Weeds compete with crops for soil moisture, along with other resources, which can impact the germination, growth, and seed production of weeds; however, this impact has not been systematically recorded and synthesized across diverse studies. To address this knowledge gap, a global meta-analysis was conducted using 1,196 paired observations from 86 published articles assessing the effect of water stress on weed germination, growth characteristics, and seed production. These studies were conducted and published during 1970 through 2020 across four continents (Asia, Australia, Europe, and North America). Imposed water stress was expressed as solution osmotic potential (ψsolution), soil water potential (ψsoil), or soil moisture as percent field capacity. Meta-analysis revealed that water stress inhibits weed germination, growth, and seed production, and the quantitative response intensified with increasing water stress. A ψsolution greater than −0.8 MPa completely inhibits germination of both grass and broadleaf weeds. A ψsolution from −0.09 to −0.32 MPa reduces weed germination by 50% compared with the unstressed condition. Moderate soil water stress, equivalent to 30% to 60% field capacity, inhibits growth characteristics (branches or tillers per plant, leaf area, leaves per plant, plant height, root, and shoot biomass) by 33% and weed seed production by 50%. Severe soil water stress, below 30% field capacity, inhibits weed growth by 51% and seed production by 88%. Although water stress inhibits weed growth, it does not entirely suppress the ability to germinate, grow, and produce seeds, resulting in weed seedbank accumulation. This creates management challenges for producers, because weed seeds can survive in the soil for many years, depending on weed species and environmental conditions. Quantitative information compiled in this meta-analysis can be instrumental to model the weeds’ multidimensional responses to water stress and designing integrated weed management strategies for reducing the weed seedbank.

Much of the agricultural area in California’s southwestern San Joaquin Valley (SJV) is prone to moisture stress and high soil-salinity conditions. Increased prevalence of glyphosate-resistant (GR) biotypes of junglerice [Echinochloa colona (L.) Link] in these environments and their ecological implications need to be further explored. Studies were conducted on GR and glyphosate-susceptible (GS) biotypes of E. colona to compare the effects of moisture and salinity stress on seed germination and salinity stress alone on growth and seed production. Intraspecific competition between the GR and GS plants was also assessed in a replacement series design experiment. With respect to germination, both biotypes were tolerant to moisture and salinity stress at germination; however, the GR biotype was more tolerant than the GS biotype. Water potential and electrical conductivity (EC) levels that reduced germination by 50% were estimated as −1.5 and −2.3 MPa and 8.5 and 12 dS m−1 for the GS and GR biotypes, respectively. The EC levels that reduced aboveground biomass by 50% were estimated as 9 and 11.5 dS m−1 for the GS and GR biotypes, respectively. Seed production was generally greater in the GR than the GS plants below 10 dS m−1. All plants produced up to 140 seeds plant−1, even at 20 dS m−1. The GR plants were more competitive and produced more aboveground dry biomass and seeds than the GS plants when grown together or alone. In conclusion, differences between these particular GR and GS biotypes to environmental stresses and intraspecific competition were noted that could have ecological implications for their prevalence in the southwestern SJV. The results also suggested that there could be high genetic variability and phenotypic plasticity in E. colona populations in the SJV and further population shifts could occur due to selection pressure from glyphosate.

Optimum germination of Canada thistle [Cirsium arvense (L.) Scop.] occurred at alternating temperatures of 20 to 30 C and 30 to 40 C and at a constant temperature of 30 C. Osmotic pressures of 7 bars and greater reduced germination, but 2% of the seeds germinated at 15 bars. Canada thistle seeds (14%) were able to germinate in NaCl concentrations of 20,000 ppmw. Light was important in seed germination, however, its effect could be overcome by adding GA3 (gibberellic acid) to the germination medium. Optimum pH for germination was between 5.8 and 7.0. Depth of planting influenced emergence; the highest percentage of seedlings emerged from depths of 0.5 to 1.5 cm. Canada thistle seedlings tolerated average soil moisture tensions of 1.3 bars and continued to grow. Canada thistle seedlings 19 days old and with two true leaves were able to resprout after top-growth removal. Regrowth was evident on 8% of the clipped plants 4 days after initial top-growth removal.

Studies were undertaken to determine effects of scarification, temperature, stratification, pH, and osmotic potential on seed germination; to determine the effect of planting depth on emergence; to describe the emergence sequence; and to quantify seedling development of bigroot morningglory. Mechanical and chemical scarification caused increased germination but cool, moist stratification did not break dormancy. Optimum germination occurred at 20 and 25 C and with alternating temperatures of 20/10 and 30/20 C. The optimum pH range for germination was between 6 and 8.5. Increasing the solution osmotic potential decreased germination linearly from 90% at −0.08 MPa to 0% at −0.8 MPa. Plant establishment was best at 2 to 4 cm and decreased at greater seeding depths. Seedling emergence was observed and recorded and found not to fit the classical models of hypogeal or epigeal emergence. Only 3% of 5-day-old seedlings sprouted after being clipped to the root crown. When seedlings were 11 days old at clipping, over 85% of the plants sprouted. These results indicate that bigroot morningglory has the potential to successfully reproduce by seed and that the rapid development of the plant should be considered when designing control programs.

Mayweed (Anthemis cotula L. # ANTCO) achenes and seed were germinated in the laboratory at constant temperatures ranging from 5 to 30 C. Maximum percent germination occurred at 20 C for both achenes and seed. Under all conditions tested, achene germination was less than seed germination. Both acid scarification for 15 min and soaking in 14 mM gibberellic acid (GA3) more than doubled achene germination. Pericarp leachate inhibited achene and seed germination only at high concentrations, indicating that inhibitors in the pericarp are not a primary cause of low germination in achenes. Optimum germination of achenes and seed occurred at pH 4.5 and over a range from pH 3 to pH 6. Achene germination was inhibited to a greater degree by moisture stress than was seed germination. It appears that structural integrity of the pericarp is the predominant factor affecting mayweed germination.

The ability of honeyvine milkweed [Ampelamus albidus (Nutt.) Britt.] to establish and develop from seed was studied in laboratory and field experiments. Optimum germination temperature was 30 C. Seed incubated at cooler temperatures and then transferred to 30 C germinated equally as well as seed incubated continually at 30 C. Germination was unaffected at moisture stress levels between 0 and −4.6 bars, but was decreased at levels between −4.6 and −12.8 bars. The optimum pH range for germination was between 5 and 7. The greatest emergence of seedlings occurred at a depth of 0.5 cm with no emergence occurring at depths greater than 5 cm. Greater emergence was obtained with a loam than sandy loam at all planting depths except 0.5 cm. Field plots seeded on May 1 gave maximum seed production. Seed production decreased with each 2-week delay in planting. Planting dates of July 10 or later produced no seed. Seed germination was affected little by delayed planting. The following spring, regrowth from plants seeded on June 12 or later was less vigorous than regrowth from plants seeded earlier.

Sorghum-almum (Sorghum almum Parod. # SORAL) is a weakly perennial, rhizomatous grass that in northern climates reproduces mainly by seeds. Environmental factors influencing seed germination and the longevity of buried seeds were studied in growth chamber and field experiments. Alternating temperatures of 20 C for 16 h and 30 C for 8 h were optimum for germination. Light was not critical to germination. Germination varied only slightly across a pH range from 5.0 to 8.8 but decreased sharply below pH 5. Osmotic potentials greater than −0.9 MPa reduced germination substantially, and no germination occurred at −1.5 MPa. Limited germination occurred at NaCl concentrations of 340 mM, and no germination occurred at 510 mM. Seeds that were either mechanically scarified or afterripened for 6 months had a higher percent germination and germination rate than untreated seeds. Sorghum-almum seedling emergence was 11% from seeding depths of 20 cm, but emergence was 67% or higher from seeding depths of 15 cm or less. In field studies, viability of seeds placed on the soil surface or buried 3 or 8 cm was 2% or less at 12 months and 0% at 18 months after burial. Viability of seeds buried 15 and 23 cm was 0.3 and 26%, respectively, at 24 months after burial. Thus, tillage that buried sorghum-almum seeds 20 cm or more could reduce emergence but would also prolong seed persistence. Shallow tillage should favor depletion of sorghum-almum seed reserves.

Net (apparent) photosynthesis rate (Pn) of jointed goatgrass (Aegilops cylindrica Host # AEGCY) leaves in the greenhouse became light saturated at a photosynthetic photon flux density (PPFD) of about 1000 μE·m–1-2·s–1 with a maximum Pn of 27 mg CO2 ·dm–2 ·h–1. Diffusive resistance to water vapor (rl) of adaxial leaf surfaces was 43% that of abaxial surfaces, in part, because stomatal density was 50% greater on adaxial leaf surfaces than on abaxial surfaces. Dark respiration rate (Rd) was 1.6 mg CO2 ·dm−2·h−1. Light compensation point (CPl) was 21 μE·m−2·s−1 and CO2 compensation point (CPc) was 32 ppmv. In the field, where light intensity and temperature were greater than in the greenhouse, leaves became light saturated for Pn at a higher intensity, and Rd and CPl were three times greater than in the greenhouse. Pn and Rd of spikes at anthesis were at least 30% less and 200% greater, respectively, than the values for leaves.

Experiments were conducted to examine the influence of adjuvant, growth stage, air temperature, and soil moisture on nicosulfuron activity, absorption, and distribution in quackgrass. Foliar absorption of 14C-nicosulfuron by quackgrass was greater in one-leaf than five-leaf plants. Total translocation of 14C-nicosulfuron was similar regardless of growth stage. However, nicosulfuron was more phytotoxic to three- and five-leaf than one-leaf quackgrass. Of the absorbed 14C, at least 71 % remained as 14C-nicosulfuron 168 h after application in three-leaf plants. 14C-Nicosulfuron absorption, translocation, and accumulation increased with increasing temperatures and was independent of soil moisture. Under adequate soil moisture conditions (-0.03 MPa), nicosulfuron activity was not influenced by temperature. Nicosulfuron efficacy was not influenced by soil moisture at a cool (11/6 C) temperature. As plant moisture stress increased, due to low soil moisture and increasing air temperature, nicosulfuron efficacy declined. Differences in nicosulfuron efficacy due to growth stage or environmental conditions could not be explained by differential 14C recovery, absorption, translocation, or accumulation. The addition of 28% urea-ammonium nitrate liquid fertilizer (UAN) to 14C-nico-sulfuron plus petroleum oil adjuvant (POA) provided greater 14C absorption than POA alone. Translocation of 14C with POA alone 168 h after treatment (HAT) was similar to POA plus UAN 24 HAT. However, 168 HAT there was no difference in the total amount of radiolabelled material translocated among the adjuvants.

Experiments were conducted in Massachusetts and New York to evaluate the potential influence of plant growth stage, spray volume, nozzle type, additional surfactant, and herbicide formulation on smooth and large crabgrass control in turf with fenoxaprop. At a well-watered site, crabgrass control with fenoxaprop was equal to or greater than with MSMA. On an irrigated, fertilized site, crabgrass growth stage did not influence fenoxaprop efficacy. Excellent control of up to 5-tiller smooth crabgrass was obtained with 0.20 kg/ha of fenoxaprop. On nonirrigated turf, fenoxaprop was less effective on tillered crabgrass than on 2- to 5-leaf weeds. Under very dry conditions, fenoxaprop was ineffective regardless of growth stage. Control with MSMA was less affected by drought than was fenoxaprop. Spray volumes, between 140 and 1120 L/ha, did not affect fenoxaprop efficacy; however, high volume applications (1120 L/ha) with floodjet nozzles were less effective than flat fan nozzle treatments in two of three tests. Added surfactant did not improve efficacy except with floodjet nozzles on a droughty site. No differences were observed between the water-based and the emulsifiable concentrate formulations of fenoxaprop. Fenoxaprop caused temporary phytotoxicity (≤20% reduction in turf quality) to established Kentucky bluegrass and perennial ryegrass.

Green foxtail [Setaria viridis (L.) Beauv. # SETVI] and proso millet [Panicum miliaceum (L.) #PANMI] growing under high water stress for 3 days before + 3 days after foliar applications of the methyl ester of haloxyfop {2-[4-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl] oxy] phenoxy] propanoic acid} developed less herbicide injury than plants growing under low water stress. There was a 32% reduction in the retention of haloxyfop sprays by proso millet when growing under high water stress than when growing under low water stress. Haloxyfop spray retention by green foxtail was not affected by the degree of water stress. The translocation of 14C out of 14C-haloxyfop-treated leaves was significantly greater in plants of both species when growing under low water stress than when growing under high water stress. The conversion of 98% of the absorbed 14C-haloxyfop-methyl to 14C-haloxyfop and unidentified polar metabolites occurred in both species within 12 h of application. The green foxtail growing under low water stress contained greater concentrations of 14C-haloxyfop than did plants growing under high water stress. Levels of 14C-haloxyfop were the same in proso millet growing under high and low water stress. The reduced injury of green foxtail and proso millet growing under high water stress from postemergence sprays of haloxyfop can be attributed to a reduction in herbicide translocation in both species, plus a reduction in spray retention by proso millet or changes in the metabolism of the herbicide in green foxtail, which results in a reduction in the concentration of haloxyfop.

Optimum temperature for germination and emergence of redvine seed in either petri dishes or soil was 35 C. Reductions in germination and emergence occurred at constant temperatures above or below this temperature. No germination or emergence occurred at temperatures above 40 or below 25 C. Germination in petri dishes first occurred on day 8, and emergence was first observed 12 days after planting in a soil medium. Maximum redvine seedling emergence of 74% occurred in soil when seed were planted 0.5 cm deep, with decreases in emergence noted at depths below 5 cm. No emergence occurred over the 35-day period evalμated when redvine seed were planted on the soil surface or at a depth of 10 cm in soil. Redvine germination was not affected by solution pH, whereas germination did not occur when osmotic stress of as little as −200 kPa was applied to seed.

The selectivity of five foliage-applied herbicides, 2,4-D [(2,4-dichlorophenoxy)acetic acid], dichlorprop [2-(2,4-dichlorophenoxy)propionic acid], glyphosate [N-(phosphonomethyl)glycine], fosamine [ethyl hydrogen (aminocarbonyl)phosphonate], and triclopyr {[(3,5,6-trichloro-2-pyridinyl)oxy] acetic acid}, applied at three phenological stages of development to five Sierran shrub species, deerbrush [Ceanothus integerrimus var. californicus (Kell.) G. T. Benson.], greenleaf manzanita (Arctostaphylos patula Greene), bearmat (Chamaebatia foliolosa Benth.), snowbrush ceanothus (Ceanothus velutinus Dougl.), and whiteleaf manzanita (Arctostaphylos viscida Parry), was compared. Treatments in the summer and fall were less effective than spring applications. Periods of herbicide susceptibility generally corresponded to times when moisture stress was low and photosynthesis was high.

Apocynum cannabinum is a native creeping perennial distributed throughout the U.S., with increasing importance in reduced tillage systems throughout the Midwest. Apocynum cannabinum has been shown to be a difficult species to control in field crops. Effective weed management is often a function of the timing of control practice. Knowledge of weed emergence patterns may be useful in predicting the optimum time of weed management. The objectives of these studies were to describe how temperature and moisture affect A. cannabinum seed germination and to describe the relationship between growing degree units (GDU) and A. cannabinum vegetative shoot emergence. At constant temperatures, seed germination was described as a sigmoidal function of temperature (r 2 = 0.83), with maximum germination (32%) from 26 to 34 C. Under alternating temperatures, seed germination increased in a linear relationship between mean temperatures of 15 and 34 C (r 2 = 0.85). Maximum seed germination (88%) occurred at a mean temperature of 34 C under alternating temperatures. The relationship between seed germination and osmotic potential between −1.0 and 0 MPa was described by a gompertz function (r 2 = 0.98). Germination at −1.0 MPa was 4% and increased in a near linear manner to the nontreated control (0 MPa), which had 80% germination. Vegetative shoot emergence in 1997 and 1998 had a sigmoidal relationship to GDU using a base temperature of 6 C (r 2 = 0.96). However, initial shoot appearance was not consistent over years, with first emergence recorded on May 21, 1997 (132 GDU), and May 5, 1998 (73 GDU). Approximately 50% of the shoots emerged before June 7, 1997 (282 GDU), and May 21, 1998 (285 GDU); therefore, optimal weed management programs will need to be initiated following this GDU accumulation.

Shoot and root growth of green foxtail [Setaria viridis (L.) Beauv. # SETVI] and yellow foxtail [Setaria lutescens (L.) Beauv. # SETLU] were compared under three moisture regimes under simulated field conditions in 1982 and 1983. An increase in water supply from 0.3 to 2.5 cm/week resulted in proportionately greater increases in the number of tillers and leaf area of green foxtail compared to yellow foxtail. In 1982, green foxtail produced approximately three times as many seed as yellow foxtail under all three water regimes, whereas under warmer conditions in 1983, green foxtail produced nearly six times as many seed as yellow foxtail under the highest water regime and more than 11 times under the lowest regime. By using a specially constructed periscope to observe root growth through clear plastic tubes implanted in the soil it was determined that the amount of available moisture had much less effect on root growth than on shoot growth of the two species. In 1982, green foxtail tended to produce more roots than yellow foxtail early in the season but as the plants matured no significant differences occurred between species. In 1983, no significant differences in total root length occurred between species at any growth stage. The roots of both species penetrated to a depth of nearly 60 cm, with the highest concentration of roots occurring at depths of 20 to 30 cm.

Optimum germination of fringed sagebrush (Artemisia frigida Willd.) occurred at alternating temperatures of 10 to 20 C. Seeds were able to germinate (15%) in NaCl concentrations of 5000 ppmw. Light was important in seed germination; however, its absence could be overcome by adding 30 ppmw GA3 (gibberellic acid) to the germination medium. Optimum pH for germination was between 5.8 and 7.0. Depth of planting influenced seedling emergence; the greatest emergence occurred when seeds were planted on the soil surface; emergence was lower when seeds were buried at any depth in the soil. Osmotic potentials of −13 bars and greater reduced germination, but 6% of the seeds germinated at −15 bars. Fringed sagebrush seedlings tolerated average plant water potentials of −10 to −19 bars and died when water potentials were decreased to −22 bars. Mature fringed sagebrush plants were capable of producing from 16500 to 190000 seeds/plant.

Maximum germination of flodman thistle [Cirsium flodmanii (Rydb.) Arthur ♯3 CIRFL] occurred at alternating temperatures of 10 to 20 and 20 to 30 C. Seeds germinated (20%) in 1.7 M NaCl. Light was important in seed germination; however, its absence could be overcome by adding 8.6 × 10-5 M GA3 (gibberellic acid) to the germination medium. The greatest seedling emergence occurred when seeds were planted on the soil surface and was lower when seeds were buried at any depth in the soil. Osmotic potentials at −0.5 MPa and greater reduced germination, but 3% of the seeds germinated at −1.3 MPa. Flodman thistle seedlings tolerated average plant water potentials of −0.9 and −1.1 MPa, but they died when the water potential was decreased to −1.5 MPa. Flodman thistle seedlings 43 days old and with four true leaves resprouted after topgrowth removal. Regrowth was evident on 75% of the clipped plants 13 days after initial topgrowth removal. Flodman thistle rosettes spread more rapidly and rosette survival was enhanced more in a weed-free nursery than in a weedy pasture.

Low soil water content for 10 to 14 days before and 7 days after herbicide application reduced control of green foxtail with fenoxaprop, fluazifop-P, haloxyfop, and sethoxydim. Withholding irrigation for 10 to 14 days before herbicide application did not reduce control of green foxtail with normal use rates of herbicides if plots were irrigated at the time of application. Low soil water content reduced the activity of sethoxydim less than the other herbicides.

Laboratory and greenhouse experiments were conducted to determine the effect of light, temperature, solution pH, solution osmotic potential, and oxygen concentration on pitted morningglory germination and radicle plus hypocotyl elongation, and seeding depth on its subsequent emergence. Daily exposure of seed to natural light resulted in lower germination than in darkness, whereas germination was not influenced by brief exposure to red or far-red light. Germination occurred over a wide range of constant temperatures, from 7.5 to 52.5 C, with optimum germination between 20 and 25 C. Germination occurred at solution pH range of 3 to 10 and was optimal from pH 6 to 8. Radicle plus hypocotyl elongation was influenced by the interaction of temperature and solution pH. A combination of acidic medium (pH 6) and high temperature (30 C) resulted in the greatest radicle plus hypocotyl length of 7.6 cm after a 7-d incubation. Germination and radicle plus hypocotyl elongation, averaged over the 15 and 30 C temperature, decreased with increasing moisture stress, with less than 3% normalized germination at −1.0 MPa. Germination was 29, 40, and 51% at 2, 10, and 20% oxygen, respectively, averaged over 15 and 30 C. Germination of seed lying on the soil surface covered with filter paper or without any cover was similar, averaging 64%. Normalized emergence, relative to germination on the soil surface, decreased with increasing burial depth to 4% emergence at 10 cm, with a mean emergence depth of 4.1 cm, averaged across two soil types.

Laboratory and greenhouse studies were conducted to determine the effect of temperature, solution pH, water stress, and planting depth on cutleaf eveningprimrose germination and emergence. Field studies were conducted to measure growth parameters of cutleaf eveningprimrose throughout the fall season. When treated with constant temperature, cutleaf eveningprimrose germinated over a range of 15 to 32 C, with the optimum germination occurring at 24 C. Onset, rate, and total germination were greatest in an alternating 20/35 C temperature regime. Germination decreased as solution pH increased, with greatest germination occurring at solution pH of 4. Germination decreased when cutleaf eveningprimrose seed was subjected to increased water stress. Emergence was optimum when seed were buried at depths of 0.5 cm. Germination decreased with increasing burial depth, and no seed emerged from a depth of 10 cm. Cutleaf eveningprimrose control was maximized when 2,4-D was applied in mixture with glyphosate or paraquat. These data suggest that cutleaf eveningprimrose can germinate and gain biomass from early March to late October. These attributes could contribute to poor control before cotton planting if preplant control applications are delayed after early March.