In the worst case scenario you'll need to get the Prosilica camera up and running from the start. The camera is always connected so what I mean by not "on" is that somehow we've closed the Prosilica Camera adl screen (the MEDM screen you see to your right) and you don't see an icon on the task bar labeled "Start Prosilica". If this indeed is the case, then alas yes...the soft EPICS Input Output Controller (or IOC) has closed up shop. Let's restart it. To do this look on the desktop for an icon labeled "Start Prosilica", the icon will look like a little camcorder (digital of course). Double click on that sucker and that should fire up the IOC. Now we need to get the camera configured properly...most of the parameters are saved automatically so there shouldn't be much to do here, but the most critical thing is to put the EPICS driver for the CCD in an acquire mode. You'll always need to do this if you restart the IOC, so go to the X26A Beamline Control adl screen and you should see that the 2nd button down on the list is "Prosilica CCD". If you press that button a screen looking remarkably similar to the one to the right should open up. We'll discuss some of the options you can set here in a moment, but let's focus on getting the camera viewable right now. We need to get the EPICS driver streaming the images from the CCD. To do this go to the Prosilica Camera adl screen that just opened and under the section labeled "Collect" there will be a label that says "Acquire" and a button next to that labeled "Start" beckoning to be pressed. If the CCD isn't streaming images the text area above these buttons will read "Done" in green. Once you press the Start button (go ahead...it's OK) this will read "Collecting" in yellow and the detector state will read acquire. You'll also see the image counter streaming the frame number. If you want you can close this adl screen for now, we'll come back to it again in a minute.

With the IOC streaming images from the Prosilica CCD the next thing we need to do is get ImageJ started, that's what we'll be using to view the images through an EPICS plugin Mark wrote. There should be an ImageJ icon on the desktop to start it up.

 ImageJ is a public domain Java image processing program inspired by NIH Image for the Macintosh. It's very widely used in the analysis of images collected using various types of microscopes so has a number of built in tools that are well suited to what we do with the optical CCD we use at the beamline. I'll let you browse the ImageJ website to get a full flavor for all it's capable of, but for our purposes let's go over how we use it to view the Prosilica image stream using Mark's areaDetector plugin.  If you successfully launched ImageJ using the desktop icon you should be presented with a toolbar like the one shown right up above, the top one...yeah...the one that says "ImageJ". To launch the areaDetector plugin select the menu option that says "Plugins" -> "EPICS_areaDetector" -> "EPICS AD Viewer" . This will launch the plugin toolbar, the bottom toolbar shown in the picture above. To get the image stream going click on the "Start" button, which will open up the display window. Voila! You should be viewing a Technicolor movie of your sample. The magnifying lens on the ImageJ toolbar lets you zoom in (left mouse button) and out (right mouse button), you can draw a crosshair with the cross-shaped tool, draw lines with the line tool, etc.

Mark has also written a companion plugin that will display a dynamically updated line profile. This is handy, for example, if you want to observe the beam profile on the YAG or ZnS phosphor in real time during focusing. To use this, draw a line through the object you want profiled then select "Plugins -> EPICS_areaDetector -> Dynamic profiler". This will open a new window that will display in real time the intensity in each pixel under the line that was drawn in the image stream.

One of the most important things we use the optical image for is to tell you where the beam is on your sample. With the old Toshiba CCD we did this with a manually adjustable X-Y crosshair. But alas...it requires an analog signal. In ImageJ this is easily done with the crosshair button. You select the tool, click on the image where the beam is, and tada...all done. The crosshair will remain in the same position even if you zoom in and out of the image. We will mark the beam position for you when we set up your experiment, but I have a feeling there will be instances where we will accidentally close the image window or erase the crosshair mark. But that's OK, it turns out that ImageJ let's you save the coordinates of the crosshair as an roi. So after we mark the beam, we we will do is save the position in your data director under the file name "Beam.roi" . If you accidentally lose the crosshair all you'll need to do is open this file using "File -> Open -> Beam.roi" and it'll return to where it was marked.

Another useful aspect of ImageJ is that it allows for scale calibration. Once an image is calibrated you'll be able to measure distances and areas in micrometers. The easiest way to do this is to open an image that has been precalibrated. Again, we'll do this for you before you start, but in case you need to reapply the scaling, simply get the image stream running as described above. Once running, open our calibrated image in ImageJ, it'll be called "X26A_Scale.tif" and it will open in a separate window. Now with this window selected choose Analyze -> Set Scale... from the ImageJ menu. A window will pop up showing the scaling for this image (basically microns per pixel), just check the box labeled "Global" and select "OK". This will apply this scaling to all open windows including the video stream. Once you've done that you can draw a line using the line tool or an area using the freehand roi tool and measure the distance or area you've defined by selecting Analyze -> Measure. You can even save an image from the video stream for posterity with a scale bar attached for future reference. To do this you'll first need a snapshot. This is actually really easy to do by simply going to the areaDetector plugin toolbar (which is most likely minimized on tha taskbar) and clicking the Snap button. With this snapshot you now have a couple of ways to get a calibrated scale bar on the image before saving it. The option I like best is to use ImageJ's scale bar tools. You can access these if they aren't open alreadey by clicking on the >> button at the rightmost side of the ImageJ toolbar and selecting Scale Bar Tools for Microscopes. This will change the set of tool buttons displayed and one of these should be a little icon that looks like a teeny weeny microscope. If you select this you'll see an option labeled X26A. Go ahead and select this and then click on the icon that looks like a scale bar with um next to it. This will pop up some menu boxes. In the first menu there's a listing for "current spatial calibration" in which you should select 5X from the drop down list. This is the objective lens we use most often. Select OK and another menu pops up asking you how big a scale bar you'd like on your image. The default is 100 um and once you've chosen you'll see a modified image with a scale bar at the bottom and various bits of information about when the frame was collected, etc. The second way to insert a scale bar is a bit simpler, simply go to "Analyze -> Tools -> Scale bar".

The Readout frame also provides control for the CCD gain (for our purposes let's consider this the image brightness). This can be varied between 1 and 22. The other area of interest I wanted to pint out here is the Collect frame from which we can adjust the image frame rate. We'll do this by adjusting the Exposure time and Acquire period. Both will affect how fast the frames update, but in general it's best to keep the exposure time as low as possible. For the GC 1360C this is 0.05. The Acquire period can then be considered the direct inverse of the frame rate and can be adjusted accordingly depending on your needs.