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Highlights d Mice discriminate unfamiliar conspecifics based on altered states (fear or relief) d Endogenous OXT release from PVN to CeA is necessary for emotion discrimination d Abolishing PVN OXT release to Nac, PFC, or CA2 does not affect emotion discrimination d Dysbindin-dependent emotion discrimination deficits are caused by reduced CeA OXTRs

Traditional methods for studying tree roots are destructive and labor intensive, but available nondestructive techniques are applicable only to small scale studies or are strongly limited by soil conditions and root size. Soil electrical resistivity measured by geoelectrical methods has the potential to detect belowground plant structures, but quantitative relationships of these measurements with root traits have not been assessed. We tested the ability of two-dimensional (2-D) DC resistivity tomography to detect the spatial variability of roots and to quantify their biomass in a tree stand. A high-resolution resistivity tomogram was generated along a 11.75 m transect under an Alnus glutinosa (L.) Gaertn. stand based on an alpha-Wenner configuration with 48 electrodes spaced 0.25 m apart. Data were processed by a 2-D finite-element inversion algorithm, and corrected for soil temperature. Data acquisition, inversion and imaging were completed in the field within 60 min. Root dry mass per unit soil volume (root mass density, RMD) was measured destructively on soil samples collected to a depth of 1.05 m. Soil sand, silt, clay and organic matter contents, electrical conductivity, water content and pH were measured on a subset of samples. The spatial pattern of soil resistivity closely matched the spatial distribution of RMD. Multiple linear regression showed that only RMD and soil water content were related to soil resistivity along the transect. Regression analysis of RMD against soil resistivity revealed a highly significant logistic relationship (n = 97), which was confirmed on a separate dataset (n = 67), showing that soil resistivity was quantitatively related to belowground tree root biomass. This relationship provides a basis for developing quick nondestructive methods for detecting root distribution and quantifying root biomass, as well as for optimizing sampling strategies for studying root-driven phenomena.

In this study, we assess the possibility of using ground penetrating radar (GPR) and electrical resistivity tomography (ERT) as indirect non-destructive techniques for root detection. Two experimental sites were investigated: a poplar plantation [mean height of plants 25.7 m, diameter at breast height (dbh) 33 cm] and a pinewood forest mainly composed of Pinus pinea L. and Pinus pinaster Ait. (mean height 17 m, dbh 29 cm). GPR measures were taken using antennas of 900 and 1500 MHz applied in square and circular grids. ERT was previously tested along 2-D lines, compared with GPR sections and direct observation of the roots, and then using a complete 3-D acquisition technique. Three-dimensional reconstructions using grids of electrodes centred and evenly spaced around the tree were used in all cases (poplar and pine), and repeated in different periods in the pine forest (April, June and September) to investigate the influence of water saturation on the results obtainable. The investigated roots systems were entirely excavated using AIR-SPADE Series 2000. In order to acquire morphological information on the root system, to be compared with the GPR and ERT, poplar and pine roots were scanned using a portable on ground scanning LIDAR. In test sections analysed around the poplar trees, GPR with a high frequency antenna proved to be able to detect roots with very small diameters and different angles, with the geometry of survey lines ruling the intensity of individual reflectors. The comparison between 3-D images of the extracted roots obtained with a laser scan data point cloud and the GPR profile proved the potential of high density 3-D GPR in mapping the entire system in unsaturated soil, with a preference for sandy and silty terrain, with problems arising when clay is predominant. Clutter produced by gravel and pebbles, mixed with the presence of roots, can also be sources of noise for the GPR signals. The work performed on the pine trees shows that the shape, distribution and volume of roots system, can be coupled to the 3-D electrical resistivity variation of the soil model map. Geophysical surveys can be a useful approach to root investigation in describing both the shape and behaviour of the roots in the subsoil.

Highlights d DS mice display microglia alterations and cognitive impairment d Depletion of microglia rescues cognitive impairment in DS mice d Acetaminophen treatment rescues microglia and cognitive impairments in DS mice d Brain samples of DS people recapitulate microglia alterations

The protein p27 plays roles that extend beyond cell-cycle regulation during cerebral cortex development, such as the regulation of neuronal migration and neurite branching via signaling pathways that converge on the actin and microtubule cytoskeletons. Microtubule-dependent transport is essential for the maturation of neurons and the establishment of neuronal connectivity though synapse formation and maintenance. Here, we show that p27 controls the transport of vesicles and organelles along the axon of mice cortical projection neurons in vitro. Moreover, suppression of the p27 ortholog, dacapo, in Drosophila melanogaster disrupts axonal transport in vivo, leading to the reduction of locomotor activity in third instar larvae and adult flies. At the molecular level, p27 stabilizes the α-tubulin acetyltransferase 1, thereby promoting the acetylation of microtubules, a post-translational modification required for proper axonal transport.

The development of the cerebral cortex requires coordinated regulation of proliferation, specification, migration and differentiation of cortical progenitors into functionally integrated neurons. The completion of the neurogenic program requires a dynamic interplay between cell intrinsic regulators and extrinsic cues, such as growth factor and neurotransmitters. We previously demonstrated a role for extrasynaptic glycine receptors (GlyRs) containing the a2 subunit in cerebral cortical neurogenesis, revealing that endogenous GlyR activation promotes interneuron migration in the developing cortical wall. The proliferative compartment of the cortex comprises apical progenitors that give birth to neurons directly or indirectly through the generation of basal progenitors, which serve as amplification step to generate the bulk of cortical neurons. The present work shows that genetic inactivation of Glra2, the gene coding the a2 subunit of GlyRs, disrupts dorsal cortical progenitor homeostasis with an impaired capability of apical progenitors to generate basal progenitors. This defect results in an overall reduction of projection neurons that settle in upper or deep layers of the cerebral cortex. Overall, the depletion of cortical neurons observed in Glra2-knockout embryos leads to moderate microcephaly in newborn Glra2-knockout mice. Taken together, our findings support a contribution of GlyR a2 to early processes in cerebral cortical neurogenesis that are required later for the proper development of cortical circuits. The cerebral cortex develops from the forebrain and contains different classes of neurons distributed within layers that are regionally organized into sensory, motor and association areas. Cerebral cortex layering arises inside-out as progenitors give birth to successive waves of pyramidal projection neurons in the dorsal telencephalon 1 and GABAergic interneurons in the ventral forebrain.2 Projection neurons migrate radially to settle in appropriate layers of the cortical plate (CP) from where they grow axonal projections towards cortical or subcortical targets. Interneurons migrate from the ganglionic eminences along multiple tangential paths to integrate local cortical networks. More generally, the development of the cortex progresses through successive steps including proliferation, specification, migration and neuronal differentiation. Disrupting the completion of one or several of these cellular events may lead to severe cortical malformations underlying neurological disorders characterized by learning and intellectual disability or epilepsy.

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