Understanding the carbohydrate dynamics of sprouting Cirsium arvense (L.) Scop. and Sonchus arvensis L. ramets can assist in optimizing perennial weed management. However, detailed knowledge about general reserve dynamics, minimum values in reserves (compensation point) and different reserve determination methods remains sparse. We present novel insights into reserve dynamics, which are especially lacking for S. arvensis. We uniquely compare root weight changes as a proxy for carbohydrates with direct carbohydrate concentration measurements using high-performance liquid chromatography (HPLC). In a greenhouse study, ramets of two sizes (20 and 10 cm) were planted in pots. Subsequent creeping roots of sprouted plants were destructively harvested and analyzed for carbohydrates 12 times between planting and flowering. Efficiency in storing carbohydrates and the replenishing rate of root weight and carbohydrates was much higher in S. arvensis than in C. arvense. Thus, our study urges to evaluate perennial weed species individually when investigating root reserves. Determining root reserves by either using root weight changes as a proxy for carbohydrates or directly measuring carbohydrate concentrations by HPLC differed in the minimum values of reserves referred to as compensation points. For both species, these minimum values occurred earlier based on root weight than based on carbohydrate concentrations. Cutting ramets into 20 or 10 cm sizes did not significantly affect carbohydrate concentration or root weight changes for both species. We conclude that any practical applications targeting perennial weeds by fragmenting roots into small ramets through belowground mechanical control must be evaluated for trade-offs in soil structure, soil erosion, and energy consumption.

Fast regrowth from deep roots and rhizomes makes it difficult to mechanically control the perennials Cirsium arvense and Tussilago farfara respectively. It is, however, not clear whether new shoots originate mainly from fragments of roots/rhizomes in upper soil layers or from an intact system below depth of soil cultivation. Here we present results from three experiments with natural infestations of C. arvense, and two with both C. arvense and T. farfara. Plots of 1 m(2) were excavated to different depths (13-25 cm), all below-ground plant parts in the topsoil were collected and thereafter fragments were either returned to or removed from the plots. Regrowth from disturbed plots with removed or returned fragments was compared. The origin of regrown shoots, that is, whether they originated from seeds, intact below-ground root/rhizome systems or returned fragments, was examined. More C. arvense shoots originated from the intact root system (48%-84%) than from root fragments (16%-52%). The final aboveground biomass was not affected by removal of the top-soil fragments. For T. farfara, a small proportion (3%) of new shoots originated from the intact rhizome system, and the rest from fragments. We conclude that the intact root system of C. arvense contributes at least as much as root fragments to regrowth after soil cultivation, which might imply that time of treatment and depth of cultivation are crucial for the effect of mechanical control. For T. farfara, the results suggest that tillage equipment with high capacity to fragment the rhizome system will contribute to efficient control.