ABSTRACT
Toxic cyanobacterial blooms have been implicated for their negative consequences on many terrestrial and aquatic organisms. Water birds belong to the most common members of the freshwater food chains and are most likely to be affected by the consumption of toxic cyanobacteria as food. However, the contribution of cyanotoxins in bird mortalities is under-studied. The aim of the study was to investigate the likely role of cyanotoxins in a mass mortality event of the Dalmatian pelican (Pelecanus crispus) in the Karla Reservoir, in Greece. Water, scum, tissues and stomach content of dead birds were examined for the presence of microcystins, cylindrospermopsins and saxitoxins by an enzyme-linked immunosorbent assay. High abundances of potential toxic cyanobacterial species and significant concentrations of cyanotoxins were recorded in the reservoir water. All examined tissues and stomach content of the Dalmatian pelicans contained significant concentrations of microcystins and saxitoxins. Cylindrospermopsin concentrations were detected in all tissues except from the brain. Our results suggest that cyanotoxins are a plausible cause for this bird mass mortality episode in the Karla Reservoir.
Subject(s)
Bacterial Toxins/toxicity , Bird Diseases/etiology , Cyanobacteria/metabolism , Alkaloids , Animals , Bacterial Toxins/metabolism , Bird Diseases/mortality , Birds , Cyanobacteria/chemistry , Cyanobacteria Toxins , Fresh Water/microbiology , Greece , Microcystins/metabolism , Microcystins/toxicity , Saxitoxin/toxicity , Uracil/analogs & derivatives , Uracil/metabolism , Uracil/toxicityABSTRACT
A biofilm material model and a procedure for numerical integration are developed in this article. They enable calculation of a composite Young's modulus that varies in the biofilm and evolves with deformation. The biofilm-material model makes it possible to introduce a modeling example, produced by the Unified Multi-Component Cellular Automaton model, into the general-purpose finite-element code ABAQUS. Compressive, tensile, and shear loads are imposed, and the way the biofilm mechanical properties evolve is assessed. Results show that the local values of Young's modulus increase under compressive loading, since compression results in the voids "closing," thus making the material stiffer. For the opposite reason, biofilm stiffness decreases when tensile loads are imposed. Furthermore, the biofilm is more compliant in shear than in compression or tension due to the how the elastic shear modulus relates to Young's modulus.
Subject(s)
Biofilms , Models, Biological , Biocompatible Materials , Biomechanical Phenomena , Elastic Modulus , Finite Element Analysis , Mathematical Concepts , Software , Tensile StrengthABSTRACT
Biofilm mechanical properties are essential in quantifying the rate of microbial detachment, a key process in determining the function and structure of biofilm systems. Although properties such as biofilm elastic moduli, yield stress and cohesive strength have been studied before, a wide range of values for the biofilm Young's modulus that differ by several orders of magnitude are reported in the literature. In this article, we use experimental data reported in Stoodley et al. [Stoodley et al., Biotechnol Bioeng (1999): 65(1):83-92] and present a methodology for the calculation of Young's modulus, which partially explains the large difference between the values reported in the literature.
Subject(s)
Bacterial Physiological Phenomena , Biofilms/growth & development , Models, Biological , Computer Simulation , Elasticity , Stress, MechanicalABSTRACT
Biofilm properties change drastically from one point to another inside the matrix, and from one minute to the next, bringing about similar variations in biofilm mechanical properties, both in time and space. In this article, we present a theory that quantifies deformation-dependent changes in the mechanical properties of a composite porous material that undergoes compression. Such changes are a result of the pores either closing (when the biofilm is under compression) or opening (when under tension). The theory borrows well-established principles of continuum mechanics and is modified to represent a biofilm composed of four different phases, three different solid biomass materials (active biomass, extracellular polymers and inert biomass) and pores. We see that, when the evolution of the volume fractions of the different phases in a uniaxial compression test is taken into account, the material "hardens" or becomes stiffer as the deformation increases, due to void closure. Once complete void closure is achieved, the material reaches its maximum stiffness. Different homogenisation schemes are presented and comparisons are performed with stress-strain calculations for all of them.