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Spatial optical coherence compares field samples at different positions, usually across a transverse plane at equal time. Two small openings separated by $d$ sample this correlation: recombine their light with nearly matched travel times and measure interferometric visibility near the central interference fringes. A narrow opening in front of a broad-spectrum lamp can improve transverse spatial optical coherence while leaving its short temporal optical coherence. These are separate controls: narrow spectral selection by itself need not make an extended source spatially coherent. MIT's lecture notes illustrate the two-opening test and these contrasting source preparations. ^[ref].

To isolate source width, stipulate a distant, narrowband source with uniform angular brightness on $-\Theta /2\le \alpha \le \Theta /2$, and mutually uncorrelated emission from distinct source directions. Here $\Theta \ll 1$ is the full angular width in radians, $\lambda$ the common wavelength, and the two openings are separated by $d$ along the same transverse direction as the source extent. Neglect amplitude differences across the openings. Each source direction contributes a phase difference approximately $2\pi d\alpha /\lambda$. Averaging its complex cross term givesThe sinc function is extended continuously to one at $q=0$. The sign convention in the exponential depends on which opening is numbered first; the symmetric model gives the same real result either way. Equal detected single-opening light intensities make the magnitude equal to interferometric visibility. A displaced source center adds a deterministic wave phase, shifting the interference fringes without changing their contrast.

The strips show $I/(I_1+I_2)=1+g_{12}^{(1)}(0)\cos \varphi$ with equal single-opening light intensities, a common phase difference coordinate $\varphi$ and no single-slit diffraction envelope. At $q=1/2$, contrast is $2/\pi \approx 0.636620$; at $q=1$, it vanishes. At $q=3/2$, the correlation is $-2/(3\pi )\approx -0.212207$: weak fringes return with bright and dark positions exchanged. For $\lambda =500\mathrm{nm}$ and $d=0.5\mathrm{mm}$, the first zero occurs at $\Theta =1\mathrm{mrad}$. This is a calculated example, not an experimental measurement or a universal source-width law.

A proposed source-width control follows directly from this model: illuminate two fixed openings with a distant adjustable luminous slit of full width $w$ at distance $R$, so $\Theta \approx w/R$ under the small-angle approximation, and hold $d$ and the spectral selection fixed. Increasing $w$ overlays more mutually incoherent, displaced interference fringe patterns. Record profiles over several near-central fringes, measure each opening separately and correct intensity imbalance as in first-order optical coherence. Restrict the recorded region so the path difference stays small compared with the optical coherence length, and resolve the fringes with the detector. Real source nonuniformity, finite opening widths and spectral spread modify the stipulated sinc function law. This protocol is a model-based extension of the verified two-opening method, not a claim that the plotted curves were measured.

Thus an extended incoherent source can give locally excellent wave interference when the sampled separation is small, and almost none when it is larger. The useful scale $d\Theta \sim \lambda$ expresses how source extent limits the aperture over which coherent addition is available. The same angular averaging explains why narrowing a source opening can recover visible interference fringes, even without narrowing its optical spectrum.

The ability of an imaging or measurement system to distinguish nearby spatial features. A resolution criterion must specify the features and measurement conditions: diffraction, noise and sampling can all limit the distinction. A small pixel spacing alone does not establish high spatial resolution; electron microscope resolution illustrates the role of wavelength and numerical aperture.

In spatial sampling of a wave, a detector records a wave at positions $x_n=np$ separated by pitch $p>0$. Angular wavenumbers differing by $2\pi m/p$, with integers $m$, give identical samples of a complex Fourier mode:This is spatial aliasing. To distinguish arbitrary sinusoids within a prescribed band, require $|k|<\pi /p$, equivalently $|{\nu }_x|<1/(2p)$, the Nyquist spatial frequency. Thus $p<{\lambda }_{\min }/2$ for the shortest allowed wavelength. At equality a sine can vanish at every sample, so phase information can be lost. The Nyquist–Shannon sampling theorem states the precise reconstruction conditions for a bandlimited function; a finite scan introduces further limitations.

The synthetic two-tone snapshot iswhere both ${\nu }_j$ count cycles per metre. The component wavelengths are $0.50\mathrm{m}$ and $0.125\mathrm{m}$. With $p=0.05\mathrm{m}$, both lie below the Nyquist spatial frequency of $10$ cycles per metre. With $p=0.10\mathrm{m}$, the $8$-cycle component aliases to the $2$-cycle component: at every $x_n=n/10$, $\cos (2\pi \cdot 8x_n)=\cos (2\pi \cdot 2x_n)$. The sampled sum is therefore indistinguishable from $1.5\cos (4\pi x)$, although the continuous curves differ between samples. Drawing lines between sample points cannot resolve this ambiguity.

For a chemical solution in a validated linear regime,where $l$ is path length in $\mathrm{dm}$ and $c$ is solute mass per final solution volume in $\mathrm{g}\mathrm{m}{\mathrm{L}}^{-1}$. These conventions give specific rotation units $\mathrm{deg}\mathrm{mL}{\mathrm{g}}^{-1}\mathrm{d}{\mathrm{m}}^{-1}$. Specify solvent, temperature $T$ and wavelength $\lambda$: specific rotation is conditional on the sample environment.^[ref]

For an original model, stipulate an unnamed enantiomer pair in the same achiral solvent at $T=20^{\circ }\mathrm{C}$ and wavelength $\lambda =589\mathrm{nm}$. Assign the positive member specific rotation $+40\mathrm{deg}\mathrm{mL}{\mathrm{g}}^{-1}\mathrm{d}{\mathrm{m}}^{-1}$, assumed constant over the modeled concentrations. With $l=1\mathrm{dm}$ and $c=0.200\mathrm{g}\mathrm{m}{\mathrm{L}}^{-1}$,These are chosen model parameters, not measured properties of a named material. Doubling only $l$ or only $c$ doubles $\alpha$ within this stipulated linear model; doubling both multiplies it by four. A real chemical solution must be checked for concentration dependence rather than assuming that $0.200\mathrm{g}\mathrm{m}{\mathrm{L}}^{-1}$ is dilute enough.

For an additive mixture containing only this enantiomer pair as solutes, put $k=[\alpha {]}_{+}$ and write $c_{+},c_{-}$ for their mass concentrations. ThenBecause enantiomers have the same molar mass, their relative mole fractions within the pair also equal their relative mass fractions: $c_{+}=x_{+}c$, $c_{-}=x_{-}c$. Thus $\alpha =klc(x_{+}-x_{-})$, which connects optical rotation to enantiomeric excess.

A spectral data cube stores intensity $I(x,y,\lambda )$ with two spatial coordinates and one spectral coordinate. The third coordinate is wavelength, not an additional spatial dimension.

Spectral emissivity compares emission with an ideal blackbody at the same temperature at a specified wavelength, or frequency under a consistently transformed convention. A hemispherical spectral emissivity uses spectral radiant exitance; a directional spectral emissivity uses spectral radiance. Always state which angular convention applies. A wavelength-selective coating can emit strongly in one band while emitting weakly elsewhere, so one band measurement does not determine total hemispherical emissivity.

Spectral luminous efficacy converts radiant flux at one wavelength to luminous flux. The candela convention fixes $K_{\mathrm{cd}}$ exactly at $540\times 10^{12}\mathrm{Hz}$, not at an exactly specified wavelength of $555\mathrm{nm}$. ^[ref]

In vacuum, that frequency corresponds to $c/(540\times 10^{12}\mathrm{Hz})\simeq 555.1712\mathrm{nm}$, using the speed of light. In standard air it is approximately $555.017\mathrm{nm}$, close to the $555\mathrm{nm}$ maximum of the photopic luminous efficiency function. Thus $K_m$ is slightly larger than $683\mathrm{lm}{\mathrm{W}}^{-1}$; using $K_m\simeq 683\mathrm{lm}{\mathrm{W}}^{-1}$ in ordinary calculations is a rounded convention. The exact anchor is $K({\lambda }_a)=683\mathrm{lm}{\mathrm{W}}^{-1}$. ^[ref]

For collected spectral radiant flux $f(\lambda )$ and a linear photodiode with spectral responsivity $r(\lambda )$, the dark-subtracted electric current is $i=\int rfd\lambda$. A reference optical spectrum $f_A$ sets the conversion $C_A$ from electric current to collected luminous flux. Applying it to another optical spectrum $f_T$ givesAssume nonzero calibration and test signals. Then $F{\Phi }_{v,\mathrm{indicated}}$ is the corrected luminous flux. Multiplying either optical spectrum by an overall positive scale leaves $F$ unchanged. If $r$ is proportional to $V$, $F=1$ for every optical spectrum. Uniformly overfilled aperture measurements use wavelength-resolved irradiance instead, multiplying the electric current expression by aperture area; the same ratio cancellation gives the illuminance correction. This is the algebra behind source-dependent calibration, rather than a new measured correction curve. ^[ref]

Spectral radiance is radiance per unit frequency or wavelength interval. Its astronomical synonym specific intensity is usually written $I_{\nu }=L_{\nu }$ or $I_{\lambda }=L_{\lambda }$; this $I_{\nu }$ is a spectral radiance, distinct from the radiant intensity $I$ in radiometry. For positive small intervals,The two expressions refer to the same spectral slice, with the positive widths related through frequency $\nu$ and wavelength $\lambda$. For frequency measured in hertz, $\mathrm{Hz}={\mathrm{s}}^{-1}$, the units are $[L_{\nu }]=\mathrm{W}{\mathrm{m}}^{-2}\mathrm{s}{\mathrm{r}}^{-1}\mathrm{H}{\mathrm{z}}^{-1}$. For wavelength measured in metres, $[L_{\lambda }]=\mathrm{W}{\mathrm{m}}^{-2}\mathrm{s}{\mathrm{r}}^{-1}{\mathrm{m}}^{-1}$. Integrating over a spectral band gives its radiance, and then multiplying by the collecting projected area and accepted solid angle gives a small uniform beam's radiant flux. A spectral measurement therefore retains information that the band-integrated power alone loses.

For an ideal blackbody, Planck's law gives $L_{\nu }=B_{\nu }(T)$ and $L_{\lambda }=B_{\lambda }(T)$ at temperature $T$, independent of outgoing direction. Its existing frequency and wavelength peaks of Planck's law illustrate why the coordinate matters. The simpler flat-band calculation below isolates that same change of variables without the thermal physics.

Spectral radiant flux resolves radiant flux by wavelength or frequency:Its units are $\mathrm{W}{\mathrm{m}}^{-1}$ per metre of wavelength or $\mathrm{W}\mathrm{H}{\mathrm{z}}^{-1}$ per hertz of frequency. A density quoted per nanometre must be integrated with wavelength intervals in nanometres; its numerical value is $10^{-9}$ times the per-metre density. The frequency and wavelength spectral radiance conversion applies equally to spectral radiant flux, through the change of variables formula:with $c$ the speed of light in vacuum and ${\Phi }_{e,\lambda }$ expressed per metre. The Jacobian determinant preserves integrated power rather than the height or location of an optical spectrum's peak.

For two explicitly synthetic optical spectra, let $x=\lambda /(1\mathrm{nm})$ and quote the following densities in $\mathrm{mW}\mathrm{n}{\mathrm{m}}^{-1}$:The triangle under $f_A$ and the rectangle under $f_B$ both have area $2\mathrm{mW}$: $200\times 0.020/2=200\times 0.010=2$. Their band radiant fluxes differ: $450$–$550\mathrm{nm}$ contains $1.5\mathrm{mW}$ of $A$, while $650$–$750\mathrm{nm}$ contains $1.0\mathrm{mW}$ of $B$. These are specified functions, not measured source spectra.

The dark-subtracted electric current of a linear photodiode isusing its spectral responsivity. The figure's stipulated $R$ gives $i_A=0.60\mathrm{mA}$ and $i_B=1.00\mathrm{mA}$ despite equal total radiant flux. Symmetry places $A$'s mean wavelength at $500\mathrm{nm}$ and $B$'s at $700\mathrm{nm}$; a linear $R$ averages to its value at that mean. A single electric current therefore cannot determine an unknown broadband radiant flux without additional spectral information or a sufficiently flat calibrated response.

For a photodiode in its linear regime, spectral responsivity is the dark-subtracted electric current per incident radiant flux in a narrow band at wavelength $\lambda$, measured in $\mathrm{A}{\mathrm{W}}^{-1}$. More generally a photodetector's readout can be electrical voltage or another quantity, with corresponding units. A broad-band readout weights the incoming optical spectrum by the detector's spectral responsivity; it is not the unweighted total incident power. ^[ref].

A spectrophotometer measures radiant power in selected wavelength bands. Comparing a chemical solution in a cuvette with a reference blank gives transmittance and absorbance.