Seasonality in embolism resistance and hydraulic capacitance jointly mediate hydraulic safety in branches and leaves of oriental cork oak (Quercus variabilis Bl.).

Seasonality in temperate regions is prominent during the era of increased climatic variability. A hydraulic trait that can adjust to seasonally changing climatic conditions is crucial for tree safety. However, little attention has been paid to the intraspecific seasonality of drought-related traits and hydraulic safety of keystone forest trees. We examined seasonal variations in the key morphological and physiological traits as well as multiple hydraulic safety margins (SMs) at the branch and leaf levels in oriental cork oak (Quercus variabilis Bl.), which is predominant in Chinese temperate forests. Pneumatic measurements indicated that, as seasons progressed, the water potential at which 50% of branch embolisms occur (P50_branch) decreased from -3.34 MPa to -4.23 MPa, with a coefficient of variation (CV) of 9.08%. Sapwood capacitance ranged from 48.19-248.08 kg m-3 MPa-1, peaking in autumn and reaching minimum in winter (CV 60.58%). Rehydration kinetics confirmed higher leaf embolism vulnerability (P50_leaf) in spring and autumn than those in summer, with values ranging from -1.06 MPa to -3.02 MPa (CV 39.85%). All leaf pressure-volume (PV) traits shifted with growth, with CVs ranging from 6.95-46.69%. Sapwood density had significant negative correlations with P50_branch and hydraulic capacitance for elastic water storage, whereas leaf mass per area was linearly associated with PV traits but not with P50_leaf. Furthermore, the branch typical SMs (difference between branch midday water potential and P50_branch) were consistently > 1.84 MPa, and vulnerability segmentation was prevalent throughout, implying a plausible hydraulic foundation for the dominance of Q. variabilis. Diverse hydraulic response patterns existed across seasons, leading to positive safety margins mediated by the aforementioned physiological traits. Although Q. variabilis exhibits a high level of hydraulic safety, its susceptibility to sudden summer droughts may increase due to global climate change.

Linking individual variability in functional brain connectivity to polygenic risk in major depressive disorder.

BACKGROUND: Major depressive disorder (MDD) is a highly heterogeneous disease, which brings great difficulties to clinical diagnosis and therapy. Its mechanism is still unknown. Prior neuroimaging studies mainly focused on mean differences between patients and healthy controls (HC), largely ignoring individual differences between patients. METHODS: This study included 112 MDD patients and 93 HC subjects. Resting-state functional MRI data were obtained to examine the patterns of individual variability of brain functional connectivity (IVFC). The genetic risk of pathways including dopamine, 5-hydroxytryptamine (5-HT), norepinephrine (NE), hypothalamic-pituitary-adrenal (HPA) axis, and synaptic plasticity was assessed by multilocus genetic profile scores (MGPS), respectively. RESULTS: The IVFC pattern of the MDD group was similar but higher than that in HCs. The inter-network functional connectivity in the default mode network contributed to altered IVFC in MDD. 5-HT, NE, and HPA pathway genes affected IVFC in MDD patients. The age of onset, duration, severity, and treatment response, were correlated with IVFC. IVFC in the left ventromedial prefrontal cortex had a mediating effect between MGPS of the 5-HT pathway and baseline depression severity. LIMITATIONS: Environmental factors and differences in locations of functional areas across individuals were not taken into account. CONCLUSIONS: This study found MDD patients had significantly different inter-individual functional connectivity variations than healthy people, and genetic risk might affect clinical manifestations through brain function heterogeneity.

Effect of NEUROG3 polymorphism rs144643855 on regional spontaneous brain activity in major depressive disorder.

PURPOSE: Our previous study identified a significant association between a single nucleotide polymorphism (SNP) located in the neurogenin3 (NEUROG3) gene and post-stroke depression (PSD) in Chinese populations. The present work explores whether polymorphism rs144643855 affects regional brain activity and clinical phenotypes in major depressive disorder (MDD). METHOD: A total of 182 participants were included: 116 MDD patients and 66 normal controls. All participants underwent resting-state functional magnetic resonance imaging (rs-fMRI) scanning at baseline. Spontaneous brain activity was assessed using amplitude of low-frequency fluctuation (ALFF). The Hamilton Depression Scale-24 (HAMD-24) and Snaith-Hamilton Pleasure Scale (SHAPS) were used to assess participants at baseline. Two-way analysis of covariance (ANCOVA) was used to explore the interaction between diagnostic groups and NEUROG3 rs144643855 on regional brain activity. We performed correlation analysis to further test the association between these interactive brain regions and clinical manifestations of MDD. RESULTS: Genotype and disease significantly interacted in the left inferior frontal gyrus (IFG-L), right superior frontal gyrus (SFG-R), and left paracentral lobule (PCL-L) (P < 0.05). ALFF values of the IFG-L were found to be significantly associated with anhedonia in MDD patients. CONCLUSION: These findings suggest a potential relationship between rs144643855 variations and altered frontal brain activity in MDD. NEUROG3 may play an important role in the neuropathophysiology of MDD.