M100 Band3 Combine 4.2.2: Difference between revisions
| Line 1: | Line 1: | ||
<div style="background-color:#E0FFFF;border:4px solid #FF9966;"> | |||
<div style="font-size:250%; color:red; text-align:center;"> | |||
This page is currently under construction. | |||
</div> | |||
<div style="font-size:200%; color:black; text-align:center"> | |||
DO NOT USE IT. | |||
</div> | |||
<div style="font-size:150%; color:black; text-align:center"> | |||
To navigate the CASAguides pages, visit [http://casaguides.nrao.edu/ | |||
casaguides.nrao.edu | |||
] | |||
</div> | |||
</div> | |||
= Overview = | = Overview = | ||
Revision as of 00:02, 10 July 2014
This page is currently under construction.
DO NOT USE IT.
To navigate the CASAguides pages, visit [http://casaguides.nrao.edu/ casaguides.nrao.edu ]
Overview
This guide describes how to combine the 7m and 12m interferometric data and then how to feather the resulting image with the total power TP image. All of the data for this SV project can be found at https://almascience.nrao.edu/alma-data/science-verification. In order to run this guide you will need to:
- Either run the 7m casaguide M100_Band3_ACA_4.1 to obtain the final 7m fully calibrated data or download the fully calibrated data: (i.e. M100_Band3_7m_CalibratedData.tgz)
- Either download the new RawUnCalibrated data for the 12m-array and run the new calibration script or download the fully calibrated data (i.e. M100_Band3_12m_CalibratedData.tgz). Note that while these are the same data that were released previously, the data reduction path has been updated to current best practices and starts from the raw data files called ASDMs (ALMA Science Data Model). Do not use the previously released uncalibrated or calibrated data.
- Either run the M100_Band3_SingleDish_4.1 guide to calibrate and image the Total Power data or download the final image (i.e. M100_TP_Image.tgz)
Confirm your version of CASA
This guide has been written for CASA release 4.1.0. Please confirm your version before proceeding.
# In CASA
version = casadef.casa_version
print "You are using " + version
if (version < '4.1.0'):
print "YOUR VERSION OF CASA IS TOO OLD FOR THIS GUIDE."
print "PLEASE UPDATE IT BEFORE PROCEEDING."
else:
print "Your version of CASA is appropriate for this guide."
Combine and Image the 7m+12m Interferometric Data
Split off CO spws
# In CASA
os.system('rm -rf m100_*m.ms.listobs')
listobs('M100_Band3_12m_CalibratedData.ms',listfile='m100_12m.ms.listobs')
listobs('M100_Band3_7m_CalibratedData.ms',listfile='m100_7m.ms.listobs')
Below are the observation and spectral window tables from the listobs.
12m data: ObservationID = 0 ArrayID = 0 Date Timerange (UTC) Scan FldId FieldName nRows SpwIds Average Interval(s) 10-Sep-2011/18:28:43.4 - 18:41:00.4 11 1 M100 1320 [0, 1, 2, 3] [6.05, 6.05, 6.05, 6.05] Spectral Windows: (4 unique spectral windows and 1 unique polarization setups) SpwID Name #Chans Frame Ch1(MHz) ChanWid(kHz) TotBW(kHz) BBC Num Corrs 0 3840 TOPO 113726.419 488.281 1875000.0 1 XX YY 1 3840 TOPO 111851.419 488.281 1875000.0 2 XX YY 2 3840 TOPO 103663.431 -488.281 1875000.0 3 XX YY 3 3840 TOPO 101850.931 -488.281 1875000.0 4 XX YY 7m data: ObservationID = 0 ArrayID = 0 Date Timerange (UTC) Scan FldId FieldName nRows SpwIds Average Interval(s) 17-Mar-2013/04:44:04.3 - 04:50:43.7 11 1 M100 168 [0, 1] [10.1, 10.1] Spectral Windows: (4 unique spectral windows and 1 unique polarization setups) SpwID Name #Chans Frame Ch1(MHz) ChanWid(kHz) TotBW(kHz) BBC Num Corrs 0 ALMA_RB_03#BB_3#SW-01#FULL_RES 4080 TOPO 111811.300 488.281 1992187.5 3 XX YY 1 ALMA_RB_03#BB_4#SW-01#FULL_RES 4080 TOPO 113686.300 488.281 1992187.5 4 XX YY 2 ALMA_RB_03#BB_1#SW-01#FULL_RES 4080 TOPO 111798.250 488.281 1992187.5 1 XX YY 3 ALMA_RB_03#BB_2#SW-01#FULL_RES 4080 TOPO 113673.250 488.281 1992187.5 2 XX YY
<figure id="12m_mosaic.png">
</figure>
<figure id="7m_mosaic.png">
</figure>
Examination of the listobs files shows that the CO is in spw=0 for the 12m data and in spws='1,3' for the 7m data. There are two spws containing CO for the 7m data because some of the data was taken with a slightly different correlator setup.
Also note that the integration time per visibility (average interval parameter in listobs) is different: 6.05s for the 12m data and 10.1s for the 7m. This will be important to know later in order to correctly weight the combined data.
Next we split out the CO spectral windows.
# In CASA
os.system('rm -rf m100_12m_CO.ms')
split(vis='M100_Band3_12m_CalibratedData.ms',
outputvis='m100_12m_CO.ms',spw='0',field='M100',
datacolumn='data',keepflags=False)
os.system('rm -rf m100_7m_CO.ms')
split(vis='M100_Band3_7m_CalibratedData.ms',
outputvis='m100_7m_CO.ms',spw='1,3',field='M100',
datacolumn='data',keepflags=False)
Also of interest is that the 12m data has 48 fields and the 7m has 24 fields (not shown in the excerpt above). The difference in number of pointings is because the 7m antennas have a FWHP (full width half power) primary beam diameter that is 12/7 times larger than the 12m antennas. One easy way to see how the mosaics compare is to install the AnalysisUtils package (see Analysis_Utilities). Then with AnalysisUtils you can make the following plots (look at the listobs to obtain the sourceid):
# In CASA
os.system('rm -rf *m_mosaic.png')
au.plotMosaic('m100_12m_CO.ms',sourceid='0',figfile='12m_mosaic.png')
au.plotMosaic('m100_7m_CO.ms',sourceid='1',figfile='7m_mosaic.png')
We see that the mosaics cover a common area but that the 7m mosaic is a bit larger. This means that the outer edges of the combined mosaic will be noisier than expected if they overlapped perfectly. Just something to look out for. If you had the case where the mosaic coverage is dramatically different, it would be best to exclude the completely non-overlapping fields from the combination.
NOTE: At this stage one would typically do continuum subtraction (if there is any). However we already know from the individual data reductions that the 3mm continuum emission is quite weak and does not significantly contribute to a 5km/s channel, so we will forgo the the continuum subtraction step. Examples of how to do this if you are so inclined are located in the 7m guide and 12m script, respectively.
Concat with 1/sigma2 scaling of Weights
<figure id="7m_WT.png">
</figure>
<figure id="12m_WT.png">
</figure>
When combining data with disparate properties it is very important that the relative weights of each visibility be in the correct proportion to the other data according to the radiometer equation. Formally, the visibility weights should be proportional to 1/sigma**2 where sigma is the variance or rms noise of a given visibility.
CASA currently scales the weights by 1/[(Tsys(i) * Tsys(j)] if calwt=True for the Tsys table applycal. To verify, we plot the weights of the 7m and 12m data. No averaging can be turned on when plotting the weights.
# In CASA
os.system('rm -rf 7m_WT.png 12m_WT.png')
plotms(vis='m100_12m_CO.ms',yaxis='wt',xaxis='uvdist',spw='0~2:200',
coloraxis='spw',plotfile='12m_WT.png')
#
plotms(vis='m100_7m_CO.ms',yaxis='wt',xaxis='uvdist',spw='0~2:200',
coloraxis='spw',plotfile='7m_WT.png')
As you can see from these plots, the weights are quite similar at this stage because the data were taken under similar weather conditions and hence Tsys.
Assuming that the 7m and 12m antennas have similar apperture and quantization efficiencies (a reasonable assumption since they were designed this way), the rms noise in a single channel for a single visibility is:
[math]\displaystyle{ \sigma_{ij}=\frac{2k}{A_{eff}} }[/math] [math]\displaystyle{ \sqrt{\frac{T_{sys,i} T_{sys,j}}{\Delta\nu_{ch} t_{ij}}} }[/math]
<figure id="Intcombo_0.193_WT.png">
</figure>
Where k is Boltzmann's constant, Aeff is the effective antenna area, Tsys,i is the system temperature for antenna i, Δνch is the channel width, and tij is the integration time per visibility.
The two key things that are different between the 7m and 12m-array data are that the effective dish Areas are different by (7/12)2 and the integration times are different by sqrt(10.1/6.05). Since dish area is in the numerator of the radiometer equation and integration time per visibility is in the denominator, and assuming WT propto 1/sigma2, the 7m weight should be scaled by: (7./12.)4 x (10.1/6.05) = 0.193 to account for the difference in telescope size and integration time per visibility.
# In CASA
# Concat and scale weights
os.system('rm -rf M100_Intcombo_0.193.ms')
concat(vis=['m100_12m_CO.ms','m100_7m_CO.ms'],
concatvis='M100_Intcombo_0.193.ms',
visweightscale=[1,0.193])
Now plot the concatenated weights to verify they are as expected.
# In CASA
os.system('rm -rf Intcombo_0.193_WT.png')
plotms(vis='M100_Intcombo_0.193.ms',yaxis='wt',xaxis='uvdist',spw='0~2:200',
coloraxis='spw',plotfile='Intcombo_0.193_WT.png')
<figure id="M100_Intcombo_0.193_vel.png">
</figure>
Some additional useful plots of the combined data (Let each plot finish before cutting and pasting next plot. If plotms gui disappears, exit CASA and restart):
amplitude as a function of uv-distance
# In CASA
os.system('rm -rf M100_Intcombo_0.193 _uvdist.png')
plotms(vis='M100_Intcombo_0.193.ms',yaxis='amp',xaxis='uvdist',spw='',
avgchannel='5000',
coloraxis='spw',plotfile='M100_Intcombo_0.193_uvdist.png')
The CO line as a function of velocity (note this plot takes a while).
# In CASA
os.system('rm -rf M100_Intcombo_0.193_vel.png')
plotms(vis='M100_Intcombo_0.193.ms',yaxis='amp',xaxis='velocity',spw='',
avgtime='1e8',avgscan=True,coloraxis='spw',avgchannel='5',
transform=True,freqframe='LSRK',restfreq='115.271201800GHz',
plotfile='M100_Intcombo_0.193_vel.png')
To see each spectral window independently, run the command again but remove plotfile, and add iteraxis='spw'.
Image Using An Automasking Technique
The commands in this section perform an iterative automasking procedure down to a user specified threshold=stop*rms where stop is typically 2-3 using the imagemode='mosaic' mode of clean. This mode automatically calculates the correct convolution of the primary beam response of the mosaic when different antenna dish diameters are present. NOTE: even if these data had only been comprised of a single pointing of 7m and 12m-array data, the imagemode='mosaic' mode would be needed to correctly image data with different antenna sizes.
The procedure outlined below takes some care to ensure that the generated masks (i) only have values of 0 or 1; (ii) are themselves masked at the minpb level. It also removes very small masked regions that are consistent with noise bumps using a function in scipy. A typical setting is to remove mask regions that are 1/2 the beam area in pixels. This is one technique under exploration for future pipeline use.
The commands have been split into multiple sections to aid cut and paste. Wait until the current one is done before starting next section. If you stop CASA and restart you will need to cut and paste again from the Define Parameters section on down.
For the long series of commands below it is important to include the beginning cpaste and ending -- in your cut and paste.
Define Parameters
Note that the parameters used here are by design the same as those used to make the stand-alone 7m-array and 12m-array images.
# In CASA
cpaste
### Initialize
import scipy.ndimage
### Define clean parameters
vis='M100_Intcombo_0.193.ms'
prename='M100_Intcombo_0.193_cube'
myimage=prename+'.image'
myflux=prename+'.flux'
mymask=prename+'.mask'
myresidual=prename+'.residual'
imsize=800
cell='0.5arcsec'
minpb=0.2
restfreq='115.271201800GHz'
outframe='LSRK'
spw='0~2'
width='5km/s'
start='1400km/s'
nchan=70
robust=0.5
phasecenter='J2000 12h22m54.9 +15d49m10'
scales=[0]
smallscalebias=0.6
### Setup stopping criteria with multiplier for rms.
stop=3.
### Minimum size multiplier for beam area for removing very small mask regions.
pixelmin=0.5
--
Make Initial Dirty Image and Determine Synthesized Beam area
The dirty image is used to determine the initial peak flux density in the cube and the beam area is used to define the minimum size of masked regions in order to exclude noise bumps from the overall mask.
# In CASA
cpaste
### Make initial dirty image
os.system('rm -rf '+prename+'.* ' +prename+'_*')
clean(vis=vis,imagename=prename,
imagermode='mosaic',ftmachine='mosaic',minpb=minpb,
imsize=imsize,cell=cell,spw=spw,
weighting='briggs',robust=robust,phasecenter=phasecenter,
mode='velocity',width=width,start=start,nchan=nchan,
restfreq=restfreq,outframe=outframe,veltype='radio',
mask='',
niter=0,interactive=F)
# Deterimine the beam area in pixels for later removal of very small mask regions
major=imhead(imagename=myimage,mode='get',hdkey='beammajor')['value']
minor=imhead(imagename=myimage,mode='get',hdkey='beamminor')['value']
pixelsize=float(cell.split('arcsec')[0])
beamarea=(major*minor*pi/(4*log(2)))/(pixelsize**2)
print 'beamarea in pixels =', beamarea
--
Find properties of the dirty image
For the long series of commands below it is important to include the beginning cpaste and ending -- in your cut and paste.
# In CASA
cpaste
### Find the peak in the dirty cube.
myimage=prename+'.image'
bigstat=imstat(imagename=myimage)
peak= bigstat['max'][0]
print 'peak (Jy/beam) in cube = '+str(peak)
### Sets threshold of first loop, try 2-4. Subsequent loops are set thresh/2
thresh = peak /4.
### If True: find the rms in two line-free channels; If False: Set rms by hand in else statement.
if True:
chanstat=imstat(imagename=myimage,chans='4')
rms1= chanstat['rms'][0]
chanstat=imstat(imagename=myimage,chans='66')
rms2= chanstat['rms'][0]
rms=0.5*(rms1+rms2)
else:
rms=0.013
print 'rms (Jy/beam) in a channel = '+str(rms)
--
Automasking Loop
On a reasonably fast computer the following will take a couple of hours for this spectral mosiac...
# In CASA
cpaste
n=-1
while (thresh >= stop*rms):
n=n+1
print 'clean threshold this loop is', thresh
threshmask = prename+'_threshmask' +str(n)
maskim = prename+'_fullmask' +str(n)
immath(imagename = [myresidual],
outfile = threshmask,
expr = 'iif(IM0 > '+str(thresh) +',1.0,0.0)',
mask=myflux+'>'+str(minpb))
if (n==0):
os.system('cp -r '+threshmask+' '+maskim+'.pb')
print 'This is the first loop'
else:
makemask(mode='copy',inpimage=myimage,
inpmask=[threshmask,mymask],
output=maskim)
imsubimage(imagename=maskim, mask=myflux+'>'+str(minpb),
outfile=maskim+'.pb')
print 'Combined mask ' +maskim+' generated.'
# Remove small masks
os.system('cp -r '+maskim+'.pb ' +maskim+'.pb.min')
maskfile=maskim+'.pb.min'
ia.open(maskfile)
mask=ia.getchunk()
labeled,j=scipy.ndimage.label(mask)
myhistogram = scipy.ndimage.measurements.histogram(labeled,0,j+1,j+1)
object_slices = scipy.ndimage.find_objects(labeled)
threshold=beamarea*pixelmin
for i in range(j):
if myhistogram[i+1]<threshold:
mask[object_slices[i]] = 0
ia.putchunk(mask)
ia.done()
print 'Small masks removed and ' +maskim +'.pb.min generated.'
os.system('rm -rf '+mymask+'')
clean(vis=vis,imagename=prename,
imagermode='mosaic',ftmachine='mosaic',minpb=minpb,
imsize=imsize,cell=cell,spw=spw,
weighting='briggs',robust=robust,phasecenter=phasecenter,
mode='velocity',width=width,start=start,nchan=nchan,
restfreq=restfreq,outframe=outframe,veltype='radio',
mask = maskim+'.pb.min',
multiscale=scales,smallscalebias=smallscalebias,
interactive = F,
niter = 10000,
threshold = str(thresh) +'Jy/beam')
if thresh==stop*rms: break
thresh = thresh/2.
# Run a final time with stop*rms if more than a little above
# stop*rms. Also make a back-up of next to last image
if (thresh < stop*rms and thresh*2.>1.05*stop*rms):
thresh=stop*rms
os.system('cp -r '+myimage+' '+myimage+str(n))
--
Notes on the Automasking procedure
This script is meant to be a possible stepping stone to optimal automasking -- it is by no means perfect and is certainly slower than optimal but feel free to try it with other datasets. Some notes below:
In addition to the final prename.image (prename.flux etc) this script produces and keeps each iteration of the various mask files which will allow you to explore how the masking proceeded as the threshold for masking and cleaning was lowered. The ones denoted "prename. fullmask*.pb.min" are the ones used in the clean steps themselves. At the end of the process the final "prename. fullmask*.pb.min" will also be stored in the prename.mask. Once you've verified you are happy with the masking, you may want to remove the prename.threshmask* and prename.fullmask* files, as they can be large for large cubes.
Additionally, before running the final loop with thresh=stop*rms the script copies the .image from the preceding clean to prename.image'n' where 'n' equals the loop number of the preceding step. So in this M100 example you will see a M100_Intcombo_0.193_cube.image and a M100_Intcombo_0.193_cube.image2 where .image is the final image and .image2 is the next to last image. This is done for convenience in the case that thresh=stop*rms is too deep such that clean diverges, you will still be left with the clean image from the preceding loop that you can further investigate to understand why clean diverged. If all goes well with the final loop, the prename.image'n' can also be deleted. Divergence at thresh=stop*rms is often a sign that the image is "dynamic range limited" in other words the rms in channels with bright emission is significantly worse than for a line-free channel.
Also note that attempts to use multiscale clean with scales of [0,5,15] on these data with this automasking script diverges -- the cause is under investigation.
Image Analysis for the 7m+12m Data
Moment Maps for 7m+12m CO (1-0) Cube
Start by examining the final image cube. Determine the start and stopping channels for the line emission -- this will be used in the "chans" parameter of immoments.
# In CASA
viewer('M100_Intcombo_0.193_cube.image')
<figure id="M100_Intcombo_0.193_cube.image.mom0.png">
</figure>
<figure id="M100_Intcombo_0.193_cube.image.mom1.png">
</figure>
Next determine the rms noise per channel and use that to exclude pixels from the moment images.
# In CASA
myimage='M100_Intcombo_0.193_cube.image'
chanstat=imstat(imagename=myimage,chans='4')
rms1= chanstat['rms'][0]
chanstat=imstat(imagename=myimage,chans='66')
rms2= chanstat['rms'][0]
rms=0.5*(rms1+rms2)
print 'rms in a channel = '+str(rms)
Next make the moment maps. For the integrated intensity: moment 0, a 2 sigma cut often considerably improves the appearance of the image with little effect on the integrated intensity as long as emission free channels are excluded. For higher order moments it is necessary to exclude all low S/N data. Typically 5-6 sigma for the higher moments works well. We also apply further masking based on the .flux image because the edges of the combined mosaic are especially noisy because the 7m mosaic is somewhat larger than the 12m mosaic as describe above (see Figures 1 & 2).
# In CASA
cpaste
os.system('rm -rf M100_Intcombo_0.193_cube.image.mom0')
immoments(imagename = 'M100_Intcombo_0.193_cube.image',
moments = [0],
axis = 'spectral',chans = '10~61',
mask='M100_Intcombo_0.193_cube.flux>0.3',,
includepix = [rms*2,100.],
outfile = 'M100_Intcombo_0.193_cube.image.mom0')
os.system('rm -rf M100_Intcombo_0.193_cube.image.mom1')
immoments(imagename = 'M100_Intcombo_0.193_cube.image',
moments = [1],
axis = 'spectral',chans = '10~61',
mask='M100_Intcombo_0.193_cube.flux>0.3',
includepix = [rms*5.5,100.],
outfile = 'M100_Intcombo_0.193_cube.image.mom1')
--
Make some figures showing the moment maps.
# In CASA
cpaste
os.system('rm -rf M100_Intcombo_0.193_cube.image.mom*.png')
imview (raster=[{'file': 'M100_Intcombo_0.193_cube.image.mom0',
'range': [-0.3,25.],'scaling': -1.0,'colorwedge': T}],
zoom={'blc': [190,150],'trc': [650,610]},
out='M100_Intcombo_0.193_cube.image.mom0.png')
imview (raster=[{'file': 'M100_Intcombo_0.193_cube.image.mom1',
'range': [1455,1695],'colorwedge': T}],
zoom={'blc': [190,150],'trc': [650,610]},
out='M100_Intcombo_0.193_cube.image.mom1.png')
--
If you plan to use your moment 0 image to make measurements, it needs to be primary beam corrected first. First we need to subimage the .flux cube to extract a single plane that can be used to primary beam correct the moment 0 image.
# In CASA
os.system('rm -rf M100_Intcombo_0.193_cube.flux.1ch')
imsubimage(imagename='M100_Intcombo_0.193_cube.flux',
outfile='M100_Intcombo_0.193_cube.flux.1ch',
chans='35')
Then primary beam correct the moment 0 image. This is the version that measurements would be made on, though the uncorrected one can be useful for figures.
<figure id="M100_Intcombo_0.193_cube.image.mom0.pbcor.png">
</figure>
# In CASA
os.system('rm -rf M100_Intcombo_0.193_cube.image.mom0.pbcor')
immath(imagename=['M100_Intcombo_0.193_cube.image.mom0', \
'M100_Intcombo_0.193_cube.flux.1ch'],
expr='IM0/IM1',
outfile='M100_Intcombo_0.193_cube.image.mom0.pbcor')
Have a look at the difference the primary beam correction makes.
# In CASA
imview (raster=[{'file': 'M100_Intcombo_0.193_cube.image.mom0',
'range': [-0.3,25.],'scaling': -1.0},
{'file': 'M100_Intcombo_0.193_cube.image.mom0.pbcor',
'range': [-0.3,25.],'scaling': -1.0}],
zoom={'blc': [190,150],'trc': [650,610]})
With the viewer open, you can flip back and forth between the images to compare them. Next, make a figure.
# In CASA
os.system('rm -rf M100_Intcombo_0.193_cube.image.mom0.pbcor.png')
imview (raster=[{'file': 'M100_Intcombo_0.193_cube.image.mom0.pbcor',
'range': [-0.3,25.],'scaling': -1.0,'colorwedge': T}],
zoom={'blc': [190,150],'trc': [650,610]},
out='M100_Intcombo_0.193_cube.image.mom0.pbcor.png')
Comparison with 12m alone Moment Maps
Below the moment maps from the 12m alone data are shown for comparison. The moment maps were made in the same way and the range and scaling for the figures are the same as that used for the 7m+12m figures. As expected the 7m+12m image shows considerably more extended emission. For comparison the 12m alone synthesized beam is 3.43"x2.38" while the 7m+12m is 3.93"x2.59".
-
Moment 0 for 12m data alone (no primary beam correction). -
Moment 0 for 12m data alone.
Convert 7m+12m Images to Fits Format
# In CASA
cpaste
os.system('rm -rf *.fits')
exportfits(imagename='M100_Intcombo_0.193_cube.image',fitsimage='M100_Intcombo_0.193_cube.image.fits')
exportfits(imagename='M100_Intcombo_0.193_cube.flux',fitsimage='M100_Intcombo_0.193_cube.flux.fits')
exportfits(imagename='M100_Intcombo_0.193_cube.image.mom0',fitsimage='M100_Intcombo_0.193_cube.image.mom0.fits')
exportfits(imagename='M100_Intcombo_0.193_cube.image.mom0.pbcor',fitsimage='M100_Intcombo_0.193_cube.image.mom0.pbcor.fits')
exportfits(imagename='M100_Intcombo_0.193_cube.image.mom1',fitsimage='M100_Intcombo_0.193_cube.image.mom1.fits')
--
Feathering the Total Power and 7m+12m Interferometric Images
Image the Total Power Data
Run listobs on the total power data to see what spw contains the CO
In CASA
os.system('rm -rf concat_m100.ms.listobs')
listobs(vis='concat_m100.ms',listfile='concat_m100.ms.listobs')
Image the TP data
In CASA
os.system('rm -rf TP_CO_cube')
sdimaging(infile='concat_m100.ms',
field=0,spw=15,
specunit='km/s',restfreq='115.271204GHz',
dochannelmap=True,
nchan=70,start=1400,step=5,
gridfunction='gjinc',imsize=[50,50],
cell=['10arcsec','10arcsec'],
outfile='TP_CO_cube')
Determine the TP Restoring Beam and Convert to Jy/beam
Next we need to determine the restoring beam size. This will depend on 3 factors
(1) The expected FWHP for the 12m TP dishes which have a -12dB taper and a Gaussian shape. This is 1.17 lambda / 12m (radians)
(2) Any broadening of the beam due to less than ideal sampling. For an antenna with -12dB taper, Nyquist = FWHM/2.4. To have less than 1% broadening the sampling should be 2 x Nyquist.
(3) The convolution of the gridding kernel with the combination of (1) and (2)
<figure id="TP_sampling.png">
</figure>
We have chosen the "gjinc" function in sdimaging because it produces the lease broadening of the effective beam. This is important because any broadening of the effective beam is equivalent to having used a smaller antenna.
For more information on these topics, see Mangum et al. 2007 (http://adsabs.harvard.edu/abs/2007A%26A...474..679M)
Two functions in the analysis utilities suite can be used to calculate the sampling of the TP data in the X and Y directions and then the final restoring beam, respectively.
In CASA
xSampling,ySampling=au.getTPSampling('concat_m100.ms',
showplot=True,plotfile='TP_sampling.png')
xSampling = 10.3766 arcsec ySampling = 15.0002 arcsec
The frequency required for au.gjincBeam is the observed sky frequency near the center of the line (not the rest frequency). The pixelsize should be the same as that used for the cell in sdimaging. The sampling parameters were determined by au.getTPSampling
In CASA
RestorBeam=au.gjincBeam(frequency=114.66,pixelsize=10,xSamplingArcsec=xSampling,ySamplingArcsec=ySampling)
The output to the terminal will be:
Theoretical primary beam FWHP = 52.5822 arcsec Expected effective restoring beam along scan = 54.4937 arcsec Expected effective restoring beam between rows = 54.9774 arcsec Geometric mean = 54.735 arcsec
Next set the restoring beam to the derived value.
In CASA
ia.open('TP_CO_cube')
ia.setrestoringbeam(major=str(RestorBeam)+'arcsec',
minor=str(RestorBeam)+'arcsec',
pa='0deg')
ia.done()
Convert the image from K to Jy assuming Jy/K = 55.0 Note currently sdimaging reports that the image it makes is in Jy/beam. This is a bug.
In CASA
os.system('rm -rf TP_CO_cube_Jy')
immath(imagename='TP_CO_cube',
expr='IM0*55.0',
outfile='TP_CO_cube_Jy')
Prepare Images for Feathering
Regrid TP image to match the shape of the 7m+12m image.
In CASA
os.system('rm -rf TP_CO_cube_Jy.regrid')
imregrid(imagename='TP_CO_cube_Jy',
template='M100_Intcombo_0.193_cube.image',
shape=[800,800,1,70],
axes=[0,1],output='TP_CO_cube_Jy.regrid')
Subimage both images to a matching size, excluding regions masked by the clean pbmin=0.2 and noisy edge pixels in the TP image. The Viewer can be used to determine a good joint region.
In CASA
os.system('rm -rf M100_Intcombo_0.193_cube.image.subim')
imsubimage(imagename='M100_Intcombo_0.193_cube.image',
outfile='M100_Intcombo_0.193_cube.image.subim',
box='230,184,604,598')
os.system('rm -rf TP_CO_cube_Jy.regrid.subim')
imsubimage(imagename='TP_CO_cube_Jy.regrid',
outfile='TP_CO_cube_Jy.regrid.subim',
box='230,184,604,598')
Creat subimaged version the mosaic response
In CASA
os.system('rm -rf M100_Intcombo_0.193_cube.flux.subim')
imsubimage(imagename='M100_Intcombo_0.193_cube.flux',
outfile='M100_Intcombo_0.193_cube.flux.subim',
box='230,184,604,598')
Multiply the TP image by the mosaic beam response of the 7m+12m image
In CASA
os.system('rm -rf TP_CO_cube_Jy.regrid.subim.depb')
immath(imagename=['TP_CO_cube_Jy.regrid.subim',
'M100_Intcombo_0.193_cube.flux.subim'],
expr='IM0*IM1',
outfile='TP_CO_cube_Jy.regrid.subim.depb')
Feather TP Cube with 7m+12m Cube
Feather with default parameters
In CASA
os.system('rm -rf M100_Feather_CO')
feather(imagename='M100_Feather_CO',
highres='M100_Intcombo_0.193_cube.image.subim',
lowres='TP_CO_cube_Jy.regrid.subim.depb')
Make Moment Maps of TP and Feathered Images
We will use the same technique as the 7m+12m image analysis above to make moment maps.
First, make moment maps for the TP image.
In CASA
myimage='TP_CO_cube_Jy.regrid.subim'
chanstat=imstat(imagename=myimage,chans='4')
rms1= chanstat['rms'][0]
chanstat=imstat(imagename=myimage,chans='66')
rms2= chanstat['rms'][0]
rms=0.5*(rms1+rms2)
os.system('rm -rf TP_CO_cube_Jy.regrid.subim.mom0')
immoments(imagename = 'TP_CO_cube_Jy.regrid.subim',
moments = [0],
axis = 'spectral',
chans = '10~61',
includepix = [rms*2.,50],
outfile = 'TP_CO_cube_Jy.regrid.subim.mom0')
os.system('rm -rf TP_CO_cube_Jy.regrid.subim.mom1')
immoments(imagename = 'TP_CO_cube_Jy.regrid.subim',
moments = [1],
axis = 'spectral',
chans = '10~61',
includepix = [rms*5.5,50],
outfile = 'TP_CO_cube_Jy.regrid.subim.mom1')
In CASA
os.system('rm -rf TP_CO_cube_Jy.regrid.subim .mom*.png')
imview (raster=[{'file': 'TP_CO_cube_Jy.regrid.subim.mom0',
'range': [-0.3,900.],'scaling': -1.0,'colorwedge': T}],
out='TP_CO_cube_Jy.regrid.subim.mom0.png')
imview (raster=[{'file': 'TP_CO_cube_Jy.regrid.subim.mom1',
'range': [1455,1695],'colorwedge': T}],
out='TP_CO_cube_Jy.regrid.subim.mom1.png')
Make moment maps for the feathered image.
In CASA
myimage='M100_Feather_CO'
chanstat=imstat(imagename=myimage,chans='4')
rms1= chanstat['rms'][0]
chanstat=imstat(imagename=myimage,chans='66')
rms2= chanstat['rms'][0]
rms=0.5*(rms1+rms2)
os.system('rm -rf M100_Feather_CO.mom0')
immoments(imagename = 'M100_Feather_CO',
moments = [0],
axis = 'spectral',
chans = '10~61',
includepix = [rms*2.,50],
outfile = 'M100_Feather_CO.mom0')
os.system('rm -rf M100_Feather_CO.mom1')
immoments(imagename = 'M100_Feather_CO',
moments = [1],
axis = 'spectral',
chans = '10~61',
includepix = [rms*5.5,50],
outfile = 'M100_Feather_CO.mom1')
In CASA
os.system('rm -rf M100_Feather_CO.mom*.png')
imview (raster=[{'file': 'M100_Feather_CO.mom0',
'range': [-0.3,25.],'scaling': -1.0,'colorwedge': T}],
out='M100_Feather_CO.mom0.png')
imview (raster=[{'file': 'M100_Feather_CO.mom1',
'range': [1455,1695],'colorwedge': T}],
out='M100_Feather_CO.mom1.png')
Primary Beam Correct the Moment 0 Image
Apply the primary beam response to the feathered image
In CASA
os.system('rm -rf M100_Intcombo_0.193_cube.flux.1ch.subimage')
imsubimage(imagename='M100_Intcombo_0.193_cube.flux',
outfile='M100_Intcombo_0.193_cube.flux.1ch.subimage',
box='230,184,604,598',
chans='35')
In CASA
os.system('rm -rf M100_Feather_CO.mom0.pbcor')
immath(imagename=['M100_Feather_CO.mom0', \
'M100_Intcombo_0.193_cube.flux.1ch.subimage'],
expr='IM0/IM1',
outfile='M100_Feather_CO.mom0.pbcor')
Create a figure of primary beam corrected moment 0.
In CASA
os.system('rm -rf M100_Feather_CO.mom0.pbcor.png')
imview (raster=[{'file': 'M100_Feather_CO.mom0.pbcor',
'range': [-0.3,25.],'scaling': -1.0,'colorwedge': T}],
out='M100_Feather_CO.mom0.pbcor.png')
Compare the Different Images
Now lets compare all the different images:
-
Primary beam corrected moment 0 for TP+7m+12m data. -
Moment 1 for TP+7m+12m data. -
Primary beam corrected moment 0 for 7m+12m data. -
Moment 1 for 7m+12m data. -
Primary beam corrected moment 0 for the 12m data .
-
Moment 1 for 12m data.
-
Primary beam corrected moment 0 for the 7m data.
-
Moment 1 for 7m data. -
Moment 0 for the TP data. -
Moment 1 for the TP data.
Last checked on CASA Version 4.1.0.
