Contributors | Affiliation | Role |
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Putnam, Hollie | University of Rhode Island (URI) | Co-Principal Investigator |
Strand, Emma | University of Rhode Island (URI) | Student |
Soenen, Karen | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
From the waters of Kāne‘ohe Bay, HI, four colonies of each coral species M. capitata and P. acuta were identified and collected under SAP 2019-60. Each of the four colonies for each species was fragmented into 30 pieces at the Hawaiʻi Institute of Marine Biology, located on Moku o Loʻe in Kāne‘ohe Bay, HI, and hot-glued to labeled plugs. (21N 157 W ; depth 1m).
Each sample was photographed using a digital camera with a red/blue/green color standard. Red/blue/green values that were extracted in ImageJ, version 1.51 (Schneider et al. 2012) from the coral were standardized to the color standards by dividing the experimental value observed in the coral against the corresponding actual recorded value from the color standards (Edmunds et al. 2003). Using the normalized intensity values from each color channel, a bleaching score was quantified as PC1 from principle components analysis of these data. As stress is prolonged and bleaching becomes more pronounced, the red/blue/green color readings from the coral will equalize around the same number because white is an equal expression of all colors. All nubbins available at each time points were used for color assessment.
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thermal_colorscore.csv (Comma Separated Values (.csv), 178.60 KB) MD5:b59e9683f571a8ddf7c3072834a54222 Primary data file for dataset ID 884220 |
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Thermal_Stress_Experiment_Color_Score_Images filename: Thermal_Stress_Experiment_Color_Score_Images_Emma_Strand.zip (ZIP Archive (ZIP), 286.59 MB) MD5:9dc5de3f06d3ae13b279e88e528b7fde Pictures of coral during a thermal stress experiment where physiology color score has been extracted from using ImageJ. |
Parameter | Description | Units |
Date | Date of measurement (Month-Day-Year) | unitless |
Timepoint | Categorical timepoint of experiment | unitless |
PLUG_ID | Plug ID indicating coral ID | unitless |
Genotype | Genotype ID | unitless |
Species | Coral species | unitless |
Photo_Number | ID of photograph taken | unitless |
Tank | Tank ID | unitless |
Treatment | Temperature treatment | unitless |
Red_Standard | Color value of red standard, raw RGB values extracted from ImageJ. | pixels |
Green_Standard | Color value of green standard, raw RGB values extracted from ImageJ. | pixels |
Blue_Standard | Color value of blue standard, raw RGB values extracted from ImageJ. | pixels |
Red_Coral | Red color in coral measurement, raw RGB values extracted from ImageJ. | pixels |
Green_Coral | Green color in coral measurement, raw RGB values extracted from ImageJ. | pixels |
Blue_Coral | Blue color in coral measurement, raw RGB values extracted from ImageJ. | pixels |
Notes | Notes | units |
Dataset-specific Instrument Name | Digital Camera |
Generic Instrument Name | Camera |
Generic Instrument Description | All types of photographic equipment including stills, video, film and digital systems. |
Dataset-specific Instrument Name | Ruler with three red, blue, and green colored bands |
Generic Instrument Name | ruler |
Generic Instrument Description | A device used for measuring or for drawing straight lines, consisting of an elongated piece of rigid or semi-rigid material marked with units for measurement. Device that allows one or more physical dimensions of a sample or specimen to be determined by visible comparison against marked graduations in units of measurement of dimension length. |
NSF Abstract:
The remarkable success of coral reefs is explained by interactions of the coral animal with its symbiotic microbiome that is comprised of photosynthetic algae and bacteria. This total organism, or "holobiont", enables high ecosystem biodiversity and productivity in coral reefs. These ecosystems are, however, under threat from a rapidly changing environment. This project aims to integrate information from the cellular to organismal level to identify key mechanisms of adaptation and acclimatization to environmental stress. Specific areas to be investigated include the role of symbionts and of epigenetics (molecular "marks" on coral DNA that regulate gene expression). These aspects will be studied in Hawaiian corals to determine whether they explain why some individuals are sensitive or resistant to environmental perturbation. Results from the proposed project will also provide significant genomic resources that will contribute to fundamental understanding of how complex biological systems generate emergent (i.e., unexpected) properties when faced with fluctuating environments. Broader impacts will extend beyond scientific advancements to include postdoctoral and student training in Science, Technology, Engineering and Mathematics (STEM). Data generated in the project will be used to train university students and do public outreach through live videos of experimental work, and short stop-action animations for topics such as symbiosis, genomics, epigenetics, inheritance, and adaptation. The research approaches and results will be shared with the public in Hawaii through the Hawaii Institute of Marine Biology education department and presentations at Hawaiian hotels, as well as at Rutgers University through its 4-H Rutgerscience Saturdays and 4-H Rutgers Summer Science Programs.
Symbiosis is a complex and ecologically integrated interaction between organisms that provides emergent properties key to their survival. Such is the case for the relationship between reef-building corals and their microbiome, a meta-organism, where nutritional and biogeochemical recycling provide the necessary benefits that fuel high reef productivity and calcification. The rapid warming and acidification of our oceans threatens this symbiosis. This project addresses how relatively stress resistant and stress sensitive corals react to the environmental perturbations of increased temperature and reduced pH. It utilizes transcriptomic, epigenetic, and microbial profiling approaches, to elucidate how corals respond to environmental challenges. In addition to this profiling, work by the BSF Israeli partner will implement powerful analytical techniques such as network theory to detect key transcriptional hubs in meta-organisms and quantify biological integration. This work will generate a stress gene inventory for two ecologically important coral species and a (epi)genome and microbiome level of understanding of how they respond to the physical environment. Acknowledgment of a role for epigenetic mechanisms in corals overturns the paradigm of hardwired genetic control and highlights the interplay of genetic and epigenetic variation that may result in emergent evolutionary and ecologically relevant properties with implications for the future of reefs. Furthermore, clarifying the joint contribution of the microbiome and host in response to abiotic change will provide an important model in metazoan host-microbiome biotic interactions.
This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |