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This markdown file reads previously created pH climatology file and uses that as the definition of the depth levels that the Argo chlorophyll a data should be aligned to. Previously created BGC data (bgc_data.rds) and metadata (bgc_metadata.rds) are loaded from the BGC preprocessed folder.
Base data qc flags are checked to ensure that the float position, pressure measurements and chlorophyll a measurements are good. Pressure is used to derive the depth of each measurement. The chlorophyll a profile is checked to ensure that significant gaps (specified by the opt_gap_limit, opt_gap_min_depth and opt_gap_max_depth) do not exist. Profiles are assigned a profile_range field that identifies the depth 1 = 614 m, 2 = 1225 m and 3 = 1600 m.
The float chlorophyll a profiles are then aligned using the spline function to match the depth levels of the climatology resulting in data frame bgc_data_chla_interpolated_clean.
ucsd_ph_clim.rds - created by load_argo_clim_pH_ucsd. This markdown aligns chlorophyll a profile to the same depths as the ph climatology
bgc_data, bgc_metadata - created by load_argo
chla_bgc_va.rds – vertically aligned ph profiles.
location of pre-prepared data
Define options that are used to determine profiles that we will us in the ongoing analysis
# Options
# opt_profile_depth_range
# The profile must have at least one chla reading at a depth <= opt_profile_depth_range[1, ]
# The profile must have at least one chla reading at a depth >= opt_profile_depth_range[2, ].
# In addition if the profile depth does not exceed the min(opt_profile_depth_range[2, ]) (i.e. 600) it will be removed.
profile_range <- c(1, 2, 3)
min_depth <- c(10, 10, 10)
max_depth <- c(614, 1225, 1600)
opt_profile_depth_range <- data.frame(profile_range, min_depth, max_depth)
# opt_gap...
# The profile should not have a gap greater that opt_gap_limit within the range defined by opt_gap_min_depth and opt_gap_max_depth
opt_gap_limit <- c(28, 55, 110)
opt_gap_min_depth <- c(0, 400, 1000)
opt_gap_max_depth <- c(400, 1000, 1600)
# opt_measure_label, opt_xlim and opt_xbreaks are associated formatting
opt_measure_label <- expression("chlorophyll a ( mg m"^"-3"~")")
opt_xlim <- c(-0.5, 2.0)
opt_xbreaks <- c(-0.5, 0, 0.5, 1.0, 1.5, 2.0)
# opt_n_prof_sel
# The selection criteria that is used against n_prof, here set to 1
# Description of n_prof usage is provided at https://argo.ucsd.edu/data/data-faq/version-3-profile-files/ the next two lines are from that page.
# The main Argo CTD profile is stored in N_PROF=1. All other parameters (including biogeochemical parameters) that are measured
# with the same vertical sampling scheme and at the same location and time as the main Argo CTD profile are also stored in N_PROF=1.
opt_n_prof_sel = 1
read pH climatology, values are provided at set depths
# climatology values (pH_clim_va) available for lat, lon, month and depth
pH_clim_va <- read_rds(file = paste0(path_argo_preprocessed, "/pH_clim_va.rds"))
# What is the max depth we are interested in
opt_profile_max_depth <- max(opt_profile_depth_range$max_depth)
# existing depth levels that we will align to
target_depth_levels <- pH_clim_va %>%
filter(depth <= opt_profile_max_depth) %>%
rename(target_depth = depth) %>%
distinct(target_depth)
rm(pH_clim_va)
gc()
read chla profile and carry out basic checks, good data.
# base data and associated metadata
bgc_data <- read_rds(file = paste0(path_argo_preprocessed, '/bgc_data.rds'))
bgc_metadata <- read_rds(file = paste0(path_argo_preprocessed, '/bgc_metadata.rds'))
# Select relevant field from metadata ready to join to bgc_data
bgc_metadata_select <- bgc_metadata %>%
filter(position_qc == 1) %>%
select(file_id,
date,
lat,
lon) %>%
mutate(year = year(date),
month = month(date),
.after = date)
# we drive alignment from pressure and chla data
# conditions
# n_prof == 1
# pres_adjusted_qc %in% c(1, 8) - pressure data marked as good
# chla_adjusted_qc %in% c(1, 8) - chla data marked as good
# !is.na(pres_adjusted) - pressure value must be present
# !is.na(chla_adjusted) - chla value must be present
bgc_data_chla <- bgc_data %>%
filter(
pres_adjusted_qc %in% c(1, 8) &
chla_adjusted_qc %in% c(1, 8) &
n_prof == opt_n_prof_sel &
!is.na(pres_adjusted) &
!is.na(chla_adjusted)
) %>%
select(file_id,
pres_adjusted,
chla_adjusted)
# join with metadata information and calculate depth field
bgc_data_chla <- inner_join(bgc_metadata_select %>% select(file_id, lat),
bgc_data_chla) %>%
mutate(depth = gsw_z_from_p(pres_adjusted, latitude = lat) * -1.0,
.before = pres_adjusted) %>%
select(-c(lat, pres_adjusted))
# ensure we have a depth, and chla_adjusted for all rows in bgc_data_chla
bgc_data_chla <- bgc_data_chla %>%
filter(!is.na(depth) & !is.na(chla_adjusted))
# clean up working tables
rm(bgc_data, bgc_metadata)
gc()
Apply the rules that are determined by options set in set_options. Profile must cover a set range and not contain gaps.
# Determine profile min and max depths
bgc_profile_limits <- bgc_data_chla %>%
group_by(file_id) %>%
summarise(
min_depth = min(depth),
max_depth = max(depth),
) %>%
ungroup()
# The profile much match at least one of the range criteria
force_min <- min(opt_profile_depth_range$min_depth)
force_max <- min(opt_profile_depth_range$max_depth)
# Apply profile min and max restrictions
bgc_apply_limits <- bgc_profile_limits %>%
filter(
min_depth <= force_min &
max_depth >= force_max
)
# Ensure working data set only contains profiles that have confrormed to the range test
bgc_data_chla <- right_join(bgc_data_chla,
bgc_apply_limits %>% select(file_id))
# Add profile type field and set all to 1.
# All profile that meet the minimum requirements are profile_range = 1
bgc_data_chla <- bgc_data_chla %>%
mutate(profile_range = 1)
for (i in 2:nrow(opt_profile_depth_range)) {
#i = 3
range_min <- opt_profile_depth_range[i,'min_depth']
range_max <- opt_profile_depth_range[i,'max_depth']
# Apply profile min and max restrictions
bgc_apply_limits <- bgc_profile_limits %>%
filter(min_depth <= range_min &
max_depth >= range_max) %>%
select(file_id) %>%
mutate (profile_range = i)
# Update profile range to i for these profiles
# bgc_data_temp <- full_join(bgc_data_temp, bgc_apply_limits) %>%
# filter(!is.na(min_depth))
bgc_data_chla <-
bgc_data_chla %>% rows_update(bgc_apply_limits, by = "file_id")
}
# Find the gaps within the profiles
profile_gaps <- full_join(bgc_data_chla,
opt_profile_depth_range) %>%
filter(depth >= min_depth &
depth <= max_depth) %>%
select(file_id,
depth) %>%
arrange(file_id, depth) %>%
group_by(file_id) %>%
mutate(gap = depth - lag(depth, default = 0)) %>%
ungroup()
# Ensure we do not have gaps in the profile that invalidate it
for (i_gap in opt_gap_limit) {
# The limits to be applied in that pass of for loop
# i_gap <- opt_gap_limit[3]
i_gap_min = opt_gap_min_depth[which(opt_gap_limit == i_gap)]
i_gap_max = opt_gap_max_depth[which(opt_gap_limit == i_gap)]
# Which gaps are greater than i_gap
profile_gaps_remove <- profile_gaps %>%
filter(gap > i_gap) %>%
filter(depth >= i_gap_min & depth <= i_gap_max) %>%
distinct(file_id) %>%
pull()
# Remonve these profiles from working data set
bgc_data_chla <- bgc_data_chla %>%
filter(!file_id %in% profile_gaps_remove)
}
# clean up working tables
rm(bgc_profile_limits, profile_gaps, profile_gaps_remove, bgc_apply_limits)
gc()
We have a set of chla profiles that match our criteria we now need to align that data set to match the depth that are in target_depth_range, this will match the range of climatology values in ucsd_clim
# create unique combinations of file_id and profile ranges
profile_range_file_id <-
bgc_data_chla %>%
distinct(file_id, profile_range)
# select variable of interest and prepare target_depth field
bgc_data_chla_clean <- bgc_data_chla %>%
select(-profile_range) %>%
mutate(target_depth = depth, .after = depth)
rm(bgc_data_chla)
gc()
# create all possible combinations of location, month and depth levels for interpolation
target_depth_grid <-
expand_grid(
target_depth_levels,
profile_range_file_id
)
# Constrain target_depth_grid to profile depth range
target_depth_grid <-
left_join(target_depth_grid, opt_profile_depth_range) %>%
filter(target_depth <= max_depth)
target_depth_grid <- target_depth_grid %>%
select(target_depth,
file_id)
# extend chla depth vectors with target depths
bgc_data_chla_extended <-
full_join(bgc_data_chla_clean, target_depth_grid) %>%
arrange(file_id, target_depth)
rm(bgc_data_chla_clean)
gc()
# predict spline interpolation on adjusted depth grid for chla location and month
bgc_data_chla_interpolated <-
bgc_data_chla_extended %>%
group_by(file_id) %>%
mutate(chla_spline = spline(target_depth, chla_adjusted,
method = "natural",
xout = target_depth)$y) %>%
ungroup()
rm(bgc_data_chla_extended)
gc()
# subset interpolated values on target depth range
bgc_data_chla_interpolated_clean <-
inner_join(target_depth_levels, bgc_data_chla_interpolated)
rm(bgc_data_chla_interpolated)
gc()
# select columns and rename to initial names
bgc_data_chla_interpolated_clean <-
bgc_data_chla_interpolated_clean %>%
select(file_id,
depth = target_depth,
chla = chla_spline)
# merge with profile range
bgc_data_chla_interpolated_clean <-
full_join(bgc_data_chla_interpolated_clean,
profile_range_file_id)
# merge with meta data
bgc_data_chla_interpolated_clean <-
left_join(bgc_data_chla_interpolated_clean,
bgc_metadata_select)
Write the interpolated chla profiles that map onto depth levels.
# Write files
# bgc_data_chla_interpolated_clean %>%
# write_rds(file = paste0(path_argo_preprocessed, "/chla_bgc_va.rds"))
# Rename so that names match if just reading existing files
chla_bgc_va <- bgc_data_chla_interpolated_clean
rm(bgc_data_chla_interpolated_clean)
gc()
Read files that were previously created ready for analysis
# read files
chla_bgc_va <- read_rds(file = paste0(path_argo_preprocessed, "/chla_bgc_va.rds"))
max_depth_1 <- opt_profile_depth_range[1, "max_depth"]
max_depth_2 <- opt_profile_depth_range[2, "max_depth"]
max_depth_3 <- opt_profile_depth_range[3, "max_depth"]
# Profiles to 600m
chla_overall_mean_1 <- chla_bgc_va %>%
filter(profile_range %in% c(1, 2, 3) & depth <= max_depth_1) %>%
group_by(depth) %>%
summarise(count_measures = n(),
chla_mean = mean(chla, na.rm = TRUE),
chla_sd = sd(chla, na.rm = TRUE))
chla_year_mean_1 <- chla_bgc_va %>%
filter(profile_range %in% c(1, 2, 3) & depth <= max_depth_1) %>%
group_by(year, depth) %>%
summarise(count_measures = n(),
chla_mean = mean(chla, na.rm = TRUE),
chla_sd = sd(chla, na.rm = TRUE))
# Profiles to 1200m
chla_overall_mean_2 <- chla_bgc_va %>%
filter(profile_range %in% c(2, 3) & depth <= max_depth_2) %>%
group_by(depth) %>%
summarise(count_measures = n(),
chla_mean = mean(chla, na.rm = TRUE),
chla_sd = sd(chla, na.rm = TRUE))
chla_year_mean_2 <- chla_bgc_va %>%
filter(profile_range %in% c(2, 3) & depth <= max_depth_2) %>%
group_by(year, depth) %>%
summarise(count_measures = n(),
chla_mean = mean(chla, na.rm = TRUE),
chla_sd = sd(chla, na.rm = TRUE))
# Profiles to 1500m
chla_overall_mean_3 <- chla_bgc_va %>%
filter(profile_range %in% c(3) & depth <= max_depth_3) %>%
group_by(depth) %>%
summarise(count_measures = n(),
chla_mean = mean(chla, na.rm = TRUE),
chla_sd = sd(chla, na.rm = TRUE))
chla_year_mean_3 <- chla_bgc_va %>%
filter(profile_range %in% c(3) & depth <= max_depth_3) %>%
group_by(year, depth) %>%
summarise(count_measures = n(),
chla_mean = mean(chla, na.rm = TRUE),
chla_sd = sd(chla, na.rm = TRUE))
# All years
chla_overall_mean_1 %>%
ggplot()+
geom_path(aes(x = chla_mean,
y = depth))+
geom_ribbon(aes(
xmax = chla_mean + chla_sd,
xmin = chla_mean - chla_sd,
y = depth
),
alpha = 0.2) +
scale_y_reverse()+
coord_cartesian(xlim = opt_xlim)+
scale_x_continuous(breaks = opt_xbreaks)+
labs(
title = paste0('Overall mean chlorophyll a to ', max_depth_1, 'm'),
x=opt_measure_label,
y='depth (m)'
)
chla_overall_mean_2 %>%
ggplot()+
geom_path(aes(x = chla_mean,
y = depth))+
geom_ribbon(aes(
xmax = chla_mean + chla_sd,
xmin = chla_mean - chla_sd,
y = depth
),
alpha = 0.2) +
scale_y_reverse()+
coord_cartesian(xlim = opt_xlim)+
scale_x_continuous(breaks = opt_xbreaks)+
labs(
title = paste0('Overall mean chlorophyll a to ', max_depth_2, 'm'),
x=opt_measure_label,
y='depth (m)'
)
chla_overall_mean_3 %>%
ggplot()+
geom_path(aes(x = chla_mean,
y = depth))+
geom_ribbon(aes(
xmax = chla_mean + chla_sd,
xmin = chla_mean - chla_sd,
y = depth
),
alpha = 0.2) +
scale_y_reverse()+
coord_cartesian(xlim = opt_xlim)+
scale_x_continuous(breaks = opt_xbreaks)+
labs(
title = paste0('Overall mean chlorophyll a to ', max_depth_3, 'm'),
x=opt_measure_label,
y='depth (m)'
)
# by years
chla_year_mean_1 %>%
ggplot()+
geom_path(aes(x = chla_mean,
y = depth))+
geom_ribbon(aes(
xmax = chla_mean + chla_sd,
xmin = chla_mean - chla_sd,
y = depth
),
alpha = 0.2) +
scale_y_reverse()+
facet_wrap(~year)+
coord_cartesian(xlim = opt_xlim)+
scale_x_continuous(breaks = opt_xbreaks)+
labs(
title = paste0('Yearly overall mean chlorophyll a to ', max_depth_1, 'm'),
x = opt_measure_label,
y = 'depth (m)'
)
chla_year_mean_2 %>%
ggplot()+
geom_path(aes(x = chla_mean,
y = depth))+
geom_ribbon(aes(
xmax = chla_mean + chla_sd,
xmin = chla_mean - chla_sd,
y = depth
),
alpha = 0.2) +
scale_y_reverse()+
facet_wrap(~year)+
coord_cartesian(xlim = opt_xlim)+
scale_x_continuous(breaks = opt_xbreaks)+
labs(
title = paste0('Yearly overall mean chlorophyll a to ', max_depth_2, 'm'),
x = opt_measure_label,
y = 'depth (m)'
)
chla_year_mean_3 %>%
ggplot()+
geom_path(aes(x = chla_mean,
y = depth))+
geom_ribbon(aes(
xmax = chla_mean + chla_sd,
xmin = chla_mean - chla_sd,
y = depth
),
alpha = 0.2) +
scale_y_reverse()+
facet_wrap(~year)+
coord_cartesian(xlim = opt_xlim)+
scale_x_continuous(breaks = opt_xbreaks)+
labs(
title = paste0('Yearly overall mean chlorophyll a to ', max_depth_3, 'm'),
x = opt_measure_label,
y = 'depth (m)'
)
Details of the number of profiles and to which depths over the analysis period
chla_histogram <- chla_bgc_va %>%
group_by(year, profile_range = as.character(profile_range)) %>%
summarise(num_profiles = n_distinct(file_id)) %>%
ungroup()
chla_histogram %>%
ggplot() +
geom_bar(
aes(
x = year,
y = num_profiles,
fill = profile_range,
group = profile_range
),
position = "stack",
stat = "identity"
) +
scale_fill_viridis_d() +
labs(title = "chlorophyll a profiles per year and profile range",
x = "year",
y = "profile count",
fill = "profile range")
sessionInfo()
R version 4.2.2 (2022-10-31)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: openSUSE Leap 15.5
Matrix products: default
BLAS: /usr/local/R-4.2.2/lib64/R/lib/libRblas.so
LAPACK: /usr/local/R-4.2.2/lib64/R/lib/libRlapack.so
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
[5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
[7] LC_PAPER=en_US.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] gsw_1.1-1 gridExtra_2.3 lubridate_1.9.0 timechange_0.1.1
[5] argodata_0.1.0 forcats_0.5.2 stringr_1.5.0 dplyr_1.1.3
[9] purrr_1.0.2 readr_2.1.3 tidyr_1.3.0 tibble_3.2.1
[13] ggplot2_3.4.4 tidyverse_1.3.2 workflowr_1.7.0
loaded via a namespace (and not attached):
[1] httr_1.4.4 sass_0.4.4 viridisLite_0.4.1
[4] jsonlite_1.8.3 modelr_0.1.10 bslib_0.4.1
[7] assertthat_0.2.1 getPass_0.2-2 highr_0.9
[10] googlesheets4_1.0.1 cellranger_1.1.0 yaml_2.3.6
[13] pillar_1.9.0 backports_1.4.1 glue_1.6.2
[16] digest_0.6.30 promises_1.2.0.1 rvest_1.0.3
[19] colorspace_2.0-3 htmltools_0.5.8.1 httpuv_1.6.6
[22] pkgconfig_2.0.3 broom_1.0.5 haven_2.5.1
[25] scales_1.2.1 processx_3.8.0 whisker_0.4
[28] later_1.3.0 tzdb_0.3.0 git2r_0.30.1
[31] googledrive_2.0.0 generics_0.1.3 farver_2.1.1
[34] ellipsis_0.3.2 cachem_1.0.6 withr_2.5.0
[37] cli_3.6.1 magrittr_2.0.3 crayon_1.5.2
[40] readxl_1.4.1 evaluate_0.18 ps_1.7.2
[43] fs_1.5.2 fansi_1.0.3 xml2_1.3.3
[46] tools_4.2.2 hms_1.1.2 gargle_1.2.1
[49] lifecycle_1.0.3 munsell_0.5.0 reprex_2.0.2
[52] callr_3.7.3 compiler_4.2.2 jquerylib_0.1.4
[55] RNetCDF_2.6-1 rlang_1.1.1 grid_4.2.2
[58] rstudioapi_0.15.0 labeling_0.4.2 rmarkdown_2.18
[61] gtable_0.3.1 DBI_1.2.2 R6_2.5.1
[64] knitr_1.41 fastmap_1.1.0 utf8_1.2.2
[67] rprojroot_2.0.3 stringi_1.7.8 Rcpp_1.0.10
[70] vctrs_0.6.4 dbplyr_2.2.1 tidyselect_1.2.0
[73] xfun_0.35