Carbon sequestration in tropical forests and water: a critical look at the basis for commonly used generalizations

Tree planting in the tropics is conducted for a number of reasons including carbon sequestration, but often competes with increasingly scarce water resources. The basics of forest and water relations are frequently said to be well understood but there is a pressing need to better understand and predict the hydrological effects of land‐use and climate change in the complex and dynamic landscapes of the tropics. This will remain elusive without the empirical data required to feed hydrological process models. It is argued that the current state of knowledge is confused by too broad a use of the terms ‘forest’ and ‘(af)forestation’, as well as by a bias towards using data generated mostly outside the tropics and for nondegraded soil conditions. Definitions of forest, afforestation and reforestation as used in the climate change community and their application by land and water managers need to be reconciled.     

Biomass and structure of planktonic communities along an air temperature gradient in subarctic Sweden

1. Air temperature will probably have pronounced effects on the composition of plankton communities in northern lake ecosystems, either via indirect effects on the export of essential elements from catchments or through direct effects of water temperature and the ice‐free period on the behaviour of planktonic organisms. 2. We assessed the role of temperature by comparing planktonic communities in 15 lakes along a 6 °C air temperature gradient in subarctic Sweden. 3. We found that the biomass of phytoplankton, bacterioplankton and the total planktonic biomass were positively related to air temperature, probably as a result of climatic controls on the export of nitrogen from the catchment (which affects phytoplankton biomass) and dissolved organic carbon (affecting bacterioplankton biomass). 4. The structure of the zooplankton community, and top down effects on phytoplankton, were apparently not related to temperature but mainly to trophic interactions ultimately dependent on the presence of fish in the lakes. 5. Our results suggest that air temperature regimes and long‐term warming can have strong effects on the planktonic biomass in high latitude lakes. Effects of temperature on the structure of the planktonic community might be less evident unless warming permits the invasion of fish into previous fishless lakes.     

Population structure in the barn swallow,Hirundo rustica: a comparison between neutral DNA markers and quantitative traits

Local adaptation to variable environments can generate clinal variation in morphological traits. Alternatively, similar patterns of clinal variation may be generated simply as a result of genetic drift/migration balance. Teasing apart these different processes is a continuing focus in evolutionary ecology. We compare genetic differentiation at molecular loci and quantitative traits to analyse the effect of these different processes in a morphological latitudinal cline of the barn swallow, Hirundo rustica, breeding across Europe. The results obtained show no structuring at neutral microsatellite loci, which contrasts with positive structuring at five quantitative morphometric traits. This supports the hypothesis that the observed morphometric cline in barn swallows is the result of selection acting in a spatially heterogeneous environment. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99 , 306–314.     

Changing our package

Starting with Volume 7, Lethaia will use its pages better by introducing a two-column type area. The amount of text published without charges will remain the same as in preceding volumes, but any optional publication charges received or profit attained will be invested in more pages. To our- authors the new arrangement implies one simple but important change, namely adjustment of published figure size to the page width (140 mm) or column width (67.5 mm) whenever possible. New elements for bibliographic identification ( biblid ) are added to the cover, article-heads, and individual pages.     

Reproductive life history variation among colour morphs of the pygmy grasshopper Tetrix subulata

Individuals of pygmy grasshoppers ( Tetrix subulata [L.] Orthoptera: Tetrigidae) exhibit genetically coded discontinuous variation in colour pattern. To determine whether reproductive performance is likely to be affected by colour pattern, this study investigated variation in body size and reproductive life-history characteristics among individuals belonging to five different colour morphs. The proportion of reproductive females (i.e. females with eggs) declined significantly as the season progressed (from 100% in mid-May to 40% in mid-June), but no such seasonal trend was apparent for body size, clutch size or egg size. Colour morphs differed significantly in body size, and these size differences accounted for most of the variation in clutch size and egg size. Colour morphs also differed in the regression of egg size on clutch size, suggesting that trade-offs between number and size of offspring might vary among morphs. Finally, I found a negative relationship across colour morphs between the proportion of females with eggs and average clutch size. This suggests that individuals belonging to certain colour morphs produce a relatively large number of clutches per unit time, at the expense of fewer offspring in each clutch, compared to other morphs. Collectively, my results indicate that different colour morphs of T. subulata may have different reproductive strategies. These differences may reflect variation in thermoregulatory capacity or differences in probability of survival induced by visual predators.     

Gyr Falcons, ptarmigan and microtine rodents in northern Sweden

A Gyr Falcon Falco rusticolus population in Northern Sweden (66°N, 17°E) was monitored from 1996 to 2002 in relation to its predator–prey interactions with its main and alternative prey species. Ptarmigan species Lagopus spp., and especially Rock Ptarmigan L. mutus , were the Gyr Falcons' most important prey and constituted more than 90% of the prey biomass. A 21-fold difference in ptarmigan abundance was found across Falcon breeding territories. However, this great variation in prey availability corresponded to only about a 10% shift in Gyr Falcon diet across territories, suggesting that the Falcons were reluctant or unable to compensate for declining ptarmigan availability by using alternative prey categories. Gyr Falcons did not respond functionally to microtine rodent abundance. Their diets were unaffected by a peak in the microtine rodent population cycle when Norwegian Lemmings Lemmus lemmus occurred in high numbers in the study area. Gyr Falcons responded numerically to their prey in two ways. First, there was a reproductive response with a significant relationship between the number of chicks fledged and the number of ptarmigan in the breeding territories. Secondly, although the Gyr Falcons did not utilize microtines as prey, there was a relationship between the microtine rodent abundance and the number of pairs that attempted to breed each year. This could be a result of an indirect community interaction, assuming that other predators switched from ptarmigan to microtines as prey, which could have had a positive effect on the breeding performance of the Gyr Falcons. The Gyr Falcons acted as true specialist predators, and their narrow food niche probably reflected a general lack of suitable alternative prey in the study area.     

Increased growth and recruitment of piscivorous perch, Perca fluviatilis, during a transient phase of expanding submerged vegetation in a shallow lake

1. In this study, we examine how a 7‐year period of expanding submerged stonewort (Chara spp.) vegetation during a shift from turbid to clear water in a shallow lake influenced individual growth and population size structure of perch (Perca fluviatilis). We expected that a shift from phytoplankton to macrophyte dominance and clear water would improve feeding conditions for perch during a critical benthivorous ontogenetic stage, and enhance the recruitment of piscivorous perch. 2. Growth analysis based on opercula showed that growth during the second year of life was significantly higher in years with abundant vegetation than in years with turbid water and sparse vegetation. Growth was not affected during the first, third and fourth year of life. Stable isotope analyses on opercula from 2‐year‐old perch showed that the increase in growth coincided with a change in carbon source in the diet. Stable nitrogen ratio did not change, indicating that the increased growth was not an effect of any change in trophic position. 3. Following the expansion of submerged vegetation, perch size range and abundance of piscivorous perch increased in central, unvegetated areas of the lake. In stands of stoneworts, however, mainly benthivorous perch were caught, and size range did not change with time. 4. Our findings provide empirical support for the notion that establishment of submerged vegetation may lead to increased recruitment of piscivorous perch, because of improved competitive conditions for perch during the benthivorous stage. This is likely to constitute a benthic‐pelagic feedback coupling, in which submerged vegetation and clear water promote the recruitment of piscivorous perch, which, in turn, may increase water clarity through top‐down effects in the pelagic.     

Titration of Photophosphorylation, Oxidative Phosphorylation and Glycolysis in Scenedesmus with Desaspidin: Regulation between Pathways and Sites for Photophosphorylation

Narrow concentration intervals were used, covering 10^?6– 10^?4M desaspidin. The interaction with glycolysis involves three steps, the inhibitor constants (K_i:s) being in turn 2.7 × 10^?5M, 1.3 × 10^?4M, and high. About 18% of total glycolysis is inhibited in each of the two first steps, and 65% left for the third reaction. After compensation for glycolysis, oxidative phosphorylation may show a sudden jump to about 10% inhibition at 1.5 × 10^?5M desaspidin, the possible K_i of the reaction starting here being very high. Correcting for glycolysis, desaspidin affects total Photophosphorylation in two steps, with the K_i values of 7.8 × 10^?5M and 4.6 × 10^?4M respectively. Inhibition in the first step is about 27% of the total photophosphorylation. By applying 10^?6M DCMU[/3-(3, 4-dichlorophenyl)-l, l-dimethy lurea], one can abolish non-cyclic photophosphorylation. Desaspidin then reacts in a single step with a K_i of 1.4 × 10^?4M. At 5 × 10^?5M DCMU, also the pseudocyclic photophosphorylation is abolished. The remaining, true cyclic photophosphorylation has a single K_i of 2.3 × 10^?5M for desaspidin. Under non-cyclic conditions, the true cyclic process contributes about 25% to total Photophosphorylation. Under pseudocyclic conditions, no cyclic photophosphorylation occurs. Under true cyclic conditions, the non-cyclic and pseudocyclic processes are inoperative. This indicates a regulative system, so that either (1) the (non-cyclic + true cyclic), (2) only the pseudocyclic, or (3) only the true cyclic systems can be traced, dependent on the level of DCMU applied. There are two sites for non-cyclic Photophosphorylation, one of them common to the pseudocyclic pathway. Cyclic photophosphorylation has a third site, different from the other two.