0.1 Introduction
The theory of organismic sets and their abstract relations, (OSR), was constructed by Nicolas
Rashevsky ([1, 2]) as a new paradigm of mathematical models of biological organization at
different hierarchical (that is, lattice-like) levels by means of mathematical sets. The first example
is that of an organismic set of zeroth order which was defined as “a finite collection S0 whose
elements correspond to (or represent) the genes gi of a cell or multi-cellular organism together with
their activities ai, biochemical products pi and corresponding inputs Ij from the environment”,
with i and j being positive integer indices spanning a finite subset N+ of the set of natural
numbers N.
0.2 Brief History
Rashevsky’s original definition ([2]) of the organismic sets of zero-th order whose elements are
genes as explained above; S0 is, therefore, perhaps the most general and simplest model of the
genome of an organism. Furthermore, OSR contains also essential relations between such
organismic sets that correspond to a biological system’s organization. Therefore, Rashevsky’s
organismic set theory is part of abstract relational biology. First order organismic sets, S1, are
then simple mathematical models of single cells in terms of both genetic (modeled by S0 whose
elements model the genes) and metabolic subsystems other than the direct products of the genes.
OSR models of multi-cellular organisms are then defined as organismic sets of second order, whose
elements are the first order organismic sets that are set-theoretical models of living cells. Further
mathematical concepts and a logic of predicates were then introduced by Rashevsky in order to
expand his theory of organismic sets to organizational, mathematical models of human
societies.
0.3 Fundamental and Practical Results of Rashevsky’s OSR
Results from such studies of relations between organismic sets in OSR were considered to be far
more important than the numerical or quantitative aspects that play such important roles in
physics and chemistry. A number of interesting results were obtained by means of standard
(Boolean) logic predicates applied to organismic sets and their relations. Further details can be
found in the publications listed below and the references cited therein. Subsequently, autopoietic
theories have enlarged upon, and also extended, the application of organismic sets to biological
systems, Ecology, societal organizations, societies and the entire set of all humans viewed from the
point of view of its activities in the broadest sense, including cultural ones, as well as the
human society interactions with its global environment. In spite of its age, the theory
of organismic sets thus appears to be today as relevant as it was 30 years ago to the
current, pressing problems of the global human society; humanity is now being faced with,
and indeed challenged by, critical global issues such as global warming, the growing
global energy crysis, and the related problem of increasing costs of food crops, as well as
food transport/manufacture/delivery/preservation that were predicted by this theory
which employs the rather simple mathematical means of the theory of sets and set-based
relations, albeit greatly enriched by the organismic contexts- biological, societal and
environmental.
0.4 Further Developments of OSR and Relational Biology Mathematical Models
In parallel with OSR developments by Rashevsky there have been related theories in abstract
relational biology such as Robert Rosen’ s theory of (M,R)-systems (MRs) and Anthony
Bartholomay’s theory of molecular sets with applications both in Mathematical Biology and
Mathematical Medicine. MRs were represented initially in terms of categories of sets and
set-theoretical maps([13, 14]). Subsequent OSR developments introduced OSR representations in
algebraic categories such as the category of algebraic theories in the sense defined by William F.
Lawvere, and also in terms of organismic supercategories [3], later defined as interpretations of
ETAS axioms ([4]). Then, a functorial construction of MRs was reported ([6, 7]) with similar
properties with those previously found for the category of automata, or sequential machines. Such
developments made then possible the formulation of a more general theory of organismic sets,
molecular sets and (M,R)-systems in terms of natural transformations of organismic structures
([8]), whose results were then compared with those obtained, or obtainable, from other network,
’net’ or automata-based theories and computer modeling of biological systems([11]);
specific examples in biology, physiology and medicine were concisely presented for arterial
systems in the lung, circulatory system in man, the human brain interactions with the
hormonal and circulation systems, neural networks, enzyme networks of the neuron, genetic
networks, tumor development (carcinogenesis), coupled biochemical oscillatory systems
and biochemical networks, chaotic subsystems in organisms and other related topics
([11, 12]).
References
[1] Rashevsky, N.: 1965, The Representation of Organisms in Terms of Predicates,
Bulletin of Mathematical Biophysics 27: 477-491.
[2] Rashevsky, N.: 1969, Outline of a Unified Approach to Physics, Biology and
Sociology., Bulletin of Mathematical Biophysics, 31: 159–198.
[3] Baianu, I.C. and M. Marinescu: 1968, Organismic Supercategories: Towards a Unitary
Theory of Systems. Bulletin of Mathematical Biophysics 30, 148-159.
[4] Baianu, I.C.: 1970, Organismic Supercategories: II. On Multistable Systems. Bulletin
of Mathematical Biophysics, 32: 539-561.
[5] Baianu, I.C.: 1971, Organismic Supercategories and Qualitative Dynamics of Systems.
Ibid., 33 (3), 339–354.
[6] Baianu, I.C.: 1973, Some Algebraic Properties of (M,R) – Systems. Bulletin of
Mathematical Biophysics 35, 213-217.
[7] Baianu, I.C. and M. Marinescu: 1974, A Functorial Construction of (M,R)– Systems.
Revue Roumaine de Mathematiques Pures et Appliquées 19: 388-391.
[8] Baianu, I.C.: 1980, Natural Transformations of Organismic Structures. Bulletin of
Mathematical Biophysics 42: 431-446.
[9] Baianu, I. C.: 1983, Natural Transformation Models in Molecular Biology., in
Proceedings of the SIAM Natl. Meet., Denver, CO.; Eprint:
http://cogprints.org/3675/ and
http://cogprints.org/3675/0l/Naturaltransfmolbionu6.pdf
[10] Baianu, I.C.: 1984, A Molecular-Set-Variable Model of Structural and Regulatory
Activities in Metabolic and Genetic Networks, FASEB Proceedings 43, 917.
[11] Baianu, I. C.: 1986–1987a, Computer Models and Automata Theory in
Biology and Medicine., in M. Witten (ed.), Mathematical Models in Medicine,
vol. 7., Ch.11 Pergamon Press, New York, 1513 -1577; URLs: CERN Preprint
No. EXT-2004-072: http://doe.cern.ch//archive/electronic/other/ext/ext-2004-072.pdf
; http://en.scientificcommons.org/1857371 .
[12] Baianu, I. C.: 1987b, Molecular Models of Genetic and Organismic Structures, in
Proceed. Relational Biology Symp. Argentina; CERN Preprint No.EXT-2004-067 and
http://doc.cern.ch/archive/electronic/other/ext/extusers/2004
67/MolecularModels-ICB3.doc.
[13] Rosen, R.: 1958a, A Relational Theory of Biological Systems Bulletin of
Mathematical Biophysics 20: 245-260.
[14] Rosen, R.: 1958b, The Representation of Biological Systems from the Standpoint of
the Theory of Categories., Bulletin of Mathematical Biophysics 20: 317-341.