Drought risk in Moldova under global warming and possible crop adaptation strategies.

This study analyzes the relationship between drought processes and crop yields in Moldova, together with the effects of possible future climate change on crops. The severity of drought is analyzed over time in Moldova using the Standard Precipitation Index, the Standardized Precipitation Evapotranspiration Index, and their relationship with crop yields. In addition, rainfall variability and its relationship with crop yields are examined using spectral analysis and squared wavelet coherence.

Preparation of SnS/MoSwith p-n heterojunction for NOsensing.

Conventional metal sulfide (SnS) gas-sensitive sensing materials still have insufficient surface area and slow response/recovery times. To increase its gas-sensing performance, MoSnanoflower was produced hydrothermally and mechanically combined with SnSnanoplate. Extensive characterization results show that MoSwas effectively integrated into SnS.

Effect of fluorine doping on the NO-sensing properties of MoSnanoflowers.

The somewhat slow recovery kinetics of NOsensing at low temperatures are still challenging to overcome. To enhance the gas sensing property, fluorine is doped to MoSnanoflowers by facile hydrothermal method. Extensive characterization data demonstrate that F was effectively incorporated into the MoSnanoflowers, and that the microstructure of the MoSnanoflowers did not change upon F doping.

Au- or Ag-Decorated ZnO-Rod/rGO Nanocomposite with Enhanced Room-Temperature NO-Sensing Performance.

To improve the gas sensitivity of reduced oxide graphene (rGO)-based NO room-temperature sensors, different contents (0-3 wt%) of rGO, ZnO rods, and noble metal nanoparticles (Au or Ag NPs) were synthesized to construct ternary hybrids that combine the advantages of each component. The prepared ZnO rods had a diameter of around 200 nm and a length of about 2 μm. Au or Ag NPs with diameters of 20-30 nm were loaded on the ZnO-rod/rGO hybrid.

Engineering of ZnO/rGO towards NO Gas Detection: Ratio Modulated Sensing Type and Heterojunction Determined Response.

Nanoscale heterostructured zinc oxide/reduced graphene oxide (ZnO/rGO) materials with p-n heterojunctions exhibit excellent low temperature NO gas sensing performance, but their doping ratio modulated sensing properties remain poorly understood. Herein, ZnO nanoparticles were loaded with 0.1~4% rGO by a facile hydrothermal method and evaluated as NO gas chemiresistor.

Convergence and divergence emerging in climatic controls of polynomial trends for northern ecosystem productivity over 2000-2018.

Recent rapid warming has caused uneven impacts on the composition, structure, and functioning of northern ecosystems. It remains unknown how climatic drivers control linear and non-linear trends in ecosystem productivity. Based on a plant phenology index (PPI) product at a spatial resolution of 0.

Cross-sectoral impacts of the 2018-2019 Central European drought and climate resilience in the German part of the Elbe River basin.

Unlabelled: The 2018-2019 Central European drought was probably the most extreme in Germany since the early sixteenth century. We assess the multiple consequences of the drought for natural systems, the economy and human health in the German part of the Elbe River basin, an area of 97,175 km including the cities of Berlin and Hamburg and contributing about 18% to the German GDP. We employ meteorological, hydrological and socio-economic data to build a comprehensive picture of the drought severity, its multiple effects and cross-sectoral consequences in the basin.

The confounding effect of snow cover on assessing spring phenology from space: A new look at trends on the Tibetan Plateau.

The Tibetan Plateau is the highest and largest plateau in the world, hosting unique alpine grassland and having a much higher snow cover than any other region at the same latitude, thus representing a "climate change hot-spot". Land surface phenology characterizes the timing of vegetation seasonality at the per-pixel level using remote sensing systems. The impact of seasonal snow cover variations on land surface phenology has drawn much attention; however, there is still no consensus on how the remote sensing estimated start of season (SOS) is biased by the presence of preseason snow cover.

The missing pieces for better future predictions in subarctic ecosystems: A Torneträsk case study.

Arctic and subarctic ecosystems are experiencing substantial changes in hydrology, vegetation, permafrost conditions, and carbon cycling, in response to climatic change and other anthropogenic drivers, and these changes are likely to continue over this century. The total magnitude of these changes results from multiple interactions among these drivers. Field measurements can address the overall responses to different changing drivers, but are less capable of quantifying the interactions among them.

New satellite-based estimates show significant trends in spring phenology and complex sensitivities to temperature and precipitation at northern European latitudes.

Recent climate warming has altered plant phenology at northern European latitudes, but conclusions regarding the spatial patterns of phenological change and relationships with climate are still challenging as quantitative estimates are strongly diverging. To generate consistent estimates of broad-scale spatially continuous spring plant phenology at northern European latitudes (> 50° N) from 2000 to 2016, we used a novel vegetation index, the plant phenology index (PPI), derived from MODerate-resolution Imaging Spectroradiometer (MODIS) data. To obtain realistic and strong estimates, the phenology trends and their relationships with temperature and precipitation over the past 17 years were analyzed using a panel data method.

Highly improved ethanol gas-sensing performance of mesoporous nickel oxides nanowires with the stannum donor doping.

Mesoporous nickel oxides (NiO) and stannum(Sn)-doped NiO nanowires (NWs) were synthesized by using SBA-15 templates with the nanocasting method. X-ray diffraction, transmission electron microscope, energy dispersive spectrometry, nitrogen adsorption/desorption isotherm and UV-vis spectrum were used to characterize the phase structure, components and microstructure of the as-prepared samples. The gas-sensing analysis indicated that the Sn-doping could greatly improve the ethanol sensitivity for mesoporous NiO NWs.

Wide bandgap mesoporous hematite nanowire bundles as a sensitive and rapid response ethanol sensor.

In this study, α-Fe2O3 nanowires were synthesized using mesoporous SBA-15 silica as the hard templates with the nanocasting method, and then mesoporous α-Fe2O3 nanowire bundles (NWBs) were separated from the well-dispersed α-Fe2O3 nanowires (NWs) by the centrifugation technique. Both samples were characterized by x-ray diffraction, transmission electron microscopy (TEM), nitrogen adsorption/desorption isotherm and UV-vis spectra. All results indicated that the α-Fe2O3 NWBs with mesoporous structure presented a higher BET surface area (95 m(2) g(-1)) and wider bandgap (2.

Preparation and Characterization of Graphene/Fe3O4 Composites by Solvothermal Method.

In the present study, graphene/Fe3O4 nanocomposites were prepared by solvothermal method using graphite oxide (GO) and FeCl3 x 6H2O as starting materials and the products were characterized by X-ray Diffraction (XRD), Scanning Electronic Microscope (SEM) and Vibrating Sample Magnetometer (VSM). Effects of Fe ion concentration, temperature and time of solvothermal reaction on the magnetic properties, microstructures and morphologies of graphene/Fe3O4 nanocomposites were investigated. The results showed that with the raising of Fe ion, particle size of the products became bigger, and saturation magnetization of the products got higher.

Isolation and crystallographic characterization of Sm@C2v(3)-C80 through cocrystal formation with Ni(II)(octaethylporphyrin) or bis(ethylenedithio)tetrathiafulvalene.

Sm@C(2v)(3)-C(80) has been separated from the carbon soot produced by electrical arc vaporization of graphite rods doped with Sm(2)O(3) and purified. Its structure has been determined by single crystal X-ray diffraction using cocrystals obtained from either Ni(II)(octaethylporphyrin) (Ni(II)(OEP)) to form Sm@C(2v)(3)-C(80)·Ni(II)(OEP)·1.68(toluene)·0.

X-ray crystallographic characterization of new soluble endohedral fullerenes utilizing the popular C82 bucky cage. Isolation and structural characterization of Sm@C3v(7)-C82, Sm@C(s)(6)-C82, and Sm@C2(5)-C82.

Three isomers of Sm@C(82) that are soluble in organic solvents were obtained from the carbon soot produced by vaporization of hollow carbon rods doped with Sm(2)O(3)/graphite powder in an electric arc. These isomers were numbered as Sm@C(82)(I), Sm@C(82)(II), and Sm@C(82)(III) in order of their elution times from HPLC chromatography on a Buckyprep column with toluene as the eluent. The identities of isomers, Sm@C(82)(I) as Sm@C(s)(6)-C(82), Sm@C(82)(II) as Sm@C(3v)(7)-C(82), and Sm@C(82)(III) as Sm@C(2)(5)-C(82), were determined by single-crystal X-ray diffraction on cocrystals formed with Ni(octaethylporphyrin).

Aqua-(2,6-dihy-droxy-benzoato-κO(1))bis-(1,10-phenanthroline-κ(2)N,N')manganese(II) 2,6-dihy-droxy-benzoate hemihydrate.

In the complex cation of the title compound, [Mn(C(7)H(5)O(4))(C(12)H(8)N(2))(2)(H(2)O)](C(7)H(5)O(4))·0.5H(2)O, the Mn(II) atom has a six-coordinate octa-hedral environment defined by one carboxyl-ate O atom belonging to a 2,6-dihy-droxy-benzoate (DHB) ligand, four N atoms from two chelating 1,10-phenanthroline mol-ecules and one water mol-ecule. The lattice water mol-ecule lies on a twofold rotation axis.

Single samarium atoms in large fullerene cages. Characterization of two isomers of Sm@C92 and four isomers of Sm@C94 with the X-ray crystallographic identification of Sm@C1(42)-C92, Sm@C(s)(24)-C92, and Sm@C3v(134)-C94.

Two isomers of Sm@C(92) and four isomers of Sm@C(94) were isolated from carbon soot obtained by electric arc vaporization of carbon rods doped with Sm(2)O(3). Analysis of the structures by single-crystal X-ray diffraction on cocrystals formed with Ni(II)(octaethylporphyrin) reveals the identities of two of the Sm@C(92) isomers: Sm@C(92)(I), which is the more abundant isomer, is Sm@C(1)(42)-C(92), and Sm@C(92)(II) is Sm@C(s)(24)-C(92). The structure of the most abundant form of the four isomers of Sm@C(94), Sm@C(94)(I), is Sm@C(3v)(134)-C(94), which utilizes the same cage isomer as the previously known Ca@C(3v)(134)-C(94) and Tm@C(3v)(134)-C(94).

Isolation of three isomers of Sm@C84 and X-ray crystallographic characterization of Sm@D(3d)(19)-C84 and Sm@C2(13)-C84.

Three isomers with the composition Sm@C(84) were isolated from carbon soot obtained by electric arc vaporization of carbon rods doped with Sm(2)O(3). These isomers were labeled Sm@C(84)(I), Sm@C(84)(II), and Sm@C(84)(III) in order of their elution times during chromatography on a Buckyprep column with toluene as the eluent. Analysis of the structures by single-crystal X-ray diffraction on cocrystals formed with Ni(II)(octaethylporphyrin) reveals the identities of two of the isomers: Sm@C(84)(I) is Sm@C(2)(13)-C(84), and Sm@C(84)(III) is Sm@ D(3d)(19)-C(84).

An optical sensor network for vegetation phenology monitoring and satellite data calibration.

We present a network of sites across Fennoscandia for optical sampling of vegetation properties relevant for phenology monitoring and satellite data calibration. The network currently consists of five sites, distributed along an N-S gradient through Sweden and Finland. Two sites are located in coniferous forests, one in a deciduous forest, and two on peatland.

Large endohedral fullerenes containing two metal ions, Sm2@D2(35)-C88, Sm2@C1(21)-C90, and Sm2@D3(85)-C92, and their relationship to endohedral fullerenes containing two gadolinium ions.

The carbon soot obtained by electric arc vaporization of carbon rods doped with Sm(2)O(3) contains a series of monometallic endohedral fullerenes, Sm@C(2n), along with smaller quantities of the dimetallic endohedrals Sm(2)@C(2n) with n = 44, 45, 46, and the previously described Sm(2)@D(3d)(822)-C(104). The compounds Sm(2)@C(2n) with n = 44, 45, 46 were purified by high pressure liquid chromatography on several different columns. For endohedral fullerenes that contain two metal atoms, there are two structural possibilities: a normal dimetallofullerene, M(2)@C(2n), or a metal carbide, M(2)(μ-C(2))@C(2n-2).

Very large, soluble endohedral fullerenes in the series La2C90 to La2C138: isolation and crystallographic characterization of La2@D5(450)-C100.

An extensive series of soluble dilanthanum endohedral fullerenes that extends from La(2)C(90) to La(2)C(138) has been discovered. The most abundant of these, the nanotubular La(2)@D(5)(450)-C(100), has been isolated in pure form and characterized by single-crystal X-ray diffraction.

Isolation and crystallographic identification of four isomers of Sm@C90.

Four isomers with the composition SmC(90) were obtained from carbon soot produced by electric arc vaporization of carbon rods doped with Sm(2)O(3). These were labeled Sm@C(90)(I), Sm@C(90)(II), Sm@C(90)(III), and Sm@C(90)(IV) in order of their elution times during chromatography on a Buckyprep column with toluene as the eluent. Analysis of the structures by single-crystal X-ray diffraction on cocrystals formed with Ni(octaethylporphyrin) reveals the identities of the individual isomers as follows: I, Sm@C(2)(40)-C(90); II, Sm@C(2)(42)-C(90); III, Sm@C(2v)(46)-C(90) and IV, Sm@C(2)(45)-C(90).

Fullerenes without symmetry: crystallographic characterization of C1(30)-C90 and C1(32)-C90.

Fullerenes are generally considered as highly symmetric, yet fullerene isomers with only C(1) symmetry, such as C(1)(30)-C(90) and C(1)(32)-C(90) whose structures are reported here, become increasingly numerous as fullerene size increases.

Bis(2,6-dihy-droxy-benzoato-κO,O)(nitrato-κO,O')bis-(1,10-phenanthroline-κN,N')dysprosium(III).

In the mononuclear title complex, [Dy(C(7)H(5)O(4))(2)(NO(3))(C(12)H(8)N(2))(2)], the Dy(III) atom is in a distorted bicapped square-anti-prismatic geometry formed by four N atoms from two chelating 1,10-phenanthroline (phen) ligands, four O atoms from two 2,6-dihy-droxy-benzoate (DHB) ligands and two O atoms from a nitrate anion. Inter-molecular π-π stacking inter-actions between the phen and DHB ligands [centroid-centroid distances = 3.542 (4) and 3.