Modularity and emergence: biology's challenge in understanding life.

This essay juxtaposes modularity and emergence in the consideration of biological systems at various scalar levels of spatio-temporal organisation. It is noted that reductionism, specialisation and modularity are basic prerequisites for understanding life. It is realised that increased progress of scientific biology in elucidating mechanisms at the level of modular components supports the accusation that the more it advances in materialistic description of details, the more it diverts from understanding the innate properties of life. It is clear that modularity, by taking the whole as the sum of its parts, is insufficient for understanding living systems. At the same time, however, there is emergence, as advocated by Robert Laughlin. Emergence after the integration of modules leads to completely new properties of individual organisms as unique unitary entities, and also of systems of organisms with synergistic and antagonistic interactions of the integrated species. The discussion is predominantly based on examples from plant biology. At hierarchically higher scalar levels emergent biological systems are networks integrating species, biotopes, ecosystems and the entire biosphere of Earth, also named Gaia by James Lovelock, in a natural scientific respect. While investigating modules remains essential, biology as a nature science needs to merge and integrate such information to be able to unfold emergence. Through efforts towards visualising and understanding emergent diversity and complexity, the research discipline of biology will provide invaluable contributions to understanding life, and thus refute the accusation that it diverts from embracing the innate properties of life.

[1]  P. Anderson More is different. , 1972, Science.

[2]  Pilar Cubas,et al.  An epigenetic mutation responsible for natural variation in ̄ oral symmetry , 2022 .

[3]  E. Schnepf Organellen-Reduplikation und Zellkompartimentierung , 1966 .

[4]  Xiaoyu Zhang The Epigenetic Landscape of Plants , 2008, Science.

[5]  Hans de Kroon,et al.  A modular concept of phenotypic plasticity in plants. , 2005, The New phytologist.

[6]  M. Palmer,et al.  Ecological Theory and Community Restoration Ecology , 1997 .

[7]  A. Bird DNA methylation patterns and epigenetic memory. , 2002, Genes & development.

[8]  J. V. Etten,et al.  Unusual Life Style of Giant Chlorella Viruses , 2003 .

[9]  M. Paulsen Genomic Imprinting in Säugetieren: Das epigenetische Gedächtnis , 2007 .

[10]  Richard J. Hobbs,et al.  Towards a Conceptual Framework for Restoration Ecology , 1996 .

[11]  E. Whitelaw,et al.  Transgenerational epigenetic inheritance: more questions than answers. , 2010, Genome research.

[12]  B. Bassler,et al.  Quorum sensing: cell-to-cell communication in bacteria. , 2005, Annual review of cell and developmental biology.

[13]  Marc-Thorsten Hütt,et al.  Dissecting the logical types of network control in gene expression profiles , 2008, BMC Systems Biology.

[14]  J. Alroy Dynamics of origination and extinction in the marine fossil record , 2008, Proceedings of the National Academy of Sciences.

[15]  G. Müller Evo–devo: extending the evolutionary synthesis , 2007, Nature Reviews Genetics.

[16]  Marc-Thorsten Hütt,et al.  Network Dynamics in Plant Biology: Current Progress in Historical Perspective , 2005 .

[17]  U. Lüttge,et al.  Evo–Devo–Eco and Ecological Stem Species: Potential Repair Systems in the Planetary Biosphere Crisis , 2013 .

[18]  Gernot Glöckner,et al.  Chromatophore Genome Sequence of Paulinella Sheds Light on Acquisition of Photosynthesis by Eukaryotes , 2008, Current Biology.

[19]  C. Suttle The significance of viruses to mortality in aquatic microbial communities , 1994, Microbial Ecology.

[20]  W. Bond,et al.  The Influence of Grazing on the Evolution, Morphology and Physiology of Plants as Modular Organisms [and Discussion] , 1991 .

[21]  P. Keeling,et al.  Organelle Evolution: What's in a Name? , 2008, Current Biology.

[22]  R. Hobbs,et al.  Ecological Restoration and Global Climate Change , 2006 .

[23]  Richard J. Hobbs,et al.  Restoration Ecology: Repairing the Earth's Ecosystems in the New Millennium , 2001 .

[24]  J. Belnap,et al.  Biological Soil Crusts: Structure, Function, and Management , 2003, Ecological Studies.

[25]  N. Butterfield,et al.  MACROEVOLUTION AND MACROECOLOGY THROUGH DEEP TIME , 2007 .

[26]  F. Esteves,et al.  Rehabilitation of a Bauxite Tailing Substrate in Central Amazonia: The Effect of Litter and Seed Addition on Flood‐Prone Forest Restoration , 2012 .

[27]  R. Bambach,et al.  A ubiquitous ~62-Myr periodic fluctuation superimposed on general trends in fossil biodiversity. I. Documentation , 2010, Paleobiology.

[28]  L. Sagan On the origin of mitosing cells , 1967, Journal of theoretical biology.

[29]  M. Watt,et al.  Rhizosphere Signals for Plant–Microbe Interactions: Implications for Field-Grown Plants , 2010 .

[30]  S. Rothstein,et al.  The role of epigenetic processes in controlling flowering time in plants exposed to stress. , 2011, Journal of experimental botany.

[31]  Werner Nachtigall,et al.  Bionik als Wissenschaft , 2010 .

[32]  Jessica A. Bolker,et al.  Modularity in Development and Why It Matters to Evo-Devo1 , 2000 .

[33]  Jian-Kang Zhu,et al.  Epigenetic regulation of stress responses in plants. , 2009, Current opinion in plant biology.