Genetic correlations for foal and studbook traits with racing traits and implications for selection strategies in the Finnhorse and Standardbred trotter.

Genetic correlations for body measurements and conformation and functional traits in foals and studbook horses with racing traits were estimated in the Finnhorse and Standardbred. Genetic response and accuracy were estimated using records of animal, half-sibs and parents in selection scenarios for racing traits, for foal and racing traits, for studbook and racing traits, and using records of animal, half-sibs and parents for foal traits and racing traits of parents. Racing time and earnings were the breeding objective. Low-to-moderate genetic correlations for body measurements and racing traits indicated that selection favours bigger horses at all ages. Being mainly favourable for the breeding objective, genetic correlations for conformation and functional traits with racing traits were highest for the foal traits of type, trot and overall grade and for the studbook traits of character and movements. Genetic correlations for foal and studbook conformation with racing traits were low in the Finnhorse and moderate to high in the Standardbred. In foals, the highest genetic correlations were for trot with racing time (-0.54) and with earnings (0.52) in the Finnhorse, and for overall grade with racing time (-0.54) and with earnings (0.54) in the Standardbred. In studbook horses, genetic correlations were high for character with racing time and earnings in the Finnhorse (-0.68, 0.61) and in the Standardbred (-0.63, 0.70), and for movements with racing time and earnings in the Finnhorse (-0.70, 0.69) and in the Standardbred (-0.90, 0.88). To increase accuracy of conformation and functional traits, foal traits would be more useful in the index with racing traits, as being less preselected than studbook traits. The foal traits (type, trot, overall grade) having moderate heritability and genetic correlations with racing traits would be useful in multi-trait index before a racing career, where the greatest gain is because of a shorter generation interval. It would be feasible to implement for AI stallions.

The use of foal and studbook traits in the breeding programmes of Finnhorse and Standardbred trotters.

Genetic correlations for body measurements and subjectively scored traits between foals and studbook horses were estimated using bivariate linear mixed models. Observations for nine foal and eleven studbook traits in Finnhorses on 6529 foals and 6596 studbook horses and in Standardbred trotters on 3069 foals and 2112 studbook horses were available from the Finnish horse breeding shows. The number of sires with progeny in both foal and studbook data was 203 in Finnhorse and 145 in Standardbred trotters. Estimates of heritability for body measurements in foals and studbook horses using univariate models were high in both breeds (0.41-0.84). Heritability estimates for subjectively scored traits using univariate models were generally higher for foals (0.08-0.46) than for studbook horses (0.06-0.21) in both breeds. Genetic correlations between foals and studbook horses for body measurements were highly positive ranging from 0.74 to 0.96 in Finnhorses and from 0.79 to 0.99 in Standardbred trotters. Low to highly positive genetic correlations between foals and studbook horses for subjectively scored traits were obtained in Finnhorse trotters, whereas in Standardbred trotters genetic correlations for subjectively scored traits varied from moderately negative to highly positive. Higher estimates of heritability for foal traits and generally high genetic correlations between the foal and studbook traits indicate that an early selection for conformation traits would be efficient in the breeding programmes.

Estimates of genetic parameters for conformation measures and scores in Finnhorse and Standardbred foals.

The aim of this study was to estimate genetic parameters for conformation measures and scores in the Finnhorse and the Standardbred foals presented in foal shows. Studied traits included height at withers and at croup, six subjectively evaluated conformation traits and overall grade. Data were from 10-year period (1995-2004) and consisted of 5821 Finnhorse foals (1-3 years old) with 7644 records and 2570 Standardbred foals (1-2 years old) with 2864 records. Variance components were estimated with REML - animal model using VCE4 program. The model included age class, year of judging, sex and region as fixed effects, and additive genetic, permanent environmental and residual as random effects. Estimates of heritability for measured traits were very high in both breeds (0.88-0.90). Estimates of heritability for conformation traits varied from 0.13 to 0.32 in the Finnhorse and from 0.06 to 0.47 in the Standardbred. In both breeds, estimates of heritability were lowest for hooves and movements at walk, and highest for type and body conformation among scored traits. Estimate of heritability for overall grade was in the Finnhorse 0.32 and in the Standardbred 0.34. Genetic correlations between overall grade and different conformation traits were 0.35-0.84 in the Finnhorse and 0.31-0.88 in the Standardbred. Thus, selection based on the overall grade would improve all studied characteristics.

Genetic parameters of milk coagulation properties and their relationships with milk yield and quality traits in Italian Holstein cows.

Milk coagulation properties (MCP) are an important aspect in assessing cheese-making ability. Several studies showed that favorable conditions of milk reactivity with rennet, curd formation rate, and curd strength, as well as curd syneresis, have a positive effect on the entire cheese-making process and subsequently on the ripening of cheese. Moreover, MCP were found to be heritable, but little scientific literature is available about their genetic aspects. The aims of this study were to estimate heritability of MCP and genetic correlations among MCP and milk production and quality traits. A total of 1,071 Italian Holstein cows (progeny of 54 sires) reared in 34 herds in Northern Italy were sampled from January to July 2004. Individual milk samples were collected during the morning milking and analyzed for coagulation time (RCT), curd firmness (a30), pH, titratable acidity, fat, protein, and casein contents, and somatic cell count. About 10% of individual milk samples did not coagulate in 31 min, so they were removed from the analyses. Estimates of heritability for RCT and a30 were 0.25 +/- 0.04 and 0.15 +/- 0.03, respectively. Estimates of genetic correlations between MCP traits and milk production traits were negligible except for a30 with protein and casein contents (0.44 +/- 0.10 and 0.53 +/- 0.09, respectively). Estimates of genetic correlations between MCP traits and somatic cell score were strong and favorable, as well as those between MCP and pH and titratable acidity. Selecting for high casein content, milk acidity, and low somatic cell count might be an indirect way to improve MCP without reducing milk yield and quality traits.

Effects of composite beta- and kappa-casein genotypes on milk coagulation, quality, and yield traits in Italian Holstein cows.

The aim of the study was to estimate the effect of the composite CSN2 and CSN3 genotypes on milk coagulation, quality, and yield traits in Italian Holstein cows. A total of 1,042 multiparous Holstein cows reared on 34 commercial dairy herds were sampled once, concurrently with monthly herd milk recording. The data included the following traits: milk coagulation time; curd firmness; pH and titratable acidity; fat, protein, and casein contents; somatic cell score; and daily milk, fat, and protein yields. A single-trait animal model was assumed with fixed effects of herd, days in milk, parity, composite casein genotype of CSN2 and CSN3 (CSN2-CSN3), and random additive genetic effect of an animal. The composite genotype of CSN2-CSN3 showed a strong effect on both milk coagulation traits and milk and protein yields, but not on fat and protein contents and other milk quality traits. For coagulation time, the best CSN2-CSN3 genotypes were those with at least one B allele in both the CSN2 and CSN3 loci. The CSN3 locus was associated more strongly with milk coagulation traits, whereas the CSN2 locus was associated more with milk and protein yields. However, because of the tight linkage between the 2 loci, the composite genotypes, or haplotypes, are more appropriate than the single-locus genotypes if they were considered for use in selection.

Quercetin derivatives are deconjugated and converted to hydroxyphenylacetic acids but not methylated by human fecal flora in vitro.

By using a batch in vitro anaerobic fecal fermentation model, we have shown that the fecal microflora can rapidly deconjugate rutin, isoquercitrin, and a mixture of quercetin glucuronides. High levels of beta,D-glucosidase, alpha,L-rhamnosidase, and beta,D-glucuronidase were present. Rutin underwent deglycosylation, ring fission, and dehydroxylation. The main metabolite, 3,4-dihydroxyphenylacetic acid, appeared rapidly (2 h) and was dehydroxylated to 3-hydroxyphenylacetic acid within 8 h. The pattern of in vitro fermentation of rutin was not changed by changing the pH (6.0 or 6.9), fermentation scale (10 or 1000 mL), or donors of the inoculum. Hydroxyphenylacetic acids were not methylated by colon flora in vitro. The colonic microflora has enormous potential to transform flavonoids into lower molecular weight phenolics, and these might have protective biological activities in the colon. The site of absorption of flavonoids and the form in which they are absorbed are critical for determining their metabolic pathway and consequent biological activities in vivo.

Analysis of aldehydes and ketones from beer as O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine derivatives.

O-(2,3,4,5,6-pentafluorobenzyl)Hydroxylamine (PFBOA) was used as a derivatization reagent for carbonyl compounds in beer. Derivatization was carried out in aqueous solution without extraction or concentration of the sample. The effects of antifoam agent, reaction time and pH on the reaction efficiency were studied. Antifoam RD, a silicone polymer-based antifoam reagent, was the best antifoaming agent since it did not cause interferences. Reaction time studies showed that the yield of aldehydes increased up to 12 hr and then decreased slightly. The yield of 3-hydroxybutanone, a test compound for ketones, increased throughout the 48 hr test period. The natural pH of beer (ca. 4.5) was favourable for the determination of carbonyl compounds as PFBOA derivatives. Higher pH values caused yield losses and some compounds, such as butanedione, 2,3-pentanedione and 5-hydroxymethyl-2-furfural, could not be measured at all in neutral or basic conditions. Carbonyl compounds were identified by GC-MS, using three different ionization techniques, electron impact ionization, chemical ionization, and negative chemical ionization. The formation of the protonated molecules by ammonia chemical ionization and formation of the negative molecular ions and [M - HF](-.) ions by negative chemical ionization permitted reliable identification of the various carbonyl compounds studied. Sixteen carbonyl compounds from the 32 standard compounds were identified in beer and 11 of the most significant were quantitated using GC-ECD. Reproducibility of quantitation for beer samples was good, the relative standard deviations varied between 2.7 and 6.7 %. The estimated detection limits of the PFBOA derivatives of the carbonyl compounds in beer varied in the range of 0.01-1 microg/dm(3).

Determination of phenolic compounds in water using membrane inlet mass spectrometry.

Two membrane inlet mass spectrometric (MIMS) methods for determining phenolic compounds in water are described and compared, namely direct analysis and analysis after acetylation of the phenolic compounds. Direct analysis of phenolic compounds in water is a very simple and rapid method and detection limits are relatively low (from 30 mug 1(-1) for phenol to 1000 mug 1(-1) for 4-nitrophenol). Analysis of phenolic compounds after aqueous acetylation is also a very simple and rapid method, and the detection limits are even two orders of magnitude lower than in the direct analysis. For example the detection limit of phenol acetate is 0.5 mug 1(-1) and that of 4-nitrophenol is 10 mug 1(-1). The acetylation method was also tested in the analysis of phenolic compounds from contaminated surface water samples.

Determination of mono- and sesquiterpenes in water samples by membrane inlet mass spectrometry and static headspace gas chromatography.

A membrane inlet mass spectrometric (MIMS) method is presented and compared with a static headspace gas chromatographic method (HSGC) for the determination of terpenes in water. The MIMS method provides a very simple and fast analysis of terpenes in water, detection limits being relatively low, from 0.2 mug l(-1) for monoterpenes to 2 mug l(-1) for geraniol. The analysis of terpenes by the HSGC (equipped with flame ionization detector, FID) method is more time-consuming and the detection limits (2 mug l(-1) for monoterpenes to 100 mug l(-1) for geraniol) are higher than with MIMS. However, the HSGC method has the advantage of determining individual mono- and sesquiterpene compounds, whereas MIMS provides only separation of different classes of terpenes. Both methods were applied to the analysis of mono- and sesquiterpenes in several condensation water samples of pulp and paper mills.

Comparison of different methods for the determination of volatile organic compounds in water samples.

The aim of this work was to compare the characteristics of three methods, membrane inlet mass spectrometry (MIMS), purge-and-trap gas chromatography-mass spectrometry (P&T) and static headspace gas chromatography (HSGC), for the determination of volatile organic compounds in water samples as used in routine analysis. The characteristics examined included linear dynamic ranges, detection limits of selected environmentally hazardous volatile organic compounds (e.g. toluene, benzene and trichloroethene) in water, required analysis time and reproducibility of the analytical methods. The MIMS and P&T methods had the lowest detection limits for all the tested compounds, ranging from 0.1 to 5 mug 1(-1). Linear dynamic ranges using the MIMS method were about four orders of magnitude and using the P&T method about two orders of magnitude. Detection limits of the HSGC method were 10-100 times higher than those of the other two methods, but the linear dynamic ranges were larger, even up to six orders of magnitude. The analysis time per sample was shortest for the MIMS method, from 5 to 10 min, and ranged around from 35 to 45 min for the HSGC and P&T methods. The reproducibilities of the methods were of the same order of magnitude, in the range of 1-13%. Agreement between the analytical results obtained for spiked samples and for environmental water samples by the three different methods was very good.

Peripheral nerve injury and Raynaud's syndrome following electric shock.

A truck driver was injured by a high-voltage line of 10,000 volts when holding a metallic bar in both hands. Initially no neurological abnormalities were found, but during the following few weeks increasing sensory and minor motor symptoms developed in the right upper extremity. After one year numbness of the right thigh and leg appeared, as well as attacks of white finger in both hands. Repeated examinations showed progressive abnormalities of the median and ulnar nerves in both hands. No other cause for Raynaud's syndrome was discovered. The late high-voltage effects, presumably indirect, are suggested to be of multifactorial etiology.

Effects of sex and age on the ossification of the collateral cartilages of the distal phalanx of the Finnhorse and the relationships between ossification and body size and type of horse.

The ossification of the collateral cartilages of the distal phalanx was evaluated in dorsopalmar radiographs of the front feet of 202 Finnhorses (101 females and 101 males, aged six months to 20 years) with reference to the sex, age, body measurements and type of horse. Ossification was more common and more extensive in females than in males from about two years of age. In females, the lateral cartilages were significantly more ossified than the medial cartilages; in males, ossification was more symmetrical in the cartilages of each foot. The amount of ossification increased rapidly during the second and third years of life, and more slowly in adults. The low positive correlation coefficients between ossification and different body measurements of the horse suggested that there was more ossification in large horses, and the correlation between chest-width in adults and the extent of ossification was statistically significant. The working type of horses showed slightly more ossification than trotters and riding horses. Ossification variables, which included ossification at both the base of the cartilage and at the possible separate centres of ossification (total ossification of individual cartilages and "possibly significant' ossification in the front feet), were found to be most satisfactory for expressing the extent of ossification.

Estimates of heritability for ossification of the cartilages of the front feet in the Finnhorse.

REASONS FOR PERFORMING STUDY: Ossification of the cartilages in the foot is common in coldblooded horses, but prevalence as well as ossification pattern varies between breeds; research on estimation of heritability for the condition has been limited. OBJECTIVES: Our purpose was to calculate estimates of 1) heritability for ossification parameters of the cartilages in the front feet of the Finnhorse and 2) genetic correlations between the different ossification parameters. METHODS: Estimates of heritability for different ossification parameters of the cartilages in the front feet and of genetic correlations between different parameters were evaluated in data consisting of dorsopalmar radiographs of the front feet and pedigree up to the fourth generation of 964 Finnhorses (age > or = 2 years; 345 females and 619 males). Ossification at the base of the cartilages and total ossification, including separate centres of ossification, were graded 0-5 according to the most proximal point of ossification and the presence of separate centres of ossification was recorded separately. The data were analysed using a model including a fixed sex-age subclass effect and a random animal effect. Variance and covariance components were estimated with the restricted maximum likelihood (REML) method assuming an animal model. RESULTS: Females had more ossification than males and this difference increased with age. The ossification in the medial cartilages progressed significantly with age in females but not in males. In the lateral cartilages, the increase in ossification with age was evident in both sexes. Separate centres of ossification were an incidental finding. Estimates of heritability for the ossification parameters varied slightly between the cartilages as well as between the front feet. For total ossification, the estimates of heritability varied between 0.31 (right lateral) and 0.50 (left medial) and were slightly higher for ossification at the base of the cartilages. High genetic correlations were found for total ossification between the medial and lateral cartilages in the foot and for parallel ossification parameters between the right and left foot. CONCLUSIONS: The estimates of heritability were relatively high, and both cartilages and front feet have a similar genetic tendency to ossify. POTENTIAL RELEVANCE: This information is useful in further studies assessing other factors contributing to the ossification process and also in the planning and modifying breeding programmes.

Inheritance of hydrocephalus in horses.

From 1974 to 1979, seven stillborn foals with internal hydrocephalus were encountered from one Standardbred trotter stallion which sired 239 registered foals. An hydrocephalic foal was also aborted by a daughter of the same stallion. One affected foal from Standardbred trotters and one from a Finnish Horses were also reported. In some cases, the condition caused severe dystocia. Based on field data, possible causes of the defect could neither be proved nor specifically overruled in individual cases. Hydrocephalus was obviously not an autosomal recessive single-locus defect, nor was it X-linked. A dominant mutation in the germ line in one of the parents or in any embryo seemed the most likely explantation for the occurrence of internal hydrocephalus in horses.

Estimates of genetic parameters for hip and elbow dysplasia in Finnish Rottweilers.

Data from 2,764 Rottweiler dogs born from 1987 to 1996 were analyzed with a Restricted Maximum Likelihood procedure using a mixed linear animal model to obtain variance component estimates for hip and elbow dysplasia. The data included 2,764 hip dysplasia and 2,278 elbow dysplasia records. Hip joints were scored as normal (0), borderline (1), slight (2), moderate (3), and severe (4, 4.5, and 5) hip dysplasia. Elbow joints were graded normal or borderline (0), slight (1), moderate (2), and severe (3) elbow dysplasia. The mean for the hip scores was 1.07 and for the elbow scores .60. Environmental effects influencing hip dysplasia were age, birth year, birth year x season interaction, and experience of the veterinarian responsible for x-raying the dog. For elbow dysplasia, statistically significant effects were age, birth year, sex of the dog, and panelist responsible for each screening. Estimates of heritability for hip and elbow dysplasia were .58 +/- .04 and .31 +/- .04, respectively, with a genetic correlation of .37 +/- .08 between the traits. Genetic improvement of almost one genetic standard deviation was observed in both traits during the 10 yr covered by the data.

Subclinical vestibular pathology in patients with noise-induced hearing loss from intense impulse noise.

Sixty patients with varying degrees of noise-induced hearing loss (NIHL) after long-term exposure to intense impulse noise from firearms, but without manifest clinical symptoms of vestibular pathology, were tested for body sway using a stable platform. The results were compared with those from 115 healthy referents examined in the same way. Subjects with NIHL showed significantly more body sway, estimated as movement of the centre of gravity in the horizontal plane, than did the referents. Subjects with more severe NIHL showed more sway than subjects with milder acoustic trauma. The results show that body sway is increased in patients with NIHL from exposure to impulse noise of high intensity in a way suggesting an exposure-effect relationship. This suggests subclinical disturbances of the vestibular system in these patients. The underlying mechanism may be simultaneous mechanical damage to both the cochlear and vestibular partitions by intense impulse noise.

Estimates of genetic parameters and environmental effects for measures of hunting performance in Finnish hounds.

Data from field trials of Finnish Hounds between 1988 and 1992 in Finland were used to estimate genetic parameters and environmental effects for measures of hunting performance using REML procedures and an animal model. The original data set included 28,791 field trial records from 5,666 dogs. Males and females had equal hunting performance, whereas experience acquired by age improved trial results compared with results for young dogs (P < .001). Results were mostly better on snow than on bare ground (P < .001), and testing areas, years, months, and their interactions affected results (P < .001). Estimates of heritabilities and repeatabilities were low for most of the 28 measures, mainly due to large residual variances. The highest heritabilities were for frequency of tonguing (h2 = .15), pursuit score (h2 = .13), tongue score (h2 = .13), ghost trailing score (h2 = .12), and merit and final score (both h2 = .11). Estimates of phenotypic and genetic correlations were positive and moderate or high for search scores, pursuit scores, and final scores but lower for other studied measures. The results suggest that, due to low heritabilities, evaluation of breeding values for Finnish Hounds with respect to their hunting ability should be based on animal model BLUP methods instead of mere performance testing. The evaluation system of field trials should also be revised for more reliability.

Medetomidine, an alpha 2-agonist, alleviates post-thoracotomy pain in dogs.

Twelve laboratory beagles underwent a routine left thoracotomy to insert permanent instrumentation. Every second dog was given 10 micrograms/kg of medetomidine, an alpha 2-agonist sedative. The rest of the animals were treated with 20 micrograms/kg of buprenorphine, an opioid agonist-antagonist, which is regularly used to treat postoperative pain in laboratory animals. The drugs were given at the end of operation (0) and 4, 8, 20, and 24 h postoperatively. Blood samples for catecholamines (adrenaline and noradrenaline) and blood gases (pCO2 and pO2) and pH were drawn immediately before any drug administration, and 30 min later. At the same time points, the pain level was subjectively evaluated using a pain score, and heart rate and rectal temperature were measured. Adrenaline and noradrenaline concentrations were lower in the medetomidine group than in the buprenorphine group. Accordingly, it was concluded that medetomidine had better analgesic effect than buprenorphine in the treated animals. This result was supported by subjective evaluation of the severity of pain, even though subjective evaluation is not considered very reliable in the present kind of open studies. pO2 was lower in the buprenorphine group than in the medetomidine group after the first injection of the analgesics. pCO2 and pH were similar in both of the groups. Medetomidine decreased heart rate after every injection, this fall and subsequent rise might be avoided by a lower dose regime. Buprenorphine did not effect heart rate. Rectal temperature did not differ in either group. It was concluded that medetomidine, and other alpha 2-agonists, possess some potential in postoperative pain alleviation.

Genetic parameters for racing records in trotters using linear and generalized linear models.

Heritability and repeatability and genetic and phenotypic correlations were estimated for trotting race records with linear and generalized linear models using 510,519 records on 17,792 Finnhorses and 513,161 records on 25,536 Standardbred trotters. Heritability and repeatability were estimated for single racing time and earnings traits with linear models, and logarithmic scale was used for racing time and fourth-root scale for earnings to correct for nonnormality. Generalized linear models with a gamma distribution were applied for single racing time and with a multinomial distribution for single earnings traits. In addition, genetic parameters for annual earnings were estimated with linear models on the observed and fourth-root scales. Racing success traits of single placings, winnings, breaking stride, and disqualifications were analyzed using generalized linear models with a binomial distribution. Estimates of heritability were greatest for racing time, which ranged from 0.32 to 0.34. Estimates of heritability were low for single earnings with all distributions, ranging from 0.01 to 0.09. Annual earnings were closer to normal distribution than single earnings. Heritability estimates were moderate for annual earnings on the fourth-root scale, 0.19 for Finnhorses and 0.27 for Standardbred trotters. Heritability estimates for binomial racing success variables ranged from 0.04 to 0.12, being greatest for winnings and least for breaking stride. Genetic correlations among racing traits were high, whereas phenotypic correlations were mainly low to moderate, except correlations between racing time and earnings were high. On the basis of a moderate heritability and moderate to high repeatability for racing time and annual earnings, selection of horses for these traits is effective when based on a few repeated records. Because of high genetic correlations, direct selection for racing time and annual earnings would also result in good genetic response in racing success.

Effects of racing on equine fertility.

Racing and fertility are connected with each other in many ways. Stress and increased body temperature induced by racing may have negative effects on fertility, but on the other hand, high quality nutrition and management of racing horses may have positive effects. Fertility may also be genetically associated with racing performance. The analysed data consisted of Finnish mating records of Standardbreds (n=33,679) and Finnhorses (n=32,731), from 1991 to 2005, and the harness racing records of both mares and stallions. Fertility was measured by foaling outcome, and racing performance was measured by best time and number of races. We used racing results from the mating year and from the entire career, to study both short-term and long-term effects of racing on fertility. The analyses were conducted with a linear mixed model, where racing was fitted as a fixed factor. In a separate bivariate analysis we measured the genetic correlation of racing and fertility, applying a threshold model for the fertility trait. For mares, racing after the first mating or more than 10 times during the mating year diminished the foaling outcome. However, racing only before the first mating or 1-5 times during the mating year had positive effects on mare fertility. Stallion fertility did not suffer from racing during the mating year. The mares with the best career racing records had the highest foaling rates, but this was probably due to preferential treatment. The genetic correlation between best racing record and fertility was favourable but weak in the Finnhorse (-0.24±0.08), and negligible in the Standardbred (-0.15±0.11).