Light field photography and microscopy

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Transcription:

Light field photography and microscopy Marc Levoy Computer Science Department Stanford University

The light field (in geometrical optics) Radiance as a function of position and direction in a static scene with fixed illumination L is radiance in watts / (m 2 steradians)

Dimensionality of the light field for general scenes 5D function L ( x, y, z, θ, φ ) in free space 4D function L (? )

Some candidate parameterizations for the 4D light field Point-on-plane + direction y L ( x, y, θ, φ ) x Two points on a sphere L (θ 1, φ 1, θ 2, φ 2 ) Points on two planes L ( u, v, s, t )

Devices for recording light fields big scenes handheld camera [Buehler 2001] small scenes array of cameras [Wilburn 2005] plenoptic camera [Ng 2005] light field microscope [Levoy 2006]

and creating Devices for recording light fields big scenes handheld camera [Buehler 2001] small scenes array of cameras [Wilburn 2005] plenoptic camera [Ng 2005] light field microscope [Levoy 2006] light field illumination

Stanford Multi-Camera Array [Wilburn SIGGRAPH 2005] 640 480 pixels 30 fps 128 cameras synchronized timing continuous streaming flexible arrangement

Synthetic aperture photography

Example using 45 cameras [Vaish CVPR 2004]

(movie is available at http://graphics.stanford.edu/projects/array)

Light field photography using a handheld plenoptic camera Ren Ng, Marc Levoy, Mathieu Brédif, Gene Duval, Mark Horowitz and Pat Hanrahan (Proc. SIGGRAPH 2005 and TR 2005-02)

Conventional versus light field camera

Conventional versus light field camera uv-plane st-plane

Prototype camera Contax medium format camera Kodak 16-megapixel sensor Adaptive Optics microlens array 125µ square-sided microlenses 4000 4000 pixels 292 292 lenses = 14 14 pixels per lens

Typical image captured by camera (shown here at low res)

Digital refocusing Σ Σ refocusing = summing windows extracted from several microlenses

Example of digital refocusing Ó 2007 Marc Levoy

Example of digital refocusing Ó 2007 Marc Levoy

Example of digital refocusing Ó 2007 Marc Levoy

Example of digital refocusing Ó 2007 Marc Levoy

Example of digital refocusing Ó 2007 Marc Levoy

Refocusing portraits (movie is available at http://refocusimaging.com) Ó 2007 Marc Levoy

Extending the depth of field conventional photograph, main lens at f / 4 conventional photograph, main lens at f / 22 light field, main lens at f / 4, after all-focus algorithm [Agarwala 2004]

Macrophotography (movie not available online) 2005 Marc Levoy

Digitally moving the observer Σ moving the observer = moving the window we extract from the microlenses Σ

Example of moving the observer

Example of moving the observer

Example of moving the observer

Moving backward and forward

Moving backward and forward

Moving backward and forward

Light Field Microscopy Marc Levoy, Ren Ng, Andrew Adams, Matthew Footer, and Mark Horowitz (Proc. SIGGRAPH 2006)

A traditional microscope eyepiece intermediate image plane objective specimen

A light field microscope (LFM) eyepiece intermediate image plane sensor 40x / 0.95NA objective 0.26µ spot on specimen 40x = 10.4µ on sensor 2400 spots over 25mm field objective specimen reduced lateral resolution on specimen = 0.26µ 12 spots = 3.1µ 125 2 -micron microlenses 200 200 microlenses with 12 12 spots per microlens

A light field microscope (LFM) eyepiece sensor intermediate image plane objective specimen

Example light field micrograph orange fluorescent crayon mercury-arc source + blue dichroic filter 16x / 0.5NA (dry) objective f/20 microlens array 65mm f/2.8 macro lens at 1:1 Canon 20D digital camera Typical image captured by camera (shown here at low res) ordinary microscope light field microscope

The geometry of the light field in a microscope objective lenses are telecentric f microscopes make orthographic views translating the stage in X or Y provides no parallax on the specimen out-of-plane features don t shift position when they come into focus front lens element size = aperture width + field width PSF for 3D deconvolution microscopy is shift-invariant (i.e. doesn t change across the field of view) 2006 Marc Levoy

Example light field micrograph (movies are available at http://graphics.stanford.edu/projects/lfmicroscope) panning sequence focal stack

Real-time viewer (movie is available at http://graphics.stanford.edu/projects/lfmicroscope/2007.html)

Other examples (movies are available at http://graphics.stanford.edu/projects/lfmicroscope) fern spore (60x, autofluorescence) Golgi-stained neurons (40x)

Zebrafish optic tectum (collaboration with Florian Engert) (movies not yet available online) genetically modified to express GFP (40x) calcium imaging of neural activity (40x)

Calcium imaging under visual stimulation (collaboration with Stephen Smith) (movie not yet available online) (Todd Anderson)

3D reconstruction 4D light field digital refocusing 3D focal stack deconvolution microscopy 3D volume data (DeltaVision) 4D light field tomographic reconstruction 3D volume data (from Kak & Slaney)

Silkworm mouth (40x / 1.3NA oil immersion) (movie is available at http://graphics.stanford.edu/projects/lfmicroscope/2005.html) 100µ slice of focal stack slice of volume volume rendering

GFP-labeled zebrafish neurons (40x / 0.8NA water immersion) focal stack deconvolved (movie not yet available online) volume rendering

Combined light field microscope (LFM) and light field illuminator (LFI) [To appear in Journal of Microscopy, 2009] applications: exotic microscope illumination reducing scattering using 3D follow spots characterizing and correcting for aberrations microscopic structured light rangefinding gonioreflectometer for opaque surfaces optical stimulation of neural tissues in 3D

Angular control over lighting brightfield image sent to projector s graphics card

Angular control over lighting brightfield (tilt due to imperfect placement of microlenses)

Angular control over lighting darkfield

Angular control over lighting headlamp

Angular control over lighting oblique

Single blond hair (10x/0.45NA) brightfield 100µ

Single blond hair (10x/0.45NA) headlamp 100µ

Single blond hair (10x/0.45NA) darkfield 100µ

Single blond hair (10x/0.45NA) headlamp 100µ

Single blond hair (10x/0.45NA) oblique 100µ

Spatial control over lighting (collaboration with Julie Theriot) 10µ Listeria monocytogenes in mouse intestine villus 6x improvement in contrast color composite with green = GFP, red = rhodamine-phalloidin

Tracking 3D bacterial motions using follow spotlights [Shenoy and Theriot] motion of Listeria monocytogenes imaged in 2µ thick chamber geometry of bacterial trajectories in 2D and 3D

Which rays contribute to a pixel as the plane of focus is changed?

Which rays contribute to a pixel as the plane of focus is changed?

Which rays contribute to a pixel as the plane of focus is changed?

Which rays contribute to a pixel as the plane of focus is changed?

Which rays contribute to a pixel as the plane of focus is changed?

Which rays contribute to a pixel as the plane of focus is changed?

Which rays contribute to a pixel as the plane of focus is changed?

Which rays contribute to a pixel as the plane of focus is changed?

Digitally refocusing the illumination (movie is available at http://graphics.stanford.edu/papers/lfillumination)

Other ideas maximize illumination over selected voxels while minimizing illumination over other voxels use algorithms from radiation treatment planning?

4D designer lighting (from [Levoy 2004])

4D designer lighting (from [Levoy 2004])

Correcting spherical aberrations digitally using light fields

Creating guide stars using programmable illumination projector camera...and using the LFM as a Shack-Hartmann sensor Gray codes aberration as a function of pupil position

Digital correction of aberrations (60 / 1.0 NA dipping objective) distilled water 10% glycerol uncorrected digitally corrected

Structured light rangefinding spatial resolution = microlens count crude 3D model combine with BRDFs / BSSRDFs to measure or parameterize new models of material appearance

Reflectance properties of biological objects (video available at http://www.mbl.edu/mrc/hanlon/video.html) (movie is available at http://graphics.stanford.edu/projects/lfmicroscope/2006.html) (Roger Hanlon) 200µ single iridiphores in live skin sample of Loligo pealeii (Lydia Mathger)

Slice of BSSRDF of single squid skin iridiphore specular component iridescence component

http://graphics.stanford.edu 2005 Marc Levoy