Globe artichoke [Cynara cardunculus L. var. scolymus (L.) Fiori] is one of the most important crops across the Mediterranean basin, where weeds are an important biotic constraint limiting crop yields. However, the effects of globe artichoke–cropping systems on weeds have been rarely tested. Following the demand for eco-friendly weed management practices, a multi-location trial (13 farms) was carried out, measuring weed seedbanks and aboveground communities within four globe artichoke–cropping systems: globe artichoke monoculture (ART), past cultivation of globe artichoke (8 to 10 yr ago) (past-ART), a globe artichoke–durum wheat (Triticum durum Desf.) rotation (ART-WHEAT), and a control where globe artichoke was never grown. Both below- and aboveground weed communities were dominated by annual therophytes, but a low correspondence was found between both types of communities. Averaged over farms, ART highly reduced both the weed soil seedbank (1,600 seeds m−2 on average) and the aboveground weed biomass (only 3.4 g dry weight m−2) compared with the control, with a decrease of 72% in the soil seedbank and 99% in the aboveground flora. Moreover, on the farms where globe artichoke was previously grown, a very low aboveground weed biomass (77% less than control) was found. In addition, ART contributed to the preservation of high levels of weed diversity (except for aboveground communities) and therefore avoided the creation of a specialized weed flora. In conclusion, we suggest the inclusion of globe artichoke into crop rotation schemes in Mediterranean agroecosystems as a sustainable tool for reducing both the soil weed seedbank and aboveground weeds, thus reducing the requirement of direct weed control methods and preserving the environment.

Cynara cardunculus (L.) seeds require incubation at fluctuating temperatures to terminate dormancy. In this study, we analysed the physiological mechanisms underlying such a requirement, focusing on the role of abscisic acid (ABA) and gibberellin (GA). As a conceptual framework, we considered the possibility that fluctuating temperatures and light trigger a similar set of hormonal processes after stimulus perception. To test this possibility, we (1) carried out hydrotime analysis of germination in seeds exposed to fluctuating temperatures (25/15°C) and constant temperature (20°C) with or without gibberellin (GA3) or red light; (2) determined the responses of seeds incubated at fluctuating or constant temperature to ABA, GA3, fluridone, an inhibitor of ABA biosynthesis, and paclobutrazol, an inhibitor of GA biosynthesis; and (3) determined the ABA content of seeds incubated at fluctuating or constant temperature. Incubation at 25/15°C or 20°C in the presence of GA3 reduced the mean base water potential [ψb(50)] of the population to a similar extent, compared to that observed with seeds incubated at 20°C without GA3. Irradiation with red light also reduced ψb(50) to a lesser extent than incubation in the presence of GA3. At all concentrations tested, exogenously applied GA3 did not promote germination of seeds incubated at 25/15°C. However, paclobutrazol inhibited germination, suggesting that fluctuating temperatures terminate dormancy through de novo GA biosynthesis. Fluctuating temperatures enhanced seed germination in the presence of ABA, but ABA content did not differ between seeds incubated at fluctuating and constant temperatures. This study provides clear evidence for the involvement of hormonal regulation in dormancy termination by fluctuating temperatures.

Seeds of Carduus acanthoides, Cynara cardunculus, Cirsium vulgare, Brassica campestris, and Sisymbrium altissimum were incubated at a range of decreasing osmotic potentials (Ψo) under fluctuating temperatures or the median temperature of the fluctuation cycle. Fluctuating temperatures promoted total seed germination in water and at reduced osmotic potential. Total germination was reduced as the Ψo decreased. However, this trend was smallest under fluctuating temperatures, signalling a higher tolerance of seeds to reduced osmotic potential. Effects of osmoticum and temperature were modelled with the hydrotime model. The parameters estimated from the model, the hydrotime constant (θH), the mean base water potential Ψb(50) and its standard deviation (σΨb) gave good descriptions of germination time courses. For all species, incubation under fluctuating temperatures shifted Ψb(50) values downwards without modifying their distribution substantially. This accounted for the greater tolerance of germination to reduced Ψo under fluctuating temperatures. To confirm that these effects were mediated by temperature fluctuations per se, the behaviour of C. acanthoides and C. cardunculus incubated at the minimum, the mean and the maximum temperature of the fluctuation cycle was also analysed. Constant maximum and minimum temperatures of the cycle did not stimulate germination, nor did they shift Ψb(50) towards more negative values. The hydrotime model provides a physiologically based quantitative description for germination promotion due to fluctuating temperature.