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Geographically selective assortment of cycles in pandemics: meta-analysis of data collected by Chizhevsky

Published online by Cambridge University Press:  11 December 2012

L. GUMAROVA
Affiliation:
Halberg Chronobiology Center, University of Minnesota, Minneapolis, MN, USA
G. CORNÉLISSEN
Affiliation:
Halberg Chronobiology Center, University of Minnesota, Minneapolis, MN, USA
D. HILLMAN
Affiliation:
Halberg Chronobiology Center, University of Minnesota, Minneapolis, MN, USA
F. HALBERG*
Affiliation:
Halberg Chronobiology Center, University of Minnesota, Minneapolis, MN, USA
*
*Author for correspondence: Dr F. Halberg, Halberg Chronobiology Center, University of Minnesota – MMC8609, 420 Delaware Street SE, Minneapolis, MN 55455, USA. (Email: halbe001@umn.edu)
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Summary

In the incidence patterns of cholera, diphtheria and croup during the past when they were of epidemic proportions, we document a set of cycles (periods), one of which was reported and discussed by A. L. Chizhevsky in the same data with emphasis on the mirroring in human disease of the ∼11-year sunspot cycle. The data in this study are based on Chizhevsky's book The Terrestrial Echo of Solar Storms and on records from the World Health Organization. For meta-analysis, we used the extended linear and nonlinear cosinor. We found a geographically selective assortment of various cycles characterizing the epidemiology of infections, which is the documented novel topic of this paper, complementing the earlier finding in the 21st century or shortly before, of a geographically selective assortment of cycles characterizing human sudden cardiac death. Solar effects, if any, interact with geophysical processes in contributing to this assortment.

Type
Original Papers
Copyright
Copyright © Cambridge University Press 2012 

INTRODUCTION

A look into the history of chronobiology, the science of the study of biological rhythms, cannot ignore the pioneering work of Alexander Leonidovich Chizhevsky [Reference Chizhevsky1Reference Chizhevsky3], who investigated the influence of the rhythms of solar activity on mass manifestations in human life: epidemics, wars, riots and other phenomena.

In particular, Chizhevsky analysed data on cholera and diphtheria in detail. Analyses of his data are not only very interesting from a historical point of view, as a reconsideration of periods found, but they remain relevant today. Despite impressive advances in the field of immunology, cholera has not disappeared from the face of the earth. According to the World Health Organization, an estimated 3·5 million cases of cholera and 100 000–120 000 cholera deaths are reported annually. Periodic outbreaks of cholera are reported in India [Reference Jain49], Africa [6Reference Harris11] and Latin America [Reference Lam1215].

Chizhevsky rightly pointed out that the disease has never disappeared from the face of the earth [3, p. 117], and what was true in his day holds good today. Vibrio cholerae is a natural inhabitant of estuarine environments in countries where cholera is epidemic or non-epidemic [Reference Chun16]. Of course, in regions of Asia, Africa, and South America, where public sanitation is poor, the disease is still endemic or epidemic. Vaccination is recommended for people living in those areas [17]. Complete protection against cholera, however, seems unlikely according to recent research by epidemiologists, since, as in the case of influenza, the genome of cholera bacteria changes during certain cycles, perhaps in keeping also with a documented bacterial coperiodism [Reference Faraone18]. Much as in the case of influenza viruses, cholera bacteria undergo a ‘shift/drift cycle’ over time, although the drift in V. cholerae is derived mainly from lateral gene transfer, most likely occurring in the natural environment in association with its plankton hosts [Reference Colwell19, Reference Constantin de Magny20]. Thus, the issue of cholera pandemics returns to the issue of cycling. Chizhevsky, in his work, pointed out the connection between cycles of cholera outbreaks and outbreaks of solar activity. Indeed, among factors causing mutation, ionizing radiation from the sun is the most potent natural source [Reference Fabrikant21].

Against this background, we meta-analysed Chizhevsky's summary first [Reference Halberg22] and then turned from the graph we used for cross-correlation [Reference Sigel23] (Fig. 1), to his actual tabulations. Modern inferential statistical methods are used [Reference Marquardt24Reference Refinetti, Cornelissen and Halberg27], as is information obtained on other biospheric time series. However, an addition and subtraction, if not a remove and/or replace approach [Reference Halberg28, Reference Cornélissen29], which is essential to examine causal relations, remains to be implemented at the periods detected.

Fig. 1. Graph of A. L. Chizhevsky on cases of cholera recorded in Moscow between 1823 and 1923, published by Sigel [Reference Sigel23]. In this graph, the original data are folded over the ∼11-year solar activity cycle. The data show a peak incidence coinciding with maximal solar activity (left panel). Taking these folded data off the published graph, an analysis by cross-correlation of cholera incidence vs. Wolf numbers (WN) yields the largest correlation coefficient at a lag of zero (right) [Reference Halberg33]. (© Halberg.)

MATERIALS AND METHODS

We used the original statistical data from Chizhevsky's book [Reference Chizhevsky3] and official reports of the World Health Organization [Reference Pollitzer59, 14] about cholera and diphtheria in Russia and in several European countries (Prussia, Switzerland, Scotland, England, Ireland, Denmark, Sweden) and in India during the span from 1823 to 1953 (details in Table 1). A combination of linear and nonlinear cosinor methods [Reference Marquardt24Reference Refinetti, Cornelissen and Halberg27] served for temporally global analyses (of a time series as a whole). Plexograms, complemented by analyses of variance of the stacked data visualized signals detected by cosinor spectra [Reference Halberg25Reference Refinetti, Cornelissen and Halberg27].

Table 1. Geographical differences in cycles with periods, τ values, in the range of 5–32 years [note τ values of ∼17 years characterizing the incidence of infectious diseases (cholera, diphtheria, croup]

CI, Confidence interval (conservative); when CI of amplitude overlaps zero, one-parameter [1p] limits are also listed.

* Linear trend removed.

From zero-amplitude (no rhythm) test.

RESULTS

Cholera in India

In considering cholera in Asia, Chizhevsky devoted considerable attention to this disease in India, tracing its history back to 1031 a.d., and noting that the first description of cholera was by Hindu writers. The description of all pandemics of cholera by Chizhevsky begins with India, but the digital statistical material presented in the book covers the span only from 1901 to 1924. We found similar statistics in the annual and consolidated reports of the WHO for the same span in a series continued up to 1961 (Fig. 2).

Fig. 2 [colour online]. Plot of yearly mortality data from cholera in India from 1901 to 1961, shown as original values (solid curve) and after removal of a linear trend (dashed curve). Data from Chizhevsky (1901–1924) and from WHO reports (1920–1961) during 1920–1924 are the same in both sources. * Prediction of outbreaks by Chizhevsky (two correct). (© Halberg.)

The above span allows a check of Chizhevsky's forecast of outbreaks of cholera:

With regard to cholera, then, generally speaking, the latter is disappearing in countries with a high state of public sanitation and hygiene. Therefore, it is difficult to expect large epidemics in the countries of Europe or North America. From 1937–1939, 1948–1950, 1959–1960 and so on, however, an epidemic or local amplifications of cholera in the East can be expected. During these years, we should expect a sharp increase in the number of deaths from cholera in those of its foci, where it has or will occur, compared with all the intermediate years [3, p. 233].

In fact an outbreak of cholera occurred in India in 1938, with a particularly high number of deaths from cholera in 1943. Further outbreaks were reported in 1948, 1953 and 1957 (Fig. 2). Chizhevsky accurately predicted outbreaks of cholera in 1938 and 1948.

Spectral analysis revealed linearly a number of components with periods of ∼30·5, ∼19·4 and ∼11·7 years (Fig. 3). However, the subsequent processing of these components by nonlinear least squares validated with statistical significance only the ∼11·7-year period (τ), and then only after removing a linear trend. Estimates of the parameters are as follows: τ = 11·67 years, 95% confidence interval (CI) 10·64–13·11 years, amplitude 70·02 ± 20·7 (in thousands of cases), P= 0·024 from one-way ANOVA after stacking data according to this period by plexogram (Fig. 4).

Fig. 3. Least squares spectrum of yearly detrended data on mortality from cholera in India during 1901–1961. The ∼11·7-year cycle is detected with statistical significance and it is validated by nonlinear least squares, the period [and its confidence interval (CI)] being estimated as 11·668 (95% CI 10·44–12·895) years, similar to the ∼11-year solar activity cycle, as suggested by Chizhevsky. (© Halberg.)

Fig. 4. In order to visualize the waveform of the ∼11·7-year cycle characterizing mortality from cholera in India during 1901–1961, the yearly detrended data were stacked over an idealized 11·7-year scale (after removal of a linear trend), using five bins (classes). The ∼11·7-year component was found to be statistically significant by one-way analysis of variance (P = 0·024). Data from Chizhevsky (1901–1924) and from WHO reports (1920–1961) during 1920–1924 are the same in both sources. (© Halberg.)

The nonlinearly validated cycle of ∼11·7 years could correspond to the ∼11-year periodicity in solar activity known as the Horrebow–Schwabe sunspot cycle. Note an additional ∼19-year component and an ∼35-year (paratridecadal) cycle known as the BEL cycle (after Brückner, Egeson and Lockyer). That the latter two could not be validated nonlinearly does not exclude their likely presence, notably since an ∼35-year (BEL) cycle was also found for diphtheria and croup in Denmark.

Cholera in Russia

Chizhevsky described the dynamics of cholera in Russia for a 100-year span: from 1823 to 1923, also indicating the number of sunspots, the Wolf numbers, during this span (Fig. 5). We were able to find data by Robert Pollitzer [Reference Pollitzer5] on the European part of Russia in the records for the same span. Where these data overlap and can be checked, they are fully consistent with each other. Hence Pollitzer's data for 1925–1926 were added to Chizhevsky's data to obtain a series spanning 104 years. After 1926, we have no data of cholera in Russia available. Since the curve of incidence during epidemics covers a very large scale, from zero case in the good years to over 1 million deaths at the epidemic's peak, the data were transformed in order to reduce the extent of lack of fit by taking their square root prior to their linear-nonlinear analysis.

Fig. 5 [colour online]. Plot as a function of time of yearly data on mortality from cholera in Russia for 104 years (1823–1926) (solid curve), compared to changes in solar activity, gauged by Wolf numbers (dashed curve). Peaks in the incidence of cholera correspond to every other peak in solar activity, suggesting the presence of a ∼22-year (Hale) cycle. Data from Chizhevsky [Reference Chizhevsky3]. (© Halberg.)

Figure 5 shows that the cholera outbreaks do not accompany each cycle of solar activity, and seem to correspond to each second peak of solar activity, with a period of ∼22 years, the Hale sunspot bipolarity cycle [Reference Hale30]. By spectral analysis, the largest peak corresponds to an ∼20·8-year period, with additional components of gradually lesser prominence having periods of ∼5·6, ∼9·0 and ∼12·7 years (Fig. 6).

Fig. 6. Least squares spectrum of yearly data on mortality from cholera in Russia (1823–1926), revealing the presence of several peaks corresponding to components with periods of ∼21, 9, and 5·6 years. Whereas the ∼9-year cycle only reaches borderline statistical significance by nonlinear analysis, the other two components are validated with statistical significance. Period estimates and their CIs (given in parentheses) are listed above their respective spectral peaks. Nonlinear result and 95% confidence interval (CI); for 1823–1924, Chizhevsky's data [Reference Chizhevsky3] were used and compared with the data of Pollitzer [Reference Pollitzer5] and added for 1924–1926. * Found for Chizhevsky originally by Vladimir Shostakovich. Footnote Borderline significance (non-overlap of zero by CI of amplitude only with one-parameter CI). (© Halberg.)

Nonlinear analyses confirmed the statistical significance of these spectral components characterizing cholera in Russia. Figure 6 shows a cycle with a period of 20·71 (95% CI 18·55–22·88) years, with an amplitude of 104·8 (95% CI 5·7–203·9) and a MESOR (midline estimating statistic of rhythm) of 108 (95% CI 38–178). Chizhevsky noted that the period of 5·5 years was calculated by Vladimir Boleslavovich Shostakovich, a Russian geophysicist [Reference Chizhevsky3]. Chizhevsky considers this period as half an 11-year (Schwabe) cycle. According to our calculations, the period is of 5·6 years (95% CI 5·5–5·8) with an amplitude of 98·3 (95% CI 13–183). The 8·95-year (95% CI 8·36–9·54) cycle is detected with statistical significance: its amplitude is 78·2 (95% CI 28·2–128·2; one-parameter limitsFootnote , as the ‘conservative’ CI slightly overlaps zero). An 11-year cycle is not statistically significant in the dynamics of cholera in Russia during 1823–1926, even when using the already too liberal approach of Marquardt's one-parameter approachFootnote .

Plexograms (Fig. 7ac) and corresponding one-way ANOVAs confirmed the statistical significance of all three components (P < 0·05) in the statistics of deaths from cholera in Russia during 1823–1826, respectively.

Fig. 7 [colour online]. (a) In order to visualize the waveform of the ∼20·7-year cycle characterizing mortality from cholera in Russia during 1823–1926, the yearly data were stacked over an idealized 20·714-year scale, using 11 bins (classes). This component is validated with statistical significance both by cosinor (P = 0·004) and by one-way analysis of variance (P < 0·001). This component corresponds to a spectral peak and is validated nonlinearly, based on the ‘conservative’ CI (see earlier footnote for explanation of conservative CI). (b) In order to visualize the waveform of the ∼5·6-year cycle characterizing mortality from cholera in Russia during 1823–1926, the yearly data were stacked over an idealized 5·62-year scale, using six bins (classes). This component is validated with statistical significance both by cosinor (P = 0·002) and by one-way analysis of variance (P = 0·015). This component corresponds to a spectral peak and is validated nonlinearly, based on the ‘conservative’ CI (see earlier footnote for explanation of conservative CI). (c) In order to visualize the waveform of the ∼9-year cycle characterizing mortality from cholera in Russia during 1823–1926, the yearly data were stacked over an idealized 8·95-year scale, using five bins (classes). This component is validated with statistical significance both by cosinor (P = 0·019) and by one-way analysis of variance (P = 0·039). This component only reached borderline statistical significance by nonlinear analysis. For 1823–1923 data from Chizhevsky [Reference Chizhevsky3] were compared with data from Pollitzer [Reference Pollitzer5] and added for 1924–1926. (© Halberg.)

Diphtheria and croup

Chizhevsky also reported on other infectious diseases, notably diphtheria and croup. Here, we show the presence of several cycles that may correspond to the ∼11-year (Horrebow–Schwabe), the ∼22-year (Hale) and the ∼35-year (BEL) cycles, among others. Such correspondence can only prompt a subtraction-addition approach [Reference Halberg28, Reference Cornélissen29]. The use of special computer programs allows us to more accurately estimate the periods. A paradecadal cycle of 8·25–12·93 years was found in Denmark, Belgium, Switzerland, Scotland, England (and Wales) and Ireland, whereas in Austria, Italy, Romania and Sweden, the period length of the most prominent cycle was between 15 and 18·8 years (Table 1). In the dynamics of diphtheria in Kherson province (then South Russia, now Ukraine), statistically significant periodicities include a point estimate of 17 years, with others of 19·4 and 21 years, but with very wide overlapping CIs so that the periods cannot be separated. In Russia, only relapsing fever in Moscow had a prominent ∼10-year period [Table 1 (bottom)], a detail qualifying even a genius like Chizhevsky. If not an ‘echo’ only to the sun, the biosphere and the noosphere it created are resonators to both the sun and the earth, among others, and the various environmental influences compete (wrangle) with one or the other dominating in different geographical regions at the same time.

DISCUSSION

In different countries, and even in neighbouring regions that were then part of Russia, point estimates of different periods are statistically significant for the cases of the infectious diseases examined here. The criteria to be considered, however, are the CIs that in the case of diphtheria in Russia are so wide as to fail to support any difference in period. CIs are indispensable, their limitations that call for their improvement notwithstanding, since judgements based only on point estimates ignore the stochastic nature of environmental and biological variables. Better CIs that also account for the aeolian nature of time structures in and around us remain to be developed. It seems possible that ruling congruence in or out by the conservative limits of Marquardt's algorithm [Reference Marquardt24] may not strictly apply, but in the want of better CIs, the latter offer a compromise with practicability. With this qualification, results of currently prevailing non-communicable diseases were presented earlier [Reference Halberg22]. By the non-overlap of the CIs of the periods, the cycle lengths differ for the same disease, sudden cardiac death in different geographical regions (Table 2). Existing geographical differences among countries differing relatively little in latitude are thus noted for both communicable and non-communicable diseases. Geomagnetic, interplanetary and solar influences may all interact (‘wrangle’) differentially in different geographical locations. We cannot speculate without further study beyond Sir Edward Appleton:

There are simple and fundamental reasons why collaborative effort is necessary in studying the influence of the sun's emanations on our own planet. First of all, the earth is round, and not flat. The result is that solar radiations do not impinge with equal effect on all regions of the earth's surface. The second reason is that the earth is constantly rotating; and, since interesting solar features may occur at any time, it is necessary to have observers at different terrestrial longitudes, in order that none of these interesting events may be missed. The third important fact is that the earth itself is a great magnet, and, because of this magnetic influence, electrified particles of solar origin are constrained to travel, not in straight lines, but along curved tracks. Sometimes the curvature of these tracks is so great that such charged particles impinge on the side of the earth's atmosphere which is further from the sun. In other words, we get solar effects at night. Moreover such effects occur with unequal intensity at different terrestrial latitudes because of the earth's magnetic qualities [Reference Appleton and Stetson31].

Table 2. Geomagnetic/geographical differences among cycles with periods in the range of 0·8–2·0 years, characterizing the incidence of myocardial infarction (MI) and sudden cardiac death*

T, Length of data series (y = years); ▵t, sampling interval (d = day, m = month); N, number of data (including 0 s); n.s., not significant.

Period and 95% confidence interval (CI) estimated by nonlinear least squares. In longer (10-year) series, a near-transyear (cycle with a period between 1·0 and 1·2 years) is detected for MIs in addition to a far-transyear. Brevity of series and lack of ordering statistical significance qualify results from Hong Kong. Note that transyears are found in 3/6 locations (P < 0·05 by linear least-squares) with a relative amplitude >12 (% of MESOR).

* With focus on transyears, with periods longer than 1·0 year (underlined; double underline for near-transyear).

International Classification of Diseases (ICD-10), code I46·1, excluding MI and sudden death of unknown or unspecified cause (except before 1999).

From linear least-squares analyses, not corrected for multiple testing. Amplitude expressed as N/day.

We can add, however, that in the language of frequencies, there are both similarities and differences among signatures of the solar wind's speed and of the antipodal index aa in the spectral region between 2 and 0·3 years (Table 3) [Reference Sidorin and Khalilov32, Reference Halberg33].

For the general reader, an annotated bibliography by John T. Burns [Reference Burns34] surveys alleged cosmic influence on influenza pandemics (p. 3), among other conditions such as Down syndrome (p. 2), suicide (p. 2), hip fractures (p. 3), myocardial infarctions (p. 5), poliomyelitis (p. 6), fetal growth (p. 7), births (p. 9) and affective disorders (p. 9). References to inferentially statistically assessed studies are also available in [Reference Halberg33, Reference Halberg, Cornélissen and Schwartzkopff35].

Table 3. Congruent* periods of helio-geomagnetics (columns 1 and 2), the estimation of 1-minute by a healthy man over 3·5 decades (column 3)

SW, Solar wind, aa, antipodal index.

* Based on weekly measurements; otherwise on daily measurements. Congruence defined by overlying or overlapping 95% confidence intervals given in parentheses. Congruence in the last column is designated as pertaining to the sun (S) or earth (E).

Solar wind/aa: 2/34 (5·882%); solar wind/1MTE: 5/34 (14·706%); aa/1MTE: 4/34 (11·765%); solar wind, aa and 1MTE all congruent: 3/34 (8·824%); No congruence: 19/34 (55·882%).

CONCLUSION

We detected cycles of different length in different geographical locations in the incidence patterns of cholera in India and Russia and of diphtheria and croup in various regions of Europe. A geographically selective assortment is thus documented for infectious diseases in the past, in keeping with such a selective assortment found earlier in recent years for sudden cardiac death. This selective assortment among decadal and multidecadal periods is also found among different variables of the same population and among and within individuals’ physiology, organ systems such as blood circulation, among variables and even among circadian characteristics such as MESOR vs. amplitude of the same variable of the same person [Reference Halberg33]. We may be dealing with genetically coded periods in the biosphere that could be driven off and on but are not consistently synchronized by competing space and earth weather, notably magnetism.

ACKNOWLEDGEMENTS

Support was received from GM-13981 (F.H.), University of Minnesota Supercomputing Institute (G.C., F.H.). The authors are greatly indebted to Professor S. Tuleukhanov of the Al-Farabi Kazakh National University for the original copy of the book The Terrestrial Echo of Solar Storms.

DECLARATION OF INTEREST

None.

Footnotes

Marquardt's algorithm [Reference Marquardt24] provides three measures of uncertainty of the period estimate and of the other parameters of the fitted model. One is an equivalent of the usual standard error and is called the ‘one-parameter’ approach. Another is called ‘conservative’ in the sense that the corresponding confidence intervals are slightly wider than the ‘true’ or ‘nonlinear’ 95% limits. The nonlinear limits, a third measure, are more complex, but generally do not differ much from the more easily derived ‘conservative’ approximation. In view of the non-stationarities of the biological data analysed, the approach called ‘conservative’ by Marquardt is actually too liberal and is used in the want of a more appropriate method that accounts for non-stationarities.

References

REFERENCES

1.Chizhevsky, AL. Les épidémies et les perturbations électromagnétiques du milieu extérieur. Paris: Éditions Hippocrate, 1938, 239 pp.Google Scholar
2.Chizhevsky, AL. Physical Factors of Historical Processes. Kaluga, Russia, 1924, pp. 72.Google Scholar
3.Chizhevsky, AL. The Terrestrial Echo of Solar Storms, 2nd edn. Moscow: Mysl, 1976, pp. 367.Google Scholar
4.Jain, M, et al. Multidrug resistant Vibrio cholerae O1 El Tor carrying classical ctxB allele involved in a cholera outbreak in South Western India. Acta Tropica 2011; 117: 152156.CrossRefGoogle Scholar
5.Pollitzer, R. Cholera. Monograph series (World Health Organization), no. 43. Geneva: World Health Organization, 1959, v. 43, 1019 pp.Google Scholar
6.WHO. World health statistics report: epidemiological and vital statistics report, 1920–1946. Geneva: World Health Organization, 1958, v. 11, pp. 616618.Google Scholar
7.WHO. World health statistics report: epidemiological and vital statistics report, 1947–1957. Geneva: World Health Organization, 1960, v. 13, pp. 360361.Google Scholar
8.Biraud, Y, Kaul, PM. Cholera: world distribution and prevalence of cholera in recent years: epidemiological and vital statistics report, 1947–1948. Geneva: World Health Organization, 1949, vol. 1, pp. 140152.Google Scholar
9.WHO. Annual epidemiological and vital statistics, 1961. Geneva: World Health Organization, 1964, 741 pp.Google Scholar
10.Mohamed, AA, et al. Molecular epidemiology of geographically dispersed Vibrio cholerae, Kenya, January 2009–May 2010. Emerging Infectious Diseases 2012; 18: 925931.CrossRefGoogle ScholarPubMed
11.Harris, JR, et al. Field evaluation of Crystal VC® Rapid Dipstick test for cholera during a cholera outbreak in Guinea-Bissau. Tropical Medicine & International Health 2009; 14: 11171121.CrossRefGoogle ScholarPubMed
12.Lam, C, et al. Evolution of seventh cholera pandemic and origin of 1991 epidemic, Latin America. Emerging Infectious Diseases 2010; 16: 11301132.CrossRefGoogle ScholarPubMed
13.Orent, W.Outbreaks around the world. Discover 2012; 33: 6969.Google Scholar
14.WHO. Annual epidemiological and vital statistics, 1961. Geneva: World Health Organization, 1964, 741 pp.Google Scholar
15.WHO. World: areas reporting cholera outbreaks, 2010–2011 (www.http://gamapserver.who.int/mapLibrary/app/searchResults.aspx). Accessed 24 January 2012.Google Scholar
16.Chun, JS, et al. Comparative genomics reveals mechanism for short-term and long-term clonal transitions in pandemic Vibrio cholerae. Proceedings of the National Academy of Sciences USA 2009; 106: 1544215447.CrossRefGoogle ScholarPubMed
17.Columbia Electronic Encyclopedia. Sixth edition. Cholera. Accessed 11 January 2011.Google Scholar
18.Faraone, P, et al. Anticipations on the deepenings of astrophysical influence on appearing of sectors in microbial colonies named CSD (some statistical correlations and reminiscences about lost CSD-data). CIFA News 2002; 31 (Suppl.): 115.Google Scholar
19.Colwell, RR. Global climate and infectious disease: the cholera paradigm. Science 1996; 274: 20252031.CrossRefGoogle ScholarPubMed
20.Constantin de Magny, G, et al. Environmental signatures associated with cholera epidemics. Proceedings of the National Academy of Sciences USA 2008; 105: 1767617681.CrossRefGoogle ScholarPubMed
21.Fabrikant, JI. Radiobiology. Chicago: Year Book Medical Publishers, 1972, pp. 421.Google Scholar
22.Halberg, F, et al. Essays on chronomics spawned by transdisciplinary chronobiology: Witness in time: Earl Elmer Bakken. Neuroendocrinology Letters 2001; 22: 359384.Google ScholarPubMed
23.Sigel, F. Vinovato solntse [The Sun is Guilty] (Dreier W, Lerche D, German translation; Göring H, scientific editor; German edition). Moscow: Verlag Mir/Leipzig: VEB Fachbuchverlag, 1975, pp. 215.Google Scholar
24.Marquardt, DW. An algorithm for least-squares estimation of nonlinear parameters. Journal of the Society for Industrial and Applied Mathematics 1963; 11: 431441.CrossRefGoogle Scholar
25.Halberg, F. Chronobiology: methodological problems. Acta Medica Romana 1980; 18: 399440.Google Scholar
26.Cornélissen, G, Halberg, F. Chronomedicine. In: Armitage, P, Colton, T, eds. Encyclopedia of Biostatistics, 2nd edn. Chichester, UK: John Wiley & Sons Ltd, 2005, pp. 796812.Google Scholar
27.Refinetti, R, Cornelissen, G, Halberg, F. Procedures for numerical analysis of circadian rhythms. Biological Rhythm Research 2007; 38: 275325.CrossRefGoogle ScholarPubMed
28.Halberg, F, et al. International BIOCOS Group. Chronobiology's progress: season's appreciations 2004–2005. Time-, frequency-, phase-, variable-, individual-, age- and site-specific chronomics. Journal of Applied Biomedicine 2006; 4: 138.CrossRefGoogle Scholar
29.Cornélissen, G, et al. Resonance of about-weekly human heart rate rhythm with solar activity change. Biologia (Bratislava) 1996; 51: 749756.Google ScholarPubMed
30.Hale, GE. Sun-spots as magnets and the periodic reversal of their polarity. Nature 1924; 113: 105112.CrossRefGoogle Scholar
31.Appleton, EV. Foreword. In: Stetson, HT. Sunspots in Action. New York: Ronald Press, 1947, pp. iiivi.Google Scholar
32.Sidorin, A, Khalilov, E (eds). Lord of Time Franz Halberg: on the 90th Anniversary of his Birth, on 5 July 2009. London: Science without Borders/International Publishing House SWB, 2011, 45 pp.Google Scholar
33.Halberg, F, et al. Integrated and as-one-goes analyzed physical, biospheric and noetic monitoring: Preventing personal disasters by self-surveillance may help understand natural cataclysms: a chronousphere (chrono-noösphere). IC GEOCHANGE (in press).Google Scholar
34.Burns, JT. Cosmic Influences on Humans, Animals, and Plants: An Annotated Bibliography. Magill Bibliographies. Lanham, MD: Scarecrow Press/Pasadena, CA: Salem Press, 1997, 203 pp.Google Scholar
35.Halberg, F, Cornélissen, G, Schwartzkopff, O.A bibliography: toward a chrononoosphere (http://2011.geocataclysm.org/pdf/franz_halberg_220811.pdf). Accessed 15 May 2012.Google Scholar
Figure 0

Fig. 1. Graph of A. L. Chizhevsky on cases of cholera recorded in Moscow between 1823 and 1923, published by Sigel [23]. In this graph, the original data are folded over the ∼11-year solar activity cycle. The data show a peak incidence coinciding with maximal solar activity (left panel). Taking these folded data off the published graph, an analysis by cross-correlation of cholera incidence vs. Wolf numbers (WN) yields the largest correlation coefficient at a lag of zero (right) [33]. (© Halberg.)

Figure 1

Table 1. Geographical differences in cycles with periods, τ values, in the range of 5–32 years [note τ values of ∼17 years characterizing the incidence of infectious diseases (cholera, diphtheria, croup]

Figure 2

Fig. 2 [colour online]. Plot of yearly mortality data from cholera in India from 1901 to 1961, shown as original values (solid curve) and after removal of a linear trend (dashed curve). Data from Chizhevsky (1901–1924) and from WHO reports (1920–1961) during 1920–1924 are the same in both sources. * Prediction of outbreaks by Chizhevsky (two correct). (© Halberg.)

Figure 3

Fig. 3. Least squares spectrum of yearly detrended data on mortality from cholera in India during 1901–1961. The ∼11·7-year cycle is detected with statistical significance and it is validated by nonlinear least squares, the period [and its confidence interval (CI)] being estimated as 11·668 (95% CI 10·44–12·895) years, similar to the ∼11-year solar activity cycle, as suggested by Chizhevsky. (© Halberg.)

Figure 4

Fig. 4. In order to visualize the waveform of the ∼11·7-year cycle characterizing mortality from cholera in India during 1901–1961, the yearly detrended data were stacked over an idealized 11·7-year scale (after removal of a linear trend), using five bins (classes). The ∼11·7-year component was found to be statistically significant by one-way analysis of variance (P = 0·024). Data from Chizhevsky (1901–1924) and from WHO reports (1920–1961) during 1920–1924 are the same in both sources. (© Halberg.)

Figure 5

Fig. 5 [colour online]. Plot as a function of time of yearly data on mortality from cholera in Russia for 104 years (1823–1926) (solid curve), compared to changes in solar activity, gauged by Wolf numbers (dashed curve). Peaks in the incidence of cholera correspond to every other peak in solar activity, suggesting the presence of a ∼22-year (Hale) cycle. Data from Chizhevsky [3]. (© Halberg.)

Figure 6

Fig. 6. Least squares spectrum of yearly data on mortality from cholera in Russia (1823–1926), revealing the presence of several peaks corresponding to components with periods of ∼21, 9, and 5·6 years. Whereas the ∼9-year cycle only reaches borderline statistical significance by nonlinear analysis, the other two components are validated with statistical significance. Period estimates and their CIs (given in parentheses) are listed above their respective spectral peaks. Nonlinear result and 95% confidence interval (CI); for 1823–1924, Chizhevsky's data [3] were used and compared with the data of Pollitzer [5] and added for 1924–1926. * Found for Chizhevsky originally by Vladimir Shostakovich. † Borderline significance (non-overlap of zero by CI of amplitude only with one-parameter CI). (© Halberg.)

Figure 7

Fig. 7 [colour online]. (a) In order to visualize the waveform of the ∼20·7-year cycle characterizing mortality from cholera in Russia during 1823–1926, the yearly data were stacked over an idealized 20·714-year scale, using 11 bins (classes). This component is validated with statistical significance both by cosinor (P = 0·004) and by one-way analysis of variance (P < 0·001). This component corresponds to a spectral peak and is validated nonlinearly, based on the ‘conservative’ CI (see earlier footnote for explanation of conservative CI). (b) In order to visualize the waveform of the ∼5·6-year cycle characterizing mortality from cholera in Russia during 1823–1926, the yearly data were stacked over an idealized 5·62-year scale, using six bins (classes). This component is validated with statistical significance both by cosinor (P = 0·002) and by one-way analysis of variance (P = 0·015). This component corresponds to a spectral peak and is validated nonlinearly, based on the ‘conservative’ CI (see earlier footnote for explanation of conservative CI). (c) In order to visualize the waveform of the ∼9-year cycle characterizing mortality from cholera in Russia during 1823–1926, the yearly data were stacked over an idealized 8·95-year scale, using five bins (classes). This component is validated with statistical significance both by cosinor (P = 0·019) and by one-way analysis of variance (P = 0·039). This component only reached borderline statistical significance by nonlinear analysis. For 1823–1923 data from Chizhevsky [3] were compared with data from Pollitzer [5] and added for 1924–1926. (© Halberg.)

Figure 8

Table 2. Geomagnetic/geographical differences among cycles with periods in the range of 0·8–2·0 years, characterizing the incidence of myocardial infarction (MI) and sudden cardiac death*†

Figure 9

Table 3. Congruent* periods of helio-geomagnetics (columns 1 and 2), the estimation of 1-minute by a healthy man over 3·5 decades (column 3)