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Bioluminescence in Focus - A Collection of Illuminating Essays, 2009: 357-385

ISBN: 978-81-308-0357-9 Editor: Victor Benno Meyer-Rochow

19 Biophotons: A clue to unravel

the mystery of “life”?
R. P. Bajpai
Sophisticated Analytical Instruments Facility, North Eastern Hill University
Shillong 793022, India

Abstract
This chapter summarises the evidence of ultraweak
emissions of so-called biophotons in connection with
living tissues irrespective of plant or animal origin
and shows that biophoton signalling between living
organisms can occur. Details are provided on how
to measure and analyse biophoton emissions. The
nature as well as salient features of the photon
emissions are being discussed. Applications of
ultraweak photon emissions are possible in the
medical field and it is concluded that ultra-weak
emissions of biophotons are representing one of the
chief characteristics of “life”. However, to what extent
Correspondence/Reprint request: Dr. R.P. Bajpai, Sophisticated Analytical Instruments Facility, North Eastern
Hill University, Shillong 793022, India. E-mail: [email protected]
358 R. P. Bajpai

such signals can be controlled by an emitter and what machinery exists in the
receiver to detect them, for the moment, remain unanswered questions. The
essay ends with some speculation on the possibility of biophotons affecting
the thinking, moods, and behaviours of human beings, linking philosophical
visions of life with the physical world.

1. Historical perspective
Alexander Gurwitsch[1] was the first to try to understand the cause of
coordinated nature of cell division in a developing organism and wondered if
coordination is achieved by some form of radiation issuing from the
developing organism[2]. He called this form of radiation mitogenic or cell
division inducing and thought that the radiation should reveal itself by
speeding up the rate of increase of cell division in a growing sample placed
near a developing organism. Gurwitsch soon discovered a sensor of
mitogenic radiation in the form of growing onion root tip where cells divide
with higher frequency[3]. The tip of one root, the emitting source, was
directed perpendicularly to a point close to the tip of second root, the
detector. The rate of cell division was assessed under a microscope and was
found to be perceptibly greater in the exposed region than on the side far
away from the source. The effect vanished on insertion of a glass plate
between the two roots but not on insertion of a quartz plate. Since glass
absorbs ultra violet (UV) radiation while quartz is transparent to it, he
suggested that mitogenic radiation probably contained UV radiation only.
Gurwitsch found another detector – a growing yeast culture, which increased
in turbidity as cells multiplied. The turbidity was measured by counting the
number of cells in a block of yeast culture embedded in agar gel. UV
radiation of weak intensity is also detected by the onset of growth in a
bacterial culture. Gurwitsch determined the spectrum of mitogenic radiation
with a quartz spectrometer and found links of different UV components with
specific biological reactions. Gurwitsch also sought and found secondary
mitogenic radiation, whose emission was stimulated by irradiation of a tissue
with the primary emanation. These were remarkable results that failed to
reproduce many times, perhaps because of the capricious nature of biological
specimens and detectors. Hollaender and Claus[4] refuted the results and the
refutation caused mitogenic radiation to become an undergrowth of science
[2]
. The interest in the subject continued to decline until the accidental
discovery of weak emission of light from germinating plants by Colli and
Fachini[5] using a photomultiplier tube. The intensity of emitted light was
more than that in black body radiation but less than the intensity expected in
forbidden transitions. The emission was therefore, called ultra weak photon
emission. A photo multiplier tube is a non- biological detector, it is more
Biophotons: A clue to unravel the mystery of “life”? 359

reliable and it gives reproducible results. Photomultiplier tubes made up of

different materials are sensitive to electromagnetic radiation in different
regions. There exist tubes capable of detecting UV or visible radiation of
nearly similar intensities. This is in contrast to the biological detectors
discovered by Gurwitsch, which were probably more sensitive to UV
radiation than photomultiplier tubes but were too insensitive to visible
radiation to detect the emission of light from living systems. Photomultiplier
detectors made the detection of weak emission of light by biological samples
a routine affair and rekindled the interest in the mitogenic radiation. Light
emission was detected many times in many varieties of plants and in diverse
species like yeast, helianthus, frog spawn, earthworms, wheat seedlings, and
garlic (Allium cepa). Quickenden in Australia[6], Popp in Germany[7] and
Inaba in Japan[8] fabricated highly sensitive dedicated photon counting
systems with extremely low noise. The measurements with the dedicated
systems established beyond doubt the phenomenon of ultra weak photon
emission in almost all living systems from bacteria to human beings.
Ultra weak emission has intriguing features. The main intriguing features
discovered in above measurements were universality, incessant emission,
ultra weak intensity, unchanging average intensity and broadband spectrum
mainly in the visible region. Universality, incessant emission and ultra weak
intensity imply that the processes responsible for photon emission occur in
every living system all the time but are either rare or involve macroscopic
structures. The rare processes may originate from some imperfections in
metabolic activities while the existence of macroscopic structures
participating in metabolic activities is a new assumption. The two
possibilities gave rise to imperfection and coherence theories of ultra weak
photon emission respectively. The imperfection theory had many
protagonists, the notable among them were Inaba[9], Quickenden[10] and
Slawinski[11]. The lone notable protagonist of the coherence theory was
Popp[12] but he never clearly specified the connection between coherence
and macroscopic structure. The unchanging intensity of the signal is
attributed to ambient amount of imperfection in imperfection theory and to
long and almost non-decaying tail of hyperbolic decay in coherence theory.
The emission in the visible range requires a mechanism to upgrade the
radiation in infra red region obtainable from biochemical energy derived from
(ATP→ ADP) and its variant reactions. The imperfection theory assigns the
job of up gradation to radicals that initiate chain reactions based on reactive
oxygen species. The coherence theory assigns it to a macroscopic structure
whose parts coordinate biochemical energy reactions occurring at different
space time locations. No specific scheme for the coordination has been
formulated so far. It is pointed out that the coherence theory does not
360 R. P. Bajpai

preclude up gradation of energy with the help of radical reactions. The

coordination needed in the successful implementation of any scheme may
arise from the dynamical behaviour of macroscopic structure. It is obvious
that above noted intriguing features cannot choose between imperfection and
coherence theories. Popp therefore, investigated the behaviour of fluctuations
in these signals by measuring photo cont distribution, the set of probabilities
of detecting different numbers of photons in a small measuring interval called
bin. Photo count distribution is expected to be normal in the imperfection
theory but not in the coherence theory. Popp observed mostly Poisson and a
few sub and super Poisson distributions. Popp considered these distributions
only indicative of quantum nature because background noise was comparable
to signals.
The convincing support to coherency theory came from the study of what
Gurwitsch called secondary emanations. Strehler and Arnold[13] were the
first to observe secondary emanations using a non-biological detector as
afterglow in photosynthetic tissues of green plants after light illumination.
The afterglow is observable for a long time and the phenomenon is called
delayed luminescence. Delayed luminescence is not restricted to
photosynthetic tissues but is a universal phenomenon of living systems
though the strength of emitted signal is higher in photo synthetic systems.
The phenomenon has also been observed in a few complex non-living
systems[14]. The distinguishing feature of a delayed luminescence signal is
the peculiar shape with two regions, decaying and non-decaying. The photon
flux in the decaying region decreases by 2 to 3 orders of magnitude in a short
time. The decaying region is followed by a long tail region in which the
photon flux is fluctuating but remains almost constant on an average. The
decaying region is easy to measure due to higher flux and further the
background noise is negligible in this region[15]. This region has been
measured in numerous systems by a large number of investigators. A
decaying region of a photon signal is usually analysed to determine the decay
constant and strength of its different exponentially decaying components. The
analysis fails and yields inconsistent and unsatisfactory values of decay
constants and strengths in delayed luminescence signals. A delayed
luminescence signal is not separable into different component decays. The
signal has a definite but peculiar shape that lacks exponential decay character.
Any definite shape other than the exponential decay means that numbers of
photons emitted at different time intervals are correlated. Some additional
mechanism must operate in living system to ensure correlation in photon
number during decay- a macroscopic time interval. The peculiar and definite
shape rules out imperfection theory. The delayed luminescence signal of a
living system is sensitive to many physiological and environmental factors
Biophotons: A clue to unravel the mystery of “life”? 361

and can pick up minute changes in these factors. The sensitivity of the signal
requires a linkage between metabolic activities and the additional
mechanism. The sensitivity suggests many potential applications of the
phenomenon of delayed luminescence. These applications have not been
actualised because of our inability to extract relevant parameters of a signal
lacking exponential decay character. We need a framework to describe the
shape of such a signal. Popp proposed a phenomenological model, in which
shape arises from dynamical evolution of photon field associated with a
living system. The classical solution of the dynamics predicts hyperbolic
shape of the photon signal. The model reproduces broad features of delayed
luminescence phenomenon and assigns the asymptotic region of hyperbolic
shape to ultra weak photon emission. The model integrates delayed
luminescence and ultra weak photon emission. The integration is formally
expressed by using a common word biophoton emission for the two photon
emissions. The two photon emissions are identified by the adjectives light
induced and spontaneous. Delay luminescence signal is light induced
biophoton signal and ultra weak photon signal is spontaneous biophoton
signal. The name “biophoton” emphasizes peculiar features and biological
relevance of signals. The model made a paradigm shift of far reaching
consequences. It was strongly resisted and its acceptance has been requiring
more and more evidence. Popp has responded by measuring the delayed
luminescence signal of many systems. He fine tuned the model to fit the
measured data. The model correctly reproduces the initial decaying portion of
a delayed luminescence signal and extracts four parameters from it. The
sensitivity of parameters, particularly the one related to the strength of signal,
has been put to use in actual applications with reasonable success. The
success, however, has not given widespread acceptance to the model because
of the ad hoc fine tuning.
The dynamical model proposed by Popp is solvable in quantum field
theory. The solution of the photon field is a squeezed state with its specifying
parameters[16] time dependent. The shape of the signal[17] has a simple
expression containing four unknown parameters. The unknown parameters
take real positive values depending on the initial conditions and emitting
system. Different values of parameters give rise to different shapes. The
model correctly reproduces the shapes of biophoton signals without any fine
tuning. The model maps the shape of biophoton signal in its parameter space.
Quite often, one combination of parameter plays the dominant role in the
mapping. This combination of parameters not only measures the shape of a
signal but provides an ordering of shapes. The success in explaining the
shape demands investigation to justify the basic assumption of the model.
The basic assumption is that a decaying biophoton signal is in a pure
362 R. P. Bajpai

quantum state. The validity of the assumption was demonstrated by

measuring the probability of no subsequent photon detection of biophoton
signal in a small interval[18]. The probability for various intervals in the
range (10 µs -100 µs) was measured at different portions of the delayed
luminescence signal emitted by a leaf. The measurements demonstrated the
quantum nature of the signal. The tail region of the signal that corresponds to
spontaneous biophoton emission was also included in the measurements. This
region permits the measurement of the probabilities of detecting different
number of photons in a measuring interval, called bin size. The measured
probabilities give valuable information about the quantum state of the signal.
The expressions of various probabilities in the squeezed state with time
dependent parameters are too complicated to calculate. We therefore,
approximate the exact squeezed state solution in the region of spontaneous
emission by an effective squeezed state specified by time independent
parameters. The approximation simplifies the calculations and permits the
estimation of the time independent parameters of squeezed state from the
photo count distribution at any bin size. The photo count distributions in a
signal measured at 14 bin sizes in the range (50ms-500ms) yielded same
estimates of squeezed state parameters[19]. The result justifies the
approximation and provides an irrefutable proof of biophoton signal in a pure
quantum state. The pure quantum state of biophoton signal implies the
existence of a quantum structure in the living system emitting the signal
because a pure quantum signal can emanate only from a quantum structure.
Further, the parameters extracted from of a biophoton signal- four from the
decaying region and four from the spontaneous emission region- are
attributes of the living system and its quantum structure. These are holistic
attributes that open up new dimensions of living systems to study and
investigate.

2. Frameworks of Analysis
A biophoton signal is experimentally determined by counting the number
of photons detected in contiguous bins of size∆. Let the number of detected
photons in a bin around the time t be n (t). The set {n (t)} of measurements at
times separated by ∆ is the digitised signal, whose shape gives the
dependence of n (t) on t. A theoretical model prescribes the functional
dependence of n (t) on t in terms of a few unknown signal specific parameters
and provides a framework to analyse digitised signals. The analysis consists
of estimating the parameters of a digitised signal. The estimation of
parameters is easier in the region in which n(t) varies with time e.g. the decay
region of a biophoton signal. The decay region is used for determining decay
Biophotons: A clue to unravel the mystery of “life”? 363

parameters of signals. The region in which n(t) does not vary with time can
estimate only one combination of parameters. However, if n(t) fluctuates in
this region and its fluctuations have definite structure, then the fluctuations
provide some additional information about the signal. The statistical
moments characterize the structure inherent in fluctuations and variance, the
second moment, is the most revealing moment. A quantity Q equal to
(variance/mean -1) was earlier used for indicating the presence of structure in
fluctuations[20] and ascertaining its nature. The set of probabilities of
detecting different number of photons in a bin, called photo count
distribution, can also characterize the structure inherent in fluctuations. This
characterization is more helpful in extracting information from a quantum
signal, in which various probabilities of detecting photons are theoretically
calculable. Photo count distributions can be measured for many bin sizes and
all distributions should yield the same estimates of the parameters of the
signal because bin size is a kinematical quantity and should not affect the
estimates of the parameters of a signal. Bin size should not affect the
estimates of parameters in decaying region as well. Robustness of estimation
to change in bin size is the test of the validity of model and the correctness of
the framework of description. Three frameworks have been used in the
analysis of biophoton signals. The important features of description in these
frameworks are given.

2.1. The conventional framework

A photon signal from an isolated system arises from the probabilistic
decay of many independent units in some excited state. The depletion of the
number of units in excited state with time confers shape to the signal. Shape
is a statistical feature, whose character has to exponential and decaying. A
living system may have more than one type of decaying units. The shape of
biophoton signal originating from exponential decay of m types of units is
given by

(1)

, where C0 is the strength of background contribution and Ci the strength of ith

decay mode with decay constant λi . A mode corresponds to the decay of one
type of units and has a definite frequency given by the energy difference
between the two states of the units. The decay constant of a mode is related to
the lifetime and width of the decaying state. The lifetime determines the
duration of decaying region. The durations of light induced biophoton signals
suggests that the contributing modes have life times of the order of 1s, which
implies sharp decaying states and discrete emission spectra. Continuous
364 R. P. Bajpai

spectrum with broad structures requires large number of decays, whose

strengths if adjusted can mimic a signal with hyperbolic decay character. The
adjustment will break down if some components are filtered out. The remnant
signal obtained after filtering out some components will have to show
exponential decay character in this framework. The framework cannot
describe non-decaying spontaneous biophoton signals for a non-decaying
signal can arise only if decaying states of every mode are continuously
replenished. The photo count distribution in the framework is expected to be
normal or Bose Einstein.

2.2. The framework of Popp

Popp[21] suggested that the shape of a light induced biophoton signal is
the consequence of dynamical evolution of a photon field given by the
Hamiltonian

(2)

, where p and q are usual canonically conjugate momentum and position

variables of photon field of frequency ω and the constant λ determines the
strength of damping. It is the Hamiltonian of a damped harmonic oscillator
with time dependent mass and frequency terms. The solution of the classical
equation of motion is

(3)

, where q0 and θ are integrating constants. The integrating constants are

signal specific parameters. The solution has a stable frequency but its
amplitude hyperbolically damped. The energy of the oscillator is proportional
to the square of amplitude. The energy is equated to the number of photons
multiplied by Planck’s constant and frequency and it gives n(t)=N0/(1+λt)2 as
the shape of signal. The analytical expression does not quite reproduce the
shape of observed signals and hence the expression is arbitrarily modified to

(4)

, where N0,λ and m are signal specific parameters giving respectively the
strength, damping, and shape of the signal and A0 gives background
contribution and should by measuring system specific but is not. The new
expression correctly reproduces small initial portion of the decay region. The
value of m in signals of different living systems is in the range 1 ≤ m ≤2. The
Biophotons: A clue to unravel the mystery of “life”? 365

model has been many successful applications based mainly on the sensitivity of
N0, the strength of signal, to various factors. NB1, the number of counts
detected in the first bin, is also a measure of signal strength. It is directly
measurable and is equally effective in various applications. Popp suggested
photo count distribution to be Poisson and quantum state to be a coherent state.

2.3. The framework of Bajpai

It is a quantum field theory framework[23] that implements the proposal
of Popp. The framework describes an electromagnetic field interacting with
living system in the interaction picture. The description has two elements,
interacting photon field operator and state vector. The Hamiltonian of eq.(2)
determines the dynamical evolution. The dynamic evolution of interacting
photon field is equivalent to the evolution of a free quasi photon field. The
creation and annihilation operators of quasi photon field are unitarily related
to creation and annihilation operators of free photon field by time dependent
coefficients. The sate vector of the interacting field is and remains a coherent
state of quasi photon field or equivalently a squeezed state of free photon
field with time dependent specifying parameters. The time dependence of the
expectation value of number of photons in the state is given by the following
expression

(5)

, where t0=λ-1 and Bi’s are three algebraic expressions of the parameters
defining a squeezed state, mode frequency ω andλ. Bi’s are independent and
take positive values only. Eq.(5) is a description of biophoton signal with
four signal specific parameters. The description contains a decaying and a
non-decaying component. The decaying component is identified with delayed
luminescence and non-decaying component with spontaneous emission. The
estimate of B0 from a digitised signal is the sum of background noise and
contribution of spontaneous biophoton emission and is expected to be signal
specific. It is further pointed out that there are many damped harmonic
oscillators that have frequency stable classical solutions. The generic
frequency stable solution is

(6)

, with any well behaved function f(t) non zero for positive t. A quantum field
theory framework can be constructed around the generic solution. The
Hamiltonian of the generic solution permits recasting into the Hamiltonian of
366 R. P. Bajpai

free quasi photon, whose coherent state is and remains a squeezed state of
photon. The shape of photon signal obtained in the dynamic evolution has
following form:

(7)

Eq.(7) permits a large variety of shapes. The choice f(t)=λ-1+t gives the
earlier form of eq.(5). The probabilities of detecting different number of
photons are not easily calculable in the squeezed state with time dependent
parameters. The problem of calculation is circumvented by assuming that the
time dependencies of parameters become very weak and ignorable in the non-
decaying. The assumption makes the probabilities of detecting different
number of photons calculable.

3. Materials and methods

The measurement of both light induced and spontaneous biophoton
signals is non invasive. The apparatus required in the measurement are a
measuring chamber, a source of stimulating radiation and a detector. The
measuring chamber is light proof with provision for the entry of stimulating
radiation and the exit of emitted photons. The stimulating radiation enters
through a window or fibre cable and its duration is controlled by a shutter.
The exit is usually through a quartz window, which is transparent to visible
radiation but opaque to UV radiation. Sample is placed in the chamber in a
sample holder made of quartz or metal that does not emit visible range
photons after exposure to stimulating radiation. The stimulating radiation is
obtained from an ordinary 100-250 watt lamp, a monochromator, or a UV
lamp. UV lamp is used mainly for stimulating cultured cells, which do not get
stimulated by visible radiation. The time of stimulation is adjustable and
varies from 5-10s. The detector is a photo multiplier tube capable of detecting
electromagnetic field of energy around 10-16 watt. The photomultiplier tube
has a large single scintillation crystal sensitive over a broad range. The actual
range depends on the material of crystal. The photomultiplier tube sensitive
in the range (350-800nm) appears most appropriate to measure biophoton
signals of botanical samples while the tube sensitive in the range (300-
600nm) is for biophoton signals of human subjects. The detector operates in
single photon mode and counts the number of photons in large number of
contiguous bins. Both, bin size and number of bins are adjustable. Spectral
decompositions of a biophoton signal are obtained by inserting band pass or
interference filters.
Biophotons: A clue to unravel the mystery of “life”? 367

The signal emitted by a living system just after stimulation is very

intense and can blind a photo multiplier tube. The measurement of light
induced biophoton signal is, therefore, made after a delay of 10ms. The delay
eliminates contributions of fluorescence signals of different materials. The
mechanical shutters controlling the entry and exit makes the number of
counts of a few initial bins erroneous in some measuring systems. The
erroneous counts in these systems are ignored and it introduces a little more
delay in measurements. One usually measures the decaying part of a signal
for 3-5 minutes using bins of sizes in the range 10-200ms. The copies of the
decaying part for measurements with higher bin sizes are obtained by
merging the observed counts in appropriate number of contiguous bins of
lower sizes. We use the copies of the signal obtained by merging up to 10
bins in the estimation of decay parameters. The calculated values in a copy
are obtained by integrating the expression over the bin size i.e. ∫n(t)dt.
Estimation is done by least square minimisation giving equal weight to all
copies. The decay parameters should not depend on the bin size and we use it
as a criterion to check the correctness of a framework. The framework (2c)
nearly fulfils this criterion while the other two frameworks show large
variations in estimated parameters with bin size. The framework (2c) will be
used in subsequent discussions. It is pointed out that many successful
applications of framework (2b) are based on the sensitivity of overall strength
of the signal to physiological and environmental factors. There are many
measures of overall strength; the total number of counts in a portion of the
signal of any length provides a measure. All measures are not equally
efficacious in bringing out the sensitivity of overall strength. The most
efficacious measure is the number of counts in the first bin, NB1. The rapid
decrease in the signal with time implies that smaller the bin size, greater the
sensitivity of NB1. The measurement of the decaying portion can be repeated
every 3 minutes and of NB1 every minute.
The measurement of spontaneous biophoton signal of a sample is made
after eliminating the effect of its stimulation by laboratory illumination. The
sample is therefore, kept in the dark chamber for at least half an hour before
the start of measurements. Photons are counted in a large number of bins of
same size. The number of bins and their size depend upon the stability of a
system. The measurements in 30000 bins of 50ms size take 25 min. The
sample should remain stable and unchanging in this duration, which is true
for samples of lichens but not for human subjects. The measurements with
bin size 50ms are used for determining digitised copies of the signal for
measurements with bin sizes varying from 50ms to 500ms in steps of 50ms.
Human subjects become restless and tense after a few minutes. The duration
of 3 min appears optimal for measurements with human subjects and
368 R. P. Bajpai

measurements in 3600 bins of 50ms can be made in this duration. The

measurements for background noise are made with the same protocol but
without a sample. The probabilities of detecting different numbers of photons
in a bin are obtained from every digitised spontaneous biophoton signal.
The probability of detecting n photons in a bin is represented by Pn for n
= 0,1, ...nmax , where nmax is the maximum number of photons detected in any
bin. The photo count distribution P is the set of probabilities {Pn}. Photons
detected in a bin come from two independent sources, biophoton signal and
background noise. As a result, the observed probabilities and signal strength
k given by the average counts in a bin are different from the probabilities and
signal strength of biophoton signal. A subscript obs, bg, or sig is added to
probabilities and signal strength to indicate whether probabilities and signal
strength are of observed signal, background noise or biophoton signal. The
properties with the subscripts obs and bg are measurable and with the
subscript sig are calculable. The three sets of properties are related. The
observed signal strength is the sum of other two signal strengths

kobs = ksig + kbg . (8)

Similarly, the observed probabilities are convolution of signal and

background probabilities

Pobs = Psig ⊗ Pbg

, (9a)

which expresses the following algebraic equations:

n
P n
obs = ∑ Psigj Pbgn − j . (9b)
j= 0

The algebraic equations can be solved recursively to obtain any Psign starting
with n=0. The procedure fails quickly due to compounding of errors of Pobs n

n n
and Pbg . The error in any Psig is higher than in Pobs
n
and their difference
increases with n. The probabilities and signal strength of a biophoton signal
are calculated by assuming the signal to be in a squeezed state. A squeezed
state α, ξ is specified by two complex parameters α and ξ or equivalently
by four real parameters, the magnitudes and phases of the two complex
parameters, i.e. α = |α| exp (iφ) and ξ = r exp (iθ). Every property calculated
in the squeezed state α, ξ is expressible by a function of four parameters.
The calculated expression of signal strength ksig(cal) is:
Biophotons: A clue to unravel the mystery of “life”? 369

2
k sig (cal ) = α + sinh 2 r (10)
.

ksig(cal) is equated to ksig that is well determined and has very small error in a
signal of constant average intensity. Eq.(10) then becomes a constraint
relation and it reduces the independent squeezed state parameters to three by
expressing |α| as a function of r and ksig. The independent parameters are
n
taken to be r, θ and φ. The calculated expression of probability Psig (cal) of
detecting n photons in a bin in the squeezed state is given by

(cal) = n α, ξ
n 2
Psig (11)

, where n is an eigen state of the number operator with eigen value n. The
scalar product of number and squeezed states for a single mode photon field
is given by[22]
n

n α, ξ =
1 ⎡1
⎢
n!cosh r ⎣ 2
⎤2 ⎡ 1 2
( )⎤
exp(iθ) tanh r ⎥ exp ⎢− α + α *2 exp(iθ) tanh r ⎥
⎦ ⎣ 2 ⎦
⎡ ⎤
⎢ α + α * exp(iθ) tanh r ⎥
× Hn (12)
⎢ (2 exp(iθ ) tanh r ) 12 ⎥
⎣ ⎦

,where α* is the complex conjugate of α and Hn is the Hermite polynomial of

n
degree n. The least square fitting of Psig n
’s to Psig ( cal ) ’s can in principle
estimate three unknown parameters but high errors in Psig n
’s make the
estimation unsatisfactory. The problem of high errors is reduced[23] in the
estimation based on the least square fitting of Pobs
n
’s to Pobs
n
(cal) ’s because the
error in Pobs
n
(cal) is much smaller than in Psign . Pobs
n
(cal) is calculated by
n
convoluting Psig ( cal ) and Pobs
n

(13)

n
Psig ( cal ) is an exact expression and is without any error. Convolution in
eq.(13) compounds only the small errors of Pbgi . The three parameters are
estimated by minimizing the function
370 R. P. Bajpai

(14)

The summation over bin size ensures that parameters common to all copies of
signal obtained by merging the counts of contiguous bins are estimated. The
minimum value Fmin obtained is an indicator of the quality of estimation.

4. Salient features of biophoton signals

Fig.1 pictorially summarizes the universal features of light induced and
spontaneous biophoton signals. The figure depicts a hypothetical biophoton
signal, whose fluctuations have been smoothed out for the sake of clarity.
Fluctuations are observed in measurements with any bin size. The smoothed
out signal is a robust curve and nearly same curve is obtained in repeating the
measurements. The figure has four distinct regions- pre stimulation, during
stimulation, decaying and tail. The flux of emitted photons is almost
unchanging in the pre-stimulation and tail regions but it changes rapidly
during stimulation and decaying regions. The regions of unchanging flux
represent spontaneous biophoton signal and the decaying region light induced
biophoton signal or delayed luminescence. The flux decreases continuously
in the decaying region. The duration of decaying region is a characteristic of

10 ms delay ( fluorescence)
500
Flu ctuation s in
Decaying Par t e ve ry bin size
( 20ms-200s)

Stimulation
75 (5-10s) Non- exp one ntial decay
Light induced e mission
Counts/s

Spontaneous Spontaneou s
25
emission emission
(10-15 min)
( for hours)
Pr e stimulation
Ba ck ground
5
Time (not to a scale )

Figure 1. Typical shape of a smoothed out biophoton signal: A hypothetical signal

summarising the main features of the different regions of biophoton signals is drawn
not to a scale.
Biophotons: A clue to unravel the mystery of “life”? 371

the emitter. It ranges from 200ms to 200s in different living systems. The
figure mentions 10-15 min as the duration of pre stimulation region but it can
be much larger in quasi stable systems that have very slow growth and decay
rates. The depicted flux of spontaneous biophoton signal is 12.2counts/s and
of background noise 8.5counts/s. The emitted photon flux is undetectable
during stimulation as it is difficult to distinguish between photons emitted by
a sample and photons stimulating the sample. The emitted flux is, therefore,
depicted by broken lines in the figure. The expected flux likely to be emitted
increases rapidly during stimulation and becomes too large in a short time.
Too large flux is depicted by a gap in the figure. The gap extends for 10ms in
the post stimulation region. The distinguishing feature of a biophoton is the
lack of exponential decay character in both, decaying and non-decaying
regions of the signal. Different living systems emit similar biophoton signals.
The signals however, differ in strength and shape. The shape and strength
seem to identify a living system. The shape and strength are sensitive to
many factors, physical, physiological, genetic, emergent and holistic.
The digitised shape of a signal N (∆t, t) is determined by repeatedly
detecting the number of photons in a fixed interval. The number N of photons
detected in the interval depends on its duration ∆t and the time of its
commencement t measured after the stimulation of the sample by light. The
number of photon detected in the first interval N (∆t, 10ms) is given a special
name NB1, where 10ms indicates the delay in the measurement. NB1 is
substantially higher than background noise and shows saturation effect with
intensity of stimulating light I and the duration of exposureτ. NB1 initially
increases with I and τ but attains its saturation value in less than one second
of exposure to normal laboratory illumination. The saturation value is
observed over wide ranges of I andτ. The other values in the digitised shape
N (∆t, t) do not follow NB1 before saturation but do attain stable values after
saturation. Repeated measurements on a sample yield same stable values of
NB1 and N (∆t, t). Only stable values will, henceforth, be considered. The
excitations of a sample by light of different wavelengths yield different
values of NB1. The dependence of NB1 on the wavelength of excitationλexc
is given by a smooth curve and that has broad structures[24]. The curve is
called excitation curve. Different samples have different excitation curves.
NB1 in a monochromatic stimulation is smaller than in the white light
stimulation. The sum of the values of NB1 obtained in monochromatic
stimulations of two or more wavelengths is greater than the value of NB1
obtained in the stimulation containing those wavelengths.
Spectral decompositions of the signal are obtained by inserting filters
prior to detection. The spectral decompositions indicate broadband emission
372 R. P. Bajpai

spectrum. The typical percentages of red, green and blue spectral components
in NB1 of a sample of young Actebularia obtained with the help of band pass
filters are 91%, 7% and 2%. The relative percentages change with the age of
the sample and are also different for different species. The influence of the
wavelength of excitation λexc on emission spectra is weak. In particular, the
delayed luminescence signal emitted by a sample excited with red light has
blue component as well. The relative percentages in the spectral components
of N (∆t, t) also have similar behaviour. Various spectral decompositions lack
exponential decay character.
The temperature of the sample affects NB1 and N (∆t, t) of its biophoton
signal. The effects on NB1 and on the counts in various regions of N (∆t, t) are
different. NB1 is maximally affected by temperature. The variation of NB1
with temperature from 1oC to 40oC was studied in samples of a lichen species
Parmelia.tinctorum using white light stimulation. NB1 decreased
monotonically and nonlinearly with the temperature of the sample in the range
1oC to 22oC. NB1 at 22oC was nearly one fifth of its value at 1oC. The value of
NB1 was specific to the temperature of the sample in the range (1oC - 22oC).
NB1 seems capable of sensing the temperature in this range with an accuracy
of 0.1oC. NB1 increased with temperature beyond 22oC, peaked at 25oC and
then decreased slowly till 40oC. The variation of temperature in this range
affected NB1 in a hysteresis like manner. Temperatures beyond 40oC inflicted
fatal damage to the sample. NB1 of a damaged sample was much smaller and
cooling a damaged sample to lower temperatures did not restored earlier values.
NB1 and N (∆t, t) depend on many other factors as well and sense
changes in those factors. NB1 is the most discriminating parameter but it uses
only the information contained at a single point of the decay curve. The
decay curve has mainly been used for estimating the smoothed out value of
NB1. The estimation procedure basically utilises only a small portion of the
decay curve because of the rapid initial decay and yields an inferior estimate
of NB1 to that obtained by averaging the results of its repeated
measurements. The decay curve has been measured in many systems but the
data are not in public domain, only the results analysed in the framework of
Popp are. The results establish the capabilities of NB1 and N (∆t, t) to
identify different physiological states of a living system. The capabilities
have many potential applications. The information contained in the entire
decay curve is utilised in the framework of Bajpai. The analysis in this
framework has been done in few systems only and it reveals that NB1 and
log(B1/B2) are very sensitive while B0 and t0 are less sensitive indicators of
various factors determining a physiological state. Both NB1 and log(B1/B2)
have higher values in signals of healthy living systems; sickness, stress and
deprivation seem to reduce their values.
Biophotons: A clue to unravel the mystery of “life”? 373

Some non-living complex systems also exhibit delayed luminescence and

emit signals lacking exponential decay. The decay curve of these systems can
also be analysed similarly. The parameters extracted from the decay curve
can identify different states of complex systems. An important application
worth mentioning is the capability of the analysis to differentiate between
sugar globuli medicated with high potency homeopathic remedies and
placebo sugar globuli [14]. The parameters extracted from N (∆t, t) in the two
types of samples are different. The parameters of medicated globuli and not
of placebo globuli change in presence of specific frequency magnetic field.
The observed changes were reversible and repeatable.
The study of fluctuations provides information about the quantum entity
present in a living system. This type of study can be made only in the region
of spontaneous biophoton emission. The study shows that the photons
emitted in different modes (or frequencies) are strongly coupled[25]. Strong
coupling implies that the probabilities of detecting different number of
photons of any mode in a bin depend only on the signal strength of the mode
and the probabilities of different modes are equal to those of composite signal
with same strength. The measured probabilities in a photon signal provide
information about its quantum state, which in case of a squeezed state is
completely determined by the signal strength and three other parameters r, θ
and φ. The four parameters have been determined in photon signals
spontaneously emitted at different anatomical locations of human
subjects[26]. The parameters show interesting patterns. The signal strength is
different at different anatomical locations in a healthy human subject but
other three parameters have same values. These parameters appear to have
same values in every healthy human subject. All three parameters are affected
by local injury, inflammation or sickness[27]. In contrast, practicing
meditation over years affect r but not θ andφ[28]. Fluctuations in the
decaying region have been studied using bins of size 10 µs. The
measurements in 1000 contiguous bins take only 10ms, in which duration the
decay of light induced biophoton signals of photo synthetic systems can be
ignored. The measurements determine the probability of detecting no photon
in 10 µs reasonably well. These measurements have been repeated
continuously over the entire decay region to obtain the dependence of
probability of no photon detection on signal strength. The measured
dependence demonstrates quantum nature of photon signal [18].

5. Implications and speculations

The experimental data summarized in the previous section provide ample
evidence of the lack of the exponential decay character in biophoton signals
emitted by isolated living systems. Only the framework of section 2.3 can
374 R. P. Bajpai

explain the smoothed out shapes of these signals. The framework envisages a
dynamic origin of the shape. The observed shape manifests an evolving
quantum squeezed state. The squeezed state in the spontaneous emission
region is specified by four real parameters, which are estimated from the
fluctuations of the signal in the region. The parameters estimated from the
smoothed out signal and from fluctuations in the spontaneous emission
region are new characteristics of a living system. The nature of new
characteristics is holistic. They open up new planes of investigation and
understanding. Let us dwell upon some obvious implications of the
spontaneous emission of photons in squeezed state. As all living systems
spontaneously emit fluctuating photon signals and fluctuations of the signal
measured in whichever living system indicate a quantum squeezed state of
the signal, one suspect that the emission of photon signal in a squeezed state
is a unique feature of a living system. Non-living systems including non-
living counterparts of living systems do not have this feature. A living system
thus, differs from its non-living counterpart in two properties, “life” and
biophoton signal. The two differing properties offer a chance to remove the
basic objection against treating living system as physical system. The
objection stems from the fact that two physical systems cannot differ in one
property alone and there has to be at least another distinguishing property law
like related to the first property in all aspects. The law like relation in all
aspects of two properties is called isomorphism. If the biophoton signal turns
out to be isomorphic to “life”, then both, a living system and its non-living
counterpart, can be physical systems. We envisage that biophoton signal is
indeed isomorphic to “life”. Isomorphism makes biophoton signal and
“life” equally mysterious. The unusual properties of biophoton signals
indicate and are law like related to the unusual features of the “life”. The
isomorphism makes the study of the biophoton signal a powerful method
for unraveling the mysteries of “life”. The study should provide complete
information about the properties of “life” and living systems. The
isomorphism shifts the emphasis of investigations from living systems to
non-living photons, which kindles the hope of measuring of every feature
of “life” because every feature of the isomorphic photon signal is
measurable. Quantum nature of biophoton signals makes “life” a quantum
phenomenon. The restriction of quantum state of photon signal to squeezed
states considerably reduces the complexity of “life” for all features of “life”
have to be expressible by the values of four real parameters. The
observation of quantum biophoton signal for macroscopic time implies that
quantum phenomenon responsible for “life” remains stable for macroscopic
time. These are broad implications that emanate from the following four
ingredients of the envisaged isomorphism:
Biophotons: A clue to unravel the mystery of “life”? 375

1. Biophoton signal emitted by a living system is a quantum photon signal.

2. The quantum photon signal is in a squeezed state.
3. The squeezed state is specified by four measurable parameters that take
continuous values.
4. The quantum photon signal exists for macroscopic time.
The ingredients are expressed as observable features of biophoton
signals. The observing of the features establishes and tests the validity of
envisaged isomorphism. The features were observed in signals emitted by
many samples of the three species of lichens and in signals emitted by human
subjects at various anatomical locations. It is ample evidence and
experimental support of isomorphism. Each feature on its own has profound
implications. The first feature is the most crucial ingredient that necessitates a
radical departure from the conventional picture of photon emission. The
conventional picture visualises photon emission of an isolated system in the
transition from higher energy state to lower energy state of a large number of
independent units-atoms, molecules or more complex structures. The
transitions of different units are probabilistic, which causes photon signal to
decay exponentially due to depletion of units in the higher energy state. The
independence of units rules out correlation among photons of the emitted
signal. A biophoton signal does not have exponential decay character and its
photo count distribution exhibit specific type of correlation. The conventional
picture cannot be valid in biophoton emission. Biophoton emission must
occur through a holistic mechanism that operates during the lifetime of a
living system. The material constituents participating in the holistic
mechanism must make up a quantum entity because only a quantum entity
emits a quantum photon signal. The first feature therefore implies the
existence a composite quantum structure of participating constituents. It will
be called quantum entity.
Molecular biology stipulates all biological properties to originate from
and be expressible by biomolecules. The quantum entity should therefore, be
a composite quantum structure of bio-molecules. A composite quantum
structure can have two types of properties, local and holistic. A local property
depends on individual constituents but not on their specific states in the
composite structure. A local property is therefore, expressible in terms of the
properties of its microscopic constituents and is called microscopic property.
Quantum framework is not necessary for its description. The classical
reductionist framework of molecular biology can correctly describe all local
properties of the quantum entity. Local properties do not reveal the presence
of quantum entity. A holistic property depends on individual constituents and
also on the state of the composite structure. The dependence of a holistic
376 R. P. Bajpai

property on the state of composite structure is correctly understood only in

the quantum framework. The classical framework has to invoke ad hoc
correlations among constituents to describe this dependence, which makes
the description macroscopic. Holistic properties are therefore, called
macroscopic properties. There is no origin of invoked correlations but it
appears knowable in some properties and unknowable in others. The
perception of origin divides the holistic properties in two classes, psyche and
consciousness. The correlations invoked to describe the properties of psyche
class can arise from exchange of information through a physical signal and
hence the origin of these correlations appears knowable. Such a signal has not
been discovered so far. Perhaps, it is a figment of imagination and exchange
of information does not occur. The classical framework will always
encounter an unbridgeable gap between perception and reality of the
properties in the psyche class. The gap was visualised earlier and called
psychosomatic gap. The correlations invoked to describe the properties of
consciousness class can arise from exchange of information in a mode that
either violates a fundamental law or requires superluminal communication
and hence the origin of these correlations appears unknowable. The
properties of consciousness class were, therefore, thought to belong to a
reality beyond science. The elusive origin of invoked correlations is the
biggest problem in understanding holistic properties of a living system. The
problem arises from the use of classical framework. The quantum framework
resolves the problem. Holistic properties are properties of a composite
quantum entity and the correlations invoked in the classical framework
contain information about the quantum state of the composite entity.
Incidentally, local properties are holistic properties not requiring any
correlation. The first feature thus implies three classes -microscopic, psyche
and consciousness- of properties in living systems. Some living systems show
another class of properties that are incomprehensible in the classical
framework and require additional inputs besides biomolecules and
correlations. These were also included in the consciousness class. The use of
the quantum framework necessitates the division of the erstwhile
consciousness class into two sub classes, soft and hard. The properties of the
soft consciousness class are comprehensible in the quantum framework and
but not of the hard consciousness class.
Mood of a living system is another ramification of the quantum entity.
Mood is an attribute ascribed in the classical framework to a living system
whose properties are different at different times or situations without an
obvious reason. The quantum framework ascribes different properties to
different states of the quantum entity. Many quantum states are available to a
quantum entity and these states have different properties. A quantum state
Biophotons: A clue to unravel the mystery of “life”? 377

can be stable or fickle to external noise. The quantum entity in the stable state
will have same properties at different times or situations but not in the fickle
state. The classical framework does not differentiate among various quantum
states and is forced to introduce an extraneous concept of mood to account
for changes in the properties of quantum entity in a fickle state due to
external noise. The envisaged isomorphism permits the detection of changing
states of quantum entity by changes in squeezed state parameters of
biophoton signal. It makes the mood measureable in living systems.
A quantum entity will participate in biological processes. Some processes
may take quantum route, in which every step in a process is a quantum
transition. Quantum route implies massive parallel processing, which means
quantum processes are faster and efficient. A biophoton signal has to emanate
from biological processes taking quantum route because of its quantum
nature. The ubiquitous presence of biophoton signal requires these biological
processes to occur at all times in every living system. The fundamental
biological processes of transcription, replication and protein synthesis occur
at all times in every living system and we suspect them to be responsible for
biophoton emission. The suspicion requires them to take quantum route.
Quantum route for fundamental biological processes was speculated earlier
for explaining the basic facts of genetic code, namely occurrence of four
types of nucleotide bases, codons made up of three nucleotides and twenty
amino acids. The explanation hinges on quantum selections made by
nucleotides and codons. A nucleotide makes quantum selection in one
transition and is able to select the desired nucleotide from four nucleotides
and not two nucleotides allowed in the classical selection. Similarly, a codon
makes quantum selection in three transitions and is able select the desired
amino acid from among twenty possible amino acids and not eight amino
acids allowed in the classical selection. The basic facts of genetic code
merely reflect optimal utilisation of resources using the most efficient
selection machinery. A necessary condition for operating the quantum
selection machinery is the existence of objects participating in selection
processes in pure quantum states. Nucleotides, codons and amino acids
should be either in pure quantum states or the constituents of a composite
structure in a pure quantum state. The latter possibility probably occurs as it
leads to the existence of quantum entity. All constituents of the composite
structure need not show quantum character all the times, only the constituents
involved in selections at an instant need show it. The relaxed requirement
permits to build a model of quantum entity in the classical framework. The
constituents of the quantum entity acquire and loose quantum character
depending on the dynamical requirement in the model. The model assumes
two states of different characters of nucleotides, amino acids and codons; one
378 R. P. Bajpai

state has classical character and the other has quantum character. The state
with classical character has lower energy and a constituent makes a transition
to higher energy state of quantum character after extracting requisite energy
from the usual biochemical machinery. The biochemical machinery increases
the number of constituents in states showing quantum character to such an
extent that they form a macroscopic object called quantum patch. A living
system has many quantum patches distributed throughout its body. Many
constituents of a quantum patch simultaneously make transition to their
classical states by emitting photon. It is a possible mechanism to up convert
biochemical energy. A quantum patch makes the transition to classical states
of its constituents after quantum selections and also because of de-cohering
interactions with local environment. Both factors restrict the growth of
number and size of quantum patches. The state of quantum entity determines
the distribution and sizes of quantum patches. The assembly of the quantum
patches makes up the quantum entity. The distribution and sizes of quantum
patches determine the spectral composition of its biophoton signal. Similar
spectral composition of biophoton signals suggests similar distributions of
number and sizes of quantum patches. Similar distributions occur because of
similar local environments in different living systems. Biophotons in the
model originate mainly in the regions where transcription, replication and
protein synthesis occur.
The second feature, namely squeezed state of quantum biophoton signal,
is established from the photo count distributions measured in a biophoton
signal at many bin sizes. The photo count distributions with different bin
sizes yield nearly same estimates of the parameters specifying a squeezed
state. The photo count distributions with various bin sizes in the range (50ms-
6s) were measured in the biophoton signal of a sample of lichen over period
of more than 5h. All of them suggested the same squeezed state of the signal.
Another reason for the squeezed state is the non-exponential decay of two to
three orders of magnitude in the intensity of a light induced biophoton signal.
The large decay is obtainable in the evolution of squeezed state but not of a
coherent state in the quantum framework. This the only model that
successfully reproduces all aspects of light induced and spontaneous
biophoton signals in a unified scheme. A squeezed state is a minimum
uncertainty state, propagates with very little expense of energy and is
detectable even if its energy is below the noise level. The emission of
quantum photon signal in a squeezed state raises many questions. How does a
living system generate such a photon signal and why? What is the role of the
signal in establishing coherence, long range order and stability in living
systems? Are living systems aware of the possibility of almost lossless
information transfer to long distances by biophoton signals? Do living systems
Biophotons: A clue to unravel the mystery of “life”? 379

extract and decipher information contained in biophoton signals? The answers

of these questions will have many implications. Even the questions suggest
clues for understanding “life” in its myriad manifestations. The first two
questions point out the need of more theoretical investigations for building a
coherent and stable quantum entity around electromagnetic field in a squeezed
state. The other two questions suggest the need of more phenomenological
investigations at this juncture particularly of the responses of living systems to
biophoton signals. A change in the rate of cell division in response to specific
biophoton signal has been observed in onion roots, yeast culture and amphibian
eggs[29]. The other living systems may respond differently and there could be
better ways of detecting responses. The technique of delayed luminescence
appears promising for it can detect minute changes in a living system. If the
response of a living system persists for a few minutes after its interaction with a
biophoton signal, then the technique can measure this response. The technique
shows the positive influence of a psychic healer on a water starved sample of
lichens from a distance. The healer probably beamed specific biophoton signal
that alleviated the problem of water starvation.
The third feature state the fact that squeezed state needs only four
parameters for its specification. It reduces the complexity of living system to
four measurable attributes. The continuous values allow the parameters to
faithfully capture the immense diversity of living systems and their moods in
the envisaged isomorphism. Mood is used in generic sense and includes all
holistic properties e.g. health, vivacity, germination capacity, etc. One
expects to find species specific patterns in quantum attributes; the attributes
of all members of a species may lie in definite ranges. One also expects to
calibrate attributes of a living system for measuring any holistic property.
The information in a squeezed state can be coded in its four parameters,
which means that the information carrying capacity of a signal in a squeezed
state is four fold to that of a signal in a coherent state. The estimates of
squeezed state parameters are different for different bin sizes in some
biophoton signals. These signals are not in squeezed states. They probably
indicate ill health.
The fourth feature- the stability of quantum photon signal for
macroscopic time- is difficult to comprehend and implement in the classical
framework. The feature allows the determination of photo count distribution
and estimation of squeezed state parameters. Photo count distribution has no
meaning if the signal changes during measurement. The living system
emitting a stable signal or rather the quantum entity responsible for emission
has to be stable as well. Two stabilities- of biophoton signal and of quantum
entity-are associated with every living system. Only the framework of
quantum field theory can implement both stabilities, still the cause and effect
380 R. P. Bajpai

linkage between the stabilities is visualized in the classical framework. There

are three possibilities of linkage: 1.The stability of biophoton signal is
primary and the instructions/information transmitted by it to spatially
separated quantum patches stabilizes the quantum entity. 2. The stability of
quantum entity is primary while biophoton signal arises from its spontaneous
acts and reflects its stability. 3. The stabilities of photon signal and of
quantum entity are at the same footing, which happens if biophoton signal
and quantum entity are in an entangled states. The mechanism for
implementing any possibility is neither known nor speculated but the e
linkage in every possibility shifts the emphasis of investigations from living
system to non-living photons. The last possibility is philosophically more
appealing. The possibility implies two equivalent descriptions of a living
system, one based on the properties of quantum entity i.e. the properties of
matter and the other based on the properties of photons i.e. the properties of
field. The state of a living system can be ascertained either by observing its
matter content as is done in various pathological and diagnostic tests or
equivalently by determining the squeezed state parameters of its biophoton
signal. Further, the state of a living system can be changed from a sick to
normal state by manipulating either matter or entangled field or a
combination of the two. The corrective measures in modern medicine are
based only on the manipulation of matter but corrective measures based on
the manipulation of field should be equally effective. The optimum strategy
for managing a sick state may involve manipulation of both types. The reason
for the success of alternative therapies in some sick subject may lie in
inadvertent manipulations of biophoton fields. There is a need to study the
relation of quantum parameters with the state of health and to find ways of
altering quantum parameters of the biophoton signal of a sick subject.
The living systems play only a passive role in above implications. They
are treated like a black box emitting biophoton signal in squeezed state. But
living systems play active roles as well. The active roles have many more
implications and permit new uses of biophoton signals. A living system
playing active roles needs to have the capability to detect a biophoton signal,
to measure its properties, to decipher the information contained in the
properties and to beam biophoton signals with desired properties if needed.
These are permissible physical capabilities but the evidence of the existence
of these capabilities in living systems is scanty and anecdotal. The
implications of capabilities are quite often considered speculative. The
capability to detect biophoton signal has been demonstrated in onion roots,
yeast cells and amphibian eggs. These system show measurable response to
some but not all biophoton signals. The response only to selective signals
implies that a living system responds only to biophoton signals whose
Biophotons: A clue to unravel the mystery of “life”? 381

squeezed state parameters lie in specific ranges and the ranges of squeezed
state parameters determine the type of a biophoton signal. There is enough
experimental evidence to support that above quoted living systems have the
capability to detect biophoton signals of the type a system emits and also of a
few more types. The evidence is extrapolated to all living systems. Every
living system detects biophoton signals similar to the one it emits but may not
show measurable response of detection. The lack of measurable response is
attributed to poor sensitivity of the detector, bad technique used in its
measurement and inappropriate properties used for its measurement. The lack
of measurable response does not preclude the existence of biophoton channel
of information transfer. Perhaps, such a channel does exist and living systems
emitting same or similar types of biophoton signals communicate among
through this channel. It is then possible to identify morphogenetic field (or its
many variants) with biophoton field of a living system. Many laboratories
routinely detect biophoton fields using non-living detectors. The information
content of the field will hopefully, be deciphered in near future. It will then
clarify many aspects of morphogenetic field.
The capability of human beings to communicate via biophoton channel
needs more careful examination because a human subject will know if it has
detected a biophoton signal and will be able to tell so to other human beings.
A human subject getting information via biophoton channel does not seem to
exist. There is a need to understand why human subjects are ignorant of their
capability to detect biophoton signals. We suggest that a new born child
senses biophoton signals emitted by other human beings but does not know
how to decipher information contained in the signals. The child also senses
photon signals received from her sensory channels and does not know how to
decipher information contained in these signals as well. She has to learn the
art of deciphering information from signals and communicating her
experiences. The signals from sensory channels are strong, classical and easy
to interpret. The society assists her in deciphering information from signals of
sensory channels and teaches her the art of communicating experiences. In
contrast, the signals of biophoton channel are weak, quantum in nature and
difficult to interpret. The society does not teach her the technique of
extracting information from a quantum signal. She starts filtering out
biophoton signals and concentrates her attention only on classical sensory
signals due to societal intervention. Perhaps after a period of bewilderment,
she associates meaning only to classical signals. The society encourages her
to ignore the obstructions caused by biophoton signals. She soon starts
treating biophoton signals as noise to be ignored. She brushes aside the innate
ability to detect biophoton signals. The innate ability, however, remains intact
and can be used in future if she learns to decipher information from quantum
382 R. P. Bajpai

biophoton signals. The learning will enable her to access information about
other objects via biophoton channel and to see invisible objects. She can be in
communion with the entire world via biophoton channel. Many religious
traditions envisage such a capability acquirable. One may not always relish
the acquiring of this capability. Imagine the horror of a person who acquires
it by chance and then starts knowing the guarded secrets of acquaintances.
Even a true narration of splendour and beauty of nature learnt via biophoton
channel will fetch him the epithet paranormal. The knowledge gained through
the additional capability will make him nonconformist. The society packs
nonconformists to solitary confinement either in jail or in jungle.
The resources required in determining the classical state of a biophoton
signal are only a small fraction of the resources required in determining its
quantum state. Classical state is characterised by one parameter-the intensity
of signal- and its determination requires the measurement of photon number
in a few large size bins. The quantum state is characterised by many
parameters and its determination requires the measurement of photon number
in many thousand bins, an assumption about the quantum state and a
procedure for estimating the parameters. Even one determination of quantum
state is a big drain on resources and many such determinations strain a living
system to the point of breakdown. Living systems therefore, avoid
determining quantum state and resort to inferences based on classical states
as often as possible. It is a survival strategy. The determination of quantum
state becomes imperative in some situations e.g. in a noisy environment, in
clogged or obstructed classical channels. The detection of some combinations
of parameters of quantum state of the signal is unaffected by noise and
clogged or obstructed classical channels hardly affect the determination of
these combinations of quantum parameters.
The capability of a living system to determine quantum state of
biophoton signals is evolutionary advantageous. The system gets access to
information of other living systems not available otherwise. The system will
know about various events and processes affecting biophoton signals of other
systems. The system will appear to have the power of remote sensing.
Perhaps, clairvoyance and extra sensory perception arise from the use of
information obtained from biophoton signals. A living system can use
biophoton channel for remote intervention if it has an additional capability to
beam coded biophoton signals that influence other systems. One wonders if
wishful thinking and blessings generate coded biophoton signals. It is feasible
but it needs experimental verification. The power of remote intervention is
achievable more easily if living system is entangled with its biophoton field.
The living system intending to intervene has to set its biophoton detecting
machinery to some desired state and wait for the detection of biophoton field
Biophotons: A clue to unravel the mystery of “life”? 383

of targeted living system in the desired state. The act of detection

accomplishes the desired intervention. The targeted living system attains the
state entangled with the detected photon state. There are many interesting
questions connected with this mode of remote intervention. Which living
systems have biophoton detection machinery? How does a living system
adjust its photon detecting machinery to a desired state? How much time does
a system wait for detection? Can a human subject acquire the capability to
detect quantum state of a biophoton signal? Do prayer, meditation, breathing
exercises and drugs help in acquiring this capability? We do not know the
answers of these questions but we suspect that answers will provide physical
basis of the phenomena like memory transcendence, paranormal perception,
remote healing and some alternative therapies.
Finally, it is conceivable that a living system capable of determining
quantum state of a biophoton signal may also have the capability to
determine quantum state of its own biophoton field. The capability will
confer the living system ability to self introspect and make mid course
correction. The implications of the ability are easy to contemplate in a system
with entangled biophoton field. The entangled biophoton field is a true and
instantaneous image of the quantum entity of the system. The system can
monitor its quantum entity by observing its biophoton field. The monitoring
provides a feedback loop to take corrective measures. The possibility to
observe and analyse oneself is the additional ingredient that can explain
supervenience of the hard problems of consciousness. The additional
ingredient integrates metaphysical and philosophical visions of life with
physical sciences.

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