Understanding the timing of weed emergence is crucial to effective management. Management practices implemented too early may fail to completely control late-emerging seedlings, whereas management practices implemented too late will suffer from low efficacy. Weed emergence times reflect biological factors, such as seed dormancy and germination requirements, as well as environmental conditions. We conducted a systematic review of studies that developed models to predict weed emergence temporal patterns. We screened 1,854 studies, 98 of which were included in the final dataset. Most of the studies included were conducted in North America (51%) or Europe (30%). A wide variety of weed species (102) and families (21) were included, and many studies modeled several weeds. Grass weeds (Poaceae) were modeled most frequently (83 instances). Most weeds (40%) had base temperature ${T_{\rm{b}}}$ values between 0 and 5 C, and 38% had base water potential ${{\rm{\psi }}_{\rm{b}}}$ ranging from −1.0 to −0.5 MPa. Most studies used empirical parametric models, such as Weibull (40%) or Gompertz (30%) models. Nonparametric and mechanistic models were also represented. Models varied in their biological and environmental data requirements. In general, empirical parametric models based on hydrothermal time (i.e., time above base temperature and water potential thresholds) represented a good balance between ease of use and prediction accuracy. Soft computing approaches such as artificial neural networks demonstrated substantial potential in situations with complex emergence patterns and limited data availability, although they (soft computing approaches) can be susceptible to overfitting. Our study also demonstrated variability in model performance and limited generalizability across species and regions. This finding underscores the need for context-specific and well-validated weed emergence models to inform management, especially in the context of climate change.

Two species of cleavers, Galium aparine L. and Galium spurium L., are known to inhabit croplands in western Canada. The latter is the more abundant of the two species. An increased abundance of these species over the most recent decades warrants a more comprehensive understanding of their developmental phenology and the cause of this increase. This study aimed to identify the base temperature and emergence characteristics of Galium spp. across different populations from western Canada. A thermal gradient plate experiment was conducted using five G. spurium populations collected from various Saskatchewan (SK) and Alberta (AB) locations. One known G. aparine reference sample was also included. A common garden experiment was conducted using the six Galium spp. populations to determine emergence characteristics. The base germination temperature identified was 2 C for all populations of G. spurium and 4 C for G. aparine. The median germination temperature for G. aparine was 8.34 C, whereas G. spurium had a similar median germination temperature of 6.5 C. Despite similar germination characteristics, the field emergence study revealed differences between populations’ initiation of emergence (150 to 250 growing degree days [GDD]) and time to 50% emergence (275 to 470 GDD) in spring. Highly variable emergence among years and populations within the year (200 to 600 GDD in 2013 and 100 to 200 GDD in 2014) were observed during fall, probably due to differences in moisture availability. Cumulative emergence among populations in fall was very low (1% to 9%) compared with spring emergence (2% to 17%). Overall, this study provides evidence for a low base temperature and differences in emergence periodicity among populations, both of which may be significant factors contributing to the seasonal success of this species.

In this study, we define the cardinal temperatures and thermal time for germination and emergence of pigeonpea genotypes. Seeds of six genotypes were subjected to constant temperatures ranging between 5 and 50°C in petri dishes with filter paper (germination) and with media (emergence) were placed in a thermal gradient plate. A nonlinear bent-stick model fitted to the rate of development to germination and emergence resulted in parameters predicting cardinal temperatures including base (Tb), optimum (To), maximum (Tm), and thermal time. Estimated Tb for 50% germination and emergence were 8.4 and 10.8°C, respectively, with no significant differences between genotypes. Optimum temperatures were 33.8 and 37.9°C for germination and emergence, respectively, with genotypes differing significantly. Thermal time for 50% germination and emergence varied significantly among genotypes. The results suggest that genotypic responses to the temperature are typical for their tropical origin and hence their suitability for cropping in summer dominant rainfall regions insubtropical Australia.

Temperature may regulate seed dormancy and germination and determine the geographical distribution of species. The present study investigated the thermal limits for seed germination of Polygonum ferrugineum (Polygonaceae), an aquatic emergent herb distributed throughout tropical and subtropical America. Seed germination responses to light and temperature were evaluated both before (control) and after stratification at 10, 15 and 20°C for 7, 14 and 28 d. Germination of control seeds was ~50% at 10 and 15°C, and they did not germinate from 20 to 30°C. The best stratification treatment was 7 d at 10°C, where seed germination was >76% in the dark for all temperatures, except at 30°C, and < 60% in light conditions. A thermal time approach was applied to the seed germination results. Base temperature (Tb) was 6.3°C for non-dormant seeds and optimal temperature (To) was 20.6°C, ceiling temperature (Tc (<50)) was 32.8°C, and thermal time requirement for 50% germination was 44.4°Cd. We concluded that a fraction of P. ferrugineum seeds is dormant, has a narrow thermal niche to germinate (10 and 15°C) and that cold stratification (10°C) alleviated dormancy and amplified the thermal range permissive for germination of the species. Consequently, P. ferrugineum is expected to occur in colder environments, for example, at high altitudes. Higher temperatures decrease the probabilities of alleviate dormancy and the ability of their seeds to germinate.

The influence of temperature and water availability on seed germination can vary across the geographic range of species with a large distribution. Betula pendula is a widely spread European tree that has differentiated into two narrowly distributed taxa, endemic to Mediterranean mountains: Betula aetnensis in Sicily and B. fontqueri in Spain and Morocco. We tested the hypothesis that the regeneration niche, expressed by temperature and water potential thresholds, varies across these species and is influenced by the local climate. Seeds were collected from six populations of B. pendula, one of B. fontqueri and two of B. aetnensis. Germination tests were conducted between 5 and 30°C. The thermal thresholds were calculated before and after cold stratification. The osmotic potential tested ranged from 0 to −1.5 MPa. Time to reach 30 and 50% of germination was calculated by fitting non-linear models. Germination was promoted by high temperatures, but the response to stratification was heterogeneous. Tb and Ψb differed between and within species. Tb ranged between 2.22 and 8.94°C for unstratified seeds. Mediterranean species had higher drought tolerance, while B. pendula showed contrasting responses to low water potential. Ψb reached a minimum value of −1.15 MPa in B. fontqueri. High temperatures influenced the Tb of unstratified seeds negatively, while, after stratification, the Tb increased with precipitation in the driest month. The heterogeneity observed could reflect higher genetic variability in marginal populations of silver birch. Knowledge of their germination ecology may be useful to mitigate future impacts of climate change on core populations of B. pendula.

Each taxon is characterized by a temperature range over which seed germination is possible and this may vary in space and time in relation to climate and ecological conditions. We used thermal modelling to test the hypothesis that thermal thresholds for seed germination can predict germination timing of Mediterranean species along an altitudinal and environmental gradient. Seeds of 18 species were collected in Sardinia from sea level to 1810 m above sea level, and germination tests were carried out at a range of constant (5 to 25°C) and alternating (25/10°C) temperatures. Different dormancy-breaking treatments [gibberellic acid (GA3), cold (C) and warm (W) stratifications and dry after ripening (DAR)] were applied. The annual pattern of soil temperatures was recorded using 24 data-loggers buried close to the study species. The logged soil temperatures distinguished ‘Mediterranean lowland’ from ‘Mediterranean mountain’ species. Although germination was >50% in untreated seeds of most species, GA3 had a positive effect in all species. C either inhibited or had a neutral effect on germination, W did not enhanced seed germination, while DAR had a positive effect only in species from coastal environments. The thermal time constant (S) for 50% germination ranged from 22 to 357°Cd (degree days) above base temperatures (Tb) of –9 to 9°C, depending on species and treatments. Mediterranean lowland species had lower Tb values compared with upland species. This study revealed significant differences in germination thresholds of Mediterranean lowland and mountain species in relation to Tb and S that probably have an impact on germination timing in the field and niche competitiveness.

Exotic annual weeds on western U.S. rangelands, including yellow starthistle, owe at least part of their invasion success to prolific seed production. Occurrence of flowering in relation to soil moisture and development of competing vegetation heavily influences reproductive output. Yellow starthistle flowers much later than associated Mediterranean invaders, which avoid summer drought by early flowering and senescence. This study used successive planting dates and four densities to investigate the influence of temperature, photoperiod, and intraspecific competition on reproductive phenology in a population of yellow starthistle from Lewiston, ID. A base temperature for seed germination of 2 C was determined by experiments at constant temperatures. Under the conditions of this study, density, photoperiod, and vernalization did not regulate reproductive development, as measured by onset of bud, flowering, and achene dispersal stages. A thermal time model adequately predicted phenology in this population of yellow starthistle. Plants emerging between October and July required about 1,240 degree days for 50% of the plants to reach bud stage, and an additional 500 and 900 degree days to flowering and achene dispersal, respectively. The relatively long time from emergence to mature achenes in this species influences management options such as prescribed fire, livestock grazing, and management of competing vegetation. Insensitiviry to photoperiod and lack of a vernalization requirement allow late germinating plants to reproduce if moisture is adequate.

Laboratory studies were conducted to describe germination and seedling elongation of Ambrosia artemisiifolia L. (common ragweed) seed. The germination process was tested for the interaction of temperature and water potential across eight thermo-periods (7.5, 12.5, 17.5, 22.5, 27.5, 32.5, 37.5, and 42.5 C) and 12 water potentials (0, −0.03, −0.06, −0.1, −0.2, −0.4, −0.6, −0.9, −1.2, −1.5, −1.8, and −2.1 mPa). The rate of seedling shoot and radicle elongation was described as a function of temperature and tested for eight day: night temperature treatments (10: 5, 15 : 10, 20 : 15, 25 : 20, 30 : 25, 35 : 30, 40 : 35, and 45 : 40 C). The rate of germination was mathematically modeled by a Weibull function. Probit analysis was used to determine the cardinal temperatures (base, optimum, and maximum) and base water potential (αb ). The base temperature (T b), optimum temperature (T opt), maximum temperature (T max), and αb for A. artemisiifolia germination were estimated as 3.6, 30.9, and 40 C and −0.8 mPa, respectively. The rates of shoot and radicle elongation were described by regression models. The T b , T opt, and T max for shoot and radicle elongation were estimated as 7.7 and 5.1, 29.5 and 31.4, and 43.0 and 44.3 C, respectively. A mathematical model describing the process of A. artemisiifolia seed germination in terms of hydrothermal time (θHT) was derived. The θHT model described the phenology of A. artemisiifolia seed germination using a single curve generated from the relationship of temperature and water potential. This model can help in predicting germination and emergence of A. artemisiifolia under field conditions.

Weed seeds were germinated in incubators at constant temperatures ranging from 4 to 32 C increments. Percent germination per day was regressed against temperature with the x-intercept representing the low threshold temperature for development. Low threshold temperatures for development (low TTD's) calculated for wild proso millet (Panicum miliaceum L. # PANMI), barnyardgrass [Echinochloa crus-galli (L.) Beauv. # ECHCG], common lambsquarters (Chenopodium album L. # CHEAL), and redroot pigweed (Amaranthus retroflexus L. # AMARE) were 6.9, 9.7, 6.0, and 10.0 C, respectively.

Thermal time models for predicting phenological development require an estimate of base temperature, an attribute not previously defined for common crupina, a Mediterranean winter annual introduced in western North America. The stage of seed germination was selected for estimating base temperature, because facilities were available for experiments over a range of constant temperatures and base temperature is relatively constant throughout the life cycle in other species. Achenes from three populations of common crupina, including two varieties, typica and brachypappa, were produced under uniform conditions. Cumulative germination was recorded at 12 h intervals for achenes in darkness and optimum moisture at 23 constant temperatures from 4 to 17 C. The time course of germination was best described by a logistic growth curve from which time to 50% germination was estimated. A parabolic model provided the best fit in a regression of germination rate (reciprocal of time to 50%) against the temperature gradient, yielding base and optimum temperatures of 1 and 10.5 C, respectively. Bootstrap confidence intervals indicated no significant difference in base and optimum temperatures in germination between the two varieties nor between two populations of var. typica of common crupina introduced in the northwestern United States.

Silky windgrass and annual bluegrass are among the most troublesome weeds in northern European winter crops, while problems with rattail fescue have been especially linked to direct-drilling practices. This study investigated the germination patterns of silky windgrass, annual bluegrass, and rattail fescue in multiple water potentials and temperature regimes. Temperature and water potential effects were similar between silky windgrass and rattail fescue, but differed from annual bluegrass. The three grass weeds were able to germinate under low water potential (−1.0 MPa), although water potentials ≤−0.25 MPa strongly delayed their germination. Silky windgrass and rattail fescue seeds were able to germinate at 1 C, while the minimum temperature for annual bluegrass germination was 5 C. Germination of silky windgrass and rattail fescue was very similar across temperature and water potentials, which implies similar emergence flushes under field conditions, allowing management interventions to follow the same scheme.

Windmillgrass is a major weed in agricultural systems in northern Australia, and it has now become more common in southern Australia. Because little information is available on the biology of this weed species in southern Australia, studies were conducted to investigate plant development and seed biology. Under irrigated field conditions in South Australia, windmillgrass required 748 to 786 growing degree days from emergence to mature seed production. Freshly harvested seed had low dormancy with 16% to 40% germination. Seeds required light exposure for germination and less than 2% germination was observed in complete darkness. Seed could germinate over a wide temperature range (10 to 40 C) with maximum germination at 20 to 25 C. At 25 to 30 C, 50% germination occurred within 27.3 to 45.5 h, and the predicted base temperature for germination of the two populations investigated ranged from 9.2 to 11.2 C. The sodium chloride concentration and osmotic potential required to inhibit germination by 50% were 51 to 73 mM and −0.27 MPa, respectively. Seedling emergence was completely inhibited by burial of seed, which is consistent with its absolute requirement for light exposure to begin germination. Under field conditions, there was no clear effect of burial depth on seed viability in the first 2 yr with average rainfall, and seeds were completely nonviable after 12 mo. However, in the third year, with low spring–summer rainfall, buried seeds (37% viability after 14 mo) persisted longer than those left on the soil surface (6% viability after 14 mo). This study provides important information on plant development and seed biology of windmillgrass that will contribute to the development of a management program for this weed species in southern Australia.

Understanding how plant traits interact with climate to determine plant niches is decisive for predicting climate change impacts. While lifespan and seed size modify the importance of germination timing, germination traits such as base temperature and base water potential directly translate climatic conditions into germination timing, impacting performance in later life stages. Yet we do not know how base temperature, base water potential, seed mass, lifespan and climate are related. We tested the relationships between base temperature and base water potential for germination, seed size and lifespan while controlling for bioclimatic regions. We also quantified the phylogenetic signal in germination traits and seed size using Pagel's λ. We used a worldwide data set of germination responses to temperature and moisture, seed size and lifespan of 240 seed plants from 49 families. Both germination temperature and moisture are negatively related to seed size. Annual plants show a negative relation between seed size and base water potential, whereas perennials display a negative relation between base temperature and seed mass. Pagel's λ highlighted the slow evolution of base temperature for germination, comparable to seed mass while base water potential was revealed to be labile. In the future, base water potential and seed mass can be used when moisture niches of plants are to be predicted. Lifespan, seed size and base temperature should be taken into account when analysing thermal limits of species distributions.

Feather fingergrass is a major weed in agricultural systems in northern Australia and has now spread to southern Australia. To better understand the biology of this emerging weed species, its growth, development, and seed biology were examined. Under field conditions in South Australia, seedlings that emerged after summer rainfall events required 1,200 growing degree days from emergence to mature seed production and produced 700 g m−2 shoot biomass. Plants produced up to 1,000 seeds panicle−1 and more than 40,000 seeds plant−1, with seed weight ranging from 0.36 to 0.46 mg. Harvested seeds were dormant for a period of about 2 mo and required 5 mo of after-ripening to reach 50% germination. Freshly harvested seed could be released from dormancy by pretreatment with 564 mM sodium hypochlorite for 30 min. Light significantly increased germination. Seed could germinate over a wide temperature range (10 to 40 C), with maximum germination at 15 to 25 C. At 20 to 25 C, 50% germination was reached within 2.7 to 3.3 d, and the predicted base temperature to germinate was 2.1 to 3.0 C. The osmotic potential and NaCl concentration required to inhibit germination by 50% were −0.16 to −0.20 MPa and 90 to 124 mM, respectively. Seedling emergence was highest (76%) for seeds present on soil surface and was significantly reduced by burial at 1 (57%), 2 (49%), and 5 cm (9%). Under field conditions, seeds buried in the soil persisted longer than those left on the soil surface, and low spring–summer rainfall increased seed persistence. This study provides important information on growth, development, and seed biology of feather fingergrass that will contribute to the development of a more effective management program for this weed species in Australia.

Weed emergence models require biological parameters such as base temperature for germination, determination of which is costly and time-consuming. Transferability of these parameters across different populations may therefore represent one of the main constraints for the development and practical use of emergence models at a large scale. A collaborative project was undertaken to assess the interpopulation variability of base temperature for germination in different European populations of velvetleaf and jimsonweed and evaluate possible applicative consequences in terms of weed control. Seeds were collected in Italy, Portugal, and Spain, and each population was then sown in every country, obtaining nine seed batches named as experimental lots. Base temperature for germination was estimated for each experimental lot to calculate lot-specific accumulation of growing degree days (GDD) under three dissimilar climatic scenarios. Threshold date (TD50) was calculated as the date when GDD accumulation of a given experimental lot surpassed the values corresponding to 50% of cumulative field emergence of seedlings. GDD accumulation and TD50 were then used as indicators to identify differences among experimental lots within each climatic scenario. No significant differences were detected among base temperatures estimated for velvetleaf experimental lots or among their patterns of accumulation of GDD and TD50 values within climatic scenarios. Each value of base temperature determined for a single experimental lot could therefore be adopted to model germination for all the lots regardless of the population of origin or cultivation site. In contrast, the population of origin affected the base temperature for jimsonweed, with significantly higher values for experimental lots of the Portuguese population. From an applicative perspective, differences among patterns of accumulation of GDD and TD50 of several experimental lots within each climatic scenario suggest the need to use population-specific values as base temperature for germination and emergence modeling of jimsonweed.

Common groundsel is an important weed of strawberry and other horticultural crops. Few herbicides are registered for common groundsel control in such crops, and understanding and predicting the timing and extent of common groundsel emergence might facilitate its management. We developed simple emergence models on the basis of soil thermal time and soil hydrothermal time and validate them with the use of field-derived data from Minnesota and Ohio. Soil thermal time did not predict the timing and extent of seedling emergence as well as hydrothermal time. Soil hydrothermal time, adjusted for shading effects caused by straw mulch in strawberry, greatly improved the accuracy of seedling emergence predictions. Although common groundsel generally emerges from sites at or near the soil surface, the hydrothermal model better predicts emergence when using hydrothermal time at 5 cm rather than 0.005 cm, probably because of the volatility of soil temperature and water potential near the soil surface.

Field experiments were conducted from 1997 through 1999 to evaluate interspecific interference between pitted morningglory at 0, 10, 16, and 62 plants m−2 and drill-seeded, glyphosate-resistant soybean as influenced by soybean population and a single glyphosate application of 1.12 kg ai ha−1. Photosynthetic rate of soybean was not influenced by pitted morningglory density or glyphosate use 2 wk after treatment (WAT). Photosynthetic rate of soybean 12 WAT was reduced by 21 and 91% with 62 treated and untreated pitted morningglory plants m−2, respectively, whereas 10 treated and untreated pitted morningglory plants m−2 had no effect on the soybean photosynthetic rate. Pitted morningglory photosynthetic rate 2 and 12 WAT was reduced by 64 and 80%, respectively, when treated with glyphosate. The reduction in the photosynthetic rate of glyphosate-treated pitted morningglory was partially attributed to shading by soybean, whereas untreated plants were fully exposed to sunlight. Glyphosate-treated pitted morningglory at 10 and 16 plants m−2 did not reduce the rate of soybean leaf area index (LAI) accumulation; however, when the density was increased to 62 pitted morningglory plants m−2, soybean LAI decreased from 1.19 to 0.88 for each accumulated 100 growing degree days. Pitted morningglory produced a maximum of 24 million seeds ha−1 in the absence of glyphosate with 217,000 soybean plants ha−1. Pitted morningglory seed production declined with increasing soybean seeding rate in the absence of glyphosate, with a 41% reduction occurring when soybean population increased from 217,000 to 521,000 plants ha−1. Seed production of treated pitted morningglory ranged from 380,000 to 700,000 seeds ha−1. Soybean seed yield was not influenced by pitted morningglory density when treated with glyphosate. Untreated pitted morningglory at 10, 16, and 62 plants m−2 reduced soybean seed yield by 47, 62, and 81%, respectively. Competitiveness of untreated soybean increased with soybean seeding rate, resulting in 22% less yield loss with 521,000 than with 217,000 plants ha−1. Soybean seed yield was not reduced by 10 and 16 glyphosate-treated pitted morningglory plants m−2, but a 9% loss in yield occurred with 62 pitted morningglory plants m−2. Averaged over all pitted morningglory densities, glyphosate-treated pitted morningglory failed to reduce soybean seed yield at each of the three soybean densities. Following a single application of glyphosate, no apparent benefit was noted from increasing the soybean population above 217,000 plants ha−1.

Field experiments were conducted at Fayetteville, AR, in 1997, 1998, and 1999 to evaluate the degree of interspecific interference between drill-seeded, glyphosate-resistant soybean and hemp sesbania as influenced by soybean population, hemp sesbania density, and a single glyphosate application. Soybean was planted at 247,000, 430,000, and 618,000 seed ha−1 with early-season emergence of 217,000, 371,000, and 521,000 plants ha−1. Hemp sesbania densities were 0, 4, 10, and 16 plants m−2 in combination with 0 and 1.12 kg ai ha−1 glyphosate applied at the V4 to V6 soybean growth stage. Untreated hemp sesbania produced a maximum of 49 million seed ha−1 with 217,000 soybean ha−1, whereas seed production of glyphosate-treated hemp sesbania ranged from 2.8 to 0.6 million seed ha−1 with 217,000 and 521,000 soybean ha−1, respectively. Soybean seed yield was reduced 43% by 16 untreated hemp sesbania m−2, while glyphosate-treated hemp sesbania did not reduce seed yield. Averaged over all untreated hemp sesbania densities, soybean yield loss was reduced from 44 to 22% by increasing the soybean population from 217,000 to 521,000 plants ha−1. Because of the absence of soybean yield loss at 521,000 soybean ha−1, this density appears beneficial when using a single application of glyphosate to provide season-long weed control. However, a single glyphosate application in combination with a high soybean density did not completely prevent hemp sesbania seed production, and the seeding rate required to achieve a stand of 521,000 plants ha−1 would not be affordable; thus, alternate management methods targeting hemp sesbania must be employed to prevent an increase in the number of seed in the soil seedbank and to prevent a potential shift in the weed spectrum.

This research investigated the temperature and light requirements for seed germination and emergence patterns of pinnate poppy, violet horned-poppy, and nodding hypecoum, three annual Papaveraceae species found in arable lands in the Mediterranean region. Two experiments performed in growth chambers (1) analyzed light (complete darkness or 12 h light) and temperature (10/5, 15/5, and 20/10 C day/night temperatures) requirements for germination, and (2) determined base temperature (Tb) for germination. An outdoor pot trial was also set up to study emergence patterns. All species showed higher germination in complete darkness than they did with a light regime, irrespective of dormancy level, time of the year, and temperature regime under which germination was tested, illustrating better germination when seeds are buried. Tb ranged from −2.6 to 0 C, depending on the species, indicating low temperature requirements for germination. Given their higher germination in daily fluctuating, rather than constant temperatures, the three Papaveraceae species should have the capacity to form persistent seed banks. These species behaved as winter annuals (from November to February) in the pot experiment and had difficulties to emerge in spring. Given that they cannot avoid autumn–winter chemical treatments, this could partially explain their regression in arable fields. These results bring new information to develop management strategies for these Papaveraceae species in agroecosystems.

Predicting weed emergence dynamics can help farmers to plan more effective weed control. The hydrothermal time concept has been used to model emergence as a function of temperature and water potential. Application of this concept is possible if the specific biological thresholds are known. This article provides a data set of base temperature and water potential of eight maize weeds (velvetleaf, redroot pigweed, common lambsquarters, large crabgrass, barnyardgrass, yellow foxtail, green foxtail, and johnsongrass). For five of these species, two ecotypes from two extreme regions of the predominant maize-growing area in Italy (Veneto and Tuscany), were collected and compared to check possible differences that may arise from using the same thresholds for different populations. Seedling emergence of velvetleaf and johnsongrass were modeled using three different approaches: (1) thermal time calculated assuming 5 C as base temperature for both species; (2) thermal time using the specific estimated base temperatures; and (3) hydrothermal time using the specific, estimated base temperatures and water potentials. All the species had base temperatures greater than 10 C, with the exception of velvetleaf (3.9 to 4.4 C) and common lambsquarters (2.0 to 2.6 C). All species showed a calculated base-water potential equal or up to −1.00 MPa. The thresholds of the two ecotypes were similar for all the studied species, with the exception of redroot pigweed, for which the Veneto ecotype showed a water potential lower than −0.41 MPa, whereas it was −0.62 MPa for the Tuscany ecotype. Similar thresholds have been found to be useful in hydrothermal time models covering two climatic regions where maize is grown in Italy. Furthermore, a comparison between the use of specific, estimated, and common thresholds for modeling weed emergence showed that, for a better determination of weed control timing, it is often necessary to estimate the specific thresholds.