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An elementary ionization-chamber charge-loss model makes the inference explicit. Let a positively charged electrode and its electrometer have effective capacitance $C$, electric potential difference $U$, and enclosed gas volume $\mathcal{V}$. Assume constant $C$, a short enough interval that collection conditions remain stable, and no multiplication of charge in the gas. If ionization produces $q$ ion pairs per unit volume per unit time and a fraction $\eta$ is collected, thenHere $e$ is the elementary charge and $I_{\mathrm{leak}}$ is the parasitic electric current through imperfect insulation. Each fully collected ion pair transfers one elementary charge through the measuring circuit; counting its two opposite carriers as two transfers would introduce a factor-of-two error. The relation follows from charge conservation, rather than from a model of the incoming particle's identity.

For an invented example, take $C=2.00\mathrm{pF}$, $\mathcal{V}=2.00\mathrm{L}$, $\eta =1$, a measured fall of $6.00\mathrm{V}{\mathrm{h}}^{-1}$, and a separately determined leakage-equivalent fall of $0.60\mathrm{V}{\mathrm{h}}^{-1}$. The leakage-subtracted fall is $5.40\mathrm{V}{\mathrm{h}}^{-1}$, soThis is about $1.87\times 10^4$ collected ion pairs per second throughout the chamber, not that many primary cosmic rays. Unknown collection losses make $\eta <1$ another uncertainty; changes in capacitance would require differentiating $Q=CU$ with both factors variable.

Gas density is a separate issue. Under a fixed radiation field, fixed gas composition and approximately constant energy deposited per unit gas mass, the volume-based ionization rate scales as $q\propto \rho$. For a vented ionization chamber, the ideal gas law gives the illustrative correctionwhere $T$ is absolute temperature. A pressure-only correction presumes equal temperature. A sealed rigid chamber instead fixes gas number density as it rises: its internal pressure may change with temperature without losing gas. This does not make its insulation, electrometer calibration or collection efficiency insensitive to temperature. Nor can dividing by gas density correct arbitrary radiation from the vessel walls or changing particle energies. Those are distinct effects, not a universal normalization recipe.

The ideal Josephson junction has a phase-dependent energyDifferentiating and using the voltage–phase relation yieldsThus the ideal pair element stores and returns energy. At $V=0$ it carries a static electric current without electrical power loss. Under a nonzero periodic drive its instantaneous power need not vanish, but its energy returns after a full phase cycle. Real junctions also have a capacitance, quasiparticle transport and an external circuit; their total losses cannot be inferred from this conservative pair term alone.

A Josephson junction couples two regions with superconductivity through a weak link. A tunnel barrier is one implementation.

The remarkable possibility is a steady electric current across an insulating barrier at zero electric potential difference. This is the DC Josephson effect, carried by coherent transfer of Cooper pairs. It differs from single-electron superconducting tunneling, which probes the quasiparticle excitation spectrum and produces a dissipative current-voltage characteristic. Both contributions can occur in the same superconducting tunnel device. Brian D. Josephson predicted the pair contribution in 1962; his paper treats transfer that leaves the quasiparticle distribution unchanged. ^[ref]

The Josephson effect turns a difference of quantum phases into a measurable electric current, and an applied electric potential difference into a rate of phase advance. The Giaever gap experiment instead turns an electric potential difference into an excitation energy scale. These complementary measurements expose two aspects of superconductivity: its coherent order parameter and its gapped quasiparticle spectrum. The microscopic pairing calculation belongs to BCS theory and the BCS gap equation. A tunnel diode uses a different device, a semiconductor p-n junction.

Adding capacitance and an external bias makes the Gauge-invariant Josephson phase dynamical. Current-biased Josephson phase dynamics explains how its trapped energy levels and escape can be measured electrically.

The incremental capacitance associated with changes of electric charge around a p-n junction. Its depletion contribution is often estimated by $C_j\simeq {\epsilon }_{s}A/W$, so an independent junction capacitance measurement can constrain the width $W$ of the depletion region under the model assumptions. Other stored electric charge, including injected minority carriers, can also contribute to a measured terminal capacitance.

The leaky integrate-and-fire model combines a passive equation for membrane potential with a firing rule. Between events, inward-positive applied electric current $I(t)$ obeyswhere $C>0$ is membrane capacitance, $g_L>0$ is the leak conductance, $R$ is the corresponding electrical resistance, and $E_L$ is the leak reversal potential. Here the leak conductance is constant. The time constant $\tau$ describes passive relaxation. When $V$ first reaches a threshold $V_{\theta }$ from below, record an action potential event and reset $V$ to $V_r<V_{\theta }$. In the version used here, hold $V=V_r$ for a fixed neuronal refractory period $t_{\mathrm{ref}}$, then resume integration. See 1.3 Integrate-And-Fire Models.

For constant $I$, with $t=0$ at the start of an integration interval and $V(0)=V_{\mathrm{initial}}$, the exact subthreshold solution isThe equilibrium point of this passive equation is $V_{\infty }=E_L+RI$. Subtracting $V_{\infty }$ leaves $d(V-V_{\infty })/dt=-(V-V_{\infty })/\tau$, explaining the exponential function. This solution applies only until a threshold event or a change in $I$. Starting below threshold, constant input produces repeated events if $V_{\infty }>V_{\theta }$; if $V_{\infty }=V_{\theta }$, the threshold is approached asymptotically and never reached at finite time.

For a worked example, chooseThese imply $g_L=10\mathrm{nS}$ and $C=200\mathrm{pF}$. All these parameters are illustrative model choices, not measurements from a particular neuron. With $I=200\mathrm{pA}$, Ohm's law gives $RI=20\mathrm{mV}$ and hence $V_{\infty }=-45\mathrm{mV}$. ThusAt threshold, $e^{-t/\tau }=1/4$, so the first event occurs after $T=20\ln 4\mathrm{ms}\approx 27.7259\mathrm{ms}$. Each subsequent cycle includes the $2\mathrm{ms}$ neuronal refractory period, givingThis is the ideal sustained firing rate; the first-event latency is $T$, not $T+t_{\mathrm{ref}}$.

With $I=100\mathrm{pA}$ instead, $RI=10\mathrm{mV}$ and $V_{\infty }=-55\mathrm{mV}$. From the same initial state, $V(t)=-55\mathrm{mV}-10\mathrm{mV}{e}^{-t/\tau }$ stays below $-50\mathrm{mV}$: no events occur, however long this current is held. The critical sustained current is $(V_{\theta }-E_L)/R=150\mathrm{pA}$; equality gives asymptotic approach rather than finite-time firing.

The leak gives old inputs progressively less influence, while capacitance prevents an ordinary finite electric current step from changing $V$ instantly. This combination makes the leaky integrate-and-fire model useful for exploring input summation, event timing and network activity at low computational cost. Its fixed parameters and reset omit the evolving voltage-gated ion channels of the Hodgkin-Huxley model, spatial integration in dendrites and mechanisms of neural adaptation. Treating a synapse as a prescribed $I(t)$ also omits its voltage-dependent driving force unless a conductance term is added. See 1.4 Limitations of the Leaky Integrate-and-Fire Model and constant-input firing rate of a leaky integrate-and-fire neuron.

Connect a passive electrical load of electrical resistance $R_L>0$ from the junction to the reference. In the steady direct current model, $R_L$ and $R_2$ share the same electric potential difference and are connected in parallel. Their equivalent electrical resistance isThis is the replacement required when a voltmeter is connected across $R_2$. The inspected teaching guide explicitly models the meter this way.^[ref]

The Kirchhoff's current law proof makes the changed assumption visible:The upper resistor carries the sum of the lower and load electric currents, so the two original resistors no longer have equal electric currents. In the stipulated $R_L=10\mathrm{k\Omega }$ example, $R_p=5\mathrm{k\Omega }$, the upper current is $2/3\mathrm{mA}$, and each lower branch carries $1/3\mathrm{mA}$.

For a digital multimeter used as a voltmeter, let its input electrical resistance on the selected voltage range be $R_m$. With no other load, set $R_L=R_m$; if an intended load is also present, use $R_L\parallel R_m$ in place of $R_L$. Two instruments connected simultaneously add two branches. Their ideal indicated value equals the voltage of this altered circuit; voltmeter loading can exist even with perfect measurement calibration. Real readout additionally has measurement uncertainty, offsets, and finite resolution. Consult the actual range and input specifications rather than assigning every digital multimeter the same $R_m$.

For an oscilloscope, the resistance-only model applies to settled direct current with a compatible input coupling setting. The oscilloscope input and cable also have capacitance; changing signals can therefore have loading that depends on frequency. A probe changes the impedance seen at its tip and the relation between tip voltage and displayed voltage; use the probe-and-input combination's specification and attenuation setting. NJIT's guide models the parallel electrical resistance and capacitance and adjusts probe compensation with a square-wave readout.^[ref]

A series circuit comprising electrical resistance $R>0$ and inductance $L>0$, placed in a parallel circuit with capacitance $C>0$, has electrical admittance $Y=(R+i\omega L{)}^{-1}+i\omega C$. Vanishing imaginary part at nonzero angular frequency gives the displayed condition, requiring $L>R^{2}C$. It defines zero voltage-current phase difference, which need not coincide exactly with the maximum of impedance magnitude when loss is present. At this frequency the electrical impedance is real and equals $L/(RC)$.

A conducting conical pendulum connected to a grounded pivot develops a motional electric potential difference $B\omega r^2/2$ between the rotation axis and a bob at radius $r$. If the bob dominates the capacitance, its electric charge is $CB\omega r^2/2$. An additional uniform vertical electric field changes both the force on that charge and, while the grounding connection remains, the background electric potential entering the charging relation. These effects must be treated consistently when calculating a first-order mechanical response.

The Field Mapper Kit (PK-9023), Product Manual 012-04346D by PASCO scientific (p. 3, Parallel plate capacitor) proposes a direct investigation of the plate-length-to-gap ratio using conductive-paper electric potential mapping. Its finite straight electrodes represent a cross-section of the plates. The apparatus is a gridded resistive sheet on a corkboard, silver-ink electrodes, pushpin electrical contacts, a $5$–$20\mathrm{V}$ direct supply capable of $25\mathrm{mA}$, and a voltmeter with input electrical resistance at least $10\mathrm{M\Omega }$. The manual specifies waiting 20 minutes for the ink to reach its maximum electrical conductivity, then checking each electrode: its internal voltage drop should be no more than $1\%$ of the applied electric potential difference.^[ref]

For the readout, keep one voltmeter lead on the reference electrode and scan the other across the sheet. Mark points having the same reading to trace an equipotential. A second method holds the two probe tips at a fixed separation and pivots them to find the largest electric potential difference; a suggested separation is one centimetre. Avoid printed grid marks when making contact.^[ref]

The inference follows from the measured electric potential, rather than assuming straight electric field lines. With probe separation $\Delta s$ and direction $\hat{\mathbf{t}}$, a local finite difference givesAn arrow toward rising electric potential follows $+\nabla \varphi$, so it must be reversed to show $\mathbf{E}$. To investigate the fringing field of a capacitor, compare contours well inside the gap with contours near and beyond the ends, then repeat at a changed gap while keeping the sheet boundary and plate length fixed. Curving contours and an outside gradient establish nonuniformity in this planar setup. Compare $-E_{y}d/V$ at recorded positions to distinguish simple voltage rescaling from geometric changes; no measured values are supplied here.

Additional useful controls are repeat reference readings to detect drift, reversal of supply polarity, and repeating selected readings with reduced probe spacing. Keep contact quality and sheet edges fixed during the aspect-ratio comparison. Finite probe separation averages the gradient; reducing it improves spatial resolution but magnifies the effect of voltage uncertainty. Voltmeter loading, imperfect ink electrodes, and inhomogeneous sheet electrical conductivity can mimic distortions. These proposed checks supplement the manufacturer's electrode check, rather than claiming a completed experiment.

The sheet carries a steady electric current. For uniform electrical conductivity, Ohm's law and electric charge conservation give the two-dimensional Laplace equation away from electrodes, as explained in conductive-paper electric potential mapping. Uncontacted sheet edges have zero normal electric current, whereas the diagram model fixes zero outer electric potential. These distinct boundary conditions must be matched before a quantitative comparison. The apparatus reveals a planar electric potential map; it does not directly measure the free-space three-dimensional capacitance of metal plates.

The 1985 spectroscopy experiment used niobium-based tunnel Josephson junctions on silicon, thermally anchored with final bias low-pass filters to a dilution refrigerator. Calibrated germanium and cobalt thermometers measured temperature. A filtered coaxial cable injected microwaves; repeated switches to nonzero electric potential difference measured escape with irradiation on and off. Bias scans at fixed microwave frequency resolved separate enhancements matching calculated unequal energy level spacings. Raising temperature merged the structure toward classical response. Junction parameters were calibrated in the classical regime; reducing the superconducting critical current with a magnetic field checked thermal readout. Parameter uncertainties limited absolute resonance positions.^[ref]

The companion escape experiment mounted a tunnel Josephson junction on an attenuating coaxial cable, cold-anchored its bias filters, ramped the electric current, and counted switches to nonzero electric potential difference. Rapid current shutoff limited heating. Classical escape and microwave resonance calibrated the superconducting critical current, capacitance and environmental loading. Low-temperature escape agreed with the quantum prediction using these calibrated parameters. A magnetic field reduced the superconducting critical current to keep the same apparatus thermally activated at lower temperature, testing excess noise. Frequency-dependent loading contributed uncertainty; the predicted damping correction was smaller than combined errors, so the experiment did not resolve that correction.^[ref]

Together these tests connect spectral structure and escape of the same kind of collective coordinate. They do not constitute a demonstration of coherent gate operations on a qubit, or prove that every macroscopic coordinate retains quantum behavior under arbitrary environmental coupling. The attraction is more concrete: a fabricated electrical circuit admits both an independently measurable classical model and quantitative quantum tests of its phase dynamics.

Membrane capacitance is the capacitance associated with separated electric charge across cell membrane. A local ideal capacitor has charging electric current $I_C=C_{m}dV/dt$. If a known actual membrane voltage change is $\Delta V$, integrating the charging transient after subtracting sustained ionic and leak components gives $C_m=\Delta V^{-1}\int I_{C}dt$. Pipette capacitance, finite patch-clamp series resistance and imperfect transient subtraction can bias the estimate. A capacitive transient is not by itself an ion channel opening.

A membrane potential can coexist with near electroneutrality in the bulk cytosol and external chemical solution. The small imbalance producing the voltage lies near the cell membrane; most positive and negative electric charges balance in the bulk.^[ref]

For a separate original capacitor model, choose a total membrane capacitance $C=5\mathrm{pF}$ and $V_m=-70\mathrm{mV}$. These are stipulated parameters, not measured properties of a particular biological cell, and this voltage is not asserted to equal the preceding $E_{\mathrm{K}}$. Model the separated electric charge relative to an uncharged reference byUsing the elementary charge $e=1.602176634\times 10^{-19}\mathrm{C}$, this representsexcess monovalent negative-charge equivalents inside. These can represent a deficit of positive ions, rather than the arrival of that many negative ions.

Independently choose an internal reservoir volume $\mathcal{V}=1\mathrm{pL}=10^{-12}\mathrm{L}$ containing $140\mathrm{mM}=0.140\mathrm{mol}{\mathrm{L}}^{-1}$ potassium, with balancing negative electric charge. With the Avogadro constant $N_A=6.02214076\times 10^{23}\mathrm{mo}{\mathrm{l}}^{-1}$, its potassium inventory isThus, if charging were entirely due to outward monovalent potassium transport, about one in $38600$ of these potassium ions would suffice. This is a comparison with the chosen potassium inventory, not a fraction of all charged particles or a measurement of spatial charge density. No shape, surface area or thickness has been inferred from the chosen capacitance and volume. The calculation illustrates why substantial voltage does not require a strongly charged bulk cytosol.

A monolithic integrated circuit has its circuit elements fabricated in or on one semiconductor die. Their connections are essential: an unconnected collection of transistors does not implement the intended electrical circuit.

An original ideal example separates function from fabrication. Connect two resistors, $R_1=10\mathrm{k\Omega }$ above $R_2=20\mathrm{k\Omega }$, in a series circuit across an ideal $3\mathrm{V}$ voltage source. With no load electric current drawn from their meeting point, Ohm's law and the Kirchhoff cycle law giveThese equations apply to either a discrete circuit or an idealized monolithic integrated circuit realizing those same electrical resistances. Integration changes construction; the electrical circuit equations still determine the output. A real load, unwanted capacitance or finite resistor tolerance changes the ideal calculation. Manufacturing many functions together also couples their fate: a fatal defect can discard an entire semiconductor die, motivating the Poisson defect yield model.

A multimeter combines measurements such as electric potential difference, electric current and electrical resistance in one instrument. Some models also measure capacitance; the supported functions and test conditions depend on the instrument. The dielectric laboratory example uses a multimeter in capacitance mode.

A neuron is a specialized biological cell that receives, integrates and transmits signals. Its shape separates places where inputs arrive from places where outputs reach other biological cells: this functional asymmetry is neuronal polarity. Understanding a neuron therefore means connecting its anatomy to changes in membrane potential, rather than treating it as a wire that merely forwards every input.

In a common multipolar neuron, branching dendrites receive inputs at synapses; the soma contains the cell nucleus and most major organelles; the axon carries signals to distant or nearby targets; and axon terminals form output contacts. All these regions belong to one biological cell enclosed by a continuous cell membrane. An axon can branch, allowing one neuron to influence several receiving biological cells.^[ref]

At an input chemical synapse, a neurotransmitter acts on a receptor, changing an electric current directly or through signal transduction.^[ref] A resulting synaptic potential contributes to synaptic integration in the dendrites and soma. In many spiking neurons, sufficiently strong depolarization recruits voltage-gated ion channels in the axon initial segment, initiating an action potential that propagates along the axon. At an output chemical synapse, calcium entry through voltage-gated ion channels promotes synaptic vesicle exocytosis, releasing neurotransmitter. An action potential is thus regenerated electrically along a cell membrane; it is not a packet of neurotransmitter travelling from the dendrites to the axon terminals.^[ref]

The compartments are specializations, not exclusive jobs. Inputs can contact the soma or axon as well as dendrites; dendrites can support active voltage-gated ion channels. Paired recordings from a pyramidal neuron's soma and dendrite or axon established that an action potential can begin in the axon and propagate back into the dendrites. The usual output direction therefore does not make every electrical signal strictly one-way.^[ref] An electrical synapse, which directly couples cytoplasms through gap junctions, also differs from the sending-and-receiving arrangement of a chemical synapse.^[ref]

Nor does every neuron have the upper diagram's shape. A bipolar neuron has two main processes, one dendrite and one axon; a multipolar neuron has several dendrites; and a pseudounipolar neuron has a single process from the soma that divides into peripheral and central branches. In the last arrangement, sensory signals can travel past the soma rather than obligatorily through it. These shape categories do not specify every neuron's receptor, connectivity or firing behavior.^[ref] Some neurons in the retina communicate through graded changes in membrane potential without generating action potentials.^[ref]

Why timing changes the computation. Synaptic integration can combine inputs at different locations, called spatial summation, and inputs arriving at different times, called temporal summation. A minimal example uses the leaky integrate-and-fire model with the illustrative parameters already given there: resting and reset membrane potential $-65\mathrm{mV}$, firing threshold $-50\mathrm{mV}$, electrical resistance $R=100\mathrm{M\Omega }$, capacitance $C=200\mathrm{pF}$, time constant $\tau =RC=20\mathrm{ms}$ and neuronal refractory period $2\mathrm{ms}$. These are chosen model values, not measured properties of a particular neuron. Before firing, a constant inward electric current $I$ starting from rest givesThe exponential function expresses the competition between charging the cell membrane's capacitance and leakage through its electrical resistance.^[ref]

Two $100\mathrm{pA}$ inputs, each lasting $40\mathrm{ms}$, produce different outputs depending on their timing. Either input alone reaches only $-56.3534\mathrm{mV}$. Applied together, they give $I=200\mathrm{pA}$ and reach threshold after $20\ln 4\mathrm{ms}\approx 27.7259\mathrm{ms}$, producing one action potential event during the pulse. If instead the second input begins $20\mathrm{ms}$ after the first ends, the earlier depolarization has partly decayed: the second pulse peaks at approximately $-55.9229\mathrm{mV}$ and neither pulse produces an action potential. The two-input protocols deliver the same total electric charge, $8\mathrm{pC}$, yet only the coincident protocol fires. Counting total input alone misses this timing dependence.

This example makes a neuron a detector of sufficiently clustered input, not a perfect logical gate: different parameters change the result. Actual dendrites introduce location-dependent filtering and active responses, and an inhibitory postsynaptic potential or shunting inhibition can change whether another input succeeds. The single-compartment leaky integrate-and-fire model omits these mechanisms.^[ref] Across connected neurons, branching axons distribute outputs while converging synapses combine inputs; spike trains can support temporal coding and rate coding, and synaptic plasticity changes the influence of an input. Connectivity and cellular dynamics together determine the computation.^[ref][ref]

Testing the connection between structure and function. Whole-cell recording connects anatomy to a measured membrane potential. In a published mouse protocol, a two-photon microscope guides solution-filled glass pipettes to neurons; an amplifier and bath reference electrode complete the electrical recording apparatus. A high-resistance seal forms against the cell membrane, then brief suction opens the membrane patch beneath the tip. In current clamp, the amplifier supplies a chosen electric current and records the resulting membrane potential, unlike voltage clamp, which controls voltage and measures electric current. The investigators used $500\mathrm{ms}$ current steps of several amplitudes to characterize excitability and firing, and negative current pulses to estimate input electrical resistance.^[ref]

The observable is a voltage trace, including graded responses and action potentials. Comparing injected electric current with that trace tests how input becomes output; it does not identify every underlying ion channel. The protocol checks access electrical resistance, which can distort voltage and action potential measurements, and includes intervals without stimulation to record spontaneous activity. In a teaching replication, repeated zero-input trials and monitoring baseline drift would provide further controls; these are recommended comparisons, not additional results attributed to the paper. A recording at the soma also cannot establish the local voltage everywhere in a branching dendrite, and this anesthetized preparation does not establish behavior in every awake neuron.^[ref]

A complementary experiment used simultaneous whole-cell recordings from the soma and an apical dendrite or axon of the same pyramidal neuron in a brain slice. The relative onset times of action potentials, together with sodium currents in excised dendrite membrane patches, supported axonal initiation followed by active propagation into dendrites. Pairing sites within one neuron is a useful comparison because it avoids confusing differences between cells with differences between compartments. Instrument timing and comparable recording quality would be essential controls when reproducing the inference. Only the published abstract was accessible here, so no unverified timing values, drug controls or channel distributions are supplied.^[ref]

An ideal open circuit permits no conduction electric current through a terminal pair, corresponding to infinite load electrical impedance. At the end of a lossless transmission line, its voltage-wave reflection coefficient is $+1$ and the terminal current is zero. Real open terminals may retain parasitic capacitance and radiation loss.

A connection that couples a measured electric potential difference into an oscilloscope. Its electrical resistance and capacitance contribute to instrument loading.

A connection in which branches share both terminal nodes and therefore the same electric potential difference. Branch electric currents add. For sinusoidal signals, the total electrical admittance is the sum of branch electrical admittances; ideal capacitances add.

A parallel-plate capacitor consists of two parallel electrical conductors with overlapping area $A$ and separation $d$. If the gap is small compared with both plate widths and is filled by a uniform material of positive permittivity $ϵ$, its capacitance is approximatelyThis neglects the fringing field of a capacitor near the plate edges. The interior electric field points from the plate of positive electric charge to the plate of negative electric charge, and is approximately uniform. ^[ref].

For a worked vacuum example, stipulate $A=0.01{\mathrm{m}}^2$, $d=0.001\mathrm{m}$, and vacuum permittivity ${ϵ}_0\approx 8.854\times 10^{-12}F/m$. This rounds the value in Fundamental Physical Constants — Complete Listing by National Institute of Standards and Technology and others. Within the approximation,At terminal electric potential difference $V=10\mathrm{V}$, the electric field magnitude is $E\simeq V/d=10^{4}V/m$, the plate electric charge magnitude is $Q=CV=0.8854\mathrm{nC}$, and the capacitor energy is $U=C{V}^2/2=4.427\mathrm{nJ}$. These numbers use the stipulated rounded vacuum permittivity; finite plates also have corrections from the fringing field of a capacitor.

The formula makes design changes easy to predict: doubling the overlapping area doubles the capacitance, and halving the gap doubles the capacitance, with permittivity fixed and the fringing field of a capacitor neglected. Doubling permittivity also doubles capacitance if the material uniformly fills the gap and remains linear. This lets a compact device store more separated electric charge at the same terminal electric potential difference.

The short derivation uses surface charge density $\sigma =Q/A$. In the interior, Gauss's law gives electric field magnitude $E\simeq \sigma /ϵ=Q/(ϵA)$. The electric potential difference is $V\simeq Ed=Qd/(ϵA)$, so dividing $Q$ by $V$ gives $C\simeq ϵA/d$. A narrow curved capacitor gap has the same leading local approximation when its width is much less than the curvature radius.

Two perfectly conducting wide strips of width $a$ and separation $d\ll a$, filled with a homogeneous nonmagnetic dielectric of absolute permittivity $\epsilon$, support a transverse electromagnetic mode. Ignoring edge fields, their distributed capacitance is $C^{\prime }=\epsilon a/d$ and distributed external inductance is $L^{\prime }={\mu }_{0}d/a$. The magnetic-energy integral ${\mu }_0(I/a{)}^{2}ad/2=L^{\prime }{I}^2/2$ gives the latter. Their characteristic impedance is $Z_0=(d/a)\sqrt{{\mu }_0/\epsilon }$ and propagation speed is $1/\sqrt{{\mu }_0\epsilon }$. These parameters are per unit length, distinct from a lumped capacitor and inductor.