Hydrodynamic disturbance and zooplankton swimming behaviour

EDITORIAL OFFICE, TAIPEI, TAIWAN, 11

A Lagrangian model of copepod dynamics: Clustering by escape jumps in turbulence

Planktonic copepods are small crustaceans that have the ability to swim by quick powerful jumps. Such an aptness is used to escape from high shear regions, which may be caused either by flow per- turbations, produced by a large predator (i.e., fish larvae), or by the inherent highly turbulent dynamics of the ocean. Through a combined experimental and numerical study, we investigate the impact of jumping behaviour on the small-scale patchiness of copepods in a turbulent environment. Recorded velocity tracks of copepods displaying escape response jumps in still water are here used to define and tune a Lagrangian Copepod (LC) model. The model is further employed to simulate the behaviour of thousands of copepods in a fully developed hydrodynamic turbulent flow obtained by direct numerical simulation of the Navier-Stokes equations. First, we show that the LC velocity statistics is in qualitative agreement with available experimental observations of copepods in tur- bulence. Second, we quantify the clustering of LC, via the fractal dimension $D_2$. We show that $D_2$ can be as low as ~ 2.3 and that it critically depends on the shear-rate sensitivity of the proposed LC model, in particular it exhibits a minimum in a narrow range of shear-rate values. We further investigate the effect of jump intensity, jump orientation and geometrical aspect ratio of the copepods on the small-scale spatial distribution. At last, possible ecological implications of the observed clustering on encounter rates and mating success are discussedComment: 13 pages, 9 figure

Two High-Nutrient Low-Chlorophyll phytoplankton assemblages: the tropical central Pacific and the offshore Perú-Chile Current

International audienceThe phytoplankton (>15 µm) composition and abundance was investigated along a ~8000 km transect between the Marquesas Islands Archipelago and the Chilean coasts off Concepción. In the southern limit of the central Equatorial Pacific (at 8° S, 141° W), in High-Nutrient Low-Chlorophyll (HNLC) warm waters, the microphytoplankton assemblage was dominated by the lightly silicified diatoms Pseudo-nitzschia delicatissima and Rhizosolenia bergonii. The morphology of these species, a small pennate diatom that exhibited a tendency to form "ball of needles" clusters and large centric diatom (>500 µm long), are interpreted as two anti-grazing strategies in an environment dominated by small micrograzers. Surprisingly, this a priori typical HNLC phytoplankton assemblage was also found in the temperate offshore waters of the Perú-Chile Current between 2000 and 600 km off Chile. This observation suggests that a common set of environmental factors (obviously other than temperature and salinity) are responsible for the establishment and maintaining of this distinctive phytoplankton in these geographically and hydrologically distant regions. Both regions are characterized by a surface nitrate-silicic acid ratio ranging from 1–3. Occasionally Rhizosolenia bergonii showed frustules anomalously fragmented, likely the result of extreme weakly silicified phytoplankton. We suggest that silicon deficiency may be responsible of the occurrence of HNLC phytoplankton assemblage in the tropical central Pacific as well as the offshore Perú-Chile Current during the austral summer

Role of kairomones in host location of the pennellid copepod parasite, Lernaeocera branchialis (L. 1767)

The life cycle of the parasitic copepod Lernaeocera branchialis involves 2 hosts, typically a pleuronectiform host upon which development of larvae and mating of adults occurs and a subsequent gadoid host, upon which the adult female feeds and reproduces. Both the copepodid and adult female stages must therefore locate and identify a suitable host to continue the life cycle. Several mechanisms are potentially involved in locating a host and ensuring its suitability for infection. These may include mechano-reception to detect host movement and chemo-reception to recognize host-associated chemical cues, or kairomones. The aim of this study was to identify the role of kairomones in host location by adult L. branchialis, by analysing their behaviour in response to fish-derived chemicals. Experiments demonstrated that water conditioned by immersion of whiting, Merlangius merlangus, elicited host-seeking behaviour in L. branchialis, whereas cod- (Gadus morhua) conditioned water did not. Lernaeocera branchialis are considered a genetically homogeneous population infecting a range of gadoids. However, their differential response to whiting- and cod-derived chemicals in this study suggests that either there are genetically determined subspecies of L. branchialis or there is some form of environmental pre-conditioning that allows the parasite to preferentially recognize the host species from which it originated

Efficient mate finding in planktonic copepods swimming in turbulence

Zooplankton live in dynamic environments where turbulence may challenge their limited swimming abilities. How this interferes with fundamental behavioral processes remains elusive. We reconstruct simultaneously the trajectories of flow tracers and calanoid copepods and we quantify their ability to find mates when ambient flow imposes physical constrains on their motion and impairs their olfactory orientation. We show that copepods achieve high encounter rates in turbulence due to the contribution of advection and vigorous swimming. Males further convert encounters within the perception radius to contacts and then to mating via directed motion toward nearby organisms within the short time frame of the encounter. Inertial effects do not result in preferential concentration, reducing the geometric collision kernel to the clearance rate, which we model accurately by superposing turbulent velocity and organism motion. This behavioral and physical coupling mechanism may account for the ability of copepods to reproduce in turbulent environments.Comment: Author's accepted manuscrip

Could dishonest banks be disciplined ?

Could a credit bureau incite banks to report correct information about their borrowers? We show that banks will choose the incorrect information sharing in the last period to increase their profits. Interestingly, however, it is shown that this strategy is optimal at the second period only if the proportion of successful projects is superior to 50%. In that case the Credit Bureau should enforce a sufficiently high penalty in order to incite banks to share information honestly. The penalty threshold that conditions the efficiency of the credit bureau’s role is endogenously derived

Could dishonest banks be disciplined ?

Could a credit bureau incite banks to report correct information about their borrowers? We show that banks will choose the incorrect information sharing in the last period to increase their profits. Interestingly, however, it is shown that this strategy is optimal at the second period only if the proportion of successful projects is superior to 50%. In that case the Credit Bureau should enforce a sufficiently high penalty in order to incite banks to share information honestly. The penalty threshold that conditions the efficiency of the credit bureau’s role is endogenously derived

From random walk to multifractal random walk in zooplankton swimming behaviour

EDITORIAL OFFICE, TAIPEI, TAIWAN, 11