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Spectroscopy with LIFU

WEAVE's LIFU fibres feed a dual-arm (blue + red) spectrograph housed on one Nasmyth platform of the WHT. A 5900-A dichroic splits the light between the blue and red arms. Dispersion is effected by inserting one of three VPH gratings in the blue arm, and one of two in the red arm, i.e. the two arms offer a total of five spectroscopic modes (blue low-res, red low-res, blue high-res 1, blue high-res 2, red high-res). The table below lists the wavelength range, spectroscopic resolution and scale (Å/pixel) expected for each. The spectroscopic resolution delivered by LIFU is half that delivered by the WEAVE MOS and mIFU modes, because the LIFU fibres have twice the diameter of the MOS/mIFU fibres.

Low-resolution High-resolution
Blue arm Red arm Blue arm Red arm
VPH grating 'B LR''R LR''B HR1''B HR2''R HR'
Wavelength range (Å) 3660-60605790-95904040-46504730-54505950-6850
Inter-CCD gap (Å) 5491-55397590-76694525-45365302-53156412-6431
Spec. resolution R for LIFU 25002500100001000010000
R in km/s 120120303030
Scale (Å pixel-1) 0.300.480.0760.0900.11
WHT/WEAVE throughput (expected) ~ 0.25 ~ 0.15 to 0.20

The spectroscopic resolutions currently being achieved routinely by LIFU (at the middle of each wavelength range) are R ~ 3000 in low-resolution mode and R ~ 11000 in high-resolution mode.

In high-resolution mode on the blue arm, observers have a choice of two possible VPH gratings, for wavelength range 4040 - 4650 Å (HR1 = 'blue') or 4730 - 5450 Å (HR2 = 'green'); they cannot be deployed simultaneously.

For any given observation, low- and high-resolution modes can't be mixed, e.g. it's not possible to observe at low resolution in the blue arm and at high resolution in the red arm. Also, a blue-arm VPH cannot be used on the red arm, or vice versa. The three allowed combinations of blue (B) + red (R) configurations for observing are thus: 'B LR' + 'R LR'; 'B HR1' + 'R HR' and 'B HR2' + 'R HR'.

The pixel scales observed during commissioning are close to the values given above.

The figure below (click to enlarge) shows the the wavelength range (and inter-CCD gap) of each of the 5 available spectroscopic configurations (in blue and red), relative to the wavelength of the dichroic cut (5900 Å, green dotted line) and a typical La Palma night-sky spectrum (black). The vertical black dotted line indicates the wavelength of the most prominent atmospheric absorption (A band, ~ 7594 Å), which falls (by design) into the inter-CCD gap when observing at low-res on the red arm.

On each arm, the spectra fall on a mosaic of two 6144 x 6160 pixel deep-depletion EEV CCDs, i.e. a total of 12288 x 6160 15-micron pixels (total area ~ 90 mm x 180 mm).

The x direction (physically, parallel to the surface of the optical bench) is spectroscopic, the y direction is 'spatial', i.e. from fibre trace to fibre trace (physically, vertical). In each arm, the inter-CCD gap is about 2.5 mm (equivalent to 170 pixels in x) (TBC).

In each arm ~ 8200 x 6140 pixels are used for science. On the blue arm, the spectra cover roughly 0 < x < 8k; and on the red arm roughly 4k < x < 10k.

The images below show LIFU low-resolution ThAr arc-lamp exposures taken with the blue arm (top, wavelength increases to left) and with the red arm (bottom image, wavelength increases to right). The exposure times were 25 and 9 sec respectively.

These images have been cropped to show most of the useful wavelength range in the x direction (7k, 8k pixels), and approximately the central third of the slit (2k pixels) in the y direction. Each white dot corresponds to an arc line (vertical bright line) detected in the spectrum from one fibre (horizontal).

In low-resolution mode (on both arms) the arc lines are straight, and nearly parallel to the y axis.

A magnified view of the centre of an image shows how the spectra are grouped in blocks of 21 in the y direction, reflecting the grouping of fibres into individual slitlets (29 of them) along the LIFU slit-head in the spectrograph.

About 2/3 of the way up this image, we see the prominent dark band of the overscans at the junction between the upper halves (4 quadrants) and the lower halves (4 quadrants) of the two 6k x 6k CCDs. Below the overscan we see the 21 fibres in each of slitlets 13 and 14 and (just below the overscan region), the first fibre of slitlet 15. The other 20 fibres of slitlet 15 are visible above the overscan. The middle fibre of the 21 in slitlet 15 is #305, the fibre which is physically at the centre of the LIFU science array.

The fibres within a slitlet are separated in the y direction by ~ 9.1 pixels. The separation between the last fibre in one slitlet to the first in the next (peak to peak) is about 19 pixels. The fibres thus span ~ (29 * 20 * 9.1) + (28 * 19) + 32 ~ 5840 pixels in the y direction.

Information about the mapping of fibre number to y pixel value, and the location in y of the central fibre of the array (#305), can be found on a separate page.

In high-res mode, the format is similar, except that the arc lines are curved (i.e. the wavelength at a given x depends on fibre number). This is a high-res ThAr arc exposure from the red arm, i.e. with VPH 'R HR' (click on image to enlarge):

On the blue arm, the hi-res spectra (i.e. with VPH 'B HR1' or 'B HR2') are similarly curved, but in the opposite direction.

The figures above indicate schematically for the blue arm (left) and the red-arm (right) the pixels used for science (yellow), masked off (grey) and corresponding to bias (8 vertical strips in green) and overscan (8 horizontal and 8 vertical strips in red). The widths of the bias and overscan strips are ~ 40 and 15 pixels respectively. The overscan strips come in pairs so e.g. the thickness in y of the central overscan strip, prominent on the detector array (as noted above) is ~ 30 pixels.

The numbering of the quadrants 'TSn' reflects that used in the FITS headers e.g. BIASSECn for n = 1 to 4.

In slow readout mode (used for most science exposures), the readout noise is typically ~ 2.8 electrons per pixel rms on the blue arm, and 2.4 rms on the red. For this readout mode the gains are approximately 1.0 on both arms.

In slow mode, with no binning, the readout time is 150 sec.

The detectors can also be read out binned (x1, x2, x4 in each direction) and/or with different readout speeds, but not all of these options are available to observers, and most are suitable only for test/commissioning purposes. See here for a table of readout times.

Three binning options are available to observers: x1, x2 or x4 in the spectral direction (x). Binning in the 'spatial' direction (y) is not offered because it would result in blending of the fibre traces.

The detectors cannot be windowed on readout.

For reasons of observing efficiency and for optimal performance from the data-reduction pipeline, there are some constraints on the allowed lengths of observing blocks (OBs, typically 1 hour for survey observations), on the lengths of individual exposures within each OB, and on the linkage betwee different OBs.

For open-time observers, the rules are set out on the WEAVE open-time pages, and in particular on the PROGTEMP-builder page, which tells open-time observers how to specify the observations required.

Cross-talk between fibres
As noted above, the separation of the fibre traces on the CCD is ~ 9.1 pixels (in the y direction). The delivered FWHM in that direction is ~ 5 pixels, small enough that the spectra can easily be traced and extracted by the CASU pipeline.

The cross-talk (at extraction) between adjacent fibres has not been characterised accurately but, with an FWHM of ~ 5 pixels, is likely be ~ few %.

Ghosting
In all 5 spectroscopic modes, each spectrum on the detector is accompanied by a faint ghost image a few pixels across, thought to be a recombination ghost. In x, the ghost image is usually located near the mid-point of the illuminated area. In y, the locations of the spectrum and ghost are roughly symmetrical about the centre (y = yc) of the illuminated area. I.e. if the spectrum is at y = yc + dy, the ghost will probably be within ~ 160 pixels of y = yc - dy. The peak counts in the ghost are typically <~ 1% the peak in the spectrum. The exact details may change as a result of the ongoing realignment of the spectrograph.

More generally, the stray-light contribution from any one object to the (non-adjacent) spectrum of any other object is expected to be < 0.5%.

Chris Benn, Lilian Domínguez, Cecilia Fariña

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Last modified: 25 August 2024

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