The Risk for Novel and Disappearing Environmental Conditions in the Baltic Sea

Future climate biogeochemical projections indicate large changes in the ocean with environmental conditions not experienced at present referred to as novel, or may even disappear. These climate-induced changes will most likely affect species distribution via changes in growth, behavior, evolution, dispersal, and species interactions. However, the future risk of novel and disappearing environmental conditions in the ocean is poorly understood, in particular for compound effects of climate and nutrient management changes. We map the compound risk of the occurrence of future novel and disappearing environmental conditions, analyze the outcome of climate and nutrient management scenarios for the world’s largest estuary, the Baltic Sea, and the potential consequences for three charismatic species. Overall, the future projections show, as expected, an increase in environmental novelty over time. The future nutrient reduction management that improves the eutrophication status of the Baltic Sea contributes to large novel and disappearing conditions. We show the consequences of novel and disappearing environmental conditions for fundamental niches of three charismatic species under different scenarios. This first step toward comprehensively analyzing environmental novelty and disappearing conditions for a marine system illustrates the urgent need to include novelty and disappearing projection outputs in Earth System Models. Our results further illustrate that adaptive management is needed to account for the emergence of novelty related to the interplay of multiple drivers. Overall, our analysis provides strong support for the expectation of novel ecological communities in marine systems, which may affect ecosystem services, and needs to be accounted for in sustainable future management plans of our oceans.

Beta bursting in the retrosplenial cortex is a neurophysiological correlate of environmental novelty which is disrupted in a mouse model of Alzheimer’s disease

The retrosplenial cortex (RSC) plays a significant role in spatial learning and memory, and is functionally disrupted in the early stages of Alzheimer’s disease. In order to investigate neurophysiological correlates of spatial learning and memory in this region we employed in vivo electrophysiology in awake, behaving mice, comparing neural activity between wild-type and J20 mice, a mouse model of Alzheimer’s disease-associated amyloidopathy. To determine the response of the RSC to environmental novelty local field potentials were recorded while mice explored novel and familiar recording arenas. In familiar environments we detected short, phasic bursts of beta (20-30 Hz) oscillations (beta bursts) which arose at a low but steady rate. Exposure to a novel environment rapidly initiated a dramatic increase in the rate, size and duration of beta bursts. Additionally, theta-beta cross-frequency coupling was significantly higher during novelty, and spiking of neurons in the RSC was significantly enhanced during beta bursts. Finally, aberrant beta bursting was seen in J20 mice, including increased beta bursting during novelty and familiarity, yet a loss of coupling between beta bursts and spiking activity. These findings, support the concept that beta bursting may be responsible for the activation and reactivation of neuronal ensembles underpinning the formation and maintenance of cortical representations, and that disruptions to this activity in J20 mice may underlie cognitive impairments seen in these animals.

RGS14 modulates locomotor behavior and ERK signaling induced by environmental novelty and cocaine within discrete limbic structures

RationaleIn rodents, exposure to novel environments or psychostimulants promotes locomotor activity. Indeed, locomotor reactivity to novelty strongly predicts behavioral responses to psychostimulants in animal models of addiction. RGS14 is a plasticity restricting protein with unique functional domains that enable it to suppress ERK-dependent signaling as well as regulate G protein activity. Although recent studies show that RGS14 is expressed in multiple limbic regions implicated in psychostimulant- and novelty-induced hyperlocomotion, its function has been studied almost entirely in the context of hippocampal physiology and hippocampusdependent behaviors.ObjectiveWe sought to determine whether RGS14 modulates novelty- and psychostimulant-induced locomotion and neuronal activity.MethodsWe assessed Rgs14 knockout (RGS14 KO) mice and wild-type (WT) littermate controls using novelty-induced locomotion (NIL) and cocaine-induced locomotion (CIL) behavioral tests with subsequent quantification of c-fos and phosphorylated ERK (pERK) induction in limbic regions that express RGS14.ResultsCompared to WT controls, RGS14 KO mice exhibited attenuated locomotor responses in the NIL test, driven by avoidance of the center of the novel environment. By contrast, RGS14 KO mice demonstrated augmented peripheral locomotion in the CIL test conducted in either a familiar or novel environment. The absence of RGS14 enhanced induction of c-fos and pERK in the central amygdala and hippocampus (areas CA1 and CA2) when cocaine was administered in a novel environment.ConclusionsRGS14 regulates novelty- and psychostimulant-induced hyperlocomotion, particularly with respect to thigmotaxis. Further, our findings suggest RGS14 may reduce neuronal activity in discrete limbic subregions by inhibiting ERK-dependent signaling and transcription.

Better model transfers require knowledge of mechanisms

Model transferability is an emerging and important branch of predictive science that has grown primarily from a need to produce ecological forecasts in the face of widespread data deficiency and escalating environmental novelty. In our recent article in Trends in Ecology and Evolution, we outlined some of the major roadblocks that currently undermine the practice of model transfers in ecology. The response of Radchuk et al. to our work stresses the value of considering ‘first principles’ in projections of ecosystem change and offers insights into outstanding challenges specific to mechanistic (synonym: process-based) models.

Locus Coeruleus and Dopamine-Dependent Memory Consolidation

Most everyday memories including many episodic-like memories that we may form automatically in the hippocampus (HPC) are forgotten, while some of them are retained for a long time by a memory stabilization process, called initial memory consolidation. Specifically, the retention of everyday memory is enhanced, in humans and animals, when something novel happens shortly before or after the time of encoding. Converging evidence has indicated that dopamine (DA) signaling via D1/D5receptors in HPC is required for persistence of synaptic plasticity and memory, thereby playing an important role in the novelty-associated memory enhancement. In this review paper, we aim to provide an overview of the key findings related to D1/D5receptor-dependent persistence of synaptic plasticity and memory in HPC, especially focusing on the emerging evidence for a role of the locus coeruleus (LC) in DA-dependent memory consolidation. We then refer to candidate brain areas and circuits that might be responsible for detection and transmission of the environmental novelty signal and molecular and anatomical evidence for the LC-DA system. We also discuss molecular mechanisms that might mediate the environmental novelty-associated memory enhancement, including plasticity-related proteins that are involved in initial memory consolidation processes in HPC.