Hemiparasitic plants obtain water and solutes from their hosts, but much remains to be learned about these transfers. We used a forest girdling experiment to investigate how leaf gas exchange, carbon and nitrogen cycling in the root hemiparasite Melampyrum lineare Desr. responded to disturbance and changes in physiology of potential host trees. By preventing belowground C allocation by 35% of the canopy, girdling decreased the starch and soluble sugar contents of bulk forest floor fine roots. Photosynthetic rates of M. lineare were statistically significantly lower in the girdled plot, but their hypothesized drivers (foliar N, stomatal conductance and transpiration) had no statistically significant differences between girdled and non-girdled plots. However, M. lineare in the girdled plot had higher foliar C concentrations and Δ14C than in the control plot, suggesting possible photosynthetic down-regulation in the girdled plot due to influx of older (e.g., host-derived) C into the leaves of M. lineare. Within the girdled plot (but not the control plot), M. lineare foliar C concentrations were positively correlated with foliar Δ14C and δ15N, suggesting that M. lineare may respond to changes in both C and N biogeochemistry during the decline of dominant canopy species.

Greenhouse experiments in central Texas assessed the relative importance of above- and belowground interactions of semidwarf Mit wheat and Marshall ryegrass during vegetative growth. One experiment used partitions to compare the effect of no (controls), aboveground only, belowground only, and full interaction for 75 d after planting (DAP) one wheat and nine ryegrass plants in soil volumes of 90, 950, and 3,800 ml. The results with the different soil volumes were similar. Wheat growth in the aboveground interaction only did not differ from controls. However, the full or belowground only interaction of wheat with ryegrass reduced wheat height, leaf number, tillering, leaf area, percent total nonstructural carbohydrates in shoot, and dry weights of leaves, stems, and roots 45 and 75 DAP compared to controls. Wheat in full and belowground interaction only did not differ from one another in growth. A replacement series experiment of 56 d also showed that the competitive advantage of ryegrass was relatively greater in root than in shoot growth. No allelopathic response of wheat to ryegrass occurred. While the tallness of the semidwarf wheat minimized aboveground interference by ryegrass, the root growth of the thinner and more fibrous roots of ryegrass greatly enhanced its belowground competitiveness.

Bentazon [3-(1-methylethyl)-(1H)-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide] was evaluated for Canada thistle [Cirsium arvense (L.) Scop. # CIRAR] control and birdsfoot trefoil (Lotus corniculatus L. ‘Norcen’) tolerance. Bentazon applied in split applications controlled more Canada thistle than a single application of equal rate in both greenhouse and field studies. Bentazon applied four times reduced the level of total nonstructural carbohydrates (TNC) in the roots of both greenhouse- and field-grown Canada thistle and increased birdsfoot trefoil injury more than bentazon applied in a single application of equal rate. All bentazon treatments caused unacceptable injury when birdsfoot trefoil was grown for seed.

Native to temperate South America, deeproot sedge has naturalized throughout the southeastern United States. Often forming dense, homogenous stands, deeproot sedge has become widespread, invasive, and potentially harmful ecologically throughout the coastal prairie ecoregion of Texas. Possessing characteristics (rapid growth, generalized habitat requirements) of other weedy congeners (purple nutsedge and yellow nutsedge), its relatively recent expansion highlights the critical need to develop effective control techniques and strategies for this species throughout this endangered ecoregion. Research was performed to delineate total nonstructural carbohydrate (TNC) trends in deeproot sedge rhizomes for development of a phenologically based schedule for herbicide applications and mechanical treatments. Overall, TNC levels were greatest in May to August and lowest from October to January, regardless of study area. Apparently, deeproot sedge exerts little energy into seed production because TNC levels were continually replenished throughout the growing season. As such, foliar-herbicide application throughout the growing season should achieve total plant kill. Conversely, deeproot sedge rhizome TNC levels never fell below 30%, even during winter, which indicates that winter mechanical treatments or winter prescribed fires will not be effective because substantial rhizome reserves are present to support resprouting during the next growing season. Beyond a priori prevention, sequential herbicide applications combined with integrated, sequential, prescribed fire and herbicide treatments will be needed for long-term deeproot sedge control throughout its geographic range.

Flame cultivation (FC) uses brief exposures of high temperature to control weeds. Three sites in southeastern Massachusetts with dewberry present were studied over a 2-yr period to determine if seasonal timing and frequency of exposure to FC would reduce dewberry stem length and biomass, both in the year of and the year following treatment, and also to evaluate whether FC treatments altered the ratio (sugar : starch) of nonstructural carbohydrates (NSC) in dewberry roots. Dewberry plants were treated with a 9-s exposure to an open-flame hand-held torch at seven different timing regimes (one application in June, July, or August or two applications in June/July, June/August, and July/August, or nontreated). After 1 yr, all treatments showed reduced aboveground dewberry biomass compared to nontreated plots. The timing and frequency of FC treatments were not significant when the weed was growing amongst cranberry vines, but were significant when weeds were treated in the absence of cranberry. Exposure to FC did not affect the ratio of NSC in roots in the year after treatment, indicating that the relative amounts allocated to each type of storage carbohydrate did not differ from nontreated plants, even though the overall amount allocated to root biomass was reduced.