6 results on '"Zachary A. Quinlan"'
Search Results
2. Coral reef biofilm bacterial diversity and successional trajectories are structured by reef benthic organisms and shift under chronic nutrient enrichment
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Kristina Remple, Nyssa J. Silbiger, Linda Wegley Kelly, Megan J. Donahue, Michael D. Fox, Zachary A. Quinlan, and Craig E. Nelson
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Water microbiology ,Coral ,Ecological succession ,Biology ,Applied Microbiology and Biotechnology ,Microbiology ,Article ,Microbial ecology ,Animals ,Reef ,geography ,geography.geographical_feature_category ,Bacteria ,Coral Reefs ,Ecology ,QR100-130 ,fungi ,Biofilm ,Nutrients ,Bacterioplankton ,Coral reef ,biochemical phenomena, metabolism, and nutrition ,Anthozoa ,Benthic zone ,Biofilms ,Nutrient pollution ,geographic locations ,Biotechnology - Abstract
Work on marine biofilms has primarily focused on host-associated habitats for their roles in larval recruitment and disease dynamics; little is known about the factors regulating the composition of reef environmental biofilms. To contrast the roles of succession, benthic communities and nutrients in structuring marine biofilms, we surveyed bacteria communities in biofilms through a six-week succession in aquaria containing macroalgae, coral, or reef sand factorially crossed with three levels of continuous nutrient enrichment. Our findings demonstrate how biofilm successional trajectories diverge from temporal dynamics of the bacterioplankton and how biofilms are structured by the surrounding benthic organisms and nutrient enrichment. We identify a suite of biofilm-associated bacteria linked with the orthogonal influences of corals, algae and nutrients and distinct from the overlying water. Our results provide a comprehensive characterization of marine biofilm successional dynamics and contextualize the impact of widespread changes in reef community composition and nutrient pollution on biofilm community structure.
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- 2021
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3. Molecular Commerce on Coral Reefs: Using Metabolomics to Reveal Biochemical Exchanges Underlying Holobiont Biology and the Ecology of Coastal Ecosystems
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Daniel Petras, Irina Koester, Craig E. Nelson, Milou G. I. Arts, Linda Wegley Kelly, Andreas F. Haas, Zachary A. Quinlan, Shayle B. Matsuda, Pieter C. Dorrestein, and Lihini I. Aluwihare
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0106 biological sciences ,0301 basic medicine ,Science ,Ecology (disciplines) ,Ocean Engineering ,QH1-199.5 ,Aquatic Science ,Biology ,microbial ecology ,Oceanography ,010603 evolutionary biology ,01 natural sciences ,03 medical and health sciences ,Metabolomics ,Microbial ecology ,biogeochemistry ,Ecosystem ,Reef ,Water Science and Technology ,Global and Planetary Change ,geography ,geography.geographical_feature_category ,Ecology ,General. Including nature conservation, geographical distribution ,Coral reef ,dissolved organic matter ,metabolomics ,Holobiont ,030104 developmental biology ,coral reefs ,coral holobiont ,Chemical database - Abstract
The rapidly advancing field of metabolomics encompasses a diverse suite of powerful analytical and bioinformatic tools that can help to reveal the diversity and activity of chemical compounds in individual organisms, species interactions, and entire ecosystems. In this perspective we use examples from studies of coral reefs to illustrate ways in which metabolomics has been and can be applied to understand coastal ecosystems. Examples of new insights that can be provided by metabolomics include resolving metabolite exchange between microbes and animals in holobiont tissues, identifying the relevant metabolite exchanges associated with the onset and maintenance of diverse bacterial endosymbionts, characterizing unknown molecules associated with coral reproductive cues, or defining the suites of compounds involved in coral-algal competition and microbialization of algal-dominated ecosystems. Here we outline sampling, analytical and informatic methods that marine biologists and ecologists can apply to understand the role of chemical processes in ecosystems, with a focus on open access data analysis workflows and democratized databases. This perspective aims to demonstrate that metabolomics tools and bioinformatics approaches which leverage open access chemical databases can provide scientists the opportunity to map detailed metabolic inventories and dynamics for a holistic view of the relationships among reef organisms, their symbionts and their surrounding marine environment.
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- 2021
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4. Species-Specific Differences in the Microbiomes and Organic Exudates of Crustose Coralline Algae Influence Bacterioplankton Communities
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Zachary A. Quinlan, Raphael Ritson-Williams, Brenna J. Carroll, Craig A. Carlson, and Craig E. Nelson
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macroalgae ,Microbiology (medical) ,Coral ,lcsh:QR1-502 ,microbiome ,Microbiology ,lcsh:Microbiology ,03 medical and health sciences ,16s rRNA gene amplicon sequencing ,parasitic diseases ,Ecosystem ,14. Life underwater ,Original Research ,030304 developmental biology ,0303 health sciences ,geography ,geography.geographical_feature_category ,biology ,030306 microbiology ,Ecology ,fungi ,technology, industry, and agriculture ,Community structure ,Coralline algae ,Coral reef ,Bacterioplankton ,dissolved organic matter ,biology.organism_classification ,crustose coralline algae ,Microbial population biology ,coral reef ecology ,Crustose - Abstract
Crustose coralline algae (CCA) are critical members of the coral reef ecosystem, yet they remain poorly studied. Recent research on CCA has shown that only a few species play a significant role in the settlement of coral larvae through either the production of chemical settlement cues or the facilitation of specific microbial communities that are hypothesized to influence coral settlement. Thus, defining how DOM exudates differ between CCA species and the bacterioplankton communities these exudates facilitate is important for understanding the role of CCA in invertebrate settlement. We conducted single day exudation experiments on two species of CCA to compare tissue microbiome community structure, DOM production and the effect of DOM on the bacterioplankton community. We collected exudates from Hydrolithon reinboldii and Porolithon onkodes in both filter-sterilized seawater and unfiltered seawater from Kāne‘ohe Bay, Hawai‘i. Our results demonstrate that while both species exude equivalent quantities of dissolved organic carbon they differ in the composition of fluorescent DOM and fostered distinct microbial communities. P. onkodes exudates facilitate more microbial OTUs associated with coral disease, whereas H. reinboldii facilitated OTUs known to produce antimicrobial compounds. Our results highlight species-specific differences in the composition of fDOM exudates of CCA and the effect of those on microbial community structure.
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- 2019
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5. Diel population and functional synchrony of microbial communities on coral reefs
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Saichetana Macherla, Emily L. A. Kelly, Craig A. Carlson, Zachary A. Quinlan, Maggie D. Johnson, Linda Wegley Kelly, Robert Edwards, Jennifer E. Smith, Brian J. Zgliczynski, Stuart A. Sandin, Douglas S. Naliboff, Sandi Calhoun, Genivaldo G. Z. Silva, Craig E. Nelson, Yan Wei Lim, Michael D. Fox, Mark J. A. Vermeij, Forest Rohwer, Andreas F. Haas, Mark Hatay, Freshwater and Marine Ecology (IBED, FNWI), and Aquatic Microbiology (IBED, FNWI)
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0301 basic medicine ,General Physics and Astronomy ,02 engineering and technology ,Organic Chemicals ,lcsh:Science ,Trophic level ,education.field_of_study ,Multidisciplinary ,geography.geographical_feature_category ,Primary producers ,Ecology ,Coral Reefs ,Microbiota ,Psychrobacter ,Coral reef ,021001 nanoscience & nanotechnology ,Halomonas ,0210 nano-technology ,geographic locations ,Environmental Monitoring ,Science ,Photoperiod ,Population ,Biology ,Article ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,Ecosystem ,14. Life underwater ,education ,Life Below Water ,Diel vertical migration ,Reef ,Ribosomal ,geography ,Pacific Ocean ,fungi ,technology, industry, and agriculture ,General Chemistry ,biochemical phenomena, metabolism, and nutrition ,Roseobacter ,030104 developmental biology ,Microbial population biology ,RNA, Ribosomal ,RNA ,lcsh:Q ,Alteromonas - Abstract
On coral reefs, microorganisms are essential for recycling nutrients to primary producers through the remineralization of benthic-derived organic matter. Diel investigations of reef processes are required to holistically understand the functional roles of microbial players in these ecosystems. Here we report a metagenomic analysis characterizing microbial communities in the water column overlying 16 remote forereef sites over a diel cycle. Our results show that microbial community composition is more dissimilar between day and night samples collected from the same site than between day or night samples collected across geographically distant reefs. Diel community differentiation is largely driven by the flux of Psychrobacter sp., which is two-orders of magnitude more abundant during the day. Nighttime communities are enriched with species of Roseobacter, Halomonas, and Alteromonas encoding a greater variety of pathways for carbohydrate catabolism, further illustrating temporal patterns of energetic provisioning between different marine microbes. Dynamic diel fluctuations of microbial populations could also support the efficient trophic transfer of energy posited in coral reef food webs., Microbes structure biogeochemical cycles and food webs in the marine environment. Here, the authors sample coral reef-associated microbes across a 24-hour period, showing clear day–night patterns of microbial populations and thus calling for more studies to consider temporal variation in microbiomes at this scale.
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- 2019
6. Nutrient pollution disrupts key ecosystem functions on coral reefs
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Kristina Remple, Michael D. Fox, Jessica K. Sevilla, Hollie M. Putnam, Megan J. Donahue, Nyssa J. Silbiger, Zachary A. Quinlan, and Craig E. Nelson
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0106 biological sciences ,010504 meteorology & atmospheric sciences ,Carbonates ,Photosynthesis ,01 natural sciences ,Hawaii ,General Biochemistry, Genetics and Molecular Biology ,Phosphates ,chemistry.chemical_compound ,Nutrient ,Nitrate ,Water Pollution, Chemical ,Animals ,Seawater ,Ecosystem ,Reef ,0105 earth and related environmental sciences ,General Environmental Science ,geography ,Global Change and Conservation ,Nitrates ,geography.geographical_feature_category ,General Immunology and Microbiology ,Coral Reefs ,Ecology ,010604 marine biology & hydrobiology ,fungi ,Ocean acidification ,General Medicine ,Coral reef ,Eutrophication ,Anthozoa ,Seaweed ,Silicon Dioxide ,Biota ,chemistry ,Nutrient pollution ,Environmental science ,General Agricultural and Biological Sciences - Abstract
There is a long history of examining the impacts of nutrient pollution and pH on coral reefs. However, little is known about how these two stressors interact and influence coral reef ecosystem functioning. Using a six-week nutrient addition experiment, we measured the impact of elevated nitrate (NO − 3 ) and phosphate (PO 3− 4 ) on net community calcification (NCC) and net community production (NCP) rates of individual taxa and combined reef communities. Our study had four major outcomes: (i) NCC rates declined in response to nutrient addition in all substrate types, (ii) the mixed community switched from net calcification to net dissolution under medium and high nutrient conditions, (iii) nutrients augmented pH variability through modified photosynthesis and respiration rates, and (iv) nutrients disrupted the relationship between NCC and aragonite saturation state documented in ambient conditions. These results indicate that the negative effect of NO − 3 and PO 3− 4 addition on reef calcification is likely both a direct physiological response to nutrients and also an indirect response to a shifting pH environment from altered NCP rates. Here, we show that nutrient pollution could make reefs more vulnerable to global changes associated with ocean acidification and accelerate the predicted shift from net accretion to net erosion.
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- 2018
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