Macroalgal blooms affect the food web of tropical coastal ecosystems impacted by fisheries.

Macroalgal bloom events have been frequent in recent years. Eutrophication and overexploitation fishing may favor blooms through nutrient availability and capturing top predators. We aim to investigate the drivers of the macroalgae blooms and their consequences on the food web of the two tropical coastal ecosystems: Porto do Mangue (with high macroalgae production) and Baía Formosa (control environment, without macroalgae), both exploited by artisanal fisheries in northeastern Brazil. The food webs are modeled using the Ecopath with Ecosim (EwE) approach. Our results suggest that fishing did not favor macroalgae blooms but rather the high concentration of nutrients added to the semi-arid conditions. Furthermore, the macroalgae bloom showed low trophic impact, so much of their biomass is transferred into detritus. However, when it decomposes, this accumulation of matter alters the structure and functioning of the ecosystem, affecting its main fish resources: shrimp and piscivorous fish. Investigating blooms is key to management.

Fractalkine protein localization and gene expression in mouse brain.

Few chemokines are expressed constitutively in the brain at detectable levels; amongst them is fractalkine. We analyzed the distribution of fractalkine in the mouse brain with the aim of giving a neuroanatomical support to the study of its physiological function. To this end, we carried out an analysis of fractalkine protein localization and gene expression. An anti-fractalkine antibody was produced and used to perform an immunohistochemical study. The results indicated a high level of fractalkine protein in cortex, hippocampus, basal ganglia, and olfactory bulb. In particular, the presence of abundant immunoreactive neurons was observed in layers II, III, V, and VI of the cortex. In the hippocampus, the CA1 region was the most intensely labeled, but immunoreactive neurons were present also in CA2 and CA3, whereas in the basal ganglia, immunoreactive cells were observed in the caudate putamen. Other brain structures such as the brainstem showed a few scattered immunoreactive cells. The presence of fractalkine immunoreactive fibers was revealed only in the olfactory bulb and in the anterior olfactory nuclei. Gene expression study results, obtained by both semiquantitative PCR and in situ hybridization, matched protein localization with the highest levels of fractalkine transcript detected in the hippocampus, cortex, and striatum. The present study showed that fractalkine protein and mRNA are constitutively expressed at a high level in forebrain structure, but are almost absent in the hindbrain. Furthermore, localization at the cellular body level would suggest a paracrine or cell-to-cell interaction role for fractalkine more than a neurotransmission modulatory function.