Draw on an Infinity Computer

7/29/2019 Draw on an Infinity Computer

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HOW TO DRAW PLANTS AND ANIMALS ON AN INFINITY COMPUTER AND

PRINT THEM OUT ON AN INFINITY PRINTER Can energy be extracted from

living shapes?

Here we will consider Batesonian combined serial and bilateral symmetry in terms

of (1) in grossone language. A common expression for bilateral symmetry in both

plants and animals will be developed from a common base of biogeographic

property graphs that decomposes the static anatomy into a kinematics of force

based historicity. These bindings permit classification of living things based on

energy contained represented. The heriarchic structure of which ensures robust

ingress and egress of access materially to the symbolized dynamics. An infinity

printer is used to create the materialization of the language.


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The use of Grossone in the experimental study of the problem of Species.

Within the perception of the difference of heredity and inheritance is a notion that

there are differences between blending and alternative inheritance hereditarily.

Here we use the experimental tool of grossone numeral systems to present this

difference and show that a direct uses of Fishers methaphor to gas theory can be

rigorously extended to Wrights network solution. Further application to social

evolution is described.

Pearson noted that blending inheritance is of the form (.5) + (.5)^2 + (.5)^3

equal to one for a lineage back to origin. Thus the abstraction of the heredity puts


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the numbers into the form to make the transition to all posterity in line with a given

invidivdual. The notion that the world is finite in grossone can substitute for this

abstraction. Thus varitations of the blending inheritance (whether (.5) or (.3) etc

etc) will depend on what infinite number the sequence stops at when the form-

making is decided originally and this will involve both the intensity of coeffient

(grossone cs) as well as the number of items as summed in the total numeralsystem per form (for purity of allelomorph combinations ). We develop the notion

of the hybrid form or heterozygote as a technological instantation of a grossone

numeral system which combines particular infinite and infintesimals (so as to pass

from one monophyla to another in a chain of them under a common set of natural

numbers that may be larger than that used for the form of specific lineage in a unity

of posterity back to another form similar but different sisterwise. Thus the

alleomorphic series studied by Wright arise in the numbers larger than grossone

which are not constructed in a particular system/lineage but are sets obtained from

that lineage. Those numbers when made into grossone (2)s and (3)s etc can result

in chained technically built solutions to be experimentally verified.

Thus we show that emendations of a grossone natural numbers system can change

the blending in Galtons law through an alternative (infinite infinitesimal

combination) into another blendable possibility. This math tool makes blending

and discrete inheritance onto one system and it becomes possible to use the gas

theory virial to move from one alleomorph distribution to another in a population.

Social selection sensu Roughgarden (which shows no preference for the purity of

the gametes genderwise) can be derived directly by differential equations types

that Fisher used but amongst the networked irreversibilites of Wright. Mayrs

condemnations of bean bag genetics is thus over. Social evolutions proposed thus

give the physiology of the process.

Divergence of the mean across generations thus becomes a matter of convergence

and divergence of the sets of grossone numbers representing the structure of

several ancestors back of that brought to account. This is accomplished with path

analysis applied. The difference of particulate mosaic inhertianance and alternative

inheritance thus is demonstrated between the coefficients gross powers combined

in on infinity computer. Galton stated that his statistical law of heredity appears to

be universally applicable to bi-sexual descent Here we apply it to multiple gender

social selections.

We come to this new theoretical tool for exploring the difference of heredity andenvironment in shaping characters by having focused on those telephonic

variations that Pearson marginalized (in the absences of reproductive selection, i.e.

the negligible correlation of fertility with the inherited character [(tetration)], and

the absence of sexual selection [(social selection)] and Wrights coefficient of

inbreeding. Pangamous mating is thus clearly defined in two level selection

processes with infinitesmail behavioral and infinite evolutionary tiers modeled. The

differences in the modes of inheritance per rate (time and form-making outside of


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biogeographic space) are thus in the same observatrion, experiment model (and the

energy exchanges booked between the elastic and inealastic collisions of the

disoncitnous and continuous inheritance per continuous anddiscontinuosu trait

(phenotypes). Grossone matheis enables friable alleomorph speperation reverted

characters in the descendets regardless of the infinity in the posterity which was

really the potential infinity in the future breeding once the space is put into the timeAND form. This was the mistake that Batesons tried unsuccessfully to rectify.

Panbiogeography was able to show up these reverted forms. One may search for

cooperative genes as well as cooperative indivudal NBS structured firms amongst

the rather rarer hypallelomorphs. The evolution of dominance is thus theorized in

the expansions of the grossone with fine arbitrary objects in infinite games no

matter the physiology or Mayrs history of evolution (1982).

If nodes and anti-nodes are defined for an entire plane and if these definitions

remain empirically self-similar across scales then the density may be approachedfrom the mass of tracks collectively irrespective of the node antinode distribution

and a notion of differential volume can be obtained as the density variance is

correlated with some point outside the plane.

The Emotional Life of Turtles A case for social evolution in the vestibular system

Astronauts know that it takes a few days get their balance back on return from

space. The buoyancy of water can make the effect of gravity rather near naught.

Water turtles of the family Emydidae (and some others but none on land) exhibit a

behavior of foreclaw motion towards others. There is increasing evidence that

turtles display emotional activites. Is it possible that this display and thetournaments or bouts that it serializes are a means for turtles to bring their

vestibular systems into congruence? This concordance could be used in various

emotional contexts creating friends, joining teams, as prenuptial bonding. The

behavior crosses species boundaries so it appears to hold to a more general effect

than simply being a reproductive species barrier kinematics. Land tortoises are

known for head bobbing. A legacy interpretation of this phenomena is akin to head

butting in mammals (limited war) as the testudines often subsequently engage in

shell on shell pushing and shoving. Could head bobbing be a means to equilibrate

the vestibular systems and the pushing that ensuses simply a physiological reflex

that occurs to force the other into a different vestibular state. Could it rather than

being an armament be instead a pleasure gradient climb (to not be put out of the

current balanced state) and thus again as with the foreclaw drumming be used in

different contexts. Thus even the sounds produced by turtles during copulation

may function in the same systematic. Can this behavior thus rather be interpreated

as cooperative interaction rather than a competitive conflict? Is the relation to

human war wrong and that to astronaut physiology right??


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If one scales the track width with set of increasing distances between any two

collection localities in a given distribution and creates a gradient percolation

representation amongst the node and antinodes defined in that space then while

the gradient will suggest linear shifting directions masses may bias whether or not

the gradients suggest a particular shape or figure. This difference will depend on


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the if the baseline rooting the masses to the tracks is one or another of if the

baseline itself is written as one amongst a finite number or is itself infinite.

Social Evolution in Salamanders From Behavior that Bonds to Bonding Behavior

Social infrastructre selection of relatively cost-free behavior over expensiveadmission tickets.

The dual role of chemistry as predicating moving forces in subsistence between

behavioral equilibria and gene pool dynamics.

Social selection presented on analogy to populations of kinetic theory gases under

elastic collisions with substantial underlying inelasticity.

Modelling on the evolutionary scale of individual based social selection sensu

Roughgarden with Grossone computations.

Switching behavior (FILO LIFO) during the evolution of the Straddle Walk in

Plethodontids (Payoff strategy of behaving in way that creates bonds to bonding

first and then behavior variation) (behavior (tail wag) then chemical bonding) to

chemical bonding then behavior (Straddle Walk).

Chemical delivery moves from posterior to anterior by climbing a higher social

selection pleasure-bonding gradient. Goes from force of water moving bonding


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chemical to internal delivery (scratch skin) to sense reception acceptance (nose).

Coalition of expensive admission tickets are replaced by ESS behaviors at lower cost

and less energy and higher efficiency Predication Plethodontids over

Salamandrids have brains more sensitive to pleasure/chemical affected neuron

circuits which are more involved with motor nerves.

Salamanders have instutionalized a transition from behavior that bonds to bonds

that behave through a norm of behavior climbed over repeated interactions.

Homoplasy - supposed developmental morphological homoplasy in salamanders

may be ESSes that are not convergent but due to infinitesimal differences optimized

both in developmental and evolutionary times and thus express different

homologies insteadthat are related to variations in higher order catastrophes. Thus

is may not be a simple distinction of selection or 'design' at workin the embedable

pattern of similarity and difference in salamanders.

Diversity of Offspring production Infrastuctures across Families

Salamandridae (98) The same fan waving neuronal signal moves both the tail and

the hand at the same time in Notopthalmus . Newts in Japan have one amino acid

difference per pond location. Western US newts will homeinto particular breeding

areas. The admission ticket winners gain coalitional strength in terms of isolating

the breeding location with membership in the coalition. Newt geography thus is
http://amphibiaweb.org/lists/Salamandridae.shtmlhttp://amphibiaweb.org/lists/Salamandridae.shtml


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ecologically part determined by successful coalition and histogeny of ornamental

badges.

Tournament-like

Displa

y


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Males direct approaching female with ticket or males approach female en mass

(frogs call females (sound vs chemical) to approach and also multiply attach)

The dorsal crest may have arose morphogenically because the chemicals remained

posterior not because of duplication vs elogantion (constraints on energy

distribution in condition rather than mode of histogeny) It is not crests and courtshipbehavior only in the correlation but crest, behavior, dominance condition,

rescource(crests and other energy needs), and geography.

The powerholding cliques enabled the formation of dorsal crests to keep behavior to

the posterior and then allopatrically and or vicariantly arose. IT was not a matter of

copy.

Ambystomatidae (32)
http://amphibiaweb.org/lists/Ambystomatidae.shtmlhttp://amphibiaweb.org/lists/Ambystomatidae.shtml


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Amphiumidae (3)

Cryptobranchidae (3)

Dicamptodontidae (4)

Hynobiidae (59)

Plethodontidae (434)
http://amphibiaweb.org/lists/Amphiumidae.shtmlhttp://amphibiaweb.org/lists/Cryptobranchidae.shtmlhttp://amphibiaweb.org/lists/Dicamptodontidae.shtmlhttp://amphibiaweb.org/lists/Hynobiidae.shtmlhttp://amphibiaweb.org/lists/Plethodontidae.shtmlhttp://amphibiaweb.org/lists/Amphiumidae.shtmlhttp://amphibiaweb.org/lists/Cryptobranchidae.shtmlhttp://amphibiaweb.org/lists/Dicamptodontidae.shtmlhttp://amphibiaweb.org/lists/Hynobiidae.shtmlhttp://amphibiaweb.org/lists/Plethodontidae.shtml


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Internal fertilization which occurs just before oviposition effectly puts the mating

not only at the time of egg laying but also directly at the place which the female

can direct. This offers more control than permitting the water currents to move the

sperm and the eggs into a location. Placement on land of the eggs also allows more

control of which geography is better. Thus Eurcyea etc just had offspring needing

larger prey items but Plethodonit Bologtogissini parental care can direct the

offspring production more so.


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thatA. ferreus courtship is distinct from typical plethodontid patterns in three

notable ways: (1) a novel, circular tail-straddling walk precedes the typical

plethodontid linear tail-straddling walk, (2) the duration of courtship is much longer

than in other plethodontids, and (3) females exhibit behaviours atypical of most

plethodontid females. We discuss the possible evolutionary and ecological

implications of these differences, some of which may have evolved in response tohabitats where space for social interactions is limited

The circular tail-straddling walk of the clouded salamander,Aneides ferreus: a deviation from the highly

conserved linear tail-straddling walk of the Plethodontidae

Authors: Sapp, Jerod R.1; Kiemnec-Tyburczy, Karen M.2

Proteidae (6)

Rhyacotritonidae (4)

Sirenidae (4)

Expensive Admission Tickets to power holding cliques.

According to social selection, ornaments and armaments evolve as signaling traits

to implement the communication needed to establish the social infrastructure from

which offspring emerge. (Alternative 2295-6) Thus the males tail evolves not as a

showy female choice target but marks the chemical pheromone wafted by the tail

as a needed gene product in the architecture of offspring raised infrastructure.

Social evolution in tail wafters is a matter of the creation of courtship semantics of
http://www.ingentaconnect.com/content/brill/amre/2011/00000032/00000002/art00009#aff_1http://www.ingentaconnect.com/content/brill/amre/2011/00000032/00000002/art00009#aff_1http://www.ingentaconnect.com/content/brill/amre/2011/00000032/00000002/art00009#aff_2http://www.ingentaconnect.com/content/brill/amre/2011/00000032/00000002/art00009#aff_2http://amphibiaweb.org/lists/Proteidae.shtmlhttp://amphibiaweb.org/lists/Rhyacotritonidae.shtmlhttp://amphibiaweb.org/lists/Sirenidae.shtmlhttp://www.ingentaconnect.com/content/brill/amre/2011/00000032/00000002/art00009#aff_1http://www.ingentaconnect.com/content/brill/amre/2011/00000032/00000002/art00009#aff_2http://amphibiaweb.org/lists/Proteidae.shtmlhttp://amphibiaweb.org/lists/Rhyacotritonidae.shtmlhttp://amphibiaweb.org/lists/Sirenidae.shtml


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selection for the pheromone cooperatively evolving with its receptor. This is a form

of gene cooperation that underlies individual cooperation. We show how the

changes in the chemistry from SPF to PMF to PRF is a form fundamental force

increased cooperation (compression penetration per cohesion elasticity) that

comes with synchronous cooperativity of the individuals. Thus gene physical

cooperation can yield further ESS stable behaviorally driven social selection.

Pria Iyer has put forth the position that ornamental prerequisite access to resources

can lead to increases in offspring production no matter the number of matings via

larger variances from individually summed fintesses inverting the logical order

otherwise thought that the condition and or dominance leads to the

rescourse/territory correlation observed empirics. These successful coalition thus

might provisionally be classified by visual differences in the ornaments and how

they are used themselves. There are single amino acid differences between newts

that correlate with specific ponds and thus if the chemicals create bonds that are

admitted by coalitions that form around expensive condition wise oranaments then

the dominance relation results from this geographic distribution of gene changes.

Changes beyond the use of the ornamental admission ticket to a less condition

expensive alternative would also have to have biogeographic consequences interms

of locations of mating offspring rearing places per establishment of dominance.

Thus dominance and condition may be different in a non-admission ticket grouping.

It may be that Ambystoma uses dominance condition irrespective of the

biogeography to establish more offspring where Plethondits use an internalization of

the ticket. One result of using dominance condition over geography (Ambystoma

travel to place to breed) may have broken down the symmetry of sex in offspring

rearing resulting in same sex (female)species and having the behavior have a

dissociated pleasure to offspring rearing bonding.

Replacement of powerful cliques by better bonding and cheaper negotiation.

Bargain begins by inverstment in somatic structure to investement in processing

behavior. Ambystomatids thus uses investment in dominance condition (using

anterior posterior behehavior )behavior over cost of admission tickest

Salamandrids use but Plethodontids use access to rescources via internal behavior

and chemicals that have moved internally from posterior to anterior. Hynobids

represent a more competitive version where many of these different cooperative

possiblites remain unresolved.

Differential access to rescources is maintained in Salamandrids by phenotypic

morphogeny but is replaced by a behavior computer of brain processing to track

with new found rescources use of streams where offspring require larger prey

items. Thus the differential access and the growth of admission ticket diffrerences

lead to energy into finding stream locations with larger prey for offspring and

makng bigger eggs. Thus the larger tails became bigger eggs and less energy

towards the ticket and more towards the bargain itself. In a sense this is the


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internalization of the classic ornament. This is not possible in the external Darwin

or Fisher Runaway which can only be explored by selection on the genes alone.

Here we see how the external fertilization and external specific ponds to reproduce

in (Salamandrids) is replaced by both an internal fertilization, internalized

ornamentation in the brain, and nonspecific streams used for offspring rearing.

Cost-Free Behaviors the Nature of Negotitations Game Theory Consequences

Behavioral dynamics need not simply mirror or not mirror gene pool dynamics but

may be associated with a gradient between a common equilibrium that can stretch

and skew the mirrored prior.

ESS where mutant can not displace concurrent genetical changing frequencies no

matter the form.

Gene Pool Dynamics and Population Level Social Selection.

Biological Norms and Institutions- Plethodontid salamanders establish a

institutionalized biological norm that puts gene cooperation and individual

cooperation into sync. SPF admission ticket based cliques are compressed into PMF

vaccinatable bonding behaviors that transitions through friable seperations onto

PRF cost-free cooperative behaviors of a tighter co-evolution. This is all one

global optimization across both preferences and strategies as it shows that the

intensity and category distinction originally erected by Price and Smith was a

function of attempts to compare animal and human behavior. Parental Investmentcan cause E_J(J) to become > E_I(J) when genes are cooperating whether by random

differences or through directed repulsion attraction gene coded specific forms used

and thus strategy stability is lost to cooperative behaviors of another preference

through changes in the payoff matrix. This is a single optimization on two vastly

different scales (behavioral and evolutionary with a changing payoff matrix).

Energy analogy and new interpretation of length of behavior relative to ESS.

Fisher Runaway modified by tetration between ticket and cost of behavior based on

length difference between tournament and display.

Fishers runaway theory where there ARE clear sex differences depends both on his

elastic and inelastic with feedback but if the notion of the display and tournament

persistence length is not intensity categorically separated but one then there may

be a continuum between the behavior and the energy used and hence energy

analogically (with differences in the form energy divisions) Tetrations between the

behavior and the ESS can scale the levels and this can be computed in grossone.


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The runaway leads to the price for the admission ticket but this need not be the

equilibriurm usedc in the actual population dynamics if the Wright network rather

than the Fisher funnel directs the irreversibility of gene acquisition in the

population/. The runaway leads to the price for the admission ticket but this need

not be the equilibriurm usedc in the actual population dynamics if the Wright

network rather than the Fisher funnel directs the irreversibility of gene acquisition inthe population/.

Nash bargain did not have a mechanism to get there (only axioms) so the climbing

of pleasure gradients is suggested as the mechanicsm. Here we suggest that the

transition from behavior to bonds to better bonding behavior occurs through this

climbing of the pleasure gradient as different chemicals are used to bond. Thus the

posterior to anterior SPF, PSM, PMF changes track the objective function of this

pleasure gradient across an entire population of demes per lineage. This resoves

the genetic conflict in the actual chemical effect of the various pheromone

chemicals. Thus the payoff matrix for SPF is less than PSM and then PMF but it

must be remembered that this is relative to the cost of the admission ticket thebehaviors used. It is not relative to the game consequence of the mixed ESS

stratigies.

One can try a particular modeling environment generated top down version of the

bottom up logic of social selection where a particular inelasticity representing the

gene kinematics of social selection (phenotypic plasticity wht genetic diversity)

wherein bothy of Wright adaptive landscape versions are modeled in a network and

Fishers notion of Sex is demoted to a gender neutral variety of narration.

Social evolution can be understood as a kind of blending energy transfer inheritance

of a Wright network othognal to Fisherian runaway as tetrations scale between

behaviors and ESSes. The notion of preference and stragey by Alger et al fail to

recognize this different kind of organon for evolutionary biological archetechtonics.

A feature of social selection is that courtship dynamics and the evolution of

ornaments are logically subordinated to an extended theory of parental investment

(Alternative 2296) The suggested salamander social evolution sequence here bears

on further scrutiny of this comment. Parental care in salamanders is skewed

towards the family Plethontidae and there one finds inter alia the loss of ornament

driven courtship based infrastructure replaced under likely increased parental

investment with a more energy efficient team bonding Which came first the

investment in young or the young that invest depends on how the gene cooperation


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and individual cooperation forces impact the effects of selection and other

population genetic forces.

Modelling on the evolutionary scale of individual based social selection sensu

Roughgarden with Grossone computations.

The particulate theory of inheritance resembles the kinetic theory of gases with its

perfectly elastic collisions, whereas the blending theory resembles a theory of gases

with inelastic collisions, and in which some outside agency is required to be

continually at work to keep the particles astir. Now if we permit on this analogy

that the gas molecule virial contributions to free path lengths may be causal with a

moving force external to the inelasticity (impenetrability). The physical

manifestation of the virial representation would be coded by forces of attractions

and repulsion in the gene parts themselves. The

external of Fisher becomes and internal (within a line of inheritance e) differentialcontribution of the repulsion vs attraction and what is astir to Fisher is within the

difference of the morphogeny vs histogeny per taxogeny and can be coordinated to

Wrights orthogonal irreversibility. This can be a global optimization bottom up

from the behavior to the ESS provided the penetrability(where genes cannot go) is

kept separate friably from the solidity(where matter can not go) else a particular

top-down approximation of the bottom up logic is in play. Fishers external runaway

turns out to be internal free paths presented and thus need not be located in the

sex difference since that is only a part of the chromosome internal difference rather

than a whole of wherein the virials symbolize.

Fisher (Genetic Theory PREFACE x) It seems impossible that full justice should bedone to the subject in this way, until there is built up a tradition of mathematical

work devoted to biological problems, comparable to the researches upon which

mathematical physicist can draw in the resolution of special difficulties

The dual role of chemistry as predicating moving forces in subsistence

between behavioral equilibria and gene pool dynamics.

http://www.sciencedirect.com/science/article/pii/S0378111908005908
http://www.sciencedirect.com/science/article/pii/S0378111908005908http://www.sciencedirect.com/science/article/pii/S0378111908005908


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http://b

ooks.google.com/books?id=pkzx2TeYYT8C&pg=RA3-PA241&lpg=RA3-

PA241&dq=sodefrin+structure&source=bl&ots=LFzN-

4Hpr9&sig=PPeOqsSYCrl_C_t4k4kkeIw5nyM&hl=en&sa=X&ei=CMxAUaLxA

8XT0wGg2oHgDQ&ved=0CF4Q6AEwCQ#v=onepage&q=sodefrin

%20structure&f=false


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http://plethodon.science.oregonstate.edu/docs/Palmeretal_2007.pdf

SPF -- PMF (3 finger loops)-- PRF (4 alpha helix)


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PMF

3 directums with sulfide line connections to 4 helicies can work by repulsions

against the sulfide connections under a general looping attraction(backbone

caused?). (Compressive force entering penetrative space (repulsing the 3 loop

attraction-repulsion forced area).

http://plethodon.science.oregonstate.edu/index.html

The 7 kDa PMF family contains more than 30 very negatively charged isoforms

representing the products of multiple genes and allelic variants. The total amounts

of various isoforms are consistent from year-to-year, but differences in the relative

levels of individual isoforms suggest their expression is differentially regulated at
http://plethodon.science.oregonstate.edu/index.htmlhttp://plethodon.science.oregonstate.edu/index.html


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the transcriptional and/or translational levels. We have purified and performed

peptide mass fingerprinting of 16 PMF isoforms, of which 8 matched our current

database of 32 unique cDNA sequences (Fig. 2). The cDNA library was prepared

from mRNA obtained from the mental glands of male P.shermani during their

courtship season. The 7 kDa pheromones have 8 conserved Cys residues (4

disulfide bonds; ~60 residues) with spacing similar to that for xenoxins and snaketoxins, but with limited sequence homology.

Close-up view of the receptor-signal interface. Amino acid positions inPRF under positive selection (blue) were mapped onto the structure of IL-6

(red), and then IL-6 was converted to this space-filling representation.

Positive selection occurs on the surface of the signal, and ?+ sites cluster at

the receptor-signal interface. (Signal-receptor structural model fromBoulanger et al. 2003; see fig. 4 of Watts et al. 2004 for details of the

mapping).

Is of the opinion that because both Salamandrids and Plethodontids have cases of

direct development (viviparity)in the Mediterranean that this must be explained

somehow and that is thought to be due to something relative to any possible

homology back to the late Jurassic when Salamandrids and Plethodontids were

thought (agreed to think) split (Zhang an Wake 2009). A narrower niche in

viviparous species may simply reflect futher direction away from SPF like

biogeography. Viviparious Salamandrids thus may posses more gene and or


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individual cooperativity than sisters. And the SPF PMF functional transit may have

reached back on this thought into the earlier Jurassic. Plethodontids may not have

originated out of applachia but they may have been related to aline that reaches

to this northern limit.

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