FEASIBILITY FOR MAPPING CARTILAGE T1 RELAXATION TIMES IN THE DISTAL METACARPUS3/METATARSUS3 OF THOROUGHBRED RACEHORSES USING DELAYED GADOLINIUM‐ENHANCED MAGNETIC RESONANCE IMAGING OF CARTILAGE (dGEMRIC): NORMAL CADAVER STUDY

Osteoarthritis of the metacarpo/metatarsophalangeal joints is one of the major causes of poor performance in horses. Delayed gadolinium‐enhanced magnetic resonance imaging of cartilage (dGEMRIC) may be a useful technique for noninvasively quantifying articular cartilage damage in horses. The purpose of this study was to describe dGEMRIC characteristics of the distal metacarpus3/metatarsus3 (Mc3/Mt3) articular cartilage in 20 cadaver specimens collected from normal Thoroughbred horses. For each specimen, T1 relaxation time was measured from scans acquired precontrast and at 30, 60, 120, and 180 min post intraarticular injection of Gd‐DTPA^2‐ (dGEMRIC series). For each scan, T1 relaxation times were calculated using five regions of interest (sites 1–5) in the cartilage. For all sites, a significant decrease in T1 relaxation times occurred between precontrast scans and 30, 60, 120, and 180 min scans of the dGEMRIC series (P < 0.0001). A significant increase in T1 relaxation times occurred between 60 and 180 min and between 120 and 180 min post Gd injection for all sites. For sites 1–4, a significant increase in T1 relaxation time occurred between 30 and 180 min postinjection (P < 0.05). Sites 1–5 differed significantly among one another for all times (P < 0.0001). Findings from this cadaver study indicated that dGEMRIC using intraarticular Gd‐DTPA^2‐ is a feasible technique for measuring and mapping changes in T1 relaxation times in equine metacarpo/metatarsophalangeal joint cartilage. Optimal times for postcontrast scans were 60–120 min. Future studies are needed to determine whether these findings are reproducible in live horses.     

Discolouration of birch wood: analysis of extractives from discoloured surface of vacuum-dried European white birch (Betula pubescens) board

A discolouration that appeared on the surfaces of a European white birch (Betula pubescens) board during vacuum drying was studied by means of colour measurements (CIEL*a*b*), elemental analysis and the analysis of extractives. The discoloured surface layer of the dried board contained substantially more methanol-soluble extractives than did the light-coloured part (50.7 mg g⁻¹ vs. 26.7 mg g⁻¹ dry wood), and the colour difference (ΔE* _ab 20.0) between the two extracts was notable. Characterization by means of GC and ¹³C NMR spectroscopy showed that the extracts contain sugars (mainly glucose and fructose), low-molecular-weight phenolic compounds, proanthocyanidins, Brauns’ lignin and fatty acid esters. Concentrations of sugars, low-molecular-weight phenols, proanthocyanidins and Brauns’ lignin were higher in the discoloured surface layer than in the light-coloured part. The yellowness of the surface layer was associated with the accumulation of low-molecular-weight phenolic extractives, and the redness with Brauns’ lignin and possibly proanthocyanidins.     

Susceptibility of Pedicularis spp. to Cronartium ribicola and C. flaccidum in Finland

Aeciospores of Cronartium ribicola and C. flaccidum were collected from several locations in Finland and used to inoculate Pedicularis spp. and some known and suspected alternate hosts in 2008–2009. In all trials, C. ribicola formed uredinia and telia on leaves of Ribes nigrum. No uredinia or telia of C. ribicola formed on older leaves of Pedicularis spp. but both uredinia and telia were found on young leaves of P. palustris ssp. palustris. Cronartium flaccidum produced uredinia and/or telia on leaves of P. palustris ssp. palustris, P. lapponica, Vincetoxicum hirundinaria and Melampyrum sylvaticum. Neither rust infected P. sceptrum‐carolinum, Vaccinium myrtillus, Calluna vulgaris or Ledum palustre. Similar to rusts in Asia and North America, the results showed that European C. ribicola exhibit more variable host reactions and wider alternate host ranges than earlier described. Pedicularis palustris may play a role in the spread of Cronartium in natural forests.