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A reticulocyte is a recently formed red blood cell retaining detectable RNA-associated material. Its maturation state differs from a fully mature erythrocyte. The proportion of reticulocytes provides information about red-cell production rather than simply the total amount of hemoglobin present.

The decreasing production function and increasing linear loss have one positive constant equilibrium $u_{\ast }$. It scales as ${\delta }^{-1/(n+1)}$ for small loss and ${\delta }^{-1}$ for large loss. With $a=n{u}_{\ast }^{n-1}/(1+u_{\ast }^n{)}^2>0$, the linear characteristic equation is $\sigma +\delta +a{e}^{-\sigma d}=0$. It has no real nonnegative root, and zero is never a root. Thus loss of stability from the zero-delay stable state must occur through a nonzero imaginary conjugate pair.

If $a>\delta$, the first crossing has $\omega =\sqrt{a^2-{\delta }^2}$ and $d_c=\arccos (-\delta /a)/\omega$. Differentiation of the characteristic equation gives $\mathrm{Re}{\sigma }^{\prime }(d_c)={\omega }^2/[(1+\delta d_c{)}^2+{\omega }^2{d}_c^2]>0$, proving transversality. If $a\le \delta$, the magnitude inequality $|\sigma +\delta |=a|e^{-\sigma d}|$ rules out a root in the closed right half-plane. The model needs an initial history on the whole delay interval. The delay represents a production/maturation lag rather than instantaneous production controlled by the current cell count.

Transient blood-forming endothelium that generates haematopoietic cells through an endothelial-to-haematopoietic transition.

The principal axes of an ellipse are the two perpendicular symmetry axes through its center of an ellipse. For a symmetric positive-definite matrix $M$, its orthonormal eigenvectors give those directions and its positive eigenvalues ${\lambda }_1,{\lambda }_2$ give semiaxis lengths ${\lambda }_1^{-1/2},{\lambda }_2^{-1/2}$. This follows by orthogonal diagonalization of the defining quadratic form. In ${\xi }^2/A^2+{\upsilon }^2/B^2=1$, the axes are already horizontal and vertical, with semiaxes $|A|,|B|$ and full lengths $2|A|,2|B|$. Equal semiaxes give a circle, for which every perpendicular pair through the center can serve.

The electric potential difference between the ground-contact points of the two feet. A ground current can make it nonzero.

The polarization of an elastic wave in an isotropic solid specifies the direction of its displacement field amplitude relative to its wavevector. The longitudinal wave component is parallel to the wavevector; the transverse wave component is perpendicular. For a real unit propagation vector $n$, $a_L=(a\cdot n)n$ and $a_T=a-a_L$. An evanescent constituent has a complex spatial derivative vector, so the corresponding amplitude ratio can be imaginary. The longitudinal and transverse constituents of a Rayleigh wave combine into ellipse particle motion at the free surface.

A shear wave in an isotropic elastic material has displacement perpendicular to its wavevector, with zero divergence for a plane wave. The Navier-Cauchy equation with inertia then reduces to $\rho {\mathbf{u}}_{tt}=\mu \Delta \mathbf{u}$, giving the displayed wave speed. At a boundary it can be generated by mode conversion from a compressional wave, even when the incident displacement is purely longitudinal.

For an isotropic elastic layer $|y|<h$ between two identical elastic half-spaces, an antiplane displacement $w=f(y)e^{i(kx-\omega t)}$ has $m^2={\omega }^2/c_{s1}^2-k^2>0$ in the layer and exterior decay rate ${\ell }^2=k^2-{\omega }^2/c_{s2}^2>0$. Hence a trapped mode has phase speed between the layer and cladding shear speeds. Continuity of displacement and shear traction gives the first displayed equation for even modes $f\propto \cos (my)$ and the second for odd modes $f\propto \sin (my)$.

In a rigid-cladding limit with nonzero decay rate, the interfaces become displacement nodes. Even transverse wavenumbers are $(n+1/2)\pi /h$, $n\ge 0$, and odd ones are $n\pi /h$, $n\ge 1$. The minimum even-mode dispersion branch is ${\omega }^2=c_{s1}^2[k^2+{\pi }^2/(4h^2)]$. When the cladding speed is finite, exterior decay remains a separate requirement; satisfying this lower cutoff alone is insufficient.

In an isotropic half-space $y<0$ with zero displacement at $y=0$, an incident longitudinal wave directed along $(\cos \alpha ,\sin \alpha )$ reflects into both longitudinal and shear waves. Let $c_p^2=(\lambda +2\mu )/\rho$ and $c_s^2=\mu /\rho$. Horizontal phase matching gives $\sin \beta =(c_s/c_p)\cos \alpha$ for a reflected shear wavevector proportional to $(\sin \beta ,-\cos \beta )$ and polarization $(\cos \beta ,\sin \beta )$. The two zero-displacement equations at the boundary give the displayed coefficients. Since $c_s<c_p$ in a stable isotropic solid, both reflected branches are propagating for every genuine incident angle $0<\alpha <\pi$, with no critical-angle obstruction for this incident-wave type. Changing to a stress-free boundary changes the amplitude equations and coefficients.

For a homogeneous isotropic plate of thickness $h$, Young's modulus $E$ and Poisson's ratio $\nu$, the bending stiffness is $D=E{h}^3/[12(1-{\nu }^2)]$. Its quadratic bending energy isIt follows by integrating the strain energy density $\frac{1}{2}{\tau }_{ij}{e}_{ij}$ through the thickness: linear bending strains are proportional to $z$, and ${\int }_{-h/2}^{h/2}{z}^{2}dz=h^3/12$. Taking a first variation and integrating by parts twice gives $D{\Delta }^{2}w=0$ without applied transverse load. Clamped boundary variations have both zero value and zero normal derivative.

A sheet-like elastic component of a vessel wall, especially prominent in the tunica media of elastic arteries.

For the unit ball and energy $W(F)=|F{|}^2+(\det F-1{)}^2$, boundary dilation $y=tx$ admits a singular incompressible radial competitor $r(R)=(R^3+t^3-1{)}^{1/3}$. Its radial stretch is $R^2/r^2$ and its double tangential stretch is $r/R$. Although the latter diverges at zero, the three-dimensional volume element makes its squared gradient integrable. Its energy is $4\pi {\int }_0^1[R^6/r^4+2r^2],dR\sim 8\pi t^2$.

The smooth homogeneous equilibrium $y=tx$ has constant stress and energy $(4\pi /3)[3t^2+(t^3-1{)}^2]$, of sixth-order growth. It is therefore beaten for large $t$ in the finite-energy Sobolev space class admitting the cavity. This conclusion depends on that class: the singular map is not continuous at the center and cannot simply be substituted as a smooth cavity-free competitor.

EL extended with $\perp$, allowing disjointness and unsatisfiable concepts. Concept satisfiability with respect to general TBoxes is P-complete.

An edge loop in a simplicial complex is an edge path whose first and last vertices are the same chosen base vertex. Consecutive repeated vertices are allowed as stationary steps. Its geometric realization is a piecewise linear based loop in the realization of the complex.

A predominantly mucous gland of the duodenum whose ducts communicate with intestinal crypts.

For the Banach space $c$ of convergent complex sequences with the supremum norm, every bounded complex-linear functional has the unique representationRestrict $F$ to $c_0$ and use coordinate duality of sequence spaces to obtain $(a_j)\in {\ell }^1$. Splitting $x$ into its constant limit sequence and a zero-limit remainder forces $a_{\infty }=F(1)-{\sum }_j{a}_j$. For the norm lower bound choose the first $N$ coordinates of $x$ with phases maximizing $a_j{x}_j$ and make its tail the constant phase maximizing $a_{\infty }\lim x$. The finite prefix and limit contributions attain their absolute values; the remaining contribution is bounded by the coefficient tail, which tends to zero. The opposite norm inequality is the triangle inequality. The index at infinity is an independent coordinate of the dual norm, rather than part of the sum of the finite-coordinate coefficients.

For a normed vector space $X$, a family $(x_i,f_i{)}_{i\in I}$ in $X\times X^{\ast }$ is biorthogonal when the displayed Kronecker-delta equations hold. Its vectors are linearly independent: applying $f_i$ to a finite linear dependence isolates its $i$th coefficient. No inner product is required, and the family need not span a dense subspace. If its linear span is dense, each prescribed coordinate functional is unique by continuity. For a countable total family, the finite sums $P_{n}x={\sum }_{i\le n}{f}_i(x)x_i$ are bounded projection operators, since biorthogonality gives $P_n^2=P_n$.

For the basis $v_j=e_1+\cdots +e_j$ obtained from a basis $e_1,\dots ,e_n$, the dual basis is obtained by successive differences of the original dual basis. Indeed, if $x={\sum }_j{c}_j{v}_j$, its original coordinates are $x_i={\sum }_{j\ge i}{c}_j$. Hence $c_i=x_i-x_{i+1}$ for $i<n$, and $c_n=x_n$. These are precisely the new coordinate linear functionals. This gives an elementary example of the inverse relation between change of basis and covector transformation under a change of basis.

For $p(X)=a+bX+c{X}^2$, the three point evaluation functionals at $0,1,-1$ form a basis of the dual space of real polynomials of degree at most two. The displayed recovery formulas express the coordinate functionals, hence the dual basis to $1,X,X^2$, as linear combinations of these evaluations. More generally distinct-node polynomial interpolation identifies values with coefficient data through an invertible Vandermonde matrix.

Suppose $u$ and $\log (1+x)u$ are Lebesgue integrable functions on $(0,\infty )$. For integers $n\ge 1$, $x+n\le n(1+x)$ gives the displayed L1 norm bound. It tends to zero because $\log n/n\to 0$, proving L1 convergence of the logarithmically weighted functions to zero. Alternatively, $|\log (n+x)u(x)/n|\le (1+\log (1+x))|u(x)|$ and pointwise convergence permit the dominated convergence theorem.

For $u(x)=\sin x/x^q$ with $1<q<2$, both integrability conditions hold. Near zero, $|\sin x|\le x$ and $\log (1+x)\le x$ give integrable bounds by powers. At infinity, $|\sin x|\le 1$ and $\log (1+x)\le \log 2+\log x$, with ${\int }_1^{\infty }{x}^{-q}\log xdx=(q-1{)}^{-2}$. The L1 norm consequently decays as $O(\log n/n)$ in Big O notation.