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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.

2018

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Abstract

This paper compares technical efficiencies (TEs) and technological gap ratios (TGRs) for dairy farms in regions of Norway, accounting for differences in working environments. We used the state-of-the-art stochastic meta-frontier approach to estimate TEs and TGRs to account for regional heterogeneity, and the ‘true’ random-effect model to account for farm effects. The dataset used was farm-level balanced panel data for 24 years (1992–2014), with 5442 observations from 731 dairy farms. The results of the analysis provide empirical evidence of small regional differences in TEs, TGRs, and input use. Furthermore, the results may provide support for the more regionally specific agricultural policy, in terms of support schemes and structural regulations.

Abstract

In this article, we estimate the progress of Total Factor Productivity (TFP) in the Norwegian grain production sector. Previous studies conducted in TFP estimation can be criticized for estimated production function relied on the assumption that the underlying technology is the same for all regions and firms face similar environmental conditions. In reality, agricultural firms in different regions resource endowment, adoption of new technology, and innovation might be different because of farmers face different production opportunities. For this study, we classified the country into two main grain producing regions with district level of development, and hence production technologies. We used farm level balanced panel data for 19 years (1996-2014) with 1463 observations from farms specialized in grain production. We applied the ‘true' fixed effect stochastic frontier model to estimate region level efficiency and source of productivity changes. The result of the analysis shows that there has been a productivity improvement in the sector, and technical change has had the main source of productivity change.

Abstract

Previous studies estimating TFP and its components have been criticized for not considering farm heterogeneity in their model. Moreover, the studies focused on the technical evaluation of a sector. However, the technical evaluation alone reveals how well farmers use the physical production process. There is a need to closely examine the cost efficiency of the farmers. In this study, we used a cost function (dual) approach to facilitating the decomposition and estimation of TFP components. Using a translog stochastic cost function, we estimated the level and source of productivity and profitability change for crop producing family firms in Norway. We used the true random effect to account for farm heterogeneity. The analysis is based on 23 years unbalanced panel data (1991-2013) from 455 crop- producing firms with a total of 3885 observations. The result indicates that average annual productivity growth rate in grain and forage production was - 0.11 % per annum during the period 1991-2013. The profit change was 0.14 % per annum.

Abstract

Previous studies estimating TFP and its components have been criticized for not considering farm heterogeneity in their model. Moreover, the studies focused on the technical evaluation of a sector. However, the technical evaluation alone reveals how well farmers use the physical production process. There is a need to closely examine the cost efficiency of the farmers. In this study, we used a cost function (dual) approach to facilitating the decomposition and estimation of TFP components. Using a translog stochastic cost function, we estimated the level and source of productivity and profitability change for crop producing family firms in Norway. We used the true random effect to account for farm heterogeneity. The analysis is based on 23 years unbalanced panel data (1991-2013) from 455 crop- producing firms with a total of 3885 observations. The result indicates that average annual productivity growth rate in grain and forage production was - 0.11 % per annum during the period 1991-2013. The profit change was 0.14 % per annum.

Abstract

This doctoral thesis incorporates an integrated framework for the measurement and analysis of the performance of Norwegian farms, focusing on crop-producing and dairy farms. Farm-level datasets were used in the analysis. The thesis comprises an introductory chapter and five independent research articles. The aim of the first article is to explore the effects of model specifications and estimate short-run and long-run inefficiency. We used the transcendental logarithmic (translog) cost function and the analysis is based on unbalanced farm-level panel data for the period 1991–2013 from 455 Norwegian farms that specialise in crop production in the Eastern and Central regions of Norway. It was found that cost efficiency scores are sensitive to how the inefficiency is modelled and interpreted. Empirical analysis demonstrates that the magnitude of long-run inefficiency (5%) is lower than the level of short-run inefficiency (6%). It would be possible to reduce crop production costs by, on average, up to 5% if shortfalls in managerial capabilities were reduced. Such shortfalls in farmers’ management abilities derive from such factors as lack of farming experience and lack of farm ownership. On the other hand, it would be possible to reduce crop production costs by up to 6% if transient inefficiencies could be eliminated. On average, actual costs could be reduced by 11% without reducing output if both forms of inefficiency were eliminated from Norwegian crop production. Policy interventions to this end might include providing training in farm-management practices, and policy changes to ease rigidity in farm ownership. The objective of the second article is to measure the economic performance of two crop-producing Norwegian farms while accounting for both unobserved heterogeneity and environmental variables. The analysis employs a translog cost function and is based on unbalanced farm-level panel data comprising 3,855 observations (1,004 observations from the central region and 2,884 from the eastern region). We found that the mean minimum costs for the period 1991–2013 were approximately 93% and 92% of the actual production costs for crop farms in the central and eastern regions, respectively. The marginal effects of crop rotation, land tenure, off-farm activity, direct government support, and experience positively correlated with the economic performance of crop farms. In both regions, the marginal contribution of these variables to economic performance increased for the period 2000–2013 compared to 1991–1999. The aim of Article 3 is to measure the contribution of productivity and price change to changes in the profitability of crop-producing family farms in Norway. The results indicate that the average annual productivity growth rate for grain and forage production decreased by 0.11% per annum over the period 1991–2013. Profits decreased by 0.14% per annum primarily due to the effect of the trend of increasing input prices and a decline in total factor productivity. Interventions to improve the productivity of farms would also improve farm profitability.

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Abstract

Marine macrophytes are the foundation of algal forests and seagrass meadows–some of the most productive and diverse coastal marine ecosystems on the planet. These ecosystems provide nursery grounds and food for fish and invertebrates, coastline protection from erosion, carbon sequestration, and nutrient fixation. For marine macrophytes, temperature is generally the most important range limiting factor, and ocean warming is considered the most severe threat among global climate change factors. Ocean warming induced losses of dominant macrophytes along their equatorial range edges, as well as range extensions into polar regions, are predicted and already documented. While adaptive evolution based on genetic change is considered too slow to keep pace with the increasing rate of anthropogenic environmental changes, rapid adaptation may come about through a set of non-genetic mechanisms involving the functional composition of the associated microbiome, as well as epigenetic modification of the genome and its regulatory effect on gene expression and the activity of transposable elements. While research in terrestrial plants demonstrates that the integration of non-genetic mechanisms provide a more holistic picture of a species’ evolutionary potential, research in marine systems is lagging behind. Here, we aim to review the potential of marine macrophytes to acclimatize and adapt to major climate change effects via intraspecific variation at the genetic, epigenetic, and microbiome levels. All three levels create phenotypic variation that may either enhance fitness within individuals (plasticity) or be subject to selection and ultimately, adaptation. We review three of the most important phenotypic variations in a climate change context, including physiological variation, variation in propagation success, and in herbivore resistance. Integrating different levels of plasticity, and adaptability into ecological models will allow to obtain a more holistic understanding of trait variation and a realistic assessment of the future performance and distribution of marine macrophytes. Such multi-disciplinary approach that integrates various levels of intraspecific variation, and their effect on phenotypic and physiological variation, is of crucial importance for the effective management and conservation of seagrasses and macroalgae under climate change.

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Abstract

Ocean warming (OW), ocean acidification (OA) and their interaction with local drivers, e.g., copper pollution, may negatively affect macroalgae and their microscopic life stages. We evaluated meiospore development of the kelps Macrocystis pyrifera and Undaria pinnatifida exposed to a factorial combination of current and 2100-predicted temperature (12 and 16 °C, respectively), pH (8.16 and 7.65, respectively), and two copper levels (no-added-copper and species-specific germination Cu- EC50). Meiospore germination for both species declined by 5–18% under OA and ambient temperature/ OA conditions, irrespective of copper exposure. Germling growth rate declined by >40%·day−1, and gametophyte development was inhibited under Cu-EC50 exposure, compared to the no-added-copper treatment, irrespective of pH and temperature. Following the removal of copper and 9-day recovery under respective pH and temperature treatments, germling growth rates increased by 8–18%·day−1. The exception was U. pinnatifida under OW/OA, where growth rate remained at 10%·day−1 before and after copper exposure. Copper-binding ligand concentrations were higher in copper-exposed cultures of both species, suggesting that ligands may act as a defence mechanism of kelp early life stages against copper toxicity. Our study demonstrated that copper pollution is more important than global climate drivers in controlling meiospore development in kelps as it disrupts the completion of their life cycle.