Now showing items 111-122 of 122
| Abstract: | Background: In order to understand the role of herbivores in trophic webs, it is essential to know
what they feed on. Diet analysis is, however, a challenge in many small herbivores with a secretive
life style. In this paper, we compare novel (high-throughput pyrosequencing) DNA barcoding
technology for plant mixture with traditional microhistological method. We analysed stomach
contents of two ecologically important subarctic vole species, Microtus oeconomus and Myodes
rufocanus, with the two methods. DNA barcoding was conducted using the P6-loop of the
chloroplast trnL (UAA) intron.
Results: Although the identified plant taxa in the diets matched relatively well between the two methods, DNA barcoding gave by far taxonomically more detailed results. Quantitative comparison of results was difficult, mainly due to low taxonomic resolution of the microhistological method, which also in part explained discrepancies between the methods. Other discrepancies were likely due to biases mostly in the microhistological analysis. Conclusion: We conclude that DNA barcoding opens up for new possibilities in the study of plant-herbivore interactions, giving a detailed and relatively unbiased picture of food utilization of herbivores. |
| URI: | http://hdl.handle.net/10037/2195 |
| Abstract: | Theoretical models predict that subordinate males should have higher sperm velocity to compensate for their disadvantaged mating role and because they experience sperm competition more frequently than dominant males. Differences in mean velocity between sperm of dominants and subordinates in the predicted direction are also documented for a few species, including the Arctic char, Salvelinus alpinus (L., 1758). Yet, this difference in mean velocity does not imply that the fastest sperm within an ejaculate, which are those most likely to fertilize eggs, swim faster in subordinates than in dominants. We studied the 5% and 10% fastest sperm cells in ejaculates of dominant and subordinate Arctic char. Before individuals attained their status, there were no differences in velocity between the fastest sperm of males that later became dominant or subordinate. Yet, after establishment of social position, subordinates showed significantly higher sperm swimming speed of the fastest cells in the first 30s post activation (i.e., at 15, 20, and 30s post activation). Males that became subordinates showed no change in sperm speed of the fast cells compared with those at pre-trial levels, whereas males that became dominant reduced the speed of their sperm (15s post activation) compared with those at pre-trial levels. Our results suggest that males which attain social dominance are unable to maintain high sperm velocity, even among the small fraction of the fastest cells. |
| URI: | http://hdl.handle.net/10037/4789 |
| Abstract: | We present an accurate, fast, simple and non-destructive photographic method to estimate wax ester and lipid content in single individuals of the calanoid copepod genus Calanus and test this method against gas-chromatographic lipid measurements. |
| URI: | http://hdl.handle.net/10037/4416 |
| Abstract: | Ingress Eutrophication is an increase in primary production due to increased nutrient supply and its consequences. In its widest sense eutrophication means any increase of nutrient availability that increases primary production. Frequently, however, eutrophication is understood exclusively as the consequence of nutrient input by anthropogenic activities. The primary consequence of eutrophication in aquatic environments is an enhancement of algal productivity and accumulation of algal biomass. Secondary consequences are changes in community structure of plankton and benthos. Man-induced eutrophication or changes in biodiversity are nothing new: they are a well-known consequence of human culture. Eutrophication phenomena accompanied all human settlements. Even in the early days of mankind human activities resulted in ecosystem changes. Several large animals such as the mammoth survived the glacial periods, but not the last one. It has been suggested that Neolithic hunters decimated this species to extinction. Similar suggestions have also been made regarding other large mammals that did not continue to exist after the last glacial. The main sewage canal in the city of Rome, ‘cloaca’, has given rise to a number of expression regarding sewage pathways in numerous languages. Since classical and medieval times there have been ‘clean-ups’ of unsanitary, plague-ridden cities. Eutrophication is thus the oldest environmental problem of human civilization and not a recent phenomenon. However, with the significant increase of human population over recent decades, eutrophication has developed from a more or less local to a global issue. Due to changes in human living conditions and the declining number of people employed in agriculture, the population in the coastal zone increases steadily. The nutrient concentration increases continually from small streams over rivers and larger lakes to the estuaries. The consequences of this, such as discoloured waters, ‘rotten’ bottom water, odour and reduced fishing yields are obvious to even a casual observer. The combined effect of increasing human population and movement to the coastal zone, the environmental pressure on rivers, estuaries and shelf regions results in an ever-increasing pressure on the entire coastal zone (Figure 1). Consequently, eutrophication turns into an escalating global phenomenon as long as the human population increases. Homo sapiens has thus a vital impacton nature that is part of its culture. As a consequence of that we have to distinguish between natural and cultural eutrophication. In most of this text the term eutrophication stands for cultural eutrophication. |
| URI: | http://hdl.handle.net/10037/2371 |
| Abstract: | History of cultural eutrophication. Cultural eutrophication is old as Homo sapiens. In particular after the introduction of agriculture and larger settlements eutrophication has been mans faithful companion. During the pre-agricultural hunting and picking stage only probably a couple million humans inhabited the world and cultural eutrophication was negligible. The 3 orders of magnitude increase in population has changed this considerably. Human population growth and mans present existence is entirely based upon the development and efficiency of agriculture. Seafood delivers only a small percentage of human food word wide (see Chapter 15). A consequence of the increased population (based on agriculture) has been large-scale cultural eutrophication. This process has accompanied all major civilisations. Mesopotamia, the Golden Crescent, the Mediterranean cultures, central Europe, North America and China all have been affected/suffered from the effects of cultural eutrophication. Some of us may dream about the good old times of the Middle ages when man lived closer to nature, when the word appeared to be ‘greener’ than today and when life was more ‘natural’. This view is based on a misunderstanding. The present eutrophication of the Baltic and North Sea was preceded by similar or even worse eutrophication periods caused by logging and the introduction of large-scale agriculture in Europe. Medieval cities were probably not only unsanitary, but contaminated by organic wastes, nutrients and heavy metals. The cultural eutrophication in major cities must have been immense, far beyond today’s imagination. A good example of the ambience of Paris in medieval times is portrayed in Patrick Suesskinds novel ‘Perfume’. Cultural eutrophication is thus not a recent phenomenon. It has continuously accompanied mans existence in variable degrees. Locally cultural eutrophication can have been far more significant than today. |
| URI: | http://hdl.handle.net/10037/2391 |
| Abstract: | Eutrophication is an increase in primary production due to increased nutrient supply and its consequences. In its widest sense eutrophication means any increase of nutrient availability that increases primary production. Frequently, however, eutrophication is understood exclusively as the consequence of nutrient input by anthropogenic activities. The primary consequence of eutrophication in aquatic environments is an enhancement of algal productivity and accumulation of algal biomass. Secondary consequences are changes in community structure of plankton and benthos. Man-induced eutrophication or changes in biodiversity are nothing new: they are a well-known consequence of human culture. Eutrophication phenomena accompanied all human settlements. Even in the early days of mankind human activities resulted in ecosystem changes. Several large animals such as the mammoth survived the glacial periods, but not the last one. It has been suggested that Neolithic hunters decimated this species to extinction. Similar suggestions have also been made regarding other large mammals that did not continue to exist after the last glacial. The main sewage canal in the city of Rome, ‘cloaca’, has given rise to a number of expression regarding sewage pathways in numerous languages. Since classical and medieval times there have been ‘clean-ups’ of unsanitary, plague-ridden cities. Eutrophication is thus the oldest environmental problem of human civilization and not a recent phenomenon. However, with the significant increase of human population over recent decades, eutrophication has developed from a more or less local to a global issue. Due to changes in human living conditions and the declining number of people employed in agriculture, the population in the coastal zone increases steadily. The nutrient concentration increases continually from small streams over rivers and larger lakes to the estuaries. The consequences of this, such as discoloured waters, ‘rotten’ bottom water, odour and reduced fishing yields are obvious to even a casual observer. The combined effect of increasing human population and movement to the coastal zone, the environmental pressure on rivers, estuaries and shelf regions results in an ever-increasing pressure on the entire coastal zone (Figure 1). Consequently, eutrophication turns into an escalating global phenomenon as long as the human population increases. Homo sapiens has thus a vital impacton nature that is part of its culture. As a consequence of that we have to distinguish between natural and cultural eutrophication. In most of this text the term eutrophication stands for cultural eutrophication. |
| URI: | http://hdl.handle.net/10037/2389 |
| Abstract: | Quantitative estimates of the fluxes and dynamics in the nutrient load on marine environments, their distribution and channelling through the food web and the effect on the increase of new production, are fundamental and constitute a prerequisite for the planning of actions for water protection measures. The Gulf of Riga is no exception. The Gulf is a semi-enclosed part of the eastern Baltic Sea, surrounded by Estonia and Latvia and has one major outlet, the Irbe Straight Sound, and one minor one, the Muhu Sound. The Gulf of Riga has a surface area of 19,000 km2, is up to 67 m deep, has a relatively simple topography and a volume of 420 km3 (Figure 19.1). The Gulf is eutrophicated and most of the pollution loads in the Gulf can be attributed to human activities in the drainage basin, which covers 135,700 km2, or more than seven times the surface area of the Gulf itself. In pelagic environments the fate of organic matter produced by an increased supply of nutrients, the regulation of vertical flux and in particular the pelagicbenthic coupling are not well known in general, let alone in the Gulf of Riga. Since the beginning of this century Estonian, Latvian, Lithuanian and Russian scientists have already carried out a substantial body of work in various disciplines in the Gulf of Riga and its drainage area (summarised by Ojaveer 1995). From 1993–1997 Nordic and Baltic scientists joined forces in an international project, the ‘Environmental Research in the Baltic Sea’, also referred to as the ‘Gulf of Riga Project’ (GoR). The objective was to study environmental problems in the Gulf and its drainage area, and to determine their impact on the rest of the Baltic Sea in general and the Baltic Proper in particular (Figure 19.2). The investigations reviewed here aim at to understand the Gulf of Riga as an ecosystem by analysing 1. the dynamics of the runoff of nutrients and their supply to the Gulf, 2. the distribution of nutrients in the Gulf, 3. the production and distribution of plankton and organic matter and 4. the processes involved in settling and the vertical export of organic matter. This chapter rests upon 14 publications from the project ‘Pelagic eutrophication and sedimentation’ (Wassmann & Tamminen, 1999); see also J. Mar. Syst, Vol 23. |
| URI: | http://hdl.handle.net/10037/2388 |
| Abstract: | Despite concerns about rapid changes in Arctic Ocean physical forcing and ecosystem function, quantitative knowledge and time series are scarce. The number of reliable physical-biological coupled models and models based on remote sensing is small. To improve our comprehension of carbon flux in the most prominent Arctic Ocean feature, the seasonal ice zone, a possible first step is to evaluate how biogeochemical cycling might develop in the future by examining conceptual models that address climate warming and seasonality in ecosystem development. Here we present three conceptual models of biogeochemical cycling and climate warming in the seasonal ice zone of the Arctic Ocean. They are designed to enhance, in a conceptual and semiquantitative manner, understanding of the possible temporal sequence of future primary production development, its spatial variation, and food availability in the most productive part of the future Arctic Ocean, including pelagic-benthic coupling. We speculate that the largest changes will take place in (a) the northern portions of today’s seasonal ice zone, which will expand to cover the entire Arctic Ocean, and (b) the southern portions, which will be exposed to more thermal stratification. The former change increases and the latter change decreases productivity and supply to the bottom. Lack of nutrient availability means that new production in the central Arctic Ocean will remain low. Blooms of ice and plankton algae may start earlier, depending on snow cover, providing more continuity in food supply for grazers in the upper water column. Weakening of today’s highly episodic primary production in the seasonal ice zone will result in lower average food concentrations for pelagic heterotrophs. We suggest that more of the available energy will be recycled in the pelagic zone, and that vertical export of biogenic matter will be less variable and of reduced quality. |
| URI: | http://hdl.handle.net/10037/3910 |
| Abstract: | Introduction. The effects of global and local changes are most prominent at the land-sea margins where presently population growth is greatest. For example, the population of coastal counties of the USA has roughly doubled since 1960 (Eos, 1992). This gives rise to increased pressure on natural resources and a large number of disturbances to coastal regions. Presently, eutrophication of coastal waters is probably the most important environmental effect (Gesamp, 1991). The effects of nutrient enrichment thoroughly change coastal ecosystems and occur virtually worldwide. Nutrients move across the land-sea margins at such high rates that coastal waters and estuaries are the most fertilized ecosystems on earth (Figure 9.1). |
| URI: | http://hdl.handle.net/10037/2390 |
| Abstract: | Background: The genus Varicellovirus (family Herpesviridae subfamily Alphaherpesvirinae) includes a group of viruses genetically
and antigenically related to bovine herpesvirus 1 (BoHV-1) among which cervid herpesvirus 2 (CvHV-2) can be of importance
in reindeer. These viruses are known to be responsible for different diseases in both wild and domestic animals. Reindeer are a
keystone in the indigenous Saami culture and previous studies have reported the presence of antibodies against
alphaherpesviruses in semi-domesticated reindeer in northern Norway. Mortality rates, especially in calves, can be very high in
some herds and the abortion potential of alphaherpesvirus in reindeer, unlike in bovines, remains unknown.
ELISA kits are the most used screening method in domestic ruminants and given the close genetic relationship between viruses
within this genus, it might be possible to use such kits to screen cervids for different alphaherpesviruses. We have compared
three different commercial ELISA kits in order to validate its use for reindeer and CvHV-2.
Methods: Three commercial bovine ELISA kits (A, B and C), using either indirect (A) or blocking (B and C) ELISA techniques to detect antibodies against BoHV-1 were tested with sera from 154 reindeer in order to detect antibodies against CvHV-2. A Spearman's rank-based coefficient of correlation (ρ) was calculated. A dilution trial was performed for all kits. A virus neutralization test using both BoHV-1 and CvHV-2 was carried out. Results: Seroprevalence was almost the same with all kits (40–41%). Despite a similar qualitative score, quantitatively kits classified samples differently and a strong correlation was only identified between Kits B and C. Blocking kits performed better in both repeatability and in the dilution trial. The virus neutralization results confirmed the ELISA results to a very high degree. Neutralizing titres ranged from 1:2 to 1:256 and from 0 to 1:16 against CvHV-2 and BoHV-1 respectively. Conclusion: Results show that the genetic and antigenic similarity between BoHV-1 and CvHV-2 enables the use of a bovine gB blocking ELISA kit to screen reindeer. The use of an ELISA kit is both cheaper and time saving, allowing screening of large populations. This study revealed a high number of positive animals against CvHV-2 and its impact and distribution in the general population should be further evaluated. |
| URI: | http://hdl.handle.net/10037/2173 |
| Abstract: | Highly repetitive sequences are the bane of genome sequence assembly, and the short read lengths produced by current next generation sequencing technologies further exacerbates this obstacle. An adopted practice is to exclude repetitive sequences in genome data assembly, as the majority of repeats lack protein-coding genes. However, this could result in the exclusion of important genotypes in newly sequenced non-model species. The absence of the antifreeze glycoproteins (AFGP) gene family in the recently sequenced Atlantic cod genome serves as an example. The Atlantic cod (Gadus morhua) genome was assembled entirely from Roche 454 short reads, demonstrating the feasibility of this approach. However, a well-known major adaptive trait, the AFGP, essential for survival in frigid Arctic marine habitats was absent in the annotated genome. To assess whether this resulted from population difference, we performed Southern blot analysis of genomic DNA from multiple individuals from the North East Arctic cod population that the sequenced cod belonged, and verified that the AFGP genotype is indeed present. We searched the raw assemblies of the Atlantic cod using our G. morhua AFGP gene, and located partial AFGP coding sequences in two sequence scaffolds. We found these two scaffolds constitute a partial genomic AFGP locus through comparative sequence analyses with our newly assembled genomic AFGP locus of the related polar cod, Boreogadus saida. By examining the sequence assembly and annotation methodologies used for the Atlantic cod genome, we deduced the primary cause of the absence of the AFGP gene family from the annotated genome was the removal of all repetitive Roche 454 short reads before sequence assembly, which would exclude most of the highly repetitive AFGP coding sequences. Secondarily, the model teleost genomes used in projection annotation of the Atlantic cod genome have no antifreeze trait, perpetuating the unawareness that the AFGP gene family is missing. We recovered some of the missing AFGP coding sequences and reconstructed a partial AFGP locus in the Atlantic cod genome, bringing to light that not all repetitive sequences lack protein coding information. Also, reliance on genomes of model organisms as reference for annotating protein-coding gene content of a newly sequenced non-model species could lead to omission of novel genetic traits. |
| URI: | http://hdl.handle.net/10037/4993 |
Now showing items 111-122 of 122
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