Summary by stock -- a commentor at ENENEWS who goes by "CodeShutdown" provided much of the information and got me going down this path.
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The below resources list is mostly a jumble of sources that I gathered together in the process of wrapping my head around the mass ocean deaths in the Pacific.
In 2016 we busted NOAA and MSM dead to rights lying about all the deaths, throwing out "Domoic Acid" as the main culprit even though when I got my hands on their real data, it only showed 1 to 3% deaths caused by Domoic Acid.
Starvation and a weakened immune system were the main culprits, as they are now.
So we know that krill are highly affected by even low levels of radiation in the environment, proven by test data on the CS134/CS137 ratio in water showing that the krill are taking CS134 to Davy Jone locker at faster rates because it kills them faster.
The disappearance of krill also allows other phytoplankton to expand. More algae. More Domoic Acid. Domoic Acid latches on to Brain Neurons and causes them to fire. But here is the real kicker, Domoic Acid acts like a chelator and can grab and carry heavy metals with it.
So any radioisotopes present can be neatly delivered right right to the brain neurons, for a wicked double whammy.
Additionally, we know that even low levels of radiation bio-magnify in Chitin, a biological structure of great importance in many ocean flora and fauna. Radiation is one of the few things that can break the tough Chitin bonds, so it can blow up the structure of animals and plants. But its destruction does not have to end just there. It can also, when close to DNA, destroy that DNA.
But it gets even "better", Chitin is also used in cell walls, where it affects the ionic and voltage gradients which are prime mechanisms that allow and tell cells how to function, change, grow.
Morphogenesis -- is the fancy way of describing how cells grow into different body parts, and so it should be obvious that having damaged Chitin in the cells is not going to be a good thing for proper cellular development.
But if you ask the "scientists" at the International Atomic Energy Association, they will explain that radiation damage can be 100% calculated by modelling the human body literally as a bag of water with energy being deposited into it. It is shameful.
So to sum it up:
- Radiation destroys chitin structure, DNA, and cell growth and bio-magnifies
- This causes a huge amount of the food chain to simply sink to the bottom
- Radiation also damages the immune system in a number of ways, particularly gut flora (70% of the immune system created in the gut) and creating hurtful immune response.
- Radiation allows more algae, and thus Domoic Acid, to be created
- Domoic acid grabs radiation and then delivers itself and the radiation directly to the brain and nervous system of sea critters, making them confused, lethargic.
- So the food chain is massively hurt, the critters are sick and can't think well, therefore they can't even hunt well for the available food.
- And we have what we are seeing in the real world.
But the military/fed funded scientists who are directed to make sure that people are smiling and unaware of the causes of the mass die-offs:
1) Test the water only, and state how there is no danger
2) Hang their hats on the ICRP radiation danger dose model (just a bag of water)
CodeShutdown
Domoic acid is a heavy metal transporter used by those toxic plankton
to modulate different metals to their needs…iron, copper… There is an
analogy; Some molds thrive in radioactive environments…they live off it.
They use melanin, and the mold is black with it.
So anyway its a
possibility, just a hypothesis, that the nuclear toxins are better
handled by the toxic algae because of the domoic acid, which gives them
an edge in the competitive world.
The domoic acid may bioconcentrate
radionuclides also, and I wonder if it is shuttled to the nervous
system. As an analog of glutamate, an excitatory neurotransmitter,
DA binds to the kainate type of glutamate receptors, but with a
binding
capacity three times greater and 20 times more powerful than kainic acid
run with it stock…call it a discovery
per code
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Chitin is a polysaccharide biological structural polymer found in
exoskeletons, like insects, crabs, beaks of squid etc, and combined with
calcium carbonate to form shells of crustaceans. It absorbs
radioactive fallout.
"radiation destruction of chitin
The change in functional composition and molecular mass of crab,
shrimp, and Antarctic shrimp (krill) chitin under the effect of ionizing
radiation has been studied….it was established that primary radicals
appear in positions 1 and 4 of the pyranose ring with subsequent
breakdown of the glycoside bond analogous to cellulose and chitosan
decay when γ-irradiated."
https://inis.iaea.org/search/search.aspx?orig_q=RN:26023735
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Kainic acid (kainate) is a natural marine acid present in some
seaweed.
Kainic acid is a potent neuroexcitatory amino acid agonist that acts by activating receptors for
glutamate, the principal excitatory neurotransmitter in the central nervous system. Glutamate is produced by the cell’s metabolic processes and there are four major classifications of glutamate receptors: NMDA receptors, AMPA receptors, kainate receptors, and the metabotropic glutamate receptors.
Kainic acid is an
agonist for
kainate receptors, a type of
ionotropic glutamate receptor. Kainate receptors likely control a sodium channel that produces
excitatory postsynaptic potentials (EPSPs) when glutamate binds.
[1]
Kainic acid is commonly injected into laboratory animal models to study the effects of
experimental ablation. Kainic acid is a direct agonist of the glutamic kainate receptors and large doses of
concentrated solutions produce immediate neuronal death by overstimulating neurons to death.
Such damage and death of neurons is referred to as an
excitotoxic lesion. Thus, in large, concentrated doses kainic acid can be considered a neurotoxin, and in small doses of dilute solution kainic acid will chemically stimulate neurons.
[2]
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Morphogenesis (from the
Greek morphê shape and
genesis creation, literally, "beginning of the shape") is the
biological process that causes an
organism to develop its shape. It is one of three fundamental aspects of
developmental biology along with the control of
cell growth and
cellular differentiation, unified in
evolutionary developmental biology (evo-devo).
The process controls the organized spatial distribution of cells during the
embryonic development of an
organism. Morphogenesis can take place also in a mature organism, in
cell culture or inside
tumor cell masses. Morphogenesis also describes the development of
unicellular life forms that do not have an embryonic stage in their life cycle, or describes the
evolution of a body structure within a
taxonomic group.
Morphogenetic responses may be induced in organisms by
hormones, by environmental chemicals ranging from substances produced by other organisms to
toxic chemicals or
radionuclides released as pollutants, and other plants, or by mechanical stresses induced by spatial patterning of the cells.
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cant wait until you realize the other part of the story stock. The
chitin acts like an ion exchange resin…and the radiation CAN break down
the chitin,
http://enenews.com/mass-death-species-found-around-fukushima-nuclear-plant-govt-disappeared-little-reproductive-success-evident-biota-around-power-plant-affected-nuclear-accident/comment-page-1#comment-746906
BUT there is a whole other path of influence. The chitin machinery
is right there on the cell wall, and several things have been discovered
which influence morphogenesis…which limb goes where…which microtubule
in the cell cytoskeleton goes which way…among which influence is the
ionic gradient and the voltage gradient.
So EVEN IF the chitin is not
degraded significantly, or if its consumed by a non chitin based
animal…it still forms a hot spot of ionic and voltage gradient which can
interfere with morphogensis on the macro and micro scale.
Indeed, ion
gradients and flow is a large factor in biochemical process and
morphogenisis. Needless to say this is a deforming potential not
directly related to DNA breaks.
In fact has been found that organisms
can select for different isotopes; "it is thought that accumulation of
radionuclide elements follows that of nonradioactive elements. However,
with the
discovery of isotope discrimination for a number of elements by a range of organisms, this may not hold true.
You arent done with your discovery process
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Jebus
"a hot spot of ionic and voltage gradient"
This fits in there.
"Collectively these data demonstrate that low-dose ionizing radiation
has an important effect on absorbing water, consuming O2 and releasing
CO2, which means the risk for embryo and endosperm development was
higher."
http://www.sciencedirect.com/science/article/pii/S0022519317302382
Embryogenesis comes to mind… -----------------------------------------------------------------
Code:
Might be a key as to how radiation directly damages immune system
besides the gut based flora route that I have already established
http://mbio.asm.org/content/3/2/e00056-12.full
Besides the role of chitin in supporting structural stability, chitin
and host enzymes with chitinase activity have an important role in host
defense and modifying the inflammatory response. Thus, chitin appears
to provide a link between the fungus and host that involves both innate
and adaptive immune responses. Recently, there has been increased
attention to the role of chitinases in the pathogenesis of allergic
inflammation, especially asthma. We review these findings and explore
the possible connection between fungal infections, the induction of
chitinases, and asthma.
So far, this seems restricted to fungal cell wall, and not cell walls in other chitin uses, but we shall see…..
Localization of chitin in algal and fungal cell walls by light and electron microscopy.
Abstract
Chitin
was visualized in cell walls after hydrolysis with potassium hydroxide
and subsequent postfixation of the deacetylated polysaccharide
(chitosan) in OsO4. Areas of chitin deposition appeared dark borwn by
light microscopy and electron dense in the electron microscope. With
this method, the presence of chitin was demonstrated in the cell walls
of the green alga Pithophora oedogonia (Montagne) Wittrock and two
fungi, Ceratocystis ulmi Buism. (C. Moreau) and Blastocladiella
emersonii Cantino and Hyatt. Most of the chitin in P. oedogonia ws found
in the crosswall disk and small amounts occurred in the outer
longitudinal walls. The septal disk of C. ulmi also contained chitin,
but significant amounts were present in the inner and outer regions of
longitudinal walls as well. Chitin was present throughout the walls of
B. emersonii. Small amounts of chitin were not easily demonstrated by
this technique, but removal of chitosan by exposure to dilute acetic
acid before osmium fixation disrupted cell wall integrity, suggesting
that small amounts of the structural polysaccharide had been removed.---------------------------------------------------------------
http://www.mdpi.com/1660-3397/11/7/2398/htm
The low iron treatment may have increased the susceptibility of
S. marinoi
to other stressors, in this case, domoic acid. Previous studies have
shown that nutrient limitation increases the susceptibility of
phytoplankton to radiation [
23,
24] and to unidentified allelopathic compounds produced by other phytoplankton [
25]. From this experiment, it is not clear whether domoic acid directly inhibits the growth of
S. marinoi or if domoic acid binds iron, and reduces iron availability to the already iron limited
S. marinoi cells
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HoTaters
Formation of excessive fibrinogen inside arteries and vessels is an
inflammatory response to a toxin, or pathogen. There may be other
causes. Kent Holtorff, M.D., discusses this in detail in a video at his
website. He discusses it in the context of an inflammatory cascade and
the long-term development of chronic disease states.
'Ho out ….
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Code say---
The cell wall of candida is composed of fibrin and chitin. I sometimes
think of humans as a kind of out of control fungal growth…but
regardless…we always have some chitin going in…we eat it, colonized by
it. Especially oceanic mammals. But I was going to mention the
fibrin…its in the back of my mind to research this because Ive noticed
more people getting thrombosis and there are some similarities of fibrin
and chitin
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Code emailed in
for what its worth....the fallout is absorbed and travels
with the MSG, and thus most assuredly with the glutamine and domoic acid, binds to the glutamine receptors and lingers
there. The glutamine is heavily tied to
mitochondria health, cancer progression, vascular inflammation, thrombosis, and
on. The key story is that science
believes without question that radiation = radiation. But we know that both
specific activity and the largely unexplored frequency and harmonics, as well
as the chemical nature of the isotope all differentiate man made radiation
from so called background. This is the hurdle...convincing young
scientists that nuclear fallout is different, worse, of
unknown biological cascade effect, promotes morbidity, not just all or nothing
hit or miss cancer, bioaccumulates in known and unknown ways and causes hot
spots on macro and micro scales
Selective distribution of radioactivity in the neonatal
mouse brain following subcutaneous administration of 14C-labeled monosodium
glutamate
Radioactivity and
its distribution in the neonatal mouse brain following subcutaneous
administration of 14C-labeled monosodium glutamate (MSG) were studied by means
of radiometry and freezing autoradiography. The brain level of radioactivity
proportionally increased and peaked at 3 hours after the injection of
radiolabeled MSG, then gradually decreased, whereas the blood level of
radioactivity rapidly increased, peaking at 50 minutes, and rapidly decreased
therafter. The radioactivity on the brain autoradiograph was less than in other
head tissues, but marked accumulation of radioactivity was observed in the
retina, lens, preoptic area, hippocampus, dorsal surface of thalamus, arcuate
nuclear region, and choroid plexus of lateral and third ventricles at 15
minutes to 24 hours. These areas, except lens and choroid plexus, correspond to
the sites of MSG-induced lesions.
