Summary Leaf dark respiration (Rd) acclimates to environmental changes. However, the magnitude, controls and time scales of acclimation remain unclear and are inconsistently treated in ecosystem models.We hypothesized thatRdand Rubisco carboxylation capacity (Vcmax) at 25°C (Rd,25,Vcmax,25) are coordinated so thatRd,25variations supportVcmax,25at a level allowing full light use, withVcmax,25reflecting daytime conditions (for photosynthesis), andRd,25/Vcmax,25reflecting night‐time conditions (for starch degradation and sucrose export). We tested this hypothesis temporally using a 5‐yr warming experiment, and spatially using an extensive field‐measurement data set. We compared the results to three published alternatives:Rd,25declines linearly with daily average prior temperature;Rdat average prior night temperatures tends towards a constant value; andRd,25/Vcmax,25is constant.Our hypothesis accounted for more variation in observedRd,25over time (R2 = 0.74) and space (R2 = 0.68) than the alternatives. Night‐time temperature dominated the seasonal time‐course ofRd, with an apparent response time scale ofc.2 wk.Vcmaxdominated the spatial patterns.Our acclimation hypothesis results in a smaller increase in globalRdin response to rising CO2and warming than is projected by the two of three alternative hypotheses, and by current models.
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Modular derivation of diverse, regionally discrete human posterior CNS neurons enables discovery of transcriptomic patterns
Our inability to derive the neuronal diversity that comprises the posterior central nervous system (pCNS) using human pluripotent stem cells (hPSCs) poses an impediment to understanding human neurodevelopment and disease in the hindbrain and spinal cord. Here, we establish a modular, monolayer differentiation paradigm that recapitulates both rostrocaudal (R/C) and dorsoventral (D/V) patterning, enabling derivation of diverse pCNS neurons with discrete regional specificity. First, neuromesodermal progenitors (NMPs) with discreteHOXprofiles are converted to pCNS progenitors (pCNSPs). Then, by tuning D/V signaling, pCNSPs are directed to locomotor or somatosensory neurons. Expansive single-cell RNA-sequencing (scRNA-seq) analysis coupled with a novel computational pipeline allowed us to detect hundreds of transcriptional markers within region-specific phenotypes, enabling discovery of gene expression patterns across R/C and D/V developmental axes. These findings highlight the potential of these resources to advance a mechanistic understanding of pCNS development, enhance in vitro models, and inform therapeutic strategies.
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- Award ID(s):
- 1648035
- PAR ID:
- 10522573
- Publisher / Repository:
- AAAS- American Association for the Advancement of Science
- Date Published:
- Journal Name:
- Science Advances
- Volume:
- 8
- Issue:
- 39
- ISSN:
- 2375-2548
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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