Time Required for Lameness Detection on an Embedded Microcomputer Based Force Plate in a Lab Based Setting

The objective of this study was to determine the minimum time required for the embedded microcomputer based force plate (force plate) to detect lameness. The force plate can be placed under an electronic sow feeder or a gestation stall to routinely assess lameness. Previous work with the force plate has required sows to remain standing in a gestation stall for longer than a typical feeding time allotment of 9 minutes to measure the force applied to each foot. Comparing sows’ weight distribution across time showed that an adjustment period is required before force distribution measurements are consistent, as the sows adapts to the force plate. When using a 30 second adjustment period, sows only needed to stand on the force plate for 210 seconds in order to have a consistent reading across time. This could create a labor reduction during research trials, and allow more data to be used from a commercial setting, than when using the previous times

Dynamic space utilization for lame and non-lame gestating sows estimated by the lying-standing sequence

peer-reviewedThe objective of this study was to estimate the dynamic space utilization for lame and non-lame sows using their lying-standing postural sequence profile. Eighty-five sows (parity 0.9 ± 1.14; range 0 to 4) were used. Sows were moved to a pen on 30, 60 and 90 days of gestation and a ceiling mounted camera was installed above the pen to record one lying-standing event per sow. Observations ceased when the sow lied and stood, or 2.5 h elapsed from recording commencement. Additionally, each sow was evaluated for walking lameness while moving from their gestation stall to the pen. Still frames were captured from the sows’ lying and standing sequences and were combined into a single image and measured by counting pixels from contouring the sows’ body (CONTOUR), overlaying a grid on the sow image and counting any square including any part of the sow (FULL-GRID) and only counting any square that was half full or more (HALF-GRID). The space utilized while turning around was calculated by measuring the sows’ length from snout to the base of the tail and using that length as the diameter of a circle (D-PIVOT), or as the radius of a circle (R-PIVOT). Parity was re-classified as 0, 1, and 2+. There were no observed differences in the dynamic space utilized to lie, stand or turn around between lame and non-lame sows (P > 0.05). On average, sows used 1.2 ± 0.47 m2 to lie and 1.3 ± 0.46 m2 to stand. There was no difference between the CONTOUR and HALF-GRID methods (P > 0.05); however, using the FULL-GRID sows required 0.3 m2 more floor area to lie and stand compared with the other measuring methods (P < 0.05). Space used to turn around differed between measuring method (P < 0.05). Sows required 1.9 ± 0.18 m2 for D-PIVOT and 7.3 ± 0.18 m2 for R-PIVOT to turn around. Space utilized to lie-down and stand-up increased as gestation progressed (P < 0.05). Under the conditions of this study, lameness did not influence dynamic space utilization; however, lameness recorded was relatively mild and might not have been sufficiently severe to significantly affect the results. These results could be important in decision-making process for housing specifications regarding US sow gestation housing

Bone cell-independent benefits of raloxifene on the skeleton: A novel mechanism for improving bone material properties

Authors' accepted manuscript. Bone Biology Laboratory http://www.iupui.edu/~bonelab/ Department of Anatomy and Cell Biology Indiana University School of Medicine Department of Biomedical Engineering IUPUIRaloxifene is an FDA approved agent used to treat bone loss and decrease fracture risk. In clinical trials and animal studies, raloxifene reduces fracture risk and improves bone mechanical properties, but the mechanisms of action remain unclear because these benefits occur largely independent of changes to bone mass. Using a novel experimental approach, machined bone beams, both from mature male canine and human male donors, were depleted of living cells and then exposed to raloxifene ex vivo. Our data show that ex vivo exposure of non-viable bone to raloxifene improves intrinsic toughness, both in canine and human cortical bone beams tested by 4-point bending. These effects are cell-independent and appear to be mediated by an increase in matrix bound water, assessed using basic gravimetric weighing and sophisticated ultrashort echo time magnetic resonance imaging. The hydroxyl groups (-OH) on raloxifene were shown to be important in both the water and toughness increases. Wide and small angle x-ray scattering patterns during 4-pt bending show that raloxifene alters the transfer of load between the collagen matrix and the mineral crystals, placing lower strains on the mineral, and allowing greater overall deformation prior to failure. Collectively, these findings provide a possible mechanistic explanation for the therapeutic effect of raloxifene and more importantly identify a cell-independent mechanism that can be utilized for novel pharmacological approaches for enhancing bone strength.The authors would like to thank Dr. Paul K. Hansma (Department of Physics, University of California, Santa Barbara), for suggesting the soaking technique and Dr. John Okasinski, Advanced Photon Source, for helping collect the WAXS data. Raloxifene was kindly provided by Eli Lilly (Indianapolis, IN, USA) under a Material Transfer Agreement to D.B.B. Eli Lilly was not involved in the study design, analyses or interpretation of the results. We are grateful to Dr. Susan J. Gunst for sharing dog tissue. Use of the Advanced Photon Source was supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. This work was supported by NIH grants to D.B.B. and M.R.A

The destruction and survival of dust in the shell around SN 2008S

SN 2008S erupted in early 2008 in the grand design spiral galaxy NGC 6946. The progenitor was detected by Prieto et al. in Spitzer Space Telescope images taken over the four years prior to the explosion, but was not detected in deep optical images, from which they inferred a self-obscured object with a mass of about 10 Msun. We obtained Spitzer observations of SN 2008S five days after its discovery, as well as coordinated Gemini and Spitzer optical and infrared observations six months after its outburst. We have constructed radiative transfer dust models for the object before and after the outburst, using the same r^-2 density distribution of pre-existing amorphous carbon grains for all epochs and taking light-travel time effects into account for the early post-outburst epoch. We rule out silicate grains as a significant component of the dust around SN 2008S. The inner radius of the dust shell moved outwards from its pre-outburst value of 85 AU to a post-outburst value of 1250 AU, attributable to grain vaporisation by the light flash from SN 2008S. Although this caused the circumstellar extinction to decrease from Av = 15 before the outburst to 0.8 after the outburst, we estimate that less than 2% of the overall circumstellar dust mass was destroyed. The total mass-loss rate from the progenitor star is estimated to have been (0.5-1.0)x10^-4 Msun yr^-1. The derived dust mass-loss rate of 5x10^-7 Msun yr^-1 implies a total dust injection into the ISM of up to 0.01 Msun over the suggested duration of the self-obscured phase. We consider the potential contribution of objects like SN 2008S to the dust enrichment of galaxies.Comment: 9 pages, 7 figures, 3 tables. rv2. To appear in MNRA

Objective evaluation of female feet and leg joint conformation at time of selection and post first parity in swine

peer-reviewedFeet and legs of replacement females were objectively evaluated at selection, i.e., approximately 150 d of age (n = 319) and post first parity, i.e., any time after weaning of first litter and before second parturition (n = 277) to 1) compare feet and leg joint angle ranges between selection and post first parity; 2) identify feet and leg joint angle differences between selection and first 3 wk of second gestation; 3) identify feet and leg joint angle differences between farms and gestation days during second gestation; and 4) obtain genetic variance components for conformation angles for the two time points measured. Angles for carpal joint (knee), metacarpophalangeal joint (front pastern), metatarsophalangeal joint (rear pastern), tarsal joint (hock), and rear stance were measured using image analysis software. Between selection and post first parity, significant differences were observed for all joints measured (P 0.8) between the front leg joints and low (<0.2) between the rear leg joints. High genetic correlations between time points indicate that the trait can be considered the same at either time point, and low genetic correlations indicate that the trait at different time points should be considered as two separate traits. Minimal change in the front leg suggests conformation traits that remain between selection and post first parity, while larger changes in rear leg indicate that rear leg conformation traits should be evaluated at multiple time periods