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Three
Assumptions
in
Neutral
Community
EcologyNeutrality
assumptionZero-Sum
assumptionPoint
mutuation
assumptionHubbell,
S.
P.
2001.
The
unified
neutral
theory
of
biodiversityand
biogeography.
-
Princeton
University
Press.第二頁,共十九頁,2022年,8月28日Relax
point
mutuation
assumption---
random
fissionspeciation?Hubbell
(2001)
stated
that
the
equilibriummetacommunity
SAD
resulting
from
random
fissionspeciation
is
a
zero-sum
multinomial.?Ricklefs
(2003)
provided
some
approximate
formulas
for
thetotal
species
richness
in
the
metacommunity
under
randomfission
speciation.?Etienne
and
Haegeman
(2010)
derive
analyticalexpressions
for
the
distribution
of
abundancesaccording
to
the
neutral
model
with
recruitment
(i.e.,dispersal
and
establishment)
limitation
and
randomfission
speciation.第四頁,共十九頁,2022年,8月28日Relax
point
mutuation
assumption---
random
fission
speciationEtienne,
R.S.
and
Bart,
Haegeman,
2010.
The
neutral
theory
biodiversity
with
random
fission
speciation.Theor
EcolFigure
5
shows
the
abundance
distributions
with
the
fitted
models.
Clearly
the
model
with
random
fission
speciation
never
performs
significantlybetter
than
the
point
mutationmodel.第五頁,共十九頁,2022年,8月28日Relax
point
mutuation
assumptionThe
metacommunity
abundance
distribution
under
random
fission
is
identical
to
thebroken-stick
abundance
distribution,
and
thus
provides
a
dynamical
explanation
for
thgrand
old
lady
of
abundance
distributions.---
random
fission
speciationThe
metacommunity
abundance
distribution
under
random
fission
:第六頁,共十九頁,2022年,8月28日Relax
point
mutuation
assumption---
speciation
rate
proportional
to
abundanceEtienne
RS,
Apol
MEF,
Olff
H,
Weissing
FJ
(2007b)
Modes
of
speciation
and
the
neutral
theory
of
biodiversity.
Oikos116:241–258.第七頁,共十九頁,2022年,8月28日Relax
point
mutuation
assumptiontion
rate:---
Protracted
speciation??
PPrroottrraacctteeddspsepceicaitaitoino:n:bybmyomdoedleilnignsgpsepceicaitaitoinoans
asgargardaudaula,lp,rportortarcatcetde,dp,rporcoecses
rsartahtehretrtanah
instana
intsatnaenotuasneventsuo
e.vent.??
SSpeciationaicep
rate:,
whe,rewheu
irsegueisren
gaelnsepreaclisapteicoina-tiinoint-iiantiitoinartaitoen.rate.第八頁,共十九頁,2022年,8月28日Relax
point
mutuation
assumption---
Protracted
speciationRosindell
et
al.,2010.
Protracted
speciation
revitalizes
the
neutral
theory
of
biodiversity.
Ecol.
Lett.
13:716-727.第九頁,共十九頁,2022年,8月28日Relax
point
mutuation
assumption---
ProtractedspeciationRosindell
et
al.,2010.
Protracted
speciation
revitalizes
the
neutral
theory
of
biodiversity.
Ecol.
Lett.
13:716-727.第十頁,共十九頁,2022年,8月28日Three
Assumptions
in
Neutral
Community
EcologyWhile
the
neutrality
assumption
is
the
heart
of
the
neutraltheory,
the
other
two
assumptions
are
assumptions
ofparticular
model
implementations
ofthe
theory,allowing
foranalytical
expressions
for
diversity
measures,
rather
than
thefundamental
assumption
of
the
theory
itself.
A
mismatchbetween
observes
and
theoretical
predictions
can,
be
due
tothese
additional
assumptions
and
therefore
cannot
beimmediately
interpreted
as
calling
for
a
rejection
of
the
neutraltheory
as
awhole.Rampal
EtienneEtienne,
R.S.
and
Bart,
Haegeman,
2010.
The
neutral
theory
biodiversity
with
random
fission
speciation.Theor
Ecol第十一頁,共十九頁,2022年,8月28日Further
study
–
niche-ovlappedHowever,
the
degree
to
which
real
ecological
communites
are
acttually
neutral
is
a
more
openquestion
(Gotelli
and
McGill,
2006).
That
is,
what
is
a
distribution
of
ecological
communitiesalong
a
continuum
form
purely
neutral,
througth
weekly
nich-structured,
to
strongly
niche-structured
(Adler,
HilleRisLambers
&
Levine
2007)?---
Different
but
equal:
the
implausible
assumption
at
the
heart
of neutral
theory,
2011In
the
present
case,
our
question
is:
when
is
the
limited
complexity
of
the
neutral
model
sufficient
to
provide
auseful
approximation
to
a
model
of
biodiversity
with
simple
niche
structure?---Theory
predicts
a
rapid
transition
from
niche-structured
to
neutralbiodiversity
pattera
speciation-rate
gradient,
2011.第十二頁,共十九頁,2022年,8月28日Further
study
–
niche-ovlappedChishom
and
Palaca
(2010)
present
an
analytical
proof
that,
in
the
limit
as
diversitybecomes
large,
a
strong
niche
model
give
rises
to
exactly
the
same
asymptotic
form
of
SAD
as
the
neutral
model.Haegeman
and
Etienne
(2011)
argue
that
their
result
is
an
artefact
because
theimodel
for
high
diversity
is
equivalent
to
an
independent-species
model.
theyanalyse
this
independent-species
model,
and
show
that
its
SADs
are
identical
toneutral
predictions
for
all
levels
of
diversity.第十三頁,共十九頁,2022年,8月28日Further
study
–
niche-ovlappedChishom
and
Palaca
(2011)
:
As
the
speciation
rate
in
the
hybrid
model
increases,
we
observe
a
surprisingly
rapid
transitionfrom
an
ecosystem
in
which
diversity
is
almost
entirely
governed
by
niche
structure
to
one
in
which
diversity
is
statisticallyindistinguishable
from
that
of
the
neutral
model.Posterior
probability
that
an
observed
species
abundance
distribution
from
the
hybrid
model
comes
from
a
neutral
model,
given
an
uninformativedichotomous
prior
that
specifies
equal
probabilities
for
the
neutral
model
and
the
pure
(broken-stick)
niche
model
(P
(neutral)
=
P(brokenstick)=0.5),
for
different
values
of
the
speciation
rate.
Other
parameters
are
m=0.1,
J=20,000,
JM=1012,
K=16.
See
text
for
model
details.
Dashedlines
show
95%
confidence
intervals
(estimated
from
20
simulations)第十四頁,共十九頁,2022年,8月28日Further
study
–
Relax
neutrality
assumptionZhou
and
Zhang
(2008):
The
neutral
theory
can
be
extended
to
explain
theseobservations
by
allowing
species
to
differ
slightly
in
their
competitive
ability(fitness).第十五頁,共十九頁,2022年,8月28日Further
study
–
Relax
neutrality
assumptionZhang
et
al.(2011)
demonstrate
how
such
a
weaker
form
of
symmetry
can
generatesignificant
macroecological
diversity
patterns,
leading
to
a
very
differentinterpretation
of
the
relation
between
Fisher’s
a
and
Hubbell’s
fundamentalbiodiversity
number.,
where第十六頁,共十九頁,2022年,8月28日Further
st
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