Systematic Modeling Approach to Selective Plugging Using In Situ Bacterial Biopolymer Production and Its Potential for Microbial-enhanced Oil Recovery

This study presents a systematic modeling approach for examining the efficiency of the MEOR process based on in situ selective plugging by bacterial biopolymer production and optimization of the nutrient injection strategy to yield the maximum oil recovery. This study focuses on modeling in situ selective plugging by the bacterial biopolymer dextran that is generated by Leuconostoc mesenteroides. Bacterial growth and dextran generation were described by a stoichiometric equation and kinetic reactions using batch model simulation. Based on the parameters for permeability reduction obtained from the sandpack model, the MEOR process was implemented in a pilot-scale system that included a highly permeable thief zone in a low-permeability reservoir. The base MEOR design yielded a 61.5% improvement of the recovery factor compared to that obtained with waterflooding. The parametric simulations revealed that the recovery efficiency was influenced by the amount of dextran, as well as the distribution of dextran, and thus, the injection strategy is critical for controlling the dextran distribution. By incorporating the results from the sensitivity analysis and optimization to determine the optimal design parameters, a 36.7% improvement of the oil recovery was achieved with the optimized MEOR process in comparison with the base case.     

The eunuch phenomenon: adaptive evolution of genital emasculation in sexually dimorphic spiders

Under natural and sexual selection traits often evolve that secure paternity or maternity through self‐sacrifice to predators, rivals, offspring, or partners. Emasculation—males removing their genitals—is an unusual example of such behaviours. Known only in insects and spiders, the phenomenon's adaptiveness is difficult to explain, yet its repeated origins and association with sexual size dimorphism (SSD) and sexual cannibalism suggest an adaptive significance. In spiders, emasculation of paired male sperm‐transferring organs — secondary genitals — (hereafter, palps), results in ‘eunuchs’. This behaviour has been hypothesized to be adaptive because (i) males plug female genitals with their severed palps (plugging hypothesis), (ii) males remove their palps to become better fighters in male–male contests (better‐fighter hypothesis), perhaps reaching higher agility due to reduced total body mass (gloves‐off hypothesis), and (iii) males achieve prolonged sperm transfer through severed genitals (remote‐copulation hypothesis). Prior research has provided evidence in support of these hypotheses in some orb‐weaving spiders but these explanations are far from general. Seeking broad macroevolutionary patterns of spider emasculation, we review the known occurrences, weigh the evidence in support of the hypotheses in each known case, and redefine more precisely the particular cases of emasculation depending on its timing in relation to maturation and mating: ‘pre‐maturation’, ‘mating’, and ‘post‐mating’. We use a genus‐level spider phylogeny to explore emasculation evolution and to investigate potential evolutionary linkage between emasculation, SSD, lesser genital damage (embolic breakage), and sexual cannibalism (females consuming their mates). We find a complex pattern of spider emasculation evolution, all cases confined to Araneoidea: emasculation evolved at least five and up to 11 times, was lost at least four times, and became further modified at least once. We also find emasculation, as well as lesser genital damage and sexual cannibalism, to be significantly associated with SSD. These behavioural and morphological traits thus likely co‐evolve in spiders. Emasculation can be seen as an extreme form of genital mutilation, or even a terminal investment strategy linked to the evolution of monogyny. However, as different emasculation cases in araneoid spiders are neither homologous nor biologically identical, and may or may not serve as paternity protection, the direct link to monogyny is not clear cut. Understanding better the phylogenetic patterns of emasculation and its constituent morphologies and behaviours, a clearer picture of the intricate interplay of natural and sexual selection may arise. With the here improved evolutionary resolution of spider eunuch behaviour, we can more specifically tie the evidence from adaptive hypotheses to independent cases, and propose promising avenues for further research of spider eunuchs, and of the evolution of monogyny.     

植食性昆虫对植物的反防御机制

本文综述了植食性昆虫对植物的反防御机制.一方面,植食性昆虫可通过其快速进化的寄主选择适应性,改变取食策略,调节生长发育的节律,以及规避自然天敌等抑制、逃避或改变植物的防御,即行为防御机制;另一方面,植食性昆虫可适应植物蛋白酶抑制剂、逃避植物防御伤信号、解毒植物次生物质,以及抑制植物阻塞反应来对植物防御进行反防御,即生理和生化防御机制.其中,昆虫抑制植物伤信号,防止植物阻塞反应是反防御机制的研究热点.昆虫反防御的研究有助于提高对昆虫-植物间协同进化关系的认识,并为害虫治理和抗虫植物的培育提供新的思路.     

Effects of oil reservoir conditions on the production of water‐insoluble Levan by Bacillus licheniformis

Bacillus licheniformis produced a water‐insoluble levan which has potential application as a selective plugging agent in microbial enhanced oil recovery (MEOR). The microorganism grew on sucrose, glucose, and fructose but produced levan only on sucrose. Plugging may thus be selectively controlled in the reservoir by substrate manipulation. B. licheniformis and a crude preparation of its extracellular enzymes were evaluated for their ability to produce levan under reservoir conditions. Oil reservoirs which have a temperature of less than 55°C, a pH between 6 and 9, a pressure less than 500 atm, and a salt concentration of 4% or less are potentially suitable. Examples of such reservoir conditions are found in Lloydminster on the Alberta‐Saskatchewan border, one of the largest Canadian oil reserves.     

Estimating and improving cold filter plugging points by blending biodiesels with different fatty acid contents

Biodiesels are alkyl esters produced by transesterification of higher fatty acids (aliphatic chains composed of 14 to 22 carbon units) from animal fats and/or vegetable oils. The cold filter plugging points (CFPP) of biodiesels are not only higher than that of petro-diesel, but they also differ from the melting point of the raw (unesterified) materials. In this study, we empirically derived equations that estimated the CFPP of a biodiesel based on its fatty acid content, using various biodiesel blends containing four methyl esters with different fatty acid compositions: soybean (SME), palm (PME), rapeseed (RME), and lard (LME). These blending ratio experiments yielded three equations that described the correlation between CFPP and fatty acid content: Y (CFPP, °C) = −3.1X (blending ratio) − 12.7 (PME/SME); Y = 2.2X − 10.7 (LME/SME); and Y = −4.0X − 13.0 (PME/RME). We also obtained the correlation between CFPP and total saturated fatty acid methyl ester content in the biodiesels: Y (CFPP, °C) = 0.449X (total saturated fatty acid methyl ester content, wt%) − 9.198. These empirical equations accurately predicted CFPP values of biodiesel compounds with known fatty acid compositions, facilitating the use of diverse biodiesels in industrial fields. The first two authors equally contributed to this work.     

Influence of the screen material on the fouling of spin filters

Mouse-mouse hybridomas (15 mum mean diameter) were cultivated in a simulated perfusion reactor with spin filter and external recirculation of the medium. Proteins at high concentrations, such as 10% foetal calf serum (FCS), were found to be not responsible by themselves for fouling, even at high recirculation rates. Stainless steel (10 mum pores) in contrast to polyamide (11 mum proes) led to a great accumulation of dead cells and nucleic acids on the screen, finally leading to fouling, as shown by biochemical and microscopic examinations. It is suggested that the high surface charge density of metals compared to polyamide is responsible for attachment of various residues. Stainless steel should rather be replaced by a resistant and nontoxic synthetic material, such as polyamide 66 which was successfully used. FCS should be avoided, since it seems to increased the fouling phenomenon. Moreover, the pore size of the screen should be carefully defined according to the wide size distribution of living and dead cells of the line used (33% of variation of the mean size in our case) as well as fragments. The purpose of the screen being to get rid of fragments and small dead cells, and not to wash too many new small cells, a good retention was achieved here by a 10-mum opening.     

Effect of microbial growth on pore entrance size distribution in sandstone cores

Summary The in situ growth of microorganisms in Berea sandstone cores preferentially plugged the larger pore entrances. The largest pore entrance sizes after microbial plugging ranged from 20 to 38 m, compared with 59 to 69 m before plugging. The pore entrance size distribution of plugged cores was shifted to smaller sizes. A mathematical model based on Poiseuille's equation was found to adequately predict permeability reductions (greater than 90%) caused by microbial growth in the large pore entries.Nomenclature Q volumetric flow rate (L ₃/t) - C orifice constant (dimensionless) - A cross-sectional area (L ₂) - g gravity (L/t ²) - h pieziometric head (L) - _s transmittivity (L ²) - R _e Reynolds number (dimensionless) - a constant (dimensionless) - density (M/L ₃) - viscosity (M/Lt) - d diameter (L) - L length (L) - P pressure change (M/L ₂)     

Mate plugging via genital mutilation in nephilid spiders: an evolutionary hypothesis

Nephilid spiders are known for gigantic females and tiny males. Such extreme sexual dimorphism and male-biased sex ratios result in fierce male–male competition for mates. Intense sperm competition may be responsible for behaviors such as mate guarding, mate binding, opportunistic mating, genital mutilation, mating plugs and male castration (eunuchs). We studied the mating biology of two phylogenetically, behaviorally and morphologically distinct south-east Asian nephilid spider species ( Herennia multipuncta, Nephila pilipes ) in nature and in the laboratory. Specifically, we established the frequencies and effectiveness of plugging (a plug is part of the male copulatory organ), and tested for male and female copulatory organ reuse. Both in nature and in the laboratory, plug frequencies were higher in H. multipuncta (75–80% females plugged) compared with N. pilipes (45–47.4%), but the differences were not significant. Plugs were single and effective (no remating) in H. multipuncta but multiple and ineffective (remating possible) in N. pilipes . In Herennia , the males plugged when the female was aggressive and in Nephila plugging was more likely when mating with previously mated and larger females. Further differences in sexual biology are complete palpal removal and higher sexual aggressiveness in Herennia (sexual cannibalism recorded for the first time), and mate binding in Nephila . Thus, we propose the following evolutionary hypothesis: nephilid plugging was ancestrally successful and enabled males to monopolize females, but plugging became ineffective in the phylogenetically derived Nephila . If the evolution of nephilid sexual mechanisms is driven by sexual conflict, then the male mechanism to monopolize females prevailed in a part of the phylogeny, but the female resistance to evade monopolization ultimately won the arms race.