the Endo something system
Everything claimed to be known is nonsense
https://youtu.be/ZtnY5EftDPo <==NASA Not As Smart As it might seem to present itself to be
https://youtu.be/XRr1kaXKBsU <<==gravity is nonsense. wrong explanation wright idea
A gyroscope (from Ancient Greek γῦρος gûros, "circle" and σκοπέω skopéō, "to look") is a device used for measuring or maintaining orientation and angular velocity. It is a spinning wheel or disc in which the axis of rotation (spin axis) is free to assume any orientation by itself. When rotating, the orientation of this axis is unaffected by tilting or rotation of the mounting, according to the conservation of angular momentum.
Mathematics:
The first and smallest transfinite ordinal number, often identified with the set of natural numbers including 0 (sometimes written {\displaystyle \omega _{0}}\omega _{0})
In set theory, ω1 is the first uncountable ordinal number (also sometimes written as Ω)
A primitive root of unity, like the complex cube roots of 1
The Wright Omega function
A generic differential form
In number theory, ω(n) is the number of distinct prime divisors of n
In number theory, an arithmetic function
In combinatory logic, the self-application combinator, (λ x. x x)
In mathematical/options finance, the elasticity of financial options
In analytical investment management, the tracking error of an investment manager
Clique number in Graph theory
Physics
Angular velocity or angular frequency
In computational fluid dynamics, the specific turbulence dissipation rate
In meteorology, the change of pressure with respect to time of a parcel of air
In circuit analysis and signal processing to represent natural frequency, related to frequency f by ω = 2πf
In astronomy, as a ranking of a star's brightness within a constellation
In orbital mechanics, as designation of the argument of periapsis of an orbit
In particle physics to represent the omega meson
Biology, biochemistry and chemistry:
In biochemistry, for one of the RNA polymerase subunits
In biochemistry, for the dihedral angle associated with the peptide group, involving the backbone atoms Cα-C'-N-Cα
In biology, for fitness
In chemistry, for denoting the carbon atom furthest from the carboxyl group of a fatty acid
In genomics, as a measure of molecular evolution in protein-coding genes (also denoted as dN/dS or Ka/Ks ratio)...In mathematics and computer science:
In complex analysis, the Omega constant, a solution of Lambert's W function
In differential geometry, the space of differential forms on a manifold (of a certain degree, usually with a superscript).
A variable for a 2-dimensional region in calculus, usually corresponding to the domain of a double integral.
In topos theory, the (codomain of the) subobject classifier of an elementary topos.
In combinatory logic, the looping combinator, (S I I (S I I))
In group theory, the omega and agemo subgroups of a p-group, Ω(G) and ℧(G)
In group theory, Cayley's Ω process as a partial differential operator.
In statistics, it is used as the symbol for the sample space, or total set of possible outcomes.
In number theory, Ω(n) is the number of prime divisors of n (counting multiplicity).
In notation related to Big O notation to describe the asymptotic behavior of functions.
Chaitin's constant.
In set theory, the first infinite ordinal number, ω
In set theory, the first uncountable ordinal number, ω1 or Ω...In physics:
For ohm – SI unit of electrical resistance; formerly also used upside down (℧) to represent mho, the old name for the inverse of an ohm (now siemens with symbol S) used for electrical conductance. Unicode has a separate code point for the ohm sign (U+2126, Ω), but it is included only for backward compatibility, and the Greek uppercase omega character (U+03A9, Ω) is preferred.
In statistical mechanics, Ω refers to the multiplicity (number of microstates) in a system.
The solid angle or the rate of precession in a gyroscope.
In particle physics to represent the Omega baryons.
In astronomy (cosmology), Ω refers to the density of the universe, also called the density parameter.
In astronomy (orbital mechanics), Ω refers to the longitude of the ascending node of an orbit...History
Ω was not part of the early (8th century BC) Greek alphabets. It was introduced in the late 7th century BC in the Ionian cities of Asia Minor to denote a long open-mid back rounded vowel [ɔː]. It is a variant of omicron (Ο), broken up at the side (), with the edges subsequently turned outward (, , , ). The Dorian city of Knidos as well as a few Aegean islands, namely Paros, Thasos and Melos, chose the exact opposite innovation, using a broken-up circle for the short and a closed circle for the long /o/.
The name Ωμέγα is Byzantine; in Classical Greek, the letter was called ō (ὦ) (pronounced /ɔ̂ː/), whereas the omicron was called ou (οὖ) (pronounced /ôː/). The modern lowercase shape goes back to the uncial form , a form that developed during the 3rd century BC in ancient handwriting on papyrus, from a flattened-out form of the letter () that had its edges curved even further upward...Omega
Last letter of the Greek alphabet
"Ω" redirects here. For the unit of electrical resistance, see Ohm.
For other uses, see Omega (disambiguation).
Omega (/ˈoʊmɪɡə, oʊˈmiːɡə, oʊˈmɛɡə, oʊˈmeɪɡə/; capital: Ω, lowercase: ω; Ancient Greek ὦ, later ὦ μέγα, Modern Greek ωμέγα) is the 24th and last letter in the Greek alphabet. In the Greek numeric system/isopsephy (gematria), it has a value of 800. The word literally means "great O" (ō mega, mega meaning "great"), as opposed to omicron, which means "little O" (o mikron, micron meaning "little").
In phonetic terms, the Ancient Greek Ω is a long open-mid o [ɔː], comparable to the "aw" of the English word raw. In Modern Greek, Ω represents the mid back rounded vowel /o̞/, the same sound as omicron. The letter omega is transcribed ō or simply o.
As the final letter in the Greek alphabet, omega is often used to denote the last, the end, or the ultimate limit of a set, in contrast to alpha, the first letter of the Greek alphabet; see Alpha and Omega.
Varieties are developed to intensify specific characteristics of the plant, or to differentiate the strain for the purposes of marketing or to make it more effective as a drug form for sale at a high tax rate. Variety names are typically chosen by their growers, and often reflect properties of the plant such as taste, color, smell, or the origin of the variety. The Cannabis strains referred to in this article are primarily those varieties with recreational and medicinal use. These varieties have been cultivated to contain a high percentage of cannabinoids. Several varieties of cannabis, known as hemp, have a very low cannabinoid content, and are instead grown for their fiber and seed.
Acapulco Gold
Acapulco Gold
Acapulco Gold is a golden-leafed Cannabis sativa strain originally from the Acapulco area of southwest Mexico.
physics, angular momentum (rarely, moment of momentum or rotational momentum) is the rotational analog of linear momentum. It is an important quantity in physics because it is a conserved quantity—the total angular momentum of a closed system remains constant. Angular momentum has both a direction and a magnitude, and both are conserved. Motorcycles, frisbees[1] and rifled bullets all owe their useful properties to conservation of angular momentum. Conservation of angular momentum is also why hurricanes[2] have spirals and neutron stars have high rotational rates. In general, conservation limits the possible motion of a system but does not uniquely determine it...Common symbols
LIn SI base unitskg m2 s−1Conserved?yes
Derivations from
other quantities
L = Iω = r × pDimensionM L2T−1 three-dimensional angular momentum for a point particle is classically represented as a pseudovector r × p, the cross product of the particle's position vector r (relative to some origin) and its momentum vector; the latter is p = mv in Newtonian mechanics. Unlike momentum, angular momentum depends on where this origin is chosen, since the particle's position is measured from it.
Angular momentum is an extensive quantity; i.e. the total angular momentum of any composite system is the sum of the angular momenta of its constituent parts. For a continuous rigid body or a fluid the total angular momentum is the volume integral of angular momentum density (i.e. angular momentum per unit volume in the limit as volume shrinks to zero) over the entire body.
Similar to conservation of linear momentum where it is conserved if there is no external force, angular momentum is conserved if there is no external torque. Torque can be defined as the rate of change of angular momentum, analogous to force. The net external torque on any system is always equal to the total torque on the system; in other words, the sum of all internal torques of any system is always 0 (this is the rotational analogue of Newton's third law of motion). Therefore, for a closed system (where there is no net external torque), the total torque on the system must be 0, which means that the total angular momentum of the system is constant. The change in angular momentum for a particular interaction is sometimes called twirl,[3] but this is quite uncommon. Twirl is the angular analog of impulse
Lumpers and splitters
Opposing factions in any discipline that has to place individual examples into rigorously defined categories
Lumpers and splitters are opposing factions in any discipline that has to place individual examples into rigorously defined categories. The lumper–splitter problem occurs when there is the desire to create classifications and assign examples to them, for example schools of literature, biological taxa and so on. A "lumper" is an individual who takes a gestalt view of a definition, and assigns examples broadly, assuming that differences are not as important as signature similarities. A "splitter" is an individual who takes precise definitions, and creates new categories to classify samples that differ in key ways.
Origin of the terms...
Origin of the terms
The earliest known use of these terms was by Charles Darwin, in a letter to Joseph Dalton Hooker in 1857: It is good to have hair-splitters & lumpers. They were introduced more widely by George G. Simpson in his 1945 work The Principles of Classification and a Classification of Mammals. As he put it:
... splitters make very small units – their critics say that if they can tell two animals apart, they place them in different genera ... and if they cannot tell them apart, they place them in different species. ... Lumpers make large units – their critics say that if a carnivore is neither a dog nor a bear, they call it a cat.
A later use can be found in the title of a 1969 paper "On lumpers and splitters ..." by the medical geneticist Victor McKusick.
Reference to lumpers and splitters in the humanities appeared in a debate in 1975 between J. H. Hexter and Christopher Hill, in the Times Literary Supplement. It followed from Hexter's detailed review of Hill's book Change and Continuity in Seventeenth Century England, in which Hill developed Max Weber's argument that the rise of capitalism was facilitated by Calvinist Puritanism. Hexter objected to Hill's "mining" of sources to find evidence that supported his theories. Hexter argued that Hill plucked quotations from sources in a way that distorted their meaning. Hexter explained this as a mental habit that he called "lumping". According to him, "lumpers" rejected differences and chose to emphasize similarities. Any evidence that did not fit their arguments was ignored as aberrant. Splitters, by contrast, emphasised differences, and resisted simple schemes. While lumpers consistently tried to create coherent patterns, splitters preferred incoherent complexity.
Usage in various fields... neuromuscular junction is a chemical synapse formed by the contact between a motor neuron and a muscle fiber. It is the site in which a motor neuron transmits a signal to a muscle fiber to initiate muscle contraction. The sequence of events that results in the depolarization of the muscle fiber at the neuromuscular junction begins when an action potential is initiated in the cell body of a motor neuron, which is then propagated by saltatory conduction along its axon toward the neuromuscular junction. Once it reaches the terminal bouton, the action potential causes a Ca2+
ion influx into the terminal by way of the voltage-gated calcium channels. The Ca2+
influx causes synaptic vesicles containing the neurotransmitter acetylcholine to fuse with the plasma membrane, releasing acetylcholine into the synaptic cleft between the motor neuron terminal and the neuromuscular junction of the skeletal muscle fiber. Acetylcholine diffuses across the synapse and binds to and activates nicotinic acetylcholine receptors on the neuromuscular junction. Activation of the nicotinic receptor opens its intrinsic sodium/potassium channel, causing sodium to rush in and potassium to trickle out. As a result, the sarcolemma reverses polarity and its voltage quickly jumps from the resting membrane potential of -90mV to as high as +75mV as sodium enters. The membrane potential then becomes hyperpolarized when potassium exits and is then adjusted back to the resting membrane potential. This rapid fluctuation is called the end-plate potential The voltage-gated ion channels of the sarcolemma next to the end plate open in response to the end plate potential. They are sodium and potassium specific and only allow one through. This wave of ion movements creates the action potential that spreads from the motor end plate in all directions. If action potentials stop arriving, then acetylcholine ceases to be released from the terminal bouton. The remaining acetylcholine in the synaptic cleft is either degraded by active acetylcholine esterase or reabsorbed by the synaptic knob and none is left to replace the degraded acetylcholine.
neuromuscular junction is a chemical synapse formed by the contact between a motor neuron and a muscle fiber. It is the site in which a motor neuron transmits a signal to a muscle fiber to initiate muscle contraction. The sequence of events that results in the depolarization of the muscle fiber at the neuromuscular junction begins when an action potential is initiated in the cell body of a motor neuron, which is then propagated by saltatory conduction along its axon toward the neuromuscular junction. Once it reaches the terminal bouton, the action potential causes a Ca2+
ion influx into the terminal by way of the voltage-gated calcium channels. The Ca2+
influx causes synaptic vesicles containing the neurotransmitter acetylcholine to fuse with the plasma membrane, releasing acetylcholine into the synaptic cleft between the motor neuron terminal and the neuromuscular junction of the skeletal muscle fiber. Acetylcholine diffuses across the synapse and binds to and activates nicotinic acetylcholine receptors on the neuromuscular junction. Activation of the nicotinic receptor opens its intrinsic sodium/potassium channel, causing sodium to rush in and potassium to trickle out. As a result, the sarcolemma reverses polarity and its voltage quickly jumps from the resting membrane potential of -90mV to as high as +75mV as sodium enters. The membrane potential then becomes hyperpolarized when potassium exits and is then adjusted back to the resting membrane potential. This rapid fluctuation is called the end-plate potential The voltage-gated ion channels of the sarcolemma next to the end plate open in response to the end plate potential. They are sodium and potassium specific and only allow one through. This wave of ion movements creates the action potential that spreads from the motor end plate in all directions. If action potentials stop arriving, then acetylcholine ceases to be released from the terminal bouton. The remaining acetylcholine in the synaptic cleft is either degraded by active acetylcholine esterase or reabsorbed by the synaptic knob and none is left to replace the degraded acetylcholine.
what we have here is a failure to communicate
ion influx into the terminal by way of the voltage-gated calcium channels. The Ca2+
influx causes synaptic vesicles containing the neurotransmitter acetylcholine to fuse with the plasma membrane, releasing acetylcholine into the synaptic cleft between the motor neuron terminal and the neuromuscular junction of the skeletal muscle fiber. Acetylcholine diffuses across the synapse and binds to and activates nicotinic acetylcholine receptors on the neuromuscular junction. Activation of the nicotinic receptor opens its intrinsic sodium/potassium channel, causing sodium to rush in and potassium to trickle out. As a result, the sarcolemma reverses polarity and its voltage quickly jumps from the resting membrane potential of -90mV to as high as +75mV as sodium enters. The membrane potential then becomes hyperpolarized when potassium exits and is then adjusted back to the resting membrane potential. This rapid fluctuation is called the end-plate potential The voltage-gated ion channels of the sarcolemma next to the end plate open in response to the end plate potential. They are sodium and potassium specific and only allow one through. This wave of ion movements creates the action potential that spreads from the motor end plate in all directions. If action potentials stop arriving, then acetylcholine ceases to be released from the terminal bouton. The remaining acetylcholine in the synaptic cleft is either degraded by active acetylcholine esterase or reabsorbed by the synaptic knob and none is left to replace the degraded acetylcholine.
She persisted
Further
Let it go
The last man standing
Failed initiations are baseline
Idling keeps the engine running
Background processes run on idle juice
molten salt reactions fuel electriobiosynthesis
Failed initiations are toe in the water tests...As there is a change in electric polarity across the membrane of the axon action potential aka nerve impulse pulses an axon response to a signal from another neuron, sodium- (Na+) and potassium- (K+) gated ion channels open and close as the membrane reaches its threshold potential. Na+ channels open at the beginning of the action potential, and Na+ moves into the axon, causing depolarization. Repolarization occurs when the K+ channels open and K+ moves out of the axon, creating reversed electric polarity between the outside of the cell and the inside. The impulse travels down the axon in one direction only, to the axon terminal where it signals other neurons. Self sustaining electric salt reactor pump.