02.02.2013 Views

EurOCEAN 2000 - Vlaams Instituut voor de Zee

EurOCEAN 2000 - Vlaams Instituut voor de Zee

EurOCEAN 2000 - Vlaams Instituut voor de Zee

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

612<br />

200 mm<br />

stages with<br />

optics and<br />

CCD camera<br />

1.9 m<br />

1000 mm stage<br />

45°<br />

1.8 m<br />

Platehol<strong>de</strong>r<br />

180mm<br />

140x100x25<br />

mirror<br />

Laser / collimator<br />

assembly<br />

Figure 4: ‘HoloScan’ hologram replay machine (off-axis configuration)<br />

• Physical Layout: Figure 4 shows a schematic of the replay system for in-line and off-axis<br />

mo<strong>de</strong>s. The replay laser (Kimmon 180mW 442nm HeCd) is mounted above the collimating<br />

optics (a reversed Galilean telescope producing a 100mm diameter beam flat to λ/5) along one<br />

arm. A set of computer controlled stepper-stages (Ealing DPS system, 1000 mm stage with 10<br />

µm steps and two 200 mm stages with 5 µm steps) carrying a vi<strong>de</strong>ocamera (JAI CV-M300<br />

CCD) is mounted along the other arm. The platehol<strong>de</strong>r is near the vertex end of the stage arm<br />

and it is possible to rapidly change the replay angle between the in-line (normal to plate) and<br />

off-axis angles. The vi<strong>de</strong>o output is captured by a ITI PC-Vision frame-grabber and then<br />

processed to clean up the image and i<strong>de</strong>ntify the true focal plane of each object within the 3dimensional<br />

sample volume.<br />

• Scanning and Data Extraction Procedure: The extraction of species distribution data is<br />

separated into three steps. Firstly, the vi<strong>de</strong>ocamera is scanned through the <strong>de</strong>pth of the sample<br />

volume (z) in a series of 0.1 mm steps. When the end is reached the camera is panned si<strong>de</strong>ways<br />

before returning to eventually scan the entire volume. For each step, the embed<strong>de</strong>d image<br />

processor receives the holographic images and processes them to clean up the noise, find<br />

plankton micro-organism and locate the true focal plane of each object within the volume. The<br />

system combines low (noise cleaning and image enhancement), middle (image segmentation,<br />

object localisation and tracking) and high level (3-d information extraction) processing<br />

modules that interact with a final high level module based on a neural net which allows species<br />

classification.<br />

System Trials and Performance<br />

The camera is in the final stages of construction. A large water tank is currently being<br />

fabricated which will encompass the front of the camera and allow completion of final<br />

laboratory testing before docksi<strong>de</strong> trials take place in August/September <strong>2000</strong>.<br />

A series of photographs of reconstructed holographic images of preserved marine plankton<br />

may be seen in Figure 5. These were recor<strong>de</strong>d in the laboratory in a Perspex tank using the<br />

camera’s laser and optical assembly. The top row of "raw" images are taken from in-line<br />

holograms (each image is 430 μm wi<strong>de</strong>). The second row of "raw" images are taken from off-

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!