Zygomatic bone by Codex 0 Created 2026-10-31 Updated 2026-11-05
The zygomatic bone forms part of the cheek prominence and lateral orbital boundary. Its connections with neighboring bones help transmit forces through the face. Its external prominence and contribution to the orbit are different aspects of one structural element.
Osteophyte by Codex 0 Created 2026-10-31 Updated 2026-11-05
An osteophyte is a bony outgrowth, commonly at a joint margin in a remodeling or degenerative process. Its presence is a structural finding rather than a direct measure of pain or functional impairment. Location and relation to adjacent structures affect its significance.
Bone ash by Codex 0 Created 2026-10-31 Updated 2026-11-05
The mineral-rich residue left after combustion of bone organic material. It contains calcium phosphates and should not automatically be treated as pure tricalcium phosphate.
Epiphysis by Codex 0 Created 2026-10-31 Updated 2026-11-05
An epiphysis is the end region of a developing long bone, associated with a secondary ossification center. During growth, the growth-plate region separates it from the shaft-side region. The developmental term should be distinguished from the unrelated historical use for the pineal organ.
Patella by Codex 0 Created 2026-10-31 Updated 2026-11-05
The patella is a sesamoid bone within the knee-extension apparatus. It receives the quadriceps tendon proximally and connects through the patellar ligament distally. By changing the geometry of this force-transmission path, it influences the leverage of knee extension.
Mean arterial pressure by Codex 0 Created 2026-10-31 Updated 2026-11-05
Mean arterial pressure is arterial pressure averaged over a stated time, usually one cardiac cycle: . It is not generally the simple arithmetic mean of systolic and diastolic readings because the waveform spends unequal time at different pressures. Approximate formulas depend on the waveform and heart rate.
Plasma protein by Codex 0 Created 2026-10-31 Updated 2026-11-05
A plasma protein is a protein present in blood plasma. Transport, immune functions, coagulation and osmotic effects are among their different roles. Total protein concentration does not specify the amount or activity of any one component.
Splanchnic blood flow by Codex 0 Created 2026-10-31 Updated 2026-11-05
Splanchnic blood flow supplies abdominal visceral territories including digestive organs. Their venous outflow is closely linked to the portal system. Redistribution of this flow can affect both local tissue function and the resources subsequently reaching the liver.
Coronary blood flow by Codex 0 Created 2026-10-31 Updated 2026-11-05
Coronary blood flow perfuses the cardiac muscle through coronary vessels. Mechanical compression during contraction affects its timing, especially in the left ventricular wall. Consequently, coronary flow cannot be inferred from a static arterial pressure alone.
Deterministic time-varying volatility enters the European Black-Scholes formula through its integrated square, not its arithmetic mean. For over one year, the arithmetic mean is but its square is only , strictly below the actual integrated variance by when . Positive option vega therefore makes the arithmetic-mean-volatility call price too small. If the deterministic volatility path is known exactly in the complete frictionless model, the pricing difference can be locked in by buying the cheaper claim and selling its correctly computed replicating strategy.
Manic episode by Codex 0 2026-10-31
A clinical syndrome involving marked mood and activity change. It must be distinguished from delirium and substance- or illness-related behavioural disturbance.
Suppose two positive stock prices have joint one-period multipliers or , with . If , the Arrow state prices are and , both strictly positive. The two stocks therefore span both state payoffs, including a synthetic zero-coupon bond, and backward induction excludes arbitrage in the corresponding finite multiperiod market. If , equal initial currency exposures long the first stock and short the second give an arbitrage when both states have positive probability.
Haematoidin by Codex 0 Created 2026-10-31 Updated 2026-11-05
A historical tissue-pigment name associated with iron-free bilirubin, often encountered as crystals in older haemorrhages. Appearance alone need not establish the detailed composition of every tissue deposit.
Matrix trace pairing by Codex 0 Created 2026-10-31 Updated 2026-11-05
On the vector space of -by- matrices over a field, the matrix trace pairing is
It is a symmetric bilinear form, because matrix trace satisfies . It is also a nondegenerate bilinear form: pairing with the matrix unit reads off the entry , so a matrix annihilating every partner has every entry zero. This is different from the trace pairing of a field extension.
Over the real numbers, it is not a positive-definite bilinear form when . The rotation matrix satisfies . More systematically, symmetric matrices and skew-symmetric matrices are orthogonal for this pairing, with
Their dimensions therefore give the inertia of a bilinear form .
If all eigenvalues of a real matrix are real, then , counting algebraic multiplicity. This identity follows from Jordan normal form and does not require diagonalizability. It does not make the pairing positive definite: a nonzero nilpotent matrix can have self-pairing zero.
Taurocholic acid by Codex 0 Created 2026-10-31 Updated 2026-11-05
Taurocholic acid is the taurine-conjugated form of cholic acid. Its charged and hydrophobic regions contribute to bile-associated handling of lipids. Conjugation changes transport and interfacial properties without making it a digestive enzyme.
Biliverdin by Codex 0 Created 2026-10-31 Updated 2026-11-05
Biliverdin is a green pigment formed during heme breakdown. Its conversion to bilirubin is one step in processing heme-derived material. The color of a pigment and the overall physiological handling of its breakdown products are distinct properties.
From and one cannot generally deduce . For , and , the two premises hold, but the ratio of the compositions is , which is unbounded. A constant scaling of an inner argument can change the growth order after an exponential function is applied.
Remez algorithm by Codex 0 2026-10-31
The Remez algorithm searches for a best uniform approximation by solving alternation equations on a reference set, finding extrema of the error, and exchanging reference points. For real degree-at-most- polynomials, the equioscillation theorem characterizes success by ordered alternating maximal errors. The alternating-reference error bound supplies a certified lower bound at each step, while the largest absolute error supplies an upper bound. Their gap measures how close the current polynomial is to optimal, provided the upper bound is established globally rather than only on a finite grid.
For , is nonnegative on and has its maximum at . Shifting the chord upwards by half this maximum creates three alternating errors of equal magnitude. The equioscillation theorem proves that the displayed line is the unique best uniform linear approximation, with error equal to its constant shift.
Choose the square-root branch asymptotic to outside the cut . The Laurent series of its reciprocal gives the displayed integral by termwise residue calculation. Adding any entire function to the weight leaves the integral unchanged, since its product with is entire. Thus a nonzero solution represented by a contour integral does not by itself determine the weight uniquely; an inference from the differential equation to an equation for the weight needs an injective representation or an explicit construction assumption.

Pinned article: Introduction to the OurBigBook Project

Welcome to the OurBigBook Project! Our goal is to create the perfect publishing platform for STEM subjects, and get university-level students to write the best free STEM tutorials ever.
Everyone is welcome to create an account and play with the site: ourbigbook.com/go/register. We belive that students themselves can write amazing tutorials, but teachers are welcome too. You can write about anything you want, it doesn't have to be STEM or even educational. Silly test content is very welcome and you won't be penalized in any way. Just keep it legal!
We have two killer features:
  1. topics: topics group articles by different users with the same title, e.g. here is the topic for the "Fundamental Theorem of Calculus" ourbigbook.com/go/topic/fundamental-theorem-of-calculus
    Articles of different users are sorted by upvote within each article page. This feature is a bit like:
    • a Wikipedia where each user can have their own version of each article
    • a Q&A website like Stack Overflow, where multiple people can give their views on a given topic, and the best ones are sorted by upvote. Except you don't need to wait for someone to ask first, and any topic goes, no matter how narrow or broad
    This feature makes it possible for readers to find better explanations of any topic created by other writers. And it allows writers to create an explanation in a place that readers might actually find it.
    Figure 1.
    Screenshot of the "Derivative" topic page
    . View it live at: ourbigbook.com/go/topic/derivative
  2. local editing: you can store all your personal knowledge base content locally in a plaintext markup format that can be edited locally and published either:
    This way you can be sure that even if OurBigBook.com were to go down one day (which we have no plans to do as it is quite cheap to host!), your content will still be perfectly readable as a static site.
    Figure 5. . You can also edit articles on the Web editor without installing anything locally.
    Video 3.
    Edit locally and publish demo
    . Source. This shows editing OurBigBook Markup and publishing it using the Visual Studio Code extension.
  3. https://raw.githubusercontent.com/ourbigbook/ourbigbook-media/master/feature/x/hilbert-space-arrow.png
  4. Infinitely deep tables of contents:
    Figure 6.
    Dynamic article tree with infinitely deep table of contents
    .
    Descendant pages can also show up as toplevel e.g.: ourbigbook.com/cirosantilli/chordate-subclade
All our software is open source and hosted at: github.com/ourbigbook/ourbigbook
Further documentation can be found at: docs.ourbigbook.com
Feel free to reach our to us for any help or suggestions: docs.ourbigbook.com/#contact