Volatile and Contact Chemical Cues Associated with Host and Mate Recognition Behavior of <Emphasis Type="Italic">Sphenophorus venatus</Emphasis> and <Emphasis Type="Italic">Sphenophorus parvulus</Emphasis> (Coleoptera: Dryophthoridae)

Beetles in the genus Sphenophorus Schönherr, or billbugs, potentially utilize both volatile and non-volatile behavior-modifying chemical signals. These insects are widely distributed across North America, often occurring in multi-species assemblages in grasses. However, details about their host- and mate-finding behavior are poorly understood. This study tested the hypothesis that volatile organic compounds from host-plants and conspecifics direct the dispersal behavior of hunting billbug S. venatus Say. Further, we characterized the cuticular hydrocarbon profiles of two widespread pest species, S. venatus and bluegrass billbug S. parvulus Gyllenhaal, to assess the potential role of contact pheromones in mate-recognition. In Y-tube olfactometer bioassays, S. venatus males were attracted to a combination of conspecifics and Cynodon dactylon host-plant material, as well as C. dactylon plant material alone. S. venatus females were attracted to a combination of male conspecifics and host-plants but were also attracted to male conspecifics alone. Field evaluation of a putative male-produced aggregation pheromone, 2-methyl-4-octanol, identified from two congeners, S. levis Vaurie and S. incurrens Gyllenhaal, did not support the hypothesis that S. venatus and S. parvulus were also attracted to this compound. Gas chromatography-mass spectrometry analysis of S. venatus and S. parvulus whole-body cuticular extracts indicated a series of hydrocarbons with qualitative and quantitative interspecific variation in addition to intraspecific quantitative variation between males and females. This study provides the first evidence that S. venatus orients toward host- and insect-derived volatile organic compounds and substantiates the presence of species-specific cuticular hydrocarbons that could serve as contact pheromones for sympatric Sphenophorus species.     

Quantifying Lipid Contents in Enveloped Virus Particles with Plasmonic Nanoparticles

Phosphatidylserine (PS) and monosialotetrahexosylganglioside (G_M1) are examples of two host‐derived lipids in the membrane of enveloped virus particles that are known to contribute to virus attachment, uptake, and ultimately dissemination. A quantitative characterization of their contribution to the functionality of the virus requires information about their relative concentrations in the viral membrane. Here, a gold nanoparticle (NP) binding assay for probing relative PS and G_M1 lipid concentrations in the outer leaflet of different HIV‐1 and Ebola virus‐like particles (VLPs) using sample sizes of less than 3 × 10⁶ particles is introduced. The assay evaluates both scattering intensity and resonance wavelength, and determines relative NP densities through plasmon coupling as a measure for the target lipid concentrations in the NP‐labeled VLP membrane. A correlation of the optical observables with absolute lipid contents is achieved by calibration of the plasmon coupling‐based methodology with unilamellar liposomes of known PS or G_M1 concentration. The performed studies reveal significant differences in the membrane of VLPs that assemble at different intracellular sites and pave the way to an optical quantification of lipid concentration in virus particles at physiological titers.     

Effects of 4-n-nonylphenol on aquatic hyphomycetes

We measured the removal of 4-n-nonylphenol (between 50 and 500 μg L⁻¹) from an aqueous solution with or without linden and oak leaf disks. More 4-n-NP was removed when the leaves were first exposed for 3 weeks in a stream, which allowed colonization by aquatic hyphomycetes. The response of fungal sporulation rates from beech, linden, maple and oak leaves to increasing levels of 4-n-NP was complex. Linear regressions were non-significant, arguing against a no-threshold model. The response at the lowest concentration (50 μg L⁻¹) was between 7% (beech) and 67% (maple) higher than in the absence of 4-n-NP, however, the difference was not significant. The number of sporulating species of aquatic hyphomycetes was significantly higher at the lowest concentration than in the control treatment without 4-n-NP. The composition of the fungal community was affected by leaf species but not by 4-n-NP concentration. The results suggest the presence of a weak hormeotic effect. The known ability of aquatic hyphomycetes and other fungi to degrade nonylphenols and related substances, combined with fungal resilience in their presence, makes decaying leaves potential candidates for bioremediation.     

Effect of a commercial freeze/tempering process on the viability of Cryptosporidium parvum oocysts on lean and fat beef trimmings

Lean and fat beef trimmings (25 cm⁻²) were inoculated with approximately 250,000 Cryptosporidium parvum oocysts, placed in commercial packages (28 kg boxes) and subjected to normal commercial processes i.e. blast frozen (to −20 °C within 60 h), stored (−20 °C, 21 days), tempered (48 h at −3 °C), and held at 0 °C for 10 h. Inoculated areas were then excised, pulsified (30 s in 50 ml PBST), and centrifuged (2500×g, 15 min). The resultant pellet was resuspended in 10 ml water and subjected to immunomagnetic separation and viability dye assay. Following the commercial freeze/tempering process the viability of the oocysts had decreased from 90.6% viable in the working stock suspension to 7.17% and 9.46% viable on lean and fat trimmings, respectively. The results of this study indicate that if C. parvum oocysts were present on beef trimmings their viability would be substantially reduced as a result of the freeze/tempering process.     

Evaluation of the effects of oxygen evolution on the capacity and cycle life of nickel hydroxide electrode materials

The effect of charge–discharge cycling on the capacity of surface-adhered nickel hydroxide (Ni(OH)₂) micro-particles is investigated in aqueous KOH by cyclic voltammetry, and compared with that for pasted nickel hydroxide electrodes. Cyclic voltammetry on adhered Ni(OH)₂ micro-particles enables rapid screening of four types of commercially available, battery-grade, nickel hydroxide samples and allows the separation of the oxidation process from the oxygen evolution reaction. With large pasted electrodes, due to their high uncompensated resistance (R_u), these processes are poorly resolved. Pasted β-nickel hydroxide electrodes with a specific capacity of between 190 and 210 mAh g⁻¹ are charged and discharged at constant currents greater than 15 C (18 mA cm⁻²). With no voltage limit in the charging profile, excess oxygen evolution occurs and capacity fading is observed within the first 50 cycles. Loss of capacity is attributed to the degradation of the electrode due to excess oxygen evolution at switching potentials greater than 0.55 V versus Hg/HgO (1 M KOH). X-ray diffraction (XRD) measurements confirm the formation of γ-NiOOH in these electrodes. Limiting the cell voltage to 1.5 V, and thereby minimizing oxygen evolution, results in no observed capacity loss within 100 cycles, and only β-Ni(OH)₂ can be detected by XRD phase analysis.     

The Biochemical Assessment of Mitochondrial Respiratory Chain Disorders

Mitochondrial respiratory chain (MRC) disorders are a complex group of diseases whose diagnosis requires a multidisciplinary approach in which the biochemical investigations play an important role. Initial investigations include metabolite analysis in both blood and urine and the measurement of lactate, pyruvate and amino acid levels, as well as urine organic acids. Recently, hormone-like cytokines, such as fibroblast growth factor-21 (FGF-21), have also been used as a means of assessing evidence of MRC dysfunction, although work is still required to confirm their diagnostic utility and reliability. The assessment of evidence of oxidative stress may also be an important parameter to consider in the diagnosis of MRC function in view of its association with mitochondrial dysfunction. At present, due to the lack of reliable biomarkers available for assessing evidence of MRC dysfunction, the spectrophotometric determination of MRC enzyme activities in skeletal muscle or tissue from the disease-presenting organ is considered the ‘Gold Standard’ biochemical method to provide evidence of MRC dysfunction. The purpose of this review is to outline a number of biochemical methods that may provide diagnostic evidence of MRC dysfunction in patients.     

Electrochemical nucleic acid-based sensors for detection of Escherichia coli and Shiga toxin-producing E. coli—Review of the recent developments

Escherichia coli are a group of bacteria that are a natural part of the intestinal flora of warm-blooded animals, including humans. Most E. coli are nonpathogenic and essential for the normal function of a healthy intestine. However, certain types, such as Shiga toxin-producing E. coli (STEC), which is a foodborne pathogen, can cause a life-threatening illness. The development of point-of-care devices for the rapid detection of E. coli is of significant interest with regard to ensuring food safety. The most suitable way to distinguish between generic E. coli and STEC is by using nucleic acid-based detection, focusing on the virulence factors. Electrochemical sensors based on nucleic acid recognition have attracted much attention in recent years for use in pathogenic bacteria detection. This review has summarized nucleic acid-based sensors for the detection of generic E. coli and STEC since 2015. First, the sequences of the genes used as recognition probes are discussed and compared to the most recent research regarding the specific detection of general E. coli and STEC. Subsequently, the collected literature regarding nucleic acid-based sensors is described and discussed. The traditional sensors were divided into four categories such as gold, indium tin oxide, carbon-based electrodes, and those using magnetic particles. Finally, we summarized the future trends in nucleic acid-based sensor development for E. coli and STEC including some examples of fully integrated devices.     

Electrochemically Induced Conformational Change of Di-Boronic Acid-Functionalized Ferrocene for Direct Solid-State Monitoring of Aqueous Fluoride Ions

While fluoride ions (F⁻) are abundant across environmental and biological systems, common procedures and potentiometric sensors for quantifying aqueous F⁻ are inefficient, time-consuming, and suffer from poor pH resiliency and high detection limits. Herein, this work reports a new di-boronic acid-functionalized ferrocene (FDBA) molecular receptor for noncovalent F⁻ recognition, toward the development of a solid-state miniaturized voltammetric fluoride sensor capable of direct and reversible F⁻ detection in drinking water (DW) (pH 6) and community water (pH 7.6–9.1) over the µg L⁻¹–mg L⁻¹ range. The associated sensing mechanism is enabled by the conformational change of FDBA from the open (charge-repelled) to closed (π-dimerized) conformation, which is facilitated by the unique linkage of two electron-accepting phenylboronic acid moieties with the electron-donating ferrocene moiety using rigid conjugated amide linkers. The square wave voltammetric (SWV) oxidation current response of the FDBA-based fluoride sensor is spectroscopically investigated, suggesting a combination of electrooxidation-triggered conformational change of FDBA on a nanocarbon-modified electrode, F⁻ anion–π interactions, and resulting electron transfer between F⁻ and FDBA. The performance of the voltammetric fluoride sensor is compared to that of a commercial liquid junction-based fluoride ion-selective electrode (F-ISE), and of a solid-contact (SC) F-ISE sensor chip, demonstrating significant advantages versus traditional potentiometric F-ISEs.     

Structure-mechanical properties correlation in bulk LiPON glass produced by nitridation of metaphosphate melts

The glassy solid electrolyte Lithium phosphorous oxynitride (LiPON) has been widely researched in thin film solid state battery format due to its outstanding stability when cycled against lithium. In addition, recent reports show thin film LiPON having interesting mechanical behaviors, especially its ability to resist micro-scale cracking via densification and shear flow. In the present study, we have produced bulk LiPON glasses with varying nitrogen contents by ammonolysis of LiPO₃ melts. The resulting compositions were determined to be LiPO_3-3z/2N_z, where 0 ≤ z ≤ 0.75, and the z value of 0.75 is among the highest ever reported for this series of LiPON glasses. The short-range order structures of the different resulting compositions were characterized by infrared, Raman, ³¹P magic angle spinning nuclear magnetic resonance, and X-ray photoelectron spectroscopies. Instrumented nano-indentation was used to measure mechanical properties. It was observed that similar to previous studies, both trigonally coordinated (N_t) and doubly bonded (N_d) N co-exist in the glasses in about the same amounts for z ≤ 0.36, the limit of N content in most previous studies. For glasses with z > 0.36, it was found that the fraction of the N_t increased significantly while the fraction of N_d correspondingly decreased. The incorporation of nitrogen increased both the elastic modulus and hardness of the glass by approximately a factor of 1.5 when N/P ratio reaches 0.75. At the same time, an apparent embrittlement of the glass was observed due to nitridation, which was revealed by nanoindentation with an extra sharp nanoindenter tip.