Calculates Pcrit (commonly understood as the threshold below which oxygen consumption rate can no longer be sustained) based on paired PO2 and MO2 values. Five Pcrit metrics are returned: the traditional breakpoint metric (broken stick regression), the nonlinear regression metric (Marshall et al. 2013), the sub-prediction interval metric (Birk et al. 2019), the alpha-based Pcrit method (Seibel et al., in prep), and the linear low O2 (LLO) method (Reemeyer & Rees 2019). To see the Pcrit values plotted, see plot_pcrit
.
calc_pcrit(
po2,
mo2,
level = 0.95,
iqr = 1.5,
NLR_m = 0.065,
MR = NULL,
mo2_threshold = Inf,
return_models = FALSE
)
a vector of PO2 values. Any unit of measurement should work, but the NLR calculation was optimized using kPa. If the NLR metric is giving you trouble, try converting to kPa using conv_o2
.
a vector of metabolic rate values. Must be the same length and corresponding to po2
.
applies to the Sub_PI
metric only. Percentage at which the prediction interval should be constructed. Default is 0.95.
applies to the Sub_PI
metric only. Removes mo2
observations that are this many interquartile ranges away from the mean value for the oxyregulating portion of the trial. If this filtering is not desired, set to infinity. To visualize which observations will be removed by this parameter, use plot_pcrit
. Default is 1.5.
applies to the NLR
metric only. Pcrit is defined as the PO2 at which the slope of the best fitting function equals NLR_m
(after the MO2 data are normalized to the 90% quantile). Default is 0.065.
applies to the alpha
and LLO
metrics only. A numeric value for the metabolic rate at which pcrit_alpha
and pcrit_LLO
should be returned. If not supplied by the user, then the mean MO2 of the "oxyregulating" portion of the curve is applied for pcrit_alpha
and NA
is returned for pcrit_LLO
.
applies to the alpha
metric only. A single numeric value above which mo2
values are ignored for alpha
Pcrit estimation. Useful to removing obviously erroneous values. Default is Inf
.
logical. Should a list of model parameters be returned along with the converged Pcrit values? Default is FALSE
.
If return_models
is FALSE
(default), a named numeric vector of Pcrit values calculated using the Alpha
, Breakpoint
, LLO
, NLR
, and Sub_PI
metrics. If return_models
is TRUE
, then a list of converged Pcrit values, along with breakpoint function parameters, the MR
value used for calculating Pcrit-alpha, a data frame of the "oxyregulating" portion of the curve, and NLR parameters are returned.
Alpha is calculated from calc_alpha
and the Pcrit corresponding to MR
is returned. This determine's the animal's oxygen supply capacity and calculates the Pcrit at any given metabolic rate of interest.
Data are fit to a broken-stick regression using segmented
.
A subset of observations are chosen only from those with an MO2 < MR
. Then, a linear model is fit through the observations and Pcrit is calculated as the PO2 at which the line reaches MR
.
Data are fit to the following functions: Michaelis-Menten, Power, Hyperbola, Pareto, and Weibull with intercept. Following the method developed by Marshall et al. 2013, the function that best fits the data (smallest AIC) is chosen and the Pcrit is determined as the PO2 at which the slope of the function is NLR_m
(by default = 0.065 following the authors' suggestion).
This metric builds off the Breakpoint
metric and results in a systematically lower Pcrit value. This is useful for applications where it is important to ensure that Pcrit is not being overestimated. It represents a reasonable lower bounded estimate of the Pcrit value for a given trial. Once the Breakpoint
Pcrit is calculated, a 95% prediction interval (can be changed with the level
argument) is calculated around the oxyregulating region (i.e. using PO2 values > breakpoint Pcrit). By default, iqr
provides some filtering of abberant observations to prevent their influence on the calculated prediction interval. Finally, the Sub_PI Pcrit value is returned at the intersection of the oxyconforming line and the lower limit of the oxyregulating prediction interval.
Marshall, Dustin J., Michael Bode, and Craig R. White. 2013. <U+201C>Estimating Physiological Tolerances - a Comparison of Traditional Approaches to Nonlinear Regression Techniques.<U+201D> Journal of Experimental Biology 216(12): 2176<U+2013>82.
Birk, Matthew A., K.A.S. Mislan, Karen F. Wishner, and Brad A. Seibel. 2019. <U+201C>Metabolic Adaptations of the Pelagic Octopod Japetella Diaphana to Oxygen Minimum Zones.<U+201D> Deep-Sea Research Part I 148: 123<U+2013>31.
Seibel et al. in prep.
Reemeyer, Jessica E., and Bernard B. Rees. 2019. <U+201C>Standardizing the Determination and Interpretation of Pcrit in Fishes.<U+201D> Journal of Experimental Biology 222(18): jeb210633.
# NOT RUN {
mo2_data <- read.csv(system.file('extdata', 'mo2_v_po2.csv', package = 'respirometry'))
calc_pcrit(po2 = mo2_data$po2, mo2 = mo2_data$mo2)
# }
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