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Publications

NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.

2023

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Abstract

The morphological ontogeny of Nanhermannia sellnicki Forsslund, 1958 is described and illustrated. In all juvenile stages the bothridial seta is minute, and two pairs of exobothridial setae are present (exa reduced to its alveolus, exp short). In the larva, the seta f1 is setiform but in the nymphs it is unobservable among cuticular tubercles. Most prodorsal and gastronotal setae of the larva are short while thouse of nymphs are long; seta in and all gastronotal and adanal setae are inserted in small individual depressions. In all instars the leg segments are oval in cross section and relatively thick, and most setae on tarsi are relatively short, thick or conical. The seta d accompanies solenidion σ on all genua, φ1 on tibia I and φ on other tibiae.

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Abstract

The morphological ontogeny of Zachvatkinibates svanhovdi A. Seniczak & S. Seniczak, 2023 is described and illustrated. The juveniles of this species are light brown with slightly darker colour on the prodorsum, gastronotal shield, surrounding of gla opening, and legs. The larva has 12 pairs of gastronotal setae, most are of medium size and barbed; the nymphs have 15 pairs, most are short and smooth. In all juveniles, the setae of c-series are inserted on unsclerotized integument. In the larva, the pygidial shield is absent but, in the nymphs, the gastronotal shield is present and the setae p2 and p3 are inserted on unsclerotized integument. In the larva, a humeral organ is absent but is present in the nymphs.

Abstract

swap is an R-package designed to help interface and work with SWAP4 model. It consists of a variety of functions that assist the user in otherwise tedious and repetitive tasks.

Abstract

The Norwegian Institute of Bioeconomy Research (NIBIO) has been working on many fronts to promote sustainable agriculture. As part of the Department of Biogeochemistry and Soil Quality, I will present initiatives and progress made by the NIBIO Institute in promoting soil organic matter persistence and sustainable agriculture in Norway and worldwide. Two major challenges have been targeted with a focus on Norway: waste generation by several industries (e.g., agriculture, forestry, and fishery) and the short time of the cropping season in the country due to climatic constraints. To solve these issues, we are working on several projects focused on re-utilizing waste products by producing organic fertilizers, optimizing these fertilizers (e.g., biochar N-enrichment), and improving current cropping systems with crop diversification. Our main objective is to investigate the benefits of these practices in improving soil quality and crop productivity and enhancing soil organic matter persistence. Our work on soil science also goes beyond Norwegian and Nordic conditions. Among our international collaborations, we are currently working on a multi-institution bilateral project between China and Norway to promote the restoration of a semi-arid ecosystem in Inner Mongolia. We are also often engaging in project proposals for promoting sustainable agriculture in tropical regions. To develop these ideas, we promote a combined approach of spectroscopy techniques in collaboration with other institutions, such as nanoscale secondary ion mass spectrometry (NanoSIMS) in partnership with the Technical University of Munich (TUM) and NMR spectroscopy in partnership with the National Research Council of Italy (CNR-Pisa). Also, our research facilities count on good infrastructure, focusing on incubations with 13C and 15N labeled amendments and 13C pulse labeling.

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Abstract

The spatial distribution of organic substrates and microscale soil heterogeneity significantly influence organic matter (OM) persistence as constraints on OM accessibility to microorganisms. However, it is unclear how changes in OM spatial heterogeneity driven by factors such as soil depth affect the relative importance of substrate spatial distribution on OM persistence. This work evaluated the decomposition and persistence of 13C and 15N labeled water-extractable OM inputs over 50 days as either hotspot (i.e., pelleted in 1 – 2 mm-size pieces) or distributed (i.e., added as OM < 0.07 µm suspended in water) forms in topsoil (0-0.2 m) and subsoil (0.8-0.9 m) samples of an Andisol. We observed greater persistence of added C in the subsoil with distributed OM inputs relative to hotspot OM, indicated by a 17% reduction in cumulative mineralization of the added C and a 10% higher conversion to mineral-associated OM. A lower substrate availability potentially reduced mineralization due to OM dispersion throughout the soil. NanoSIMS (nanoscale secondary ion mass spectrometry) analysis identified organo-mineral associations on cross-sectioned aggregate interiors in the subsoil. On the other hand, in the topsoil, we did not observe significant differences in the persistence of OM, suggesting that the large amounts of particulate OM already present in the soil outweighed the influence of added OM spatial distribution. Here, we demonstrated under laboratory conditions that the spatial distribution of fresh OM input alone significantly affected the decomposition and persistence of OM inputs in the subsoil. On the other hand, spatial distribution seems to play a lower role in topsoils rich in particulate OM. The divergence in the influence of OM spatial distribution between the top and subsoil is likely driven by differences in soil mineralogy and OM composition.

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Abstract

The molecular diversity of the source substrate has been regarded as a significant controller of the proportion of plant material that is either mineralized or incorporated into soil organic matter (SOM). However, quantitative parameters to express substrate molecular diversity remain elusive. In this research, we fractionated leaves, twigs, bark, and root tissues of 13C-enriched eucalypt seedlings into hot water extractables (HWE), total solvent (acetone) extractables (TSE), a cellulosic fraction (CF), and the acid unhydrolyzable residue (AUR). We used 13C NMR spectroscopy to obtain a molecular diversity index (MDI) based on the relative abundance of carbohydrate, protein, lignin, lipid, and carbonyl functional groups within the biochemical fractions. Subsequently, we obtained artificial plant organs containing fixed proportions (25%) of their respective biochemical fractions to be incubated with soil material obtained from a Haplic Ferralsol for 200-days, under controlled temperature (25 ± 1 ◦C) and moisture adjusted to 70–80% of the soil water holding capacity. Our experimental design was a randomized complete block design, arranged according to a factorial scheme including 4 plant organs, 4 biochemical fractions, and 3 blocks as replicates. During the incubation, we assessed the evolution of CO2 from the microcosms after 1, 2, 3, 4, 7, 10, 13, 21, 28, 38, 45, 70, 80, 92, 112, 148, 178 and 200 days from the start of the incubation. After the incubation, soil subsamples were submitted to a density fractionation to separate the light fraction of SOM (LFOM) i.e., with density <1.8 g cm 3. The heavy fraction remaining was submitted to wetsieving yielding the sand-sized SOM (SSOM) and the mineral-associated SOM (MAOM), with particle-size greater and smaller than 53 μm, respectively. We found that HWE and AUR exhibited comparatively higher MDIs than the TSE and CF. During the incubation, HWE and CF were the primary sources of 13C-CO2 from all plant organs and after 92 days, the respiration of the TSE of bark and roots increased. Otherwise, the AUR contributed the least for the release of 13C-CO2. There were no significant relationships between the MDI and the amount of 13C transferred into the LFOM or SSOM. Otherwise, the transfer of 13C into the MAOM increased as a linear-quadratic function of MDI, which in turn was negatively correlated with the total 13C-CO2 loss. Overall, the MDI exerted a stronger control on the 13C-labeled MAOM than on 13C-CO2 emissions, highlighting the need to improve our ability to distinguish and quantify direct plant inputs from those of microbial origin entering soil C pools.

Abstract

The aim of this study was to contribute to development of organic fertiliser products based on fish sludge (i.e. feed residues and faeces) from farmed smolt. Four dried fish sludge products, one liquid digestate after anaerobic digestion and one dried digestate were collected at Norwegian smolt hatcheries in 2019 and 2020. Their quality as fertilisers was studied by chemical analyses, two 2-year field experiments with spring cereals and soil incubation combined with a first-order kinetics N release model. Cadmium (Cd) and zinc (Zn) concentrations were below European Union maximum limits for organic fertilisers in all products except one (liquid digestate). Relevant organic pollutants (PCB7, PBDE7, PCDD/F + DL-PCB) were analysed for the first time and detected in all fish sludge products. Nutrient composition was unbalanced, with low nitrogen/phosphorus (N/P) ratio and low potassium (K) content relative to crop requirements. Nitrogen concentration in the dried fish sludge products varied (27–70 g N kg-1 dry matter), even when treated by the same technology but sampled at different locations and/or times. In the dried fish sludge products, N was mainly present as recalcitrant organic N, resulting in lower grain yield than with mineral N fertiliser. Digestate showed equally good N fertilisation effect as mineral N fertiliser, but drying reduced N quality. Soil incubation in combination with modelling is a relatively cheap tool that can give a good indication of N quality in fish sludge products with unknown fertilisation effects. Carbon/N ratio in dried fish sludge can also be used as an indicator of N quality.