Write , and assume these scales are nonzero. The two reference liquidus relations imply . For the similarity variable and front ,
Thus a temperature profile has and . Each heat equation becomes . The solute diffusion equation becomes , with
This Lewis number compares thermal and solutal diffusivities. Inside the mushy layer, gives . The wall and far-field conditions become and as .
At the moving phase boundary, equality of temperatures gives . Equality of concentrations gives . Therefore the dimensionless parameters with the convention used here are
Neither concentration nor temperature offsets should be dropped when enforcing continuity. In particular can be negative. If , then : this is the inverse Stefan number, although the paper calls its Stefan number.
To check every factor of two in the flux conditions, divide the thermal Stefan condition by , and the solute balance by . This gives
Finally and imply . This is marginal equilibrium at a mush-liquid boundary. Together these calculations produce all the rescaled differential equations and all three interface balances.
Maintain the latest five temperature readings in a circular buffer, together with their running sum. The following C programming language code spells out the message passing interface rather than assuming a particular library: send(dst,&m) is a blocking synchronous message passing send; receive(src,&m) receives from the specified sender or ANY and returns the sender's identity; sendrec(dst,&m) atomically sends the request and waits for that sender's reply in the same message object. Successful, reliable operations are assumed. Message contents are copied by the interface.
enum { ANY = -1, TIMER = 1, TEMP = 2 };
enum { PULSE, PING, REQUEST, REPLY };
typedef struct {
    int type;
    int period_ms;
    double value;
} Message;

extern void send(int dst, const Message *m);
extern int receive(int src, Message *m);
extern void sendrec(int dst, Message *m);

void smooth(void) {
    double history[5] = {0};
    double sum = 0;
    int count = 0, next = 0;
    Message m = { .type = PULSE, .period_ms = 1000 };
    send(TIMER, &m);                 /* subscribe once */

    for (;;) {
        int sender = receive(count < 5 ? TIMER : ANY, &m);
        if (sender == TIMER && m.type == PING) {
            Message t = { .type = REQUEST };
            sendrec(TEMP, &t);       /* matching REPLY contains t.value */
            if (count == 5)
                sum -= history[next];
            else
                ++count;
            history[next] = t.value;
            sum += t.value;
            next = (next + 1) % 5;
        } else if (count == 5 && m.type == REQUEST) {
            Message answer = { .type = REPLY, .value = sum / 5.0 };
            send(sender, &answer);
        }
    }
}
Before the fifth reading, selective reception from TIMER prevents premature client requests from being accepted. Such clients wait at their synchronous sends; they are not given a partial arithmetic mean. Thereafter the operating-system process receives both timer messages and client requests. Each accepted PING initiates one measurement; each accepted client request returns the arithmetic mean of the five most recently completed measurements, without initiating another measurement or changing the circular buffer.
The loop invariant is that count is the number of valid readings, capped at five, sum is their sum, and next is the next unused slot during startup or the oldest slot afterwards. Removing the overwritten reading and adding the new one preserves this loop invariant. Each update and reply uses time complexity and storage, since the window length is fixed. Under timely sensor replies, timer delivery and process scheduling, measurements are initiated once per second. The next parts explain failures of these timing assumptions; the code does not promise one-second sampling when the sensor itself cannot sustain it.
The diffusion equation is linear, so superposition gives
Each term separately satisfies the equation, and their sum recovers the stated initial data at . Its e-folding times are , so implies . The shorter-wavelength oscillation loses a given fraction of its amplitude first. It approaches zero exponentially rather than disappearing at a finite instant. This preferential damping explains smoothing of fine-scale temperature structure.
For an approximately isotropic elastic solid,
where is bulk modulus, is shear modulus and is mass density. Five relevant controls are:
These controls interact: a dense rock is not automatically faster if its moduli are also different.
An activity model is required in addition to the two compositions. Use ideal multisite mineral activity: independent ideal Fe–Mg mixing on the three relevant sites per formula unit gives
The garnet/biotite activity ratio is . All other solids are pure, so the dimensionless reaction quotient is
With the same pressure-corrected numerator as in part b,
Diluting the magnesian product endmember more strongly than the reactant favors the forward dehydration and lowers its equilibrium temperature. The powers of three count Fe–Mg mixing sites, not three formula units of either mineral. Nonideal site interactions or site partitioning would change these activities. If ideal mixing of whole formula units rather than sites were intended, activities would instead be and ; composition alone does not select that different model. The calculation explicitly adopts the conventional ideal-site interpretation.
With water fugacity coefficient , use bar. Retain the same ideal mineral-site activities, giving
Hence
The lower fluid chemical fugacity stabilizes the water-bearing products of the forward dehydration relative to the ideal-gas calculation and lowers the required temperature by about K. Here the stated fugacity coefficient is treated as a given constant for evaluating the equilibrium.
For , direct differentiation again gives and . Thus it satisfies the heat equation. Moreover,
vanishes at both endpoints for integer , proving the homogeneous Neumann boundary conditions. Now gives the nonzero constant mode , which does not decay. It represents conserved mean temperature in an insulated plate.
The reference to part “(c)(i)” in the source is circular; the relevant modes are those verified in part (b)(i). Linearity of the heat equation and its homogeneous Dirichlet boundary conditions allows superposition of those modes:
Match the initial uniform interior temperature using the orthogonality of the Fourier sine series:
Thus for even integers and for odd integers , giving
For every , the exponential factor makes the series and the derivatives needed in the heat equation converge uniformly on later time intervals. At , the Fourier sine series equals at interior points but zero at the endpoints: the instantaneous cooling boundary condition is incompatible with the pre-immersion endpoint values. This corner mismatch is physically the idealization of an instantaneous bath contact and does not invalidate the solution for .
Figure 1.
Cooling profiles in a zero-temperature bath and the mean temperature retained after insulation
. Details.
After bath cooling followed by insulated equilibration, the remaining mean temperature is conserved: integrating the insulated heat equation gives
For constant density, specific heat capacity and cross-section, this is conservation of energy. Its Fourier cosine series has a constant mode equal to the initial integral average; every nonconstant mode decays. Therefore the eventual uniform temperature is
For each mode with an odd integer index in part (c), . Integrating the bath-cooled series yields
For , uniform convergence justifies termwise integration; the result also follows by dominated convergence of the summable positive coefficients. As a check, gives for zero bath time, and as . More bath time strictly lowers the retained average temperature when and .
Effective stress and frictional strength generally increase with depth through the shallow crust undergoing brittle fracture. At , small overburden and often weak, fractured near-surface materials limit the shear stress and elastic energy that can accumulate. Some shallow materials also undergo stable sliding rather than unstable earthquake nucleation. Near , a locked fault prone to brittle fracture can sustain a much larger differential stress before frictional instability releases stored elastic energy.
This depth is plausibly near the lower, strong part of the seismogenic layer: below it, increasing temperature eventually promotes material creep across the brittle-ductile transition. Once nucleated at depth, a dynamic finite-source rupture can propagate into shallow regions that could not independently nucleate the same event. Depth alone does not determine the nucleation point: local pore pressure, frictional stability and stress heterogeneity also matter.
For pure phases at the reference pressure , the Gibbs energy of reaction is . Chemical equilibrium requires , so
The reaction is muscovite dehydration to sanidine, corundum and water; its positive standard entropy of reaction makes the product assemblage favored at high temperature under this constant-property approximation.
Use the pressure correction to a mineral reaction for the solids, and the gas thermodynamic activity for water. These are separate contributions: do not also add a gas-volume pressure correction after including . For this reaction,
At with pure solids and an ideal gas, and the solid-activity ratio is one. Therefore
and
The pressure unit in the solid term is bar, matching the supplied . The gas logarithm is dimensionless because . High water chemical fugacity opposes dehydration and raises the equilibrium temperature substantially.
The fugacity coefficient gives . Keep the same solid thermodynamic activities and pressure correction to a mineral reaction as in part (c), changing only the water chemical fugacity:
The lower water chemical fugacity makes the dehydrated assemblage more favorable, so the equilibrium temperature decreases by about . This direction is a useful independent check on the logarithm's sign.
For an approximately isotropic rock, the P wave and S wave speeds are
where is bulk modulus, is shear modulus, and is density. Five important controls are:
The measured core seismic velocities should therefore be checked against in-situ saturation, effective stress, and temperature; laboratory values need not transfer unchanged offshore.
The result predicts initial failure in a uniform material under the assumed principal-stress orientations. The actual Figure 3 is a present-day NW–SE cross section through a thick, heterogeneous Alpine stack, extending to about 50 km depth. It contains near-horizontal basal stretches, curved ramps, tightly bent contacts, and steep structures in the internal zones around Viso and the Dora Maira complex. It does not show a single undeformed conjugate pair newly formed in horizontal uniform rock.
Several processes explain the departures:
Finally, a section shows apparent dip unless it is perpendicular to fault strike. For an ideal plane, , where is the angle between the section direction and fault strike. Obliquity can make a plane look shallower, but cannot on its own explain an apparent dip steeper than its true dip. Do not infer that each black curve is a currently active brittle earthquake fault.
Let be the Fourier transform of the initial temperature. Solving the scalar linear ordinary differential equation gives
Recover using the Fourier inversion theorem, with inverse factor for this two-dimensional convention. Equivalently, take the convolution of the initial data with the two-dimensional heat kernel. On a periodic square, the same exponential applies to each discrete Fourier mode, with and .
The line references below use the original listing's line numbers.
For this linear homogeneous problem, the exponential update is exact for the retained modes, apart from roundoff error. It is not a forward Euler method step and does not require the explicit finite-difference diffusion stability restriction. Sampling, periodic modelling and spatial resolution still matter.
The wave equation is second order in time. Even one normal mode obeys a second-order ordinary differential equation, so its initial displacement and initial velocity are independent data. Physically they specify stored elastic deformation and the initial motion.
The heat equation is first order in time; its initial temperature already fixes the instantaneous time derivative through the spatial Laplacian. It needs one initial field. In either case spatial boundary conditions remain necessary and are not substitutes for initial data. Classical fixed-end string data must satisfy the appropriate endpoint compatibility, including and, when endpoint velocities exist, .
Mammalian endothermy probably emerged through several interacting changes along the synapsid stem, and its precise onset remains disputed because the fossil proxies measure different aspects of physiology. Endothermy concerns substantial metabolic heat production; homeothermy concerns relatively constant body temperature. A large animal can have relatively stable temperature without a mammalian metabolic rate, while an endothermic animal can display heterothermy. These distinctions prevent a single temperature estimate or anatomical character from being treated as a complete diagnosis.
The physiological problem is a heat balance. In a deliberately simplified steady-state model:
where is metabolic energy turnover, external work, effective thermal conductance of an animal, body and ambient temperature, and evaporative heat loss. Maintaining a warm body in a cool environment can involve increased metabolism, reduced conductance, behaviour, or a combination. For example, and a difference imply of non-evaporative heat loss in this illustrative model. The numbers are not a reconstruction of a fossil animal.
Along the synapsid lineage, increased sustained activity would require coordinated oxygen uptake, transport and use, greater food processing and sufficient energy assimilation. More effective locomotor construction, ventilation and circulation could support greater aerobic capacity, while insulation would reduce the cost of retaining the resulting heat. Shivering thermogenesis and later forms of non-shivering thermogenesis can contribute in living mammals. Brown adipose tissue in many living placental mammals cannot simply be assigned to early therapsids; a modern mechanism need not have been the ancestral one. Similarly, an expanded secondary palate or an altered limb posture is compatible with increased performance but is not a direct measurement of resting metabolism.
The time sequence must be reconstructed from several lines of evidence. Early synapsids lack the complete modern mammalian package, whereas various therapsids and cynodonts show changes in growth, feeding and respiratory anatomy before the mammalian crown radiation. Rapidly deposited fibrolamellar bone supports rapid growth, but fast-growing ectotherms and the influence of size and environment prevent a unique inference of endothermy. Growth interruptions can reflect seasonality or resource shortage rather than a categorical physiological boundary. Nasal structures interpreted as respiratory nasal turbinates could reduce water and heat loss during high ventilation, but identifying their precise form and separating respiratory from olfactory roles in fossils is difficult.
Preserved hair supplies direct evidence of insulation in some later fossils. Castorocauda, a Middle Jurassic mammaliaform, preserves integument alongside an aquatic anatomical specialization. [ref] This establishes that a fur-bearing covering existed by that time, not when insulation first evolved or whether its original function was thermal. Sensory and protective functions can precede elaboration for heat conservation. Direct preservation is particularly valuable, but its late appearance in the sampled record is not proof of biological absence in older lineages.
Stable isotope analysis has suggested earlier elevated thermometabolism. Comparing oxygen-isotope compositions of therapsid apatite with those of coexisting tetrapods, one study inferred differences in physiology and proposed elevated thermometabolism in several Permo-Triassic therapsid groups. [ref] The comparison is stronger than analysing one isolated animal because coexisting taxa constrain aspects of the environment. Nevertheless, body water, drinking source, habitat, evaporation and diagenesis affect the isotopic signal. The proposed middle-to-late Permian origin is an interpretation using a physiological framework, not a thermometer reading of an observed living cynodont.
A contrasting biomechanical approach uses the temperature dependence of endolymph properties and the dimensions of the semicircular canals. Calibration against living animals and application to fossil inner ears supported a relatively abrupt transition around 233 million years ago in the Late Triassic, near the origin of mammaliamorphs. [ref] This offers a quantitative prediction from a different anatomical system. However, body size, activity, reconstruction and the adequacy of the living calibration remain relevant. A change in a temperature-sensitive inner-ear proxy need not coincide exactly with the first increment in metabolic heat production or the first insulating covering. The disagreement with earlier isotope-based interpretations should therefore be tested, rather than erased by choosing the preferred date.
There are several plausible selective explanations. The aerobic capacity hypothesis proposes that selection for sustained locomotor performance raised maximum oxygen consumption, with elevated resting metabolism and heat production linked to that change. Comparative measurements of resting and maximum oxygen use underpin this proposal. [ref] A major issue is the strength and evolutionary direction of the relationship: high resting expenditure is expensive, and an association among living species does not prove which change led historically. Selection for thermal independence, nocturnal activity or performance in fluctuating climates provides related benefits, but “the climate became colder” is not sufficient unless the energetic costs and available food are considered.
A parental care hypothesis instead emphasizes selection for controlling the developmental environment and supplying offspring. Improved provisioning endurance and more stable incubation or offspring temperatures could favour increased metabolic capacity and heat retention. [ref] This gives concrete reproductive benefits that might offset energetic costs, while remaining a hypothesis about historical selective circumstances. The evidence required includes relationships among care, thermal performance and reproductive success, not merely the fact that living mammals both care for young and are endothermic. Activity, parental investment, insulation and environmental variability could reinforce one another, so the explanations need not be mutually exclusive.
The most secure account is a mosaic physiological transition with increasingly effective energy supply, heat production and heat retention. A Late Triassic onset of a more fully mammalian condition is a specific supported hypothesis, while earlier therapsid evidence indicates that parts of the transition may be older. fossil anatomy and chemistry constrain when particular features existed; the selective reasons require functional and comparative tests and remain less directly observable.