A genetic basis for the manipulation of sink-source relationships by the galling aphid Pemphigus batae.

We examined how the galling aphid Pemphigus batae manipulates resource translocation patterns of resistant and susceptible narrowleaf cottonwood Populus angustifolia. Using carbon-14 ((14)C)-labeling experiments in common garden trials, five patterns emerged. First, although aphid galls on resistant and susceptible genotypes did not differ in their capacity to intercept assimilates exported from the leaf they occupied, aphids sequestered 5.8-fold more assimilates from surrounding leaves on susceptible tree genotypes compared to resistant genotypes. Second, gall sinks on the same side of a shoot as a labeled leaf were 3.4-fold stronger than gall sinks on the opposite side of a shoot, which agrees with patterns of vascular connections among leaves of the same shoot (orthostichy). Third, plant genetic-based traits accounted for 26% of the variation in sink strength of gall sinks and 41% of the variation in sink strength of a plant's own bud sinks. Fourth, tree susceptibility to aphid gall formation accounted for 63% of the variation in (14)C import, suggesting strong genetic control of sink-source relationships. Fifth, competition between two galls was observed on a susceptible but not a resistant tree. On the susceptible tree distal aphids intercepted 1.5-fold more (14)C from the occupied leaf than did basal aphids, but basal aphids compensated for the presence of a distal competitor by almost doubling import to the gall from surrounding leaves. These findings and others, aimed at identifying candidate genes for resistance, argue the importance of including plant genetics in future studies of the manipulation of translocation patterns by phytophageous insects.

The impact of two gall-forming arthropods on the photosynthetic rates of their hosts.

The impact of herbivores on host plant photosynthetic rates can range from negative to positive. While defoliation by chewing herbivores can result in increases in photosynthesis followed by compensatory growth, other herbivore guilds, such as mesophyll feeders which damage photosynthetic leaf tissues, almost always reduce photosynthetic rates. The impact of galling herbivores on host photosynthesis has rarely been examined, even though the limited tissue disruption and the strong metabolic sinks induced by gall-forming herbivores could potentially stimulate photosynthetic rates. I examined the hypothesis that gall-inducing herbivores could stimulate photosynthesis in neighboring leaves in response to increased sink-demand by the gall. To address this hypothesis, I measured photosynthetic rates of galled leaves or leaflets, neighboring ungalled leaves or leaflets, and ungalled leaves or leaflets on ungalled shoots on naturally growing Prunus serotina (wild cherry) and Rhus glabra (smooth sumac). The leaves of wild cherry were galled by an eriophyid mite, Phytoptus cerasicrumena; the leaves of smooth sumac by an aphid, Melaphis rhois. I found that both species reduced the photosynthetic rates of the leaves or leaflets they galled from 24 to 52% compared to ungalled leaves in ungalled areas of the plants. Contrary to my hypothesis, mite galls on wild cherry reduced photosynthesis of neighboring ungalled leaves within the same shoot by 24% compared to ungalled leaves on gall-free shoots. Aphid galls on sumac leaflets did not significantly alter the photosynthetic rates of neighboring leaflets relative to ungalled leaves on ungalled shoots. Although gall-formers would appear to have the potential to stimulate photosynthesis in the same manner as defoliating herbivores, i.e., by increasing sink demand relative to source supply, I found only negative impacts on photosynthesis. I suggest that sink competition for nutrients between developing leaves and growing gall tissue may account for the negative impacts of sink-inducing gallers on photosynthesis.

Manipulation of food resources by a gall-forming aphid: the physiology of sink-source interactions.

We examined the capacity of the galling aphid, Pemphigus betae, to manipulate the sink-source translocation patterns of its host, narrowleaf cottonwood (Populus angustifolia). A series of 14C-labeling experiments and a biomass allocation experiment showed that P. betae galls functioned as physiologic sinks, drawing in resources from surrounding plant sources. Early gall development was dependent on aphid sinks increasing allocation from storage reserves of the stem, and later development of the progeny within the gall was dependent on resources from the galled leaf blade and from neighboring leaves. Regardless of gall position within a leaf, aphids intercepted 14C exported from the galled leaf (a non-mobilized source). However, only aphid galls at the most basal site of the leaf were strong sinks for 14C fixed in neighboring leaves (a mobilized source). Drawing resources from neighboring leaves represents active herbivore manipulation of normal host transport patterns. Neighboring leaves supplied 29% of the 14C accumulating in aphids in basal galls, while only supplying 7% to aphids in distal galls. This additional resource available to aphids in basal galls can account for the 65% increase in progeny produced in basal galls compared to galls located more distally on the leaf and limited to the galled leaf as a food resource. Developing furits also act as skins and compete with aphid-induced sinks for food supply. Aphid success in producing galls was increased 31% when surrounding female catkins were removed.