Fine partitioning of epiphyte habitat within Johansson zones in tropical Australian rain forest trees

For over three decades, the Johansson zones have been widely used in epiphyte studies as a way of stratifying the host tree into habitat zones. The usefulness of this system, however, has been questioned. We test the effectiveness of the Johansson zones by grouping epiphyte species by the substrate and microclimatic attributes of their individual occurrences and assessing the fidelity of these groups to the Johansson zones. Habitat characteristics were recorded for every individual epiphyte on 30 trees in the lower montane rain forests of northeastern Australia. Twenty‐four epiphyte species were agglomerated into four groups using Ward's method. Group 4 was highly distinct and included shade‐loving species and nomadic vines from the lower zones of the host trees. Group 3 contained species from the most exposed habitats. Group 1 had higher light levels and lower substrate thickness than Group 2, yet both groups had close to identical distributions over the Johansson zones. This suggests that groups of epiphyte species may utilize different micro‐sites within the same zone. While the Johansson zones are a useful tool in epiphyte studies, finer partitioning of habitat within the host tree may be missed.     

Quantitative analysis of lignocaine and metabolites in equine urine and plasma by liquid chromatography–tandem mass spectrometry

In this paper, a method for the sensitive and reproducible analysis of lignocaine and its four principal metabolites, monoethylxylidide (MEGX), glycylxylidide (GX), 3-hydroxylignocaine (3-HO-LIG), 4-hydroxylignocaine (4-HO-LIG) in equine urine and plasma samples is presented. The method uses liquid chromatography coupled to tandem mass spectrometry operating in electrospray ionisation positive ion mode (+ESI) via multiple reaction monitoring (MRM). Sample preparation involved solid-phase extraction using a mixed-mode phase. The internal standard adopted was lignocaine-d₁₀. Lignocaine and its metabolites were successfully resolved using an octadecylsilica reversed-phase column using a gradient mobile phase of acetonitrile and 0.1% (v/v) aqueous formic acid at a flow rate of 300 μL/min. Target analytes and the internal standard were determined by using the following transitions; lignocaine, 235.2 > 86.1; 3-HO-LIG and 4-HO-LIG, 251.2 > 86.1; MEGX, 207.1 > 58.1; GX, 179.1 > 122.1; and lignocaine-d₁₀, 245.2 > 96.1. Calibration curves were generated over the range 1–100 ng/mL for plasma samples and 1–1000 ng/mL for urine samples. The method was validated for instrument linearity, repeatability and detection limit (IDL), method linearity, repeatability, detection limit (MDL), quantitation limit (LOQ) and recovery. The method was successfully used to analyse both plasma and urine samples following a subcutaneous administration of lignocaine to a thoroughbred horse.     

Haplotypes versus genotypes on pedigrees

Background  

Genome sequencing will soon produce haplotype data for individuals. For pedigrees of related individuals, sequencing appears to be an attractive alternative to genotyping. However, methods for pedigree analysis with haplotype data have not yet been developed, and the computational complexity of such problems has been an open question. Furthermore, it is not clear in which scenarios haplotype data would provide better estimates than genotype data for quantities such as recombination rates.     

EVALUATION OF GRIP LOSS—A Factor of Permanent Partial Disability in California: Summation and Conclusions of the Subcommittee for Study of Grasping Power of the Committee on Industrial Health and Rehabilitation of the California Medical Association

Loss of grasping power is a ratable factor of permanent partial disability by the Industrial Accident Commission of the State of California. The ratings that issue therefrom are based upon the proportion of grasping power actually lost as a result of the injury sustained. The conditions which most frequently impair grasping power are, (1) amputation; (2) limited motion of digits, wrists, forearm, elbow or shoulder; (3) pain; (4) muscular weakness. The examining physician can greatly facilitate proper rating if he carefully and fully reports data needed by the I.A.C. Grip readings should be measured by the most precise instrument which can be obtained. Makeshift devices such as using a blood pressure cuff are not acceptable. A committee of the California Medical Association appointed to study the subject of loss of grip for purposes of establishing compensation rating, concluded that a dynamometer that registers pounds force is preferable to one registering pressure.     

A modified metal-ion affinity chromatography procedure for the purification of histidine-tagged recombinant proteins expressed in Drosophila S2 cells

We have developed a modified method of immobilized metal-ion affinity chromatography (IMAC) that can be used for the purification of histidine-tagged proteins from conditioned medium containing free copper ions. Classical methods of IMAC purification, using resins such as Ni-NTA, have proven inefficient for this type of purification and require multiple steps due to the interference of divalent copper ions with the binding of His-tagged protein to the charged resin. In contrast, this modified IMAC procedure, using chelating Sepharose instead of Ni-NTA, enables efficient purification from copper-containing medium in a single step. This method appears to rely upon a preferential interaction of protein-copper complexes with immobilized chelating resin. We have utilized this method to purify active, His-tagged murine interleukin 12 from the conditioned medium of Drosophila S2 cells coexpressing recombinant p40 and His-tagged p35 subunits and for the purification of the extracellular domain of the erythropoietin receptor. This method should be applicable to the purification of a wide variety of His-tagged fusion proteins expressed in Drosophila cells and in other systems where free metal ions are present.