Ecophysiology of the kleptoplastidic dinoflagellate Shimiella gracilenta: I. spatiotemporal distribution in Korean coastal waters and growth and ingestion rates

To explore the ecophysiological characteristics of the kleptoplastidic dinoflagellate Shimiella gracilenta, we determined its spatiotemporal distribution in Korean coastal waters and growth and ingestion rates as a function of prey concentration. The abundance of S. gracilenta at 28 stations from 2015 to 2018 was measured using quantitative realtime polymerase chain reaction. Cells of S. gracilenta were detected at least once at all the stations and in each season, when temperature and salinity were 1.7–26.4°C and 9.9–35.6, respectively. Moreover, among the 28 potential prey species tested, S. gracilenta SGJH1904 fed on diverse prey taxa. However, the highest abundance of S. gracilenta was only 3 cells mL-1 during the study period. The threshold Teleaulax amphioxeia concentration for S. gracilenta growth was 5,618 cells mL-1, which was much higher than the highest abundance of T. amphioxeia (667 cells mL-1). Thus, T. amphioxeia was not likely to support the growth of S. gracilenta in the field during the study period. However, the maximum specific growth and ingestion rates of S. gracilenta on T. amphioxeia, the optimal prey species, were 1.36 d-1 and 0.04 ng C predator- 1 d-1, respectively. Thus, if the abundance of T. amphioxeia was much higher than 5,618 cells mL-1, the abundance of S. gracilenta could be much higher than the highest abundance observed in this study. Eurythermal and euryhaline characteristics of S. gracilenta and its ability to feed on diverse prey species and conduct kleptoplastidy are likely to be responsible for its common spatiotemporal distribution.

Sexual Reproduction in Dinoflagellates—The Case of Noctiluca scintillans and Its Ecological Implications

Noctiluca scintillans is a larger, bioluminescent red-tide dinoflagellate (400–1,000 μm in diameter) that reproduces by sexual or asexual reproduction (binary fission). The process of sexual reproduction in N. scintillans has been thoroughly studied, but the ecological role and the mechanism of shifting from asexual to sexual reproduction have not been fully elucidated. It is believed, however, that sexual reproduction occurs when N. scintillans faces environmental stress. In this study, we tried to determine which factors drive N. scintillans to undergo sexual reproduction and we considered sexual reproduction’s ecological role. We cultured N. scintillans under different conditions of temperature, N. scintillans cell concentration, prey concentration, cultivation time, cultivation volume, light exposure time and physical vibration (simulated wave motion), and counted gametocyte mother cells every 24 h to calculate how the sexual reproduction rate changed over the experimental period. Rises in the sexual reproduction rate or the concentration of gametocyte mother cells only occurred in response to large variations in prey concentration, typically after the exponential phase of N. scintillans population growth. A noticeable upsurge in gametocyte mother cells, from 1% or less to nearly 10% of the total N. scintillans population, occurred when the prey concentration fell below ∼400 cells/mL. This implies that a sudden decrease in prey concentration induces more N. scintillans to shift from trophonts to gametocyte mother cells. We suggest that sexual reproduction may occur in N. scintillans as a response to the post-bloom situation when the dinoflagellate’s food supply has been dramatically depleted, producing large numbers of gametes for an alternative mode of survival after the end of each bloom.

Interactions Between the Kleptoplastidic Dinoflagellate Shimiella gracilenta and Several Common Heterotrophic Protists

The newly described dinoflagellate, Shimiella gracilenta, is known to survive for approximately 1 month on the plastids of ingested prey cells during starvation, indicating kleptoplastidy. To understand the population dynamics of this dinoflagellate in marine planktonic food webs, its growth and mortality rate due to predation should be assessed. Thus, we investigated the feeding occurrence of eight common heterotrophic protists on S. gracilenta. We also determined the growth and ingestion rates of Oxyrrhis marina and the naked ciliate, Rimostrombidium sp. on S. gracilenta as a function of the prey concentration. The common heterotrophic dinoflagellates (HTDs) Gyrodinium dominans, O. marina, and Pfiesteria piscicida and a naked ciliate Rimostrombidium sp. were able to feed on S. gracilenta; whereas the HTDs Aduncodinium glandula, Gyrodinium jinhaense, Oblea rotunda, and Polykrikos kofoidii were not. Shimiella gracilenta supported positive growth of O. marina and Rimostrombidium sp. but did not support that of G. dominans and P. piscicida. With increasing prey concentrations, the growth and ingestion rates of O. marina and Rimostrombidium sp. on S. gracilenta increased and became saturated. The maximum growth rates of O. marina and Rimostrombidium sp. on S. gracilenta were 0.645 and 0.903 day−1, respectively. Furthermore, the maximum ingestion rates of O. marina and Rimostrombidium sp. on S. gracilenta were 0.11 ng C predator day−1 (1.6 cells predator−1 day−1) and 35 ng C predator day−1 (500 cells predator−1 day−1), respectively. The maximum ingestion rate of O. marina on S. gracilenta was lower than that on any other algal prey reported to date, although its maximum growth rate was moderate. In conclusion, S. gracilenta had only a few common heterotrophic protist predators but could support moderate growth rates of the predators. Thus, S. gracilenta may not be a common prey species for diverse heterotrophic protists but may be a suitable prey for a few heterotrophic protists.

A three dimensional, full life cycle, anchovy and sardine model for the North Aegean Sea (Eastern Mediterranean): Validation, sensitivity and climatic scenario simulations

We present the development of a 3D full-lifecycle, individual-based model (IBM) for anchovy and sardine, online coupled to an existing hydrodynamic/biogeochemical low-trophic level (LTL) model for the North Aegean Sea. It was built upon an existing 1D model for the same species and area, with the addition of a horizontal movement scheme. In the model, both species evolve from the embryonic stage (egg+yolk sac larva) to the larval, juvenile, and adult stages. Somatic growth is simulated with the use of a “Wisconsin” type bioenergetics model and fish populations with an adaptation of the ‘super individuals’ (SI) approach. For the reference simulation and model calibration, in terms of fish growth and population biomass, the 2000-2010 period was selected. Interannual biomass variability of anchovy was successfully represented by the model, while the simulated biomass of sardine exhibited low variability and did not satisfactorily reproduce the observed interannual variability from acoustic surveys. The spatial distribution of both species’ biomass was in relatively good agreement with field data. Additional single-species simulations revealed that species compete for food resources. Temperature sensitivity experiments showed that both species reacted negatively to a temperature increase. Anchovy, in particular, was more affected since its spawning and larval growth periods largely overlap with the period of maximum yearly temperature and low prey concentration. Finally, simulation experiments using IPCC climatic scenarios showed that the predicted temperature increase and zooplankton concentration decrease in the future will negatively affect anchovy, resulting in sardine prevalence.

On the sensitivity of plankton ecosystem models to the formulation of zooplankton grazing

Model representations of plankton structure and dynamics have consequences for a broad spectrum of ocean processes. Here we focus on the representation of zooplankton and their grazing dynamics in such models. It remains unclear whether phytoplankton community composition, growth rates, and spatial patterns in plankton ecosystem models are especially sensitive to the specific means of representing zooplankton grazing. We conduct a series of numerical experiments that explicitly address this question. We focus our study on the form of the functional response to changes in prey density, including the formulation of a grazing refuge. We use a contemporary biogeochemical model based on continuum size-structured organization, including phytoplankton diversity, coupled to a physical model of the California Current System. This region is of particular interest because it exhibits strong spatial gradients. We find that small changes in grazing refuge formulation across a range of plausible functional forms drive fundamental differences in spatial patterns of plankton concentrations, species richness, pathways of grazing fluxes, and underlying seasonal cycles. An explicit grazing refuge, with refuge prey concentration dependent on grazers’ body size, using allometric scaling, is likely to provide more coherent plankton ecosystem dynamics compared to classic formulations or size-independent threshold refugia. We recommend that future plankton ecosystem models pay particular attention to the grazing formulation and implement a threshold refuge incorporating size-dependence, and we call for a new suite of experimental grazing studies.

Foraging modes and movements of Oncorhynchus mykiss as flow and invertebrate drift recede in a California stream

Salmonids frequently adapt their feeding and movement strategies to cope with seasonally fluctuating stream environments. Oncorhynchus mykiss tend to drift-forage in higher velocity habitat than other salmonids, yet their presence in streams with seasonally low velocity and drift suggests behavioral flexibility. We combined 3-D videogrammetry with measurements of invertebrate drift and stream hydraulics to investigate the drivers of O. mykiss foraging mode and movement during the seasonal recession in a California stream. From May to July (2016), foraging movement rate increased as prey concentration and velocity declined; however, movement decreased in August as pools became low and still. In May, 80% of O. mykiss were drift-foraging, while by July, over 70% used search or benthic-foraging modes. Velocity and riffle crest depth were significant predictors of foraging mode, while drift concentration was a poor univariate predictor. However top ranked additive models included both hydraulic variables and drift concentration. A drift-foraging bioenergetic model was a poor predictor of foraging mode. We suggest that infall and benthic prey, as well as risk aversion, may influence late-summer foraging decisions.

Salinity and prey concentration on larviculture of killifish Hypsolebias radiseriatus (Cyprinodontiformes: Rivulidae)

The aim of this study was to investigate the tolerance of Hypsolebias radiseriatus larvae to different salinities, and the effects of different prey concentrations and water salinities on the larviculture of this species. Salinity tolerance was tested by subjecting newly-hatched larvae to 96 hours of osmotic shock testing (experiment I) and gradual acclimatization (experiment II) of the following salinities: freshwater (control), 2, 4, 6 and 8 g of salt L-1. A third experiment (experiment III) evaluated three water salinities (S0 - freshwater, S2 - 2 g of salt L-1 and S4 – 4 g of salt L-1) and three initial daily prey concentrations (100, 300 and 500 artemia nauplii larva-1). In experiments I and II, survival was only influenced by the salinity of 8 g of salt L-1 (p < 0.01). After 35 days, weight was only influenced by prey concentration (p < 0.05), with the highest value being with 500 artemia nauplii larva-1. The lowest survival was for 4 g of salt L-1 and for 100 artemia nauplii larva-1. H. radiseriatus larviculture can be carried out in salinity of up to 2 g of salt L-1 and initial daily prey concentrations with 500 artemia nauplii larva-1.

Ecophysiological traits of mixotrophic Strombidium spp

Ciliates represent an important trophic link between nanoplankton and mesoplankton. Many species acquire functional chloroplasts from photosynthetic prey, being thus mixotrophs. Little is known about which algae they exploit, and of the relevance of inorganic carbon assimilation to their metabolism. To get insights into these aspects, laboratory cultures of three mixotrophic Strombidium spp. were established and 35 photosynthetic algal species were tested as prey. The relative contributions of ingestion and photosynthesis to total carbon uptake were determined, and responses to prey starvation were studied. Ciliate growth was supported by algal species in the 2–12 μm size range, with cryptophytes and chlorophytes being the best prey types. Inorganic carbon incorporation was only quantitatively important when prey concentration was low (3–100 μgCL−1), when it led to increased gross growth efficiencies. Chla specific inorganic carbon uptake rates were reduced by 60–90% compared to that of the photosynthetic prey. Inorganic carbon uptake alone could not sustain survival of cultures and ciliate populations declined by 25–30% during 5 days of starvation. The results suggest that mixotrophy in Strombidium spp. may substantially bolster the efficiency of trophic transfer when biomass of small primary producers is low.