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Successful reproduction is critical to the growth and persistence of marine fish populations, yet how changes in the environment influence reproduction remains largely unknown. We explored how shifting ocean conditions influenced larval production in four species of long-lived, live-bearing rockfish (Sebastes spp.) in the California Current. Brood fecundity, body size, and environmental information were analyzed from the mid-1980s through 2020. Interannual variation in brood fecundity was greater than 50% in the single-brooding yellowtail rockfish (S. flavidus) and widow rockfish (S. entomelas). Brood fecundity varied less in chilipepper (S. goodei) and bocaccio (S. paucispinis), two species capable of multiple broods per year. In these two species, interannual fecundity variability is more likely to depend on the number of broods produced than on brood size alone. In all four species, brood fecundity was positively correlated with maternal length and body condition. Variable ocean conditions influenced the strength of maternal size effects by year. These results provide evidence for reproductive plasticity and environmental effects on fecundity, with implications for changes in population reproductive potential with climate change. 

The neocortex is functionally organized into layers. Layer four receives the densest bottom up sensory inputs, while layers 2/3 and 5 receive top down inputs that may convey predictive information. A subset of cortical somatostatin (SST) neurons, the Martinotti cells, gate top down input by inhibiting the apical dendrites of pyramidal cells in layers 2/3 and 5, but it is unknown whether an analogous inhibitory mechanism controls activity in layer 4. Using high precision circuit mapping, in vivo optogenetic perturbations, and single cell transcriptional profiling, we reveal complementary circuits in the mouse barrel cortex involving genetically distinct SST subtypes that specifically and reciprocally interconnect with excitatory cells in different layers: Martinotti cells connect with layers 2/3 and 5, whereas non-Martinotti cells connect with layer 4. By enforcing layer-specific inhibition, these parallel SST subnetworks could independently regulate the balance between bottom up and top down input.