Borehole Equilibration: Testing a New Method to Monitor the Isotopic Composition of Tree Xylem Water in situ

Forest water use has been difficult to quantify. One promising approach is to measure the isotopic composition of plant water, e.g., the transpired water vapor or xylem water. Because different water sources, e.g., groundwater versus shallow soil water, often show different isotopic signatures, isotopes can be used to investigate the depths from which plants take up their water and how this changes over time. Traditionally such measurements have relied on the extraction of wood samples, which provide limited time resolution at great expense, and risk possible artifacts. Utilizing a borehole drilled through a tree's stem, we propose a new method based on the notion that water vapor in a slow-moving airstream approaches isotopic equilibration with the much greater mass of liquid water in the xylem. We present two empirical data sets showing that the method can work in practice. We then present a theoretical model estimating equilibration times and exploring the limits at which the approach will fail. The method provides a simple, cheap, and accurate means of continuously estimating the isotopic composition of the source water for transpiration

Thermal imaging of increment cores: a new method to estimate sapwood depth in trees

The cells in tree sapwood form a network of interconnected conduits which enables the transport of water and nutrients from the tree roots to the canopy. Sapwood depth must be assessed when tree water use is estimated from sap flow velocities. However, current approaches to assess sapwood depth are either not applicable universally, or require expensive instruments, the application of chemicals or laborious field efforts. Here, we present a new method, which estimates sapwood depth by thermal imaging of increment cores. Using a low-cost thermal camera for mobile devices, we show that the sapwood-heartwood boundary is detectable by a sharp increase in temperature. Estimated sapwood depths agree with dye estimates (R-2 = 0.84). We tested our approach on a broad range of temperate and tropical tree species: Quercus robur, Pinus sylvestris, Swietenia macrophylla, Guazuma ulmifolia, Hymenaea courbaril, Sideroxylon capiri and Astronium graveolens. In nearly all species, the methods agreed within 0.6 cm. Thermal imaging of increment cores provides a straightforward, low-cost, easy-to-use, and species-independent tool to identify sapwood depth. It has further potential to reveal radial differences in sapwood conductivity, to improve water balance estimations on larger scales and to quickly develop allometric relationships

Continuous in situ measurements of water stable isotopes in soils, tree trunk and root xylem: Field approval

Rationale New methods to measure stable isotopes of soil and tree water directly in the field enable us to increase the temporal resolution of obtained data and advance our knowledge on the dynamics of soil and plant water fluxes. Only few field applications exist. However, these are needed to further improve novel methods and hence exploit their full potential. Methods We tested the borehole equilibration method in the field and collected in situ and destructive samples of stable isotopes of soil, trunk and root xylem water over a 2.5-month experiment in a tropical dry forest under natural abundance conditions and following labelled irrigation. Water from destructive samples was extracted using cryogenic vacuum extraction. Isotope ratios were determined with IRIS instruments using cavity ring-down spectroscopy both in the field and in the laboratory. Results In general, timelines of both methods agreed well for both soil and xylem samples. Irrigation labelled with heavy hydrogen isotopes clearly impacted the isotope composition of soil water and one of the two studied tree species. Inter-method deviations increased in consequence of labelling, which revealed their different capabilities to cover spatial and temporal heterogeneities. Conclusions We applied the novel borehole equilibration method in a remote field location. Our experiment reinforced the potential of this in situ method for measuring xylem water isotopes in both tree trunks and roots and confirmed the reliability of gas permeable soil probes. However, in situ xylem measurements should be further developed to reduce the uncertainty within the range of natural abundance and hence enable their full potential

Engineered Ovalbumin Nanoparticles for Cancer Immunotherapy

Ovalbumin (OVA) is a protein antigen that is widely used for eliciting cellular and humoral immune responses in cancer immunotherapy. As an alternative to solute OVA, engineering approach is developed herein towards protein nanoparticles (pNPs) based on reactive electrospraying. The resulting pNPs are comprised of polymerized OVA, where individual OVA molecules are chemically linked via poly(ethylene glycol) (PEG) units. Controlling the PEG/OVA ratio allows for fine‐tuning of critical physical properties, such as particle size, elasticity, and, at the molecular level, mesh size. As the PEG/OVA ratio decreased, OVA pNPs are more effectively processed by dendritic cells, resulting in higher OT‐I CD8+ cells proliferation in vitro. Moreover, pNPs with lower PEG/OVA ratios elicit enhanced lymphatic drainage in vivo and increased uptake by lymph node macrophages, dendritic cells, and B cells, while 500 nm OVA pNPs show poor draining lymph nodes delivery. In addition, pNPs with lower PEG/OVA ratios result in higher anti‐OVA antibody titers in vivo, suggesting improved humoral immune responses. Importantly, OVA pNPs result in significantly increased median survival relative to solute OVA antigen in a mouse model of B16F10‐OVA melanoma. This work demonstrates that precisely engineered OVA pNPs can improve the overall anti‐tumor response compared to solute antigen.As an alternative to solute antigens for cancer immunotherapy, protein nanoparticles (pNPs) comprised of polymerized antigen linked by poly(ethylene glycol) units are developed based on reactive electrospraying. This engineering approach allows fine tuning the physico‐chemical properties of pNPs such as particle size, elasticity, and mesh size. These properties are related to pNPs enhanced antigen‐specific immune responses and improved anti‐tumor efficacy.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/163384/3/adtp202000100-sup-0001-SuppMat.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/163384/2/adtp202000100.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/163384/1/adtp202000100_am.pd

Hydration and Solvent Exchange Induced Swelling and Deswelling of Homogeneous Poly(N-isopropylacrylamide) Microgel Thin Films

Widmann T, Kreuzer LP, Hohn N, et al. Hydration and Solvent Exchange Induced Swelling and Deswelling of Homogeneous Poly(N-isopropylacrylamide) Microgel Thin Films. LANGMUIR. 2019;35(49):16341-16352.The investigation of the response kinetics of smart colloidal microgel films is crucial for their optimization to enable advanced applications. We study the classical thermoresponsive microgel model system N-isopropylacrylamide cross-linked with N,N'-methylenebisacrylamide. Without the typically used polyelectrolyte coating of the substrate, thin microgel films are prepared in a single spin-coating step. Atomic force microscopy measurements reveal an extremely dense packing, resulting in a homogeneous compact thin film of microgel particles. The hydration kinetics of these films in H2O and D2O atmospheres as well as the kinetics of the solvent exchange between both water species are investigated with in situ time-of-flight neutron reflectometry (TOF-NR) and in situ Fourier-transform infrared (FTIR) spectroscopy. With accounting for a nonconstant humid atmosphere, the intrinsic diffusion dynamics of water molecules into the thin microgel film are modeled and the specific time constant tau and the effective Flory-Huggins interaction parameter chi(eff) are determined. Comparing the results in H2O and D2O atmospheres, TOF-NR and FTIR spectroscopy results show an increased affinity of the microgel films toward H2O as compared to D2O. From the FTIR spectroscopy data, we further identify different kinetics of intermolecular processes and order them according to their temporal evolution