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Biology subjects

Garcia Munoz, A.

Publications and source records attributed to Garcia Munoz, A..

3 recordsLinked to original sources

Recreational climbing alters cliff soil chemistry and plant-associated fungal communities

O_LICliffs are environmentally extreme yet biodiversity-rich ecosystems that harbour specialist plants, many endemic and threatened. Plant persistence in these nutrient-poor substrates may depend on tightly linked soil- and root-associated microbial communities, which remain poorly understood. These interactions may become increasingly important with the global expansion of recreational climbing. While physical climbing impacts on vegetation are documented, potential chemical effects, from the use of climbing chalk (magnesium carbonate), on soil properties and plant-associated microbiota remain unknown. C_LIO_LIWe sampled soils and roots beneath cliff-specialist and generalist plants, and unvegetated soils, across climbed and unclimbed routes in northern, central, and southern Spain. Soil physicochemical properties were quantified, fungal communities were characterized using ITS-metabarcoding, and structural equation modelling was used to disentangle direct and indirect effects. C_LIO_LIClimbing increased soil pH and altered soil chemical properties, driving shifts in fungal diversity and functional composition in soil and roots. The relative read abundance of root-associated symbiotrophic fungi declined, whereas arbuscular mycorrhizal fungi and pathogens increased in climbed cliffs. Overall effects were consistent, with cliff-specialist plants mediating nutrient and fungal shifts. C_LIO_LIur findings show that climbing can reshape cliff soil chemistry and fungal communities, with potential cascading consequences for plant functional performance, nutrient dynamics, and ecosystem resilience. C_LI

ecology↗

Reproductive isolation emerges from coordinated barriers during mating system divergence in plants

Background and AimsUnderstanding how reproductive barriers combine to restrict gene flow remains a central challenge in speciation research. Although reproductive isolation is inherently a composite process, most empirical studies have focused on individual barriers in isolation, limiting our ability to capture their joint effects particularly in systems undergoing evolutionary transitions such as shifts in mating system. MethodsHere, we provide a comprehensive, life-cycle-wide quantification of reproductive isolation between two closely related species of the Erysimum incanum complex that differ strikingly in mating system: the predominantly selfing E. incanum and the outcrossing E. wilczekianum. Key ResultsBy integrating ecological, phenological, behavioural, and post-pollination components, we show that total reproductive isolation is nearly complete (T{approx}0.999), but overwhelmingly driven by pre-pollination barriers. Ecogeographical differentiation and, most prominently, pollinator-mediated isolation dominate, with pollinators exhibiting a strong bias toward E. wilczekianum. Floral traits linked to mating system divergence, particularly flower size, emerge as key drivers of assortative mating, supporting their role as "magic traits" coupling ecological divergence with reproductive isolation. In contrast, post-pollination barriers are weaker but strongly asymmetric. Hybrid seed formation is largely prevented when E. wilczekianum acts as the maternal parent, consistent with expectations from mating system differences, whereas reciprocal crosses are relatively successful. Despite reduced germination, hybrids display enhanced growth and no evidence of hybrid breakdown, suggesting that intrinsic incompatibilities remain incomplete. ConclusionsThese findings reveal that mating system divergence restructures the entire architecture of reproductive isolation rather than acting as a single barrier. More broadly, our results highlight that early-stage speciation can be driven by coordinated shifts in ecological and reproductive traits, emphasizing the need for integrative approaches to fully understand how barriers interact to generate species boundaries.

plant biology↗

Integrated genomic and epigenetic profiling reveals RAS pathway as a key driver of odontogenic tumors

Odontogenic tumors (OTs) are highly proliferative lesions with a low number of driving mutations, suggesting that concurrent alternative molecular mechanisms could support their extensive proliferation capacity. In this study, we analyzed 94 tissue samples from 79 patients with OTs and 15 healthy controls to explore their genetic and epigenetic alterations. Whole Exome Sequencing identified the BRAF V600E mutation in 75% of patients. A mutational hotspot analysis of six key genes (NRAS, EGFR, BRAF V600E, SMO L412, SMO W535, KRAS Q22K, PTCH1 R602*, and PTCH1 W129) revealed a high mutational rate, particularly in BRAF (91%), with 90% of BRAF V600E-positive patients being ameloblastomas. DNA methylation in the promoters of nine tumor-related genes (RB1, RASSF1A, BRCA1, BRCA2, MSH2, MLH1, MGMT, TIMP3, BRAF) was assessed in 67 OT patients and 15 controls. Five CpG sites showed significant hypermethylation (p<0.05; FDR q<0.05), notably in RASSF1A (cg50378469, cg50378539) and TIMP3 (cg33197381, cg33197394, cg33197400). Somatic hypermethylation of the full promoter was detected in RASSF1A (8 patients, mean methylation: 17.5%), BRCA1 (3 patients, mean methylation: 11.7%), and MLH1 (1 patient, mean methylation: 2%). Interestingly, 76.5% of BRAF V600E-positive patients had RASSF1A promoter hypermethylation. A strong correlation between BRAF V600E mutation and RASSF1A hypermethylation was detected. Our results might imply a synergistic effect of the BRAF V600E mutation and RASSF1A hypermethylation as determinants in the RAS pathway. These findings, together with observations from other studies, suggest that the RAS pathway is a key axis in OT biology.

genomics↗