Colony-Level 3D Photogrammetry Reveals That Total Linear Extension and Initial Growth Do Not Scale With Complex Morphological Growth in the Branching Coral, Acropora cervicornis
Abstract:The ability to quantify changes in the structural complexity of reefs and individual coral colonies that build them is vital to understanding, managing, and restoring the function of these ecosystems. However, traditional methods for quantifying coral growth in situ fail to accurately quantify the diversity of morphologies observed both among and within species that contribute to topographical complexity. Three-dimensional (3D) photogrammetry has emerged as a powerful tool for the quantification of reefscape c… Show more
“…For volume averages, these ranged from 0.65% to 11.25% (overall mean 5.5%, mm range), with small and large CVs at 3.55% and 8.77%. These CVs are on-par or lower compared to SfM methods, which are deemed within suitable ranges of a few mm to cm (SA: 1.5%, V: 2% Ferrari et al, 2017; 14%-15% Lange & Perry, 2020; SA: 3.7% and V: 5.7% Million et al, 2021).…”
Several sampling and measurement strategies have been developed to assess biological forms in three dimensions, including corals. However, the effectiveness (in speed and precision) of current three‐dimensional (3D) methods in scanning and model construction are challenging at small scales (μm–mm).
In this paper, a practical 3D scanning and model construction tool using an intra‐oral dental scanner was assessed to measure the surface area and volume of coral juveniles across multiple species. Intra‐oral scanners using confocal imaging are fast, precise to the μm scale and safe to use with live tissue, thereby eliminating the need to harm or kill the animals. The trial was conducted at the National Sea Simulator at the Australian Institute of Marine Science.
High‐quality 3D scans of individual coral juveniles were successfully generated and integrated automatically into high‐resolution (μm) mesh from point clouds. The attained average scanning efficiency was <2 min/individual, without a significant difference in speed given coral complexity or between live colonies or dead coral skeletons.
Overall, this fast and precise system could become a promising tool for marine environmental surveys and restoration initiatives. This tool also removes the need to sacrifice animals for measurement analysis, thereby increasing conservation and animal welfare.
“…For volume averages, these ranged from 0.65% to 11.25% (overall mean 5.5%, mm range), with small and large CVs at 3.55% and 8.77%. These CVs are on-par or lower compared to SfM methods, which are deemed within suitable ranges of a few mm to cm (SA: 1.5%, V: 2% Ferrari et al, 2017; 14%-15% Lange & Perry, 2020; SA: 3.7% and V: 5.7% Million et al, 2021).…”
Several sampling and measurement strategies have been developed to assess biological forms in three dimensions, including corals. However, the effectiveness (in speed and precision) of current three‐dimensional (3D) methods in scanning and model construction are challenging at small scales (μm–mm).
In this paper, a practical 3D scanning and model construction tool using an intra‐oral dental scanner was assessed to measure the surface area and volume of coral juveniles across multiple species. Intra‐oral scanners using confocal imaging are fast, precise to the μm scale and safe to use with live tissue, thereby eliminating the need to harm or kill the animals. The trial was conducted at the National Sea Simulator at the Australian Institute of Marine Science.
High‐quality 3D scans of individual coral juveniles were successfully generated and integrated automatically into high‐resolution (μm) mesh from point clouds. The attained average scanning efficiency was <2 min/individual, without a significant difference in speed given coral complexity or between live colonies or dead coral skeletons.
Overall, this fast and precise system could become a promising tool for marine environmental surveys and restoration initiatives. This tool also removes the need to sacrifice animals for measurement analysis, thereby increasing conservation and animal welfare.
“…Specifications for model building and all scripts can be found at https://github.com/wyattmillion/Coral3DPhotogram. 3D models were imported into Meshlab v2020.6 (103) to measure four growth-related traits following protocols described in Million et al (102) and detailed in the Supplementary Methods: TLE, SA, V, and V inter . We assessed the final shape of colonies that survived to T12 with no detectable fragmentation by calculating SA-to-V and TLE-to-V ratios, in addition to packing, convexity, and sphericity (59).…”
Section: Methodsmentioning
confidence: 99%
“…Ten coral genets maintained long-term (5+ years) at Mote Marine Laboratory's in situ coral nursery (Table S10) were outplanted in a multi-site transplant study under FKMNS permits 2015-163-A1 and 2018-035. In April 2018, 270 coral (mean TLE of 8.4 cm) ramets representing 10 genets (27 ramets per genet) affixed to concrete pucks were photographed following Million et al (102) and manually measured for TLE immediately before transplantation to nine active restoration sites (Table S1, Fig. 1).…”
Section: Experimental Designmentioning
confidence: 99%
“…Photographs taken in situ were used to generate individual 3D models of each coral ramet in Metashape 1.5.4 (Agisoft LLC, St. Petersburg, Russia) using a high-throughput pipeline (102). Specifications for model building and all scripts can be found at https://github.com/wyattmillion/Coral3DPhotogram.…”
Genotype-by-environment interactions (GxE) indicate that variation in organismal traits cannot be explained by fixed effects of genetics or site-specific plastic responses alone. For tropical coral reefs experiencing dramatic environmental change, identifying the contributions of genotype, environment, and GxE on coral performance will be vital for both predicting persistence and developing restoration strategies. We quantified the impacts of G, E, and GxE on the morphology and survival of the endangered coral, A. cervicornis, through an in situ transplant experiment exposing common garden (nursery) raised clones of ten genotypes to nine reef sites in the Florida Keys. By fate-tracking outplants over one year with colony-level 3D photogrammetry, we uncovered significant GxE on coral size and survivorship indicating that no universal winner exists in terms of colony performance. Moreover, the presence of GxE also implies the existence of intraspecific variation in phenotypic plasticity. Rather than differences in mean trait values, we find that individual-level morphological plasticity is adaptive in that the most plastic individuals also exhibited the fastest growth and highest survival. This indicates that adaptive morphological plasticity may continue to evolve, influencing the success of A. cervicornis and resulting reef communities in a changing climate. As focal reefs are active restoration sites, the knowledge that variation in phenotype is an important predictor of performance can be directly applied to restoration planning. Taken together, these results establish A. cervicornis as a system for studying the eco-evolutionary dynamics of phenotypic plasticity that also can inform genetic- and environment-based strategies for coral restoration.
“…Emerging approaches, using underwater photogrammetry and structure-from-motion (SfM) software to create three-dimensional (3D) models of coral colonies [ 12 , 13 ], are now helping to address many of the above analytical constraints. Recent studies explored colony-scale growth patterns by either measuring extension, surface area or volume repeatedly for the same colony [ 14 , 15 ] or by overlying models from subsequent years and directly quantifying the change in dimensions [ 16 ]. Besides being non-invasive and thus allowing repeated measurements of the same coral colony over many years, photogrammetry-based methods are providing novel ways to quantify a whole range of different colony-scale growth metrics and to analyse intra-colony variability in growth.…”
Coral growth is an important metric of coral health and underpins reef-scale functional attributes such as structural complexity and calcium carbonate production. There persists, however, a paucity of growth data for most reef-building regions, especially for coral species whose skeletal architecture prevents the use of traditional methods such as coring and Alizarin staining. We used structure-from-motion photogrammetry to quantify a range of colony-scale growth metrics for six coral species in the Mexican Caribbean and present a newly developed workflow to measure colony volume change over time. Our results provide the first growth metrics for two species that are now major space occupiers on Caribbean reefs, Agaricia agaricites and Agaricia tenuifolia. We also document higher linear extension, volume increase and calcification rates within back reef compared to fore reef environments for four other common species: Orbicella faveolata, Porites astreoides, Siderastrea siderea and Pseudodiploria strigosa. Linear extension rates in our study were lower than those obtained via computed tomography (CT) scans of coral cores from the same sites, as the photogrammetry method averages growth in all dimensions, while the CT method depicts growth only along the main growth axis (upwards). The comparison of direct volume change versus potential volume increase calculated from linear extension emphasizes the importance of assessing whole colony growth to improve calcification estimates. The method presented here provides an approach that can generate accurate calcification estimates alongside a range of other whole-colony growth metrics in a non-invasive way.
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