Context dependency in interference competition among birds in an endangered woodland ecosystem

Aim

Much research has quantified species responses to human-modified ecosystems. However, there is limited work on how human-modified ecosystems may reshape competitive interactions between species. Using a 19-year study across 3 million ha, we aimed to answer the question: Are levels of interference competition between bird species context dependent and influenced by habitat structure and productivity? We focussed on the hyper-aggressive behaviour of the Noisy Miner (Manorina melanocephala), which is recognized as a key threatening process for other woodland bird species in Australia. Whether environmental conditions such as amount of forest cover and net primary productivity (NPP) mediate the Noisy Miners' impact remains untested at large spatiotemporal scales.

Location

Temperate woodlands of south-eastern Australia.

Methods

We gathered data on bird site occupancy from repeated surveys of field sites and assembled satellite data on tree cover and NPP. We constructed Bayesian multi-species occupancy/detection models of bird species in woodland patches and tested the fixed and interactive effects of Noisy Miner presence, the amount of tree cover, NPP, and time. We quantified the responses of 31 species, many with known interactions with the Noisy Miner documented previously at fine spatial scales.

Results

We identified negative associations between the Noisy Miner and 18 bird species, including, unexpectedly, both small and large bodied taxa. Site occupancy in some species was influenced by interactions between Noisy Miner presence and increasing amounts of tree cover or productivity. For some species, interference competition by the Noisy Miner is context-dependent and mitigated by increasing tree cover and/or increasing NPP.

Main Conclusions

Our analyses revealed that woodland bird conservation in our study region will be promoted by protecting refugia characterized by areas of high NPP and high tree cover. Preventing vegetation clearing that reduces tree cover could reduce interference competition by the Noisy Miner on parts of the remaining woodland bird community, including species of conservation concern.     

In vitro estimation of the rate of hexose phosphorylation, by sequential pulsing with [3H]- and [14C]2-deoxy-D-glucose

The rate of phosphorylation of 2-deoxy-D-glucose (2dGlc) was determined by incubating Schistosoma mansoni in vitro in [3H]2-deoxy-D-glucose; 60 sec after exposure to the [3H]dGlc, [14C]dGlc was added to the medium, and metabolic activity was arrested at 2 min by immersion of the tissue in ice-cold silicone oil. Column chromatographic separation of the neutral [3H]- and [14C]dGlc from the [3H]- and [14C]2-deoxy-D-glucose-6-phosphate permitted estimation of the quantity of [3H]dGlc phosphorylated in 2 min, and the proportion of [14C]dGlc phosphorylated in 1 min; thus a phosphorylation rate was determined from a single tissue sample. In male schistosomes derived from mouse infections 4.4 +/- 0.8% of the dGlc was phosphorylated each minute, and 4.2 +/- 0.9% in the females. Lower rates of phosphorylation were measured in schistosomes taken from hamsters where males phosphorylated 2.4 +/- 1.1% of the dGlc each minute, and in females 2.7 +/- 1.0%. These studies suggest the high rate of hexose utilization by schistosomes compares to the conscious rat brain, where 11% of the dGlc is phosphorylated each minute.     

Inhibition of plasma membrane NADH dehydrogenase by adriamycin and related anthracycline antibiotics

Doxorubicin (adriamycin) is cytotoxic to cells, but the biochemical basis for this effect is unknown, although intercalation with DNA has been proposed. This study suggests that the cytotoxicity of this drug may be due to inhibition of the plasma membrane redox system, which is involved in the control of cellular growth. Concentrations between 10^–6–10^–7 M adriamycin inhibit plasma membrane redox reactions >50%. AD32, a form of adriamycin which does not intercalate with DNA, but is cytotoxic, also inhibits the plasma membrane redox system. Thus, the cytotoxic effects of adriamycin, which limit its use as a drug, may be based on the inhibition of a transplasma membrane dehydrogenase involved in a plasma membrane redox system.     

Insulin control of a transplasma membrane NADH dehydrogenase in erythrocyte membranes

A study of NADH ferricyanide reductase activity in oriented vesicles or open ghosts of human and porcine erythrocytes shows that the dehydrogenase activity can have three types of orientation in the membrane. There is activity which responds only to acceptors and NADH exclusively on the inside face, or exclusively on the outer surface. There is also activity which requires exposure of both sides of the membrane and thus is transmembranous. The transmembrane activity is inhibited by insulin, whereas the internal and external enzymes do not respond to insulin. The transmembrane dehydrogenase can be a basis for proton transport in the plasma membrane.     

Diferric transferrin reductase in the plasma membrane is inhibited by adriamycin

Diferric transferrin which is often necessary for growth of cells is reduced by the transplasma membrane electron transport system of HeLa cells with release of ferrous iron outside the cell. Reduction of external diferric transferrin is reflected in oxidation of internal NADH. Adriamycin, an antitumor drug, inhibits diferric transferrin reduction by the HeLa cells and inhibits concomittant oxidation of cytosolic NADH at concentrations, 10(-8)-10(-6)M, which inhibit cell growth. Isolated liver plasma membranes have an NADH diferric transferrin reductase activity which is inhibited by similar adriamycin concentrations. We propose that inhibition of cell growth by adriamycin can be based on inhibition of transplasmalemma diferric transferrin reductase.