Interspecific interactions and biomass allocation among grassland plant species

Although a handful of studies have shown how interspecific interactions may influence plant shoot to root ratios, the issue of how these interactions influence biomass partitioning among coexisting plant species remains largely unexplored. In this study, we determined whether a given plant species could induce other plant species to allocate relative biomass to each of four zones (aboveground, and three soil depth layers) in a different manner to what they would otherwise, and whether this may influence the nature of competitive or facilitative interactions amongst coexisting plant species. We used a glasshouse study in which mixtures and monocultures of ten grassland plant species were grown in cylindrical pots to determine the effects of plant species mixtures versus monocultures on the production of shoots and of roots of other species for each of three soil depths. Across all experiments, stimulation of production in mixtures was far less common than suppression of production. Different plant species shifted their allocation to shoots or roots at different depths, suggesting that interspecific interactions can either: (1) increase the ratio of deep to shallow roots, perhaps because competition reduces root growth in the uppermost part of the soil profile; or (2) decrease this ratio by reducing plant vigour to such an extent that the plant cannot produce roots that can reach deep enough to exploit resources at lower depths. Further, these results suggest that there are instances in which competition may have the potential to enforce resource partitioning between coexisting plant species by inducing different species to root at different depths to each other.     

The timing of the electromyogram in the lateral myotomes of mackerel and saithe at different swimming speeds

Electromyogram (EMG) signals from two points at about 40% L and 65% L ( L = length) in the left latera1 muscle of mackerel ( Scomber scombrus L.) L = 28–33 cm a nd saithe ( Pollachius virens L.) L = 42–50 cm were recorded synchronously with films of steady straight swimming motions. In both species, the duration of EMG activity at both electrodes, remains a constant proportion of the tail cycle period Tat all the tail beat frequencies between 1–8 and 13 Hz. In mackerel and saithe respectively: onset of EMG activity at the front was 74% T and 77% T before the left-most tail blade position and fronl EMG-onset occurred 15% T and 18% T before rear onset. The duration of the EMG burst is longer at the front position (41% T and 47% T ) than at the rear (25% T and 27% T ), At all swimming speeds the wave of electrical activation of the muscle travelled between the two electrodes 25% L apart at a velocity between 1.5 and 1.6 L T ⁻¹. Frequencies of spikes within the burst of EMG activity rose from 30–40 Hz at 2 T s⁻¹ to 50–80 Hz at 8 T s⁻¹. In muscle at 40%L EMG-onset happens at phase 30° just after muscle strain at this point reaches its resting length while lengthening (360°). At 65% L EMG-onset occurs earlier in the strain cycle-350° just before the muscle reaches it resting length while lengthening (360°). This could represent within the length of the fish, a phase shift of up to 90° in the EMG-onset in relation to the muscle strain cycle. These timings are discussed in relation to optimized work output and a single instant of maximum bending moment all along the left side of the body.     

Life history variation in Campanula americana (Campanulaceae): population differentiation

Genetic variation in life history traits has important consequences for life-history evolution. Here we report the results of a greenhouse experiment investigating the broad sense genetic basis of variation in life history traits within and among five populations of Campanula americana distributed along a latitudinal gradient. The populations exhibit differentiation for a number of morphological traits (seed weight, number of branches, final plant size, number of capsules) and the phenological traits, days to emergence, days to bolting, the onset of flowering, and the duration of flowering. Families within populations differed only in days to emergence and seed weight. These results suggest that the life history differences among populations are genetically based. In addition, two life history types—winter annuals and biennials—have previously been reported from natural populations of Campanula americana. This experiment identified a third type—summer annuals from the Florida population.     

A gradient of BMP activity specifies dorsal-ventral fates in early Xenopus embryos.

BMP-4 is an extracellular signalling molecule belonging to the TGF-beta superfamily that plays a central role in dorsoventral patterning in vertebrate gastrulae. We review the evidence indicating that BMP-4 acts as a morphogen, specifying dorsoventral positional values in a concentration-dependent manner. An activity gradient of BMP-4 is established not by simple diffusion from a localised source, but by diffusion of inhibitory binding proteins that act on a uniform level of BMP-4 protein. These in turn are regulated by the activity of tolloid-related metalloproteases, such as Xenopus xolloid and zebrafish tolloid.     

Burst swimming speeds of mackerel, Scomber scombrus L.

Burst swimming speeds were measured in mackerel 0.275–0.380 m long by filming newly caught fish, first released into a large shore-sited tank, using a high-speed cine camera and real time TV camera. The highest speed was 5.50 m s⁻¹ or 18 body length per second ( b.l . s⁻¹) in a 0.305 m long mackerel at 12° C. The recorded maximum tail beat frequency of 18 Hz agrees well with 19 Hz predicted from the measured contraction time of 0.026 s for the anterior lateral swimming muscle. The stride length was close to 1 B.L.; the power, calculated from the drag, was 4.53 W, and, calculated from the muscle used, was 5.07 W; all suggesting that the mackerel is swimming close to its physiological limit.     

Parental Feeding Style and the Inter‐generational Transmission of Obesity Risk

Objective: This study was designed to determine whether a community sample of obese mothers with young children used different feeding styles compared with a matched sample of normal‐weight mothers. Four aspects of feeding style were assessed: emotional feeding, instrumental feeding (using food as a reward), prompting/encouragement to eat, and control over eating. Research Methods and Procedures: Participants were from 214 families with same‐sex twins; 100 families in which both parents were overweight or obese and 114 in which both parents were normal weight or lean. Results: We found that obese mothers were no more likely than normal‐weight mothers to offer food to deal with emotional distress, use food as a form of reward, or encourage the child to eat more than was wanted. The obese and normal‐weight mothers did differ on “control”; obese mothers reported significantly less control over their children's intake, and this was seen for both first‐born and second‐born twins. Twin analyses showed that these differences were not in response to children's genetic propensities, because monozygotic correlations were no greater than dizygotic correlations for maternal feeding style. Discussion: These results suggest that the stereotype of the obese mother, who uses food in nonnutritive ways so that her child also becomes obese, is more likely to be myth than fact. However, the results raise the possibility that lack of control of food intake might contribute to the emergence of differences in weight.