Neural Network Recognition of Marine Benthos and Corals
Abstract
:1. Introduction
2. The Future of Coral Reefs
3. Application of CNN and DBN
4. Applications to the Study of Corals
- Underwater image photography, followed by de-noising (preprocessing step), due to different challenges to quality (motion blurring, color attenuation, refracted sunlight patterns, sky color variation, scattering effects, presence of particles, etc.). The obtained raw images must be enhanced in order to visualize the coral species in detail for the steps to follow [37].
- Feature extraction: for images of different coral species, one needs to find salient features in each species in order to identify and reliably distinguish it from other species [38], avoiding errors due to illumination, rotation, size, view angle, camera distance, etc.
- The extracted features are used as input for DL [39].
5. Published Coral Classifications Based on Machine Learning
- Beijbom et al. (2012) [45] showed that their proposed method accurately estimates coral coverage across diverse reef sites and over multiple years, these offer timely and powerful potential for large scale coral reef analysis. The proposed algorithm accurately estimates coral coverage across locations and years, thereby taking a significant step towards reliable automated coral reef image annotation.
- Shihavuddin et al. (2013) [46] obtained better results by using a selective combination of various preprocessing steps, feature extraction methods, kernel mappings, priori designing a single method for all datasets. Using mosaic images, their method for large continuous areas resulted in 83.7% overall accuracy.
- Elawady, (2015) [39] presents the first application of DL techniques especially CNN in under-water image processing. He investigated CNN in handling noisy large-sized images, manipulating point-based multi-channel input data. Hybrid image patching procedure for multi-size scaling process across different square based windowing around labeled points.
- Mahmood et al. (2016) [48] proposed to use pre-trained CNN representations extracted from VGGnet with a 2-layer MLP classifier for coral classification. They also introduced a local-SPP approach to extract features at multiple scales to deal with the ambiguous class boundaries of corals. They then combined automated CNN based features with manually acquired hand-crafted features, while dealing effectively with the class imbalance problem.
- Mahmood et al. (2016a) [55] applied pre-trained CNN image representations extracted from VGGnet to a coral reef classification problem. They investigated the effectiveness of their trained classifier on unlabeled coral mosaics and analyzed the coral reef of the Abrolhos Islands in order to quantify the coral coverage and detect a decreasing trend in coral population automatically.
- Mahmood et al. (2017) [34] showed that the ResFeats data, extracted from the deeper layers of a ResNet performs better than the shallower ResFeats. They experimentally confirmed that their proposed approach consistently outperforms the CNN off-the-shelf features. Finally, they improved the state-of-the-art accuracy of the Caltech101, Caltech-256, and MLC datasets.
- Gómez-Ríos et al., (2018) [49] achieved state-of-the art accuracies using different variations of ResNet on the two small coral texture datasets, EILAT and RSMAS. They showed that using a simpler network, like ResNet-50, performs better than a more complex network, like DenseNet-121 or DenseNet-161 provided the datasets are small. When considering the impact of data augmentation, there is little benefit obtained from using such techniques.
- Williams et al. (2019) [54] used CoralNet to annotate points with an automated-analysis algorithm to achieve at least 90% certainty of a classification. CoralNet includes 822 data sets consisting of over 700,000 images. The site implements sophisticated computer vision algorithms, based on deep neural networks that allow researchers, agencies, and private partners to rapidly annotate benthic survey images. The site also serves as a repository and collaboration platform for the scientific community.
6. Discussion
7. Conclusions
- Working with “big data” in order to address the urgent ecological need of classifying corals.
- So far, the classification of corals has been performed by using outdated painstaking, time consuming manual methods, which highly limit its performance and usefulness. As a result, current coral reef species censuses are usually limited to single reefs [61]. That does not allow comparison among different reefs and their responses to specific stressors. However, Cleary et al. [62,63,64] present evidence to the contrary. A further important goal is to refine discrimination acuity and reliability sufficiently to use photographic images of larger reef sectors. A complementary possibility will be to extract large data sets from continuous film transects, all the above will be achievable only by the combination between NN future capabilities with cloud large data set storage volume.Furthermore, the painstaking nature of coral censuses limits the possibility of non-specialized technicians to gather large amounts of temporarily sequential data sets that can track decline and/or recovery of reefs in response to different IPCC scenarios and bioremediation measures.The usefulness of future, more refined NN will allow such comparisons and their analyses.The impressive power of NN in advanced application to plants has already been demonstrated [33].
- Developing and applying the automatic methods of machine based DL neuronal networks for classifying corals and using future large dataset solutions, where programs are made freely available to allow researchers anywhere to use their own images to train the algorithms then run their own analysis will help monitoring the global reefs health all over the world. An additional, sorely needed, but achievable development would be the possibility of NN to identify different age colonies of the same species, in order to follow population level processes, crucial for recruitment and inter-specific competition outcomes.
- Using video transects, rather than stills, as the image source.
- Allow recognition of different ages of the same coral species in order to extract population dynamics features such as population age structure and recruitment or decline of species.
- Calculate species diversity parameters from the image sets.
- Construct trend lines from sequential photo surveys of the same reef providing future likely outcomes.
- Estimate reef health based on bleaching and mortality.
Author Contributions
Acknowledgments
Conflicts of Interest
References
- Field, M.E.; Cochran, S.A.; Evans, K.R. U.S. Coral Reefs; Imperiled National Treasures; 025-02; USGS U.S. Geological Survey Fact: Reston, VA, USA, 2002. Available online: https://pubs.usgs.gov/fs/2002/fs025-02/ (accessed on 12 November 2019).
- Roberts, C.M.; McClean, C.J.; Veron, J.E.N.; Hawkins, J.P.; Allen, G.R.; McAllister, D.E.; Mittermeier, C.G.; Schueler, F.W.; Spalding, M.; Wells, F.; et al. Marine biodiversity hotspots and conservation priorities for tropical reefs. Science 2002, 295, 1280–1284. [Google Scholar] [CrossRef] [Green Version]
- Schumacher, H.; Zibrowius, H. What is hermatypic? A redefinition of ecological groups in corals and other organisms. Coral Reefs 1985, 4, 1–9. [Google Scholar] [CrossRef]
- Jones, C.G.; Lawton, J.H.; Shachak, M. Organisms as Ecosystem Engineers. In Ecosystem Management; Springer: New York, NY, USA, 1994; pp. 130–147. [Google Scholar]
- Brandt, K. Uber die symbiose von algen und tieren. Arch. Anat. Physiol. 1883, 1, 445–454. [Google Scholar]
- Odum, H.T.; Odum, E.P. Trophic structure and productivity of a windward coral reef community on Eniwetok Atoll. Ecol. Monogr. 1955, 25, 291–320. [Google Scholar] [CrossRef]
- Iluz, D.; Fermani, S.; Ramot, M.; Reggi, M.; Caroselli, E.; Prada, F.; Dubinsky, Z.; Goffredo, S.; Falini, G. Calcifying response and recovery potential of the brown alga Padina pavonica under ocean acidification. ACS Earth Space Chem. 2017, 1, 316–323. [Google Scholar] [CrossRef]
- Burns, T.P. Hard-coral distribution and cold-water disturbances in South Florida: Variation with depth and location. Coral Reefs 1985, 4, 117–124. [Google Scholar] [CrossRef]
- Dubinsky, Z.; Iluz, D. Corals and Light: From Energy Source to Deadly Threat. In The Cnidaria, Past, Present and Future: The World of Medusa and Her Sisters; Goffredo, S., Dubinsky, Z., Eds.; Springer: Cham, Switzerland, 2016; pp. 469–487. [Google Scholar]
- Goreau, T.F. The physiology of skeleton formation in corals. I. A method for measuring the rate of calcium deposition by corals under different conditions. Biol. Bull. 1959, 116, 59–75. [Google Scholar] [CrossRef] [Green Version]
- Cohen, A.L.; McCorkle, D.C.; de Putron, S.; Gaetani, G.A.; Rose, K.A. Morphological and compositional changes in the skeletons of new coral recruits reared in acidified seawater: Insights into the bio mineralization response to ocean acidification. Geochem. Geophys. Geosyst. 2009, 10. [Google Scholar] [CrossRef] [Green Version]
- Anthony, K.R.N.; Kline, D.I.; Diaz-Pulido, G.; Dove, S.; Hoegh-Guldberg, O. Ocean acidification causes bleaching and productivity loss in coral reef builders. Proc. Natl. Acad. Sci. USA 2008, 105, 17442–17446. [Google Scholar] [CrossRef] [Green Version]
- Fox, H.E.; Pet, J.S.; Dahuri, R.; Caldwell, R.L. Recovery in rubble fields: Long-term impacts of blast fishing. Mar. Pollut. Bull. 2003, 46, 1024–1031. [Google Scholar] [CrossRef]
- Wood, E. Collection of Coral Reef Fish for Aquaria: Global Trade, Conservation Issues and Management Strategies; Marine Conservation Society: Ross-on-Wye, UK, 2001. [Google Scholar]
- Downs, C.A.; Kramarsky-Winter, E.; Segal, R.; Fauth, J.; Knutson, S.; Bronstein, O.; Pennington, P. Toxicopathological effects of the sunscreen UV filter, oxybenzone (benzophenone-3), on coral planulae and cultured primary cells and its environmental contamination in Hawaii and the US Virgin Islands. Arch. Environ. Contam. Toxicol. 2016, 70, 265–288. [Google Scholar] [CrossRef] [PubMed]
- Longcore, T.; Rich, C. Ecological light pollution. Front. Ecol. Environ. 2004, 2, 191–198. [Google Scholar] [CrossRef]
- Wielgus, J.; Balmford, A.; Lewis, T.B.; Mora, C.; Gerber, L.R. Coral reef quality and recreation fees in marine protected areas. Conserv. Lett. 2010, 3, 38–44. [Google Scholar] [CrossRef]
- Littler, M.M.; Littler, D.S.; Brooks, B.L. Harmful algae on tropical coral reefs: Bottom-up eutrophication and top-down herbivory. Harmful Algae 2006, 5, 565–585. [Google Scholar] [CrossRef]
- Fabricius, K.E. Effects of terrestrial runoff on the ecology of corals and coral reefs: Review and synthesis. Mar. Pollut. Bull. 2005, 50, 125–146. [Google Scholar] [CrossRef] [PubMed]
- Heery, E.C.; Hoeksema, B.W.; Browne, N.K.; Reimer, J.D.; Ang, P.O.; Huang, D.; Alsagoff, N. Urban coral reefs: Degradation and resilience of hard coral assemblages in coastal cities of East and Southeast Asia. Mar. Pollut. Bull. 2018, 135, 654–681. [Google Scholar] [CrossRef]
- West, J.M.; Salm, R.V. Resistance and resilience to coral bleaching: Implications for coral reef conservation and management. Conserv. Biol. 2003, 17, 956–967. [Google Scholar] [CrossRef] [Green Version]
- Gorbunov, M.Y.; Falkowski, P.G. Photoreceptors in the cnidarian hosts allow symbiotic corals to sense blue moonlight. Limnol. Oceanogr. 2002, 47, 309–315. [Google Scholar] [CrossRef]
- Tamir, R.; Lerner, A.; Haspel, C.; Dubinsky, Z.; Iluz, D. The spectral and spatial distribution of light pollution in the waters of the northern Gulf of Aqaba (Eilat). Sci. Rep. 2017, 7, 42329. [Google Scholar] [CrossRef] [Green Version]
- LeCun, Y.; Bengio, Y.; Hinton, G. Deep learning. Nature 2015, 521, 436–444. [Google Scholar] [CrossRef]
- He, K.; Zhang, X.; Ren, S.; Sun, J. Delving Deep into Rectifiers: Surpassing Human-Level Performance on ImageNet Classification. In Proceedings of the IEEE International Conference on Computer Vision, Copenhagen, Denmark, 6 February 2015; pp. 1026–1034. [Google Scholar]
- Ciregan, D.; Meier, U.; Schmidhuber, J. Multi-Column Deep Neural Networks for Image Classification. In Proceedings of the 2012 IEEE Conference on Computer Vision and Pattern Recognition (CVPR), Providence, RI, USA, 16–21 June 2012; pp. 3642–3649. [Google Scholar]
- Sun, Y.; Chen, Y.; Wang, X.; Tang, X. Deep Learning Face Representation by Joint Identification-Verification. In Proceedings of the Advances in Neural Information Processing Systems (1988–1996), Montreal, QC, Canada, 8–13 December 2014. [Google Scholar]
- Taigman, Y.; Yang, M.; Ranzato, M.A.; Wolf, L. DeepFace: Closing the Gap to Human-Level Performance in Face Verification. In Proceedings of the 2014 IEEE Conference on Computer Vision and Pattern Recognition, Columbus, OH, USA, 23–28 June 2014; pp. 1701–1708. [Google Scholar]
- Wan, L.; Zeiler, M.; Zhang, S.; LeCun, Y.; Fergus, R. Regularization of Neural Networks Using DropConnect. In Proceedings of the 30th International Conference on Machine Learning, Atlanta, GA, USA, 16–21 June 2013; pp. 1058–1066. [Google Scholar]
- LeCun, Y.; Bottou, L.; Bengio, Y.; Haffner, P. Gradient-based learning applied to document recognition. Proc. IEEE 1998, 86, 2278–2324. [Google Scholar] [CrossRef] [Green Version]
- Wang, T.; Wu, D.J.; Coates, A.; Ng, A.Y. End-to-end Text Recognition with Convolutional Neutral Networks. In Proceedings of the 21st International Conference on Pattern Recognition (ICPR2012), Tsukuba, Japan, 11–15 November 2012; pp. 3304–3308. [Google Scholar]
- Coates, A.; Carpenter, B.; Case, C.; Satheesh, S.; Suresh, B.; Wang, T.; Ng, A.Y. Text Detection and Character Recognition in Scene Images with Unsupervised Feature Learning. ICDAR 2011, 11, 440–445. [Google Scholar] [CrossRef] [Green Version]
- Reyes, A.K.; Caicedo, J.C.; Camargo, J.E. Fine-Tuning Deep Convolutional Networks for Plant Recognition. In Proceedings of the Working Notes of CLEF 2015 Conference, Toulouse, France, 8–11 September 2015. [Google Scholar]
- Mahmood, A.; Bennamoun, M.; An, S.; Sohel, F. Resfeats: Residual Network Based Features for Image Classification. In Proceedings of the 2017 IEEE International Conference on Image Processing (ICIP), Beijing, China, 17–20 September 2017; pp. 1597–1601. [Google Scholar]
- Lee, H.; Pham, P.T.; Largman, Y.; Ng, A.Y. Unsupervised Feature Learning for Audio Classification Using Convolutional Deep Belief Networks. In Proceedings of the Advances in Neural Information Processing Systems 22 (NIPS 2009), Vancouver, BC, Canada, 10–12 December 2009; pp. 1096–1104. [Google Scholar]
- Christin, S.; Hervet, E.; Lecomte, N. Applications for deep learning in ecology. bioRxiv 2018, bioRxiv334854. [Google Scholar] [CrossRef]
- Ravikiran, C.; Prasad, V.; Rehna, V.J. Enhancing Underwater Gray Scale Images Using a Hybrid Approach of Filtering and Stretching Technique. Int. J. Adv. Eng. Manag. Sci. 2015, 1, 3. [Google Scholar]
- Pizarro, O.; Rigby, P.; Johnson-Roberson, M.; Williams, S.B.; Colquhoun, J. Towards Image-Based Marine Habitat Classification. In Proceedings of the OCEANS, Basel, Switzerland, 15–18 September 2008; pp. 1–7. [Google Scholar]
- Elawady, M. Sparse Coral Classification Using Deep Convolutional Neural Networks (VIBOT 2014). arXiv 2015, arXiv:1511.09067v1. [Google Scholar]
- Johnson-Roberson, M.; Kumar, S.; Williams, S. Segmentation and Classification of Coral for Oceanographic Surveys: A Semi-Supervised Machine Learning Approach. In Proceedings of the OCEANS—Asia Pacific, Singapore, 16–19 May 2006; pp. 1–6. [Google Scholar]
- Lowe, D.G. Object Recognition from Local Scale-Invariant Features. In Proceedings of the 7th IEEE International Conference on Computer Vision, Kerkyra, Greece, 20–27 September 1999; Volume 2, pp. 1150–1157. [Google Scholar]
- O’Hara, S.; Draper, B.A. Introduction to the Bag of Features paradigm for image classification and retrieval. arXiv 2011, arXiv:1101.3354. [Google Scholar]
- Stokes, M.D.; Deane, G.B. Automated processing of coral reef benthic images. Limnol. Oceanogr. Methods 2009, 7, 157–168. [Google Scholar] [CrossRef]
- Yang, J.; Liu, C.J.; Zhang, L. Color space normalization: Enhancing the discriminating power of color spaces for face recognition. Pattern Recognit. 2010, 43, 1454–1466. [Google Scholar] [CrossRef]
- Beijbom, O.; Edmunds, P.J.; Kline, D.I.; Mitchell, B.G.; Kriegman, D. Automated Annotation of Coral reef Survey Images. In Proceedings of the 2012 IEEE Conference on Computer Vision and Pattern Recognition (CVPR), Providence, RI, USA, 16–21 June 2012. [Google Scholar]
- Shihavuddin, A.S.M.; Gracias, N.; Garcia, R.; Gleason, A.C.; Gintert, B. Image-based coral reef classification and thematic mapping. Remote Sens. 2013, 5, 1809–1841. [Google Scholar] [CrossRef] [Green Version]
- Tanaka, J.W.; Presnell, L.M. Color diagnosticity in object recognition. Percept. Psychophys. 1999, 61, 1140–1153. [Google Scholar] [CrossRef] [Green Version]
- Mahmood, A.; Bennamoun, M.; An, S.; Sohel, F.; Boussaid, F.; Hovey, R.; Kendrick, G.; Fisher, R.B. Coral classification with hybrid feature representations. In Proceedings of the IEEE International Conference on Image Processing (ICIP), Phoenix, AZ, USA, 25–28 September 2016. [Google Scholar]
- Gómez-Ríos, A.; Tabik, S.; Luengo, J.; Shihavuddin, A.S.M.; Krawczyk, B.; Herrera, F. Towards highly accurate coral texture images classification using deep convolutional neural networks and data augmentation. arXiv 2018, arXiv:1804.00516. [Google Scholar] [CrossRef] [Green Version]
- Szegedy, C.; Vanhoucke, V.; Ioffe, S.; Shlens, J.; Wojna, Z. Rethinking the Inception Architecture for Computer Vision. In Proceedings of the IEEE Computer Society Conference on Computer Vision and Pattern Recognition, Vegas, NV, USA, 26 June–1 July 2016; pp. 2818–2826. [Google Scholar]
- He, K.; Zhang, X.; Ren, S.; Sun, J. Identity Mappings in Deep Residual Networks. In Proceedings of the European Conference on Computer Vision, Amsterdam, The Netherlands, 11–14 October 2016; Springer: Cham, Switzerland, 2016; pp. 630–645. [Google Scholar]
- Huang, G.; Liu, S.; van der Maaten, L.; Weinberger, K.Q. CondenseNet: An Efficient DenseNet Using Learned Group Convulutions. Group 2017, 3, 11. [Google Scholar]
- Beijbom, O.; Edmunds, P.J.; Roelfsema, C.; Smith, J.; Kline, D.I.; Neal, B.P.; Chan, S. Towards automated annotation of benthic survey images: Variability of human experts and operational modes of automation. PLoS ONE 2015, 10, e0130312. [Google Scholar] [CrossRef] [PubMed]
- Williams, I.D.; Couch, C.S.; Beijbom, O.; Oliver, T.A.; Vargas-Angel, B.; Schumacher, B.D.; Brainard, R.E. Leveraging Automated Image Analysis Tools to Transform Our Capacity to Assess Status and Trends of Coral Reefs. Front. Mar. Sci. 2019. [Google Scholar] [CrossRef] [Green Version]
- Mahmood, A.; Bennamoun, M.; An, S.; Sohel, F.; Boussaid, F.; Hovey, R.; Kendrick, G.; Fisher, R. Automatic annotation of coral reefs using deep learning. In Proceedings of the OCEANS 2016 MTS/IEEE Monterey, Monterey, CA, USA, 19–23 September 2016; pp. 1–5. [Google Scholar] [CrossRef] [Green Version]
- Loya, Y. Community structure and species diversity of hermatypic corals at Eilat, Red Sea. Mar. Biol. 1972, 13, 100–123. [Google Scholar] [CrossRef]
- Samoilys, M.A.; Carlos, G. Determining methods of underwater visual census for estimating the abundance of coral reef fishes. Environ. Biol. Fishes 2000, 57, 289–304. [Google Scholar] [CrossRef]
- Shaish, L.; Abelson, A.; Rinkevich, B. How plastic can phenotypic plasticity be? The branching coral Stylophora pistillata as a model system. PLoS ONE 2007, 2, e644. [Google Scholar] [CrossRef]
- Kaandorp, J.A.; Koopman, E.A.; Sloot, P.M.; Bak, R.P.; Vermeij, M.J.; Lampmann, L.E. Simulation and analysis of flow patterns around the scleractinian coral Madracis mirabilis (Duchassaing and Michelotti). Philos. Trans. R. Soc. Lond. Ser. B Biol. Sci. 2003, 358, 1551–1557. [Google Scholar] [CrossRef] [Green Version]
- Goffredo, S.; Caroselli, E.; Mattioli, G.; Pignotti, E.; Dubinsky, Z.; Zaccantia, F. Inferred level of calcification decreases along an increasing temperature gradient in a Mediterranean endemic coral. Limnol. Oceanogr. 2009, 54, 930–937. [Google Scholar] [CrossRef] [Green Version]
- Hoey, A.S.; Bellwood, D.R. Limited functional redundancy in a high diversity system: Single species dominates key ecological process on coral reefs. Ecosystems 2009, 12, 1316–1328. [Google Scholar] [CrossRef]
- Cleary, D.F.; De Vantier, L.; Vail, L.; Manto, P.; de Voogd, N.J.; Rachello-Dolmen, P.G.; Hoeksema, B.W. Relating variation in species composition to environmental variables: A multi-taxon study in an Indonesian coral reef complex. Aquat. Sci. 2008, 70, 419–431. [Google Scholar] [CrossRef]
- Cleary, D.F.; Polónia, A.R.; Renema, W.; Hoeksema, B.W.; Wolstenholme, J.; Tuti, Y.; de Voogd, N.J. Coral reefs next to a major conurbation: A study of temporal change (1985–2011) in coral cover and composition in the reefs of Jakarta, Indonesia. Mar. Ecol. Prog. Ser. 2014, 501, 89–98. [Google Scholar] [CrossRef] [Green Version]
- Cleary, D.F.R.; Polónia, A.R.M.; Renema, W.; Hoeksema, B.W.; Rachello-Dolmen, P.G.; Moolenbeek, R.G.; Hariyanto, R. Variation in the composition of corals, fishes, sponges, echinoderms, ascidians, molluscs, foraminifera and macroalgae across a pronounced in-to-offshore environmental gradient in the Jakarta Bay–Thousand Islands coral reef complex. Mar. Pollut. Bull. 2016, 110, 701–717. [Google Scholar] [CrossRef] [PubMed]
Dataset | Shihavuddin’s Method | Inception v3 | ResNet-50 | ResNet-152 | DenseNet-121 | DenseNet-161 |
---|---|---|---|---|---|---|
Eilat | 95.79% | 95.25% | 97.85% | 97.85% | 91.03% | 93.81% |
RSMAS | 92.74% | 96.03% | 97.67% | 97.95% | 89.73% | 91.10% |
Author | Dataset | Classifier | Classes | Accuracy | Number of Images |
---|---|---|---|---|---|
Beijbom et al. (2012) [45] | Based on Moorea Labeled Corals dataset (MLC) – from the island of Moorea in French Polynesia. That is a subset of the MCR LTER packaged for computer vision research. The MLC dataset is available at http://vision.ucsd.edu/data. | Support vector machines (SVM) along with filters and a texture descriptor. | 9 classes: including 5 coral genera: Acropora, Pavona, Montipora, Pocillopora, Porites are marked by triangles, non-coral substrates, Crustose Coralline Algae, Turf algae, Macroalgae, and Sand by circles. | accuracy on the MLC 2008 + 2009⇒ 2010 83.10% | 2055 images collected over three years: 2008, 2009 and 2010. |
Shihavuddin et al. (2013) [46] | Used six standard datasets: Moorea Labeled Corals (MLC), EILAT dataset, RSMAS and 3 more. | Support vector machines SVM multiclass, KNN, a neural network or probability density weighted mean distance technique. | 8 benthos types of classes on MLC dataset: sand, urchin, branches type I, brain coral, favid, branches type II, dead coral and branches type III. | Accuracy on MLC dataset:85.5% whereas all the other compared methods attained less than 80% On the Red Sea mosaic image, overall accuracy of 83.7%, which is at least 8% higher than the other methods tested. | |
Elawady, (2015) [39], Mahmood et al. (2016) [48] | Moorea Labeled Corals (MLC) and Atlantic Deep Sea (ADS) | Sparse classification for coral species using supervised DL method called CNNs. | 2 classes distinguish between: heathy to bleached coral reefs. MLC classes: 9 coral/non-coral classes These classes are classified into 5 coral classes (Acropora “Acrop”, Pavona “Pavon”, Montipora “Monti”, Pocillopora “Pocill”, and Porites “Porit”) and 4 non-coral classes (Crustose Coralline Algae “CCA”, Turf algae “Turf”, Macroalgae “Macro”, and Sand “Sand” | First work that used CNNs for coral classification was of Elawady, (2015) [39] 55% accuracy on the two datasets. they used ResFeats-50+ sCNN classifier 78.8%ResFeats-152+ sCNN classifier 80.0% ResFeats-152+ PCA-SVM 80.8% | ADS 50 images are expertly annotated (200 labeled points per image) clarifying different types of Lophelia coral habitats and the surrounding soft sediment Logachev mounds (Rockall Trough). The target nine classes are classified into 5 coral classes “Dead Coral” “Encrusting White Sponge”, “Leiopathes Species”, and “Rubble Coral” and 4 non-coral classes: “Boulder”, “Darkness”, “Gravel”, and “Sand” |
Mahmood et al. (2016a) [55] | Moorea Labeled Corals (MLC) BENTHOZ-2015 | 5 Classes: bare ground, seagrass meadows, algal cover, sponges, and coral reefs (i.e., coral/non-coral classification) | 77.90% VGGnet with a 2-layer MLP classifier (trained with the MLC dataset) | 400,000 images and associated sensor data collected by an autonomous vehicle over Australia | |
Mahmood et al. (2017) [34] | Moorea Labeled Corals (MLC) | 9 MLC classes | CNNs along with hand-crafted features. VGGnet pre-trained on ImageNet. Accuracy 84.50% | For Trainng—87,428 images from the year 2008, and 43,832 for testing. | |
Gómez-Ríos et al. (2018) [49] | EILAT and RSMAS | Three CNNs: Inception v3, ResNet and DenseNet. | Discrimination among structural groups such as a few branched and brain corals. Eilat contains: 8 classes RSMAS contains: 14 classes | Accuracy (see Table 1) | EILAT: 1123 images. RSMAS: 776 images. |
Williams et al. 2019 [54] | CoralNet -machine-learning image analysis tool consists of 822 data sets | Classification by functional group and by training within habitat types | Separate classes for coral-rich, pavement, boulder, or “other” habitats | automated-analysis algorithm is at least 90% certain of a classification | 700,000 images |
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Share and Cite
Raphael, A.; Dubinsky, Z.; Iluz, D.; Netanyahu, N.S. Neural Network Recognition of Marine Benthos and Corals. Diversity 2020, 12, 29. https://doi.org/10.3390/d12010029
Raphael A, Dubinsky Z, Iluz D, Netanyahu NS. Neural Network Recognition of Marine Benthos and Corals. Diversity. 2020; 12(1):29. https://doi.org/10.3390/d12010029
Chicago/Turabian StyleRaphael, Alina, Zvy Dubinsky, David Iluz, and Nathan S. Netanyahu. 2020. "Neural Network Recognition of Marine Benthos and Corals" Diversity 12, no. 1: 29. https://doi.org/10.3390/d12010029
APA StyleRaphael, A., Dubinsky, Z., Iluz, D., & Netanyahu, N. S. (2020). Neural Network Recognition of Marine Benthos and Corals. Diversity, 12(1), 29. https://doi.org/10.3390/d12010029