Sampling and identifying marine zooplankton

stretch_gulper44

Zooplankton can be subdivided into two major groups. Holoplankton (for example, copepods and krill) spend their entire lives as plankton, and thus provide major food sources for pelagic fisheries. Meroplankton (for example, the larvae of barnacles, mussels, annelids, and fish) spend only part of their life as plankton. These larvae and juveniles typically provide the dispersal mechanisms for sessile adult organisms, such as reef-building corals, shellfish and worms, or for economically important benthic species such as crabs, lobsters and rockfish. Knowing when (seasonally) and where (inshore or offshore) dispersal occurs is essential to maximizing the productivity of commercial species and designing marine protected areas. Traditionally, surveys of zooplankton abundance and diversity are conducted from research vessels. More economical and efficient methods are needed to guide the recommendations of fisheries managers and conservation agencies.

Zooplankton are notoriously difficult to sample. Despite opportunities for mixing, individual zooplankton are tiny and species are often patchily distributed. Coastal oceans are physically dynamic, high-energy environments. Winds, currents and upwelling fronts affect the availability of nutrients and distribution of food that control zooplankton growth and dispersal. To address the difficulties posed by spatial patchiness and temporal variability, we developed the SIMZ program to explore more efficient methods for zooplankton sampling and identification.

stretch_gulper26Traditionally, tow-nets are used to sample plankton along paths through the water. Because these paths often traverse smaller environmental patches, they frequently lack the precision needed to associate the distribution and abundance of zooplankton species with particular physical and biological processes. To better assess the spatial patchiness in zooplankton abundance, MBARI engineers have equipped the Dorado AUV with 20 gulpers, 1.6 L bottles that rapidly inhale discrete water samples. The AUV is equipped with sensors (for example, temperature, salinity, and chlorophyll fluorescence) and onboard computer software can then instruct the Gulper AUV to recognize and autonomously sample specific environmental patches, such as upwelling fronts or chlorophyll thin layers. This “surgical” approach to ocean sampling allows SIMZ researchers to study the effects of specific physical processes on zooplankton distribution and diversity.

Visual identification and enumerate of zooplankton species under a microscope is time consuming and requires considerable taxonomic expertise. We have developed high-throughput molecular methods to quickly identify the diverse taxa present in marine samples. Yet, metagenomic methods based on a limited number of genetic markers are not perfect. We still need to vet these methods by comparing our results with data obtained by morphological taxonomic assessments. Likewise, small sample volumes obtained by the Gulper AUV system also tend to miss low-abundance organisms and some organisms with behaviors aimed at escaping predators. Despite the present shortcomings, these new sampling and molecular methods have succeeded in obtaining very precise data on zooplankton associations with specific environmental features.

The SIMZ program has generated massively diverse molecular and physical oceanographic data that are difficult to manage and analyze in traditional contexts. The molecular data alone from a single Gulper sample can return hundreds of thousands of DNA sequences, and 20 to 40 samples can be taken in a single day. The need to combine the metagenomic and environmental data in a comprehensive database has played a large role in motivating development of the Spatial Temporal Oceanographic Query System (STOQS) at MBARI. This system enables researchers to more easily visualize, manage and analyze data from the diverse sources employed under SIMZ.

Relevant publications

McCann M, Schramm R, Cline D, Michisaki R, Harvey J, Ryan J (2014). Using STOQS (The spatial temporal oceanographic query system) to manage, visualize, and understand AUV, glider, and mooring data. Autonomous Underwater Vehicles (AUV), Institute for Electrical and Electronics Engineers Oceanic Engineering Society Meeting, Oxford, Massachusetts. http://dx.doi.org/10.1109/auv.2014.7054414

Ryan JP, Harvey JBJ, Zhang Y, Woodson CB (2014). Distributions of invertebrate larvae and phytoplankton in a coastal upwelling system retention zone and peripheral front. Journal of Experimental Molecular Biology and Ecology 459: 51–60. http://dx.doi.org/10.1016/j.jembe.2014.05.017

Harvey JBJ (2014). A 96–well plate format for detection of marine zooplankton with the sandwich hybridization assay. In: Stricker, S.A. and D. Carroll (Eds.), Methods in Molecular Biology: Developmental biology of the sea urchin and other marine invertebrates. Humana Press Inc., New York. http://dx.doi.org/10.1007/978-1-62703-974-1_18

Das J, Harvey JBJ, Py F, Vathsangam H, Graham R, Rajan K, and Sukhatme GS (2013). Hierarchical probabilistic regression for AUV-based adaptive sampling of marine phenomena. Proceedings of the 2013 Institute for Electrical and Electronics Engineers International Conference on Robotics and Automation, Karlsruhe, Germany. http://dx.doi.org/10.1109/icra.2013.6631377

Harvey JBJ, Djunaedi AF and Vrijenhoek RC (2013). Validation of a sandwich hybridization assay for marine copepod detection. Journal of Experimental Molecular Biology and Ecology 446: 306–310. http://dx.doi.org/10.1016/j.jembe.2013.06.005

Zhang Y, Ryan JP, Bellingham JG, Harvey JBJ and McEwen RS (2012). Autonomous detection and sampling of water types and fronts in a coastal upwelling system by an autonomous underwater vehicle. Limnology Oceanography: Methods 10: 934–951. http://dx.doi.org/10.4319/lom.2012.10.934

Harvey JBJ, Ryan JP, Marin III R, Preston CM, Alvarado N, Scholin CA and Vrijenhoek RC (2012). Robotic sampling, in situ monitoring and molecular detection of marine zooplankton. Journal of Experimental Molecular Biology and Ecology 413: 60–70. http://dx.doi.org/10.1016/j.jembe.2011.11.022

Ryan JP, Johnson SB, Sherman A, Rajan K, Py F, Thomas H, Harvey JBJ, Bird L, Paduan JD and Vrijenhoek RC (2010). Mobile autonomous process sampling within coastal ocean observing systems. Limnology and Oceanography Methods 8: 394–402. http://dx.doi.org/10.4319/lom.2010.8.394

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