Germination of annual ryegrass seeds (Lolium rigidum Gaud.) as influenced by temperature, light, storage environment, and age

1972 ◽  
Vol 23 (5) ◽  
pp. 779 ◽  
Author(s):  
D Gramshaw

Germination of Lolium rigidum seeds, in the light (12 hr day length) and in the dark, at constant temperatures of 12, 18, and 24°C and an alternating temperature of 24/12° (12 / 12 hr), was studied in freshly harvested seeds and in seeds stored for 18 weeks. In freshly harvested seeds the highest germinability (80%) was recorded at 12° in either light or dark and at 24/12° in the light. After 18 weeks' storage, a germinability of between 95 and 100% was observed at 12° and 24/12° in the dark and at 24° and 24/12° in the light. In another experiment in which seeds from a different source were used, seeds kept in six different environments and recovered at 3-weekly intervals during a 21 week post-harvest period were examined for germinability and germination rate. The six environments were: storage in a room, storage in a 60/15°C temperature cabinet, and four field treatments in which seeds were buried 0.2 and 1.0 cm under both a bare and a mulched soil surface. Germination was tested in the light and in the dark at an alternating temperature of 24/12°. Major increases in seed germinability with age occurred during the first 9 weeks after harvest. The different environments influenced the relationship between seed age and germinability only during the first 9 weeks. Seeds located 0.2 cm beneath either a bare or a mulched soil surface during summer germinated at a faster rate than seeds kept in the other environments. These findings are discussed in relation to the germination behaviour of seeds in the field.

1976 ◽  
Vol 27 (6) ◽  
pp. 779 ◽  
Author(s):  
D Gramshaw

Germination of Lolium rigidum seeds, in the light (12 hr day length) and in the dark, was studied at constant and alternating (12/12 hr) temperatures in the range 8–35°C. Seeds had after-ripened for 22 weeks. Different constant temperature optima for germinability were found: 27° in light and 11° in dark. Germinability at alternating temperatures in darkness was determined solely by the minimum temperature of the alternation, and there was no response to thermoperiodicity per se. In contrast, light and alternating temperature appeared to interact to increase germinability, although the highest germinability occurred only when the maximum temperature was close to the optimum constant temperature, i.e. about 27°. Germination in both light and dark was most rapid where either the constant or the average temperature of an alternating regime was between 18 and 29°. Below 18° germination rates decreased markedly, and at 8°, rates were one-third of those at 18°. Seeds germinated more slowly in light than in darkness at all temperatures, but the differences were small relative to the effects of low temperatures.In another study, seeds collected from plants naturalized in eight different localities in the cereal belt of Western Australia and subsequently planted together in two contrasting environments were examined for germinability at 24/12°C in light and dark 18 weeks after harvest. Dark germinability differed between seed sources but not between planting sites, and ranged between 78 and 93%. Exposure of germinating seeds to light substantially alleviated dormancy in seeds from all sources.


Weed Science ◽  
2004 ◽  
Vol 52 (6) ◽  
pp. 968-975 ◽  
Author(s):  
Robert S. Gallagher ◽  
Kathryn J. Steadman ◽  
Andrew D. Crawford

The effect of hydration (priming) treatment on dormancy release in annual ryegrass seeds from two populations was investigated. Hydration duration, number, and timing with respect to after-ripening were compared in an experiment involving 15 treatment regimens for 12 wk. Seeds were hydrated at 100% relative humidity for 0, 2, or 10 d at Weeks 1, 6, or 12 of after-ripening. Dormancy status was assessed after each hydration treatment by measuring seed germination at 12-hourly alternating 25/15 C (light/dark) periods using seeds directly from the hydration treatment and seeds subjected to 4 d postpriming desiccation. Seeds exposed to one or more hydration events during the 12 wk were less dormant than seeds that remained dry throughout after-ripening. The longer hydration of 10 d promoted greater dormancy loss than either a 2-d hydration or no hydration. For the seed lot that was most dormant at the start of the experiment, two or three rather than one hydration event or a hydration event earlier rather than later during after-ripening promoted greater dormancy release. These effects were not significant for the less-dormant seed lot. For both seed lots, the effect of a single hydration for 2 d at Week 1 or 6 of after-ripening was not manifested until the test at Week 12 of the experiment, suggesting that the hydration events alter the rate of dormancy release during subsequent after-ripening. A hydrothermal priming time model, usually used for modeling the effect of priming on germination rate of nondormant seeds, was successfully applied to dormancy release resulting from the hydration treatments.


1977 ◽  
Vol 28 (1) ◽  
pp. 81 ◽  
Author(s):  
D Gramshaw ◽  
WR Stern

Annual ryegrass–subterranean clover pastures that produced about 5000 kg total dry weight per hectare and 23,500 ryegrass seed per sq metre in spring were grazed by sheep at different stocking rates during summer. Intensive stocking equivalent to about 3000 sheep days ha-1 reduced seed numbers by 20%. Under continuous grazing, about 70% of the seed produced in spring fell readily to the ground during summer. The remaining seed was firmly held in seed heads, and apparently sheep ate mainly this component. Less than 1% of the seed ingested was voided in the faeces. No significant changes in seed numbers over summer were observed in ungrazed pasture. Subsequently, at the break of season in autumn, germination of seeds was examined in situ near the soil surface. The summer grazing history of pastures influenced the percentage of seeds that germinated; more seeds germinated in heavily than in leniently grazed pastures. Whether the pasture was leniently or heavily grazed, there was little effect on germination of shed seeds. Seeds in seed heads were found to germinate more slowly than seeds shed to the soil surface. Seedling emergence in autumn was regulated mainly by the interrelationship between the germination rate of the seed population, depending on summer-early autumn rains, and the period for which favourable moisture conditions prevailed at the soil surface after rain began in autumn. In the field, temperature and light appeared to be unimportant in influencing germination at the break of season. Dynamics of seed and seedling numbers in annual ryegrass pastures in a Mediterranean type environment, particularly at the break of season, are discussed.


1987 ◽  
Vol 27 (4) ◽  
pp. 525 ◽  
Author(s):  
PM Kloot

The ability of Hordeum glaucum to germinate and initially grow faster than Lolium rigidum was found to be influenced by the soil's physical state and its chemical characteristics. Glasshouse studies showed that the replacement of Lolium by Hordeum in undisturbed situations was due to the advantage of the latter having awned florets which anchor and lever the seed on smooth, compacted surfaces. Soil disturbance produces a broken surface upon which Hordeum has no advantage over Lolium. Hordeum is also able to germinate under higher osmotic pressures than is Lolium. Higher osmotic pressures will arise on stock camps and on alkaline soils where the salts are of biological and pedological origin respectively. Glasshouse and field observations showed that the top 3 mm of the soil surface are drier and more saline than the soil profile generally as indicated from measurements on soil cores. In undisturbed soil this surface layer will favour the dominance of Hordeum over Lolium. In cultivated soil the layer will be diluted throughout the depth of cultivation.


1995 ◽  
Vol 35 (1) ◽  
pp. 67 ◽  
Author(s):  
GS Gill

Annual ryegrass (Lolium rigidum) samples from the cropping belt of Western Australia were screened for herbicide resistance in 1992 and 1993. There was a strong relationship between the number of applications of a herbicide group and development of resistance in ryegrass populations. Resistance was detected in all populations that received >7 applications of aryloxyphenoxypropionate (AOPP) and cyclohexanedione (CHD) herbicides or >4 applications of sulfonylurea (SU) herbicides. Some AOPP-resistant populations had also developed crossresistance to SU herbicides, a group with a different mode of action. Inclusion of pasture in the rotation had little effect on the relationship between the number of applications of the AOPP and SU herbicides and development of resistance. A subset of 33 populations was chosen to determine the response of triasulfuron-resistant populations to sulfometuron, a nonselective SU herbicide which has been shown to be effective against metabolic-type resistance. All triasulfuron-resistant populations were found to be resistant to sulfometuron, possibly due to insensitive acetolactate synthase (ALS) in these ryegrass populations. Some of these SU-resistant populations were also resistant to the imidazolinone herbicide imazethapyr, another ALS inhibitor. However, there were several populations with a high level of SU resistance that were still susceptible to imazethapyr.


2004 ◽  
Vol 55 (7) ◽  
pp. 787 ◽  
Author(s):  
Kathryn J. Steadman ◽  
Gavin P. Bignell ◽  
Pippa J. Michael

Experiments were performed to determine whether the dormancy release effect of hydrated storage in darkness (dark-stratification) is common amongst annual ryegrass populations and has the potential to occur under field conditions. Dormant seeds from all populations tested (22) became sensitive to light during dark-stratification, enabling them to germinate when subsequently exposed to light. Under controlled temperature (25/15°C), light (12-h photoperiod), and hydration (solidified agar-water) conditions, more seeds germinated by 28 days if the first 14 days were in darkness followed by exposure to light for 12 h per day than if they were exposed to light throughout or darkness throughout. Constraint over the conditions imposed during dark-stratification and germination was gradually reduced to investigate whether the dormancy release effect was diminished. Dark-stratification was effective in promoting germination when performed under natural diurnal temperatures, and burial in moist soil provided suitable conditions for dark-stratification to occur. The surface of moist soil, with natural diurnal temperatures and sunlight, was suitable for germination of dark-stratified seeds. Dark-stratification is a quick and effective means to enhance the sensitivity of dormant annual ryegrass seeds to light, enabling the majority of the population to germinate. However, large quantities of light are required to promote germination of dark-stratified seeds, so buried seeds must be moved to the soil surface to allow exposure to adequate light for germination.


2013 ◽  
Vol 23 (2) ◽  
pp. 133-140 ◽  
Author(s):  
Xiaowen Hu ◽  
Tingshan Li ◽  
Juan Wang ◽  
Yanrong Wang ◽  
Carol C. Baskin ◽  
...  

AbstractAlthough seed dormancy of temperate legumes is well understood, less is known about it in species that grow in subalpine/alpine areas. This study investigated dormancy and germination of four Vicia species from the Tibetan Plateau. Fresh seeds of V. sativa were permeable to water, whereas those of V. angustifolia, V. amoena and V. unijuga had physical dormancy (PY). One year of dry storage increased the proportion of impermeable seeds in V. angustifolia, but showed no effect on seed coat permeability in V. amoena or V. unijuga. Seeds of all four species also had non-deep physiological dormancy (PD), which was especially apparent in the two annuals at a high germination temperature (20°C). After 1 year of storage, PD had been lost. The hydrotime model showed that fresh seeds obtained a significantly higher median water potential [Ψb(50)] than stored seeds, implying that PD prevents germination in winter for seeds dispersed without PY when water availability is limited. After 6 months on the soil surface in the field, a high proportion of permeable seeds remained ungerminated, further suggesting that PD plays a key role in preventing germination after dispersal. Addition of fluridone, an inhibitor of abscisic acid (ABA) biosynthesis, evened-out the differences in germination between fresh and stored seeds, which points to the key role of ABA biosynthesis in maintaining dormancy. Further, fresh seeds were more sensitive to exogenous ABA than stored seeds, indicating that storage decreased embryo sensitivity to ABA. On the other hand, the gibberellic acid GA3 increased germination rate, which implies that embryo sensitivity to GA is also involved in seed dormancy regulation. This study showed that PY, PD or their combination (PY+PD) plays a key role in timing germination after dispersal, and that different intensities of dormancy occur among these four Vicia species from the Tibetan Plateau.


2002 ◽  
Vol 42 (2) ◽  
pp. 111 ◽  
Author(s):  
R. Stanton ◽  
J. Piltz ◽  
J. Pratley ◽  
A. Kaiser ◽  
D. Hudson ◽  
...  

A trial was conducted to investigate the survival and digestibility of annual ryegrass (ARG) seed (Lolium rigidum L.) eaten by sheep and cattle. Sheep (n= 8) and cattle (n = 8) were fed a basal diet containing 1:1 lucerne chaff:oaten chaff with (ARG) or without (control) the inclusion of 20% total dry matter of annual ryegrass seed in a changeover design. Intake was restricted to 17 g/kg liveweight. Digestibility of the control diet was lower (P<0.01) for sheep than cattle. Annual ryegrass seed was present (P<0.01) in the faeces of both sheep and cattle within 24 h of first ingestion. Some 10.8 and 32.8% of seed ingested was excreted by sheep and cattle respectively, with 3.9% (sheep) and 11.9% (cattle) remaining germinable. Annual ryegrass seed continued to be excreted by both sheep and cattle up to 5 days after removal from the diet. Dry matter digestibility of the annual ryegrass diet was 53% in cattle.


1990 ◽  
Vol 94 (3) ◽  
pp. 1180-1186 ◽  
Author(s):  
John M. Matthews ◽  
Joseph A. M. Holtum ◽  
David R. Liljegren ◽  
Barbara Furness ◽  
Stephen B. Powles

Sign in / Sign up

Export Citation Format

Share Document