Population genetics of the black ant Formica lemani (Hymenoptera: Formicidae)

Colony kin structure and spatial population structure were studied in multiple populations of the ant Formica lemani , using allozymes and DNA microsatellites. Average genetic relatedness between nestmate workers varied little between populations ( r  = 0.51–0.76), indicating that the average colony kin structure was relatively simple. Worker genotypes could not be explained with a single breeding pair in all nests, however, and the distribution of relatedness estimates across nests was bimodal, suggesting that single- and multi-queen colonies co-occur. We studied spatial population structure in a successional boreal forest system, which is a mixture of different aged habitats. Newly clear-cut open habitat patches are quickly colonized by F. lemani , where it is able to persist for a limited number of generations. Newly-founded populations showed signs of a founder effect and spatial substructuring, whereas older populations were more homogenous. This suggests that new populations are founded by a limited number of colonizers arriving from more than one source. Genetic differentiation among local populations was minor, indicating strong migration between them. There were, however, indications of both isolation by distance and populations becoming more isolated as habitat patches grew older.  © 2009 The Linnean Society of London, Biological Journal of the Linnean Society , 2009, 97 , 247–258.     

Effects of temperature and sediment properties on benthic CO2 production in an oligotrophic boreal lake

1. Temperature and many other physical and chemical factors affecting CO₂ production in lake sediments vary significantly both seasonally and spatially. The effects of temperature and sediment properties on benthic CO₂ production were studied in in situ and in vitro experiments in the boreal oligotrophic Lake Pääjärvi, southern Finland. 2. In in situ experiments, temperature of the water overlying the shallow littoral sediment varied seasonally between 0.5 and 15.7 °C, but in deep water (≥20 m) the range was only 1.1–6.6 °C. The same exponential model (r² = 0.70) described the temperature dependence at 1.2, 10 and 20 m depths. At 2.5 and 5 m depths, however, the slopes of the two regression models (r² = 0.94) were identical but the intercept values were different. Sediment properties (wet, dry, mineral and organic mass) varied seasonally and with depth, but they did not explain a significantly larger proportion of variation in the CO₂ output rate than temperature. 3. In in vitro experiments, there was a clear and uniform exponential dependence of CO₂ production on temperature, with a 2.7‐fold increase per 10 °C temperature rise. The temperature response (slope of regression) was always the same, but the basic value of CO₂ production (intercept) varied, indicating that other factors also contributed to the benthic CO₂ output rate. 4. The annual CO₂ production of the sediment in Lake Pääjärvi averaged 62 g CO₂ m^?2, the shallow littoral at 0–3 m depth releasing 114 g CO₂ m^?2 and deep profundal (>15 m) 30 g CO₂ m^?2. On the whole lake basis, the shallow littoral at 0–3 m depth accounted for 53% and the sediment area in contact with the summer epilimnion (down to a depth c. 10 m) 75% of the estimated total annual CO₂ output of the lake sediment, respectively. Of the annual production, 83% was released during the spring and summer. 5. Using the temperature‐CO₂ production equations and climate change scenarios we estimated that climatic warming might increase littoral benthic CO₂ production in summer by nearly 30% from the period 1961–90 to the period 2071–2100.     

Post-emergence migration of stoneflies (Plecoptera) into the nearby forest

Abstract. 1. The post-emergence lateral migration of both sexes of eight stonefly species was examined in a dystrophic, fourth-order forest river in eastern Finland.
2. For this purpose, 7351 stonefly adults were collected with eighteen trunk funnels positioned in rows of six at distances of approximately 1, 15 and 60 m from the river. A further 1880 adults were also caught from the vegetation of the bank zone by sweep netting and with slit traps.
3. The species could be grouped into two types with respect to migration distance: Isoperla difformis, I.grammatica and Leuctra fusca tended to stay in the bank area, whereas Nemoura flexuosa, N.avicularis, Amphinemura borealis, L.hippopus and N.cinerea tended to disperse into the forest, so that the majority were found some distance away from the shore.
4. The males of the leuctrids, N.flexuosa and N.cinerea migrated farther than the females.
5. The sex ratio was significantly biased in all species except N.flexuosa. The isoperlids, leuctrids and A.borealis showed a significant predominance of females in the trunk funnel catches, but males were significantly dominant in N.avicularis and N.cinerea. The material caught by other methods reversed the ratio for I.difformis and N.avicularis. Comparison of the sex ratios of the species with other reports revealed marked variation and deviation from unity, much of which could be attributed to bias introduced by the sampling methods.
6. Lateral migration seems to be the first phase in the colonization cycle, although the latter as such was not studied here. Adults of Euholognatha species migrate farther than those of Systellognatha, a difference of which may be due to their ability to feed as adults.     

Statistical Distribution of Stomatal Apertures of Vicia faba and Hordeum vulgare and the Spannungsphase of Stomatal Opening

Plants of Vicia faba and Hordeum vulgare were grown in growthboxes with 7 mW cm^–2 PAR, 14 h day/10 h night, at 22/20°C. Stomata of attached leaves were measured under controlledconditions by means of an optical microscope and the distributionfunctions of the widths of pores were established. For Viciafaba they appeared to be symmetrical bell-shaped functions.In the process of stomatal opening or closure the shape of thedistribution remained constant, its maximum sliding left andright along the aperture axis. This result has been interpretedto mean that increments or decrements of apertures were equalfor all stomata independent of their individual apertures. Theconclusion has been drawn that the ‘driving force’is evenly distributed, equal for all stomata, and varies withinwider limits than is possible for stomatal apertures. Stomatalopening is limited by the closed state from below and by ananatomically possible maximum aperture from above.