Cladoceran community responses to biomanipulation and re‐oligotrophication in Lake Vesijärvi,Finland, as inferred from remains in annually laminated sediment

1. We studied the role of zooplankton in biomanipulation and the subsequent recovery phase in the Enonselkä basin of Lake Vesijärvi, using subfossil cladocerans in annually laminated sediment. Measures to restore the Enonselkä basin included reduction in external nutrient loading and mass removal of plankti‐ and benthivorous fish. Water clarity increased and the lake changed from a eutrophic to a mesotrophic state. However, some signs of increased turbidity were observed after 5–10 years of successful recovery. 2. Annual laminae in a freeze core sample were identified and sliced, based on the seasonal succession of diatoms. Cladoceran remains and rotifer eggs were counted, and Daphnia ephippia and Eubosmina and Bosmina ephippia and carapaces were measured. Annual changes in pelagic species composition were studied with principal component analysis. Individual species abundance, size measurements and various cladoceran‐based indices or ratios (commonly used to reconstruct changes in trophic state and fish predation) were tested for change between four distinct periods: I (1985–1988) dense fish stocks, poor water quality; II (1989–1992) fish removal; III (1993–1997) low fish density, improved water quality; IV (1998–2002) slightly increased fish density and poorer water quality. 3. After the removal of fish, the mean size of Daphnia ephippia and Eubosmina crassicornis ephippia and carapaces increased significantly. In contrast, the percentage of Daphnia did not increase. When based on ephippia, the ratio Daphnia/(Daphnia + E. crassicornis) increased, but the interpretation was obscured by the tolerance of fish predation by small Daphnia and by the fact that bosminids were the preferred food of roach. Moreover, ephippial production by E. crassicornis decreased in recent years. 4. The abundance of Diaphanosoma brachyurum and Limnosida frontosa increased significantly after the fish population was reduced, while that of Ceriodaphnia and rotifers decreased. 5. The expanding littoral vegetation along with improved water clarity was clearly reflected in the concentration of littoral species in the deep sediment core. The species diversity index for the entire subfossil community also increased. 6. The period of faltering recovery was characterised by greater interannual variability and an increased percentage of rotifers. Nevertheless, the mean sizes of Daphnia ephippia and E. crassicornis ephippia and carapaces indicated a low density of fish. The deteriorating water quality was apparently related to multiple stressors in the catchment after rehabilitation, such as intensified lakeshore building, as well as to exceptional weather conditions, challenging the management methods in use.     

Indirect carbon dioxide emissions from producing bioenergy from forest harvest residues

Forest harvest residues are important raw materials for bioenergy in regions practicing forestry. Removing these residues from a harvest site reduces the carbon stock of the forest compared with conventional stem‐only harvest because less litter in left on the site. The indirect carbon dioxide (CO₂) emission from producing bioenergy occur when carbon in the logging residues is emitted into the atmosphere at once through combustion, instead of being released little by little as a result of decomposition at the harvest sites. In this study (1) we introduce an approach to calculate this indirect emission from using logging residues for bioenergy production, and (2) estimate this emission at a typical target of harvest residue removal, i.e. boreal Norway spruce forest in Finland. The removal of stumps caused a larger indirect emission per unit of energy produced than the removal of branches because of a lower decomposition rate of the stumps. The indirect emission per unit of energy produced decreased with time since starting to collect the harvest residues as a result of decomposition at older harvest sites. During the 100 years of conducting this practice, the indirect emission from average‐sized branches (diameter 2 cm) decreased from 340 to 70 kg CO₂ eq. MWh^?1 and that from stumps (diameter 26 cm) from 340 to 160 kg CO₂ eq. MWh^?1. These emissions are an order of magnitude larger than the other emissions (collecting, transporting, etc.) from the bioenergy production chain. When the bioenergy production was started, the total emissions were comparable to fossil fuels. The practice had to be carried out for 22 (stumps) or four (branches) years until the total emissions dropped below the emissions of natural gas. Our results emphasize the importance of accounting for land‐use‐related indirect emissions to correctly estimate the efficiency of bioenergy in reducing CO₂ emission into the atmosphere.     

Optimization of cryptic coloration in heterogeneous habitats

We present a theoretical approach to the optimization of crypsis in heterogeneous habitats. Our model habitat consists of two different microhabitats, and the optimal combination of crypsis in the microhabitats is supposed to maximize the probability of escaping detection by a predator. The probability of escaping detection for a prey is a function of: (i)degree of crypsis, (ii) probability of occurrence in the microhabitats and (iii) probability of encountering a predator in the microhabitats. Because crypsis is background-specific there is a trade-off between crypsis in two visually different microhabitats. Depending on the nature of the trade-off, the optimal coloration is either a compromise between the requirements of the differing microhabitats or entirely adapted to only one of them. An increased risk of predation in one of the microhabitats favours increased crypsis in that microhabitat. Because the trade-off constrains possible optimal solutions, it is not possible to predict the optimal coloration only from factors (i)-(iii). However, habitat choice may fundamentally change the situation. If minimizing predation risk does not incur any costs, the prey should exclusively prefer the microhabitat where it has a lower probability of encountering a predator and better crypsis. The implications of these results for variation in cryptic coloration and polymorphism are discussed.     

Alternative Concepts of Reproductive Effort, Costs of Reproduction, and Selection in Life-History Evolution

An outline for an organismic theory of reproductive tacticsis presented to develop the demographic theory of optimal reproductivetactics into a more realistic theory of life-history evolution.Reproductive effort—denned as the proportion of resourcesinvested in reproduction—and the costs in somatic investmentdo not automatically result in survival costs. Both the conditionswhere survival costs are produced and the conditions where reproductioncan take place without survival costs are specified. Compensationand threshold hypotheses are put forward to allow weaker correlationsbetween reproduction and survival than the trade-off hypothesis,which assumes direct impacts by reproductive effort on survival.Furthermore, reproductive tactics are unlikely to be mouldedby the demographic forces of selection only. An empirical exampleis shown where residual reproductive value played no significantrole in the evolution of reproductive tactics. Selection probablyoperates not on separate life-history traits but on whole organismsthrough their entire life-history. The structural and physiologicalintercouplings between separate traits can result in phenotypicopportunity sets where selection can mould life-history traitsonly within the constraints of the opportunity sets. Optimizationtheory has provided an efficient technique for modelling andmaking predictions. However, organismic selection does not necessarilyoptimize adaptive strategies but eliminates unfit strategies.Life-history theory, and evolutionary theory in general, canbe developed along alternative logical lines when differenthypotheses are generated on how selection operates.     

Increased nest predation in a declining and threatened Temminck's Stint Calidris temminckii population

We measured nesting success of the Temminck's Stint Calidris temminckii along the Finnish Bothnian Bay coast during 19 breeding seasons (1983–2001) and conducted a population census (1999–2002). We found 105 pairs, showing a marked decline from the previous survey (170 pairs 1987–95). Of the 424 'known-fate' nests, 47% hatched. Depredation caused 79.9% of the nest losses. Nesting failures increased from 1983–91 to 1992–2001 owing to a rise in nest predation. The proportion of failed nests that failed because of predation rose from 48.9 to 87.7%. When only depredated nests were considered as losses, Mayfield nest survival probability over the incubation period dropped from 69 to 31% (461 nests). This pattern emerged both in man-made and in natural habitats. Survival probability was independent of habitat type (natural vs. man-made). In an experiment involving videotaping of dummy nests, Common Gull Larus canus and Ruddy Turnstone Arenaria interpres were found to be the most important egg predators.     

Should ecological factors affect the evolution of age at maturity in freshwater clams?

We studied the evolution of age at maturity in freshwater clams of the genus Anodonta in relation to their ecology. We analysed an age-structured density-dependent population dynamics model, which we developed for freshwater clams, using several different options for density dependence. As evolutionary optimality criteria we applied both the maximization of a fitness measure (either intrinsic rate of increase or expected lifetime fecundity) and the concept of evolutionarily stable strategies (ESSs). All three evolutionary criteria yielded estimates which were too high for the optimal age at maturity in a deterministic model with a constant survival rate. The predictions are improved when size-selective predation is included in the model. Mature clams also face a risk of infection by castrating parasites, which would select for delayed maturity. Variable newborn survival selects for earlier reproduction, though the observed levels of stochasticity probably have a negligible effect.     

Species traits explain recent range shifts of Finnish butterflies

This study provides a novel systematic comparative analysis of the species characteristics affecting the range margin shifts in butterflies towards higher latitudes, while taking phylogenetic relatedness among species into account. We related observed changes in the northern range margins of 48 butterfly species in Finland between two time periods (1992–1996 and 2000–2004) to 11 species traits. Species with positive records in at least ten 10 km × 10 km grid squares (in the Finnish National Butterfly Recording Scheme, NAFI) in both periods were included in the study. When corrected for range size change, the 48 butterfly species had shifted their range margins northwards on average by 59.9 km between the study periods, with maximum shifts of over 300 km for three species. This rate of range shifts exceeds all previously reported records worldwide. Our findings may be explained by two factors: the study region is situated in higher latitudes than in most previous studies and it focuses on the period of most prominent warming during the last 10–15 years. Several species traits exhibited a significant univariate relationship with the range margin shift according to generalized estimation equations (GEE) taking into account the phylogenetic relatedness among species. Nonthreatened butterflies had on average expanded their ranges strongly northwards (84.5 km), whereas the distributions of threatened species were stationary (−2.1 km). Hierarchical partitioning (HP) analysis indicated that mobile butterflies living in forest edges and using woody plants as their larval hosts exhibited largest range shifts towards the north. Thus, habitat availability and dispersal capacity of butterfly species are likely to determine whether they will be successful in shifting their ranges in response to the warming climate.     

The fragmented Atlantic rain forest of Brazil: size, shape and distribution of forest fragments

The geographical characteristics of a total of 1839 forest fragments surrounded by sugar cane fields were studied in the Brazilian Atlantic rain forest region of the northeastern state of Pernambuco. The size and shape of the fragments as well as inter-fragment distances and the effects of varying edge width were examined using a geographical information system. The analyses show that the fragments are relatively small and close to each other. Approximately 48% of the rain forest fragments are <10 hectares, while only about 7% are >100 hectares. Forest fragments are close to each other, as fragments located 50m or less apart formed groups that included ca. 50% of the total forest area. At 350m inter-fragment distance, 98% of the rain forest area was included in groups of fragments. Due to the small size and irregular shape of the fragments, the total area of edge zone exceeds that of the interior habitat when the edge width is ca. 60m. At an edge width of 300m ca. 94% of the total fragment area is edge zone. For conservation purposes, ways of establishing networks of forest fragments connected by corridors and stepping stone fragments are demonstrated using GIS. Simulations using these techniques show that reforestation of sugar cane fields between the forest fragments would considerably increase the area of interior forest habitat and connectivity between fragments.