bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2021,
Volume and Issue:
unknown
Published: Dec. 21, 2021
Abstract
Under
gametophytic
self-incompatibility
(GSI),
plants
are
heterozygous
at
the
locus
(
S
-locus)
and
can
only
be
fertilized
by
pollen
with
a
different
allele
that
locus.
The
last
century
has
seen
heated
debate
about
correct
way
of
modeling
diversity
in
GSI
population
was
never
formally
resolved.
Starting
from
an
individual-based
model,
we
derive
deterministic
dynamics
as
proposed
Fisher
(1958),
compute
stationary
-allele
frequency
distribution.
We
find
distribution
Wright
(1964)
is
close
to
our
theoretical
prediction,
line
earlier
numerical
confirmation.
Additionally,
approximate
invasion
probability
new
-allele,
which
scales
inversely
number
resident
-alleles.
Lastly,
use
estimate
size
plant
empirically
obtained
spectrum,
complements
existing
estimator
Our
expression
resolves
long-standing
approximation
-alleles
paves
statistical
developments
for
estimation
based
on
frequencies.
PLoS Computational Biology,
Journal Year:
2023,
Volume and Issue:
19(8), P. e1011364 - e1011364
Published: Aug. 14, 2023
The
use
of
an
antibiotic
may
lead
to
the
emergence
and
spread
bacterial
strains
resistant
this
antibiotic.
Experimental
theoretical
studies
have
investigated
drug
dose
that
minimizes
risk
resistance
evolution
over
course
treatment
individual,
showing
optimal
will
either
be
highest
or
lowest
concentration
possible
administer;
however,
no
analytical
results
exist
help
decide
between
these
two
extremes.
To
address
gap,
we
develop
a
stochastic
mathematical
model
dynamics
under
treatment.
We
explore
various
scenarios
density
regulation
(bacterial
affects
cell
birth
death
rates),
modes
action
(biostatic
biocidal).
derive
for
survival
probability
subpopulation
until
end
treatment,
size
at
carriage
time
it
is
replaced
by
sensitive
one
after
verify
with
simulations.
find
scenario
mode
are
important
determinants
subpopulation.
Resistant
cells
survive
best
when
competition
reduces
biocidal
antibiotics.
Compared
analogous
deterministic
model,
population
reached
type
larger
slightly
reduced
loss
cells.
Moreover,
obtain
prediction
maximizes
cells,
which
dosage
(not)
administer.
Our
amenable
experimental
tests
link
within
host
scales
in
epidemiological
models.
Ecology and Evolution,
Journal Year:
2021,
Volume and Issue:
11(11), P. 5857 - 5873
Published: May 1, 2021
Abstract
Continuum
limits
in
the
form
of
stochastic
differential
equations
are
typically
used
theoretical
population
genetics
to
account
for
genetic
drift
or
more
generally,
inherent
randomness
model.
In
evolutionary
game
theory
and
ecology,
however,
this
method
is
less
frequently
study
demographic
stochasticity.
Here,
we
review
use
continuum
ecology
evolution.
Starting
with
an
individual‐based
model,
derive
a
large
size
limit,
(stochastic)
equation
which
called
limit.
By
example
Wright–Fisher
diffusion,
outline
how
compute
stationary
distribution,
fixation
probability
certain
type,
mean
extinction
time
using
context
logistic
growth
equation,
approximate
quasi‐stationary
distribution
finite
population.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: May 17, 2024
This
paper
focuses
on
the
maximum
speed
at
which
biological
evolution
can
occur.
I
derive
inequalities
that
limit
rate
of
evolutionary
processes
driven
by
natural
selection,
mutations,
or
genetic
drift.
These
limits
link
variability
in
a
population
to
rates.
In
particular,
high
variances
fitness
and
quantitative
trait
allow
for
fast
changes
trait's
average.
contrast,
low
makes
less
susceptible
random
due
The
results
this
article
generalize
Fisher's
fundamental
theorem
selection
dynamics
mutations
drift,
via
trade-off
relations
constrain
rates
arbitrary
traits.
be
used
probe
questions
various
biology
ecology
settings.
They
apply,
instance,
within
across
species
bacteria
strains.
apply
any
trait,
e.g.,
from
species'
weights
lengths
DNA
strands.
The American Naturalist,
Journal Year:
2024,
Volume and Issue:
unknown, P. 000 - 000
Published: Sept. 18, 2024
AbstractTheoretical
studies
from
diverse
areas
of
population
biology
have
shown
that
demographic
stochasticity
can
substantially
impact
evolutionary
dynamics
in
finite
populations,
including
scenarios
where
traits
are
disfavored
by
natural
selection
nevertheless
increase
frequency
through
the
course
evolution.
Here,
we
analytically
describe
eco-evolutionary
populations
first
principles.
We
investigate
how
noise-induced
effects
alter
fate
which
total
size
may
vary
stochastically
over
time.
Starting
a
generic
birth-death
process,
derive
set
stochastic
differential
equations
(SDEs)
individuals
bearing
discrete
traits.
Our
recover
well-known
descriptions
dynamics,
such
as
replicator-mutator
equation,
Price
and
Fisher's
fundamental
theorem
infinite
limit.
For
our
SDEs
reveal
predictably
bias
trajectories
to
favor
certain
traits,
phenomenon
call
"noise-induced
biasing."
show
biasing
acts
two
distinct
mechanisms,
"direct"
"indirect"
mechanisms.
While
direct
mechanism
be
identified
with
classic
bet-hedging
theory,
indirect
is
more
subtle
consequence
frequency-
density-dependent
stochasticity.
lead
evolution
proceeding
direction
opposite
predicted
By
extending
generalizing
some
standard
genetics,
thus
appears
alongside,
interacts
with,
well-understood
forces
neutral
drift
determine
nonconstant
size.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: July 12, 2022
Population
turnover,
a
key
trait
shaped
by
the
organism’s
life
history
strategy,
plays
an
important
role
in
eco-evolutionary
dynamics
fixing
timescale
for
individual
birth
and
death
events
as
well
determining
level
of
demographic
stochasticity
related
to
growth.
Yet,
standard
theory
population
genetics,
models
heavily
used
data
analysis,
have
largely
ignored
turnover.
Here
we
propose
reformulation
genetics
starting
from
first
principles
show
that
turnover
is
evolutionarily
important.
We
derive
general
stochastic
differential
equation
frequency
competing
birth-death
processes
determine
appropriate
corrections
essential
results
regarding
fixation,
establishment,
substitution
mutants.
Our
reveal
how
both
absolute
relative
rates
influence
evolution.
further
describe
deterministic
selection,
flux,
which
operates
small
populations.
Finally,
analyse
evolution
mean
it
explains
mechanisms
underlying
transitions.
In
conclusion,
our
explicitly
life-history
strategies,
stochasticity,
ecological
feedback,
are
inseparably
intertwined,
thus
calling
unified
development
death.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 17, 2024
Abstract
Transposable
elements
are
DNA
sequences
that
can
move
and
replicate
within
genomes.
Broadly
speaking,
two
element
types
exist:
autonomous
elements,
which
encode
the
necessary
enzymes
for
transposition,
nonautonomous
rely
on
these
produced
by
their
transposition.
Nonautonomous
have
been
proposed
to
regulate
transposable
numbers,
is
a
possible
explanation
continued
transposition
activity
over
long
evolutionary
times.
However,
previous
modeling
studies
indicate
interactions
between
usually
result
in
extinction
of
one
type.
Here,
we
study
stochastic
model
allows
stable
coexistence
elements.
We
determine
conditions
derive
an
analytical
expression
stationary
distribution
copy
showing
fluctuations
number
stationarity.
find
variances
each
be
expressed
as
function
averages
covariance,
enabling
data
comparison
validation.
These
results
suggest
besides
silencing
or
domestication
regulated
may
alternative
outcome
could
example
explain
co-evolutionary
history
LINE1
Alu
human
ancestry.
Theoretical Population Biology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 1, 2024
Infinitely
many
distinct
trait
values
may
arise
in
populations
bearing
quantitative
traits,
and
modelling
their
population
dynamics
is
thus
a
formidable
task.
While
classical
models
assume
fixed
or
infinite
size,
which
the
total
size
fluctuates
due
to
demographic
noise
births
deaths
can
behave
qualitatively
differently
from
constant
density-dependent
dynamics.
In
this
paper,
I
present
stochastic
field
theory
for
eco-evolutionary
of
finite
one-dimensional
traits.
derive
equations
that
describe
evolution
densities,
frequencies,
mean
value
any
population.
These
recover
well-known
results
such
as
replicator-mutator
equation,
Price
gradient
limit.
For
populations,
intricate
interplay
between
natural
selection,
noise-induced
feedback,
neutral
genetic
drift
determining
evolutionary
trajectories.
My
methods
use
ideas
statistical
physics,
calculus
variations,
SPDEs,
providing
alternative
complement
measure-theoretic
martingale
approach
more
common
literature.
Ecology,
Journal Year:
2022,
Volume and Issue:
103(9)
Published: May 13, 2022
Abstract
Understanding
the
mechanisms
of
ecological
community
dynamics
and
how
they
could
be
affected
by
environmental
changes
is
important.
Population
dynamic
models
have
well
known
parameters
that
describe
key
characteristics
species
such
as
effect
noise
demographic
variance
on
dynamics,
long‐term
growth
rate,
strength
density
regulation.
These
are
also
central
for
detecting
understanding
in
communities
species;
however,
incorporating
vital
into
challenging.
In
this
paper,
we
demonstrate
generalized
linear
mixed
specified
intercept‐only
with
different
random
effects
can
used
to
fit
abundance
distributions.
Each
has
an
ecologically
meaningful
interpretation
either
describing
general
species‐specific
responses
stochasticity
time
or
space,
variation
rate
carrying
capacity
among
species.
We
use
simulations
show
accuracy
estimation
depends
regulation
discrete
population
dynamics.
The
covariance
parameters,
corresponding
statistical
uncertainties,
demonstrated
case
studies
fish
bat
communities.
find
heterogeneity
main
factor
spatial
temporal
similarity
both
studies.