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1.
Fig. 8

Fig. 8. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

Averaged density values (cells/mm2) for photoreceptors (red symbols) and ganglion cells (blue symbols) as a function of retinal eccentricity.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.
2.
Fig. 1

Fig. 1. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

Adaptive optics multiphoton microscope. AO module, adaptive optics module (Hartmann-Shack wavefront sensor and deformable mirror); PMT, photomultiplier tube.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.
3.
Fig. 5

Fig. 5. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

(a, b) Reconstructed volume renderings of the chicken central retina: top (a) and bottom (b) views. Diagonal cross-section (c) and transversal tomography (d) computed from (a). A different false color has been chosen for a better visualization.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.
4.
Fig. 7

Fig. 7. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

Photoreceptor density values (cells/mm2) as a function of retinal eccentricity. The black line fitted to the data gives a significant linear decrease with increasing retinal eccentricity (p< 0.0001). Linear fit: y = −175x + 20675.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.
5.
Fig. 6

Fig. 6. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

TPEF images of the ganglion cells and photoreceptors of a chicken retina for different retinal eccentricities (12° (left), 50° (middle) and 85° (right). Ganglion cells (upper panels); photoreceptors (bottom panels). Scale bar: 50 μm.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.
6.
Fig. 9

Fig. 9. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

Values of maximum anatomical resolving power (c/deg) in the chick retina as a function of retinal eccentricity computed using Eq. (1). An example of an image corresponding to the Fourier transform of a photoreceptor mosaic is shown on the left. Linear fit: y = −0.03x + 7.15.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.
7.
Fig. 2

Fig. 2. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

Microscopy images of different chicken retinal layers acquired with a bright-field microscope and a 20x objective. Nerve fibers (a), ganglion cells (b), inner nuclear layer (c), and photoreceptors (oil droplets, see text) (d). Scale bar: 50 µm.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.
8.
Fig. 4

Fig. 4. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

TPEF in chicken retinal tissues. (a) The same transversal XZ section of a chicken retina as in Fig. 3a. (b)-(g) TPEF images acquired with a 100x objective for the same retinal area as in Fig. 3; (b) ganglion cells; (c and d) inner nuclear layer; (e) outer plexiform layer; (f) outer nuclear layer and (g) photoreceptors. Scale bar: 25 μm.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.
9.
Fig. 3

Fig. 3. From: Analysis of the chicken retina with an adaptive optics multiphoton microscope.

(a) Histological transversal section of a fixed and stained chicken retina. (b)-(g) TPEF images of the different retinal layers acquired with a 20x objective: nerve fibers (b), ganglion cells (c), inner plexiform layer (d), inner nuclear layer (e), outer nuclear layer (f), and photoreceptors (oil droplets, see text) (g). Images correspond to a retinal eccentricity of about 30 deg. TPEF signal is exclusively due to the local endogenous fluorescence (autofluorescence). Scale bar: 50 µm.

Juan M. Bueno, et al. Biomed Opt Express. 2011 June 1;2(6):1637-1648.

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