"Primeval Code" reactivated:
Living archetypes of plants and animals created at the
laboratory.
Biography:
In laboratory experiments the researchers the Dr. Guido Ebner
and Heinz Schürch exposed cereal seeds and fish eggs to an
"electrostatic field" – in other words, to a high voltage
field, in which no current flows. Unexpectedly primeval
organisms grew out of these seeds and eggs: a fern that no
botanist was able to identify; primeval corn with up to twelve
ears per stalk; wheat that was ready to be harvested in just
four to six weeks. And giant trout, extinct in Europe for 130
years, with so-called salmon hooks. It was as if these
organisms accessed their own genetic memories on command in
the electric field,
The Swiss pharmaceutical group patented the process – and then
stopped the research in 1992. Why? The discovery was soon
forgotten, without the global scientific community taking any
notice. But this changed: In collaboration with the
researchers involved – or rather their sons - author Luc
Bürgin has for the first time now disclosed in detail how the
principle of this revolutionary bio-experiment works.
Nevertheless many scientists who think along conventional
lines may remain sceptical about this inexplicable biological
effect. But now for the first time, renowned German expert
botanists such as Professor Edgar Wagner of the University of
Freiburg and Professor Gunter Rothe from the University of
Mainz make positive statements about it in the book. Rothe
even had replicated the Ciba experiments in detail at his
university in 2001 – and was successful. And also for the
first time, even a Nobel laureate – the world-famous Swiss
microbiologist Werner Arber – is taking up the cudgels for
this controversial discovery. Back then, Arber had given an
expert opinion on the Ciba experiments in person in the
laboratory. The professor said to the author: "I was
impressed!"
After Guido Ebner and Heinz Schürch both passed away
unexpectedly in 2001, their experiments were continued by
Guido Ebner's son, Daniel – himself a biologist – on a private
basis. Daniel M. Ebner (studies of biology, chemistry and
biostatics at the Universities of Basel and Montreal) works as
Management Consultant at the Swiss Arcondis company ("Art of
Consulting and Development for Information System",
CH-Reinach) in the fields of pharmaceutical validation
processes and information technology. At the WMF 2008 he
will present facts, reasonings and perspectives of the
discovery of his father. Ebner’s involvement belongs
especially in the practical usage of the discovery for food
production of countries in the Third World.
Examples of re-created plants and animals will be presented
live for the public at the WMF 2008!
The "Primeval Code"
The ecological alternative
to the controversial genetically engineered seeds of the
international agro-multinationals
Title of the lecture of Daniel M. Ebner, Switzerland, at the
"World Mysteries Forum" 2008 in Basel:
"Primeval Code" -
reactivated!
Can the global food problem at last be solved without using
genetic engineering? This new book by Swiss journalist Luc
Bürgin unveils the secret of a sensational biological
discovery at the pharmaceutical giant Ciba (now Novartis),
which unfortunately has been ignored by the experts up to the
present day. In laboratory experiments the researchers there
Dr. Guido Ebner and Heinz Schürch exposed cereal seeds and
fish eggs to an "electrostatic field" in other words, to a
high voltage field, in which no current flows.
Unexpectedly primeval organisms grew out of these seeds and
eggs: a fern that no botanist was able to identify; primeval
corn with up to twelve ears per stalk; wheat that was ready to
be harvested in just four to six weeks. And giant trout,
extinct in Europe for 130 years, with so-called salmon hooks.
It was as if these organisms accessed their own genetic
memories on command in the electric field, a phenomenon, which
the English biochemist, Rupert Sheldrake, for instance
believes is possible.
The Swiss pharmaceutical group patented the process and then
stopped the research in 1992. Why? Because "primeval cereals"
generated by an electric field, in contrast to modern strains
of seeds, require hardly any fertilisers or pesticides i.e.
crop protection agents, sold as priority products by Ciba at
that time. The discovery was soon forgotten, without the
global scientific community taking any notice.
In collaboration with the researchers involved or rather their
sons, in this book, the author has for the first time now
disclosed in detail how the principle of this revolutionary
bio-experiment works. Previously unpublished research reports,
64 exclusive photos, English-language patent specifications
and interviews document the "Primeval Code" in all its
aspects.
Nevertheless many scientists who think along conventional
lines may remain sceptical about this inexplicable biological
effect. But now for the first time, renowned German expert
botanists such as Professor Edgar Wagner of the University of
Freiburg and Professor Gunter Rothe from the University of
Mainz make positive statements about it in the book. Rothe
even had replicated the Ciba experiments in detail at his
university in 2001 and was successful. And also for the first
time, even a Nobel laureate the world-famous Swiss
microbiologist Werner Arber is taking up the cudgels for this
controversial discovery. Back then, Arber had given an expert
opinion on the Ciba experiments in person in the laboratory.
The professor said to the author: "I was impressed!"
Indeed, Guido Ebner and Heinz Schürch appear to have
discovered a biological method of effectively creating
antecedents from progeny without using genetic engineering. Or
as both researchers put it: "Our experiments do not involve a
mutation of the organism in question, which in the case of
genetic engineering involves channelling an additional gene
into the organism. No entirely new organism is created. In the
electrostatic field, only the gene expression is altered the
retrieval of the existing gene. That is something different."
In addition to corn and trout experiments, the results of
experiments with wheat were also amazing: thus the cereal
exposed to the electrostatic field developed new proteins,
which people looked for in the original wheat to no avail.
Furthermore, it surprisingly produced much larger roots than
the control group. This had the advantage of allowing the
crops to grow far more rapidly. And occasionally in these
experiments, a variant emerged which resembled the genetic
antecedents of the wheat. Thus, a meadow grass-like
arrangement of ear shoots and small narrow leaves was
observed, for example.
"In the case of our 'manipulated' wheat, growth was so rapid
that it was ripe in four weeks instead of the usual seven
months", Heinz Schürch recalled. "However one has to say that
although the ears and stalks were somewhat smaller, there were
more ears per plant. The actual benefit is that we could
cultivate this wheat in regions where spring and summer are
short where conventional wheat cannot be grown at all." In
this case, one can also cheerfully refrain from using
pesticides and herbicides: "The pests that have adapted to the
growth process of normal wheat have not yet developed when we
harvest our wheat as early as four to eight weeks after
planting."
The Third World in particular could benefit from this method
of cultivation that is both environmentally friendly and
inexpensive. For "primeval cereals" from an electric field
yield more than modern genetically engineered varieties and do
not require fertilisers. Furthermore, it is completely natural
and thus healthier. It can be grown by anybody at minimal
cost.
After Guido Ebner and Heinz Schürch both passed away
unexpectedly in 2001, their experiments were continued by
Guido Ebner's son, Daniel himself a biologist – on a private
basis. He now wants to export this electric field technology
to Africa as soon as possible, as part of an aid project, with
the assistance of the former assistant to the UN Food
Representative, Professor Jean Ziegler, in order to make it
available to local farmers free of charge, as an ecological
alternative to the controversial genetically engineered seeds
of the international agro-multinationals.
The Experiments by Ciba Geigy - An Untold
Story
A factual report of Carl R. and Steffen Jachulke
after a television report of H. Heisterkamp on the topic
"Biological experiments with the electric field"
Prologue
It seems a fantastic world in which we were introduced to our
children through stories, pictures and story books. It seems
no less fantastic, as we see today is foreign to us drawings
or engravings of plants or animals of prehistoric times.
Living creatures on our planet thousands of years ago, or even
millions of years existed. Oversized trees and animals that
are long gone. I would not have believed it possible that
animals from a bygone era in our reality is to get today. It
can be done! This report shows how and where this has happened
and what peculiarities connected with it.
A scientific sensation
With an entertainment program of the Swiss television (super
hit on 17/12/1988) it was made public. Million spectators have
witnessed, as Showmaster Kurt Felix introduced two
researchers.
Figure -- The two guests in the show, Kurt Felix Law;
the two researchers in the close-up.
Guido Ebner and Heinz Schürch, two scientists in the research
and development at one of the 10 largest chemical companies in
the world - Ciba-Geigy. The Swiss company sells chemical
products and services in three markets. Health, agriculture
and industry.
Research results were presented which were to remain under
wraps at the moment. Plants can be changed by an electrostatic
field in such a way that they grow as millions of years ago.
So a step backwards in their evolutionary history experienced.
From a traditional male fern with its feathery leaves had
turned around a Hirschzungenfarn tapering, tongue-like leaves.
Some scientists call this Ciba-Geigy also Urfarn fern.
Figure -- Left is the common male fern. Right: the
experimental result of the electric field of the treated
spores Wurmfarns. In addition, a petrified image.
Plants from prehistoric times, perhaps, could do from the time
of the dinosaurs, perhaps even from the time before ... The
scientists conjecture. Anyway, it's a time warp back in
evolutionary history with the help of our common fern spores,
reproductive cells, ie from the time now treated in an
electric field. Performed in the research laboratories of the
chemical company in Basel.
Figure -- Section of a still living Artvertreters of
Hirschzungen ferns
What the public has been presented is just one part of the
experiments. They also experimented with other crops (mainly
wheat), even with fish. For example, experiments with corn.
In Petri dishes artificial soil and water was tested together
with maize kernels, which were then placed in an electrostatic
field. Static electric fields, stress fields in which no
current flows. There exists a DC voltage up to several
thousand volts, depending on the experimental arrangement.
What alchemists dreamed before several hundreds of years,
actually, the general doctrine is to spite. A Nobel
Prize-breaking discovery.
Figure -- Assistants help prepare the dishes. On the right is
an experimental dish on a high-voltage electrodes.
For three days the corn grains are drawn into the air and
water-sealed Petri dishes in an electric field, then continue
to grow the seeds, like any other plant in a pot or in the
greenhouse. The result after normal growing season is a corn
with a particularly high number of pistons in a heap, where
normally found only in maize is a piston.
Figure --- Heinz Schürch is in the preparation of an
experimental approach. Left is the experimental set-up to see
in which an electric field is applied.
The corn "remembers" how it was. No genetic engineering, no
use of chemicals.
Supposed benefits:
- Higher germination
- Increased resistance to pests and harsh climatic conditions
- No agrotoxics
Figure -- Left is a conventional hybrid form. Right in the
electric field grown maize. Noteworthy is the fact that up to
5 flasks grow in one spot.
Corn in today's agriculture
Used are hybrid varieties, hybrid varieties so highly
cultivated, and highly sensitive to their semen can not be
used. I.e. The farmer must be buy new seeds every year, not
only for corn.
The seed production in turn is dominated by multinationals in
the food, agricultural chemicals and petroleum industries. The
same companies that sell and fertilizers, pesticides and
herbicides to farmers. For the chemical industry is a billion
dollar business.
It is the chemistry that the way of agriculture and food
destined. At least now suddenly becomes clear what the tests
actually Ciba-Geigy.
The Basel-based chemical giant, annual sales at about 22
billion Swiss Francs 94 000 employees. Each employee sold
statistically for 235 000 Swiss Francs in chemistry. Research
on and with the electrostatic field is, with the eyes of the
chemical businessman, has called sawing the branch on which it
sits.
Because the findings show, it's possible without chemistry. At
least in many areas. The significance of the research result
lies in the fact that the hereditary characteristics have been
lost through breeding or degeneration, can bring out again and
activate.
Experiments with higher
organisms
In this context the most spectacular attempt at Ciba-Geigy had
been made this time around with ordinary commercially
available rainbow trout. In the laboratory, the females are
taken for this purpose the eggs.
Figure -- Removal of the eggs of the female. Right, the eggs
are subjected to the retort of an artificial insemination.
Figure -- Placing the fertilized eggs in a suitable
experimental setup for the rearing of young fish
These eggs are artificially inseminated and subsequently
exposed for 4 weeks to an electrostatic field. The
experimental arrangement is designed as before with fern and
corn.
Solothurn in Switzerland, in a fish farm. In one of the fish
tanks of the treatment in the electrostatic field that emerged
animals. In another pool, the untreated normal trout. Same
source, different fish?
Here's the proof:
Figure -- Conventional rainbow trout, known fish shop and
restaurant, 2-4 years old. They move slowly, are almost tame.
Colors are visible only weak upper and lower jaws are not very
pronounced. They often have only rudimentary teeth.
Figure -- DC Old Trout emerged from the experiments with the
static electric fields. They are 1/3 larger, heavier,
fleshier, stronger. You have more and stronger teeth are
remarkably strong colors. In adult males of the lower jaw as
in wild salmon is at the front is formed into a powerful hook.
A statement from the press
office of Ciba
The investigative body of the fish Confederation in Berne
described the animals as an archetype of the trout, which was
about 150 years ago practically extinct. There is no
scientific explanation, it is not until today. Neither the
trout, even in plants. Also a scientific sensation!
Over again, as in plants, a conflict of interest with
Ciba-Geigy. The sale of drugs for the fish part of the
business. The trout, however, need not, therefore, no
business.
European Patent Office in Munich. Three years ago the Swiss
announced a patent on their invention. Patent applicant is
Ciba-Geigy, the inventor, the guests from the show, Kurt
Felix, Guido Ebner and Heinz Schürch. The patent specification
states:
"The present invention relates to a novel process which leads
to permanent useful and desirable properties in fish that
would otherwise not at all or only with considerable
additional costs are generated.
The simplicity of the process measures learns the rearing of
freshwater and saltwater fish, a drastic improvement.
The first thing you'll notice a significantly higher hatching
rate, which often occurs an increase of 100 to 300 percent.
Quite significant is their extremely high survival rate. This
becomes more evident if one does without any drug treatment.
In addition, the treated fish, with the same diet, increase
much more rapidly in weight and size and for sale as food fish
available. "
Unbeatable ... properties, unimagined possibilities.
The Swiss chemical giant is doing what he does, he stopped the
research. The patent now rests in the drawers of the European
Patent Office and its imitation is prohibited.
After the financial report Ciba-Geigy is the world leader in
crop protection, their sales rising every year. No
experiments? Trout "blue" as usual?
In the annual report of the entity:
"The business activities of Ciba Geigy's long-term livelihood
oriented towards."
From the press office, it was then:
"Ciba has given up by now all these studies, there have been
no further scientific work undertaken in this area because
they can not be assigned to one of the priority research areas
of the company. For this reason, the research industry in
many, many interesting approaches in exploratory projects will
be dropped. "
On 17/12/1988, Kurt Felix then told Swiss television on the
experiment before it was discontinued.
US5048458 // EP0351357
Method of breeding fish
Inventor: EBNER GUIDO [CH] // SCHUERCH HEINZ [CH]
Applicant: CIBA GEIGY CORP [US]
EC: A01K61/00G
IPC: A01K61/00 // (IPC1-7):A01K63/00
There is disclosed a novel method which, based on the brief
application of electrostatic fields, induces lasting useful
and desirable properties in fish, which properties cannot
otherwise be induced at all or can only be induced by dint of
substantial additional investment in time and material
resources. The simplicity of the measures proposed in this
invention and the significant results obtained will
revolutionize the breeding of fish, especially edible fish,
but also ornamental fish.
The present invention relates to a novel method which, based
on the brief application of electrostatic fields, induces
lasting useful and desirable properties in fish, which
properties cannot otherwise be induced at all or can only be
induced by dint of substantial additional investment in time
and material resources. The simplicity of the method of this
invention and the significant results obtained make it
possible to improve very substantially the breeding of
freshwater and saltwater fish, especially of edible fish and
also of ornamental fish.
The method of the present invention essentially comprises
exposing early development stages of fish, such as juvenile
fish or preferably eggs, before, during or after
fertilisation, especially eggs in early phases of cell
division, for a short time to electrostatic fields, without
the flow of electric currents. It is particularly preferred to
use eggs during or immediately after fertilisation.
Specifically, in the practice of this invention, tanks
(aquaria) filled with freshwater or saltwater and containing
the fish or eggs, and consisting preferably of electrically
non-conductive material (insulator), are placed between the
electrodes of a capacitor. A directcurrent voltage of one to
tens of thousands of volts is then applied to said electrodes.
Instead of using the non-conductive aquarium material, it is
of course also possible to use electrodes which are provided
with an insulating layer and to immerse these electrically
insulated capacitor plates direct in the tanks. Of sole
importance is that the electrodes of the capacitor are
insulated against the freshwater or saltwater acting as
dielectric medium. As no currents flow in this apparatus, no
perceptible loss of energy is observed. Hence energy is not a
cost factor in this invention.
A further essential feature of this invention is that, because
no electric current flows, the chemical identity of the system
"fish" does not undergo change.
Interest in the investigation of parameters which exert a
direct or indirect activity on physico-chemical interactions
in living organisms has so far centered almost exclusively on
the influence of temperature, pressure, electromagnetic
radiation and electrodynamic fields (alternating fields). In
contrast, far less attention has been paid, for example, to
the investigation into possible interactions of electrostatic
fields on the development of higher organisms, especially
fish.
Only recently have reports become more frequent on the
possible effects of gravitation and magnetic fields on
biological systems. Thus, for example, Goodman and Henderson
[Bioelectromagnetics, 7: 23-29, 1986] have found indications
that a correlation exists between electromagnetic fields and
the rate of transcription in biological material, the rate
being influenced favourably by the applied electromagnetic
field so that enhanced transcription results.
In contrast, it would appear that the possibility that
electrostatic fields might also have an influence on the
course of physico-chemical interactions in organisms,
especially also in early development phases, has so far been
ruled out from the start. Hence there have to date been no
reports on the possible effect of electrostatic fields on the
development of fish.
Experiments have, however, been described (C.A. 95: 165 987b;
Vosyliene et al.), in which trout (Salmo iridens) and carp
(Cyprinus carpio) were exposed over long periods to field
strengths of 0.03-0.08 V/cm and 0.06-0.10 V/cm. These
experiments dealt principally with the influence of the
voltage applied on brain development and the excretion of
noradrenalin, depending additionally on the season.
The reason why there has been so little investigation into the
effects of electrostatic fields may primarily be that, in the
light of conventional teaching, it has been assumed that an
electrostatic field in a medium filled with charge carriers is
shielded by the spontaneous formation of an electric double
layer and consequently remains inert in its effect.
This teaching is based essentially on the equation formulated
by C. Gouy and D. L. Chapman, according to which the actual
thickness of a diffuse double layer for an electrolyte is
##EQU1## wherein d=the thickness of the double layer
F=the Faraday constant
.epsilon.=the dielectric constant
R=the universal gas constant
T=the absolute temperature, and
i=the nature of the ions of concentrations ci and valences zi.
Surprisingly, this prejudice has now been overcome with
respect to fish in the practice of this invention by the
application of simple measures.
In contradistinction to the conventional teaching elaborated
above, the aim has now for the first time been successfully
achieved, within the scope of this invention, of providing a
method by which it is possible to induce in fish lasting
desirable and useful changes, which method is based on a
modification of physico-chemical interactions induced by the
effect of an electrostatic field.
As previously stated, this aim can be achieved most simply by
exposing juvenile fish or fertilised fish eggs to an
electrostatic field, such that the physico-chemical
interactions which take place during cell division and
differentiation, and which it is desired to modify with the
aid of the method of this invention, take place under the
influence of a defined electrostatic field under controlled
conditions.
Accordingly, the present invention relates to a method of
inducing desirable and useful properties in fish, which
comprises a) exposing early development stages of fish to an
electrostatic field, such that the physico-chemical reactions
which it is desired to modify take place under the influence
of a defined electrostatic field under controlled conditions,
but without thereby changing the chemical identity of the
system itself, and
b) keeping said early development stages of fish in said
electrostatic field for a period of time necessary for a
stable development of the desired modification.
Throughout this specification, the expression "early
development stages of fish" shall be understood as meaning all
stages starting from the egg (egg cell), preferably the
fertilised egg, through the different embryonic stages right
up to the hatchable or hatched juvenile fish. These are the
stages of frequent cell division and differentiation in which
the electrostatic fields produce favourable and lasting
results.
Especially preferred in this connection are fish eggs which
are actually fertilised in the static field or which are
exposed to the influence of an electrostatic field only after
fertilisation -- most preferably directly after.
A favourable, and therefore within the scope of this invention
preferred, period of time during which these early development
stages remain in the electrostatic field, is the time until
the eggs ripen, especially until they hatch. This period of
time will normally depend on external conditions, for example
water temperature, the oxygen concentration and the like, but
most especially on the species of fish.
Afterwards, the juvenile fish are transferred to larger tanks,
as is usual in fish breeding, where they mature to a desired
growth stage.
The really surprising feature is that these juvenile fish
which have been pretreated in the described manner and
transferred to normal breeding tanks differ significantly from
untreated control groups.
Firstly, a substantially higher hatching rate of the treated
fish eggs is observed, with frequently an increase of 100 to
300% and even higher values being achieved. Secondly, these
juvenile fish make a far more agile and more vital impression
than the untreated comparison fish. Very significant is their
markedly higher survival rate which extends not only to their
first few days, but virtually to their entire life cycle. This
feature becomes all the more marked if all medication is
dispensed with. For it is then observed that, in the first few
days and weeks, the untreated control group (not exposed to an
electrostatic field) is at least twice as heavily reduced by
the non-artifically inhibited and naturally occurring
population of pathogens as the fish that have been exposed to
treatment with an electric field. In addition, the treated
fish, while receiving identical feeding, grow in weight and
size far faster and reach adulthood significantly earlier, and
hence can be transferred to natural waters or are available
for marketing as edible or ornamental fish. Further, no
deleterious changes in the progeny of these treated fish are
observed. On the contrary, a certain element of the vitality
seems to be transferable to the progeny.
All in all, the fish treated by the method of this invention
are substantially more vital than the untreated comparison
fish and reach adulthood earlier. For the fish breeder this
means a reduction in the consumption of medicaments and
antibacterial agents, even to the extent of dispensing with
such substances completely, a perceptibly more efficient
utilisation of the fish feed employed, and a shortened rearing
phase. These are advantages which no other expedient at
present known is able to afford.
The mechanism on which the method of this invention is based
is at present not known and will require elucidation in the
future.
On the whole, the application of the method of this invention
results surprisingly, for example, in a favourable change in
the development and growth efficiency, in the morphogenesis,
possibly in the gene expression patterns, in proneness to
stress, resistance to pathogens, and many other
characteristics.
A primary object of this invention is accordingly the
provision of a method of enhancing the efficiency of the
development and breeding of freshwater and saltwater fish.
Especially preferred is a method of enhancing the efficiency
of the development and growth of edible fish.
Also falling within the scope of this invention are the fish
themselves in which change has been induced by the application
of the method of this invention, which fish have an enhanced
development of growth efficiency, and the progeny thereof,
provided these latter still have a novel and characteristic
property of at least one of the parents in which change has
been induced by the method of this invention.
Within the scope of this invention, an enhanced development
and growth will be understood as meaning, for example, an
increase in the hatching rate and an enhancement of the growth
rate.
A further object of the present invention is the provision of
a method which modifies the specific stress reactions of fish
in desirable and useful manner, especially such that the
treated fish are more robust and reach adulthood faster.
Thus, for example, it is possible to reduce very substantially
the susceptibility of fish to diseases by the application of
the method of this invention, and so to breed the fish under
conditions which would normally be critical to their health
and which would not permit a normal and controlled
development.
Hence the present invention also relates to fish whose
specific reactions to specific stress parameters are modified
in a desirable and useful manner by the application of the
method of this invention, especially those fish which exhibit
increased resistance to pathogens.
More particularly, it is an object of the present invention to
provide a method of vitalising fish, which comprises
a) exposing fertilised fish eggs to an electrostatic field,
without flow of current, or fertilising eggs in said field,
b) adjusting the field strength to values in the range from 1
V/cm to 10@5 V/cm, and
c) maintaining the electrostatic field until the juvenile fish
hatch or mature.
The fertilisation step can, of course, also be carried out in
apparatus of this invention (aquarium with electrodes) with
the voltage already applied.
In the practice of this invention, the electrostatic field is
preferably produced between the electrically insulated plates
of a capacitor.
The field strength of the electrostatic field is determined by
the following equation:
E=U/d
where U is the potential difference between the capacitor
plates, and d is the distance between the plates.
The potential difference U is produced by a high-tension
generator. Any kind of high-tension generator may be used in
the method of this invention. Preferred high-tension
generators are those based on the transformer principle with
rectifier.
The preferred potential difference within the scope of this
invention is from 1.0 V (volt) to 10@5 (V) volt.
For the application of the method of this invention to fish
eggs, potential differences of 1 V to 20 000 V, preferably of
100 V to 10 000 V, are used. Most preferred is a potential
difference of 500 V to 3 000 V.
The distance between the plates of the capacitor depends on
the dimensions of the aquarium, and is, for example, from 0.01
mm to 1 mm, but is preferably from 1 cm to 10 cm.
In practice, the field strength of the electrostatic field at
the given distance between the plates of the capacitor is
regulated by the strength of the voltage produced by a
high-tension generator.
In the practice of this invention, the field strengths are
preferably from 1 V/cm to 10 000 V/cm, more preferably from 50
V/cm to 5 000 V/cm but, most preferably, from 500 V/cm to 1
000 V/cm.
For the application of the method of this invention, it is
most preferred to use biological material which has a high
rate of division and/or still exhibits little differentiation,
for example cells capable of division. Specifically, suitable
biological material in the context of this invention comprises
fertilised of unfertilised eggs as well as early embryonic
stages right up to hatchable juvenile fish.
The rate of fertilisation and hatching of fish eggs can be
significantly enhanced under the influence of an electrostatic
field.
All these foregoing particulars cited by way of
exemplification are solely intended to illustrate the
invention and in no way restrict the subject matter thereof.
Most particularly, it is an object of the present invention to
provide a method wherein the development of the fertilised
eggs to juvenile fish takes place in an electrostatic field in
which the field strengths may vary preferably from 10 V/cm to
3 000 V/cm. Field strengths of 500 V/cm to 1500 V/cm, more
particularly of 500 V/cm to 1 000 V/cm, are especially
preferred.
First and foremost, the invention provides a method of
enhancing the growth and development efficiency of fish, which
method comprises enhancing the fertilisation, hatching and
survival rate as well as the growth of fish by
a) treating fish eggs with male sperm,
b) placing the treated eggs in incubators in which an
electrostatic field is produced,
c) providing field strengths for the electrostatic field of 10
V/cm to 3 000 V/cm,
d) removing the juvenile fish, after hatching, from the sphere
of influence of the electrostatic field, and
e) rearing said juvenile fish by methods which are known per
se.
The treatment of the fish in the electrostatic field in the
practice of this invention is preferably effected in special
incubators which, in the bottom and in the cover, contain
built-in electrodes which are water-tight and insulated and
are connected to a source for producing a high direct-current
voltage, and with the aid of which an electrostatic field can
be produced inside the incubators. It is, of course, possible
to use any other experimental apparatus for treating the fish,
provided it meets the basic conditions as set forth above.
After the juvenile fish have hatched, the electric field is
removed and the further rearing of the juvenile fish is
continued by conventional methods free from the influence of
an electric field.
Contrary to all theory, and hence extremely surprisingly, it
has been found that, compared with the controls, the juvenile
fish which have hatched in the electric field have, in
addition to a substantially enhanced fertilisation and
hatching rate, further advantageous properties which then also
develop after removal of the electric field and influence the
further development of the fish.
These further advantageous properties comprise, for example,
an enhanced rate of growth compared with the controls.
Furthermore, the treated fish, compared with the controls,
have a markedly enhanced vitality.
The present invention further relates to the use of the method
of this invention for modifying specific stress reactions of
fish.
Particularly preferred fields of use relate to the enhancement
of resistance to stress, for example to specific environmental
factors such as increased salt concentrations in the culture
medium, limitation of specific nutrients, limitation of light
and/or oxygen, acceptance of pollution and the like.
One of the most frequent stress factors in the living
environment is deficiency stress, where one or more factors
can simultaneously have a limiting effect.
Deficiency stress occurs as soon as one or more of the factors
essential for optimum growth or development, for example
light, supply of oxygen/carbon dioxide, supply of nutrients,
vitamins and the like, attain suboptimum values. The
consequence is that the affected organism is no longer able to
maintain to the full its ability to generate the syntheses
essential for optimum development and growth, resulting
initially in a retardation of growth. If this deficiency
stress continues for a prolonged period of time, it results in
an impairment of essential functions, leading then as a rule
to early onset of senescence and hence ultimately to the death
of the affected organism.
Not only a deficiency, but also a superfluity, of specific
crucial factors is able to trigger stress reactions. Increased
salt concentrations in the nutrient medium leads, for example,
to a rise in the osmotic value in the medium and,
consequently, to a loss of fluid in the cells present therein,
owing to the onset of osmosis and hence to cell shrinkage. The
loss of fluid can usually be compensated for to a certain
extent by self-regulatory steps taken by the affected
organisms. But if a critical threshold is exceeded, then this
will result in the death of the cells.
The method of this invention can, in principle, be applied to
all species of fish, but preferably to species that are bred
on a commercial scale. In this connection, the treatment of
edible fish is of particular importance, as it is expected
that production costs can be reduced very considerably with
the aid of the method of this invention.
To illustrate the somewhat general nature of the foregoing
description and to contribute to a better understanding of the
invention, reference will now be made to specific working
Examples which are non-limitative in character, unless special
attention is drawn to them. The same applies to all
particulars of an exemplary nature which are contained in the
foregoing description.
NON-LIMITATIVE WORKING
EXAMPLES
PRODUCING THE ELECTROSTATIC
FIELD -- EXPERIMENTAL APPARATUS
All experiments hereinafter described are carried out in
electrostatic fields which are produced between the plates of
a capacitor.
The electric field strength is given by the equation
E=U/d
where
U is the potential difference (voltage) between the capacitor
plates, and
d is the distance between the capacitor plates.
The voltage is generated by means of a high-tension generator
which operates on the principle of a transformer with
rectifier, normally using voltage differences from 500 volt to
12 000 volt.
The distance between the plates will depend on the dimensions
of the test tanks used in the individual experiments. Normally
the variable parameters U and d will be chosen such that the
field strengths of the electrostatic field are from 250 V/cm
to 1500 V/cm.
The present invention also relates to an apparatus for the
treatment of early development stages of fish with electric
fields, said apparatus comprising
a) a tank suitable for holding the early development stages of
fish in aqueous medium, and
b) a source for producing a voltage and, connected therewith,
an arrangement of electrodes suitable for producing an
electrostatic field in at least a part of the volume
surrounded by the tank, which process is characterized in that
the arrangement of electrodes is electrically insulated
against the medium contained in the tank and is preferably
arranged in form of capacitor plates, and that the source of
voltage is a source of a direct-current voltage.
Example 1: Effect of an
Electrostatic Field on the Development of Fish
It is possible to influence favourably the development of
animal organisms with the aid of an electrostatic field, as
will be demonstrated in the following experiment carried out
with rainbow trout.
1.1 Experimental Apparatus
(FIG. 1)
BRIEF DESCRIPTION OF THE
DRAWING
FIG. 1 is a diagram of a preferred form of the invention,
being an incubator with a source for an electrostatic field.
Trout eggs (1) in batches of 1000 are treated in tanks with
male sperm and immediately placed in incubators. The
incubators consist of 1 liter plexiglass tanks (2) measuring
31.5.times.28.5.times.4.5 cm. Aluminium electrodes (3) which
are sealed air- and water-tight are built into the cover and
bottom of the containers (see FIG. 1).
The incubators are connected to a spring water (4) system of
10 DEG-12 DEG C. and the electrodes are connected to a
high-tension generator (5) (FUG HCN 14-12500, available from
Weter, Schaffhausen, Switzerland). The voltage applied is 215
volt and the space between the plates is 3 cm, so as to
provide a field strength of 716 V/cm between the electrodes.
The fertilisation and ripening of the eggs takes place in this
apparatus. The eye stage is reached after ca. 4 weeks, and the
brood hatches after ca. 8 weeks.
After hatching, the brood is transferred to tanks measuring
50.times.50.times.15 cm with laminar flow and the electric
field is removed, so that the further development of the
juvenile fish may take place free from the influence of the
field.
1.2 Results
Table 4 shows that the number of juvenile fish which have
hatched under the influence of the electrostatic field is
markedly greater than that of the controls.
Compared with the controls, the number of fish which perished
after hatching and after 5 weeks was reduced by about half
with aid of the field.
In addition, a growth increase effect of the field can also be
detected. The size of the juvenile fish hatched under the
influence of the electrostatic field, 10 weeks after hatching,
is from 30 to 40% higher than that of the control fish (q.v.
Table 1).
______________________________________
with field
free from field
tank 1 tank 2
______________________________________
hatched juvenile fish
140 244 469
perished after hatching
37 14 19
perished after 5 weeks
10 5 6
size after 10 weeks
2.6 cm 3.4 cm 3.6 cm
______________________________________
The fish incubated in the field exhibit a markedly greater
vitality.
Transparent sheet
Inventor: EBNER GUIDO DR [CH] // HEFTI HEINZ DR [CH]
Applicant: CIBA GEIGY AG [CH]
EC: A01G9/14E // C08K5/00P4
IPC: A01G9/14 // C08K5/00 // C09K11/02
The invention relates to transparent sheets containing a
fluorescent substance, characterised in that the fluorescent
substance absorbs light of the wavelength 300 to 400 nm and
fluoresces a wavelength range from 430 to 470 nm and in that
the sheet contains the fluorescent substance in such an amount
that, in daylight, the transmission in the wavelength range
from 430 to 470 nm is amplified by more than 10%, and to a
process for improving the photosynthesis rate of
chlorophyll-containing cells and plants, to processes for
preparing the sheet of the invention, and to an arrangement
for improving the photosensitive rate.
Description
The invention relates to transparent film containing a
fluorescent substance with a fluorescence maximum of about 450
nm, their use for increasing the rate of photosynthesis and
for influencing plant growth as well as methods for their
preparation.
There are already partially transparent films become known
containing dyes or fluorescent dyes for influencing plant
growth.
The Swiss patent CH 515 957 relates to transparent foils or
sheets, which in addition to the usual auxiliaries, a dye up
with a minimum permeability in the range of 380 590 nm and a
maximum permeability of 660 to 750 nm.
Similarly, it is suggested in the Austrian Patent AT-270 288,
to improve plant growth through the field of red light
(600-700 nm) fluorescent dyes that are applied to suitable
carriers.
This is followed by the on off of EP-A-00 77 496 known method
in which light of wavelength 470 to 600 nm is absorbed by
means of fluorescent dyes and emits in the range of 600-700
nm.
These, from the prior art devices and methods, is based on the
principle of action to stimulate the rate of photosynthesis
chlorophyll plants by an extra supply of light of wavelength
600-700 nm.
In contrast, the invention proposes to stimulate the rate of
photosynthesis plant chlorophyll by light starting from
fluorescent substances having an absorption in the range of
300-400 nm (near UV) and an emission in the range of 430 to
470 nm.
As carrier material for the fluorescent substances, a
transparent film is proposed.
The invention thus relates to transparent film containing a
fluorescent substance, characterized in that the fluorescent
material absorbs light of wavelength of 300 to 400 nm and a
wavelength range fluorescing from 430 to 470 nm and that the
film the fluorescent substance in an amount such nm that is
enhanced with natural light transmittance in the wavelength
range of 430 to 470 to more than 10%.
Fluorescent substances of the aforementioned type are known
per se (described, for
, In "Fluorescent Whitening Agents", A. Müller, eds.
, Georg Thieme Verlag, Stuttgart, 1975) and used in numerous
industrial areas for improving the color properties using.
According to the invention, those fluorescent substances are
used, in the near UV range (300 to 400 nm) absorption and thus
received excitation energy in the range of 430 to 470 nm,
preferably 430 to 450 or 450-470, especially 440-460,
especially in the range 445-460 nm emit.
By applying the fluorescent substance on a transparent film,
the transmission of daylight in the aforementioned areas by at
least 10%, depending on the optical quality of the film, the
amount of fluorescent material and its quantum yield, the
relation and the light amount of UV light of wavelength
300-400 nm and the light quantity of the incident light onto
the film in the aforementioned intervals within 430 to 470 nm,
a gain by fluorescence of more than 20, 50 or even 100% is
achieved.
As a reinforcement of the transmission through the
fluorescence is understood with simultaneous irradiation with
UV light in the range of 300 to 400 nm measured increase in
the amount of light in each specified area on the fluorescence
of the light source side facing away from the film.
Daylight source is the overcast sky or the radiation matched
the overcast sky artificial light source.
Routinely, the spectral composition of daylight in the
measuring apparatus by means of a standardized simulated
daylight source D65 (A. Brocker in "Fluorescent Whitening
Agents", Thieme 1975, p 23).
Transparent films are films with a light transmission of over
70%, preferably over 90% in the range of 400 to 700 nm
In an especially advantageous manner are suitable transparent
film with a light transmission maximum in the range of 400-500
nm and 600-700 nm
According to the invention can in principle each slide using
the aforementioned criteria to find the light transmittances
met.
In particular, films made from the following classes of
polymers are suitable: polyester, polyvinyl chloride,
polyolefins such as polyethylene, polypropylene, polyamides,
polystyrene, polyacrylates, regenerated cellulose, such as
cellophane ™ or polyacetates.
As fluorescent substances are in principle all substances
which absorb at 300-400 nm and whose emission maximum in the
range of 430-470 nm, suitable.
In addition, preferred are those substances which are in the
respective selected polymer material molecularly dispersible.
Particularly suitable are fluorescent substances of the
following classes of compounds:
2,5-bis-benzoxazol-2-yl-thiophene,
4,4-bis-benzoxazole-2-yl-stilbene,
4-phenyl-4'-benzoxazol-2-yl-stilbene,
4,4-distyryl biphenyls,
1,4-bis-benzoxazol-2-yl-naphthalenes,
1,2-bis-benzoxazol-2-yl-ethenes,
4,4-bis (diphenyl-1 ,3,5-triazinyl)-stilbene,
4,4-bis (5-phenyl-1 ,3,4-oxazol-2-yl)-stilbene,
3,7-Disubstituted coumarins or
substituted naphthalenes.
The following compounds are proposed:
# 1: 4,4-bis-benzoxazol-2-yl-stilbene of formula
EMI12.1
# 2: 2,5-bis-benzoxazol-2-yl-thiophene of the formula
EMI12.2
# 3: 2,5-bis-(5-tert-butyl-benzoxazol-2-yl)-thiophene of the
formula
EMI12.3
# 4: 4,4-di-(2-methoxy-beta-styryl)-biphenyl of the formula
EMI12.4
No. 5: 4,4 '-disubstituted biphenyls of the formula
EMI12.5
# 6: 1,4-bis-benzoxazol-2-yl-naphthalene of formula
EMI13.1
# 7: 1,4-bis-(5-methoxycarbonyl-benzoxazol-2-yl)-stilbene of
formula
EMI13.2
No. 8: 4,4-bis-[5 - (4-tert-butyl) phenyl-1
,3,4-oxadiazol-2-yl]-stilbene of formula
EMI13.3
No. 9: 4,4-bis-[4,6 - (p-tolyl) -1,3,5-triazin-2-yl]-stilbene
of formula
EMI13.4
# 10: min 4-phenyl-4 - (5-tert-butyl) benzoxazol-2-yl-stilbene
of formula
EMI14.1
# 11: 1,2-bis-(5-methylbenzoxazole-2-yl)-ethene of the formula
EMI14.2
No. 12: 7 - (benzo [c] benzotriazol-2-yl)-3-phenylcoumarin of
the formula
EMI14.3
No. 13: 1 - [4 - (2-cyanoethenyl)-phenyl] -2 -
(naphthalen-1-yl)-ethene of the formula
EMI14.4
# 14: 4 - (O-methoxyiminomethyl) -4 min-cyanoethenyl-stilbene
of formula
EMI14.5
According to the invention usable fluorescent substances may
be applied by known methods to the serving as a carrier
transparent film.
Must be ensured in the selection of appropriate procedures,
that the fluorescent material primarily on the transparent
substrate in a molecular dispersed distribution (dissolved) is
present.
A particularly suitable method may be mentioned, for small and
medium-sized batches: the transfer printing, dipping and
coating processes for medium and large batches: the
incorporation of the fluorescent substance in the polymer as
well as diving and painting activities.
When transferring pressure from the fluorescent material is a
first - given support material - usually made of cotton or
tissue paper existing one.
The printable transparent film is then brought into close
contact with the carrier material.
The excretion of the fluorescent substance in the film is
then, as usual, at transfer pressure, effected by heating
under contact.
Many polymers swell under the action of suitable solvents and
can take up dissolved in the solvent substances that remain
then distributed by removing the solvent in the polymer
molecularly.
By means of this effect can be the fluorescent materials by
dip-coating process and solvent baths with solvents or with
molecularly incorporated into the film transparende.
In a particularly advantageous manner, the fluorescent
substance to be incorporated before the film production and as
an additive in the polymer material.
In this case, both the fluorescent agent may be incorporated
by melting or mixing in the production of film serving
granules or it is added during film extrusion in a
conventional manner as other additives and thus dissolved in
the melt of the polymer.
Also, the fluorescent substances are added at the stage of
polymerization or polycondensation.
Depending on the polymeric support material in which they are
contained, the emission maxima of the fluorescent substances
vary within certain limits.
Are particularly suitable for polyester compounds 1, 2, 6, 7
and 9 to 14
Polyamides are particularly suitable for compounds 8 and 10
The compounds 3, 4 and 6 are preferably polyvinyl chloride or
polyolefins.
Compound 5 is particularly suitable for regenerated cellulose.
The transparent sheets can contain not only the registration
according to still another fluorescent materials commonly used
in film production assistants and additives such as
plasticizers, stabilizers, supporting tissue, hardeners, etc.
to a limited extent, UV-absorbers.
The concentration of fluorescent substances in the film is
determined by the respective desired reinforcing effect and
can be determined by simple preliminary tests.
In general, the fluorescent agent is present in concentrations
of 0.01 to 1% distributed in molecularly disperse before
serving as carrier material film.
The principle underlying the invention can be used as a light
amplification in the range of 430 nm understood to 470.
In this range the short-wavelength absorption maximum of
chlorophyll.
Accordingly, the inventive films can be found to stimulate the
rate of photosynthesis chlorophyll cell systems used.
In addition to land-based plants can especially in aqueous
medium living cell systems, such as algae, are advantageously
affected by the application according to transparent film in
its growth.
The inventive films are particularly suitable for use in
agriculture, horticulture or fruit.
The application according to the foils are attached in a known
manner between the plants and the light source, usually
daylight so that the largest part of the incident on the plant
light passes through the film and into the type described
above by means of fluorescence in the 430 470 nm is amplified.
In practical application, the films can therefore over the
seed-containing soil or on the plant or placed by means of
suitable constructions in a conventional manner used as plant
tunnel or greenhouse covers are.
The inventive films are particularly suitable for the limited
light availability, especially on cloudy days to improve by
fluorescence light: depending on the particular plant variety,
a certain amount of light are assumed to be the lowest
threshold, below which the rate of photosynthesis of the plant
or the chlorophyll-containing cell is no longer sufficient to
the plant or the cell alive.
Due to an orienting test (Example 2b), this value in the range
of about 1000 mu W cm <-2> for watercress are accepted
as a test plant.
Measurements of the intensity of daylight under overcast skies
(Example 2c) show that under the conditions occurring in
temperate latitudes often a covered sky the limit is already
reached.
By fluorescence light can offer for the plant usable in the
range of 430-470 nm can be increased to such a degree that the
light intensity does not drop below the critical level for
plant growth.
Example 1
Film: Melinex polyester film type 0, manufacturer ICI, film
thickness 75 microns
Fluorescent substance - 2,5-bis-benzoxazol-2-yl-thioben of the
formula
EMI17.1
- 1 - [4 - (2-cyanoethenyl)-phenyl] -2 -
(naphthalen-1-yl)-ethene of the formula
EMI18.1
- 4 - (O-methoxyiminomethyl) -4 min-cyanoethenyl-stilbene of
formula
EMI18.2
Photometer:
Kerry 219 - Photometer Lamps:
Halogen-tungsten lamp, 150 watt, Xenophot, Osram, HLX 64 640
The fluorescent substance is applied to the HT process on the
film.
For use, the polyester film is colored with a content of 0.1%
of the aforementioned compound.
The liquor ratio is 1: 50, being used as the dispersant 1 g /
l P Irgasol.
The dyebath is heated in a pressure vessel within 30 min from
40 to 130 ° C and maintained for 30 min at 130 ° C.
After obtaining the film is rinsed with acetone.
The transmission values ??at 430, 440, 450, 460 and 470 nm are
shown in Table I:
Table I
EMI19.1
Example 2 influencing plant growth by fluorescent light
Example 2a: Normalization of daylight lamp
As a daily source of light a 100-W light bulb-type plants
Ormalight is used.
Which is in the range 25 to 150 cm measured light energy in
Table II:
Distance [cm] Light energy [mu watts. cm <-2>]
(uncorrected)
25 4600 50 1500 75 870 100 530 125 420 150 240
Example 2b: Determination of the limiting light offer
In a darkened chamber in pots sown seeds of watercress
illuminated with a daylight lamp in accordance with Example 2
in 25, 50, 75, 100, 125 and 150 cm from the top.
After 4 weeks the condition of the plants is evaluated.
The illuminated from 25 to 50 cm from plants develop normally,
while the dead are from 75, 100, 125 and 150 cm illuminated
plants.
Example 2c: Determination of the amount of daylight in heavily
overcast sky
On 4
June 1984 at 9.00 shall be measured with a UDT Radiometer 140
X in Basel / Switzerland, the amount of light, such as: total
light (300-700 nm): 1200 mu W cm <-2> UV portion
(300-400 nm): 120 mu W cm <-2> proportion of visible
(400-700 nm): about 1080 mu W cm <-2>
Example 2d: Plant growth with insufficient daylight and
additional fluorescent light
Daylight source: lamp according to Example 2a UV light source:
UV lamps from Camag (Catalog No. 29 230) with an emission
maximum at 366 nm
UV filter: To ensure that no visible light is guided by the UV
sources of the experimental arrangement, the outlet openings
with UV filters type UV-11 (transmission range 250-400 nm) and
the Schott Schleifer covered.
Investigated films: film A Melinex polyester film type = 0,
manufacturer ICI, film thickness 75 mu.
Film B = film according to Example 1, containing 0.1% of
compound 2 foil C = film according to Example 1, containing
0.1% of compound 12 film D = Film according to Example 1,
containing 0.1% of compound 13
The seeds sown in pots of watercress in a dark room between
two sides established UV light sources, which are coated with
transparent fluorescent films prepared, and their growth with
a blank sample (film A) were compared.
The entire experimental arrangement is from the top of the
distance 75 cm irradiated with a daylight lamp in Example 2a.
The growth of test plants will be evaluated weekly.
The irradiated through the films B, C and D watercress
developing normally, with a strong preference for the lateral
growth direction to the UV light sources is observed for.
Apart from the plants develop up to the 9th
Week in which the experiment was terminated normally.
The irradiated film A by water cress sprouts initially grow
normally and straight up.
In the second week, shows a strong "fear growth."
In the third week the plants begin to wither and die off in
the fourth week.
US6238663
Method for treating
hyperkeratotic disease with a Halobacterium halobium
lysate
Inventor:EBNER GUIDO [CH]
Applicant: INST OF PHARMACEUTICAL RES AG [US]
EC: A01G7/04 // C12N13/00
IPC: A01G7/04 // A01K67/00 // A61K31/07