This package, is a data only package, part of a suite, which has package ‘photobiology’ at its core. Please visit (https://www.r4photobiology.info/) for more details. For more details on plotting spectra, please consult the documentation for package ‘ggspectra’, and for information on the calculation of summaries and maths operations between spectra, please, consult the documentation for package ‘photobiology’.
library(photobiology)
library(photobiologySensors)
library(photobiologyWavebands)
eval_ggspectra <- TRUE
library(ggspectra)
In this brief User Guide we describe how to re-scale the normalized spectra, and how to access individual spectra or subsets of spectra.
Spectra in the package are contained in one collection:
sensors.mspct
contains spectral data for various types of
broadband sensors.
In addition to the objects containing the data itself, several character vectors of names of spectra are provide to facilitate the retrieval of subsets of spectra.
The response_spct
member objects in
sensors.mspct
can be accessed through their names or
through a numeric index. As the numeric indexes are likely to change
with updates to the package, their use is discouraged. Names as
character strings should be used instead. They can also be retrieved
with method names()
.
## [1] "ams_TSL254R" "ams_TSL257"
## [3] "Analytik_Jena_UVX25" "Analytik_Jena_UVX31"
## [5] "Analytik_Jena_UVX36" "apogee_s2_131_FR"
## [7] "apogee_s2_131_R" "apogee_sq_100X"
## [9] "apogee_sq_500" "apogee_sq_610"
## [11] "apogee_su_200" "Berger_UV_Biometer"
## [13] "DeltaT_BF5" "flat_e"
## [15] "flat_q" "KIPP_CUV_5"
## [17] "KIPP_PQS1" "KIPP_UVS_A"
## [19] "KIPP_UVS_B" "KIPP_UVS_E"
## [21] "LICOR_LI_190SA" "LICOR_LI_200"
## [23] "LICOR_LI_210" "LICOR_LI_190"
## [25] "LICOR_LI_190R" "LICOR_LI_210R"
## [27] "sglux_TOCON_blue4" "sglux_SG01D_A"
## [29] "sglux_SG01D_B" "sglux_SG01D_C"
## [31] "sglux_SG01L" "Skye_SKE510"
## [33] "Skye_SKL310" "Skye_SKP210"
## [35] "Skye_SKP215" "Skye_SKR110_FR"
## [37] "Skye_SKR110_R" "Skye_SKS1110"
## [39] "Skye_SKU421" "Skye_SKU421a"
## [41] "Skye_SKU430a" "Skye_SKU440a"
## [43] "SolarLight_501_Biometer_high_UVA" "SolarLight_501_Biometer_low_UVA"
## [45] "SolarLight_501_Biometer_typical" "Solarmeter_SM60"
## [47] "Specmeters_3415F" "Thies_E1c"
## [49] "Vishay_VEML6075_UVA" "Vishay_VEML6075_UVB"
## [51] "Vital_BW_20"
We can use a character string as index to extract an individual
response_spct
object.
## Object: response_spct [182 x 2]
## Wavelength range 380.76093-797.90271 nm, step 0.5007704-4.006164 nm
## Label: LICOR LI 190R light sensor
## Time unit 1s
##
## # A tibble: 182 × 2
## w.length s.e.response
## <dbl> <dbl>
## 1 381. 0.00164
## 2 385. 0.00405
## 3 386. 0.00653
## 4 387. 0.00775
## 5 388. 0.0110
## 6 389. 0.0130
## 7 393. 0.0305
## 8 397. 0.0529
## 9 398. 0.0626
## 10 398. 0.0738
## # ℹ 172 more rows
## Object: response_spct [182 x 2]
## Wavelength range 380.76093-797.90271 nm, step 0.5007704-4.006164 nm
## Label: LICOR LI 190R light sensor
## Time unit 1s
##
## # A tibble: 182 × 2
## w.length s.e.response
## <dbl> <dbl>
## 1 381. 0.00164
## 2 385. 0.00405
## 3 386. 0.00653
## 4 387. 0.00775
## 5 388. 0.0110
## 6 389. 0.0130
## 7 393. 0.0305
## 8 397. 0.0529
## 9 398. 0.0626
## 10 398. 0.0738
## # ℹ 172 more rows
Be aware that according to R’s rules, using single square brackets
will return a response_mspct
object possibly of length one.
This statement is not equivalent to the one in the chunk immediately
above.
## Object: response_mspct [1 x 1]
## --- Member: LICOR_LI_190R ---
## Object: response_spct [182 x 2]
## Wavelength range 380.76093-797.90271 nm, step 0.5007704-4.006164 nm
## Label: LICOR LI 190R light sensor
## Time unit 1s
##
## # A tibble: 182 × 2
## w.length s.e.response
## <dbl> <dbl>
## 1 381. 0.00164
## 2 385. 0.00405
## 3 386. 0.00653
## 4 387. 0.00775
## 5 388. 0.0110
## 6 389. 0.0130
## 7 393. 0.0305
## 8 397. 0.0529
## 9 398. 0.0626
## 10 398. 0.0738
## # ℹ 172 more rows
##
## --- END ---
We can subset sensors.mspct
object by indexing with
vectors of character strings. The package provides some predefined ones,
and users can easily define their own, either as constants or through
computation. Here we use a vector defined by the package.
## Object: response_mspct [1 x 1]
## --- Member: Berger_UV_Biometer ---
## Object: response_spct [21 x 2]
## Wavelength range 279.872-378.458 nm, step 3.311-5.284 nm
## Label: Berger UV Biometer light sensor
## Time unit 1s
##
## # A tibble: 21 × 2
## w.length s.e.response
## <dbl> <dbl>
## 1 280. 0.747
## 2 285. 0.912
## 3 290. 1
## 4 295. 0.985
## 5 300. 0.770
## 6 305. 0.471
## 7 310. 0.215
## 8 315. 0.0782
## 9 320. 0.0263
## 10 325. 0.00845
## # ℹ 11 more rows
##
## --- END ---
More generally one can search for matching names within the collection of spectra.
## Object: response_mspct [1 x 1]
## --- Member: Berger_UV_Biometer ---
## Object: response_spct [21 x 2]
## Wavelength range 279.872-378.458 nm, step 3.311-5.284 nm
## Label: Berger UV Biometer light sensor
## Time unit 1s
##
## # A tibble: 21 × 2
## w.length s.e.response
## <dbl> <dbl>
## 1 280. 0.747
## 2 285. 0.912
## 3 290. 1
## 4 295. 0.985
## 5 300. 0.770
## 6 305. 0.471
## 7 310. 0.215
## 8 315. 0.0782
## 9 320. 0.0263
## 10 325. 0.00845
## # ℹ 11 more rows
##
## --- END ---
Set algebra operations can be used with the indexing vectors as each vector describes a single property: color, brand, type, etc.
## Object: response_mspct [1 x 1]
## --- Member: LICOR_LI_190 ---
## Object: response_spct [194 x 2]
## Wavelength range 381.85375-798.83668 nm, step 0.5005798-4.004638 nm
## Label: LICOR LI 190 light sensor
## Time unit 1s
##
## # A tibble: 194 × 2
## w.length s.e.response
## <dbl> <dbl>
## 1 382. 0.0272
## 2 382. 0.0291
## 3 383. 0.0310
## 4 384. 0.0349
## 5 386. 0.0425
## 6 389. 0.0559
## 7 390. 0.0613
## 8 390. 0.0650
## 9 391. 0.0689
## 10 392. 0.0766
## # ℹ 184 more rows
##
## --- END ---
The spectra are normalized, and consequently, several summaries expressed in absolute units are undefined, and trigger errors. Summaries like ratios which are not affected by normalization are allowed and valid. The data have been normalized as the measuring conditions used are not all the same, and in many cases not well characterized (e.g. distance to nearby reflecting walls, or exact alignment of the spectrometer input optics with respect to light sources).
What we will do in this section is to rescale the spectral data so that after conversion a given target value for a summary quantity will be true. As an example, we will rescale one spectrum so that it yields a response of 100 mol-1 m2for the range 400 to 700 nm.
my.spct <- fscale(sensors.mspct$LICOR_LI_190R,
range = PhR(),
q_response,
target = 100,
set.scaled = FALSE)
q_response(my.spct, PhR())
## R[/q]_PhR
## 100
## attr(,"time.unit")
## [1] "second"
## attr(,"radiation.unit")
## [1] "total photon response"
## R[/q]_]UVA.ISO
## 0.3119866
## attr(,"time.unit")
## [1] "second"
## attr(,"radiation.unit")
## [1] "total photon response"
If we want to treat the rescaled spectral data, as if they were true
readings with no scaling we can reset the attribute with method
setScaled()
. With method getScaled()
we can
test if a spectrum has been scaled.
## [1] FALSE
If for some obscure reason we want to simply “pretend” that the spectral data have not been normalized, we can permanently override the attribute on a copy of the data. Most of the time this is a very bad idea!
## R[/q]_Total
## 49405060
## attr(,"time.unit")
## [1] "second"
## attr(,"radiation.unit")
## [1] "total photon response"
Using autoplot()
methods for spectra defined in package
‘ggspectra’ annotated plotting is automatic. The defaults can be easily
changed, please see the documentation in package ‘ggspectra’.
Using the ggplot()
method for spectra from package
‘ggspectra’ plus geometries and statistics from
package ‘ggplot2’ we gain additional control on the design.
ggplot(sensors.mspct$LICOR_LI_190R, unit.out = "photon") +
geom_hline(yintercept = 1, colour = "red") +
geom_hline(yintercept = c(0.9, 1.1), colour = "red", linetype = "dotted") +
geom_line(linetype = "dashed") +
scale_y_s.q.response_continuous(breaks = c(0, 0.5, 1)) +
scale_x_wl_continuous() +
theme_classic()
ggplot(diffusers.lst$bentham.D7, aes(angle.deg, response)) +
geom_line() +
geom_line(aes(y = cos(angle.deg * pi / 180)), linetype = "dotted", color = "red") +
scale_x_continuous(name = "Angle (degrees)", breaks = c(-90, -60, -30, 0, 30, 60, 90)) +
scale_y_continuous(name = "Response (/1)") +
theme_classic()
As response_mspct
is a class derived from
list
, and response_spct
is derived from
tibble::tible
which is a (mostly) compatible
reimplementation of data.frame
the data can be used very
easily with any R function.
## w.length s.e.response
## 1 380.7609 0.001644911
## 2 384.7671 0.004052161
## 3 386.2694 0.006525339
## 4 386.7702 0.007746274
## 5 388.2725 0.011006905
## 6 388.7733 0.013019329
Of course attach
and with
also work as
expected.
## Object: response_spct [6 x 2]
## Wavelength range 380.76093-388.77325 nm, step 0.5007704-4.006164 nm
## Label: LICOR LI 190R light sensor
## Time unit 1s
##
## # A tibble: 6 × 2
## w.length s.e.response
## <dbl> <dbl>
## 1 381. 0.00164
## 2 385. 0.00405
## 3 386. 0.00653
## 4 387. 0.00775
## 5 388. 0.0110
## 6 389. 0.0130
## [1] 798.8367
## [1] 381.8537 798.8367