Literature DB >> 34987769

Interpreting airborne pandemics spreading using fractal kinetics' principles.

Panos Macheras1,2, Athanasios A Tsekouras2,3, Pavlos Chryssafidis1,2.   

Abstract

Introduction  The reaction between susceptible and infected subjects has been studied under the well-mixed hypothesis for almost a century. Here, we present a consistent analysis for a not well-mixed system using fractal kinetics' principles.  Methods  We analyzed COVID-19 data to get insights on the disease spreading in absence/presence of preventive measures. We derived a three-parameter model and show that the "fractal" exponent h of time larger than unity can capture the impact of preventive measures affecting population mobility.  Results  The h=1 case, which is a power of time model, accurately describes the situation without such measures in line with a herd immunity policy. The pandemic spread in four model countries (France, Greece, Italy and Spain) for the first 10 months has gone through four stages: stages 1 and 3 with limited to no measures, stages 2 and 4 with varying lockdown conditions. For each stage and country two or three model parameters have been determined using appropriate fitting procedures. The fractal kinetics model was found to be more akin to real life.  Conclusion  Model predictions and their implications lead to the conclusion that the fractal kinetics model can be used as a prototype for the analysis of all contagious airborne pandemics. Copyright:
© 2021 Macheras P et al.

Entities:  

Keywords:  COVID-19; SI model; airborne pandemics; fractal kinetics; herd immunity policy

Mesh:

Year:  2021        PMID: 34987769      PMCID: PMC8686328          DOI: 10.12688/f1000research.53196.1

Source DB:  PubMed          Journal:  F1000Res        ISSN: 2046-1402


Introduction

Recently, Jewell et al. criticized the predictive models of the COVID-19 pandemic. This rigorous analysis justifies the first portion of the famous quote by George Box “All models are wrong, some of them are useful”. All epidemiological models used in practice have a common origin, namely, the famous Kermack–McKendrick model. We argue in this work that their poor predictive power originates from the erroneous hypothesis of the “well-mixed” epidemiological system; this hypothesis is crucial for the validity of the differential equations, which describe the “reaction” between susceptible ( S) and infected ( I) subjects. We also argue that the violation of this hypothesis results in a wrong perception and definition of the basic reproductive number R 0 of epidemiological models, which denotes the number of secondary infections produced by a single infection. People worldwide are concerned about the uncontrolled “exponential” spread of a disease, yet it is not clear or justified if this description is correct. In fact, an alternative “power” model based on an adjustable exponent of time has been proposed. We expand this approach by first questioning the ‘well-mixed” hypothesis and introducing a “fractal kinetics’” approach which yields, as a special case, the “power” model. This model relies on fractal kinetics’ principles that are suitable for the study of reactions and diffusion processes in insufficiently mixed media. In the same vein, we explored all theoretical aspects of the fractal kinetics’ SI model and applied it for the description of the time evolution of the COVID-19 pandemic in several countries. Our results support that this “conceptual change” from classical to fractal kinetics principles offers a novel, useful approach for the analysis of airborne pandemics data and justifies the second portion of George Box quote above.

Theory

The “reaction” of susceptible-infected individuals under homogeneous conditions. In the Kermack–McKendrick model, the studied population is divided into susceptible, S, infectious, I and recovered, R, sub-populations while the relevant terms SI and SIR model were coined a long time ago. For each one of the sub-populations, specific ordinary differential equations are written based on the principles of chemical kinetics. These equations rely on the law of mass action which states that the rate of the chemical reaction is directly proportional to the product of concentrations of the reactants. However, this law applies under the strict hypothesis that the studied chemical reaction takes place under well-stirred conditions. This dogma applies well in chemical systems and validates the use of time-independent reaction rate constants and molar concentrations of the reactants in the reaction rate expressions. Obviously, the well-mixed hypothesis cannot be applied to epidemiological models since individuals, unlike molecules in a stirred solution, do not mix homogeneously; this is particularly so when preventive measures are applied. This, in turn, makes the mathematical formalism used so far questionable and the derived estimates of the relevant parameters, e.g., R 0, a very rough approximation of reality. In fact, R 0 cannot capture time-dependent variations in the transmission potential; the time course of an epidemic can be partly described by the effective reproduction number, R( t), which is a time-dependent parameter defined as the actual average number of secondary cases per primary case at time t: where S( t) and S( 0) are the numbers of susceptible subjects at time t and zero, respectively. Eq. 1 shows that R( t) relies on an estimate of R 0, which is usually derived from the early phase data of the pandemic. R 0 is also crucial for the calculations of herd immunity. The current SIR models for the ongoing COVID-19 epidemic include additional features to the classical SIR model, namely, the probability of death in the vulnerable fraction of the population, infectious period, and a time from infection to death are included. The basic reproduction number, R 0, and all variables and parameters of the model are expressed as Gaussian distributions around previously estimated means. However, R( t) is used extensively as a reliable measure of a pathogen’s transmissibility. The “reaction” of susceptible-infected individuals under heterogeneous conditions. In 1988, Kopelman introduced the concept of fractal reaction kinetics for reactions taking place under topological constraints. Under these heterogeneous conditions, time-dependent coefficients k( t) and not rate constants govern the rate of the reaction process. Numerous disciplines study rate processes with this approach. It is also very appropriate in studying the “reaction” of susceptible-infected individuals under “real-life” conditions. Consider two rooms of the same size shown in Figure 1 with the same “concentration” of 10 unmovable susceptible subjects and two COVID-19 infected subjects. The probability for SARS-CoV-2 transmission is much higher in the left-hand side room, because the distance for seven of the susceptible subjects from the two infected subjects is much smaller than the “critical distance” associated with the bimolecular reactions of fractal kinetics. On the contrary, only one of the susceptible subjects is within “critical distance” from infected subjects of the right-hand side room. The static picture depicts the equivalency of the social distancing (1.5 meters applied during the Covid-19 pandemic) with the “pair up” and “critical distance” concepts of fractal kinetics. Intuitively, if the subjects in the two rooms start moving, virus transmission will increase as a function of time and will be dependent on the trajectory of each individual. Obviously, continuous movement of the subjects in the two rooms sweeping the available space would result in the transmission of the disease to all susceptible subjects in accordance with the “well-mixed” hypothesis. This means that the “well-mixed” system is just a single limiting case of the myriad heterogeneous space/time configurations of the individuals in a population.
Figure 1.

Probability considerations for virus transmission based on the “pair-up” and “critical distance” concepts of bimolecular reactions in fractal kinetics.

Although the number of infected (red) and susceptible subjects (green) is the same in both rooms, the instantaneous probability for virus transmission is 7/10 and 1/10 for the left- and right-hand side room, respectively.

Probability considerations for virus transmission based on the “pair-up” and “critical distance” concepts of bimolecular reactions in fractal kinetics.

Although the number of infected (red) and susceptible subjects (green) is the same in both rooms, the instantaneous probability for virus transmission is 7/10 and 1/10 for the left- and right-hand side room, respectively. These considerations lead us to the following very important conclusions relevant to airborne pandemics. The time evolution of pandemics described by the classical SI and SIR models, which are based on the well-mixed hypothesis, are very crude approximations of reality. The use of a fixed R 0 value, is inadequate for capturing the transmission dynamics. The use of R( t) can capture time-dependent variations in the transmission potential, but is heavily dependent on the R 0 estimate. In real-life conditions, the transmission of the disease is not only dependent on time, but also on the topology/movement associated with susceptible/infected individuals. The importance of the “initial conditions” for fractal reaction kinetics has been delineated. In pandemics, the corresponding “initial conditions” are “patient zero” at the epicenter of the country of pathogen’s origin as well as “patient zeros” of the first humans infected in different countries. For the COVID-19 pandemic specifically, since most of the infected subjects are asymptomatic during the initial phase of the disease spreading, no precautions are taken. During this initial period, which lasts until social distancing measures are applied, disease spreading follows a “herd immunity” style, which we call “herd kinetics”. Similarly, we coin the term “fractal kinetics” for the disease spreading when containment measures are imposed. The fractal kinetics’ SI model for epidemic spreading relies on the following equation: where I( t) is the cumulative fraction of infected individuals at time t, β is a parameter proportional to the probability of an infected individual to infect a healthy one and h is the fractal dimensionless exponent associated with fractal kinetics. The core assumption of the model is that societies as complex systems will exhibit self-organization as a reaction to the emergence of a pandemic wave, enforcing preventive measures and increasing public awareness. Thus, instead of an infection rate constant, the fractal SI model uses a rate factor β/t decreasing of time. The solution of Eq. 2 gives I( t) as a function of time: where c is a parameter which determines the fraction of individuals that will become infected eventually. By substituting we introduce parameter α of inverse time dimension, which changes Eq. 3 into 4, namely: In the limit t → ∞ we find: The “well-mixed” model, described by Eq. 2 with h = 0, has a limiting value of I( t) equal to one as a result of a completely susceptible population. However, this is not a realistic feature for all pandemics that have appeared so far. Eq. 5 reveals that the plot of I( t) versus time for h > 1 reaches a plateau equal to 1/(1 + c) (see Figure 2), which is a reasonable feature for all pandemics. For the special case h = 1, Eq. 6 (also plotted in Figure 2) is derived which describes what we call “herd kinetics” not only because no precautions or measures are taken, but also because the rate of increase of infected subjects progressively diminishes in a similar fashion when a “herd immunity” policy is implemented:
Figure 2.

Simulated curves for the infected population fraction generated from Eqs. 4 and 6.

Parameter values used: h = 0, β = 0.064, c = 790; h = 1, β = 3, c = 4.4 × 10 5; h = 2.5, α = 0.018 (time) −1, c = 6. Marks on the curves are inflection points.

Simulated curves for the infected population fraction generated from Eqs. 4 and 6.

Parameter values used: h = 0, β = 0.064, c = 790; h = 1, β = 3, c = 4.4 × 10 5; h = 2.5, α = 0.018 (time) −1, c = 6. Marks on the curves are inflection points. A linearized form of Eq. 6 is as follows: where the slope β is an “apparent” dimensionless transmissibility rate constant during the “herd kinetics” period; the term “apparent” is used to underline its proportional dependency to the probability of an infected individual to infect a healthy one (see Eq. 2). At t = 1, hence ln t = 0, we get: Theoretically, the value of I( t = 1) corresponds to the “initial conditions”, i.e., the fraction of infected individuals at the first day of the pandemic; since the real “time zero” is unknown, c 1 is proportional to the number of total (asymptomatic and symptomatic) infected cases from the real time zero to time t = 1 day, when the first case was confirmed. We use the notation c 1 to distinguish it from c appearing in Eqs. 5, 6 and 7. In all pandemics, a characteristic time is observed when the daily number of confirmed infected cases does not increase anymore and starts declining; this corresponds to the inflection point t ip. When h > 1, an estimate for t ip can be obtained by equating the second derivative of Eq. 4 to zero and solving the resulting equation for time. Lacking an analytical solution, this equation can only be solved numerically. For the special case h = 0, t ip, can be derived from Eq. 4: The following t .ip can be derived from Eq. 2, under “herd kinetics” conditions ( h = 1): The inflection points for the three examples considered, h = 0, h = 1 and h = 2.5 are shown on the simulated curves of Figure 2. Inflection points denote when a curve changes from being convex (upwards) to concave (downwards), i.e., the confirmed infected new cases remain temporarily constant and then start to drop. If the value of parameter c is low, all cases reach the asymptotic limit of 1. However, in real-life conditions the limiting value of the cumulative fraction of infected individuals, I( t) is always much smaller than 1. This epidemiological evidence (fact) can be explained only by the fractal kinetics SI model as shown in Figure 2. The curve of the example considered using h = 2.5 reaches the plateau value of 0.125, i.e., 12.5% of the population will be infected eventually. For h > 1, the I( t) corresponding to the inflection time point, I ( t ip) can be derived from Eq. 4 using the t ip estimate in the denominator of Eq. 4. The t ip estimate is obtained by equating the second derivative of Eq. 4 to zero and solving numerically the resulting equation. For h = 0: while for h = 1: During the time course of the pandemics, an estimate for the time of the termination or close to the termination of the spreading is desperately needed as early as possible. An estimate for the time of 90% termination, t 90% for h > 1, can be derived from Eq. 4 using I( t) = 0.90/(1 + c):

Methods

Fits to COVID-19 data

The best fits of Eqs. 4 and 6 to the data were obtained by maximizing the R 2 of the two adjacent periods. By anchoring the date of each country’s lockdown decision (or any similar form of draconian measure) and moving forward in time, the Levenberg–Marquardt algorithm of least squares was implemented. The lockdown dates are close or very close to the transition from herd kinetics to fractal kinetics and vice versa. A minimum value of R 2 = 0.985 was set as a criterion of goodness of fit and every value higher than that was accepted. The turning time data point at which the best R 2 value began to diminish was rejected and its prior time data point was accepted. From that time segment and further on the consequent kinetic profile was fitted to the data points until the plateau of quasi-steady state was reached. The fitting discontinuities observed in the kinetics between the distinct periods ( e.g., from second to third period for France) are associated with the fact that I( t) values at the boundary of the two periods were not equalized in our fitting methodology. Between the quasi-steady state and the beginning of the second herd period a 10% change of the number of cumulative infected cases at one week interval was sought in order to establish the commencement of a second viral wave and the reproduction of the according fitting procedure. Data acquisition, modelling and simulations were programmatically implemented with Python language and its respective libraries.

Results

In our previous studies on COVID-19 data analysis, we applied the fractal kinetic SI model ( Eq. 3) assuming that fractal kinetics commences at time zero. However, reconsideration of the topological characteristics of the virus transmission in the light of Eq. 4 led us to the realization that a “herd kinetics’” period precedes the “fractal kinetics’” period. Exponent β drives the kinetics during the “herd kinetics” stage and is the analogue of R 0 for a not well-mixed system. But, unlike R 0, β is not associated with the expected number of cases directly generated by one case in a population. During the “fractal kinetics” period, parameter α in Eq. 4 governs the rate of the disease, while the prevailing spatial conditions are reflected on the h value. During this period, a meaningful parameter for the rate of the process is the half-life, t ½ = ln2/ α.

The “Herd-Fuzzy-Fractal-Herd-Fuzzy-Fractal” (HFF) 2 kinetic motif

Initially, virus transmission takes place under “herd kinetics’” conditions ( Eq. 6, Figure 3A). This prevails until the first preventive measures are imposed; these can be followed by a lockdown decision. The preventive measures and the lockdown status induce a gradual reduction in the rate of the disease spread, i.e., “fractal kinetics” starts operating ( Eq. 4, h>1, Figure 3B). The transition from herd kinetics ( Eq. 6) to fractal kinetics ( Eq. 4, h>1) can be gradual during this fuzzy period, with both equations operating concurrently. The prevalence of fractal kinetics during the lockdown period results in an asymptotic approach of I( t) to the steady state, i.e., I( t) = (1+ c) -1 (see Eq. 5, Figure 3B); according to Eq. 4 the higher the value of the fractal exponent of time h, the more rapid is the approach of I( t) to the steady state. This pattern we call “Herd-Fuzzy-Fractal” (HFF) kinetic motif. When the confirmed new cases reach a steady state, governments relax lockdown rules. In theory, when such a decision is taken, the termination of the first wave of the pandemic has been accomplished. However, the relaxation of lockdown measures in conjunction with the large number of infected individuals at steady state can, after a while, initiate a second wave of the pandemic leading to the application of new preventive measures and new lockdown rules. Consequently, a second wave of the disease emerges ( Figures 3C and 3D); hence, the (HFF) 2 kinetic motif.
Figure 3.

A schematic of the “Herd-Fuzzy-Fractal-Herd-Fuzzy-Fractal” (HFF) 2 kinetic motif of COVID-19 pandemic.

The gray line segments indicate fuzzy periods. A–D. Subplots correspond to the four distinct periods of the kinetic motif. Equations and parameter values used: A: Eq. 6, β = 8, c = 3 × 10 16; B: Eq. 4, h = 4.5, α = 0.012 (time) −1, c = 240; C: Eq. 6, β = 1.18, c = 119350; D: Eq. 4, h = 8, α = 3.35 × 10 −3(time) −1, c = 20.

A schematic of the “Herd-Fuzzy-Fractal-Herd-Fuzzy-Fractal” (HFF) 2 kinetic motif of COVID-19 pandemic.

The gray line segments indicate fuzzy periods. A–D. Subplots correspond to the four distinct periods of the kinetic motif. Equations and parameter values used: A: Eq. 6, β = 8, c = 3 × 10 16; B: Eq. 4, h = 4.5, α = 0.012 (time) −1, c = 240; C: Eq. 6, β = 1.18, c = 119350; D: Eq. 4, h = 8, α = 3.35 × 10 −3(time) −1, c = 20.

Analysis of COVID-19 data

We focused on the data of four model countries, namely, France, Greece, Italy, and Spain. Figure 4 shows for each one of the four countries, the fittings of Eqs. 6 and 4 to herd- and fractal-kinetics’ periods’ data, respectively. Parameter estimates derived are listed in Table 1. High R values listed in this Table indicate that the model of Eqs. 4 and 6, for all four countries, is in excellent agreement with the disease data except Italy’s fourth fractal kinetics’ period data.
Figure 4.

Best fits (solid lines) of Eqs. 6 and 4 for the herd kinetics periods and fractal kinetics periods, respectively, to data (points) for France, Greece, Italy and Spain.

The data correspond from time zero up to 10 December 2020. The gray line segments indicate fuzzy periods.

Table 1.

Estimates for the parameters of Eqs 6 and 4 derived from the fittings to herd kinetics periods and fractal kinetics periods data respectively, of France, Greece, Italy and Spain.

Estimates of the secondary parameters t ip, t 90%, steady state infected fraction are also listed.

ParametersFranceGreeceItalySpain
β herd1 11.69 ± 0.092.38 ± 0.067.87 ± 0.1311.09 ± 0.19
α fractal 2 (days) −l 0.01 ± 4.89 × 10 −5 0.02 ± 1.96 × 10 −4 0.012 ± 1.69 × 10 −5 0.01 ± 3.33 × 10 −5
h fractal 2 4.71 ± 0.092.93 ± 0.064.39 ± 0.0215.14 ± 0.06
c fractal 2 386.52 ± 2.563227 ± 30.19238 ± 0.36184 ± 0.54
β herd 3 5.08 ± 0.083.80 ± 0.041.17 ± 0.023.56 ± 0.04
α fractal 4 (days) −1 0.003 ± l.348 × 10 −5 0.003 ± 4.055 × 10 −5 high uncertainty value 0.003 ± 5.62 × 10 −5
h fractal 4 16.11 ± 0.549.01 ± 0.42 high uncertainty value 6.28 ± 0.43
c fractal 4 25.50 ± 0.2953.58 ± 2.61 high uncertainty value 17.96 ± 0.94
R 1 2 I 0.9990.9940.9970.996
R 2 2 I 0.9900.9930.9990.996
R 3 2 I 0.9840.9910.9920.993
R 4 2 I 0.9950.9960.9950.991
t ip (estimated - observed) (days) II 17.6–1824.4–25 high uncertainty value 21.5–23
t 90% (days) III 31.9 ± 1.467.1 ± 4.2 high uncertainty value 63.6 ± 6.1
I( t→∞) IV 0.038 ± 0.0010.018 ± 0.001 high uncertainty value 0.053 ± 0.003

I: coefficient of determination.

II: estimated from numerical solution of second derivative.

III: estimated from equation 13.

IV: estimated from equation 5.

Best fits (solid lines) of Eqs. 6 and 4 for the herd kinetics periods and fractal kinetics periods, respectively, to data (points) for France, Greece, Italy and Spain.

The data correspond from time zero up to 10 December 2020. The gray line segments indicate fuzzy periods.

Estimates for the parameters of Eqs 6 and 4 derived from the fittings to herd kinetics periods and fractal kinetics periods data respectively, of France, Greece, Italy and Spain.

Estimates of the secondary parameters t ip, t 90%, steady state infected fraction are also listed. I: coefficient of determination. II: estimated from numerical solution of second derivative. III: estimated from equation 13. IV: estimated from equation 5. For the first herd kinetics’ period, the estimate for β herd 1 in Greece was found to be 2.38 ± 0.06, which is much smaller than for the other three countries. This is in agreement with the remarkably lower initial I(t) profile of Greece in Figure 4. We should emphasize the valid estimation of the parameter β herd1 for all countries studied. This is clear proof that the initial phase follows a power of time function ( Eq. 6) which is contrary to the general belief that the initial phase increases exponentially. This subexponential increase has been observed in the early phase of COVID-19 spreading in different parts of China. During the first fractal kinetics’ period, the estimate for α fractal 2 in Greece was also higher, 0.02 ± 2 × 10 −4 (days) −1 compared with 0.010–0.012 (days) -1 found for the other three countries. This leads to a shorter half-life of 42 days for Greece compared with an average of 63 days for the three other countries; this, coupled with the earlier lockdown rules imposed in Greece, explains the more rapid approach to the steady state ( Figure 4). The fractal exponent h fractal 2 was smaller in Greece, 2.93 ± 0.06, while for France, Italy and Spain it was 4.71 ± 0.09, 4.39 ± 0.02, 5.14 ± 0.06, respectively ( Table 1). On the contrary, the estimate for c fractal 2 in Greece 3227 ± 30.19 was roughly ten-times higher than in the other three countries, resulting in much lower I( t) steady-state value. All countries remained in a slightly moving upwards quasi-steady state for 2–3 months ( Figure 4). This period was followed by a gradually increasing phase in the number of confirmed infected cases. Relaxed rules led to higher population mobility. All countries re-entered a herd kinetics’ period (blue concaving upwards segment in Figure 4). The estimates for β herd 3 were found 1.17 ± 0.02, 3.56 ± 0.04, 3.80 ± 0.04, 5.08 ± 0.08 for Italy, Spain, Greece and France, respectively, in full agreement with the visually increasing “curvature” of the blue concaving upwards segment of the four countries. All countries imposed preventive measures and lockdown rules several times ( Figure 4). For France, Greece and Spain a remarkably similar reliable estimate for α fractal 4, 0.003 (days) −1 was found; this is indicative of a slow process with a half-life of 231 days. However, different h fractal 4 estimates, 16.11 ± 0.54 , 9.01 ± 0.42 and 6.28 ± 0.43 were found for France, Greece, and Spain , respectively. Assuming that the conditions will not change in the next time period, predictions, based on the parameter estimates of the fourth fractal kinetics period for the steady-state value and t 90%, can be made for the three countries ( Table 1). On the contrary, the fitting of Eq. 4 to Italy’s fourth fractal kinetics’ period data was not equally successful and reliable parameters estimates for h fractal 4, α fractal 4 and c fractal 4 were not derived ( Table 1). This is due to the fact that the point of inflection has not been reached yet and therefore the fitting algorithm cannot converge to reliable parameters estimates. The estimates for t ip reported in Table 1 for France, Greece and Spain correspond to time (days) from the commencement of the fourth fractal kinetics’ period. These estimates were found to be in agreement with the observed values, which is an additional piece of evidence for the validity of the fractal model. An estimate for Italy’s t ip was not obtained for reasons mentioned above. Besides, the fourth fractal kinetics period data were used to predict the t 90% (expressed in days from the commencement of this period) and the final steady-state (1/(1+ c)) for France, Greece and Spain ( Table 1).

Analysis of COVID-19 data for countries deviating from the (HFF) 2 kinetic motif

A large number of countries, besides the four analyzed, followed the (HFF) 2 kinetic motif shown in Figure 4, e.g., Australia, China, Germany, Austria, United Kingdom. Yet, several countries did not exhibit the (HFF) 2 motif, lacking a second wave and followed a “herd-fuzzy-fractal” (HFF) kinetic motif. Argentina and Brazil are examples of countries where strict/mild preventive measures were either not applied or did not work effectively. Both countries exhibit an (HFF) kinetic motif, Figure 5. Parameter values determined: Argentina, 1 st stage: ( h = 1), β = 1.929 ± 0.028; 2 nd stage: h = 2.189 ± 0.043, α = (1.754 ± 0.067) × 10 −3 (days) −1, c = 3.61 ± 0.38; Brazil, 1 st stage: ( h = 1), β = 4.633 ± 0.017; 2 nd stage: h = 2.892 ± 0.023, α = (4.044 ± 0.017) × 10 −3 (days) −1, c = 21.86 ± 0.24.
Figure 5.

I( t) versus time plots for Argentina and Brazil.

Xs mark the implementation of mild preventive measures. The gray lines indicate the fuzzy period after the X point.

I( t) versus time plots for Argentina and Brazil.

Xs mark the implementation of mild preventive measures. The gray lines indicate the fuzzy period after the X point. On the other hand, some countries exhibited a more complex pattern, which deviates from the (HFF) 2 and (HFF) motifs. Infection data for USA did not follow either the (HFF) 2 or the (HFF) kinetic motif. The I( t) time profile never reached a steady state and the shape of the curve indicates a deformed three-wave like kinetic profile ( Figure 6). Probably both types of kinetics (herd and fractal) run concurrently for most of the time throughout the course of the pandemic, with the contribution of each varying with time. This is most likely due to different COVID-19 policy containment measures followed in different states around the country. Sweden intentionally applied the herd immunity strategy during the COVID-19 pandemic. An initial herd-kinetics type continuous increase in the number of total infected cases reached a point of inflection around 20 July 2020, followed by a slower rate of increase of infected cases, ( Figure 6). Since neither strict measures nor lockdown rules were applied at that time, the shape of the curve should be attributed to a fractal kinetics-like self-organization of the society. A rather sharp increase after 10 September 2020 can be attributed to the increased mobility of the individuals since no relaxation measures were taken close to this date.
Figure 6.

Confirmed infected cases for USA and Sweden.

Confirmed infected cases for USA and Sweden.

Implications

The above results ( Figures 2, 3, Table 1) demonstrate that the fractal kinetics SI model is more akin to real life. Since the well-mixed hypothesis is the crux of the matter of the epidemiological models, the use of not well-mixed hypothesis has important implications, which can metamorphosize airborne pandemics; these implications are discussed and itemized (designated with italics) below.

The reproductive number

The reproductive number, R 0 is not needed for the initial growth of the disease being incompatible with the not well-mixed hypothesis, Figure 1. Limitations associated with the estimation of R , can be found in numerous publications. Our results show that the time exponent β of Eq. 6 controls the time evolution of the disease throughout the initial herd kinetics’ period. In other words, β drives the initial phase of the disease spreading being the slope of Eq. 7, i.e. a linearized form of Eq. 6. The predominant role of β during the herd kinetics’ period can be also concluded from Eq. 12, which explicitly shows that the infected population fraction at the inflection point, I( t) is solely dependent on β. Although R 0 and β are different, however, they can be used complementary to each other during the initial stages of the pandemics. Estimates for β derived from the analysis of herd kinetics’ period data at two time points from 100 countries are shown in Figure 7 and Table 2. The degree of uncertainty (standard deviation) for the estimates was found in most cases small; this was accompanied with high correlation coefficients (not shown). Overall, the estimates derived from the longer period of 35 days seem to be either similar or higher or significantly higher than these derived from the analysis of the shorter period (10 days) data. For some countries, the small number of confirmed infected cases in the first 10 days did not allow the estimation of β. In view of the diversity and variability of data presented in Figure 7, we quote the median values derived from the analysis of 100 countries, 2.44 (0.25–12.24) and 1.34 (0.20–6.13) for the β estimates corresponding to 35 and 10 days, respectively.
Figure 7.

A bar plot of 100 countries based on the estimates with standard deviations for β, derived from the nonlinear regression analysis of data using Eq. 6.

Data of 10 and 35 days, after the first reported case, were analyzed. See also Table 2.

Table 2.

β values and associated uncertainties ( σ) and fitting corresponding coefficients of determination ( R) derived from nonlinear regression analysis of data from 100 countries using Eq. 6.

Data of 10 and 35 days, after the first reported case, were analyzed. Part of these results is shown in Figure 7. Blanks are due to fragmented data that prevented the fitting procedure to converge.

#Country β 35 σ(β 35 ) N R β 10 σ(β 10 ) N R
1United Arab Emirates1.1540.107360.995820.6730.14517110.979075
2Qatar1.3290.126320.996391.2580.1177380.988578
3Singapore1.2940.054360.996491.3890.14623110.992743
4Lebanon3.10.067320.999144.0120.56454110.998925
5Israel5.8910.136330.999742.2820.39644100.99666
6Azerbaijan3.7430.093290.999352.0710.2279450.992274
7Algeria3.8790.079310.999423.8940.4451890.998676
8South Africa1.8910.129340.998042.6050.4331590.997136
9United States of America1.9860.286360.998251.240.22384110.991278
10Canada0.920.094360.994170.6520.07839110.978231
11Egypt4.4180.169320.9995511
12Australia0.6830.043360.991280.950.12042110.986863
13Yemen5.3730.144360.9997111
14Saudi Arabia2.5920.064330.998842.9550.3409780.997505
15Afghanistan3.4360.174260.999197
16Iraq3.0480.093340.999141.7260.10908110.994959
17South Korea5.90.27360.999970.9960.15335110.987751
18Thailand1.50.089360.997220.990.23089110.987646
19Iran2.2830.053360.998624.1980.17418110.999016
20Turkey2.8750.043340.999053.7650.161190.998585
21Vietnam0.6920.065360.991431.6020.35587110.994278
22Philippines0.2470.034330.975410.6230.09151110.977024
23Japan2.3970.183360.998740.320.15916110.957422
24Bangladesh6.540.369300.999781.0840.2102650.975912
25Pakistan3.0920.118310.999120.8170.1581970.975079
26Indonesia2.2810.036290.998432.8480.3250550.995896
27India7.20.15360.999830.4280.07002110.966147
28China1.1880.072310.995620.9420.6056560.975897
29Antigua and Barbuda0.9130.046360.99411.1370.18016110.99
30Barbados1.4870.049340.997090.5930.1382690.971
31Bahamas0.3340.04310.979631.1530.2672160.982289
32Suriname2.0950.093340.998350.3810.1059490.956115
33Guyana1.4890.109350.997140.8020.05252100.981859
34Jamaica0.8560.03360.993551.2750.07792110.991663
35Uruguay2.4680.029360.99881.920.13438110.995809
36Panama1.7150.049350.997731.1680.09999100.989569
37Costa Rica1.9210.038360.998151.7350.21188110.995005
38El Salvador0.9280.046360.994240.4460.1619110.967419
39Nicaragua1.6410.052320.997430.7840.111770.973687
40Paraguay1.7550.087340.997781.5250.2257390.992582
41Honduras2.8430.098270.998891.8940.4631130.982547
42Dominican Republic2.5410.032330.99881.6730.1452380.992942
43Cuba1.50.058360.997221.2460.25306110.991344
44Haiti2.430.052350.998740.8520.11752100.983297
45Bolivia3.0110.099310.999080.8640.092280.979807
46Equador2.6750.088360.998961.2450.10828110.991338
47Guatemala3.2330.058350.999242.3240.12754100.996768
48Chile0.8310.039360.993281.1330.31607110.989937
49Venezuela5.3610.255350.99972.4160.186100.996989
50Peru2.6240.066330.998861.920.2085480.994462
51Argentina2.5630.04320.99882.0360.1756770.994346
52Colombia0.7510.078360.9922911
53Mexico4.8140.125360.999645.3480.90313110.999395
54Brazil1.420.053350.996891.7890.17175100.994858
55San Marino1.0510.072300.994610.5850.2151750.94762
56Liechtenstein1.240.046240.995163
57Monaco2.5390.057360.998851.7170.14569110.994915
58Iceland2.0650.239280.99812.9040.7679160.996674
59Belarus10.440.415360.999921.3710.30641110.992587
60United Kingdom2.2120.099290.998341.7070.2141550.988902
61Luxembourg1.1480.064360.995781.8670.15733110.995599
62Montenegro2.6670.071270.998760.9420.6056760.975901
63North Macedonia3.5380.065340.999351.7430.231790.994102
64Moldova2.5560.048350.998851.6430.21845100.994054
65Hungary3.4380.086360.999336.1380.86169110.999545
66Switzerland1.4910.031350.997153.1690.15303100.998181
67Slovenia1.8530.045350.9982.8220.08282100.997738
68Slovakia3.3580.057330.999271.2640.1613680.988674
69Serbia2.8870.105270.998924
70Lithuania2.1020.066320.99831.8450.1895470.993247
71Latvia1.8550.059360.998042.6880.25161110.997706
72Malta1.7990.056330.997832.7980.5765180.997231
73Georgia2.1140.074310.998284.3620.6600670.998736
74Estonia1.8820.046340.998021.3040.1180290.990376
75Cyprus2.8840.066360.999092.9920.27071110.998119
76Czechia9.1350.462360.999911
77Belgium2.1940.037270.998252
78Armenia1.6670.042360.997661.280.09468110.991712
79Albania4.10.112330.999491.0130.04827100.987014
80Croatia1.4970.027340.997121.7250.1010690.993996
81Bulgaria7.20.15360.999830.4280.07002110.966147
82China2.4320.051360.998770.9950.1101110.987732
83Kazakhstan0.3750.161360.9831611
84Russia4.5310.075340.999592.1660.4326690.995986
85Romania3.1110.149260.999032
86Ukraine2.8750.043340.999053.7650.161190.998585
87Turkey2.3460.034340.998643.4930.328390.998361
88Greece7.5631.321340.9998411
89Finland2.5320.049360.998852.8880.1294110.997991
90Norway2.1910.082360.998522.8570.21442110.99795
91Denmark3.2440.054340.999231.9160.2674390.995004
92Ireland3.50.061360.999353.750.12038110.998774
93Netherlands3.1920.02340.999212.5330.1742490.996984
94Poland3.4180.098360.999332.1760.13686110.99664
95Portugal12.240.159360.999940.320.15915110.957416
96Spain1.8040.419360.997950.4540.077110.967925
97France8.1390.145360.9998711
98Italy10.040.991360.999910.7880.06693110.982925
99Germany10.460.196360.9999211
100Sweden3.7990.114360.999443.2110.41481110.998352

A bar plot of 100 countries based on the estimates with standard deviations for β, derived from the nonlinear regression analysis of data using Eq. 6.

Data of 10 and 35 days, after the first reported case, were analyzed. See also Table 2.

β values and associated uncertainties ( σ) and fitting corresponding coefficients of determination ( R) derived from nonlinear regression analysis of data from 100 countries using Eq. 6.

Data of 10 and 35 days, after the first reported case, were analyzed. Part of these results is shown in Figure 7. Blanks are due to fragmented data that prevented the fitting procedure to converge.

Exponential versus power growth

The classical phraseology “ the exponential growth of the disease” used by medical doctors, scientists and laymen is questionable. This phrase is related to the approximate solution of the SIR model, which is an exponential function, when the parameter of the recovery rate is equal to zero. Based on our theoretical results and the good fittings of Eq. 6 to data of herd kinetics’ period ( Figure 4), “the herd kinetics’ period seems to obey a power of time function”. According to Eq. 2, β drives the disease spreading when h = 1 and the rate of infection is inversely proportional to time. This is in agreement with the real-life conditions because of the continuous reduction of the probability of infection as a function of time ( β/ t). However, the resemblance of the I( t) profiles of the classical, h = 0 and the special case h = 1 in Figure 2 makes the discernment of the kinetics of the initial phase difficult. Herd immunity Herd immunity calculations rely on an estimate for R 0 and syllogisms based on the relative magnitude, λ = R( t)/ R 0, which is the proportion of the population that is susceptible to catching the disease. If preventive measures are not applied, an estimate for the time needed to reach a certain level of the infected population fraction, e.g., I( t) = 0.6 ensuring herd immunity can be obtained from Eq. 7. Assuming an infected individual at time t=1, i.e., , where N is the population of the country, then, from Eq. 7, we get c = N − 1 ≈ N. Hence, the time t hi needed to reach a certain level of herd immunity I ( t hi) under non preventive measures is Figure 8 shows t hi as a function of β and N assigning I ( t hi) = 0.6. It can be seen that population size has a mild effect, whereas the apparent transmissibility constant β severely reduces t hi. Eq. 14 can be used at the initial stages of the pandemics and requires only a valid estimate for β. This will certainly provide valuable information for authorities, if coupled with estimates of the mortality rate and deaths, prior to a decision for a herd-immunity policy. Caution should be exercised with the use of Eq. 14, since it can be applied only under the strict assumption of herd kinetics operating throughout the entire period of the disease spreading. The example of Sweden ( Figure 6) shows that societies can exhibit self-organization and move to a fractal kinetics’ mode.
Figure 8.

A contour plot based on Eq. 14 showing the time required to reach herd immunity level I ( t hi) = 0.6 for various values of parameter β and population size N.

A contour plot based on Eq. 14 showing the time required to reach herd immunity level I ( t hi) = 0.6 for various values of parameter β and population size N. Deviation from the herd kinetic profile after the imposition of lockdown Cumulative data of infected people from nine countries (Austria, Belgium, Denmark, France, Germany, Italy, Spain, Switzerland, United Kingdom) were gathered and analyzed under two different prisms. Analysis was broken down into two parts, before and after imposition of strict preventive measures (lockdown) ( Figure 9). For the first period, the herd kinetic motif where h = 1 ( Eq. 6) was found to be adequate, whereas after lockdown clearly fails. The latter period was also analyzed using the fractal kinetic motif of h > 1 with very persuasive goodness of fit ( Figure 9). In all cases, R 2 was greater than 0.98. This pictorial divergence shows that after implementing mobility restrictions the evolution of the pandemic could not be captured by a power law expression, but rather by a fractal kinetic one ( Eq. 4) which eventually leads to a plateau of cumulative cases.
Figure 9.

I( t) versus time plots for Austria, Belgium, Denmark, France, Germany, Italy, Spain, Switzerland, United Kingdom.

The blue dots represent cumulative infected cases up to lockdown datum points. The orange lines depict the power fit to these data. Purple dots represent data after lockdown imposition whereas the purple lines are their superimposed fractal fits. Red lines depict the hypothetical power fit to the aforementioned data points in the event that Covid-19 propagation followed a power law pattern. R 2 values for all nine countries were measured higher than 0.98.

I( t) versus time plots for Austria, Belgium, Denmark, France, Germany, Italy, Spain, Switzerland, United Kingdom.

The blue dots represent cumulative infected cases up to lockdown datum points. The orange lines depict the power fit to these data. Purple dots represent data after lockdown imposition whereas the purple lines are their superimposed fractal fits. Red lines depict the hypothetical power fit to the aforementioned data points in the event that Covid-19 propagation followed a power law pattern. R 2 values for all nine countries were measured higher than 0.98. Model predictions According to Jewell et al., the ability of current models to predict is very poor. Our work demonstrates that the herd kinetics’ period is described by Eq. 6, while the kinetic motif “herd-fuzzy-fractal” should be taken into account in the modeling work. Apparently, these approaches have not been implemented so far. Roughly, predictions during the herd kinetics’ period can be based on a valid estimate for β, Eq. 6. Under preventive measures, valid estimates for the parameters of the model ( Eq. 4, h>1) can be derived and used for predictive purposes provided that data beyond the point of inflection are available (see Table 1).

Conclusions

Since the early days of epidemics’ modeling, a great deal of work has been done and now there is a change of paradigm. Interestingly, the results of our work are in full agreement with the basic conclusion of the most recent, extensive and elegant COVID-19 study based on the effective reproduction number R( t), “… that major non-pharmaceutical interventions—and lockdowns in particular—have had a large effect on reducing transmission”. Our approach quantifies this large effect on the basis of Eq. 4, which captures the dynamics of the disease under “herd kinetics’” and “fractal kinetics’” conditions. In addition, our herd kinetics’ period results are in full agreement with the observations of the distinctive subexponential increase of confirmed cases during the early phase of the epidemic in China, contrasting an initial exponential growth expected for an unconstrained outbreak. The present fractal SI model can be extended to its SIR analogue, with the caveat that the corresponding differential equations require numerical solution. In conclusion, the fractal kinetics SI model with the kinetically established herd period as well as the (HFF) 2 or (HFF) kinetic motifs opens up a new era in the field of epidemiological models for airborne pandemics. This is a timely and interesting contribution to the study of the dynamics of the COVID-19. Since some models do not capture well the dynamics, it is considered a fractional principle. Fractal and fractional models have considered, for example in Ndaïrou et al. (2021 ) and Bushnaq et al. (2021 ). I would recommend to continue this approach with updated data. Is the work clearly and accurately presented and does it cite the current literature? Partly If applicable, is the statistical analysis and its interpretation appropriate? Yes Are all the source data underlying the results available to ensure full reproducibility? Yes Is the study design appropriate and is the work technically sound? Yes Are the conclusions drawn adequately supported by the results? Yes Are sufficient details of methods and analysis provided to allow replication by others? Yes Reviewer Expertise: Pure and Applied Mathematics, Biomathematics I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard. Thanks for the opportunity to review this manuscript. This article by Panos Macheras, Athanasios A. Tsekouras and Pavlos Chryssafidis gives a consistent analysis for a not well-mixed system using fractal kinetic principles. They derived a three arameter model and show that the fractal exponent of time larger than unity can capture the impact of preventive measures affecting population mobility, and lead to the conclusion that the fractal kinetics model can be used as a prototype for the analysis of all contagious airborne pandemics. Overall, The study is well-designed and data analyses are well performed. Is the work clearly and accurately presented and does it cite the current literature? Yes If applicable, is the statistical analysis and its interpretation appropriate? I cannot comment. A qualified statistician is required. Are all the source data underlying the results available to ensure full reproducibility? Yes Is the study design appropriate and is the work technically sound? Yes Are the conclusions drawn adequately supported by the results? Yes Are sufficient details of methods and analysis provided to allow replication by others? Yes Reviewer Expertise: NA I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard. Overall this is an important contribution, pointing out the occasionally fallacious assumption in epidemiological theories of a “well stirred” population. While in many chemical reactions “well stirred” conditions are met, or taken care of to be met, the adoption in the standard epidemiology approaches of a similar condition is questionable. While it may be a good approximation for an animal model, or for a primitive society where no precautions against infection are practiced, this is questionable for a modern society, where isolation of the sick and preventive measures by the healthy, e.g., wearing masks, are a standard, or even mandated modus operandi. This justifies rejecting the “classical reaction kinetics” model and replacing it by a “non-classical reaction kinetics” model, which was originally called “fractal reaction kinetics” (Ref 8). While with the new model more adjustable parameters are introduced, which should be emphasized by the authors, the agreement with the spread of Covid in a large number of countries is impressive. So is the agreement of the classical limit (“h=0”) with the spread of the pandemic in Sweden, where no preventive restrictions were adopted, with the aim of reaching “herd immunity” (an animal model). Minor Comments: Explain better the definition of the last factor in Eq. 1. Explain better the definition of the last factor in Eq. 2. Also discuss the positive vs. negative values of h. Straighten out and explain eq. 3. Carefully define “alpha” in eq. 4. In Eq. 6, explain wherefrom comes “11”. Eq. 8, ditto. Eq. 10, ditto. Eq. 12, explain wherefrom comes “12”. Eq. 13, explain wherefrom comes “11”. Clarify eq. 14. Is the work clearly and accurately presented and does it cite the current literature? Yes If applicable, is the statistical analysis and its interpretation appropriate? Yes Are all the source data underlying the results available to ensure full reproducibility? Yes Is the study design appropriate and is the work technically sound? Yes Are the conclusions drawn adequately supported by the results? Partly Are sufficient details of methods and analysis provided to allow replication by others? Yes Reviewer Expertise: NA I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above. Response to comments by R. Copelman. We thank the reviewer for his constructive critique. Regarding the minor comments and questions, we have the following replies to each point raised. Explain better the definition of the last factor in Eq. 1. Response: This equation is presented in detail in Ref. 11. Explain better the definition of the last factor in Eq. 2. Also, discuss the positive vs. negative values of h. Response: [1- I( t)] is the fraction of the susceptible population. Negative h values don't come up in actual data. Straighten out and explain eq. 3. Response: Eq. 3 is described in Ref. 7. Carefully define “alpha” in eq. 4. Response: See line above Eq. 4. In Eq. 6, explain wherefrom comes “11”. Response: What does "11" stand for? There is no "11" in Eq. 6. Eq. 6 is derived from Eq. 3 by taking the limit h->1 and implementing L'Hopital's rule, i.e., taking the derivative of numerator and denominator in the exponent and then taking the limit. We will clarify the point in the next version of the text. Eq. 8, ditto. Response: Eq. 8 is derived from Eq. 7 after doing some straightforward algebra. Eq. 10, ditto. Response: The derivation of Eq. 10 is described right before Eq. 9 and repeated before Eq. 11. Eq. 12, explain wherefrom comes “12”. Response: Eq. 12 is derived from Eq. 6 following the procedure described before Eq. 9. Eq. 13, explain wherefrom comes “11”. Response: Eq. 13 is derived from Eq. 4 by setting the right-hand side of the latter equal to 0.9 times I( t->infinity) and solving for t. Clarify eq. 14. Response: Eq. 14 tells us when the fraction of infected individuals will reach a certain level given the size of the population and exponent β. Here again, we will add a brief explanation in the updated version of the text.
  20 in total

1.  Michaelis-Menten kinetics under spatially constrained conditions: application to mibefradil pharmacokinetics.

Authors:  Kosmas Kosmidis; Vangelis Karalis; Panos Argyrakis; Panos Macheras
Journal:  Biophys J       Date:  2004-09       Impact factor: 4.033

2.  Fractal pharmacokinetics of the drug mibefradil in the liver.

Authors:  J Fuite; R Marsh; J Tuszyński
Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2002-08-13

Review 3.  Gastrointestinal drug absorption: is it time to consider heterogeneity as well as homogeneity?

Authors:  P Macheras; P Argyrakis
Journal:  Pharm Res       Date:  1997-07       Impact factor: 4.200

4.  Carrier-mediated transport can obey fractal kinetics.

Authors:  P Macheras
Journal:  Pharm Res       Date:  1995-04       Impact factor: 4.200

5.  Fractal-like kinetics of the solid-state anaerobic digestion.

Authors:  Zhi-Wu Wang; Fuqing Xu; Karthik R Manchala; Yewei Sun; Yebo Li
Journal:  Waste Manag       Date:  2016-04-25       Impact factor: 7.145

6.  Estimating the effects of non-pharmaceutical interventions on COVID-19 in Europe.

Authors:  Seth Flaxman; Swapnil Mishra; Axel Gandy; H Juliette T Unwin; Thomas A Mellan; Helen Coupland; Charles Whittaker; Harrison Zhu; Tresnia Berah; Jeffrey W Eaton; Mélodie Monod; Azra C Ghani; Christl A Donnelly; Steven Riley; Michaela A C Vollmer; Neil M Ferguson; Lucy C Okell; Samir Bhatt
Journal:  Nature       Date:  2020-06-08       Impact factor: 49.962

7.  Fractal-like kinetics of intracellular enzymatic reactions: a chemical framework of endotoxin tolerance and a possible non-specific contribution of macromolecular crowding to cross-tolerance.

Authors:  Catalin Vasilescu; Mircea Olteanu; Paul Flondor; George A Calin
Journal:  Theor Biol Med Model       Date:  2013-09-14       Impact factor: 2.432

8.  A fractal kinetics SI model can explain the dynamics of COVID-19 epidemics.

Authors:  Kosmas Kosmidis; Panos Macheras
Journal:  PLoS One       Date:  2020-08-11       Impact factor: 3.240

9.  Effective containment explains subexponential growth in recent confirmed COVID-19 cases in China.

Authors:  Benjamin F Maier; Dirk Brockmann
Journal:  Science       Date:  2020-04-08       Impact factor: 47.728

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