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Randomly branched polymers and conformal invariance
Jeffrey Miller, Keith De’Bell
To cite this version:
Jeffrey Miller, Keith De’Bell. Randomly branched polymers and conformal invariance. Journal de
Physique I, EDP Sciences, 1993, 3 (8), pp.1717-1728. �10.1051/jp1:1993211�. �jpa-00246827�
Classification Physics Abstracts
5.40 5.70J 36.20C
Randomly branched polymers and conformal invariance
Jeffrey
D. Miller(I)
and Keith De'Bell(~)
(1)
Service de Physique Thdorique de Saclay, 91191 Gif-sur-Yvette Cedex, France (~) Trent University, Department of Physics, Peterborough, Ontario K9J 788 Canada(Received
I December 1992, rev~sed 3 March 1993, accepted 27 April1993)
Abstract We show that the field theory that describes randomly branched polymers does
not have the structure one expects of a two-dimensional conformal field theory. In particular,
we show that the lowest dimension operator in the theory cannot be primary. We show
more- over that the free field theory obtained by setting the potential equal to zero in the branched polymer theory is not even classically conformally invariant. Finally, we present numerical data for the exponent
0(a),
defined byTN(«)
+~
l~N~~l"J+~,
whereTN(«)
is number of distinctconfigurations of a branched polymer rooted near the apex of a cone with apex angle a. The data indicate that
0(a)
is not linear inlla,
providing further evidence that correlation func- tions which generate randomly branched polymers do not transform simply under conformaltransformations.
1 Introduction.
It is
widely
believed that statistical mechanical systems at the critical point of a second orderphase
transition areconformally
invariant on scales muchlarger
than anymicroscopic
distanceiii (~).
Intwo-dimensions,
where the conformalalgebra
is infinitedimensional,
conformal invarianceplaces
strong constraints on the fixedpoint
correlation functions. Theanalysis
of these constraints,starting
with the paper ofBelavin, Polyakov,
and Zamolodchikov [2], has lead to a rathercomplete understanding
of thelarge
distance behavior of twc-dimensionalcritical theories [3].
As is
well-known,
thelarge
distance behavior of certain randomgeometrical
systems exhibit criticalfluctuations,
and can be describedby
continuum field theories. The conformal proper- ties in two dimensions of most of thesesystems-linear polymers,
branchedpolymers
with fixedtopology,
thetapolymers, percolation,
densepolymers,
etc. arefairly
well understood [4].(1)
More precisely, translational, rotational, and scale invariance, in systems with only short rangeinteractions, are thought to imply conformal invariance.
1718 JOUIIIiAL DE PHYSIQUE I N°8
Randomly
branchedpolymers
[5] are a notableexception (~).
It is not known which conformal fieldtheory
describes them, or even whetherthey
are describedby
a conformal fieldtheory
at all.Numerical work indicates that
randomly
branchedpolymers
behaveanomalously
under con~formal transformations. The rates of
decay
of correlation functions in astrip,
for systems thatare
conformally
invariant in thebulk,
aresimply
related to thescaling
dimensions of the operators that appear in the correlation functions [6].Extremely
accurate transfer matrix cal- culations of lattice animals(which
are believed to be in the sameuniversality
class as branchedpolymers)
in thestrip
[7]yield
correlationlengths
which do not seem to beproportional
to any of the known exponents in the branchedpolymer problem. Also,
numerical enumerations ofrandomly
branchedpolymers
in thewedge
[8] indicate that the exponent0w(a),
definedby TJ~(a)
+~
A~N~°(")+I,
whereTJ~(a)
is number of distinctconfiguratations
of a branchedpolymer
rooted near the apex of a cone with apexangle
a, is not linear inlla
unlike whatone finds in
conformally
invariant systems, like linearpolymers
[9].Previous theoretical
investigations
of branchedpolymers
have also encounteredproblems
inregard
to thequestion
of conformal invariance.Duplantier, Kostov,
and Saleur have solved the branchedpolymer problem
on a random lattice [10]. These authorscalculate,
on a random lat- tice, universalproperties
ofpolymer partition
functions. Unlike the case of other(conformally invariant) geometrical
systems that can be solved on a random latticeill], however,
thesepartition
functions cannotalways
beinterpreted
in terms of correlation functions ofscaling
operators.Furthermore,
unlike the case of linearpolymers
orpercolation,
it is not clear in thiscase how to relate the
quantities
calculated on the random lattice to thecorresponding
quan~tities in the
plane.
Thiscorrespondence
should exist in theories that areconformally
invariant [12]. Saleur [13] has alsopointed
out that the violation of naivehyperscaling
in the branchedpolymer
fieldtheory (discussed below), together
with finite sizescaling
in astrip
of widthL,
leads to an Ldependence
for thesingular
part of the branchedpolymer
free energy that is atvariance with what one expects in a conformal field
theory.
In this paper we address the
question
of conformal invariance of branchedpolymers by studying
the structure of the continuum fieldtheory
that describes theirscaling
behavior.This field
theory
was first studied within the context of theepsilon expansion
around the upper critical dimension of branchedpolymers,
d~ =8, by Lubensky
and Isaacson [5].Later,
Parisi and Sourlas [14] showed that thistheory
is, up toperturbatively
irrelevant operators,supersymmetric.
A consequence of the supersymmetry is that certain correlation functions of the branchedpolymer
fieldtheory
in d dimensions areequal
to correlation functions in the fieldtheory
that describe theYang~Lee edge singularity
[15] near its upper critical dimension of six in d 2 dimensions(~). Although
theoriginal
paper of Parisi and Sourlasonly
demonstrated the supersymmetry near the upper critical dimension of the branchedpolymer problem,
and thenonly perturbatively,
there isgood
reason to believe that the supersymmetry and its consequence dimensional reduction to theYang-Lee edge problem persist
all the way down to d= 2.
First,
thepredictions
of dimensional reduction in two and three dimensions for the exponent0,
which governs the number of branchedpolymer configurations,
theprediction
in three dimensions for the exponent u which governs the radius of
gyration
[14], and theprediction
for thescaling
form of thepair
correlation function also in three dimensionsii?]
areall well confirmed
by
numerical work.Second,
there exists asupersymmetric
latticemodel,
(~) A randomly branched polymer is a tree(no loops)
on a regular lattice. Each tree witha given number of bonds is taken be equally probable [5].
(~) We emphasize that one can prove non-perturbatively that
a Parisi-Sourlas supersyrr~metry implies dimensional reduction [16] the only question is whether the theory in question is really super~
symmetric.
due to
Shapir
[18], which holds in alldimensions,
and which has as its continuum limit the Parisi-Sourlas fieldtheory, again
up to operators which areperturbatively
irrelevant.We therefore take this field
theory
as ourstarting point.
Ourassumptions
are,explicitly,
that the supersymmetry and the operator content of the Parisi-Sourlas field
theory persist
down to dimension d
= 2. In
light
of the aboveremarks,
thisassumption
appears to be agood
one. Thequestion
that we would then like to answer is whether these twoassumptions
are
compatible
with conformal invariance.By
conformalinvariance,
we mean herehaving
the structure of a conformal fieldtheory,
with the operators of thetheory arranged
in conformal families(highest weight representations
of the Virasoroalgebra),
the lowest dimension operator in eachfamily being
aprimary
operator [2].In order that the branched
polymer
fieldtheory
has this structure, it is clear that the lowest dimension operator in thetheory
must beprimary.
For if this operator were notprimary, (and
if the
theory
had the usual structure of a conformal fieldtheory),
it would have to be the descendent of another operator with lowerscaling dimension,
andby assumption
there is no lower dimension operator.The
precise question
that we want to ask then is whether the lowest dimension operator in the branchedpolymer theory,
the operator which appears in all of the branchedpolymer
generating functions,
isprimary.
We find that it is not, and thus conclude that thistheory
does not have the structure that one expects of a conformal fieldtheory.
To show
this,
we assume that the lowest dimension operator in thetheory
isprimary
andshow, by conformally mapping
theplane
to the cone, that one then obtains inconsistent pre- dictions for the exponent0(a)
definedby TN(a)
+~A~N~°(")+I,
whereTN(a)
is number of distinctconfigurations
of a branchedpolymer
rooted near the apex of a cone with apexangle
£X.
To further
investigate
thequestion
of conformal invariance in thismodel,
we also consider the free fieldtheory
obtainedby setting
thepotential equal
to zero in the branchedpolymer
field
theory.
We show that thistheory
is not evenclassically conformally
invariant. The reason for this is that the free Parisi~sourlastheory
isessentially
ahigher
derivative Gaussiantheory,
and it is known
that,
inhigher
derivativetheories,
scale invariance does notimply
conformalinvariance [19]. It is
important
toemphasize
that the freetheory
nolonger
describes branchedpolymers,
evennon-self-avoiding
ones. That the freetheory
is not evenclassically conformally
invariant
is,
inlight
of theproblems
that arise in theinteracting theory, however, suggestive.
Finally,
we present numerical enumerations ofrandomly
branchedpolymers
in the cone. Acone is a
wedge
withopposite
sidesidentified,
and isconformally
related to thepunctured plane.
If the lowest dimension operator in the branchedpolymer problem
wereprimary,
the exponent0(a)
in the cone would besimply
related to the exponent 0 in theplane
and to the apexangle
o. Moreprecisely, 0(a)
would be be linear in Ila.
Our enumerations indicate that this linear relation does not hold.The
plan
of this paper is as follows. In section 2 we discuss the fieldtheory
that describesrandomly
branchedpolymers,
in section 3 we show that the lowest dimension operator in thistheory
is notprimary,
in section 4 we show that the free Parisi-Sourlastheory
is notconformally
invariant, in section 5 we present our results for the exponent0(a)
obtainedby
exact ennumerations of branchedpolymers
in the cone, and in section 6 we restate ourconclusions.
1720 JOURNAL DE PHYSIQUE I N°8
2. Structure of Parisi~sourlas field
theory.
The effective Hamiltonian of the field
theory
that describes the universalproperties
ofrandomly
branched
polymers
near their upper critical dimension [5] can be written [14]HB.p
=/ d~rlw(-V~#
+
V'(#))
+W~
+
~l(-V~
+V"(#))lbl. (i)
where
V(#)
=
)r#~
+i)#~. #
and w arecommuting scalars;
~b and 1i anti-commute. HB.P. is invariant under the supersymmetry transformations
b#
=
-aepxH~b,
bw=
2aep6H~b,
b~b = 0, andbli
=
a(epxHw 2ep6H#)
where a is ananti-commuting
number and ep anarbitrary
vector[20].
We take this fieldtheory
as ourstarting point,
and inparticular
assume, for the reasonsgiven
in theintroduction,
and as is usual(~),
that the operator content of thetheory
in twodimensions is that of the field
theory
definedby equation (I).
The supersymmetry
imposes
relations between the correlation functions of thetheory.
Forour purposes, the
following
identities are useful(<(r)w(o))
=(~b(r)I(o))
=
4$1<(r)<(o)). (2)
FYom these
equations
it follows that the thescaling
dimensions ~~, xw, x~, and x~ of the fields#, w, ~b, and are related
by
x~=xw-2=x~-I=x~-1. (3)
#
is therefore the lowest dimension field in HB.P:In accordance with the discussion in the
introduction,
the field#
must beprimary
if the fieldtheory
describedby equation (I)
is to have the usual structure of a conformal fieldtheory.
Given that
#
isprimary,
it follows fromequation (2)
thatw =
kV~#
+ Q(4)
where &l is a sum of
primary
operators, and the constant k= This is because in
x~
a conformal field
theory
the twopoint
function of operatorsbelonging
to different conformal families isalways
zero; since(#w)
is not zero, w must have a term thatbelongs
to the conformalfamily
of#.
Since thescaling
dimension of w is x~ + 2, this term must be a descendent of#
at level two, and theonly
descendent of#
at level two which is also a scalar isV~#. Likewise,
&lmust be the sum of
primary
operators, since if iD has a term which is notprimary,
that term must be the descendent of another operator withscaling
dimension xw n where n is apositive integer.
Butagain
there is no such operator in thetheory (other
than#;
&l is acommuting
variable and therefore cannot be a first
generation
descendent of ~bor1i).
It isimportant
to note that conformal invariancetogether
withequation (2) imply
that w=
kV~#
+ iD holds asan operator
identity,
and notjust
as anequality
in theplane.
(~) For example, the lowest dimension fields, # and #~
(the
spin and energyoperators),
of the scalar #~ theory that describes the Ising model in sufficiently high dimensions correspond to primaryoperators in two dimensions; the lowest field dimension field, #, in the #~ theory that describes the
Yang-Lee theory [15] corresponds to a primary operator [21]; and the lowest dimension "operator" in the n - 0
O(n)
model, which generates linear polymers, corresponds to a primary operator.3. Lowest dimension field not
primary.
We now show that
#
cannot beprimary.
The correlation function(#(r)w(0))
is thegenerating
function for the number
wN(r)
ofrandomly
branchedpolymer configurations
with N bondscontaining
the sites 0 and r[17,18]
(#(r)Ld(0))
+~
/~ dNe~"~KfWN(r). (5)
Here K is a
fugacity
for the number of bonds in thepolymer,
K~ is the(non-universal)
value of thefugacity
at which the averagepolymer
size in the fixedfugacity
ensemblediverges,
ande measures the deviations of K from K~: e
=
~
Equation (5)
holds for esmall,
and+~
means that both sides of the
equation
have thesane leading singular
behavior. In thescaling
region
we expect(#(r)#(0))
=
~~~/~~,
where the correlationlength (
+~ e~" FYom
equation
r 4
(2), (#(r)w(0))
=
~j~~)j. Using
thisscaling
form andintegrating
both sides ofequation IS)
with respect to r
a~~d~hen taking
the inverseLaplace
transform with respect to e we have~nunrooted
~
~N
~f-@~
)N ~fu(d-2x~-2)-3 (~)
N j~
c
where T@~~°°~~~ is the number of unrooted branched
polymers
of size N in theplane,
and£~ wN(r)
=
N~T]~~°°~~~. Setting
d= 2 and
using
theapproximate
value of u= 0.64 [7] and
the exact value of 0
= [14], we find x~ = -I
Iv
R -1.5. The field#
therefore hasnegative scaling
dimension.Under the
assumption
that#
isprimary
we can also calculate the exponent0(a),
definedby
TN(a)
+~
l~N~°(")+I,
whereTN(a)
is the the total number ofrandomly
branchedpolymer configurations
rooted near the apex of a cone with apexangle
a (~). To calculate0(o)
we needj
to know
(#w)
in the cone. The transformation z -(
= z2« maps theplane
onto the cone.Since, by assumption, #
isprimary,
we have atcriticality
(<(Zl)<(22))Plane
"i)(Zl)i~~i)(22)i~~(<(<1)<(<2))cone (7)
so
that,
(§~((1)§~((2))cone "
())~~~'(l'~~ ~~~~'(2(~~
~~~~ m m~
(~~
'(l" (2"
~~where we have normalized
#
so that(#(r)#(0))plane
"fi.
FYom equation(4)
it then followsr
that
(~((l)~J((2))cone
"
(§~((1)(ki7~~
+ld))cone
"k~)2 (~((l
)§~((2))cone(9)
where we used the
orthogonality
of#
and &l to obtain the secondequality. Combining equations (8)
and(9)
thengives
(§~((1)~J((2))cone ~~(2 (~~
~~~~~~~~~~ ~~~~~~~~~ ~ ~~~~j(~ _~f
(2x~
~~~~
(~) A cone can be thought of as a wedge in the plane, with opposite sides identified. By apex angle
We mean the angle in the plane between the two sides of the wedge.
1722 JOURNAL DE PHYSIQUE I N°8
The correlation function
(#((i)w((2))cone
is the thegenerating
function for the total number of branchedpolymers
in the cone. This statement is trueregardless
of whether we put#
inthe bulk and w near the apex or w near the apex and
#
in the bulk. On the otherhand,
wesee from
equation (10)
that the exponent0(a) depends
on whether#
or w is near the apex.For if we put w in the
bulk,
thatis,
if weintegrate
over(2, holding (i
fixed and near the apex of the cone, we find0(a)
= 2~'~
(II
a
while if
integrate
over(i holding (2
fixed we findsomething different, namely 0(a)
= 2~'~
2u
(12)
for a < 27r. Since we obtain different answers for
0(o) depending
on whether we put#
or wnear the apex,
equation (10)
cannot be correct: the correlation function(#w)
in the cone is notequal
to the conformal transformation of(#w)
in theplane,
under the assumption that#
transforms as aprimary
operator. There are in fact two additionalproblems
withequations (II)
and(12):
1) the the coefficient of27rla
isnegative, implying
that the smaller the apexangle,
the greater the number of rootedpolymer configurations,
which isimpossible,
and2)
the exponent0(a)
inequation (12) jumps discontinuously
from one at a = 27r to about1/3
for ajust
smaller than 27r. Such ajump
seemsunlikely,
and in any case is in the wrong direction(0(a)
should increase as adecreases).
A final
point
must beconsidered, namely
that the cone is notconformally
related to theplane,
but to thepunctured plane.
In mosttheories,
the distinction between theplane
and thepunctured plane
is irrelevant. A puncture in the continuumtheory corresponds
to a finite size hole in the latticetheory.
The presence of the holechanges
the interactions between sitesvariables,
and socorresponds
to the presence of an energy like operator. The energy operatoron the lattice can be written as a sum of operators in the continuum
theory.
Ingeneral,
oneexpects every operator in the continuum
theory
to appear in this sum unless it is forbidden to do soby
some symmetry. The lowest dimension operator in the sum is the mostrelevant,
and dominates the
large
distancephysics.
In most theories the lowest dimension operator with thesane
symmetryas the energy operator is the
identity
operator, so a defect in the lattice does notchange
thelarge
distance behavior of correlation functions. But in thetheory
weare
considering (and
in theYang-Lee theory)
the operator#
has the same symmetry as the energy operator and has a smallerscaling
dimension than theidentity
operator,If, therefore,
#
appears in the sum(and
there is no symmetry which forbids it fromdoing so)
thelarge
distance behavior of correlation functions on a lattice with a
single
defect would be different from the behavior of correlation functions on theperfect
lattice. In the continuum this means that correlation functions in theplane
would not be the same as those in thepunctured plane.
The exponent 0 in the
punctured plane,
or on a lattice with a finite sizehole,
would therefore be different from 0 in theplane.
Since correlation functions in the cone areconformally
related to those in thepunctured plane, they
would also bemodified,
as wouldpredictions
for0(a).
This
proposal,
whileraising interesting questions,
has a number ofproblems. First,
it is difficult to see how the presence of a finite size hole on the lattice could alter the exponent 0.To check
this,
we have enumerated all branchedpolymer configurations (rooted
near theorigin)
with twelve and fewer bonds on a square lattice with the site at the
origin
removed. Branchedpolymer configurations containing
theorigin
were disallowed. The ratio of the number ofpolymer configurations
in the presence of the puncture to the number in theplane
appears to converge to a constant near 0A as the number of bonds in thepolymer
increases. This indicates that the defect does notchange
0.Second,
we expect that the presence of the puncture shouldnot affect the
boundary
conditions atinfinity.
Thus the state, atinfinity
should still be theSL(2, C)
invariant vacuum, I.e. the statecorresponding
to theidentity
operator. In the Hilbert spaceformulation,
the statecorresponding
to the operator#
is an energyeigenstate,
and isorthogonal
to theSL(2, C)
invariant vacuum. Hence thepartition
function Z should not be affectedby
the puncture. Correlationfunctions, however,
will now have an extra#(0)
inserted in them. Since we are interested in twopoint functions,
the correlation functions with the extra insertion of#(0)
are three point functions and arecomputable. Performing
these computations,one can show
explicitly
that the correlation function(#w)
in thepunctured plane
stilldepends
on whether
#
or w is put at theorigin.
4. Free Parisi-Sourlas
theory
notconformally
invariant.In order to
gain insight
into whatmight
go wrong with conformal invariance in the branchedpolymer theory,
we consider here thesimplest theory
with a Parisi-Sourlas supersymmetry.This is obtained
by setting
thepotential V(#)
in equation(I) equal
to zero. Thecommuting
fields#
and w thendecouple
from theanti~commuting
fields~b and @.
Moreover,
the fermion part of the free Hamiltonian HF has the form of anordinary
Gaussianmodel,
and isconformally
invariant with ~b and 1i
transforming
asprimary
fields with conformal dimension zero. Theremaining
part of the freetheory
isHF
=/ d~x[w(-V~#)
+ ~w~].(13)
2
or,
integrating
out the field w,HF "
d~r(V~#)~ (14)
a
higher
derivative Gaussiantheory.
ForHF
to be scaleinvariant, #
must havescaling
dimen~sion -I, or conformal dimension
-1/2.
Let us assume, as we did for the branchedpolymers,
that#
transforms under conformal transformations as aprimary
operator.Then,
under thetransformation z - z +
e(z),
4(~, 2)
~(i ))~~/~(i ))~~/~#(~'~l' (is)
Taking
into account the transformation of the measure d~r and the derivatives6~,
we find thevariation in HF
~
~~~
/ ~~~~i~~~
~~~~~~~~~ ~ ~'~'~' ~~~~
If
e(z)
is constant,corresponding
to atranslation,
or linear in z,corresponding
to a dilatationor
rotation, bHF
vanishesidentically,
while ife(z)
isquadratic
in z, theintegrand
is a totalderivative,
and so bHF vanishes in this case as well. These three transformations generate thespecial
conformal group,SL(2, C).
On the otherhand,
theintegrand
is not a total derivative for moregeneral
conformal transformations.Thus, assuming
that#
isprimary,
the action inequation (14)
is invariant under the groupSL(2,C),
transformationsmapping
theplane
toitself,
but not invariant under the full conformal group in two dimensions.Furthermore,
there is no way to transform#
so thatbHF
" 0. To see
this,
suppose that under z - z +e(z)
<(z z)
-(i t)-~/~(i t)~/~<(z z)
+b<(z z). (17)
JOURNAL DE PHYSIQUE J T 3,N. 8, AUGUST 1993 62
1724 JOURNAL DE PHYSIQUE I N°8
with
b#
linear in#
and e. ThenbHF
=/ d~rl( ~j)i~ (3#)(63#)
+
2(33#)(63b#))
+ C-Cl(18)
In order for
bHF
tovanish,
we need to chooseb#
in such a way that theintegrand
is a total derivative.Considering
the first term inequation (18)
we see that this isonly possible
ifb#
is of the formae(z)6#
+b6e(z)#.
But we cannot add a term of this kind to the transformation law for#,
because this hasalready
been fixedby
translational and scale invariance(that
is to say, if we add term of this form to transformation law for#,
HF will not be invariant under thespecial
conformalgroup).
Thus there is no way to transform#
so thatbHF
" 0 under
general
conformal transformations. Hence the
simplest theory
with a Parisi-Sourlas supersymmetry is notconformally
invariant even at the classical level. It seemslikely
that this is related to theproblems
with conformal invariance encountered in the morecomplicated interacting theory
that describes branchedpolymers.
5 Numerical results.
In
light
of the discussion in sectionthree,
it is of interest to know thedependence
of the exponent0(a)
on the thereciprocal
of the coneangle
a for branchedpolymers
confined to acone. For linear
polymers,
one finds [9], as asimple
consequence of the fact that thegenerating
function for a linear
polymer
is the correlation function of twoprimary
operators, an exponent that is linear in Ilo.
In the case athand,
we do not know what to expect,because,
as wehave shown in section 3, the
generating
function forrandomly
branchedpolymers
is not the correlation function ofprimaries,
or of aprimary
and a descendent. Aprevious analysis
ofexact enumeration data [8] for branched
polymers
confined to awedge
found a non-linearrelation between the exponent and the inverse cone
angle.
Itis, however,
worthstudying
branched
polymers
in the cone, because the cone, unlike thewedge,
isconformally
related to the(punctured) plane.
We have
analysed
exact enumeration data for lattice trees confined to a cone. The cone is formedby applying cyclic boundary
conditions to awedge,
cut froma square
lattice,
in such a way thatcorresponding
lattice sites on the two boundaries of thewedge
become identified asa
single
site on the surface of the cone. The number of(weak) embeddings
of trees rooted at the apex of the cone were enumerated for trees with up to 16 vertices.We assume that the number of trees on the surface of the cone
diverges
asTN(o)
+~
l'~N~°(")+~ (19)
1 is the
growth
constant for lattice trees on the square lattice and is the same for trees confined to awedge
or cone as it is for trees in the bulk lattice [22]. Theyth
moment of thegenerating
function for
TN(o)
will therefore have critical behaviour describedby
G~Y)(x)
=£TNX'~NY
+~ (x~x)~+Y~° (20)
N
From
previous
work [23], the value of x~ is known to be +o,00001 Xc "1/~
" °.~~~~~(21)
-0.00002
To obtain estimates of
0(a)
a Baker-Hunter confluentsingularity analysis
[24] wasapplied
tothe exact enumeration data at each of the cone
angles
considered. This type ofanalysis
wasused since we expect the presence of confluences in the
generating
function for lattice trees [25].The initial
analysis
used the central estimate of x~given
aboveand,
since0(o)
isbigger
thanunity
for the smallerangles,
thefirst,
second and third moments of thegenerating
functionwere
analysed
[8]. The results are shown in table I. As this type ofanalysis
may be sensative to the value of x~assumed,
we alsoperformed
ananalysis
which eliminates the need tospecify
x~.To do this the ratio of the number of
embeddings
in the bulk lattice TN and thecorresponding
number of
embeddings
in a cone withwedge angle
a,TN (a),
was formedTN "
TN/TN(a)
+~
N°(")~° (22)
Table I. Estimates of
0(o)
for various coneangles
o. Columns labelled 1, 2 and 3 tabulate results obtained from thefirst,
second and third moment of thegenerating
functionrespectively.
The column labelled 4 tabulates the results obtained
by taking
the ratio of the number of trees in the bulk lattice to the number on the cone.Angle
1 2 3 490° 2.091 2.134 2.126 2.l14
+0.017 +0.025 +0.017 +0.014
12i° 1.98 1.96 1.85 1.852
+0.ll +0.09 +0.03 +0.007
143° 1.85 1.83 1.78 1.73
+o.06 +o.os +o.io +o.09
180° 1.55 1.551 1.550 1.553
+o.02 +o.oos
±((((
+o.oio233° 1.418 1.4080 1.39 1.39
+0.010 +0.0007 +0.09 +0.04
270° 1.2539 1.250 1.252 1.236
+0.0012 +0.006 +0.004 +0.014
The
generating
function for these ratios has a critical behaviorgiven by
~
(~) £
~
~N
~ (~ ~)l+@(a)-@
(~~)
r N
N
This has the
advantage
that the criticalpoint (x~
=I)
is knownexactly
and it is not necessary to usehigher
moments as the exponent isalways
greater than I. Theresulting
estimates of0(a)
are shown in column 4 of table 1.1726 JOURNAL DE PHYSIQUE I N°8
In most cases the
spread
in the central estimates of0(a)
in the columns of tableI,
for agiven
value of a, is
comparable
with the error estimate in asingle
column obtainedby considering
the variation in the estimate from different Pad4
approximants
to the Baker-Hunterauxillary
function. In order to make a
comparison
with theexpected
linear relation we take the overall estimate of0(a)
to have a central valuegiven by
an average, over the columns of tableI,
of the central estimates and error bounds such that all of the central estimates fall within thesebounds. These values are
plotted against
Ila
infigure
I. Evenallowing
for somedegree
ofsubjectivity
in the value of the error bounds the estimates of0(a)
areclearly
not consistent with a linearrelationship (although
we cannotaltogether
rule out short series effects as thereason for this deviation from a linear
relation).
2.2
~
4l
1.8
§
Sin)
~~ olA @
1.2 ~
l 8
0.00i 0.004 0 006 0.008 0.01 0 012
1In
Fig. I. Overall estimates of @(a) plotted against I
la.
The bulk value of= I has been included
as the value for a
= 360°.
6. Conclusions.
In this paper we have considered whether
randomly
branchedpolymers
areconformally
in- variant, We have shown that the usual structure of conformal fieldtheories,
in which the lowest dimension operator in thetheory
isprimary,
does not hold. This rules out the moststraightforward
formulation of conformal invariance for branchedpolymers.
We also showed that the free Parisi-Sourlas Hamiltonian is not evenclassically conformally invariant,
because it isessentially
ahigher
derivativetheory.
This isinteresting,
because thishigher
derivativetheory
is thesimplest
local scale invarianttheory
that one can write down which is not alsoconformally
invariant. It seemslikely
that the lack of conformal invariance in the freetheory
is related to the
problems
that arise in theinteracting
branchedpolymer theory. Finally,
from numerical ennumerations, we showed that0(a)
is not linear in the inverse coneangle
a, as is the case when thegenerating
function is a correlation function of primaries, or of aprimary
and a descendent.We would like to conclude with several remarks.
First,
our results rest on theassumption
that the supersymmetry and operator content of the Parisi-Sourlas fieldtheory,
valid neareight dimensions, persist
down to two dimensions. As noted in theintroduction,
thepredictions
of thesupersymmetric
formulation agreeextremely
well with numerical work in two and three di-mensions,
so that theseassumptions
seem to begood
ones.They
are neverthelessassumptions.
Second,
it would be nice to have a betterunderstanding
of the role ofboundary
conditions intheories,
like this one, that havenegative
dimension operators. As we discussed in section4,
theexistence of
negative
dimension operators makes the relationbetween,
forexample,
theplane
and the
punctured plane
ratherambiguous. Finally,
the reason forproblems
with conformal invariance may be related tonon-unitarity
of the model. Since thetheory
isnon~unitary,
the Hamiltonian in the Hilbert space formulation of theproblem
is notHermitian,
and therefore need not bediagonalizable.
If H is notdiagonalizable,
the usual arrangement of operators inconformal field theories in
highest weight representaions
of the Virasoroalgebra
[2] would beimpossible.
Acknowledgements.
J.M. thanks John
Cardy
forsuggesting
thisproblem
tohim,
and for manyhelpful
conversa~tions. He also thanks Mark Goulian for
discussions,
and BertrandDuplantier,
Ivan Kostov and Hubert Saleur forexplaining
theirunpublished
work to him. This work wassupported,
in part,by
NSF Grant PHY 86-14185 and the Natural Sciences andEngineering
Research Council ofCanada.
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