Climate reconstruction from paired oxygen-isotope analyses of chironomid larval head capsules and endogenic carbonate (Hawes Water, UK) - Potential and problems

Temperature and the oxygen isotopic composition (δ18O) of meteoric water are both important palaeoclimatic variables, but separating their influences on proxies such as the δ18O of lake carbonates is often problematic. The large temperature variations that are known to have occurred in the northern mid-latitudes during the Late Glacial make this interval an excellent test for a novel approach that combines oxygen-isotope analyses of chironomid larval head capsules with co-occurring endogenic carbonate. We apply this approach to a Late Glacial lake sediment sequence from Hawes Water (NW England). Oxygen-isotope values in chironomid head capsules show marked variations during the Late Glacial that are similar to the oxygen isotope record from endogenic carbonate. However, summer temperature reconstructions based on the paired isotope values and fractionation between chironomids and calcite yield values between −20 and −4 °C, which are unrealistic and far lower than reconstructions based on chironomid assemblages at the same site. The composition of a limited number of samples of fossil chironomid larval head capsules determined using Pyrolysis gas-chromatography mass spectrometry indicates the presence of aliphatic geopolymers, suggesting that diagenetic alteration of the head capsules has systematically biased the isotope-derived temperature estimates. However, a similar trend in the isotope records of the two sources suggests that a palaeoclimate signal is still preserved

Phenotyping of Left and Right Ventricular Function in Mouse Models of Compensated Hypertrophy and Heart Failure with Cardiac MRI

Background: Left ventricular (LV) and right ventricular (RV) function have an important impact on symptom occurrence, disease progression and exercise tolerance in pressure overload-induced heart failure, but particularly RV functional changes are not well described in the relevant aortic banding mouse model. Therefore, we quantified time-dependent alterations in the ventricular morphology and function in two models of hypertrophy and heart failure and we studied the relationship between RV and LV function during the transition from hypertrophy to heart failure. Methods: MRI was used to quantify RV and LV function and morphology in healthy (n = 4) and sham operated (n = 3) C57BL/6 mice, and animals with a mild (n = 5) and a severe aortic constriction (n = 10). Results: Mice subjected to a mild constriction showed increased LV mass (P0.05). Animals with a severe constriction progressively developed LV hypertrophy (P<0.001), depressed LVEF (P<0.001), followed by a declining RVEF (P<0.001) and the development of pulmonary remodeling, as compared to controls during a 10-week follow-up. Myocardial strain, as a measure for local cardiac function, decreased in mice with a severe constriction compared to controls (P<0.05). Conclusions: Relevant changes in mouse RV and LV function following an aortic constriction could be quantified using MRI. The well-controlled models described here open opportunities to assess the added value of new MRI techniques for the diagnosis of heart failure and to study the impact of new therapeutic strategies on disease progression and symptom occurrence

Myocardial perfusion MRI shows impaired perfusion of the mouse hypertrophic left ventricle

There is growing consensus that myocardial perfusion deficits play a pivotal role in the transition from compensated to overt decompensated hypertrophy. The purpose of this study was to systematically study myocardial perfusion deficits in the highly relevant model of pressure overload induced hypertrophy and heart failur

Abundance of lipids in differently sized aggregates depends on their chemical composition

Evidence for a vital role of soil mineral matrix interactions in lipid preservation is steadily increasing. However, it remains unclear whether solvent-extractable (‘free’) or hydrolyzable (‘bound’) lipids, including molecular proxies, e.g., for cutin and suberin, are similarly affected by different stabilization mechanisms in soil (i.e., aggregation or organo-mineral association). To provide insights into the effect of these stabilization mechanisms on lipid composition and preservation, we investigated free and bound lipids in particulate and mineral soil fractions, deriving from sand- and silt-/clay-sized aggregates from a forest subsoil. While free lipids accumulated in sand-sized aggregates, the more complex bound lipids accumulated in silt- and clay-sized aggregates, particularly in the respective mineral fractions < 6.3 µm (fine silt and clay). The presence of both, cutin and suberin markers indicated input of leaf- and root-derived organic matter to the subsoil. Yet, our cutin marker (9,10,ω-trihydroxyoctadecanoic acid) was not extracted from the mineral aggregate compartments < 6.3 µm, perhaps due to its chemical structure (i.e., cross-linking via several hydroxy groups, and thus higher ‘stability’, in macromolecular structures). Combined, these results suggest that the chemical composition of lipids (and likely also that of other soil organic matter compounds) governs interaction with their environment, such as accumulation in aggregates or association with mineral soil compartments, and thus indirectly influences their persistence in soil

Abundance of lipids in differently sized aggregates depends on their chemical composition

Evidence for a vital role of soil mineral matrix interactions in lipid preservation is steadily increasing. However, it remains unclear whether solvent-extractable (‘free’) or hydrolyzable (‘bound’) lipids, including molecular proxies, e.g., for cutin and suberin, are similarly affected by different stabilization mechanisms in soil (i.e., aggregation or organo-mineral association). To provide insights into the effect of these stabilization mechanisms on lipid composition and preservation, we investigated free and bound lipids in particulate and mineral soil fractions, deriving from sand- and silt-/clay-sized aggregates from a forest subsoil. While free lipids accumulated in sand-sized aggregates, the more complex bound lipids accumulated in silt- and clay-sized aggregates, particularly in the respective mineral fractions < 6.3 µm (fine silt and clay). The presence of both, cutin and suberin markers indicated input of leaf- and root-derived organic matter to the subsoil. Yet, our cutin marker (9,10,ω-trihydroxyoctadecanoic acid) was not extracted from the mineral aggregate compartments < 6.3 µm, perhaps due to its chemical structure (i.e., cross-linking via several hydroxy groups, and thus higher ‘stability’, in macromolecular structures). Combined, these results suggest that the chemical composition of lipids (and likely also that of other soil organic matter compounds) governs interaction with their environment, such as accumulation in aggregates or association with mineral soil compartments, and thus indirectly influences their persistence in soil

Plant- or microbial-derived? A review on the molecular composition of stabilized soil organic matter

Soil organic matter (SOM) represents a major reservoir of stored carbon (C). However, uncertainties regarding the composition and origin of stabilized SOM hinder the implementation of sustainable management strategies. Here, we synthesize data on the contribution of plant- and microbial-derived compounds to stabilized SOM, i.e., aggregates and mineral-associated organic matter (MAOM), and review the role of environmental factors influencing this contribution. Extrapolating amino sugar concentrations in soil based on molecular stoichiometry, we find that microbial necromass accounts for ~50% (agroecosystems) or less (forest ecosystems) of the C stabilized within aggregates and MAOM across studies. This implies that plant biomolecules, including lipids, lignin, and sugars, might account for a substantial portion (≥50%) of the organic matter protected by minerals and aggregates. Indeed, plant-specific sugars and lipids can each account for as much as 10% of organic C within mineral soil fractions, and most reported quantities of plant-specific lipids and lignin in mineral soil fractions are likely underestimates due to irreversible sorption to minerals. A relatively balanced contribution of plant and microbial biomolecules to stabilized SOM in aggregates and MAOM is inconsistent with recent suggestions that stable SOM is comprised mostly of microbial compounds. Land use and soil type appear to profoundly affect the contribution of plant and microbial compounds to stabilized SOM. Consistent with studies of bulk soils, favorable conditions for microbial proliferation in grasslands or fertile Chernozems or Luvisols appear to increase the contribution of microbial compounds, while less favorable conditions for microbial proliferation in forest soils or Podzols/Alisols appear to favor the abundance of plant compounds in stabilized SOM. Combined with a tight link between substrate quality and the abundance of microbial compounds in stabilized SOM, and a potentially inverse relationship between substrate quality and the abundance of plant compounds, these results provide evidence that plant biomolecules might be preferentially stabilized by organo-mineral interactions in some ecosystems. Various areas warrant further research. For example, difficulties in distinguishing direct and indirect effects of temperature and precipitation on the composition of stabilized SOM may be overcome by long-term observational studies that include climate manipulations. Knowledge gaps in the contribution of plant and microbial compounds to stabilized SOM in soil layers below 30 cm depth may simply be closed by extending the sampling depth. Moreover, a refined focus on soil fauna, with potentially strong effects on microbial and plant compounds in stabilized SOM, will provide new insights into SOM dynamics. Future studies should quantify both microbial and plant biomolecules in mineral soil fractions to allow direct comparisons and overcome limitations in existing data. For example, because biomarker-based estimates of microbial-derived C can only indirectly estimate the maximum amount of plant-derived C, exhaustive studies of plant biomarker concentrations could be conducted, including estimates of plant-specific lipids, sugars, and lignin (and biomarkers released following mineral dissolution). Generally, more integrative studies, e.g., combining molecular and isotopic tracers of organic matter inputs with targeted sampling of mineral fractions, are required to improve knowledge of the formation and persistence of stabilized SOM

Aquatic weeds as novel protein sources: Alkaline extraction of tannin-rich Azolla

The aquatic weed Azolla is a potential protein crop due to its prolific growth and high protein content, supported entirely by nitrogen-fixing symbionts. Alkaline protein extraction at pH 8 followed by acid precipitation allowed recovery of 16–26% of the biomass nitrogen, while at pH 10.5 nitrogen recovery improved to 35–54%. This pH effect was typical of ferns of the family Salviniaceae, and may be explained by high concentrations of condensed tannins (CTs) in the biomass that precipitate protein at mild pH. Two approaches were tested to increase protein yield and reduce protein binding by CTs. Pre-extraction with aqueous acetone (70 v/v%) removed 76–85% of the CTs and subsequent alkaline extraction at pH 12.5 and 95 °C recovered 38% of the biomass nitrogen. Extraction with 1.5% of PEG as a CT-binding agent, also permitted to recover 38% of the nitrogen, under milder conditions of pH 8 and 45 °C

Multiscale microbial preservation and biogeochemical signals in a modern hot-spring siliceous sinter rich in co2 emissions, Krýsuvík geothermal field, Iceland

The microbial communities inferred in silica sinter rocks, based on multiscale morphological features (fabrics and textures) and the presence of lipid biomarkers and their carbon isotopic composition, are evaluated in the Krýsuvík geothermal area of Iceland. Close to vent environments (T > 75 °C and pH 1.7‒3), stream floors are capped with homogeneous vitreous crusts and breccia levels, with no distinct recognizable silicified microbes. About 4 m far from the vents (T 75‒60 °C and pH 3‒6) and beyond (T < 60 °C and pH 6‒7.6), microbial sinters, including wavy and palisade laminated and bubble fabrics, differ between abandoned meanders and desiccated ponds. Fabric and texture variances are related to changes in the ratio of filament/coccoid silicified microbes and associated porosity. Coatings of epicellular silica, less than 2 µm thick, favor identification of indi-vidual microbial filaments, whereas coalescence of opal spheres into agglomerates precludes recognition of original microbial textures and silicified microbes. Episodic fluctuations in the physico-chemical conditions of surface waters controlled the acidic hydrolysis of biomarkers. Wavy laminated fabrics from pond margins comprise fatty acids, mono-and dialkyl glycerol, mono-and di-ethers, monoalkyl glycerol esters and small traces of 10-methyl branched C16 and C18 fatty acids and archaeol, indicative of intergrowths of cyanobacteria, Aquificales, and sulfate reducing bacteria and methanogenic archaea. In contrast, wavy laminated fabrics from abandoned meanders and palisade laminated fabrics from ponds differ in their branched fatty acids and the presence vs. absence of bacteriohopanetetrol, reflecting different cyanobacterial contributions. δ13C values of biomarkers range from −22.7 to −32.9‰, but their values in the wavy (pond) and bubble fabrics have much wider ranges than those of the wavy (meander), palisade, and vitreous fabrics, reflecting dissolved inorganic carbon (DIC) sources and a decrease in13C downstream outflow channels, with heavier values closer to vents and depleted values in ponds

Multiscale microbial preservation and biogeochemical signals in a modern hot-spring siliceous sinter rich in co2 emissions, Krýsuvík geothermal field, Iceland

The microbial communities inferred in silica sinter rocks, based on multiscale morphological features (fabrics and textures) and the presence of lipid biomarkers and their carbon isotopic composition, are evaluated in the Krýsuvík geothermal area of Iceland. Close to vent environments (T > 75 °C and pH 1.7‒3), stream floors are capped with homogeneous vitreous crusts and breccia levels, with no distinct recognizable silicified microbes. About 4 m far from the vents (T 75‒60 °C and pH 3‒6) and beyond (T < 60 °C and pH 6‒7.6), microbial sinters, including wavy and palisade laminated and bubble fabrics, differ between abandoned meanders and desiccated ponds. Fabric and texture variances are related to changes in the ratio of filament/coccoid silicified microbes and associated porosity. Coatings of epicellular silica, less than 2 µm thick, favor identification of indi-vidual microbial filaments, whereas coalescence of opal spheres into agglomerates precludes recognition of original microbial textures and silicified microbes. Episodic fluctuations in the physico-chemical conditions of surface waters controlled the acidic hydrolysis of biomarkers. Wavy laminated fabrics from pond margins comprise fatty acids, mono-and dialkyl glycerol, mono-and di-ethers, monoalkyl glycerol esters and small traces of 10-methyl branched C16 and C18 fatty acids and archaeol, indicative of intergrowths of cyanobacteria, Aquificales, and sulfate reducing bacteria and methanogenic archaea. In contrast, wavy laminated fabrics from abandoned meanders and palisade laminated fabrics from ponds differ in their branched fatty acids and the presence vs. absence of bacteriohopanetetrol, reflecting different cyanobacterial contributions. δ13C values of biomarkers range from −22.7 to −32.9‰, but their values in the wavy (pond) and bubble fabrics have much wider ranges than those of the wavy (meander), palisade, and vitreous fabrics, reflecting dissolved inorganic carbon (DIC) sources and a decrease in13C downstream outflow channels, with heavier values closer to vents and depleted values in ponds

Preferential degradation of leaf- vs. root-derived organic carbon in earthworm-affected soil

Earthworms are integral parts of many ecosystems and may play a decisive role in determining whether soils function as carbon (C) sink or source. However, information on how earthworms affect the composition and stability of soil organic matter (SOM) is scarce. Particularly their effect on organic matter deriving from leaves and roots with distinct composition and, thus, susceptibility to decomposition and stabilization remains unclear. Here, we combine cutin- and suberin-derived lipids as specific markers for leaf- and root-derived SOM with their 13C composition and physical fractionations of soil. We show that earthworms overprint the protective role of organo-mineral associations and aggregates to favor the accumulation of root- relative to leaf-derived SOM. This gradual accumulation contributes to the often-observed dominance of root-derived organic matter in soil and emphasizes the need to consider molecular level effects of earthworms on SOM dynamics