the most general statement about it I know is the Osterwalder-Schrader reconstruction theorem showing the correspondence between Euclidean and Lorentzian n-point functions under $t\mapsto \mathrm{i}\tau$
Your latter option is what is meant - the perturbation series is an expansion in loop orders, and the power of $\alpha$ is what counts the loop order.
From en.wikipedia.org/wiki/Quantum_electrodynamics > if we want to calculate the probability amplitude for an electron to get from A to B, we must take into account all the possible ways: all possible Feynman diagrams with those endpoints. [...] we have a fractal-like situation
The fine structure constant is the scaling factor of that giant fractal Feynman diagram: as we zoom in, the contribution of a sub-diagram at zoom level n+1 is worth ~1/137 a sub-diagram at level n. So it doesn't take many levels before the sub-diagrams have negligible effect.
This makes perturbation theory in QED tractable. But figuring out the details was certainly worth a Nobel prize for Feynman, Schwinger, and Tomonaga.
In contrast, QCD perturbations don't work like that, which makes QCD much harder
@nickbros123 Ok. But even if you're not ready for all the details, it's good to get a rough qualitative feel for what's going on. So discussing it here in Chat is probably ideal.
But it's probably a Good Idea to discuss it with people like ACM, rather than me. ;)
I know nothing about perturbation theory to be honest. my only exposure to quantum is through a 1 sem long introductory quantum chemistry course. The context of my question was purely based on the approach one takes to explain molecules of the kind of H2, where we add the wave functions of 2 H2+ in a linear combination.
@Mr.Feynman I meant it! I fear the day where someone asks me to explain how exactly spinors and Wick rotation interact in the cases where the Euclidean and Lorentzian spinor reps don't correspond to each other in obvious ways (e.g. one has Majoranas and the other doesn't)
@Slereah that's how Wick rotation is often presented - as a continuous rotation - but I don't think that's actually how one should think about it on a mathematical level
well, the theorem just says "Under the following conditions, the analytic continuations of the Euclidean n-point functions are the n-point functions of a Lorentzian theory at pure imaginary $t$"
it doesn't assign any meaning to the value of these function "in between", i.e. at arbitary complex values
of course "intuition" wants to say that at 45° we have something like a 50-50 mixture of Euclidean and Lorentzian but I don't think that's what's going on
I don't understand why I can just decide to analytically continue my function and then consider the imaginary axis
We get decreasing exponential this way, sure. It looks like some ad hoc manipulation to get what they want, though
@ACuriousMind If you mean that I could analytically continue that function, yes. The problem is that I don't see why it is allowed here - without changing the meaning of that expression - and it doesn't change anything
@ACuriousMind Mhh... But at the beginning we have $t\in\mathbb{R}$, then by analytical continuation $\mathbb{R}\ni t\to t'\in\mathbb{C}$ and we now consider the line $t'=i\tau$ with $\tau\in\mathbb{R}$
in the end this weird continuation just disappears again because you end up with a contour integral that you can deform again to go along the real axis
Maybe I'm not explaining well what I don't understand. My problem is that this formal manipulation is done to lead to decreasing exponential and take the dominant term, that is the least suppressed. It looks like something ad hoc to get what we want
We couldn't have excluded the other terms of the sum without that machinery
The only thing that would look "legit" to me would be to write $\mathbb{R}\ni t=-i\tau$ without analytical continuation, which would not help because it would make $\tau$ imaginary and nothing would really change in my expression above (so I couldn't exclude the exponential). If I analytically continue, it works but the thing I'm left with after the analytical continuation is not (?) what I had in the first place
If it were just rewriting the real $t$ in another way I would understand we are just rewriting things differently, analytical continuation looks like more than just rewriting here
Unless you too mean that "formal manipulation" is more than just "rewriting in another form"
hello, i have a question about the following photo. In this equation, i am trying to figure out how the solution to the first component of 2.8 is 2.10. i see that we can write F in terms of A, which is by definition of the electromagnetic field tensor as i understand it? Then, i see that j can be written in terms of the wave function and gamma matrices, but i do not see how we unite these into one equation whose solution is 2.8?
yes this is kind of what i am struggling with -- why we would want to represent it in this way? because if i write out this equation in component form, it naively to me at least looks like it would be very easy to solve? but i think i am missing something
> A more accurate way of saying what is in my 1988 paper is that I look at the twistor space of orthogonal complex structures over a 4d Riemannian manifold, and try and identify the electroweak U(2) as the subgroup of SO(4) at each point in twistor space that commutes with the complex structure.
🤔
> Analytic continuation between Minkowski and Euclidean space-time can be naturally performed, since twistor geometry provides their joint complexification.
For single particle QM, the Greens function (for any system with energy eigenstates $\psi_n(X)$) takes the form $$ G(X,Y) = \sum_n \frac{{\psi_n}(X){\psi_n^*}(Y)}{E-E_n} $$ i.e. there is a pole at each excited energy level of the system.
The same thing appears to be happening in QFT except the poles from the excitations above the vacuum are either a multiparticle state (that contributes to a branch cut) or an isolated pole at $P^2=M^2$. As a function of $E$ (which is what we are interested in in non-rel QFT), this amounts to a continuum of poles for every allowed $\mathbf{k}$ value at $E =\pm \sqrt{ \mathbf{k}^2 - M^2}$ (i.e. the pole gives the dispersion relation in the language of non-rel QFT).
In the case of unstable particles, we will get a pole in the 2nd Reimann sheet (the unphysical sheet) which will affect the spectral function in the physical sheet. If we associate the pole with a particle, we will get a decomposition of the particle into propagators of free particles over a range of masses I think
I'm not sure the last but is correct. I need to go over it properly
Tho is some cases, we leave the time as imaginary. e.g. in quantum statistical mechanics. The idea there is that the temperature stuff really behaves like the quantum theory of imaginary time
If the wavefunction of a free particle is $e^{\imath P^\mu X_\mu}$, then maybe the wavefunction for $1$ unstable particle could be $\int \mathrm{d} s \rho(s) e^{\imath P^\mu (s) X_\mu}$ where $\rho(s)$ is the spectral function on the physical sheet associated with the pole in the 2nd Reimannian sheet
If the pole is shifted slightly, then there will be an isolated spectral function away from the branch cut associated with the multiparticle states
@DIRAC1930 relativistically it is not really clear what "the wavefunction" even means - remember there are no good relativistic position operators
@Obliv it's wrong/nonsense - what does $D$ mean, differentiation with respect to what variable? and something like $f(x)\int f(x)\mathrm{d}x$ is always suspect notation - a variable ($x$) should not occur both as a free variable and an integration variable
@Obliv I mean the variable behind the $\mathrm{d}$
@DIRAC1930 what about it?
there are contexts where it makes sense to talk about a particle wavefunction like that, particularly in the "hacky" viewpoints of "relativistic QM"
which ultimately turns out to be inconsistent in various places which is what we need QFT for
this progression non. rel. QM -> rel. QM -> QFT is pretty tricky and we need to be careful which descriptions are appropriate at what stage
I don't think it is useful to mix-and-match these various descriptions, in particular I almost never want to think about a "wavefunction" in a QFT context, except when I'm trying to match QFT with the QM description
@Acuriousmind they are of $x$ values, I'm trying to solve $a_1(x)\frac{dy}{dx} + a_0(x)y = g(x)$ but I solved the homogeneous case to get $y=ce^{-\int P(x)dx}$ where $P(x) = \frac{a_0(x)}{a_1(x)}$
I know you're just going to multiply by an integrating factor but I'm just working through it myself to make more sense of it
I just wanted to take the derivative of the soln. to the homogeneous case
when you integrate with respect to a variable you "remove" it: $\int_{-\infty}^\infty f(x)\mathrm{d}x$ is not a function, it is just a number
I don't think you are using integral signs correctly
when you write $\int f(x)\mathrm{d}x$ you seem to mean "the antiderivative of $f$ w.r.t. $x$", but the standard way to write that with integral notation is $F(x) = \int_c^x f(z)\mathrm{d}z$ for some constant $c$
if the integral is supposed to be a function of $x$ the $x$ needs to appear in the limit, not as the integration variable
OTOH, I am sympathetic to Obliv's original notation. But you do need to be explicit about what happens with the constant of integration. Also, it's much more common to do stuff like $y(t)=\int_0^t f(x) dx$, where $x$ is a dummy variable.
nvm I don't remember how to construct riemann sums lol
The integral notation is just shorthand for the associated infinite riemann sum anywho
so regardless, the idea is then you have nonhomogeneous case $\frac{dy}{dx} + P(x)y = g(x)$ and you divide both sides by $\frac{dy}{dx}$ the derivative of the soln. to the homogeneous case?
Actually I know the EV bomb was done, not sure if the three box paradox was applied as an experiment
EV bomb without the bomb
The peculiar things have to do with weak values that apparently tell you something "paradoxical" about the state of the system in between two measurements
When i first read about double slit experiment, i had a similar idea that the electron cud actually interact with the electrons in the future. Using this "interaction thru time", the pattern got made :P
It was becuz the book said "electron r fired one by one. So they cant interact"
I think the analogy between non-rel and rel is the same. In non-rel a particle is identified as an excitation that satisfies a dispersion relation $\tilde{E}(k)$ which is system dependent e.g. for a free particle we have $E=k^2/2m$ which is just the non rel limit of the dispersion relation $P^2=M^2$ minus the rest energy. In rel QFT, the renormalization condition is enforcing $P^2=M^2$ because that's all it can be from physical experiments
I'll see what happens when I have an unstable particle in it's rest frame and see it's modes in terms of the spectral function
@RyderRude It's fun speculating about that. After studying a bit of GR I started thinking, maybe on such a small scale, the entire manifold is just waving around so the wave functions are just waves in the manifold or something
@geocalc33 It is customary to ask without prior notice
In physics, a wave packet (or wave train) is a short "burst" or "envelope" of localized wave action that travels as a unit. A wave packet can be analyzed into, or can be synthesized from, an infinite set of component sinusoidal waves of different wavenumbers, with phases and amplitudes such that they interfere constructively only over a small region of space, and destructively elsewhere.
Each component wave function, and hence the wave packet, are solutions of a wave equation. Depending on the wave equation, the wave packet's profile may remain constant (no dispersion, see figure) or it may change...
So I thought it didn't matter which side of the equation the cosmological constant was one (did it emerge from geometry or the stress energy tensor). However, then I remembered the weak , strong, null, etc energy conditions. Now, if I presume the cosmological constant emerged from the stress ener...
I understand you get $D[\frac{dy}{dx}ce^{-\int P(x) dx} + y P(x) ce^{-\int P(x) dx}] = ce^{-\int P(x) dx}g(x)$ which you can rearrange and simplify to $D[yy_c]$ on the left hand side
how is the differential operator $D = \frac{d}{dx}$ defined ? It maps a set of functions to another set, with the notion of $D[xy] = x'y + y'x$, $D[x+y] = x' + y'$ etc
it's associative in function addition but not function multiplication?