Effects of manganese, copper and lead on Selenastrum capricornutum and Chlorella stigmatophora

Algal assays were conducted to observe the responses of Selenastrum capricornutum and Chlorella stigmatophora to the metals manganese, copper and lead, added singly or in combination to both artificial media and natural waters. A 50% reduction in the total algal cell volume of Selenastrum in standard algal assay medium (SAAM) occurred by the addition of either 3.1 mg manganese 1⁻¹ 85 μg copper 1⁻², or 140 μg lead 1⁻¹. For Chlorella grown in 28 ppt artificial seawater plus full SAAM nutrients, the corresponding numbers were 50mg manganese 1⁻¹, 70 μg copper 1⁻¹ or 700 μg lead 1⁻¹. Of the metals tested, only lead was found in higher concentrations in urban and agricultural runoff than at least one of these levels.Theoretical considerations show that a product model is a more reasonable reference for no-interaction than an additive model for experiments in which toxic metals are added in combination. Combination experiments, in which any combination of the three metals act at the same time, indicate (1) synergism between manganese and copper, (2) antagonism between manganese and lead, and (3) antagonism between copper and lead. As to the manganese-lead interaction, it is shown that the lead-induced inhibition of cell division is offset, partially for Selenastrum and completely for Chlorella by the addition of manganese.     

Potentially harmful secondary metabolites produced by indoor Chaetomium species on artificially and naturally contaminated building materials

The presence of the fungal genus Chaetomium and its secondary metabolites in indoor environments is suspected to have a negative impact on human health and well‐being. About 200 metabolites have been currently described from Chaetomium spp., but only the bioactive compound group, chaetoglobosins, have been screened for and thus detected in buildings. In this study, we used a liquid chromatography high‐resolution mass spectrometry approach to screen both artificially and naturally infected building materials for all the Chaetomium metabolites described in the literature. Pure agar cultures were also investigated to establish differences between metabolite production in vitro and on building materials as well as in comparison with non‐indoor reference strains. On building materials, six different chaetoglobosins were detected in total concentrations of up to 950 mg/m² from Chaetomium globosum along with three different chaetoviridins/chaetomugilins in concentrations up to 200 mg/m². Indoor Chaetomium spp. preferred wood‐based materials over gypsum, both in terms of growth rate and metabolite production. Cochliodones were detected for the first time on all building materials infected by both C. globosum and Chaetomium elatum and are thus candidates as Chaetomium biomarkers. No sterigmatocystin was produced by Chaetomium spp. from indoor environment.     

Domestic and agricultural contributions to the inputs of phosphorus and nitrogen to Lough Neagh

Loadings of nitrogen and phosphorus from the major river catchments that contribute to Lough Neagh have been measured for the years 1971–1974. Analysis of this data indicated that there was a very significant correlation between soluble ortho-P loadings and the human but not the animal population densities of the catchments. The land drainage and agricultural contribution of soluble ortho-P to Lough Neagh was 0.14 kg P-ha⁻¹·yr⁻¹ which was about 25% of the measured soluble ortho-P loading to the Lough. It was estimated that the introduction of phosphorus removal treatment at sewage works connected to populations greater than 2000 could curtail 50% of the phosphorus available to support algal growth in the Lough. There was a good correlation between nitrogen fertilisers usage in Northern Ireland and the nitrate concentration in the major rivers.     

Detergent phosphorus and algal growth

The total biomass of Chlorella pyrenoidosa (two strains) Chlamydomas reinhardtii. Euglena gracilis. Anabaena flos-aquae and Plectonenema boryanum was determined after the algae were grown in waters from Sylvan, Pleasant and Pidgeon Lakes (all in northeastern Indiana) that had been supplemented with 0.1, 1 or 10% sewage effluents (Indianapolis and Crawsfordsville, Indiana). Biomass was found not to be significantly decreased when the total phosphorus was reduced by alkaline treatment from 7.20-3.50 mg l⁻¹ (50 per cent reduction) for the Crawfordsville effluents. In another series of experiments Chlorella pyrenoidosa was grown in Sugar Creek water (west central Indiana) to which had been added 0.1. 1 or 10% sewage effluents that originated from a motel treatment system. Reactive sewage phosphorus was reduced from 15.4 to 7.44 mg l⁻¹ (57 per cent reduction) by supplying the motel with non-phosphorus cleaning products. No significant reduction in algal growth was observed. Only when effluents were advanced treated so that reactive phosphorus levels were below 1.2 mg l⁻¹ (92 per cent reduction) was algal growth significantly decreased.     

Heavy metals in animals of Lake Balaton

Hg, Cd, Cu, Pb, Zn, Fe and Mn concentrations were measured in Chironomidae larvae, Crustacea plankton, as well as in various organs of mussels and fishes collected from the open water area of Lake Balaton. The values were comparatively low. However, there were significant differences in the metal concentrations of species and tissue.Most Cd was found in the gill of Unio pictorum L., most Pb, Zn and Mn in the gill of Anodonta cygnea L., most Cu in Crustacea plankton and in the liver of Abramis brama L., and most Hg and Fe in Chironomidae larvae. Low concentrations occurred in fishes, the lowest in the flesh of Stizostedion lucioperca L.Accumulation of metals in organs as compared with their concentration in the lake water was in the range of 3.4 × 10²−2.6 × 10³ for Hg; 7.0 × 10²−6.8 × 10³ for Cd; 3.3 × 10²−9.7 × 10³ for Cu; 6.9 × 10²−8.1 × 10³ for Zn; 1.5 × 10³−2.4 × 10⁴ for Pb; 3.5 × 10²−3.1 × 10⁴ for Fe; and 5.0 × 10¹−3.5 × 10⁵ for Mn.     

A quantitative investigation of the reaction of ozone with p-toluenesulfonic acid in aqueous solution as a model compound for anionic detergents

The reaction of ozone with p-toluenesulfonic acid (PTA) at initial pH 3 and 12 in aqueous solutions (25°C) has been studied at initial concentration 1 mmol l⁻¹ and ozone dose is 24 mg min⁻¹ 1. and 11 mg min⁻¹ 1. respectively. The substrate elimination follow a zero order rate law. A 98% p-toluenesulfonic acid reduction requires at least 7 mol O₃ per mol PTA, however to remove 100% PTA the consumption of ozone increases to 16 mmol O₃ per mmol PTA. At this point a 28% reduction of DOC and a 74% COD reduction was achieved.The PTA decomposition is quicker at higher ozone flow rate, but the specific ozone consumption increases also. As oxidation products the following compounds were identified and their quantitative variations as function of ozonation time were measured: methylglyoxal, acetic acid, formic acid, pyruvic acid, oxalic acid, H₂SO₄ and H₂O₂. As byproduct mesoxalic acid was identified. At pH 12 lactic acid as a further oxidation product was observed.Balances of carbon, sulfur and methyl as well of the acid equivalents indicate one or more intermediates with a sulfonic acid group. These intermediates with a proportion of about 20% disappear after 100% PTA elimination. On account of these results a reaction mechanism is discussed.     

Detoxification of seawater used for gas scrubbing in the steel industry

Cyanide ion present in seawater after scrubbing blast furnace and coke ovens gases can be removed by sedimentation of hexacyanoferrate complexes followed by oxidation of residual cyanide with Caro's acid. Zinc ion is removed at the same time by adsorption on the hexacyanoferrate/hydrous ferric oxide precipitate.Sulphide is precipitated as ferrous sulphide, then oxidised by atmospheric oxygen. At 25°C and using an Fe/CN ratio of 1·00, initial concentrations of 50 mg l⁻¹ of CN⁻ and 10 mg l⁻¹ of Zn²⁺ in seawater are reduced to 5–7 mg l⁻¹ and 0·1 mg l⁻¹. Subsequent treatment with H₂SO₅/CN = 1·2 reduces the [CN⁻] to 0·1 mg l⁻¹.Treatment of a combined blast furnace/coke ovens effluent ([CN⁻] = 24 mgl⁻¹, [Zn²⁺] = 4·0 mgl⁻¹) with Fe/CN = 1·5 reduced [CN⁻] to 0·2 mg l⁻¹ and [Zn²⁺] to <0·1 mgl⁻¹. Subsequent treatment with H₂SO₅/CN = 2·0 reduced [CN⁻] to 0·2 mg l⁻¹. The process operates best in the pH range 7–9 and so is not affected by the buffer characteristics of seawater.