2 datasets found
  1. n

    Respiration_chambers/raw_log_files and combined datasets of biomass and...

    • cmr.earthdata.nasa.gov
    • researchdata.edu.au
    • +1more
    Updated Dec 18, 2018
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    (2018). Respiration_chambers/raw_log_files and combined datasets of biomass and chamber data, and physical parameters [Dataset]. http://doi.org/10.26179/5c1827d5d6711
    Explore at:
    Dataset updated
    Dec 18, 2018
    Time period covered
    Jan 27, 2015 - Feb 23, 2015
    Area covered
    Description

    General overview The following datasets are described by this metadata record, and are available for download from the provided URL.

    • Raw log files, physical parameters raw log files
    • Raw excel files, respiration/PAM chamber raw excel spreadsheets
    • Processed and cleaned excel files, respiration chamber biomass data
    • Raw rapid light curve excel files (this is duplicated from Raw log files), combined dataset pH, temperature, oxygen, salinity, velocity for experiment
    • Associated R script file for pump cycles of respirations chambers

    ####

    Physical parameters raw log files

    Raw log files 1) DATE= 2) Time= UTC+11 3) PROG=Automated program to control sensors and collect data 4) BAT=Amount of battery remaining 5) STEP=check aquation manual 6) SPIES=check aquation manual 7) PAR=Photoactive radiation 8) Levels=check aquation manual 9) Pumps= program for pumps 10) WQM=check aquation manual

    ####

    Respiration/PAM chamber raw excel spreadsheets

    Abbreviations in headers of datasets Note: Two data sets are provided in different formats. Raw and cleaned (adj). These are the same data with the PAR column moved over to PAR.all for analysis. All headers are the same. The cleaned (adj) dataframe will work with the R syntax below, alternative add code to do cleaning in R.

    Date: ISO 1986 - Check Time:UTC+11 unless otherwise stated DATETIME: UTC+11 unless otherwise stated ID (of instrument in respiration chambers) ID43=Pulse amplitude fluoresence measurement of control ID44=Pulse amplitude fluoresence measurement of acidified chamber ID=1 Dissolved oxygen ID=2 Dissolved oxygen ID3= PAR ID4= PAR PAR=Photo active radiation umols F0=minimal florescence from PAM Fm=Maximum fluorescence from PAM Yield=(F0 – Fm)/Fm rChl=an estimate of chlorophyll (Note this is uncalibrated and is an estimate only) Temp=Temperature degrees C PAR=Photo active radiation PAR2= Photo active radiation2 DO=Dissolved oxygen %Sat= Saturation of dissolved oxygen Notes=This is the program of the underwater submersible logger with the following abreviations: Notes-1) PAM= Notes-2) PAM=Gain level set (see aquation manual for more detail) Notes-3) Acclimatisation= Program of slowly introducing treatment water into chamber Notes-4) Shutter start up 2 sensors+sample…= Shutter PAMs automatic set up procedure (see aquation manual) Notes-5) Yield step 2=PAM yield measurement and calculation of control Notes-6) Yield step 5= PAM yield measurement and calculation of acidified Notes-7) Abatus respiration DO and PAR step 1= Program to measure dissolved oxygen and PAR (see aquation manual). Steps 1-4 are different stages of this program including pump cycles, DO and PAR measurements.

    8) Rapid light curve data Pre LC: A yield measurement prior to the following measurement After 10.0 sec at 0.5% to 8%: Level of each of the 8 steps of the rapid light curve Odessey PAR (only in some deployments): An extra measure of PAR (umols) using an Odessey data logger Dataflow PAR: An extra measure of PAR (umols) using a Dataflow sensor. PAM PAR: This is copied from the PAR or PAR2 column PAR all: This is the complete PAR file and should be used Deployment: Identifying which deployment the data came from

    ####

    Respiration chamber biomass data

    The data is chlorophyll a biomass from cores from the respiration chambers. The headers are: Depth (mm) Treat (Acidified or control) Chl a (pigment and indicator of biomass) Core (5 cores were collected from each chamber, three were analysed for chl a), these are psudoreplicates/subsamples from the chambers and should not be treated as replicates.

    ####

    Associated R script file for pump cycles of respirations chambers

    Associated respiration chamber data to determine the times when respiration chamber pumps delivered treatment water to chambers. Determined from Aquation log files (see associated files). Use the chamber cut times to determine net production rates. Note: Users need to avoid the times when the respiration chambers are delivering water as this will give incorrect results. The headers that get used in the attached/associated R file are start regression and end regression. The remaining headers are not used unless called for in the associated R script. The last columns of these datasets (intercept, ElapsedTimeMincoef) are determined from the linear regressions described below.

    To determine the rate of change of net production, coefficients of the regression of oxygen consumption in discrete 180 minute data blocks were determined. R squared values for fitted regressions of these coefficients were consistently high (greater than 0.9). We make two assumptions with calculation of net production rates: the first is that heterotrophic community members do not change their metabolism under OA; and the second is that the heterotrophic communities are similar between treatments.

    ####

    Combined dataset pH, temperature, oxygen, salinity, velocity for experiment

    This data is rapid light curve data generated from a Shutter PAM fluorimeter. There are eight steps in each rapid light curve. Note: The software component of the Shutter PAM fluorimeter for sensor 44 appeared to be damaged and would not cycle through the PAR cycles. Therefore the rapid light curves and recovery curves should only be used for the control chambers (sensor ID43).

    The headers are PAR: Photoactive radiation relETR: F0/Fm x PAR Notes: Stage/step of light curve Treatment: Acidified or control

    The associated light treatments in each stage. Each actinic light intensity is held for 10 seconds, then a saturating pulse is taken (see PAM methods).

    After 10.0 sec at 0.5% = 1 umols PAR After 10.0 sec at 0.7% = 1 umols PAR After 10.0 sec at 1.1% = 0.96 umols PAR After 10.0 sec at 1.6% = 4.32 umols PAR After 10.0 sec at 2.4% = 4.32 umols PAR After 10.0 sec at 3.6% = 8.31 umols PAR After 10.0 sec at 5.3% =15.78 umols PAR After 10.0 sec at 8.0% = 25.75 umols PAR

    This dataset appears to be missing data, note D5 rows potentially not useable information

    See the word document in the download file for more information.

  2. m

    R codes and dataset for Visualisation of Diachronic Constructional Change...

    • bridges.monash.edu
    • researchdata.edu.au
    zip
    Updated May 30, 2023
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    Gede Primahadi Wijaya Rajeg (2023). R codes and dataset for Visualisation of Diachronic Constructional Change using Motion Chart [Dataset]. http://doi.org/10.26180/5c844c7a81768
    Explore at:
    zipAvailable download formats
    Dataset updated
    May 30, 2023
    Dataset provided by
    Monash University
    Authors
    Gede Primahadi Wijaya Rajeg
    License

    Attribution-NonCommercial-ShareAlike 4.0 (CC BY-NC-SA 4.0)https://creativecommons.org/licenses/by-nc-sa/4.0/
    License information was derived automatically

    Description

    PublicationPrimahadi Wijaya R., Gede. 2014. Visualisation of diachronic constructional change using Motion Chart. In Zane Goebel, J. Herudjati Purwoko, Suharno, M. Suryadi & Yusuf Al Aried (eds.). Proceedings: International Seminar on Language Maintenance and Shift IV (LAMAS IV), 267-270. Semarang: Universitas Diponegoro. doi: https://doi.org/10.4225/03/58f5c23dd8387Description of R codes and data files in the repositoryThis repository is imported from its GitHub repo. Versioning of this figshare repository is associated with the GitHub repo's Release. So, check the Releases page for updates (the next version is to include the unified version of the codes in the first release with the tidyverse).The raw input data consists of two files (i.e. will_INF.txt and go_INF.txt). They represent the co-occurrence frequency of top-200 infinitival collocates for will and be going to respectively across the twenty decades of Corpus of Historical American English (from the 1810s to the 2000s).These two input files are used in the R code file 1-script-create-input-data-raw.r. The codes preprocess and combine the two files into a long format data frame consisting of the following columns: (i) decade, (ii) coll (for "collocate"), (iii) BE going to (for frequency of the collocates with be going to) and (iv) will (for frequency of the collocates with will); it is available in the input_data_raw.txt. Then, the script 2-script-create-motion-chart-input-data.R processes the input_data_raw.txt for normalising the co-occurrence frequency of the collocates per million words (the COHA size and normalising base frequency are available in coha_size.txt). The output from the second script is input_data_futurate.txt.Next, input_data_futurate.txt contains the relevant input data for generating (i) the static motion chart as an image plot in the publication (using the script 3-script-create-motion-chart-plot.R), and (ii) the dynamic motion chart (using the script 4-script-motion-chart-dynamic.R).The repository adopts the project-oriented workflow in RStudio; double-click on the Future Constructions.Rproj file to open an RStudio session whose working directory is associated with the contents of this repository.

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(2018). Respiration_chambers/raw_log_files and combined datasets of biomass and chamber data, and physical parameters [Dataset]. http://doi.org/10.26179/5c1827d5d6711

Respiration_chambers/raw_log_files and combined datasets of biomass and chamber data, and physical parameters

AAS_4127_Respiration_chambers_1

Explore at:
Dataset updated
Dec 18, 2018
Time period covered
Jan 27, 2015 - Feb 23, 2015
Area covered
Description

General overview The following datasets are described by this metadata record, and are available for download from the provided URL.

  • Raw log files, physical parameters raw log files
  • Raw excel files, respiration/PAM chamber raw excel spreadsheets
  • Processed and cleaned excel files, respiration chamber biomass data
  • Raw rapid light curve excel files (this is duplicated from Raw log files), combined dataset pH, temperature, oxygen, salinity, velocity for experiment
  • Associated R script file for pump cycles of respirations chambers

####

Physical parameters raw log files

Raw log files 1) DATE= 2) Time= UTC+11 3) PROG=Automated program to control sensors and collect data 4) BAT=Amount of battery remaining 5) STEP=check aquation manual 6) SPIES=check aquation manual 7) PAR=Photoactive radiation 8) Levels=check aquation manual 9) Pumps= program for pumps 10) WQM=check aquation manual

####

Respiration/PAM chamber raw excel spreadsheets

Abbreviations in headers of datasets Note: Two data sets are provided in different formats. Raw and cleaned (adj). These are the same data with the PAR column moved over to PAR.all for analysis. All headers are the same. The cleaned (adj) dataframe will work with the R syntax below, alternative add code to do cleaning in R.

Date: ISO 1986 - Check Time:UTC+11 unless otherwise stated DATETIME: UTC+11 unless otherwise stated ID (of instrument in respiration chambers) ID43=Pulse amplitude fluoresence measurement of control ID44=Pulse amplitude fluoresence measurement of acidified chamber ID=1 Dissolved oxygen ID=2 Dissolved oxygen ID3= PAR ID4= PAR PAR=Photo active radiation umols F0=minimal florescence from PAM Fm=Maximum fluorescence from PAM Yield=(F0 – Fm)/Fm rChl=an estimate of chlorophyll (Note this is uncalibrated and is an estimate only) Temp=Temperature degrees C PAR=Photo active radiation PAR2= Photo active radiation2 DO=Dissolved oxygen %Sat= Saturation of dissolved oxygen Notes=This is the program of the underwater submersible logger with the following abreviations: Notes-1) PAM= Notes-2) PAM=Gain level set (see aquation manual for more detail) Notes-3) Acclimatisation= Program of slowly introducing treatment water into chamber Notes-4) Shutter start up 2 sensors+sample…= Shutter PAMs automatic set up procedure (see aquation manual) Notes-5) Yield step 2=PAM yield measurement and calculation of control Notes-6) Yield step 5= PAM yield measurement and calculation of acidified Notes-7) Abatus respiration DO and PAR step 1= Program to measure dissolved oxygen and PAR (see aquation manual). Steps 1-4 are different stages of this program including pump cycles, DO and PAR measurements.

8) Rapid light curve data Pre LC: A yield measurement prior to the following measurement After 10.0 sec at 0.5% to 8%: Level of each of the 8 steps of the rapid light curve Odessey PAR (only in some deployments): An extra measure of PAR (umols) using an Odessey data logger Dataflow PAR: An extra measure of PAR (umols) using a Dataflow sensor. PAM PAR: This is copied from the PAR or PAR2 column PAR all: This is the complete PAR file and should be used Deployment: Identifying which deployment the data came from

####

Respiration chamber biomass data

The data is chlorophyll a biomass from cores from the respiration chambers. The headers are: Depth (mm) Treat (Acidified or control) Chl a (pigment and indicator of biomass) Core (5 cores were collected from each chamber, three were analysed for chl a), these are psudoreplicates/subsamples from the chambers and should not be treated as replicates.

####

Associated R script file for pump cycles of respirations chambers

Associated respiration chamber data to determine the times when respiration chamber pumps delivered treatment water to chambers. Determined from Aquation log files (see associated files). Use the chamber cut times to determine net production rates. Note: Users need to avoid the times when the respiration chambers are delivering water as this will give incorrect results. The headers that get used in the attached/associated R file are start regression and end regression. The remaining headers are not used unless called for in the associated R script. The last columns of these datasets (intercept, ElapsedTimeMincoef) are determined from the linear regressions described below.

To determine the rate of change of net production, coefficients of the regression of oxygen consumption in discrete 180 minute data blocks were determined. R squared values for fitted regressions of these coefficients were consistently high (greater than 0.9). We make two assumptions with calculation of net production rates: the first is that heterotrophic community members do not change their metabolism under OA; and the second is that the heterotrophic communities are similar between treatments.

####

Combined dataset pH, temperature, oxygen, salinity, velocity for experiment

This data is rapid light curve data generated from a Shutter PAM fluorimeter. There are eight steps in each rapid light curve. Note: The software component of the Shutter PAM fluorimeter for sensor 44 appeared to be damaged and would not cycle through the PAR cycles. Therefore the rapid light curves and recovery curves should only be used for the control chambers (sensor ID43).

The headers are PAR: Photoactive radiation relETR: F0/Fm x PAR Notes: Stage/step of light curve Treatment: Acidified or control

The associated light treatments in each stage. Each actinic light intensity is held for 10 seconds, then a saturating pulse is taken (see PAM methods).

After 10.0 sec at 0.5% = 1 umols PAR After 10.0 sec at 0.7% = 1 umols PAR After 10.0 sec at 1.1% = 0.96 umols PAR After 10.0 sec at 1.6% = 4.32 umols PAR After 10.0 sec at 2.4% = 4.32 umols PAR After 10.0 sec at 3.6% = 8.31 umols PAR After 10.0 sec at 5.3% =15.78 umols PAR After 10.0 sec at 8.0% = 25.75 umols PAR

This dataset appears to be missing data, note D5 rows potentially not useable information

See the word document in the download file for more information.

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