Crystal growth kinetics as an architectural constraint on the evolution of molluscan shells
Author(s) -
Vanessa Schoeppler,
Robert Lemanis,
Elke Reich,
Tamás Pusztai,
László Gránásy,
Igor Zlotnikov
Publication year - 2019
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1907229116
Subject(s) - biomineralization , constraint (computer aided design) , shell (structure) , kinetics , evolutionary biology , crystal growth , nanotechnology , geology , materials science , paleontology , biology , physics , geometry , chemistry , classical mechanics , crystallography , composite material , mathematics
Molluscan shells are a classic model system to study formation-structure-function relationships in biological materials and the process of biomineralized tissue morphogenesis. Typically, each shell consists of a number of highly mineralized ultrastructures, each characterized by a specific 3D mineral-organic architecture. Surprisingly, in some cases, despite the lack of a mutual biochemical toolkit for biomineralization or evidence of homology, shells from different independently evolved species contain similar ultrastructural motifs. In the present study, using a recently developed physical framework, which is based on an analogy to the process of directional solidification and simulated by phase-field modeling, we compare the process of ultrastructural morphogenesis of shells from 3 major molluscan classes: A bivalve Unio pictorum , a cephalopod Nautilus pompilius , and a gastropod Haliotis asinina We demonstrate that the fabrication of these tissues is guided by the organisms by regulating the chemical and physical boundary conditions that control the growth kinetics of the mineral phase. This biomineralization concept is postulated to act as an architectural constraint on the evolution of molluscan shells by defining a morphospace of possible shell ultrastructures that is bounded by the thermodynamics and kinetics of crystal growth.
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