<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wioland H</submitter><funding>European Research Council</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>341-345</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4869837</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12</volume><pubmed_abstract>Despite their inherent non-equilibrium nature1, living systems can self-organize in highly ordered collective states2,3 that share striking similarities with the thermodynamic equilibrium phases4,5 of conventional condensed matter and fluid systems. Examples range from the liquid-crystal-like arrangements of bacterial colonies6,7, microbial suspensions8,9 and tissues10 to the coherent macro-scale dynamics in schools of fish11 and flocks of birds12. Yet, the generic mathematical principles that govern the emergence of structure in such artificial13 and biological6-9,14 systems are elusive. It is not clear when, or even whether, well-established theoretical concepts describing universal thermostatistics of equilibrium systems can capture and classify ordered states of living matter. Here, we connect these two previously disparate regimes: Through microfluidic experiments and mathematical modelling, we demonstrate that lattices of hydrodynamically coupled bacterial vortices can spontaneously organize into distinct phases of ferro- and antiferromagnetic order. The preferred phase can be controlled by tuning the vortex coupling through changes of the inter-cavity gap widths. The emergence of opposing order regimes is tightly linked to the existence of geometry-induced edge currents15,16, reminiscent of those in quantum systems17-19. Our experimental observations can be rationalized in terms of a generic lattice field theory, suggesting that bacterial spin networks belong to the same universality class as a wide range of equilibrium systems.</pubmed_abstract><journal>Nature physics</journal><pubmed_title>Ferromagnetic and antiferromagnetic order in bacterial vortex lattices.</pubmed_title><pmcid>PMC4869837</pmcid><funding_grant_id>247333</funding_grant_id><funding_grant_id>1130206</funding_grant_id><pubmed_authors>Wioland H</pubmed_authors><pubmed_authors>Goldstein RE</pubmed_authors><pubmed_authors>Woodhouse FG</pubmed_authors><pubmed_authors>Dunkel J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ferromagnetic and antiferromagnetic order in bacterial vortex lattices.</name><description>Despite their inherent non-equilibrium nature1, living systems can self-organize in highly ordered collective states2,3 that share striking similarities with the thermodynamic equilibrium phases4,5 of conventional condensed matter and fluid systems. Examples range from the liquid-crystal-like arrangements of bacterial colonies6,7, microbial suspensions8,9 and tissues10 to the coherent macro-scale dynamics in schools of fish11 and flocks of birds12. Yet, the generic mathematical principles that govern the emergence of structure in such artificial13 and biological6-9,14 systems are elusive. It is not clear when, or even whether, well-established theoretical concepts describing universal thermostatistics of equilibrium systems can capture and classify ordered states of living matter. Here, we connect these two previously disparate regimes: Through microfluidic experiments and mathematical modelling, we demonstrate that lattices of hydrodynamically coupled bacterial vortices can spontaneously organize into distinct phases of ferro- and antiferromagnetic order. The preferred phase can be controlled by tuning the vortex coupling through changes of the inter-cavity gap widths. The emergence of opposing order regimes is tightly linked to the existence of geometry-induced edge currents15,16, reminiscent of those in quantum systems17-19. Our experimental observations can be rationalized in terms of a generic lattice field theory, suggesting that bacterial spin networks belong to the same universality class as a wide range of equilibrium systems.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Apr</publication><modification>2026-05-05T16:35:21.228Z</modification><creation>2019-03-27T02:13:54Z</creation></dates><accession>S-EPMC4869837</accession><cross_references><pubmed>27213004</pubmed><doi>10.1038/nphys3607</doi></cross_references></HashMap>