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Absolute cross-sectional area measurements in quantitative coronary arteriography by dual-energy DSA.

Recent studies have emphasized the limitations of conventional coronary angiography. These limitations include the lack of correlation between the severity of coronary stenosis as estimated from coronary angiograms and the actual severity of stenotic lesions measured in postmortem hearts. As a result, attempts have been made to quantitate luminal dimension more precisely. The application of quantitative digital subtraction angiography (DSA) in the assessment of coronary artery lesion dimension has been limited by cardiac and respiratory motion artifacts. We have reported previously on a motion-immune dual-energy (DE) cardiac mode in which kVp and filtration are switched at 30 Hz. To assess the potential advantages of a videodensitometric technique for quantification of absolute vessel cross-sectional area (CSA), three different quantitative coronary arteriography (QCA) algorithms were compared. The three algorithms under comparison were a videodensitometric (V) algorithm, which does not require any geometric assumption for absolute vessel CSA measurement, and videodensitometric (VC) and edge detection (ED) algorithms, which do require the assumption of circular cross-section for CSA measurements. A cylindrical vessel phantom (0.5-4.75 mm in diameter) and a crescentic vessel phantom, producing 25% to 90% area stenosis, were imaged over the chest of a humanoid phantom. The low- and high-energy images were corrected for scatter and veiling glare before energy subtraction. For CSA measurements in crescentic vessel phantoms, the V algorithm produced significantly improved results (slope = 0.87, intercept = 0.51 mm2, r = .95) when compared to the VC (slope = 1.05, intercept = 4.19 mm2, r = .75) and the ED (slope = 1.57, intercept = 5.21 mm2, r = .60) algorithms.

Algorithms↗

Implications of the linear pressure-natriuresis relationship and importance of sodium sensitivity in hypertension.

Although the concept of the pressure-natriuresis curve is very clear, considerable confusion concerning its importance and utility in understanding the pathophysiology of hypertension persists. We recently showed that the pressure-natriuresis curve could be considered linear. In this brief review, we would like to stress the advantages of treating it as a line. Its linear approximation simplifies understanding of the sodium sensitivity of the blood pressure and mechanisms of hypertension. The blood pressure can be expressed as the sum of two components: the non-sodium-sensitive component determined by the x intercept of the pressure-natriuresis curve and the sodium sensitive one determined by the product of the reciprocal of the slope and the amount of sodium intake. Theoretically, it can be affected in two different ways to cause hypertension; either a parallel shift along the blood pressure axis toward a higher blood pressure level due to the increase in the x intercept or a decrease in the slope. The parallel shift induces non-sodium-sensitive hypertension, whereas the decrease in slope induces sodium-sensitive hypertension. Thus, the linear approximation makes the definition of the sodium sensitivity of the blood pressure very clear and, furthermore, suggests that mechanisms of hypertension can be clarified if the determinants of the x intercept and the slope of the pressure-natriuresis curve are known. A clear definition of sodium sensitivity allows us to study its importance as a marker of a greater risk of renal and cardiovascular complications.

Animals↗

ULFS-49 causes bradycardia without decreasing right ventricular systolic and diastolic performance.

The effects of ULFS-49, a new calcium channel blocker, on right ventricular (RV) systolic and diastolic performance were evaluated in nine anesthetized, closed-chest dogs by load-insensitive indexes. ULFS-49 (0.3 mg/kg) decreased heart rate (HR) from 76 +/- 25 to 47 +/- 11 beats/min (p less than 0.01) and cardiac output (CO) from 1.89 +/- 0.62 to 1.42 +/- 0.72 L/min (p less than 0.01), as RV free wall end-diastolic area increased from 486 +/- 126 to 581 +/- 45 mm2 (p less than 0.01) and RV end-diastolic volume increased from 66.6 +/- 26.4 to 85.3 +/- 28.5 ml (p less than 0.05). Pacing at 100 beats/min ablated these hemodynamic and dimensional changes. RV free wall contractility was assessed by the slope and midrange intercept values of the relation between RV end-systolic pressure (Pes) and end-systolic free wall area (Aes) and between RV free wall segmental work (SW) and end-diastolic area (Aed). RV free wall stiffness was measured by exponential fit of the RV end-diastolic pressure (Ped)-Aed points during caval occlusion. With pacing at 100 beats/min, the slope of the Pes-Aes relationship was unchanged by ULFS-49 (0.52 +/- 0.29 vs. 0.60 +/- 0.35 mm Hg/mm2) as was the midrange intercept (382.3 +/- 114.7 vs. 387.1 +/- 121.5 mm2). After administration of ULFS-49, the slope of the SW-Aed relation increased from 31.8 +/- 14.4 to 37.3 +/- 17.7 mm Hg.mm2 (p less than 0.05) without changing the midrange intercept (410.5 +/- 108.1 mm2 vs. 413.0 +/- 107.0 mm2). Similarly, neither the position nor curvature of the Ped-Aed relation was changed by ULFS-49. These data demonstrate that ULFS-49 causes significant bradycardia and increases the size of the right ventricle without directly depressing RV free wall systolic or diastolic performance.

Animals↗

Relationship between % heart rate reserve and % VO2 reserve in treadmill exercise.

For exercise prescription purposes, it is often assumed that % heart rate reserve (%HRR) provides equivalent intensities to %VO2max. However, a recent study from this laboratory demonstrated that during cycling exercise %HRR is not equivalent to %VO2max, but is instead equivalent to a percentage of the difference between resting and maximal VO2, i.e., % VO2reserve (%VO2R). The current study examined these relationships during treadmill exercise. Fifty adults performed Bruce protocol treadmill tests to exhaustion. For each subject, data obtained at rest, at the end of each stage, and at maximum were used to determine linear regressions of %HRR versus %VO2max, and of %HRR versus %VO2R. For %HRR versus %VO2max the mean intercept and slope were -6.1+/-0.7 and 1.10+/-0.01, respectively, with a mean r of 0.990+/-0.002. For %HRR versus %VO2R, the mean intercept and slope were 1.5+/-0.6 and 1.03+/-0.01, respectively, with a mean r of 0.990+/-0.002. Both regressions differed statistically from the line of identity (i.e., intercept of 0 and slope of 1). However, the regression of %HRR versus %VO2R was significantly closer (P < 0.001 ) to the line of identity than was the regression of %HRR versus %VO2max. We conclude that %HRR should be considered as an indicator of %VO2R, not %VO2max, when prescribing treadmill exercise, as was previously concluded for cycling exercise.

Adolescent↗

Multilevel modeling of a clustered continuous outcome: nurses' work hours and burnout.

BACKGROUND: Multilevel models were designed to analyze data generated from a nested structure (e.g., nurses within hospitals) because conventional linear regression models underestimate standard errors and, in turn, overestimate test statistics. OBJECTIVES: To introduce 2 types of multilevel models, the random intercept model and the random coefficient model, to describe the correlation among observations within a cluster, and to demonstrate how to identify the superior model. METHOD: The conceptual and mathematical bases for the 2 multilevel model types are presented. Intraclass correlation is defined and assessment of model fit is detailed. An empirical example is presented in which average work hours per week and burnout are analyzed using data from 4,320 staff nurses clustered in 19 hospitals. RESULTS: Average work hours were positively associated with nurse burnout. The multilevel models corrected the problem of underestimated standard errors in conventional linear regression models. Graphs displaying the hospital-level differences illustrated the 2 multilevel model types. Although the multilevel models corrected the underestimation of standard errors, the results did not differ substantively for the conventional or the 2 multilevel models. The intraclass correlation coefficient was .044, indicating that the extent of shared variance among nurses in a hospital was low. The random intercept model fit the data better than did the random coefficient model. CONCLUSIONS: Multilevel models provide a more accurate and comprehensive description of relationships in clustered data than do conventional models, by correcting underestimated standard errors, by estimating components of variance at several levels, and by estimating cluster-specific intercepts and slopes.

Burnout, Professional↗

Post-test quality control for the single blood sample technique in glomerular filtration rate measurement in children.

BACKGROUND: While the value of the single blood sample (SBS) method for estimating 51Cr-EDTA plasma clearance has been repeatedly demonstrated, some nuclear medicine physicians are still reluctant to use it because of the lack of quality control parameters. PURPOSE: To present a post-test quality control procedure for the SBS technique in children. METHODS: In addition to the SBS clearance calculated using the specific paediatric SBS method, three artificial slope intercept (ASI) method clearances were calculated by assuming the distribution volume as, respectively, 20%, 25% and 30% of body weight. By dividing the injected activity by the distributional volume, the initial plasma concentrations (A0,30%, A0,25% and A0,20%) were calculated. Using these A0 values and the available single sample, ASI clearances were calculated by using the classical slope-intercept method. The working hypothesis of this approach was as follows. In the absence of significant errors, the three ASI clearance values should be close to that of the SBS method. This hypothesis has been tested using both simulated and patients' data. RESULTS: The results of the simulated study showed that an error in the injected dose produced variable differences between SBS and ASI clearances depending on the clearance values. The effect of an error on the plasma sample also varied as a function of the clearance values. The analysis of patient data revealed that the ASI approach allowed the identification of patients in whom the classical slope-intercept method suggested the presence of a possible error. CONCLUSION: A post-test quality control procedure for the SBS GFR measurement is presented. When the SBS clearance shows a difference with the ASI method (> 10 ml . min(-1) per 1.73 m2), the presence of an error is highly probable. A smaller difference, however, does not exclude erroneous data.

Child↗

Fixation disparity analysis of oculomotor imbalance.

A device and method for measuring forced vergence fixation disparity curves in clinical situations are described. Phoria, vergence, and fixation disparity are measures of different functions of the oculomotor system. In decreasing order of diagnostic effectiveness, four features of the fixation disparity curve are curve type, slope, Y-intercept, and X-intercept. Patients with exophoria and non-Type I curves are likely to have ocular discomfort. The steeper the curve, the more likely the patient is to have symptoms. However, Type IV curves are usually flat, and many of these patients do have symptoms. Patients with Type I curves respond well to visual training, but those with Type II curves generally need lenses or prisms to obtain relief. The Y-intercept gives information that is particularly useful in exophoric patients. A complete analysis of the oculomotor system requires measurement of both phoria/vergence and fixation disparity.

Eyeglasses↗

Problems with use of the end systolic pressure-volume slope as an indicator of left ventricular contractility: an alternate method.

The use of end-systolic elastance as a parameter of left ventricular contractility is based on a theory put forward by Sagawa and is limited by an assumed linearity of the model for a time varying compliance. A major problem is the contractility-dependent curvilinearity of the end-systolic pressure-volume relationship (ESPVR), which may result in intercept volumes that are below a passive unstretched volume. Based on the experimental data of Burkhoff et al., we demonstrate the reasons for the lack of correlation of the slope (k) of the end-systolic pressure (P(es))-volume (V(es)) relationship with ventricular contractility. A parabolic relation, P(es) = a x V(es)2 + b x V(es) + c, was used for approximation of the ESPVRs, as proposed by Burkhoff et al., and the slope (k = 2 x a x V(es) + b), together with the volume axis intercepts (V0), calculated for the tangents for all P(es)/V(es) points of the ESPVRs. The results demonstrate the volume range dependence of the slope and V0 of linear regression lines. However, intercepts of the ESPVRs tangents with a midrange constant pressure line (e.g., 80 mmHg or 100 mmHg) justify the use of the shift of the end-systolic pressure-volume relationship as a parameter of left ventricular contractility. This method appears to be valid over a much wider range of end-systolic volumes than is the use of the slope alone.

Animals↗

Monte carlo simulation of the mixed alkali effect with cooperative jumps

In our previous works on molecular dynamics (MD) simulations of lithium metasilicate (Li2SiO3), it has been shown that the long time behavior of the lithium ions in Li2SiO3 has been characterized by the component showing the enhanced diffusion (Levy flight) due to cooperative jumps. It has also been confirmed that the contribution of such component decreases by interception of the paths in the mixed alkali silicate (LiKSiO3). Namely, cooperative jumps of like ions are much decreased in number owing to the interception of the path for unlike alkali-metal ions. In the present work, we have performed a Monte Carlo simulation using a cubic lattice in order to establish the role of the cooperative jumps in the transport properties in a mixed alkali glass. Fixed particles (blockage) were introduced instead of the interception of the jump paths for unlike alkali-metal ions. Two types of cooperative motions (a pull type and a push type) were taken into account. Low-dimensionality of the jump path caused by blockage resulted in a decrease of a diffusion coefficient of the particles. The effect of blockage is enhanced when the cooperative motions were introduced.

Journal Article↗

Effects of covariate measurement error in the initial level and rate of change of an exposure variable.

When repeated measures of an exposure variable are obtained on individuals, it can be of epidemiologic interest to relate the slope of this variable over time to a subsequent response. Subject-specific estimates of this slope are measured with error, as are corresponding estimates of the level of exposure, i.e., the intercept of a linear regression over time. Because the intercept is often correlated with the slope and may also be associated with the outcome, each error-prone covariate (intercept and slope) is a potential confounder, thereby tending to accentuate potential biases due to measurement error. Under a familiar mixed linear model for the exposure measurements, we present closed-form estimators for the true parameters of interest in the case of a continuous outcome with complete and equally timed follow-up for all subjects. Generalizations to handle incomplete follow-up, other types of outcome variables, and additional fixed covariates are illustrated via maximum likelihood. We provide examples using data from the Multicenter AIDS Cohort Study. In these examples, substantial adjustments are made to uncorrected parameter estimates corresponding to the health-related effects of exposure variable slopes over time. We illustrate the potential impact of such adjustments on the interpretation of an epidemiologic analysis.

Acquired Immunodeficiency Syndrome↗

How dogs navigate to catch frisbees.

Using micro-video cameras attached to the heads of 2 dogs, we examined their optical behavior while catching Frisbees. Our findings reveal that dogs use the same viewer-based navigational heuristics previously found with baseball players (i.e., maintaining the target along a linear optical trajectory, LOT, with optical speed constancy). On trials in which the Frisbee dramatically changed direction, the dog maintained an LOT with speed constancy until it apparently could no longer do so and then simply established a new LOT and optical speed until interception. This work demonstrates the use of simple control mechanisms that utilize invariant geometric properties to accomplish interceptive tasks. It confirms a common interception strategy that extends both across species and to complex target trajectories.

Animals↗

Characteristics of the inhibition of rat brain monoamine oxidase in vitro by MD780515.

The inhibiton of type A and B MAO in rat forebrain crude membrane preparation by MD780515, (3-(4-[(3-cyanophenyl)methoxy]phenyl)-5-(methoxymethyl)-2-oxazolidinone-Centre de Recherche Delalande, France) has been investigated in vitro with 5-hydroxytryptamine and beta-phenylethylamine as substrates. The inhibition of the high-affinity binding of [3H]harmaline, a specific marker of type A MAO, was also studied. In the experimental conditions used, MD780515 appeared to be a pure mixed MAO inhibitor (MAOI) of 5-HT deamination, both Km and Vmax being altered [Ki (Dixon) = Ki, (slope) = 2 nM; Ki (intercept) = 12 nM]. Phenylethylamine oxidation could be considered to be noncompetitively inhibited by MD780515 (Ki (slope) = 78 nM; Ki (intercept) = 103 nM). Dixon and intercept replots were hyperbolic, suggesting that, at high concentrations, PEA could be deaminated by both forms of MAO. This hypothesis was confirmed by biphasic inhibition curves of 80 microM-PEA obtained when MD780515, clorgyline, harmaline and deprenyl were used at MAOIs. MD780515 was a potent inhibitor (IC50 = 1-2 nM) of [3H]harmaline binding. Comparatively, clorgyline, 'cold' harmaline and Lilly 51641 inhibited 3H ligand binding, with IC50 of 5, 7 and 40 nM respectively. In conclusion, MD780515 is a reversible, specific and potent type A MAOI.

Animals↗

Homogeneous substrate-labeled fluorescent immunoassay for carbamazepine.

Carbamazepine is an anticonvulsant drug useful in the management of epilepsy. Because of the narrow therapeutic range, serum carbamazepine monitoring is useful for ensuring adequate drug therapy without toxicity. We report the development of a homogeneous substrate-labeled fluorescent immunoassay for carbamazepine in human serum. A carbamazepine fluorogenic reagent (FR) has been synthesized. Upon hydrolysis by beta-galactosidase, the nonfluorescent FR produces a fluorescent product. This enzymic hydrolysis sin inhibited when the FR binds with antibody against carbamazepine. The inhibition is relieved when carbamazepine competes with FR for available antibody binding sites. Thus, increasing levels of carbamazepine result in increasing levels of fluorescence that can be conveniently monitored with any conventional fluorometer. For low, medium, and high control sera (4, 12, and 16 micrograms carbamazepine/ml), the within-run coefficient of variation for the assay is 5.5%, 1.6%, and 2.9%, respectively, while the respective between-run coefficients of variation are 3.5%, 1.9%, and 2.3%. Fifty-three clinical serum samples were assayed by the SLFIA, gas chromatography (GC), high pressure liquid chromatography (HPLC), and an enzyme immunoassay method. The SLFIA method compares favorably with the HPLC technique (r - 0.97, slope = 1.10, y-intercept = 1.21), the enzyme immunoassay (r = 0.98, slope = 1.07, y-intercept = 0.82), and the GC method (r = 0.95, slope = 1.01, y-intercept = -0.03).

Antibodies↗

O(2) delivery and the venous P(O(2))-O(2) uptake relationship in pump-perfused canine muscle.

Under the conditions of both an increased red cell affinity for O(2) at a constant rate of O(2) delivery (arterial O(2) content x flow) and a decrease in the rate of O(2) delivery induced by hypoxic hypoxia at constant blood flow, we have obtained a linear relationship between the partial pressure of O(2) in the muscle venous effluent (P(v,)(O(2))) and O(2) uptake (.V(O(2))). The relationship is described by the equation .V(O(2)) = D(a) x P(v,)(O(2)) + .V(O(2)conv)) where D(a) is the apparent O(2) diffusion capacity and .V(O(2)conv)) is O(2) delivery-limited .V(O(2)), and D(a) x P(v,)(O(2)) represents the O(2) diffusion-limited .V(O(2)) .V(O(2)diff)). From these observations, we propose the hypothesis that .V(O(2)) consists of two additive values, .V(O(2)conv)) and .V(O(2)diff)). The mechanism underlying the reduction in .V(O(2)) that is induced by reducing O(2) delivery to markedly below the .V(O(2)conv)) value has only been investigated using a model based on the single compartment of diffusion-limited .V(O(2)), and has not been investigated in terms of this additive .V(O(2)) model. The single compartment analysis appears to overestimate the role of O(2) diffusion in limiting the reduction of .V(O(2)) that occurs in response to a decrease in O(2) diffusion capacity, as reflected by the .V(O(2))/P(v,)(O(2)) ratio. To gain better insight into the mechanism involved, we altered the rate of O(2) delivery by changing arterial P(O(2)) from normoxia (with inhalation of air) to hypoxia (by inhalation of 10-11 % O(2)) and blood flow (with high and low flow rates (n = 7 for both groups), and very low and ischaemic flow rates (n = 4 for both groups)) in pump-perfused dog gastrocnemius preparations during tetanic isometric contractions at 1 Hz. As rates of O(2) delivery were reduced from 23.2 to 10.9 ml min(-1) (100 g)(-1), significant decreases in P(v,)(O(2)) and .V(O(2)) were observed (P < 0.05). From the data of P(v,)(O(2)) and .V(O(2)) values within this range of O(2) delivery rates, we obtained the regression equation .V(O(2)) = 0.22 x P(v,)(O(2)) + 8.14 (r = 0.58). From the equation, the intercept of the .V(O(2))-axis was significantly different from zero (P < 0.05), in accordance with the observation that the .V(O(2)) /P(v,)(O(2)) ratio (ml min(-1) (100 g)(-1) Torr(-1)) increased from 0.54 to 1.35 (P < 0.05). However, at extremely low rates of O(2) delivery (5.6 and 7.3 ml min(-1) (100 g)(-1) the .V(O(2))/P(v,)(O(2)) ratio was 1.51 and 2.80 (P < 0.05), respectively. This indicates a break in the linear .V(O(2))-P(v,)(O(2)) relationship as the rate of O(2) delivery was reduced to below the .V(O(2)conv)) value of the .V(O(2))-axis intercept. These results suggest that the reduction in .V(O(2)) caused by extreme reductions in the rate of O(2) delivery is not attributable to a reduction in O(2) diffusion capacity, as expected from the .V(O(2))/P(v,)(O(2)) ratio, but to a reduction in the O(2) delivery-limited .V(O(2)) component, as evaluated by the .V(O(2))-axis intercept of the linear .V(O(2))-P(v,)(O(2)) relationship.

Animals↗

'Off' tails of intramembrane charge movements in frog skeletal muscle in perchlorate-containing solutions.

1. Charge movements in response to hyperpolarizing ('off') voltage-clamp steps were examined in frog skeletal muscle fibres in the presence of 8 mM-perchlorate. 2. The appearance of prolonged 'off' decays, of duration 50-100 ms coincided with those of slow 'q gamma' charge transfers in preceding 'on' transients. 3. Charge was conserved in the presence of perchlorate whether testing or pre-pulse voltages were varied. Additionally, steady-state charge as a function of voltage was independent of the direction from which the voltage was reached. 4. 'Off' recoveries were most prolonged at voltages around -90 to -100 mV and became less marked with depolarization. 5. Charging currents in response to hyperpolarizing steps that intercepted prolonged ('q gamma') 'on' decays showed reduced slow 'off' tails but intact 'off' decays at early times. 6. Transients elicited by depolarizing steps that intercepted 'off' tail currents showed decreased slow 'on' components. By varying the time at which 'off' responses were so intercepted, it was shown that 'off' tails can require well over 100 ms to attain a steady state in perchlorate. 7. Prolonged depolarization to a holding potential of -30 mV inactivated delayed ('q gamma') components in both 'on' and 'off' responses but left the more rapid ('q beta') decays intact. 8. These observations are easier to reconcile with parallel systems responsible for independent early ('q beta') and delayed ('q gamma') transients in both 'on' and 'off' steps than with the existence of 'q beta' and 'q gamma' transitions in a causal sequence.

Action Potentials↗

Extending the theory of dash running.

I extend the theory of dash running by allowing resisting force to be proportional to any positive power of speed and by allowing the runner to be tractive-force-limited at the beginning of the dash and developable-force-limited subsequently. I solve the equation of motion and express the maximum value of developable force as a function of limiting dash velocity, resisting-force/velocity exponent, and indoor and outdoor-track asymptotic intercept times (the intercepts with the time axis of asymptotic lines that are fitted to the distance-time curves) and limiting tractive coefficients. For a 20-yr-mean world record limiting dash velocity of 10.33 m/s and indoor and outdoor asymptotic intercept times of 0.617 and 0.265 s, I find that a composite dash world record holder is tractive-force-limited on indoor tracks, that limiting indoor tractive coefficient is about 0.9, and that the maximum value of developable force exceeds 2.0 times the record holder's weight.

Biophysical Phenomena↗

A cross-linguistic investigation of locus equations as a phonetic descriptor for place of articulation.

A previous study [H. Sussman, H. McCaffrey, and S. Matthews, J. Acoust. Soc. Am. 90, 1309-1325 (1991)] of American English CV coarticulation showed a remarkably linear relationship between onset frequencies of F2 transitions, plotted on the y axis, in relation to the F2 midvowel "target" frequencies, plotted on the x axis, for CVC tokens with initial [b d g] and ten medial vowel contexts. Slope and y-intercept values of regression functions fit to these scatterplots ("locus equations") were shown to serve as statistically powerful phonetic descriptors of place of articulation. The present study extends the locus equation metric to three additional languages--Thai, Cairene Arabic, and Urdu--having both two and four place contrasts for syllable-initial voiced stops. A total of 14 speakers (Thai = 6, Arabic = 3, Urdu = 5) produced 1740 CVC tokens that were acoustically analyzed using MacSpeech Lab II. Strong linear regression relationships were found for every stop category across all speakers. Slopes and y intercepts systemically varied as a function of place of articulation. Cross-language comparisons of stop place categories were performed but variability of slope and y intercept means tempered conclusions concerning the existence of CV "phonetic hot spots."

Adult↗

Dry-heat destruction of Bacillus subtilis spores on surfaces: effect of humidity in an open system.

Bacillus subtilis var. niger spores were tested for dry-heat resistance on stainless-steel strips hung in an oven. Heat resistance was dependent on the relative humidity before and during treatment, which in turn affected the water content of the spores. Higher humidities increased the heat resistance of the spores. D-values ranged from 16.1 min for spores conditioned at <2% relative humidity (RH) and treated at 0.34% RH to 37.6 min for spores conditioned at 89% RH and treated at 1.1% RH. The y-intercept of the regression line ranged from 6.94 x 10(4) for spores conditioned and treated at the low humidities to 2.00 x 10(5) for spores conditioned at 89% RH and treated at 0.34% RH. For a constant value of N(0), the y-intercept appears to be lowered by low-humidity conditions. The statistic log y(0)/log N(0) is used to measure the downward displacement of the regression line. Values obtained in this experiment range from 0.90 for spores conditioned at <2% RH and treated at 0.34% RH to 1.04 for spores conditioned at <2% RH and treated at 1.1% RH. A combination of linear regression and analysis of variance methods was used for data analysis. The former estimates D-values and y-intercepts, whereas the latter is sensitive to differences between treatments.

Analysis of Variance↗