Individual differences in explicit and implicit visuomotor learning and working memory capacity

The theoretical basis for the association between high working memory capacity (WMC) and enhanced visuomotor adaptation is unknown. Visuomotor adaptation involves interplay between explicit and implicit systems. We examined whether the positive association between adaptation and WMC is specific to the explicit component of adaptation. Experiment 1 replicated the positive correlation between WMC and adaptation, but revealed this was specific to the explicit component of adaptation, and apparently driven by a sub-group of participants who did not show any explicit adaptation in the correct direction. A negative correlation was observed between WMC and implicit learning. Experiments 2 and 3 showed that when the task restricted the development of an explicit strategy, high WMC was no longer associated with enhanced adaptation. This work reveals that the benefit of high WMC is specifically linked to an individual’s capacity to use an explicit strategy. It also reveals an important contribution of individual differences in determining how adaptation is performed

Combined effects of feeding enriched rotifers and antibiotic addition on performance of striped trumpeter (Latris lineata) larvae

Striped trumpeter have a complex and extended larval phase and are difficult to culture. Two experiments were conducted in replicated, 300-l hemispherical tanks to determine if larval survival, growth, bacterial or fatty acid profile were improved by feeding non-enriched rotifers or rotifers enriched with algae or commercially available products, as well as the effect of an antibiotic, oxytetracycline (OTC). Larvae were stocked at 25 l1 and 15 l1 and reared until Day 16 and Day 19 in Experiments 1 and 2, respectively. In Experiment 1, the feeding treatments were non-enriched rotifers, or rotifers enriched on algae, DHA Selco (a fish oil based emulsion) or RotiMac (dried Schizochytrium). There were no significant differences in mean survival (FSD) across treatments, which were generally low at 14.6F5.2%. Larvae reared on rotifers fed DHA Selco and RotiMac, had significantly higher proportions of incorporated DHA but no significant increase in growth. In Experiment 2, larvae were fed rotifers enriched on DHA Selco or AlgaMac 2000 and reared with or without the daily addition of 25 mg l1 OTC. At Day 19, there was significantly higher survival for larvae reared on AlgaMac 2000 and OTC, (37.4F5.6%), than DHA Selco and OTC, (16.0F7.4%), AlgaMac 2000 without OTC (7.0F8.0) and DHA Selco without OTC (3.3F1.2). Larvae reared with OTC were larger (279F58 Ag and 7.4F0.2 mm) than without OTC (177F40 Ag and 6.3F0.2 mm). The addition of antibiotics did not significantly influence fatty acid profiles of larvae. There were no significant differences in the percentage of DHA, 27.6F2.8%, EPA 4.6F1.0% or ARA 4.9F0.4%. Larvae reared with OTC had significantly less dgrey gutT (a measure of intestinal dysfunction). The results indicated that bacterial infection was a major source of mortality in striped trumpeter larvae and compromised larval growth. Assessment of the bacterial flora indicated that antibiotic use reduced the bacterial load, but did not eliminate potential pathogens. Our study suggests that microbial control has a greater influence than lipid nutrition on the survival and growth of larvae during the rotifer feeding stage

Influences of Dietary n-3 Long Chain PUFA on Body Concentrations of 20:5n-3, 22:5n-3 and 22:6n-3 in Larvae of a Marine Teleost Fish from Australian Waters, the Striped Trumpeter (Latris lineata)

We determined the effect of dietary long-chain (≥C20) PUFA (LC-PUFA), 20:5n-3 and 22:6n-3, on larval striped trumpeter (Latris lineata) biochemistry through early development and during live feeding with rotifers (Brachionus plicatilis). Rotifers were enriched using seven experimental emulsions formulated with increasing concentrations of n-3 LC-PUFA, mainly 20:5n-3 and 22:6n-3. Enriched rotifer n-3 LC-PUFA concentrations ranged from 10–30 mg/g dry matter. Enriched rotifers were fed to striped trumpeter larvae from 5 to 18 d post-hatch (dph) in a short-term experiment to minimize gross deficiency symptoms such as poor survival that could confound results. No relationships were observed between larval growth or survival with dietary n-3 LC-PUFA at 18 dph. The larval FA profiles generally reflected those of the rotifer diet, and significant positive regressions were observed between most dietary and larval FA at 10, 14, and 18 dph. The major exception observed was an inverse relationship between dietary and larval 22:5n-3. The presence of 22:5n-3 in elevated amounts when dietary 22:6n-3 was depressed suggests that elongation of 20:5n-3 may be occurring in an attempt to raise body concentrations of 22:6n-3. We hypothesize that accumulation of 22:5n-3 might be an early indicator of 22:6n-3 deficiency in larval fish that precedes a reduction in growth or survival. A possible role of 22:5n-3 as a biochemical surrogate for 22:6n-3 is discussed