The seed science community currently defines germination as radicle emergence of 2 mm from the dispersal unit. Consequently, most seed researchers abruptly terminate germination experiments after radicle emergence, concluding that the seed has germinated. However, this approach underestimates epicotyl dormancy and often leads to dormancy misclassification, or worse, a failure to identify epicotyl dormancy altogether. To address these limitations, we propose extending germination studies to the point of first leaf emergence; we term this the “full germination” period. Our methodology involves germinating fully matured, freshly collected seeds and depending on the time required for radicle emergence, the seeds are categorized into (1) viviparous, where seeds germinate prematurely while they are still attached to the parent plant or within the fruit; (2) Morphological dormancy (MD) or Non-dormant (ND), where seeds germinate within 30 days; and (3) physiological dormancy (PD) and morphophysiological dormancy (MPD), where germination does not occur within 30 days. The absence of shoot emergence within 30 days following radicle protrusion indicates the presence of epicotyl dormancy. Thus, species initially classified as ND, MD, or viviparous may be miscategorized if shoot emergence is not assessed. Likewise, seeds exhibiting PD or MPD may possess an additional epicotyl dormancy component, possibly leading to placing them in incorrect subclass or level. A comprehensive assessment of shoot development is imperative for accurate dormancy characterization. We strongly recommend monitoring seed germination until first true leaf emergence should be adopted to ensure correct conclusions about dormancy, plant life cycles and ecological adaptations.

Purple nutsedge is a competitive and persistent perennial weed in the agronomic and horticultural cropping systems of the southeastern United States. Its management is a challenge during the growing season due to its ability to propagate vegetatively through underground rhizomes and tubers. Therefore, effective herbicide programs are needed that can check the spread of purple nutsedge and protect crop yields. Greenhouse experiments were conducted in 2024 to evaluate the response of purple nutsedge at two different growth stages (10 to 15 cm and 15 to 20 cm heights) to herbicides currently labeled for use in Mississippi cropping systems. Herbicides tested were glyphosate at 1,260 g ai ha–1, glufosinate at 672 g ai ha–1, bentazon at 1,680 g ai ha–1, halosulfuron at 69.5 g ai ha–1, and trifloxysulfuron at 6.9 g ai ha–1. Glyphosate was the most effective herbicide against purple nutsedge, providing >90% control, followed by halosulfuron, which provided 70% to 90% control at both growth stages. New shoot emergence was highest when glufosinate and bentazon were applied, and no new shoots emerged when glyphosate and halosulfuron were applied. More new shoots were observed when glufosinate and bentazon were applied when plants were 15 to 20 cm high compared to 10 to 15 cm. Shoot regrowth at 21 d after cutting the aboveground shoots indicated similar trends. A reduction of >90% in shoot and root biomass was observed when glyphosate, halosulfuron, and trifloxysulfuron were applied, whereas glufosinate and bentazon applications resulted in 50% less biomass reduction. Overall, herbicide efficacy against purple nutsedge was greater when plants were treated at the recommended height of 10 to 15 cm rather than 15 to 20 cm. The study results indicated that both herbicide mode of action and application timing are important for better purple nutsedge management in cropping systems.

Carolina redroot [Lachnanthes caroliniana (Lam.) Dandy] is a frequent weed of New Jersey cranberry (Vaccinium macrocarpon Aiton) bogs that competes with the crop for nutritional resources. Studies were conducted in 2018 to determine the effects of planting depth, soil moisture, lighting conditions, rhizome water content, and duration of rhizome submersion under water on L. caroliniana shoot emergence, vegetative growth, and rhizome development. Only planting depth greater than 12 cm significantly reduced shoot emergence (54%), biomass shoot and root production (27% and 65%, respectively), and rhizome formation (65%) compared with a 2-cm depth. Complete inhibition of new rhizome production was observed when the rhizome water content dropped to 30%. Soil moisture ≤30% decreased shoot biomass by ≥53% compared to 60% soil moisture, but marginally affected root biomass and had no impact on rhizome formation. Rhizome submersion for at least 120 d had minor effect on shoot emergence but reduced plant biomass by ≥28% and completely inhibited the formation of rhizomes. Finally, shading did not influence emergence but had a more dramatic effect on root and shoot biomass, which were reduced by 53% and 75%, respectively, and prevented the development of new rhizomes. This study demonstrates the plasticity of L. caroliniana to drought stress or long-lasting flooding conditions, therefore preventing consideration of cranberry bed temporary flooding or limitation of irrigation volume and frequency as viable management options. Sanding would not provide a layer of material sufficiently thick for reducing L. caroliniana shoot emergence. Reducing the quantity of light reaching the soil with black tarps or promoting rapid crop canopy closure are options that can complement the use of mesotrione for controlling L. caroliniana. Future research should address the practicality of these options, especially in bogs with low L. caroliniana pressure when early-summer weed regrowth occurs following dissipation of PRE herbicide activity.

Laboratory and greenhouse studies were conducted to determine the effect of temperature, soil moisture, light, planting depth, and rhizome water content on shoot emergence and vegetative growth of alligatorweed. Optimum shoot emergence and growth occurred at constant 30 C, and no shoot emergence was found below constant 5 C. A maximum shoot emergence of 93% occurred at constant soil moisture of 30% with temperatures of 10 to 35 C. Shoot emergence and growth decreased as rhizome water content decreased, and shoot emergence did not occur below a rhizome water content of 20%. Shoot emergence and growth decreased with burial depth; shoot emergence was above 90% when rhizomes were buried 0.5 to 1.0 cm deep compared to 16% when they were buried 18 cm deep. Alligatorweed shoot emergence and vegetative growth were not significantly affected by light. In the fields, shoot emergence began in late March and culminated in May and June. These data help explain why this species is most commonly found in crop fields, orchards, roadsides, rivers, lakes, ponds, and irrigation canals. This information may aid in the development of more effective management measures, such as bringing alligatorweed rhizomes to the surface or below 20 cm deep to restrain its emergence and growth at winter or summer plowing.

Cogongrass is a noxious perennial grass that has invaded many countries in the tropical and subtropical regions of the world. Its management has been a significant challenge because of large rhizome and bud reserves in the soil. The emergence pattern of this weed under field conditions has received little attention. Field trials were conducted in 2002 and 2003 in the humid forest zone of southeastern Nigeria to model shoot emergence. The experiment had four treatments: (1) count and tag crop-free cogongrass shoots, (2) count and suppress crop-free cogongrass shoots with paraquat, (3) count and cut crop-free cogongrass shoots, and (4) count and cut cogongrass shoots in cultivated corn. The rationale for these treatments was to determine the effect of different monitoring techniques on shoot emergence of cogongrass. The development of the model was based on hydrothermal time, which was calculated from soil moisture and soil temperature at a 2-cm depth. A Weibull function was fitted to cumulative percent shoot emergence values of Treatment 4 and hydrothermal time. The model closely fit the observed pattern of cogongrass shoot emergence (r 2 = 0.95, n = 36). It also predicted shoot emergence satisfactorily in six treatments (r 2 > 0.85, P < 0.001, n = 7 in each treatment) that simulated farmers' practices in southwestern Nigeria. This is the first model developed for cogongrass shoot emergence based on hydrothermal time under field observations. The model should facilitate further analyses of cogongrass emergence patterns and the timing of its management.

Although it has been speculated that seeds of the gymnosperm family Podocarpaceae have an underdeveloped embryo, no detailed studies have been done to definitively answer this question. Our purpose was to determine if embryos in seeds of two species of Podocarpaceae, Podocarpus costalis and Nageia nagi, from Taiwan are underdeveloped and to examine the kind of dormancy the seeds have. Embryos in fresh seeds of P. costalis were 4.6 ± 0.5 mm long, and they increased in length by about 54% before radicle emergence (germination), demonstrating that the embryo is underdeveloped at seed maturity. Seeds germinated to >90% at 30/20, 25/15 and 25°C in light in ≤ 4 weeks, without any cold stratification pretreatment. Thus, seeds of P. costalis have morphological dormancy (MD). Embryos in fresh seeds of N. nagi were 7.4 ± 0.8 mm long and they increased in length by about 39% before radicle emergence (germination) occurred, indicating that the embryo is underdeveloped at seed maturity. Seeds germinated to < 25% at 30/20 and 25°C in light in 4 weeks but to >90% at the same temperatures in 12 weeks. Thus, most seeds of N. nagi have morphophysiological dormancy (MPD). Although underdeveloped embryos are considered to be a primitive condition in seed plants, they also occur in the most advanced orders. The occurrence of underdeveloped embryos in Podocarpaceae documents that they are not restricted to a basal clade in gymnosperms.