Cold mountain stream chironomids (Diptera) of the genus Diamesa indicate both historical and recent climate change.

Chironomids of the genus Diamesa (Meigen, 1835, Diptera: Chironomidae) inhabit cold, oxygen-rich running waters. We have investigated the presence of Diamesa and other freshwater macroinvertebrates at 22 stream sampling sites in 3 European high mountain regions (the Central Pyrenees, the Ötztal Alps, and the Tatra Mountains) to establish suitable temperature conditions for Diamesa dominance. It has been generally accepted that their high abundance was linked to the presence of glaciers; however, we have shown that in the Tatra Mountains, where there are no glaciers, the conditions for the dominance of Diamesa species are created due to permanent snowfields, the geographical orientation of the valley and shading by the surrounding high peaks. The historical connection of Diamesa to glaciers was investigated from the paleolimnological records of subfossil chironomid assemblages from the Bohemian Forest, where glaciers disappeared before or during the Late Glacial period. As expected, water temperature seems to be the main driver of Diamesa distribution, and we determined that the relative abundance of Diamesa species was significantly higher at the sites with a mean July water temperature below 6.5 °C. The Diamesa-dominated stream communities seems to be endangered due to ongoing climate warming and this assumption is supported by our paleolimnological results from the Bohemian Forest lakes, where Diamesa has disappeared due to warming of lake inflows at the beginning of the Holocene. These findings strengthen the former suggestions that some Diamesa species could be used as an indicator for tracking recent environmental changes in vulnerable ecosystems of cold mountain streams.

Molecular and morphological characterisation of larvae of the genus Diamesa Meigen, 1835 (Diptera: Chironomidae) in Alpine streams (Ötztal Alps, Austria).

Diamesa species (Diptera, Chironomidae) are widely distributed in freshwater ecosystems, and their life cycles are closely linked to environmental variables such as temperature, water quality, and sediment composition. Their sensitivity to environmental changes, particularly in response to pollution and habitat alterations, makes them valuable indicators of ecosystem health. The challenges associated with the morphological identification of larvae invoke the use of DNA barcoding for species determination. The mitochondrial cytochrome oxidase subunit I (COI) gene is regularly used for species identification but faces limitations, such as similar sequences in closely related species. To overcome this, we explored the use of the internal transcribed spacers (ITS) region in addition to COI for Diamesa larvae identification. Therefore, this study employs a combination of molecular markers alongside traditional morphological identification to enhance species discrimination. In total, 129 specimens were analysed, of which 101 were sampled from a glacier-fed stream in Rotmoostal, and the remaining 28 from spring-fed streams in the neighbouring valleys of Königstal and Timmelstal. This study reveals the inadequacy of utilizing single COI or ITS genes for comprehensive species differentiation within the genus Diamesa. However, the combined application of COI and ITS markers significantly enhances species identification resolution, surpassing the limitations faced by traditional taxonomists. Notably, this is evident in cases involving morphologically indistinguishable species, such as Diamesa latitarsis and Diamesa modesta. It highlights the potential of employing a multi-marker approach for more accurate and reliable Diamesa species identification. This method can be a powerful tool for identifying Diamesa species, shedding light on their remarkable adaptations to extreme environments and the impacts of environmental changes on their populations.

Energy status of chironomid larvae (Diptera: Chironomidae) from high alpine rivers (Tyrol, Austria).

Chironomids (non-biting midges) inhabit almost every wet or semi-wet continental environment on Earth with probably 10,000 different species. Species occurrence and composition are undoubtedly limited by environmental harshness and food availability being reflected in their energy stores. Most animals store energy as glycogen and lipid. They enable the animals to survive adverse situations and to continue growth, development, and reproduction. This general statement is also true for insects and also particularly true for chironomid larvae. The rationale behind this research was, that probably any stress, any environmental burden, and any harmful influence increases the energy requirement of individual larvae depleting energy stores. We developed new methods to measure the glycogen and lipid content in small tissue samples. Here we show how to apply these methods to single chironomid larvae to demonstrate their energy stores. We compared different locations of the high Alpine rivers along harshness gradient densely populated and dominated by chironomid larvae. All samples show very low energy stores without any major differences. We found glycogen concentrations below 0.01% of dry weight (DW) and lipid concentrations below 5% of DW irrespective of the specific sampling point. These values are among the lowest ever observed in chironomid larvae. We demonstrate that individuals living in extreme environment are stressed leading to reduced energy stores in their bodies. This appears to be a general feature of high altitude regions. Our results provide new insights and a better understanding of population and ecological dynamics in harsh mountainous areas, also in view of a changing climate.

Diverse effects of accelerating climate change on chemical recovery of alpine lakes from acidic deposition in soil-rich versus scree-rich catchments.

The current recovery of mountain lakes from atmospheric acidification is increasingly affected (both accelerated and/or delayed) by climate change. We evaluated long-term trends in the ionic composition of 30 lakes situated in the alpine zone of the Tatra Mountains, and compared the rates of their recovery with model (MAGIC) simulations done 20 years ago for the 2003-2020 period. The observed recovery was faster than the model forecast, due to greater reductions in acidic deposition than projected. Trends in water composition were further modified by climate change. Rising temperatures increased the length of the growing season and retention of inorganic N and SO42- more in soil-rich compared with soil-poor catchments. In contrast, elevated precipitation and an increase in rainfall intensity reduced water residence time in soils, and consequently reduced N retention, especially in soil-poor catchments. It is likely that increases in rainfall intensity and annual number of days without snow, along with air temperatures fluctuating around the freezing point elevated the physical erosion of rocks, especially in high-elevation, steep, and scree-rich areas where rocks are not thermally insulated and stabilized by soils. Weathering of exposed accessory calcite in the eroded granodiorite bedrock was a source of Ca2+ and HCO3-, while S-bearing minerals likely contributed to lake water SO42- and partly mitigated its deposition-related decrease in scree-rich catchments. The extent of climate effects on changes in the water composition of alpine lakes recovering from acidic deposition thus depended on elevation and cover of soil and scree in catchments. Our results highlight the need for incorporating dominant climate-related process into existing process-based models to increase their reliability in predicting the future development of lake water composition.

Climate Change Increasing Calcium and Magnesium Leaching from Granitic Alpine Catchments.

Climate change can reverse trends of decreasing calcium and magnesium [Ca + Mg] leaching to surface waters in granitic alpine regions recovering from acidification. Despite decreasing concentrations of strong acid anions (-1.4 µeq L-1 yr-1) during 2004-2016 in nonacidic alpine lakes in the Tatra Mountains (Central Europe), the average [Ca + Mg] concentrations increased (2.5 µeq L-1 yr-1), together with elevated terrestrial export of bicarbonate (HCO3-; 3.6 µeq L-1 yr-1). The percent increase in [Ca + Mg] concentrations in nonacidic lakes (0.3-3.2% yr-1) was significantly and positively correlated with scree proportion in the catchment area and negatively correlated with the extent of soil cover. Leaching experiments with freshly crushed granodiorite, the dominant bedrock, showed that accessory calcite and (to a lesser extent) apatite were important sources of Ca. We hypothesize that elevated terrestrial export of [Ca + Mg] and HCO3- resulted from increased weathering caused by accelerated physical erosion of rocks due to elevated climate-related mechanical forces (an increasing frequency of days with high precipitation amounts and air temperatures fluctuating around 0 °C) during the last 2-3 decades. These climatic effects on water chemistry are especially strong in catchments where fragmented rocks are more exposed to weathering, and their position is less stable than in soil.

Effects of acidic deposition on in-lake phosphorus availability: a lesson from lakes recovering from acidification.

Lake water concentrations of phosphorus (P) recently increased in some mountain areas due to elevated atmospheric input of P rich dust. We show that increasing P concentrations also occur during stable atmospheric P inputs in central European alpine lakes recovering from atmospheric acidification. The elevated P availability in the lakes results from (1) increasing terrestrial export of P accompanying elevated leaching of dissolved organic carbon and decreasing phosphate-adsorption ability of soils due to their increasing pH, and (2) decreasing in-lake P immobilization by aluminum (Al) hydroxide due to decreasing leaching of ionic Al from the recovering soils. The P availability in the recovering lakes is modified by the extent of soil acidification, soil composition, and proportion of till and meadow soils in the catchment. These mechanisms explain several conflicting observations of the acid rain effects on surface water P concentrations.

Spatial distribution of polychlorinated biphenyls in High Tatras lake sediments.

The objective of the present study was to gain insight on the spatial distribution of seven polychlorinated biphenyl (PCB) congeners in the High Tatras mountain range in Eastern Europe. Twenty high mountain lakes were sampled on their top-core sediment. Despite the relative uniform composition of PCB congeners among the lakes, there are important differences in the observed concentrations. Moderate top-core sediment concentrations of PCB congeners were observed (1.9 to 38 ng/g dw for ∑PCB) in comparison to other high mountain or Arctic areas. The variation in PCB concentrations can partly be explained by a possible altitudinal effect, resulting in higher PCB concentrations at higher (colder) altitudes. Part of this enhanced accumulation of PCBs could be caused by external factors (topography and meteorology) and internal lake factors (sediment dynamics). Many of these factors were not quantified for all individual lakes and their influence could, therefore, only be studied for some.

Long-range transported atmospheric pollutants in snowpacks accumulated at different altitudes in the Tatra Mountains (Slovakia).

Persistent organic pollutants (POPs), including polychlorobiphenyls (PCB), endosulfans, hexachlorocyclohexanes (HCHs), hexachlorobenzene (HCB), polybromodiphenyl ethers (PBDEs), and polycyclic aromatic hydrocarbons (PAHs), were analyzed in snowpack samples collected along an altitudinal gradient (1683-2634 meters above sea level) in the High Tatra Mountains (Slovakia). All analyzed compounds were found at all altitudes, pointing to their global distribution. The presence of PBDEs, particularly BDE 209, in the snowpack samples is especially relevant, as it reflects the air transport capacity of this low volatile, very hydrophobic pollutant to remote mountain regions. The most abundant compounds at all altitudes were PAHs, with mean values ranging from 90 to 300 ngL(-1), 1 order of magnitude higher than concentrations of other compounds. PCBs (sum of PCB 28, 52, 101, 118, 153, 138, and 180) and BDE 209 were the dominant organohalogen pollutants, with concentrations from 550 to 1600 pg L(-1) and from 670 to 2000 pgL(-1), respectively. Low brominated PBDEs, endosulfans, HCHs and HCB were consistently found in all samples at lower concentrations. The concentrations of these compounds correlated positively with altitude (i.e., negatively with temperature), which is consistent with cold-trapping effects. The regression coefficients were positive and statistically significant (p < 0.05) for all compounds except BDE 209, endosulfan sulfate, HCB and α-HCH. Contrariwise, the concentrations of BDE 209 and endosulfan sulfate exhibited a statistically significant positive correlation with total particle amount, which agrees with long-range atmospheric transport associated to aerosols according to the physical-chemical properties of these compounds. Snow specific surface area, which determines the maximum amount of each organic compound that can be sorbed by snow, proved utile for describing the distribution of the more volatile compounds, namely α-HCB and HCB, in the snowpack.

Polycyclic aromatic hydrocarbons in lake sediments from the High Tatras.

European alpine lake systems are used as indicators of air quality over the continent. Preliminary data showed high polycyclic aromatic hydrocarbons (PAH) loads in the High Tatras (Eastern Europe) in comparison to other mountain regions. Here, insight on the spatial distribution of PAH is provided from analysis of top-core sediments of 27 alpine lakes distributed along the High Tatras. Top-core sediment concentrations were higher than those in deep-cores, and they were higher than those observed in other European high mountain regions. The PAH profiles were uniform and comparable to those observed in aerosols and snow, indicating that atmospheric deposition was the predominant PAH input pathway to the lakes. Good agreement between estimated atmospheric deposition and sedimentation fluxes was observed. However, in several lakes in the western range higher sediment fluxes may correspond to higher PAH depositions levels. The higher concentrations may also reflect inputs from potential emission source areas.

Atmospheric polycyclic aromatic hydrocarbons in remote European and Atlantic sites located above the boundary mixing layer.

BACKGROUND, AIM AND SCOPE: Ambient air concentrations of polycyclic aromatic hydrocarbons (PAH) were determined at five elevated mountain sites on the European continent and the Atlantic Ocean. All sites can be considered remote background areas since they are situated above the timberline and they lack local emission sources of these compounds. RESULTS AND DISCUSSION: Average gas phase concentrations of SigmaPAH were 165, 1,475, 1,553, 1,822 and 4,443 pg m(-3) for Tenerife, Pyrenees, Central Norway, Tyrolean Alps and High Tatras, respectively. Particulate phase concentrations were 55, 70, 383, 196 and 708 pg m(-3), respectively. The PAH profiles of samples from the different sites are very similar, being typical of PAH mixtures after long-range atmospheric transport. Part of the fluctuations in PAH concentrations are explained by the influence of temperature on the particulate/gas phase partitioning. CONCLUSION: The differences in PAH levels between sites, with the lowest concentrations found in Tenerife and the highest in the High Tatras, suggest the geographical influence of regional emissions on the sites, especially in the cold periods and for the sites in the eastern sector of the European continent. This is supported by air mass back-trajectories analysis for the samples on the different sites. The influence of the continent is not detectable in the case of the elevated site of Tenerife where the free troposphere has been sampled. The results in this study are consistent with the PAH levels found in soils and/or high mountain lake sediments from these areas.

Altitudinal gradients of PBDEs and PCBs in fish from European high mountain lakes.

A first case of temperature-dependent distribution of polybromodiphenyl ethers (PBDEs) in remote areas is shown. Analysis of these compounds in fish from Pyrenean lakes distributed along an altitudinal transect shows higher concentrations at lower temperatures, as predicted in the global distillation model. Conversely, no temperature-dependent distribution is observed in a similar transect in the Tatra mountains (Central Europe) nor in fish from high mountain lakes distributed throughout Europe. The fish concentrations of polychlorobiphenyls (PCBs) examined for comparison showed significant temperature correlations in all these studied lakes. Cold trapping of both PCBs and PBDEs concerned the less volatile congeners. In the Pyrenean lake transect the concentrations of PCBs and PBDEs in fish were correlated despite the distinct use of these compounds and their 40 year time lag of emissions to the environment. Thus, temperature effects have overcome these anthropogenic differences constituting at present the main process determining their distributions. These cases of distinct PBDEs and PCBs behavior in high mountains likely reflect early stages in the environmental distribution of the former since they have been under secondary redistribution processes over much shorter time than the latter.

Long-term trends and spatial variability in nitrate leaching from alpine catchment-lake ecosystems in the Tatra Mountains (Slovakia-Poland).

Relationships between catchment characteristics of 31 alpine lakes and observed trends in lake water concentrations of nitrate were evaluated in the Tatra Mountains. Nitrate concentrations increased from background levels <4 microeql(-1) in the 1930s to maxima (up to 55 microeql(-1)) in the 1980s, after which they declined to 4-44 microeql(-1) by the late 1990s. In-lake nitrate concentrations correlated negatively with parameters characterising catchment-weighted mean pools (CWM; kgm(-2)) of soil, i.e. with percent land cover with meadow and soil depth, and positively with grade of terrain, annual precipitation, and the highest elevation in the catchment. The CWM pool of soil and annual precipitation explained together 65% of the current spatial variability in nitrate concentrations. Denitrification and direct N deposition on surface area explained 14% of the variability. Increased atmospheric N deposition and declining net N retention in soils were responsible for long-term changes in nitrate concentrations. Long-term decline in %N retention in soils decreased along with the estimated decline in C:N ratios (from 21 to 18 on average during the last 70 years). An empirical model linking nitrate concentrations in different types of alpine Tatra Mountain lakes to four independent variables (CWM soil pool, annual precipitation, increased N deposition, and average trend in soil C:N ratios) explained 80% of the observed spatial and temporal nitrate variability over the period 1937-2000.

Atmospheric semivolatile organochlorine compounds in European high-mountain areas (central Pyrenees and high Tatras).

Atmospheric samples from two European high-mountain areas showed similar composition of semivolatile organochlorine compounds (SOC), such as polychlorobiphenyls (PCBs), DDTs, endosulfans, hexachlorobenzene (HCB), and hexachlorocyclohexanes (HCHs). Nearly all compounds were predominantly found in the gas phase and only the less volatile such as some PCBs (e.g., 149, 118, 153, 138, and 180) were found in higher abundance in the particulate phase. HCB, 49-85 pg m(-3), is the dominant SOC. This compound is only found in the gas phase exhibiting uniform concentrations irrespective of season and air mass origin. SOC of present use, like HCHs and endosulfans, were found in higher concentrations in the warm periods, 32-46 and 4-10 pg m(-3) in the gas + particulate phases, respectively, reflecting their seasonal pattern of use in many European countries. PCB and 4,4'-DDE, 39-42 and 4-6 pg m(-3) in the gas + particulate phases, respectively, also showed a seasonal trend despite neither the former nor the precursor of the latter (4,4'-DDT) being manufactured with their use drastically restricted since the 1980s. The seasonal differences are mainly due to a higher occurrence of air masses with strong continental inputs in the warm than in the cold periods. In this respect, samples whose air masses traveled at the high troposphere (backward air mass trajectories >6000 m) have been observed to carry considerably smaller PCB and 4,4'-DDE loads (9.3 +/- 2.8 and 0.4 +/- 0.05 pg m(-3), respectively) than overall average.