Physical activity and behavior of a centrarchid fish, Micropterus salmoides (Lacépède), during spawning

Abstract – The spawning behavior of male and female largemouth bass Micropterus salmoides (Lacépède) was studied in central Illinois during the spring of 1998 to examine patterns of muscular activity associated with different spawning related behaviors and to evaluate whether electromyogram (EMG i ) telemetry could be used to detect spawning activity. Fish were implanted with EMG i transmitters (8 females, 16 males) on April 7, prior to the initiation of spawning, and were released in four 0.10-ha earthen research ponds. Continuous EMG i records, underwater videography and additional visual observations for one pair of EMG i tagged fish were collected throughout the entire spawning event, allowing us to quantify behavioral correlates of physical activity. Male EMG i activity patterns were only correlated with female patterns during courting and periods of male aggression toward the female. Overall, EMG i activity was highest for the female during shuddering (gamete deposition), whereas male EMG i activity was similarly high during periods of nest excavation, shuddering and post-spawn parental care activities. During spawning, female EMG i activity was positively correlated to shuddering. Average daily EMG i activities for females peaked on the day of spawning. As a result of their engagement in parental care activities, male activity continued to rise even after spawning was completed. EMG i telemetry appears to be a useful technique for monitoring the reproductive activity of largemouth bass, especially in areas of high cover or turbid water or during low light conditions. This technology permitted us to quantify and contrast the activity patterns associated with different spawning related activities, information that will be required to construct accurate, gender-specific bioenergetics models for this species.     

Molecular epidemiology of avian pathogenic Escherichia coli (APEC) isolated from colisepticemia in poultry

The molecular biology and epidemiology of 150 avian pathogenic Escherichia coli strains (APEC) isolated from septicemic poultry in Germany was investigated by serotyping, pulsed field gel electrophoresis (PFGE), and polymerase chain reaction (PCR). Only 49.6% of the isolates could be grouped to serogroups O1, O2, and O78. Macrorestriction analyses data revealed two large clonal groups (clusters I and II) among the APEC strains with a similarity of 60.9% to each other. An association between restriction pattern and serogroup or origin of the strains was only present in a few subgroups of each clusters I and II, but was not evident. In contrast, our data revealed distinct combinations of virulence-associated genes in that 51.2% of the O2-strains harboured a combination of the genes fyuA, irp2, iucD, tsh, vat, fimC, and colV and 36.4% of the O78-strains possessed the same gene combination with exception of vat. With 34 different gene combinations the non-O1, -O2, -O78 isolates revealed a higher variability in their virulence gene pattern than O1-, O2-, and O78-strains with 6, 13, and 9 patterns, respectively. Our data indicate only a limited association between the virulence gene pattern and the serogroup of APEC strains and question the sensitivity of O-typing for APEC identification without the application of further diagnostic tools. Although a limited number of APEC clones exist, horizontal gene transfer seems to be common in these pathogens. These findings strengthen further research on the population structure of APEC and may be the reason for the lack of clear definition of this common E. coli pathotype.     

Polarization of PAR proteins by advective triggering of a pattern-forming system

In the Caenorhabditis elegans zygote, a conserved network of partitioning-defective (PAR) polarity proteins segregates into an anterior and a posterior domain, facilitated by flows of the cortical actomyosin meshwork. The physical mechanisms by which stable asymmetric PAR distributions arise from transient cortical flows remain unclear. We present evidence that PAR polarity arises from coupling of advective transport by the flowing cell cortex to a multistable PAR reaction-diffusion system. By inducing transient PAR segregation, advection serves as a mechanical trigger for the formation of a PAR pattern within an otherwise stably unpolarized system. We suggest that passive advective transport in an active and flowing material may be a general mechanism for mechanochemical pattern formation in developmental systems.     

Soil nitrogen dynamics after slurry injection in field trials: Evaluation of a soil sampling strategy

Slurry injection below maize seeds is a rather new application technique developed to improve the nitrogen use efficiency of liquid organic manure. To enable the characterization of the spatial and temporal soil mineral nitrogen (SMN) dynamics after slurry injection, the present study aims to develop an appropriate soil sampling strategy. Three consecutive experiments were conducted. The first testing of the soil sampling approach was conducted in an existing field trial where the slurry was injected down to a depth of 12 cm (upper rim) below the soil surface. The soil profile (75 cm wide) centered below the maize row was sampled grid‐like to a depth of 90 cm. Around the injection zone, soil monoliths (SM) were sampled using a purpose‐built soil shovel. Below the SMs and in the interrow space (15 and 30 cm distance to the row) a standardized auger procedure was performed. The second experiment aimed at improving the sampling strategy with a focus on sample homogenization quality and necessary sample sizes per pooled sample. Furthermore, the risk of a carryover of slurry components along the soil core due to drilling an auger through a slurry band was analyzed. In the third experiment this improved sampling strategy was validated. Results from the first testing of the sampling procedure showed that the strategy is suitable, although some problems occurred (especially the high spread in values among the replications causing high coefficients of variation (CV) of mostly 40–60%). The improvement trial revealed that due to the high gradient of SMN concentration in the direct range of the injection zone an intensive homogenization of these samples is required. Suitable sample sizes (twelve auger samples and six soil monolith samples per pooled sample) have to be collected to obtain reliable SMN values. Drilling an auger through a slurry band to sample subjacent soil layers has to be avoided. Following this enhanced sampling strategy, in the final validation trial the spread in values were considerably reduced and resulted in CV values of mostly < 20%. The developed sampling strategy enables the characterization of the spatial and temporal SMN dynamics when slurry has been band‐injected below a maize row. The method can be transferred to other row crops and different slurry injection spacing.