Search for: All records

Abstract Corals are under siege by both local and global threats, creating a worldwide reef crisis. Cryopreservation is an important intervention measure and a vital component of the modern coral conservation toolkit, but preservation techniques are currently limited to sensitive reproductive materials that can only be obtained a few nights per year during spawning. Here, we report the successful cryopreservation and revival of cm-scale coral fragments via mL-scale isochoric vitrification. We demonstrate coral viability at 24 h post-thaw using a calibrated oxygen-uptake respirometry technique, and further show that the method can be applied in a passive, electronics-free configuration. Finally, we detail a complete prototype coral cryopreservation pipeline, which provides a platform for essential next steps in modulating post-thaw stress and initiating long-term growth. These findings pave the way towards an approach that can be rapidly deployed around the world to secure the biological genetic diversity of our vanishing coral reefs. 

Coral reefs are declining worldwide primarily because of bleaching and subsequent mortality resulting from thermal stress. Currently, extensive efforts to engage in more holistic research and restoration endeavors have considerably expanded the techniques applied to examine coral samples. Despite such advances, coral bleaching and restoration studies are often conducted within a specific disciplinary focus, where specimens are collected, preserved, and archived in ways that are not always conducive to further downstream analyses by specialists in other disciplines. This approach may prevent the full utilization of unexpended specimens, leading to siloed research, duplicative efforts, unnecessary loss of additional corals to research endeavors, and overall increased costs. A recent US National Science Foundation-sponsored workshop set out to consolidate our collective knowledge across the disciplines of Omics, Physiology, and Microscopy and Imaging regarding the methods used for coral sample collection, preservation, and archiving. Here, we highlight knowledge gaps and propose some simple steps for collecting, preserving, and archiving coral-bleaching specimens that can increase the impact of individual coral bleaching and restoration studies, as well as foster additional analyses and future discoveries through collaboration. Rapid freezing of samples in liquid nitrogen or placing at −80 °C to −20 °C is optimal for most Omics and Physiology studies with a few exceptions; however, freezing samples removes the potential for many Microscopy and Imaging-based analyses due to the alteration of tissue integrity during freezing. For Microscopy and Imaging, samples are best stored in aldehydes. The use of sterile gloves and receptacles during collection supports the downstream analysis of host-associated bacterial and viral communities which are particularly germane to disease and restoration efforts. Across all disciplines, the use of aseptic techniques during collection, preservation, and archiving maximizes the research potential of coral specimens and allows for the greatest number of possible downstream analyses. 

Reversing coral reef decline requires reducing environmental threats while actively restoring reef ecological structure and function. A promising restoration approach uses coral breeding to boost natural recruitment and repopulate reefs with genetically diverse coral communities. Recent advances in predicting spawning, capturing spawn, culturing larvae, and rearing settlers have enabled the successful propagation, settlement, and outplanting of coral offspring in all of the world's major reef regions. Nevertheless, breeding efforts frequently yield low survival, reflecting the type III survivorship curve of corals and poor condition of most reefs targeted for restoration. Furthermore, coral breeding programs are still limited in spatial scale and species diversity. Here, we highlight four priority areas for research and cooperative innovation to increase the effectiveness and scale of coral breeding in restoration: (1) expanding the number of restoration sites and species, (2) improving broodstock selection to maximize the genetic diversity and adaptive capacity of restored populations, (3) enhancing culture conditions to improve offspring health before and after outplanting, and (4) scaling up infrastructure and technologies for large‐scale coral breeding and restoration. Prioritizing efforts in these four areas will enable practitioners to address reef decline at relevant ecological scales, re‐establish self‐sustaining coral populations, and ensure the long‐term success of restoration interventions. Overall, we aim to guide the coral restoration community toward actions and opportunities that can yield rapid technical advances in larval rearing and coral breeding, foster interdisciplinary collaborations, and ultimately achieve the ecological restoration of coral reefs. 

Abstract Coral reefs are threatened by anthropogenic climate change, which causes ocean acidification and warming that can result in coral death and the loss of genetic diversity on reefs around the world. Global efforts to secure the genetics of threatened populations using cryopreservation and biobanking are underway but are limited to coral sperm and larvae, available only during brief annual spawning events. Methods to cryopreserve adult coral tissues to enable biobanking activities year‐round are urgently needed, but are challenging due to the presence of a calcium carbonate skeleton and algal symbionts within the tissues, and chill sensitivity. In this study, vitrification and laser nanowarming permitted successful recovery of adult coral tissues in a novel sample type, the single‐polyp microfragment. Fluorescence and confocal microscopy shows clearly defined green fluorescent protein auto‐fluorescence around the polyp mouth post‐warming, with an overall survival rate of 39.7 ± 7.4% at 24 h post‐warming and 23.3 ± 9.7% at 1 month, but relatively few algal symbionts are present in the tissues, indicating poor survival of these cells. These proof‐of‐concept results provide a basis for continued research and development of a field‐ready protocol for cryopreservation of adult coral tissues, which will be essential to prevent extinctions and support reef restoration.