Light-scattering methods for modelling algal particles as a collection of coated and/or nonspherical scatterers

Ocean reflectance or ocean colour measurements are an important tool for oceanographic studies of phytoplankton dynamics. Theoretical models based on homogeneous, spherical particles underestimate algal backscattering and thus reflectance values. It is our understanding that more advanced light-scattering methods must be employed, both for refractive index retrieval (Mie, Aden–Kerker) with inverse models, and for backscattering calculations (Extended Boundary Condition Method, EBCM). The measured optical properties of a monospecific bloom of the marine brown tide pelagophyte Aureococcus anophagefferens are used to compare the effects of assuming various simulated particle geometries. Computational results from polydisperse, coated spherical particles show results that compare better to experimental reflectance values than calculations based on homogeneous spheres. No noticeable change in simulated reflectance values is observed when a randomly oriented coated spheroidal (rather than spherical) geometry is assumed for the particle population. Our results suggest that a layered spherical geometry, based on Aden–Kerker theory, can adequately reproduce experimentally determined light-scattering properties even supposedly shape-sensitive properties such as the backscattering coefficient.     

A chemostat model of resource competition and allelopathy

Presented is a chemostat model in which one microbial population excretes a poison that increases the mortality of another, with toxin production increasing as the growth rate of the toxic species decreases. The model is intended to explore the role of allelopathy in blooms of harmful algae, such as red tide (Karenia brevis) and golden algae (Prymnesium parvum). This study introduces the model and its biological basis, and proceeds to the analysis of its asymptotic states. All theoretical results are supported by a set of numerical simulations. A discussion of biological conclusions and similarities to other mathematical models is also presented.     

高效色谱-电感耦合等离子体质谱法分析海藻类海产品中砷的形态

采用阴(Hamilton PRP-X100柱)阳(Dionex Ionpac CS-10柱)离子交换色谱-电感耦合等离子体质谱联用技术,分别以pH 10.3的20 mmol/L NH4HCO3和pH 2.0的5 mmol/L吡啶溶液为流动相,建立了As(Ⅲ)、As(Ⅴ)、一甲基砷酸(MMA)、二甲基砷酸(DMA)、砷甜菜碱AsB、砷糖PO4、砷糖OH、砷糖SO3、砷糖SO4砷形态的分析方法。采用微波消解法和超声溶剂提取法对不同海域10种紫菜和海带产品进行前处理,对As含量及其化学形态进行分析。实验表明,样品总砷的质量分数为1.7～38.7 mg/kg,样品萃取物中,As糖PO4和As糖OH为As的主要形态,其含量分别占可提取As的6.5%～67.7%和12.9%～86.2%,海带样品萃取物中还有As糖SO3和DMA被检测,其含量分别占可提取As的13.0%～52.1%和5.9%～17.4%。在紫菜和海带海藻类产品中,含As的化合物主要是毒性较低的有机砷。     

Structures and absolute stereochemistry of nipponallene and neonipponallene, new brominated allenes from the red alga Laurencia nipponica

Two new natural brominated allenes named as nipponallene 1 and neonipponallene 2 were isolated from the red alga Laurencia nipponica, collected near the Russian shore of the Sea of Japan (Troitsa Bay). The structures and absolute stereochemistry of 1 and 2 were elucidated using NMR spectroscopy, chemical transformations, modified Mosher’s method and on the basis of biogenetic understanding.     

Biologically Active Metabolites from Marine Organisms

The authors' chemical studies on the secondary metabolites from marine organisms are summarized. From marine sponges, algae and soft corals grown in the South China Sea, thirty five compounds were isolated. Their structures were elucidated mainly on the basis of spectral evidence. The biological activities of dysamides, 1–6 , stelletin 21 and lactone 23 are reported.     

Algal biotechnology

The review gives a general outline of macro and microalgal biotechnology. The main methods by which algae are cultivated and harvested are described. The first section deals with the environmental factors affecting mass culture and the principles governing the design and operation of mass cultivation systems. The second section gives the main current and potential uses of algae: in wastewater treatment, a source of food and feed, an energy source, and in the production of common and fine chemicals, such as polysaccharides, lipids, glycerol, pigments, and enzymes. Pharmaceutical uses of algae are described, and their potential as a source of novel biologically-active compounds is discussed. Future developments and the great potential of algae are considered.     

Modeling equilibrium and kinetics of metal uptake by algal biomass in continuous stirred and packed bed adsorbers

Physical and chemical characterization of algae Gelidium particles shows a gel structure, with two major binding groups, carboxylic and hydroxyl groups, with an affinity constant distribution for protons, well described by a Quasi-Gaussian distribution suggested by Sips. A continuous model, considering a heterogeneous distribution of the carboxylic groups, determined by potentiometric titration experiments, was able to predict equilibrium data at different pH. The metal uptake capacity decreases with the solution pH, suggesting that competition exists between hydrogen ions, present in high concentrations for low pH values, and metal ions. For high ionic strengths, adsorption sites will be surrounded by counter ions and partially lose their charge, which weakens the contribution of the electrostatic binding and decreases the overall adsorption. A small influence of the temperature in the adsorption process was observed. Batch kinetic experiments were also performed, at different pH values, and results were well fitted by a mass transfer model, considering the intraparticle diffusion resistance given by the linear driving force model (LDF). Continuous stirred adsorber (CSTA) and packed bed column configurations were also tested for metal adsorption. The biosorbent regeneration was achieved by contacting it with strong acid (0.1 M HNO₃). A mass transfer model was applied with success to describe the biosorption/desorption process in CSTA and packed bed column, considering the equilibrium given by the Langmuir equation/mass action law and film and intraparticle diffusion resistances.     

Isolation and characterization of a photosystem I-associated antenna (LHC I) and a photosystem I—core complex from the chlorophyll c-containing alga Pleurochloris meiringensis (Xanthophyceae)

A photosystem (PS) I holocomplex was isolated from Pleurochloris meiringensis Vischer (Xanthophyceae) using sucrose density centrifugation. This complex exhibited a fluorescence emission maximum at 715 nm, which is in accordance with the long wavelength emission of whole cells. The complex was further dissociated into a core complex and a light-harvesting protein (LHC I). The core protein contains mainly Chl a and β-carotene, is 8.25 times enriched in P700 and has its main emission maximum at 715 nm. Therefore, the longest wavelength emission of P. meiringensis is due to the PS I core, which is in contrast to higher plants. The LHC I differs from LHC II with regard to its polypeptide pattern as well as its spectral properties. The arrangement of antennae is discussed in relation to the regulation of energy transfer between the photosystems.     

基于定量遥感反演的内陆水体藻类监测

叶绿素作为衡量湖泊富营养化的重要指标,利用遥感技术对其进行实时动态监测具有重要意义。以太湖为例,通过对水体实测光谱和水质采样数据的分析,建立了光谱反射率比值与叶绿素a浓度的回归模型。结果显示,700 nm附近波段与625 nm附近波段所构建的比值模型R2最高,710 nm以后波段与其他可见光波段所构建的比值模型的R2会随可见光波长的增大而逐渐下降。在高光谱遥感估算模型的基础上,应用同步MODIS卫星遥感数据进行了太湖叶绿素a浓度的空间分布反演,并基于MODIS绿度指数建立了太湖藻华水体信息提取模型,从叶绿素a浓度估算和藻华信息提取两个方面实现了太湖藻类空间分布特征的定量反演,为太湖等大型内陆水体藻类的实时定量遥感监测提供了新的研究思路。     

Identification of dimethylarsinoyl-riboside derivatives in seaweed by pneumatically assisted electrospray tandem mass spectrometry

Pneumatically-assisted electrospray tandem mass spectrometry (ES MS/MS) was proposed as a technique for the identification of dimethylarsinoyl-riboside derivatives (arsenosugars) in seaweed (Laminaria). Conditions for the acquisition of MS and MS/MS spectra were optimized. A size-exclusion HPLC (SE HPLC) step was developed for the purification of algal extracts prior to ES MS. The arsenosugar fraction was found to elute prior to the majority of other arsenic compounds. The identity of the compounds expected to be arsenosugar compounds was confirmed by the collision induced dissociation (CID) of the relevant protonated molecule ions. An independent confirmation of the identity of analytes was obtained by two-dimensional (size-exclusion–anion exchange) HPLC–ICP MS with signal identification by spiking with the appropriate arsenosugar standards.