Understanding the quality of seed dispersal effectiveness of frugivorous species can elucidate how endozoochory structures tropical forests. Large seeds, containing more resources for growth, and gut passage by frugivores, which remove seed pulp, both typically enhance the speed and probability of germination of tropical seeds. However, the interaction of seed size and gut passage has not been well studied. We assessed the role of two species of toucans (Ramphastos spp.) in seed germination of the tropical tree Eugenia uniflora, which produces seeds that vary considerably in size (3.7–14.3 mm), using 151 control and 137 regurgitated seeds in germination trials. We found that toucan regurgitation did not increase germination success, although 93.4% germinated compared to 76.8% of control seeds; however, larger seeds germinated more often at faster rates. Although only marginally significant, germination rates were 3.6× faster when seeds were both large and regurgitated by toucans, demonstrating that toucan regurgitation can disproportionally benefit larger E. uniflora seeds. As tropical forests are increasingly disturbed and fragmented by human activities, the ability of toucans to continue providing seed dispersal services to degraded habitats may be vital to the persistence of many tropical plants that contain larger seeds and depend on larger dispersers.

Leucaena [Leucaena leucocephala (Lam.) de Wit] is a perennial weed in more than 25 countries, including Australia. Knowledge regarding the seed biology of L. leucocephala could help in making weed management decisions. Experiments were conducted to study the effect of hot water (scarification), alternating temperatures, heat stress, salt stress, water stress, and burial depth on seed germination of two populations of L. leucocephala collected from Toowoomba and Gatton, Australia. The optimum duration of hot water treatment to break the hard seed coat dormancy was 2 min for both populations. The highest germination (92% to 98%) was recorded at 35/25 C for both populations, and similar germination occurred at 30/20 C. The Toowoomba population recorded greater germination at low temperature (15/5 to 25/15 C) than the Gatton population. Additionally, the Gatton population had higher germination than the Toowoomba population after 5 min of exposure to temperatures of up to 100 C, suggesting that the Gatton population may be more tolerant to heat stress. Germination was completely inhibited at pretreatment (5 min) temperatures of 150 to 250 C. The Toowoomba population recorded 17% greater germination than the Gatton population at a high salt concentration (160 mM NaCl), indicating its greater salt tolerance. At low moisture stress (−0.1 and −0.2 MPa), higher germination was observed in the Toowoomba population than in the Gatton population, whereas germination was similar for both populations at higher water stress levels (−0.4 MPa or lower). Germination was similar for both populations at shallow depths (0 and 1 cm) but higher emergence was recorded for the Toowoomba population at 2 to 8 cm than the Gatton population. Differential germination behaviors of both populations suggest that they adapted differently in their respective local environments. Knowledge gained from this study will help in formulating integrated management practices for L. leucocephala.

Sweet acacia [Vachellia farnesiana (L.) Willd.] is a problematic thorny weed species in several parts of Australia. Knowledge of its seed biology could help to formulate weed management decisions for this and similar species. Experiments were conducted to determine the effect of hot water (scarification), alternating temperatures, light, salt stress, and water stress on seed germination of two populations of V. farnesiana and to evaluate the response of its young seedlings (the most sensitive developmental stage) to commonly available postemergence herbicides in Australia. Both populations responded similarly to all the environmental factors and herbicides; therefore, data were pooled over the populations. Seeds immersed in hot water at 90 C for 10 min provided the highest germination (88%), demonstrating physical dormancy in this species. Seeds germinated at a wide range of alternating day/night temperatures from 20/10 C (35%) to 35/25 C (90%), but no seeds germinated at 15/5 C. Germination was not affected by light, suggesting that seeds are nonphotoblastic and can germinate under a plant canopy or when buried in soil. Germination was not affected by sodium chloride (NaCl) concentrations up to 20 mM, and about 50% of seeds could germinate at 160 mM NaCl, suggesting high salt tolerance ability. Germination was only 13% at −0.2 MPa osmotic potential, and no seeds germinated at −0.4 MPa, suggesting that V. farnesiana seeds may remain ungerminated until moisture conditions have become conducive for germination. A number of postemergence herbicides, including 2,4-D + picloram, glufosinate, paraquat, and saflufenacil, provided >85% control of biomass of young seedlings compared with the non-treated control treatment. Knowledge gained from this study will help to predict the potential spread of V. farnesiana in other areas and help to integrate herbicide use with other management strategies.

The distribution of sicklepod (Cassia obtusifolia L.) and coffee senna (Cassia occidentalis L.) in the United States is similar and both species are increasing as problems within their range. Sicklepod is a problem in 11 southern states and increasing in 12 while coffee senna is a problem in 7 states and increasing in 8 states. Both species germinated over a wide range of temperature. Germination characteristics were similar in the range of 15 to 36 C. Germination of coffee senna was drastically reduced at 39 C by Rhizopus sp. Seedling growth was similar for both species and was maximum from 30 to 36 C. Both species have a hard seedcoat. Abrasion for 5, 10, or 15 s, puncturing with a needle, and sulfuric acid were all effective in initiating germination. Both species emerged from a soil depth of 12.5 cm; however, emergence of sicklepod was more rapid than coffee senna with 63% of the sicklepod seedlings emerging from 2.5 cm after only 3 days.

Hemp sesbania [Sesbania exaltata (Raf.) Cory] was more tolerant to induced moisture stress than soybean [Glycine max (L.) Merr.] with osmotic potentials of −4 and −2 bars, respectively, required to reduce germination. Hemp sesbania germinated at temperatures of 15 to 40 C with optimum germination occurring at 30 to 40 40 C. Seed dormancy was caused by impermeable seed coats. Acid scarification of 45 and 60 min and mechanical scarification 20 and 30 s gave maximum germination. Scarification increased water absorption. Light had no effect on germination. As oxygen content increased from 0 to 21%, germination of unscarified seed increased from 5 to 39%, but germination did not increase as oxygen increased from 21 to 100%. Hemp sesbania and soybean emerged from depths up to 12 cm with maximum emergence occurring at the 1- and 3-cm depths. Hemp sesbania emerged faster and in greater numbers at all depths than soybean.

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.

Seed of three weed species collected from the grain bins of combines while standing hard red winter wheat was harvested germinated better than hand-harvested seed. Combine-harvested curly dock seed germinated from 4 to 24% more than hand-harvested seed. Curly dock seed harvested with a commercial-type combine germinated better than those harvested with a small-plot combine. Harvesting slimleaf lambsquarters and Venice mallow seed with a commercial-type combine also enhanced germination compared to hand-harvested seed.

Observations in a citrus grove indicated that hairy beggarticks numbers were higher in plots receiving thiazopyr alone or thiazopyr with oxyfluorfen than in nontreated plots. At 120 days after treatment (DAT), approximately 90% more hairy beggarticks plants had emerged in plots receiving thiazopyr at 0.56 kg ai/ha than in nontreated plots. A tank mix of thiazopyr plus oxyfluorfen, each at 0.56 kg/ha, resulted in a 55% increase in hairy beggarticks number at 120 DAT. Greenhouse studies using seeds collected from sites with or without herbicide history produced similar results. Oxyfluorfen at 0.28 kg/ha stimulated seed germination but injured seedlings by 47% or more at 36 DAT when applied at higher rates. Thiazopyr applied at 0.56 kg/ha antagonized the preemergence activity of oxyfluorfen at 0.28 or 0.56 kg/ha. Thiazopyr at 1.12 kg/ha stimulated hairy beggarticks germination by 37% compared with nontreated containers.

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.

Concentrated sulfuric acid (H2SO4) scarification of balloonvine (Cardiospermum halicacabum L.) for 3 h reduced balloonvine seed coat thickness by 25%, and resulted in increased water absorption and maximum germination. Germination of balloonvine occurred at temperatures of 15 to 40 C with optimum germination occurring at 35 C. Intact balloonvine seed was more sensitive to simulated moisture stress than soybean [Glycine max (L.) Merr. ‘Bragg’]. No balloonvine germination occurred at osmotic potentials of −2 bars and less with intact seeds. Balloonvine seed with seed coats removed germinated at osmotic potentials of −8 bars. Maximum emergence of balloonvine occurred at the 1- and 3-cm depths with limited emergence at a depth of 12 cm.

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.

Laboratory and greenhouse studies were conducted to determine the effect of several environmental factors on seed germination and seedling emergence of the invasive weed Pueraria lobata (kudzu). Germination occurred over a range of alternating temperatures from 15/6 to 35/25 C. Seed germinated equally well in alternating light/darkness and continuous darkness. At all temperature regimes, percentage germination was much greater for hand-scarified seed (95 to 100%) than for nonscarified seed (7 to 17%), indicating that P. lobata seed possesses physical dormancy. Germination exceeded 51% in solutions with pH 5 to 9. Maximum germination (99%) was observed in distilled water at pH 5.4. Germination was greatly reduced in solutions with osmotic potentials below −0.4 MPa (28% at −0.6 MPa, and 13% at −0.9 MPa); no germination was observed at −1.3 MPa. Percentage emergence was greater than 45% at burial depths in soil of 0.5 to 10 cm, with maximal emergence (72 to 85%) at depths of 0.5 to 4 cm. Seed sown on the soil surface had low seedling emergence (< 13%). No seedlings emerged when seed was exposed to flooding for 7 d or more. Pueraria lobata seed is capable of germinating in a variety of climatic and edaphic conditions, but flooding may severely limit establishment of stands by seed.

Sicklepod (Cassia obtusifolia L. ♯3 CASOB) seed were obtained from 10 locations in nine southern states, and plants were grown in a nursery for 3 yr. In field experiments, plant height, seed per pod, number of seed per plant, and number of pods per plant varied among seed sources and years. The vegetative growth phase, as measured from emergence to the initiation of the first floral buds, was approximately 30 days shorter for plants grown from the Tennessee source than for those grown from seed collected in Alachua, FL, in all 3 yr. Hand-harvested seed from plants grown from the 10 seed sources that were planted in 1982 were planted beside the original source sicklepod seed in 1983, and both flowered at approximately the same time, indicating self-fertilization. Percent germination of hand-harvested sicklepod seed from the 10 sources ranged from 2 to 11% for 1981 and 3 to 23% for 1982.

Showy crotalaria (Crotalaria spectabilis Roth) seed dormancy was due to seed coat impermeability to water. The seed coats became impermeable during later stages of maturation on the plant. When incubated immediately after harvest, 9% of the mature, black seeds (11% water content) imbibed water and germinated. The remaining 91% had impermeable coats and did not germinate. After dry storage for 3 months at 23 C, 24% of the seeds imbibed water and germinated. Seeds of another seed lot, which contained seeds of different maturity stages, attained 47% imbibition and germination after storage for 1 yr. The dry, less mature green seeds had a higher percentage (51%) of permeable seeds than did the black seeds (31%) from the same lot. Several seed coat treatments induced imbibition of water and germination of previously impermeable seeds. Effective treatments included piercing of seed coats, scarification with sandpaper, soaking in 70 C water, and simply applying pressure on the strophiole area. Covering the pressed strophiole with petroleum jelly significantly blocked imbibition and indicated that water entered the seeds at only the pressed area. However, studies indicated natural loss of impermeability in showy crotalaria seeds may occur at other sites as well.

Treatments that enhanced the germination of dormant seed of dwarf spikerush [Eleocharis coloradoensis (Britt.) Gilly] the most were chilling seed at 2 C for 3 months and then scarifying with sodium hypochlorite, scarifying seed and then chilling wet seed at 7 C for 3 months, or chilling wet seed at 2 C for 24 months. Percentage of germination for these treatments were 58, 56, and 65%, respectively. Scarifying seed with sodium hypochlorite after they had been chilled wet for 12 to 24 months at 2 C reduced germination. Other treatments that significantly enhanced germination were chilling seed wet for 4 months at 2 C, scarifying dry-stored seed with a 5.25% solution of sodium hypochlorite for 10 h, and soaking seed in concentrated hydrochloric acid for 24 min. These latter treatments resulted in germination percentages of 35, 33, and 35, respectively. Eighty percent of the viable seed usually germinated within 10 days, and when germination was poor, seed lacked embryos or were empty. Dormancy appeared to be due to an impermeable seed coat and not to a germination inhibitor.

To understand the role of the seed coat in regulation of houndstongue seed dormancy, the effects of manipulation of seed coat integrity on seed germination and O2 uptake were studied. The results suggest that the seed coat of this weed regulates dormancy in part by interfering with the diffusion of O2 to the embryo. Scanning electron microscopy showed a network of ridges on the seed coat surface that were partially dissolved following 1.5 min of sulphuric acid scarification. Mechanical scarification removed fragments of the seed coat surface. Both scarification treatments stimulated seed germination. Supply of an elevated level of O2 also stimulated seed germination. O2 uptake by seeds imbibed in O2-saturated water was 150% higher than that for seeds imbibed in air-saturated water. Although all treatments that stimulated seed germination also stimulated O2 uptake, there was a lack of a consistent, quantitative relationship between increases in O2 uptake and seed germination in various experiments. This suggests that limitation of O2 availability to the embryo is not the only factor involved in regulation of houndstongue seed dormancy by the seed coat. Mechanical restriction of embryo expansion by the seed coat may also be important. Methanol-insoluble phenolics constituted < 1% of the total phenolic pool in the embryo. Their potential oxidation could not account for more than a small fraction of the previously reported massive stimulation of O2 uptake by the embryo upon decoating. The present O2 uptake and seed germination studies indicate that not all of the large increase in O2 uptake following decoating is essential for houndstongue seed germination.

The optimum pH for germination of smallflower morningglory (Jacquemontia tamnifolia (L.) Griseb. # IAQTA] seed was 8.0. A scarification time of 25 to 60 s using a drum scarifier with medium grit provided the best germination, and the optimum temperature for germination was 35 to 40C. However, the optimum temperature for growth was 25 to 35C, with reductions in growth occurring above or below this range. Emergence after 14 days was 81 and 49% at planting depths of 1.5 and 10 cm, respectively. Shade levels of 30 to 92% reduced smallflower morningglory growth by 38 to 87% compared to plants grown in full sunlight.

The effects of acid scarification, prechilling, summer irrigation, and root extract stimulant from faba bean plants grown during different seasons on crenate broomrape seed dormancy and germination were determined. Immersion of 6- to 12-mo old seed in 0.5 to 5 N H2SO4 solution from 1 to 20 min increased germination by 20%. Similarly, seed pretreatment at temperatures between −4 and 6 C increased germination, regardless of the pretreatment duration. Results suggest that the hard seed coat is an important dormancy mechanism in newly formed crenate broomrape seeds. Summer irrigation did not substantially change the germination capacity of crenate broomrape seeds. The germination stimulant activity of the root extract from faba bean plants grown during different seasons varied considerably, decreasing in this order: autumn > winter > spring > summer. This suggests an ecological adaptation of crenate broomrape to its main host crop.

Fall panicum (Panicum dichotomiflorum Michx.) seed were found to be dormant at harvest. This dormancy was overcome by an after-ripening period of 17 to 22 weeks, alternating germination temperatures (10 C for 16 h and 30 C for 8 h), stratification, and mechanical or chemical scarification. Soaking seed in gibberellic acid (GA3) or thiourea for 1 day, or washing seed in running tap water for up to 96 h before seed were placed in a germinator, had no effect on dormancy. In the greenhouse, fall panicum emergence was greatest (82%) when seed were placed on the growth media surface. The maximum number of seedlings (39%) emerged in the field when seed were placed 1.3 cm below the soil surface, although some emerged from as deep as 5.1 cm.

Laboratory studies were conducted to determine the effect of various factors on germination of tropical soda apple. Tropical soda apple seed were found to be moderately photoblastic with 30% germination occurring in the dark. Germination increased in response to green (545 nm) and red light (650 nm) to 75 and 66%, respectively, indicating phytochrome regulation. No germination occurred in response to blue (450 nm) and far-red light (750 nm). Germination increased from 4 to 64% between 10 to 30 C, but no germination was found at 5 and 40 C. Maximum germination occurred at 30 C. A second degree polynomial (Y= −48.7 + 7.9X – 0.2X2, R2 = 0.76) best fit the data. Seed germinated over a broad range of pH (2 to 14) with the highest germination occurring at pH 8 and no germination occurring at pH 2 and 14 (Y = −63.3 + 30.5X – 1.9X2, R2 = 0.95). Seed germination declined as osmotic potential increased from 0 to −1.0 MPa (Y = 76.7 – 12.9X + 5.2X2, R2 = 0.87). Seedling emergence was maximum from depth of 3 to 6 cm, but no seedling emergence occurred when seed were planted below 12 cm (Y = 10.2 + 17.8X – 1.6X2, R2 = 0.93). Optimum germination occurred at a depth of 5.6 cm. Mechanical and sulfuric acid scarification increased the rate of germination but not the overall percentage. Tap water or hot water increased the rate of germination 26% and KNO3, GA3, or ethephon increased it 53%. Tropical soda apple seed germinated in response to variable environmental and edaphic conditions which could allow establishment in diverse ecosystems.