{"data":[{"id":"10.48321/d14de07d3b","type":"dois","attributes":{"doi":"10.48321/d14de07d3b","identifiers":[],"creators":[{"nameType":"Personal","affiliation":["University of Oklahoma"],"name":"Joshua Wimhurst","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","schemeUri":"https://orcid.org","nameIdentifier":"https://orcid.org/0000-0002-2606-3910"}]}],"titles":[{"lang":"en-US","title":"Understanding the North American Monsoon - A Two-Step AI-Assisted Approach for Ensemble Modeling and Stakeholder-Informed Experimentation on Mesoscale Phenomena"}],"publisher":"DMPTool","container":{},"publicationYear":2026,"subjects":[],"contributors":[],"dates":[],"language":"en","types":{"schemaOrg":"CreativeWork","resourceTypeGeneral":"OutputManagementPlan","citeproc":"article","bibtex":"misc","ris":"GEN","resourceType":"Data Management Plan"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":null,"rightsList":[],"descriptions":[{"descriptionType":"Abstract","description":"The North American Monsoon (NAM) has been the subject of much climatological research over the last 25 years. However, model depictions of its small-scale climate dynamics, such as moisture transport from the Gulf of California, orographic uplift, and timing of late-season monsoon retreat, remain as gaps in current understanding of the NAM’s behavior and subsequent socioeconomic impacts. We propose value-added exists in incorporating outputs of General Circulation Model (GCM) simulations of the NAM into seasonal forecasting for the region, specifically for climate scientists, farmers, and managers tasked with water resource planning. To that end, we propose to develop a two-step Artificial Intelligence (AI)-assisted approach to incorporating stakeholder knowledge and needs into climatological studies of the NAM. The first step of this approach is training and refining a Retrieval-Augmented-Generation enhanced Large Language Model (RAG-LLM) that generates domain-specific responses about the NAM. The RAG-LLM's corpus consists of scientific literature about the NAM, along with transcripts from focus groups and interviews with regional stakeholders who possess tacit knowledge about the NAM’s local impacts and modeling limitations. Critical knowledge gaps about the NAM are to be revealed by the RAG-LLM from this corpus, such as a recommended GCM ensemble for NAM simulations specifically, and model experiments to conduct based on stakeholder needs. The second step is to statistically downscale the recommended GCM ensemble using an Extreme Gradient Boosting (XGBoost) machine learning algorithm to conduct these stakeholder-identified model experiments and achieve explicit representation of the NAM’s hard-to-resolve climate dynamics. The expected outcomes of these experiments are historical simulations of NAM behavior that more closely agree with reanalysis products than non-downscaled GCM data, and spatiotemporal representations of the NAM’s effects on the Southwest United States (US) of direct relevance to stakeholder needs. This application of RAG-LLM and XGBoost to conduct high-resolution model experiments that address climatological unknowns among stakeholders and within the literature could be transferred to studies of any mesoscale atmospheric phenomenon in the US.","lang":"en"}],"geoLocations":[],"fundingReferences":[{"funderIdentifierType":"ROR","funderName":"National Science Foundation (nsf.gov)","funderIdentifier":"https://ror.org/021nxhr62"}],"url":"https://dmphub.uc3prd.cdlib.net/dmps/10.48321/D14DE07D3B","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-23T04:21:10Z","registered":"2026-06-23T04:21:11Z","published":null,"updated":"2026-06-30T00:05:41Z"},"relationships":{"client":{"data":{"id":"cdl.cdl","type":"clients"}}}},{"id":"10.5281/zenodo.7777962","type":"dois","attributes":{"doi":"10.5281/zenodo.7777962","identifiers":[{"identifier":"oai:zenodo.org:7777962","identifierType":"oai"}],"creators":[{"nameType":"Personal","affiliation":["Université de Genève"],"givenName":"Elliot","familyName":"Jiwani-Brown","name":"Jiwani-Brown, Elliot","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-7744-3756"}]},{"nameType":"Personal","affiliation":["Université de Genève"],"givenName":"Matteo","familyName":"Lupi","name":"Lupi, Matteo","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-2351-6371"}]}],"titles":[{"title":"LOTOS code inputs for local earthquake tomography of the Irazú-Turrialba volcanic complex, Costa Rica"}],"publisher":"Zenodo","container":{},"publicationYear":2023,"subjects":[{"subject":"LET"},{"subject":"Tomography"},{"subject":"Costa Rica"},{"subject":"Volcano"}],"contributors":[],"dates":[{"date":"2023-06-30","dateType":"Issued"}],"language":null,"types":{"schemaOrg":"Dataset","resourceTypeGeneral":"Dataset","citeproc":"dataset","bibtex":"misc","ris":"DATA","resourceType":""},"relatedIdentifiers":[{"relationType":"IsVersionOf","relatedIdentifier":"10.5281/zenodo.7777961","relatedIdentifierType":"DOI"}],"relatedItems":[],"sizes":[],"formats":[],"version":null,"rightsList":[{"rightsIdentifierScheme":"SPDX","rightsUri":"https://creativecommons.org/licenses/by/4.0/legalcode","schemeUri":"https://spdx.org/licenses/","rights":"Creative Commons Attribution 4.0 International","rightsIdentifier":"cc-by-4.0"}],"descriptions":[{"descriptionType":"Abstract","description":"Local earthquake seismic tomography model for Jiwani-Brown, E., Koulakov, I., Muñoz-Burbano, F., Pacheco, J., Mora, M., \u0026 Lupi, M. (2023). Comparing local and ambient seismic tomographic methods to infer the plumbing system of the Irazú-Turrialba volcanic complex, Costa Rica. \n\n\nThe tomography model presented in the paper are obtained using the LOTOS code by Koulakov (2009). Input files for running of LOTOS code adapted for Windows OS. More details on the LOTOS code can be found atwww.ivan-art.com/science/LOTOS"}],"geoLocations":[],"fundingReferences":[{"funderIdentifierType":"Crossref Funder ID","funderName":"Swiss National Science Foundation","funderIdentifier":"10.13039/501100001711","awardTitle":"GENERATE - GEophysical and Numerical Experiments for Reservoir Analysis and fluid-Transported Energy","awardNumber":"166900"}],"url":"https://zenodo.org/doi/10.5281/zenodo.7777962","contentUrl":null,"metadataVersion":1,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2023-03-28T11:57:25Z","registered":"2023-03-28T11:57:26Z","published":null,"updated":"2026-06-30T00:02:42Z"},"relationships":{"client":{"data":{"id":"cern.zenodo","type":"clients"}}}},{"id":"10.6082/uchicago.15048","type":"dois","attributes":{"doi":"10.6082/uchicago.15048","identifiers":[{"identifier":"oai:uchicago.tind.io:15048","identifierType":"Other"}],"creators":[{"nameType":"Personal","affiliation":["University of Chicago"],"givenName":"Anchita","familyName":"Addhya","name":"Addhya, Anchita","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0009-0007-2443-3926"}]}],"titles":[{"title":"Laser Manipulation of Quantum Defects in Diamond Nanostructures"}],"publisher":"University of Chicago","container":{},"publicationYear":2025,"subjects":[{"subject":"diamond"},{"subject":"nanophotonics"},{"subject":"laser-writing"},{"subject":"strain tuning"},{"subject":"color centers"},{"subject":"cavity-coupling"}],"contributors":[{"nameType":"Personal","givenName":"Alex","familyName":"High","name":"High, Alex","nameIdentifiers":[],"contributorType":"Supervisor","affiliation":[]},{"nameType":"Personal","givenName":"F. 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To address these challenges, this thesis presents advancements in the laser-driven creation and manipulation of quantum defects in diamond nanostructures. Leveraging the interaction of a pulsed laser with diamond nanophotonic resonators, we generate defects in photonic cavities with enhanced efficiency and scalability. Additionally, we introduce a novel, all-optical approach to tailor the optical properties of quantum defects in diamonds. We also explore the effect of cavity interactions of excitons and trions in 2D materials. Chapter 1 introduces the foundational concepts of color centers in diamond, focusing on nitrogen-vacancy (NV-) centers and Group IV color centers and their integration with nanophotonic cavities. We review established methods for creating these defects and provide an overview of the emerging technique of ultrafast laser writing in diamond. Chapter 2 outlines our experimental setups, especially our custom-built confocal microscope, its several functions throughout our experiments and integration with a pulsed laser-writing setup. Chapter 3 details the fabrication and characterization of integrated nanophotonic devices on our novel thin-film diamond platforms both by direct etching as well as hybrid integration with titanium dioxide (TiO2) devices. We present the processes for creating structures like ring resonators, nanopillars, and bullseye antennas, highlighting the challenges and solutions in achieving high-quality devices compatible with color center integration. Chapter 4 demonstrates cavity-enhanced laser writing as a novel method for creating quantum defects in diamond membranes, highlighting reduced (picojoule) pulse energies compared to laser writing in bulk diamond, thereby relaxing system and substrate requirements. Chapter 5 presents an avenue for optical tuning of germanium-vacancy (GeV-) color centers in a suspended diamond membrane, using pulsed laser irradiation to achieve permanent shifts of the zero-phonon line (ZPL), without the need of complex device integration. Chapter 6 explores the cavity-engineering of exciton and trion lifetimes and emission linewidths in monolayer molybdenum diselenide (MoSe2). Chapter 7 and 8 summarize the key findings and outlines future research directions of cavity-enhanced laser-writing. The work presented in this dissertation significantly contributes to the advancement of quantum technologies by introducing and characterizing novel methods for creating and manipulating quantum defects in diamond using laser engineering. These findings pave the way for the development of more efficient, scalable, and integrated quantum devices."}],"geoLocations":[],"fundingReferences":[{"funderName":"U.S. Department of Energy","awardTitle":"National Quantum Information Science Research Centers"},{"funderName":"National Science Foundation","awardTitle":"Hybrid Quantum Architectures and Networks"},{"funderName":"National Science Foundation","awardTitle":"Kadanoff-Rice 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The system is controlled via the SounderSuite software package which consists of the EchoControl Server to interface directly with the echosounder hardware and peripheral devices, and the EchoControl Client to provide the primary user interface for echogram visualization."}],"geoLocations":[],"fundingReferences":[{"funderIdentifierType":"Crossref Funder ID","funderName":"U.S. National Science Foundation","funderIdentifier":"10.13039/100000001","awardTitle":"Management and Operations of the JOIDES Resolution as a Facility for the International Ocean Discovery Program (IODP)","awardNumber":"1326927"}],"url":"https://zenodo.org/doi/10.5281/zenodo.21047409","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"api","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":1,"versionOfCount":0,"created":"2026-06-29T21:57:28Z","registered":"2026-06-29T21:57:28Z","published":null,"updated":"2026-06-29T21:57:28Z"},"relationships":{"client":{"data":{"id":"cern.zenodo","type":"clients"}}}},{"id":"10.5281/zenodo.21047410","type":"dois","attributes":{"doi":"10.5281/zenodo.21047410","identifiers":[{"identifier":"oai:zenodo.org:21047410","identifierType":"oai"}],"creators":[{"nameType":"Personal","givenName":"Susan Q.","familyName":"Lang","name":"Lang, Susan Q.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0003-0873-6082"}],"affiliation":[]},{"nameType":"Personal","givenName":"Andrew","familyName":"McCaig","name":"McCaig, Andrew","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-7416-4911"}],"affiliation":[]},{"nameType":"Personal","givenName":"Peter","familyName":"Blum","name":"Blum, Peter","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-5282-0690"}],"affiliation":[]},{"nameType":"Personal","givenName":"Natsue","familyName":"Abe","name":"Abe, Natsue","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-2734-0035"}],"affiliation":[]},{"nameType":"Personal","givenName":"William","familyName":"Brazelton","name":"Brazelton, William","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0003-0933-0148"}],"affiliation":[]},{"nameType":"Personal","givenName":"Rémi","familyName":"Coltat","name":"Coltat, Rémi","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-9474-1584"}],"affiliation":[]},{"nameType":"Personal","givenName":"Jeremy R.","familyName":"Deans","name":"Deans, Jeremy R.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-6249-8244"}],"affiliation":[]},{"nameType":"Personal","givenName":"Kristin L.","familyName":"Dickerson","name":"Dickerson, Kristin L.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0009-0005-8131-7812"}],"affiliation":[]},{"nameType":"Personal","givenName":"Marguerite","familyName":"Godard","name":"Godard, Marguerite","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0003-3097-5135"}],"affiliation":[]},{"nameType":"Personal","givenName":"Barbara E.","familyName":"John","name":"John, Barbara E.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-7518-8736"}],"affiliation":[]},{"nameType":"Personal","givenName":"Frieder","familyName":"Klein","name":"Klein, Frieder","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-9560-5093"}],"affiliation":[]},{"nameType":"Personal","givenName":"Rebecca","familyName":"Kuehn","name":"Kuehn, Rebecca","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-2430-280X"}],"affiliation":[]},{"nameType":"Personal","givenName":"Kuan-Yu","familyName":"Lin","name":"Lin, Kuan-Yu","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-6856-613X"}],"affiliation":[]},{"nameType":"Personal","givenName":"C. Johan","familyName":"Lissenberg","name":"Lissenberg, C. Johan","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-7774-2297"}],"affiliation":[]},{"nameType":"Personal","givenName":"Haiyang","familyName":"Liu","name":"Liu, Haiyang","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-7055-3482"}],"affiliation":[]},{"nameType":"Personal","givenName":"Ethan L.","familyName":"Lopes","name":"Lopes, Ethan L.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-7359-0353"}],"affiliation":[]},{"nameType":"Personal","givenName":"Toshio","familyName":"Nozaka","name":"Nozaka, Toshio","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-6724-9706"}],"affiliation":[]},{"nameType":"Personal","givenName":"Andrew J.","familyName":"Parsons","name":"Parsons, Andrew J.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-7538-9418"}],"affiliation":[]},{"nameType":"Personal","givenName":"Vamdev","familyName":"Pathak","name":"Pathak, Vamdev","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-9571-6161"}],"affiliation":[]},{"nameType":"Personal","givenName":"Mark K.","familyName":"Reagan","name":"Reagan, Mark K.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0003-1628-4194"}],"affiliation":[]},{"nameType":"Personal","givenName":"Jordyn A.","familyName":"Robare","name":"Robare, Jordyn A.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-9133-8485"}],"affiliation":[]},{"nameType":"Personal","givenName":"Ivan P.","familyName":"Savov","name":"Savov, Ivan P.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0003-4218-4365"}],"affiliation":[]},{"nameType":"Personal","givenName":"Esther","familyName":"Schwarzenbach","name":"Schwarzenbach, Esther","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-4549-4660"}],"affiliation":[]},{"nameType":"Personal","givenName":"Olivier J.","familyName":"Sissmann","name":"Sissmann, Olivier J.","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-9372-1779"}],"affiliation":[]},{"nameType":"Personal","givenName":"Gordon","familyName":"Southam","name":"Southam, Gordon","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-8941-1249"}],"affiliation":[]},{"nameType":"Personal","givenName":"Fengping","familyName":"Wang","name":"Wang, Fengping","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0002-3429-8410"}],"affiliation":[]},{"nameType":"Personal","givenName":"C. Geoffrey","familyName":"Wheat","name":"Wheat, C. Geoffrey","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","nameIdentifier":"0000-0001-8858-1310"}],"affiliation":[]}],"titles":[{"title":"IODP Expedition 399 Bathymetry"}],"publisher":"International Ocean Discovery Program","container":{},"publicationYear":2025,"subjects":[{"subject":"International Ocean Discovery Program"},{"subject":"IODP"},{"subject":"JOIDES Resolution"},{"subject":"Expedition 399"},{"subject":"Site U1309"},{"subject":"Site U1601"},{"subject":"Atlantis Massif"},{"subject":"deep biosphere"},{"subject":"serpentinization"},{"subject":"Lost City hydrothermal field"},{"subject":"peridotite mantle"},{"subject":"detachment fault"}],"contributors":[{"nameType":"Organizational","name":"International Ocean Discovery Program","nameIdentifiers":[],"contributorType":"DataCollector","affiliation":[]}],"dates":[{"date":"2025-05-03","dateType":"Issued"}],"language":null,"types":{"schemaOrg":"Dataset","resourceTypeGeneral":"Dataset","citeproc":"dataset","bibtex":"misc","ris":"DATA","resourceType":""},"relatedIdentifiers":[{"relationType":"IsDocumentedBy","resourceTypeGeneral":"Text","relatedIdentifier":"10.14379/iodp.proc.399.2025","relatedIdentifierType":"DOI"},{"relationType":"IsVersionOf","relatedIdentifier":"10.5281/zenodo.21047409","relatedIdentifierType":"DOI"}],"relatedItems":[],"sizes":[],"formats":[],"version":null,"rightsList":[{"rightsIdentifierScheme":"SPDX","rightsUri":"https://creativecommons.org/licenses/by/4.0/legalcode","schemeUri":"https://spdx.org/licenses/","rights":"Creative Commons Attribution 4.0 International","rightsIdentifier":"cc-by-4.0"}],"descriptions":[{"descriptionType":"Abstract","description":"The Knudsen CHIRP 3260 is the primary sub-bottom profiler and bathymetric echosounder used on the JOIDES Resolution starting on Transit 396T (October 2021). The system utilizes 3.5 kHz and 12 kHz frequency transducers housed in the ship's forward sonar dome. The system is controlled via the SounderSuite software package which consists of the EchoControl Server to interface directly with the echosounder hardware and peripheral devices, and the EchoControl Client to provide the primary user interface for echogram visualization."}],"geoLocations":[],"fundingReferences":[{"funderIdentifierType":"Crossref Funder ID","funderName":"U.S. National Science Foundation","funderIdentifier":"10.13039/100000001","awardTitle":"Management and Operations of the JOIDES Resolution as a Facility for the International Ocean Discovery Program (IODP)","awardNumber":"1326927"}],"url":"https://zenodo.org/doi/10.5281/zenodo.21047410","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"api","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":1,"created":"2026-06-29T21:57:28Z","registered":"2026-06-29T21:57:28Z","published":null,"updated":"2026-06-29T21:57:28Z"},"relationships":{"client":{"data":{"id":"cern.zenodo","type":"clients"}}}},{"id":"10.5061/dryad.cjsxksngm","type":"dois","attributes":{"doi":"10.5061/dryad.cjsxksngm","identifiers":[],"creators":[{"nameType":"Personal","affiliation":["Emory University"],"name":"Boddu, Satya Spandana","nameIdentifiers":[]},{"nameType":"Personal","affiliation":["Emory University"],"name":"Martini, K. Michael","nameIdentifiers":[]},{"nameType":"Personal","affiliation":["Emory University"],"name":"Nemenman, Ilya","nameIdentifiers":[]},{"nameType":"Personal","affiliation":["Emory University"],"name":"Vega, Nic","nameIdentifiers":[{"nameIdentifierScheme":"ORCID","schemeUri":"https://orcid.org","nameIdentifier":"https://orcid.org/0000-0002-9929-6109"}]}],"titles":[{"title":"Variance in \u003cem\u003eC. elegans\u003c/em\u003e gut bacterial load suggests complex host-microbe dynamics"}],"publisher":"Dryad","container":{},"publicationYear":2026,"subjects":[{"schemeUri":"https://web-archive.oecd.org/2012-06-15/138575-38235147.pdf","subject":"FOS: Biological sciences","subjectScheme":"fos"},{"schemeUri":"https://github.com/PLOS/plos-thesaurus","subject":"Caenorhabditis elegans","subjectScheme":"PLOS Subject Area Thesaurus"},{"schemeUri":"https://github.com/PLOS/plos-thesaurus","subject":"Stochastic processes","subjectScheme":"PLOS Subject Area Thesaurus"},{"schemeUri":"https://github.com/PLOS/plos-thesaurus","subject":"Microbiome","subjectScheme":"PLOS Subject Area Thesaurus"},{"schemeUri":"https://github.com/PLOS/plos-thesaurus","subject":"Population ecology","subjectScheme":"PLOS Subject Area Thesaurus"}],"contributors":[],"dates":[{"date":"2025-12-26T19:58:01Z","dateType":"Created"},{"date":"2025-12-26T19:58:02Z","dateType":"Submitted"},{"date":"2026-06-29T00:00:00Z","dateType":"Issued"},{"date":"2026-06-29T00:00:00Z","dateType":"Available"}],"language":"en","types":{"schemaOrg":"Dataset","resourceTypeGeneral":"Dataset","citeproc":"dataset","bibtex":"misc","ris":"DATA","resourceType":"dataset"},"relatedIdentifiers":[{"relationType":"IsCitedBy","relatedIdentifier":"10.1371/journal.pcbi.1013110","relatedIdentifierType":"DOI"},{"relationType":"IsCitedBy","relatedIdentifier":"10.1101/2024.12.09.627557","relatedIdentifierType":"DOI"}],"relatedItems":[],"sizes":["16192299 bytes"],"formats":[],"version":"3","rightsList":[{"rightsIdentifierScheme":"SPDX","rightsUri":"https://creativecommons.org/publicdomain/zero/1.0/legalcode","schemeUri":"https://spdx.org/licenses/","rights":"Creative Commons Zero v1.0 Universal","rightsIdentifier":"cc0-1.0"}],"descriptions":[{"descriptionType":"Abstract","description":"Variation in bacterial composition inside a host is a result of complex\n dynamics of microbial community assembly, but little is known about these\n dynamics. To deconstruct the factors that contribute to this variation, we\n used a combination of experimental and modeling approaches. We found that\n demographic stochasticity and stationary heterogeneity in the host\n carrying capacity or bacterial growth rate are insufficient to explain\n quantitatively the variation observed in our empirical data. Instead, we\n found that the data can be understood if the host-bacteria system can be\n viewed as stochastically switching between high and low growth rates\n phenotypes. This suggests the dynamics significantly more complex than\n logistic growth used in canonical models of microbiome assembly. We\n develop mathematical models of this process that can explain various\n aspects of our data. We highlight the limitations of snapshot data in\n describing variation in host-associated communities and the importance of\n using time-series data along with mathematical models to understand\n microbial dynamics within a host."},{"descriptionType":"TechnicalInfo","description":"# Description of the data and file structure for: Variance in C. elegans\n gut bacterial load suggests complex host-microbe dynamics All the data\n required to generate the figures are assumed to be in a subfolder named\n \"Data\" and all the corresponding code is assumed to be in a\n subfolder named \"code\". These folders are provided as\n \"Data.zip\" and \"code.zip\". Output Numpy data files\n (.npy) for Maximum likelihood estimation (Figure 3) are also in the\n subfolder \"code\". \"GreenBeadFeed1219.csv\" is derived\n from a Biosorter output data file, in which each row is one event detected\n by the machine. In Biosorter data, NAs appear when a label is irrelevant\n and where a channel summary statistic was not calculated. Files include\n machine-reported columns: * \"Id\" - Unique index of each event\n within the run * \"Time\" - Time of event relative to start of run\n * \"Plate\", \"Row\", and \"Column\" - IFF objects\n were sorted into a multi-well plate from this run, the plate number, row,\n and column of the destination for the event * \"SourceWell\" - IFF\n samples were taken out of a multi-well plate, the row + column of the well\n associated with the event * \"Clog\" - Binary variable indicating\n whether the machine clogged on this event * \"Sorted\" - Code\n indicating sort status of the event. \"0\" if not sorted;\n \"6\" if sorted as a clean, single event. * \"InRegions\"\n - Binary string indicating the gates into which an event fell, from right\n to left. The number of digits is equal to the total number of gates\n defined during a run. The right-most position is gate R1 (all acquired\n events) and will be 1 for all saved events. In the standard setup used for\n these experiments, the second position from right (gate R2) is defined on\n extinction and time of flight (TOF) to include adult-sized worms.\n Subsequent gates are typically defined in part on fluorescence. *\n \"TOF\" - Time of flight. Time required for the object to pass\n through the detector. * \"Extinction\" - Roughly, the amount of\n light (here, using 488 nm laser) blocked by the object, integrated over\n time of flight. Similar to absorbance. *\n \"Green\",\"Yellow\", and \"Red\" - Integrated\n emitted signal intensity over the total length of the object, in arbitrary\n units. Not all channels may have been recorded/reported, in which case\n values appear as NA. *\n \"PHExtinction\",\"PWExtinction\",\"PCExtinction\"\n - Peak height (PH), peak width (PW), and peak integrated volume (PC) for\n the dominant peak in the extinction channel. Any statistics not calculated\n appear as NA. *\n \"PHGreen\",\"PWGreen\",\"PCGreen\" - Same peak\n statistics for green fluorescence channel. *\n \"PHYellow\",\"PWYellow\",\"PCYellow\" - Same peak\n statistics for yellow fluorescence channel. *\n \"PHRed\",\"PWRed\",\"PCRed\" - Same peak\n statistics for red fluorescence channel. In data file\n \"GreenBeadFeed1219.csv\", each row therefore represents one\n individual worm. Columns are as described above for Biosorter standard\n files, plus: * \"Host\" - Genotype of the worm host *\n \"Concentration\" and \"Rep\" - Unused fields *\n \"Bact\" - Bacterial food provided in addition to inert beads\n (\"none\" or \"HKOP50\", the latter indicating heat-killed\n E. coli OP50) * \"SourceRow\" and \"SourceColumn\" - IFF\n samples were taken out of a multi-well plate, the row + column of the well\n associated with the event, as separate colums * \"Beads\" -\n Relative concentration of inert fluorescent beads to which worms were\n exposed, as described in Methods Data files \"CFU Mapping.csv\",\n \"LowInh24.csv\", and \"Inhibition_compiled.csv\" were\n derived by merging Biosorter data with corresponding plating data. Each\n row represents one individual adult worm. Columns are: * Condition -\n Treatment condition. Chloramphenicol-treated worms are labeled as\n \"CMXX\", where \"XX\" is the concentration of antibiotic\n in ug/mL * Time - Time on antibiotic, in hours (string) * timefit - Time\n after sorting, in hours (numeric) * Row and Column - Biosorter data\n columns, as described above * Gate - Fluorescence gate associated with\n each worm, translated from the original binary string * TOF, Extinction,\n and Green - Biosorter data columns, as described above * logGreen -\n log10-transformed total green fluorescence (Green) * CFU/worm and logCFU -\n CFU count-derived data columns, as described above Data files\n \"Migration_Compiled.csv\",\n \"Migration_run2_Compiled.csv\", and\n \"Migration_T0_fill.csv\" were extracted from Biosorter data and\n used for model fitting. * Time - Time since sorting of pre-colonized adult\n worms, in hours (string) * timefit - As \"Time\" (numeric) * Row,\n Column, Sorted, InRegions - Biosorter data columns, as described above *\n Condition - Type of worm sorted (high/mid/low fluorescence) and treatment\n (+/- re-feeding with live fluorescent bacteria) * Gate - Fluorescence gate\n associated with each worm, translated from the original binary string *\n TOF, Extinction, and Green - Biosorter data columns, as described above *\n logGreen - log10-transformed total green fluorescence (Green) In data file\n \"WormShedCFU.csv\", each row represents one individual worm.\n Columns are: * \"Bact\" - Abbreviation used for bacterial genus\n +species * \"Run\" - Unique index of the replicate run from which\n these data were taken * \"Date\" - Date of the experiment, as\n YYYYMMDD * \"Row\" and \"Column\" - Destination well into\n which the worm was sorted, if sorted as single worms * \"Time\" -\n Time after sorting, in hours (string) * \"InfectTime\" - Duration\n of exposure to the infecting bacteria * \"Bin\" - Coarse\n fluorescence bin from which each worm was sorted (low, mid. high) *\n \"ID\" - Unique index of each worm within run * \"Count\"\n - Number of colonies counted after serial dilution and plating of worm\n digest * \"D\" - 10-fold dilution at which colonies were counted *\n \"CFU\" and \"logCFU\" - Raw and log10-transformed\n CFU/worm calculated from plating data In files containing colony forming\n unit (CFU) data for worm native microbiome members (MYb27.csv, MYb45.csv,\n MYb53.csv, MYb71.csv, MYb120.csv, MYb238.csv, MYbSpecies.csv), each row\n represents one individual worm. Empty rows containing NA values for CFU\n and logCFU were added as placeholders when needed to achieve a rectangular\n data structure for plotting. Files include columns: * MYbSp - Species ID\n of the bacteria * Time - Time (in hours) * CFU - Colony forming units\n (CFUs) in the intestine, as determined by serial dilution and plating *\n logCFU - Log10-transformed CFU data. When CFU count was 0, logCFU is also\n assigned a value of 0 for plotting. Files \"MYb71 CD.csv\" and\n \"MYb120 CD.csv\" contain CFU data from experiments where worms\n were exposed to different densities of bacteria during colonization. *\n Density - Bacterial density, in CFU/mL * Time - Time in hours over which\n worms were exposed to colonizing bacteria (numeric) * CFU - Colony forming\n units (CFUs) in the intestine, as determined by serial dilution and\n plating * logCFU - Log10-transformed CFU data. When CFU count was 0,\n logCFU is also assigned a value of 0 for plotting. File\n \"invitro_082819.csv\" contains plate reader data from an\n experiment in which optical density at 600 nm (OD600) was read over time\n as a proxy for microbial growth. * \"T_hours\" and\n \"T_mins\" indicate the time since the start of run, in hours and\n minutes respectively * \"Blank\" - OD600 data in the blank well\n (media only) * \"BactSpecies_Replicate\" - All remaining columns\n are named in this format and contain OD600 data for the indicated\n replicate well of the indicated bacterial species # Sharing/access\n information Link to other publically accessible source of the data and\n code: *\n [https://github.com/veganm/varianceinwormgut.git](https://github.com/veganm/varianceinwormgut.git) # Code/software Analysis notebooks are independent and can be run in any order. Analyses were done with the following package versions: ``` - python: 3.11.4 - matplotlib: 3.7.1 - scikit-learn: 1.3.0 - pandas: 1.5.3 - numpy: 1.24.3 - scipy: 1.10.1 - seaborn: 0.12.2 ``` ## Figure 1 Figure 1 in the main text is generated in notebook \"WormMatters_Fig1.ipynb\" using data files: * MYbSpecies.csv - datafile with bacterial loads inside worms for all the bacterial species * invitro_082819.csv - datafile with bacterial growth outside the worm * MYb71.csv - datafile with bacterial loads for the species MYb71 * MYb120.csv - datafile with bacterial loads for the species MYb120 ## Figure 2 Figure 2 in the main text is generated in notebook \"HetCarryingCap_fig2.ipynb\" using data files: * MYb71 CD.csv - datafile with bacterial loads for the species MYb71 at different colonization densities * MYb120 CD.csv - datafile with bacterial loads for the species MYb120 at different colonization densities ## Figure 3 Figure 3 in the main text is generated in notebook \"HetGrowthCol_Fig3.ipynb\" using data files: * MYb71.csv - datafile with bacterial loads for the species MYb71 * MYb120.csv - datafile with bacterial loads for the species MYb120 Bacteria-specific MLE parameters for the logistic growth model are generated in notebooks \"MLE Gridsearch for MYb71.ipynb\" and \"MLE Gridsearch for MYb120.ipynb\" using the same data files. The resulting likelihood values are saved as Numpy files \"likelihoodvals_MYb71.npy\" and \"likelihoodvals_MYb120.npy\", and parameters are saved as \"allparameters_MYb71.npy\" and \"allparameters_MYb120.npy\". ## Figure 4 Figure 4 in the main text is generated in notebook \"Inhibition_Fig4.ipynb\" using data file: * Inhibition_compiled.csv - datafile with bacterial loads for MYb14 under varying levels of chloramphenicol inhibition (25-500 ug/mL) and over time ## Figure 5 Figure 5 in the main text is generated in notebook \"Migration_Fig5.ipynb\" using data files: * Migration_compiled.csv - datafile with Biosorter data for worms colonized with MYb14-GFP, 24 and 48 hours after being sorted into \"low\" and \"high\" GFP gates * Migration_T0_fill.csv - datafile with Biosorter data for the initial population of MYb14-GFP colonized worms, from which the initial low/high sort was carried out ## Figure 6, 8, and 9 Figures 6, 8, and 9 in the main text are generated in notebook \"MultistabilityModelSimulations_Fig6.ipynb\". No data files are called. ## Figure 7 The GFP to CFU mapping in Figure 7 is generated in notebook \"MappingGFPtoCFU.ipynb\" using data files: * CFU Mapping.csv - datafile with bacterial loads for the species MYb14 and the corresponding GFP reads in the experiment shown in Figure 6 in SI. * LowInhT24.csv - datafile with bacterial loads for the species MYb14 and the corresponding GFP reads in the lowest-inhibition condition (chloramphenicol 25 ug/mL, no inhibition of bacterial growth inside worms) also shown in Figure 4 ## SI Text ### Figure A in SI Text. Bacterial load in individual worms over time. Figure A is generated in notebook \"SI_Monocolonization.ipynb\" and calls data files: * MYb27.csv * MYb45.csv * MYb53.csv * MYb238.csv each of which contains data for bacterial loads of the indicated species in individual worms, in the same format as used in Figure 1. ### Figure B in SI Text. Fluorescent bead accumulation in adult worms Figure B is generated in R script \"SI_GreenBeadAccumulationN2.R\" and calls data file: * GreenBeadFeed1219.csv - datafile with Biosorter data for N2 worms allowed to ingest green fluorescent beads ### Figure C in SI Text. Bacterial load distributions under additional levels of inhibition of growth within hosts. Figure C is generated in notebook \"SI_Inhibition.ipynb\" using data file: * Inhibition_compiled.csv - datafile with bacterial loads for MYb14 under varying levels of chloramphenicol inhibition (25-500 ug/mL) and over time. Also used in Figure 4. ### Figure D in SI Text. Bacterial load switching between modes in an additional experimental run Figure D is generated in notebook \"SI_Migration.ipynb\" using data file: * Migration_run2_Compiled.csv - datafile with Biosorter data for worms colonized with MYb14-GFP as in Figure 5, but representing an independent run of the experiment ### Figure E. State switching in N2 adults colonized with Salmonella enterica LT2 Figure E is generated in R script \"SI_SEStateSwitch.R\" using data file: * WormShedCFU.csv - datafile containing bacterial load data from a separate set of experiments, including colonization (bacterial load) data for individual worms exposed to GFP-labeled Salmonella enterica and sorted into low- and high-GFP bins ### Figure F. Probability distributions of GFP and CFU data Figure F is generated in notebook \"MappingGFPtoCFU.ipynb\" using data files as in Figure 7. ### Figure G (Predictions of dynamics in the 6th order polynomial potential (5th order force) model) and H (Predictions of dynamics in the state switching model) Figures G and H are generated in notebook \"MultistabilityModelSimulations_Fig6.ipynb\". 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echosounder used on the JOIDES Resolution starting on Transit 396T (October 2021). The system utilizes 3.5 kHz and 12 kHz frequency transducers housed in the ship's forward sonar dome. The system is controlled via the SounderSuite software package which consists of the EchoControl Server to interface directly with the echosounder hardware and peripheral devices, and the EchoControl Client to provide the primary user interface for echogram visualization."}],"geoLocations":[],"fundingReferences":[{"funderIdentifierType":"Crossref Funder ID","funderName":"U.S. National Science Foundation","funderIdentifier":"10.13039/100000001","awardTitle":"Management and Operations of the JOIDES Resolution as a Facility for the International Ocean Discovery Program (IODP)","awardNumber":"1326927"}],"url":"https://zenodo.org/doi/10.5281/zenodo.21046539","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"api","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-29T21:22:57Z","registered":"2026-06-29T21:22:57Z","published":null,"updated":"2026-06-29T21:22:57Z"},"relationships":{"client":{"data":{"id":"cern.zenodo","type":"clients"}}}}],"meta":{"total":83478,"totalPages":400,"page":1},"links":{"self":"https://api.datacite.org/dois?query=fundingReferences.funderName%3A%22National+Science+Foundation%22","next":"https://api.datacite.org/dois?page%5Bnumber%5D=2\u0026page%5Bsize%5D=25\u0026query=fundingReferences.funderName%3A%22National+Science+Foundation%22"}}