Potential age of aquatic Oligochaeta

The maximum lifetime of species with exclusively sexual reproduction covers 5–15 years or even more in aquaria, although most specimens die consecutively earlier. The zooids of paratomic species live some weeks or months, their clones usually less than a year, rarely for some years. In the species with facultative architomy (fragmentation) the clonal age also exceeds that of the individual, both lasting for several years. The actual lifetime of worms in nature may be shorter than in cultures.     

DNA fingerprinting reveals relation between tail ornaments and cuckoldry in barn swallows, Hirundo rustica

In an experimental study in Denmark, it was previously foundthat male barn swallows (Hirundo rustica) with elongated tailstreamers obtained an apparent fitness advantage through earlierpairing, an increased frequency of second clutches, and highertotal reproductive success per season. In a parallel study offive barn swallow colonies in Ontario, Canada, we also foundthat elongated males paired earlier and thus were apparentlypreferred by females. Now, using DNA fingerprinting on familiesfrom two of those Ontario colonies, we show that five elongatedmales fathered only 59% of the offspring in their nests, whereassix shortened males fathered 96% of their nestlings. Thus, althoughelongated males were clearly preferred by females at the timeof pair formation, tail elongation may have hampered the abilityof a male to guard his mate, resulting in an increase in extrapairfertilizations (EPFs). A significant negative correlation betweenthe number of EPFs and natural tail length in this experimentalstudy also suggests that tail streamer length may reflect malequality. (Behav Ecol 1990; 2: 90–98)     

Inbreeding,energy use and sexual signaling

Genetic quality and energy metabolism are expected to have an effect on the level of energetically costly sexual signaling. To explore this we manipulated genetic quality of male decorated crickets (Gryllodes sigillatus) by inbreeding and measured the resting metabolic rate and total energy budget of males. We also measured several aspects of the sexual signaling of males: probability to initiate calling, latency, amount of call bouts, first call bout duration, mean call bout duration and total time spent calling. Inbreeding increased the latency and lowered the first and mean call bout duration. Moreover, the resting metabolic rate had a positive effect, and body mass a negative effect on first call bout duration and mean call bout duration. Our results, suggest that sexual signals are indicative of genetic quality but are also dependent on the physical properties of individuals.     

Evolution of Hsp90 expression in Tetrahymena thermophila (Protozoa, Ciliata) populations exposed to thermally variable environments

Evolutionary consequences of thermally varying environments were studied in the ciliated protozoan Tetrahymena thermophila. Replicated lines were propagated for 60 days, a maximum of 500 generations, in stable, slowly fluctuating (red spectrum), and rapidly fluctuating (blue spectrum) temperatures. The red and blue fluctuations had a dominant period length of 15 days and two hours, respectively. The mean temperature of all time series was 25 degrees C and the fluctuating temperatures had the same minimum (10 degrees C), maximum (40 degrees C), and variance. During the experiment, population sizes and biomasses were monitored at three-day intervals. After the experiment, carrying capacity and maximum growth rate were measured at low (15 degrees C), intermediate (25 degrees C), and high (35 degrees C) temperatures for each experimental line. Physiological changes in the lines were assessed by measuring the expression of stress-induced heat shock protein Hsp90 at 25 degrees C, 35 degrees C, and 39 degrees C. Population sizes and biomasses showed no differences between stable, blue, or red temperature treatments during the experiment. Also, after the experiment, mean carrying capacities and maximum growth rates were comparable in the stable, blue, and red temperature treatments. The expression of Hsp90 was higher in lines from the blue environment than in lines from the stable environment. Lines from the red environment had an intermediate level of Hsp90 expression. This supports the hypothesis that inducible thermotolerance and expression of canalizing genes can evolve in response to rapidly varying environments. Furthermore, we found correlative evidence of benefits and disadvantages of high Hsp90 expression. Lines with high expression of Hsp90 had an increased growth rate at the highest temperature when food resources were not limiting growth. At low and intermediate temperatures the same lines had the lowest carrying capacities.     

Variation in needle-trace diameter in respect of needle morphology in five conifer species

Needle traces have been used for revealing historical changes in needle longevity of Pinus sylvestris L. and Picea abies (L.) H. Karst. In this paper we compared the needle-trace diameter of five conifer species [Abies sibirica Ledeb., Picea abies, Pinus sylvestris, Pseudotsuga menziesii (Mirb.) Franco and Taxus baccata L.] in respect of needle size. In case of P. sylvestris, we studied how needle-trace diameter varied among different growing sites and among different shoots within a site, and related that variation to needle morphology and structure. Pinus sylvestris had the greatest diameter of needle traces (mean±SD =233±30 m) followed by T. baccata (141±19 m) and P. menziesii (121±30 m). The smallest needle-trace diameter was in A. sibirica (85±21 m) and P. abies (80±18 m). Among species, the needle-trace diameter was strongly correlated with needle length (r =0.93, P <0.05). Within P. sylvestris, the needle-trace diameter was significantly affected by location (P <0.001) and varied significantly among shoots within a location (P <0.001). The shoots of P. sylvestris which had greater average diameter of needle traces, tended to have longer (r =0.36, P <0.05), wider (r =0.55, P <0.05) and heavier (r =0.64, P <0.05) needles with greater stomatal density (r =0.55, P <0.05). Although our results do not allow the use of needle-trace diameter to predict properties of needle structure at the present stage, they nevertheless indicate general trends and point to a need for further studies.     

Experimental evolution of evolutionary potential in fluctuating environments

Variation is the raw material for evolution. Evolutionary potential is determined by the amount of genetic variation, but evolution can also alter the visibility of genetic variation to natural selection. Fluctuating environments are suggested to maintain genetic variation but they can also affect environmental variance, and thus, the visibility of genetic variation to natural selection. However, experimental studies testing these ideas are relatively scarce. In order to determine differences in evolutionary potential we quantified variance attributable to population, genotype and environment for populations of the bacterium Serratia marcescens. These populations had been experimentally evolved in constant and two fluctuating environments. We found that strains that evolved in fluctuating environments exhibited larger environmental variation suggesting that adaptation to fluctuations has decreased the visibility of genetic variation to selection.     

Global diversity of polychaetes (Polychaeta; Annelida) in freshwater

A literature review of Polychaeta (Annelida) including Aphanoneura (the oligochaete-like Aeolosomatidae and Potamodrilidae), living in freshwater yielded 168 species, 70 genera and 24 families representing all of the major polychaete clades, but less than 2% of all species. The best-represented families were, in order, Nereididae, Aeolosomatidae, Sabellidae, Spionidae and Histriobdellidae. Fourteen families were represented by a single species and genus. Regions supporting the highest diversity of freshwater polychaetes were in order, Palaearctic, Neotropical, Oriental, Nearctic, Australasian, and Afrotropical. More than half of all species and genera inhabitat lakes and rivers, followed by lagoons/estuaries, which have a high proportion of euryhaline species, and inland seas. Less common, atypical polychaete habitats include subterranean waters, the hyporheic zone of rivers and plant container habitats (phytotelmata). At least three distinct ecological/historical processes appear to account for the colonisation of continental waters: invasion of a clade prior to the break-up of Gondwana, as in Aphanoneura, Namanereis, Stratiodrilus, and Caobangia; relatively recent stranding of individual species (relicts); and the temporary visitation of euryhaline species. Guest editors: E. V. Balian, C. Lévêque, H. Segers & K. Martens Freshwater Animal Diversity Assessment