Dynamics of water-extractable phosphorus during the degradation of Microcystis aeruginosa by four bacteria species

We carried out a laboratory experiment for studying the dynamics of water-extractable phosphorus release during the decomposition of dead Microcystis aeruginosa driven by the four bacteria strains. Our results showed that water-extractable phosphorus had significant correlation to alkaline phosphatase but without obvious correlation to acid phosphatase, suggesting that alkaline phosphatase was the primary enzyme decomposing organic phosphorus. Also, water-extractable phosphorus exhibited an obvious correlation to pH, indicating that the alkaline environment contributed to the release of water-extractable phosphorus. The quantity of bacteria hardly correlated to the release of water-extractable phosphorus for all species. This could result from decrease of bacterial quantity after consumption of substrate in closed system. Obvious variation in water-extractable phosphorus was observed across the strains in two water treatments. Sporolactobacillus sp. and Bacillus macerans had the strongest ability for decomposing organic phosphorus among five strain treatments in the lake water. In the distilled water, Bacillus sp. had the strongest ability to degrade organic phosphorus. In both water treatments, mixed species exhibited intermediate ability for decomposing organic phosphorus. It was true that water quality strongly affected the release of phosphorus by regulating phosphatase activity.     

Soluble fractions of phosphorus compounds and alkaline phosphatase activity in loch creran and loch etive,Scotland

Reactive phosphorus, polyphosphate, monophosphate ester, dissolved organic phosphorus, and alkaline phosphatase activity were measured in Loch Creran and Loch Etive. Argyll, Scotland during the spring outburst of 1976. In addition, data on chlorophyll a, phacopigment, and salinity were obtained on each occasion.The mean levels of reactive phosphorus initially present in Loch Creran and Loch Etive were 0.50 and 0.22 μg-at. PO₄?P/I, respectively. As the diatom bloom progressed, it fell below the limit of detection. The mean values of polyphosphate were between 0.05–0.08 μg-at. PO₄?P/l in Loch Creran and 0.04 μg-at. PO₄?P/l in Loch Etive, and although present at the initiation and decline of the bloom, it was absent when chlorophyll a was high and the reactive phosphorus was low or undetectable. Monophosphate ester, was found in Loch Creran only, and then in the same concentration as that of the polyphosphate fraction. The mean levels of the dissolved organic phosphorus in Loch Creran and Loch Etive ranged between 0.08–0.18 μg-at. PO₄-P/l and 0.05–0.08 μg-at. PO₄?P/l, respectively. Alkaline phosphatase activity was detected when there was no reactive phosphorus in the water: the highest values in Loch Creran and Loch Etive were 0.003 and 0.005 I.U. of enzyme/4 ml of sample, respectively. The highest mean values of chlorophyll a were 8.0 μg/l in Loch Creran, and 6.0 μg/l in Loch Etive. The mean percentages of phaeopigment fluctuated between 20–55% in Loch Creran and 30–65% in Loch Etive. The highest values were found at the end of the bloom. The mean surface salinities ranged from 22.0 to 31.0‰ in Loch Creran and 3.7 to 17.0‰ in Loch Etive. The lowest values were recorded at the end of the bloom. The statistical treatment of the data, suggests a strong relationship between zooplankton grazing and levels of dissolved phosphorus compounds and phaeopigment.     

太湖不同解有机磷菌株胞外碱性磷酸酶活性对蓝藻碎屑的响应

浮游细菌胞外碱性磷酸酶在湖泊磷循环过程中具有关键作用, 但其与生物可利用性磷和颗粒态有机质之间的关系尚未得到充分的研究。研究以从太湖沉积物分离的3 株解有机磷细菌(OPB)和东湖水中OPB菌群为实验对象, 以蓝藻干物质为颗粒态有机质, 系统分析了模拟条件下OPB 的数量、不同大小颗粒所表现的胞外碱性磷酸酶活性(APA)与不同形态磷的浓度及其相互关系。从总体上讲, APA 与OPB 数量显著正相关, 且明显反比于溶解反应性磷(SRP)浓度, 在模拟实验过程中, 不同菌株(群)所对应的SRP 浓度均显著不同, 故其解磷能力各异。从绝对活性及其在总活性中所占的比例来看, 各处理间小颗粒(0.22—3.0 μm)APA亦明显不同, 而大颗粒(>3.0 μm)APA和溶解态(8 CFU/mL), SRP 浓度逐渐增加。实验后期(20—33 d)细菌数量大幅度减少, 且伴随SRP 和溶解态有机磷浓度的显著升高。因此, 在缺磷且富含颗粒态有机质的条件下, OPB 将产生胞外碱性磷酸酶, 分解有机磷, 进而满足其大量生长的需要, 同时有效改变溶解态磷的形态与生物可利用性。       

Molecular Response of the Bloom-Forming Cyanobacterium, Microcystis aeruginosa, to Phosphorus Limitation

Cyanobacteria blooms caused by species such as Microcystis have become commonplace in many freshwater ecosystems. Although phosphorus (P) typically limits the growth of freshwater phytoplankton populations, little is known regarding the molecular response of Microcystis to variation in P concentrations and sources. For this study, we examined genes involved in P acquisition in Microcystis including two high-affinity phosphate-binding proteins (pstS and sphX) and a putative alkaline phosphatase (phoX). Sequence analyses among ten clones of Microcystis aeruginosa and one clone of Microcystis wesenbergii indicates that these genes are present and conserved within the species, but perhaps not the genus, as phoX was not identified in M. wesenbergii. Experiments with clones of M. aeruginosa indicated that expression of these three genes was strongly upregulated (50- to 400-fold) under low inorganic P conditions and that the expression of phoX was correlated with alkaline phosphatase activity (p < 0.005). In contrast, cultures grown exclusively on high levels of organic phosphorus sources (adenosine 5′-monophosphate, β-glycerol phosphate, and d-glucose-6-phosphate) or under nitrogen-limited conditions displayed neither high levels of gene expression nor alkaline phosphatase activity. Since Microcystis dominates phytoplankton assemblages in summer when levels of inorganic P (P_i) are often low and/or dominate lakes with low P_i and high organic P, our findings suggest this cyanobacterium may rely on pstS, sphX, and phoX to efficiently transport P_i and exploit organic sources of P to form blooms.     

Distribution of alkaline phosphatase genes in cyanobacteria and the role of alkaline phosphatase on the acquisition of phosphorus from dissolved organic phosphorus for cyanobacterial growth

Phosphorus is a vital nutrient for cyanobacterial growth. Aside from dissolved inorganic phosphorus, dissolved organic phosphorus (DOP) is used by cyanobacterial species via the activity of alkaline phosphatase (APase), which likely plays an important role in acquiring phosphorus for algal growth in the same manner as it does in other bacteria. In this work, APase genes phoA, phoD, and phoX were found distributed in the cyanobacterial strains included in the algal genome collection of the NCBI database. PhoX has a wider distribution than the classical phoA and phoD. Furthermore, multiple types of APase genes were simultaneously identified in a single strain or genome. Anabaena flos-aquae FACHB-245 was selected as a typical strain to study the performance of cyanobacteria growing on DOP. In algal growth involving AMP or lecithin, APase regulates the release of phosphorus from DOP as confirmed by the relative quantification of phoD and phoX expression levels. Our results confirmed that the distribution of APase is prevalent in cyanobacteria and thus provides a new insight into the potential role of cyanobacterial APase on phosphorus acquisition in natural environment.     

Intraspecific variability in response to phosphorus depleted conditions in the cyanobacteria Microcystis aeruginosa and Raphidiopsis raciborskii

Phosphorus loading plays an important role in the occurrence of cyanobacterial blooms and understanding how this nutrient affects the physiology of cyanobacteria is imperative to manage these phenomena. Microcystis aeruginosa and Raphidiopsis raciborskii are cyanobacterial species that form potentially toxic blooms in freshwater ecosystems worldwide. Blooms comprise numerous strains with high trait variability, which can contribute to the widespread distribution of these species. Here, we explored the intraspecific variability in response to phosphorus depleted conditions (P-) testing five strains of each species. Strains could be differentiated by cell volume or genetic profiles except for those of the same species, sampling location and date, though these presented differences in their response to (P-). Although differently affected by (P-) over 10 days, all strains were able to grow and maintain photosynthetic activity. For most M. aeruginosa and R. raciborskii strains growth rates were not significantly different comparing (P+) and (P-) conditions. After ten days in (P-), only one M. aeruginosa strain and two R. raciborskii strains showed reduction in biovolume yield as compared to (P+) but in most strains chlorophyll-a concentrations were lower in (P-) than in (P+). Reduced photosystem II efficiency was found for only one R. raciborskii strain while all M. aeruginosa strains were affected. Only two M. aeruginosa and one R. raciborskii strain increased alkaline phosphatase activity under (P-) as compared to (P+). Variation in P-uptake was also observed but comparison among strains yielded homogeneous groups comprised of representatives of both species. Comparing the response of each species as a whole, the (P-) condition affected growth rate, biovolume yield and chlorophyll yield. However, these parameters revealed variation among strains of the same species to the extent that differences between M. aeruginosa and R. raciborskii were not significant. Taken together, these results do not support the idea that R. raciborskii, as a species, can withstand phosphorus limitation better than M. aeruginosa and also point that the level of intraspecific variation may preclude generalizations based on studies that use only one or few strains.     

Diel changes in the alkaline phosphatase activity of bacteria and phytoplankton in the hypereutrophic Villerest reservoir (Roanne,France)

The diel changes of the size fractioned alkaline phosphatase activity (APA) were studied in relation to several abiotic and biotic factors in Villerest reservoir (located on the Loire river, near the city of Roanne, France), bihourly during two days in July 1992. The APA measured in this work exceeded considerably those reported in the literature, suggesting that dissolved mineral phosphorus was not available to microorganisms. At 1 m, the APA was primarily due to bacteria which actively assimilated organic P compounds released by photosynthetic algal metabolism. At 5, 10 and 20 m, the APA was predominantly algal. The high concentrations in SRP (soluble reactive phosphorus) would indicate that orthophosphates were not bioavailable. The reverse (i. e availability to phytoplankton) would have resulted in undetectable levels of P-PO _inf4 ^sup3– due to the massive proliferation of algae in Villerest reservoir.     

Ecological significance of phosphomonoesters and phosphomonoesterase activity in a small Mediterranean river and its estuary

In 1998, the concentration of phosphomonoesters, a biologically available fraction of the dissolved organic phosphorus pool, was measured along Palmones River (a small Mediterranean river in Southern Spain) and its estuary. Due to the extremely low phosphomonoester concentration in the river (usually under detection limits by analytical procedures), a method using chromatographic cartridges to concentrate this compound was used. Phosphomonoester concentration was usually in the nanomolar range, although values up to 6 m were measured in a sampling station near an effluent of domestic sewage and a cellulose pulp plant. Concentrations were always lower than the dissolved reactive phosphorus (mostly orthophosphate). Phosphomonoesters represented a variable percentage of the dissolved organic phosphorus, from negligible percentages up to 56%. Besides, a highly significant correlation between these two phosphorus fractions was found.In addition, phosphomonoesterase (alkaline phosphatase) activity was measured in the water and macrophytobenthos (both algae and aquatic phanerogams) along the river and the estuary. In water, most of the phosphatase activity upstream was regarded as soluble. This was confirmed by the difficulty of performing kinetic studies in the unfiltered samples. On the contrary, the phosphomonoesterase activity in the estuary was attributed to different size fractions, suggesting that phosphomonoesters are used actively as a phosphate source by bacteria and phytoplankton, with relative contributions depending on the sampling period.     

Alkaline phosphatase activity in Protogonyaulax tamarensis

A non-toxic strain of the marine dinoflagellate Protogonyaulaxtamarensis (= Gonyaulax tamarensis has been isolated from abloom in the Adriatic Sea, off the Emilia-Romagna coast. Culturesof the cells were grown in the laboratory in enriched seawaterat various initial ambient orthophosphate (P_i concentrations,ranging from 0.3 to 40.5 µM. The growth rate varied from0.3 to 0.8 divisions day^–1 depending on the P_i concentration.Alkaline phosphatase activity was inversely proportional toambient P levels. From measurements of kinetic parameters, thebinding of the artificial substrate p-nitrophenylphosphate tothe P.tamarensis alkaline phosphatase was quite strong (K_m=50µM). Maximal activity was observed at pH 8.4, althoughthe pH-activity curve was broad, in contrast to that of otheralkaline phosphatases. Protogonyaulax tamarensis alkaline phosphatase,measured over a 24h period, exhibited an apparent diurnal fluctuationin activity, in common with the enzyme from other dinoflagellates.     

Analysis of the effect of plant growth regulators and organic elicitors on antibacterial activity of <Emphasis Type="Italic">Eucomis autumnalis</Emphasis> and <Emphasis Type="Italic">Drimia robusta</Emphasis> ex vitro-grown biomass

The effects of plant growth regulators (PGRs) and organic elicitors (OEs) on in vitro propagation of Eucomis autumnalis was established. Three-year-old ex vitro grown plants from organogenesis of E. autumnalis and somatic embryogenesis (previously reported protocol) of Drimia robusta were investigated for antibacterial activity. In vitro propagation from leaf explants of E. autumnalis was established using different PGRs and OE treatments for mass propagation, biomass production and bioactivity analysis to supplement the use of wild plant material. Prolific shoots (16.0?±?0.94 shoots per explant) were obtained with MS (Murashige and Skoog in Physiol Plant 15:473–497, 1962) medium containing 100 mg l^?1 haemoglobin (HB), 10 µM benzyladenine (BA) and 2 µM naphthaleneacetic acid (NAA). The shoots were rooted effectively with a combination of 2.5 µM indole-3-acetic acid and 5.0 µM indole-3-butyric acid. The plantlets were successfully acclimatized in a vermiculite-soil mixture (1:1 v/v) in the greenhouse. Three-year-old ex vitro-grown E. autumnalis and D. robusta plants derived via organogenesis and somatic embryogenesis respectively exhibited antibacterial activity and varied with PGR and OE treatments, plant parts and bacteria. The leaves of E. autumnalis ex vitro-derived from a combination of HB, BA and NAA followed by the individual treatments of BA and HB gave the best antibacterial activities (<?1 mg ml^?1: minimum inhibitory concentration from 0.098 to 0.78 mg ml^?1) against all tested pathogenic bacteria (Bacillus subtilis, Enterococcus faecalis, Micrococcus luteus, Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa). The bulbs of D. robusta ex vitro-derived from solid culture with 10 µM picloram, 1 µM thidiazuron and 20 µM glutamine exhibited good antibacterial activity against E. faecalis, M. luteus and S. aureus when compared with other treatments and mother plants. The ex vitro-grown E. autumnalis and D. robusta biomass produced with PGRs along with OE treatments confirmed a good potent bioresource and can be used as antibacterial agents. The in vitro plant regeneration of E. autumnalis and D. robusta protocols and ex vitro plants could be used for conservation strategies, bioactivity and traditional medicinal use.     

Plant growth regulator induced phytochemical and antioxidant variations in micropropagated and acclimatized Eucomis autumnalis subspecies autumnalis (Asparagaceae)

Eucomis species is a valuable plant with both medicinal and horticultural potential. The current study evaluated the role of plant growth regulator (PGR) on growth, phytochemicals, and antioxidant activity in Eucomis autumnalis subspecies autumnalis. Five cytokinins including topolins and benzyladenine (BA) at 2 µM in combination with varying (0–15 µM) concentrations of naphthalene acetic acid (NAA) were tested. In vitro regenerants were acclimatized in the greenhouse for 4 months. Highest number of shoots (9 shoots/explant) was observed with 15 µM NAA alone or when combined with BA. Acclimatized plants derived from the 15 µM NAA treatment had the highest number of roots, largest leaf area and biggest bulbs. While applied PGRs increased the iridoids and condensed tannins in the in vitro regenerants, total phenolics and flavonoids were higher in the PGR-free treatment. Among the in vitro regenerants, 5 µM NAA and 2 µM BA treatments produced the best antioxidant activity in the DPPH (55 %) and beta-carotene (88 %) test systems, respectively. A remarkable carry-over effect of the PGR was conspicuous in the phytochemical levels and antioxidant activity of the 4-month-old plants. In addition to the optimized micropropagation protocols, the current findings present a promising potential for manipulating the type and concentration of applied PGRs to improve phytochemical production and hence medicinal value in E. autumnalis subspecies autumnalis.     

Characterization of ectoenzyme activity and phosphate-regulated proteins in the coccolithophorid Emiliania huxleyi

Three phosphate-regulated proteins in the coccolithophorid Emilianiahuxleyi were detected by the biotinylation of cell-surface proteins.Two of these phosphate-regulated proteins have reduced denaturedmolecular weights near 110 000 Da (118 078 and 110 541, respectively),while the third, and most abundant, is 69 087 Da. Inductionof the three proteins and the common marker of phosphate stress,alkaline phosphatase activity, occur in the presence of <0.25µM inorganic phosphate in batch culture. Phosphate-regulatedproteins and enzyme activity differed among E. huxleyi strains.Alkaline phosphatase is an enzyme commonly induced by phytoplanktonin response to phosphate stress in order for cells to scavengeinorganic phosphate from organic sources. In E. huxleyi, thisenzyme activity and the phosphate-regulated proteins are rapidlylost when phosphate is added back to phosphate-stressed cultures.This contrasts with the slower loss of alkaline phosphataseactivity in the dinoflagellate Prorocentrum minimum. The presenceof the three phosphate-regulated proteins and enzyme activityappear to differ somewhat among E. huxleyi strains. Based onthese differences between strains, kinetic data, growth experimentsand enzyme activities, the 69 087 Da protein may be a phosphatasewith a high specificity for 5'-nucleotides.     

Salmon‐derived nutrient and organic matter fluxes from a coastal catchment in southeast Alaska

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Phosphatases; origin,characteristics and function in lakes

Phosphatases catalyze the liberation of orthophosphate from organic phosphorus compounds. The total phosphatase activity in lake water results from a mixture of phosphatases localized on the cell surfaces of algae and bacteria and from dissolved enzymes supplied by autolysis or excretion from algae, bacteria and zooplankton. External lake water phosphatases usually have pH optima in the alkaline region. Acid phosphatases generally seem to be active in the internal cell metabolism. The synthesis of external alkaline phosphatases is often repressed at high phosphate concentrations and derepressed at low phosphate concentrations. Phosphatase activity has therefore been used as a phosphorus deficiency indicator in algae and in natural plankton populations. The possibilities for this interpretation of phosphatase activity in lake water are limited, however, and this is discussed. The in situ hydrolysis capacity, i.e. the rate by which orthophosphate is released from natural substrates, is unknown. However, we advocate that this process is important and that the rate of substrate supply, rather than phosphatase activity, limits the enzymatic phosphate regeneration.     

The calcified puparium of the face fly, Musca autumnalis (Diptera: Muscidae)

The general composition of the calcified puparium of Musca autumnalis was determined. Ash-weight analyses show that 62% of the puparium is inorganic material. The major components of the puparium are calcium, magnesium, phosphate and carbonate. Calcium and magnesium phosphate are the predominant salts in the puparium, with a lesser contribution by their respective carbonates. Scanning electron microscopy revealed that the exocuticle was the site of calcification in the puparium. Inorganic analyses of the insoluble salt isolated from face fly larvae showed it to be compositionally identical with the puparial salt. Major organic components of the puparium are lipid, chitin and protein. The presence of carbonic anhydrase and alkaline phosphatase activity in post-feeding larvae was confirmed.     

Phosphorus Scavenging in the Unicellular Marine Diazotroph Crocosphaera watsonii

Through the fixation of atmospheric nitrogen and photosynthesis, marine diazotrophs play a critical role inthe global cycling of nitrogen and carbon. Crocosphaera watsonii is a recently described unicellular diazotroph that may significantly contribute to marine nitrogen fixation in tropical environments. One of the many factors that can constrain the growth and nitrogen fixation rates of marine diazotrophs is phosphorus bioavailability. Using genomic and physiological approaches, we examined phosphorus scavenging mechanisms in strains of C. watsonii from both the Atlantic and the Pacific. Observations from the C. watsonii WH8501 genome suggest that this organism has the capacity for high-affinity phosphate transport (e.g., homologs of pstSCAB) in low-phosphate, oligotrophic systems. The pstS gene (high-affinity phosphate binding) is present in strains isolated from both the Atlantic and the Pacific, and its expression was regulated by the exogenous phosphate supply in strain WH8501. Genomic observation also indicated a broad capacity for phosphomonoester hydrolysis (e.g., a putative alkaline phosphatase). In contrast, no clear homologs of genes for phosphonate transport and hydrolysis could be identified. Consistent with these genomic observations, C. watsonii WH8501 is able to grow on phosphomonoesters as a sole source of added phosphorus but not on the phosphonates tested to date. Taken together these data suggest that C. watsonii has a robust capacity for scavenging phosphorus in oligotrophic systems, although this capacity differs from that of other marine cyanobacterial genera, such as Synechococcus, Prochlorococcus, and Trichodesmium.     

Nutrient Utilization Strategies of Algae and Bacteria after the Termination of Nutrient Amendment with Different Phosphorus Dosage: A Mesocosm Case

The impacts of nutrient amendment termination on the growth strategies of algae and bacteria were conducted in experimentally designed mesocosm in which two different phosphorus (P) dosages were treated. The algal community composition did not change greatly in Group A (low phosphorus) and Group B (high phosphorus). In Group A, the secretion of bacterial alkaline phosphatase (AP) after nutrient termination stimulated bacterial phosphorus acquisition, which caused the decrease in algal phosphorus levels, in terms of the increase of bacterial abundance and bacterial production, as well as the decrease in chlorophyll a and particulate organic carbon. The algal collapse resulted in dissolved organic carbon secretion, further fuelling bacterial growth. In Group B, excess phosphorus input urged algae to store phosphorus as poly-phosphate. When phosphorus input ceased, in order to maintain their used high phosphorus demand, algae strengthened to gain phosphorus through the hydrolysis of dissolved organic phosphorus in water column and ploy-phosphate inside the cells by AP, evidenced by high algal alkaline phosphatase activity, algal growth continuation, and bacterial growth decline. These facts indicated that phosphorus content should reduce to a lower level than expected, so that algal bloom can be effectively controlled in eutrophic water bodies.     

Mixed plantations of Metasequoia glyptostroboides and Bischofia polycarpa change soil fungal and archaeal communities and enhance soil phosphorus availability in Shanghai,China

Soil degradation has been found in urban forests in Shanghai, especially in the pure plantations. Mixed plantations are considered to improve soil quality because they can stimulate organic matter cycling and increase soil carbon and nutrient content. Although soil microbes play crucial roles in regulating soil biogeochemical processes, little is known about how mixed plantations affect soil microbial communities, including bacteria, archaea, and fungi. Here, we evaluated soil chemical properties, abundances and compositions of soil bacterial, archaeal, and fungal communities, and enzyme activities in pure and mixed Metasequoia glyptostroboides and Bischofia polycarpa plantations, located in Shanghai, China. The results showed that soil available phosphorus content in the mixed plantation of M. glyptostroboides and B. polycarpa was significantly higher than that in pure plantations, while no significant difference was observed in the content of soil organic carbon, total and available nitrogen, total and available potassium among the three studied plantations. We found higher fungal abundance in the mixed plantation, when compared to both pure plantations. Moreover, fungal abundance was positively correlated with the content of soil available phosphorus. No significant difference was found in the abundance and diversity of bacterial and archaeal community among the three studied plantations. A similarity analysis (ANOSIM) showed that mixed plantation significantly altered the community composition of archaea and fungi, accompanied with an increase of alkaline phosphatase activity. However, ANOSIM analysis of bacterial communities showed that there was no significant group separation among different plantations. Overall, results from this study indicated that fungal and archaeal communities were more sensitive to aboveground tree species than bacterial community. Moreover, mixed plantations significantly increased the activity of alkaline phosphatase and the content of soil available phosphorus, suggesting that afforestation with M. glyptostroboides and B. polycarpa is an effective way to alleviate phosphorus deficiency in urban forests in Shanghai, China.     

不同稻蟹生产模式对土壤活性有机碳和酶活性的影响

采取田间定位试验与室内分析相结合的方法,研究了有机稻蟹、常规稻蟹与单作水稻生产模式对土壤活性有机碳和酶活性的影响。结果表明,与单作水稻模式相比,有机稻蟹模式下的土壤总有机碳(TOC)、活性有机碳(LOC)、中活性有机碳(MLOC)、高活性有机碳(HLOC)含量及碳库管理指数(CMI)均显著或者极显著提高,且有机肥用量越大,效果越显著;有机稻蟹模式显著提高了土壤过氧化氢酶、脲酶、转化酶及碱性磷酸酶活性,与2009年相比,2010年中量有机肥稻蟹模式(M3)的LOC和MLOC含量增幅最高,分别达10.11%和5.14%;低量有机肥稻蟹模式(M4)的脲酶和碱性磷酸酶活性增幅最为明显,分别达80.25%和46.62%;常规稻蟹模式各指标的变化也有其类似的规律,但均明显低于有机稻蟹模式。相关分析表明,TOC、LOC、MLOC与4种土壤酶活性呈显著或者极显著正相关,相关系数最低为0.584*(P<0.05),最高可达0.940**(P<0.01)。因此,有机稻蟹生产模式不仅能显著提高土壤有机质的数量和质量,而且能增加土壤酶活性,提高土壤肥力。     

5′-Nucleotidase Activity in a Eutrophic Lake and an Oligotrophic Lake

Differences in enzymatic hydrolysis of dissolved organic phosphorus and subsequent phosphorus uptake were compared by using dual-labeled (γ-³²P and 2-³H) ATP in oligotrophic Lake Michigan and a moderately eutrophic lake in southeastern Michigan. More than 50% of the phosphate that was hydrolyzed was immediately taken up into bacterium-sized particles in the eutrophic lake and at a near-shore site in Lake Michigan. Less than 50% of the hydrolyzed phosphate was taken up into bacterium-sized particles at an offshore site in Lake Michigan. It is hypothesized that differences in size-fractionated uptake were the result of greater phosphorus utilization capacity in bacteria in habitats where loading of organic carbon is greater. Substantial isotope dilution of labeled phosphate uptake by unlabeled phosphate occurred, which implied that the phosphate was hydrolyzed extracellularly in both systems. Comparable nucleotidase activities were measured in the eutrophic lake and Lake Michigan, but the significance of the phosphate regenerated relative to particulate phosphorus pools was an order of magnitude greater in Lake Michigan. Seventy percent of the nucleotidase activity was inhibited by 100 μM phosphate in the eutrophic lake, which suggests that most hydrolysis was by phosphatase. Therefore, nucleotidase activity may be more important to phosphorus regeneration in oligotrophic habitats than phosphatase activity.