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Feyen, J.

Publications and source records attributed to Feyen, J..

2 recordsLinked to original sources

Laser scanning identifies large trees as a major source of uncertainty in mangrove carbon accounting

BackgroundMangrove forests are crucial ecosystems which support biodiversity, protect coastlines and store vast amounts of carbon. Mangrove conservation and protection rely on accurate carbon accounting to unlock investment. However, the allometric equations underpinning these carbon estimates remain poorly constrained, particularly for the large trees. MethodsWe used terrestrial laser scanning (TLS) to estimate the biomass of 187 mangrove stems across Suriname, Panama, Colombia and Jamaica, including 84 stems >20 cm DBH. TLS-derived biomass estimates were used to evaluate local, regional and pantropical allometric equations. ResultsMost diameter-based allometric equations underestimated biomass by 8-65%. Equations additionally incorporating tree height performed better, but still underestimated biomass by 12-16% on average. Applying alternative allometries to a representative mangrove inventory from Panama produced biomass estimates ranging from 80 to 200 Mg ha-{superscript 1}, demonstrating that allometric uncertainty alone can generate more than a two-fold difference in estimated carbon stocks. ConclusionsCurrent allometric equations systematically underestimate the biomass of large mangrove trees and are therefore likely to underestimate mangrove carbon stocks. TLS provides a practical, non-destructive approach for expanding biomass datasets and improving allometric equations. Reducing allometric uncertainty should be a priority for strengthening blue carbon accounting and mangrove conservation.

ecology↗

Deconvolution Of Hematopoietic Stem/Progenitor Cell Signaling Predicts Inflammatory Niche Remodeling To Be A Determinant Of Tissue Failure And Outcome In Human AML

Cancer initiation is orchestrated by interplay between tumor-initiating cells and their stromal/immune environment. Here, by adapted scRNAsequencing, we decipher the predicted signaling between tissue-resident hematopoietic stem/progenitor cells (HSPCs) and their neoplastic counterparts with their native niches in the human bone marrow. LEPR+ stromal cells are identified as central regulators of hematopoiesis through predicted interactions with all cells in the marrow. Inflammatory niche remodeling and the resulting deprivation of critical HSPC regulatory factors is predicted to repress distinct high-output HSC subsets in NPM1-mutated AML, with relative resistance of clonal cells. Stromal gene signatures reflective of niche remodeling are associated with reduced relapse rates and favorable outcome after chemotherapy, across all genetic risk categories. Elucidation of the intercellular signaling defining human AML, thus, predicts that inflammatory remodeling of stem cell niches drives tissue repression and clonal selection, but may pose a vulnerability for relapse-initiating cells in the context of chemotherapeutic treatment. statement of significanceTumor-promoting inflammation is considered an enabling characteristic of tumorigenesis, but mechanisms remain incompletely understood. By deciphering the predicted signaling between tissue-resident stem cells and their neoplastic counterparts with their environment, we identify inflammatory remodeling of stromal niches as a determinant of normal tissue repression and clinical outcome in human AML. Key pointsO_LIA comprehensive taxonomy of the predicted interactions between LEPR+ stromal niches, HSPCs and adaptive/innate immune cells in the human NBM. C_LIO_LIInflammation-associated decline of stromal niches in AML represses residual normal hematopoiesis with relative resistance of leukemic cells. C_LIO_LIInflammatory decline of stromal niches is associated with reduced relapse risk and favorable outcome. C_LI

cancer biology↗