Unboxing the Buried Seeds of My Belonging

2016 ◽  
Vol 57 (9) ◽  
pp. e153-e156
Author(s):  
Tori Vasquez ◽  
Brenda Sendejo
Keyword(s):  
Buried Seeds

Light Requirements of Buried Seeds

Nature ◽  
1967 ◽  
Vol 213 (5076) ◽  
pp. 600-601 ◽  
Author(s):  
G. WESSON ◽  
P. F. WAREING
Keyword(s):  
Light Requirements ◽  
Buried Seeds

scholarly journals The influence of soil moisture on losses of buried seeds to fungi

2003 ◽  
Vol 24 (5-6) ◽  
pp. 255-263 ◽  
Author(s):  
Michelle Schafer ◽  
Peter M Kotanen
Keyword(s):  
Soil Moisture ◽  
Buried Seeds

Interspecific variation in extraction of buried seeds within an assemblage of sparrows

Oikos ◽  
2000 ◽  
Vol 88 (3) ◽  
pp. 574-584 ◽  
Author(s):  
David M. Whalen ◽  
Bryan D. Watts
Keyword(s):  
Interspecific Variation ◽  
Buried Seeds

Seed softening, imbibition time, and seedling establishmentin yellow serradella

2002 ◽  
Vol 53 (9) ◽  
pp. 1011 ◽  
Author(s):  
G. B. Taylor ◽  
C. K. Revell
Keyword(s):  
Marked Effect ◽  
Soil Surface ◽  
First Year ◽  
Large Numbers ◽  
Buried Seeds ◽  
Ornithopus Compressus ◽  
Intermediate Time ◽  
Softening Process ◽  
Viable Seeds ◽  
The Times

The first (preconditioning) and final stages of seed softening were studied over a 4-year period in 4 lines of yellow serradella (Ornithopus compressus L.): cvv. Santorini and Charano, and accessions GEH72-1A and GRC5045-2-2. Pods grown in 1997 were collected in December (start of summer) and placed on the soil surface or buried at a depth of 1 cm. Measurements of seed softening between years were made from pod samples removed in June each year. The progress of preconditioning and seed softening within the first 3 years was determined from samples taken at the end of February. Numbers of soft and viable seeds were determined from each sampling. Preconditioned seeds were identified by subjecting seeds to 7 gradual diurnal temperature cycles of 48/15°C in darkness before testing for permeability. Seed softening was markedly accelerated by pod burial in all 4 lines, with most buried seeds of GEH72-1A and Santorini softening during the first year. Seed softening was slower in GRC5045-2-2 and Charano, approaching a constant annual rate over the 4 years of the experiment. Despite this marked effect of burial the differences between lines in rates of softening of buried seeds were sufficient to have important implications for persistence under some management systems. Most seeds of all lines softened between February and June, indicating that shallow pod burial could be delayed in these lines until at least the end of February to promote the final stage of seed softening. Although large numbers of seeds of GEH72-1A and GRC5045-2-2 had preconditioned at the soil surface by the end of February, few went on to complete the softening process by June, when most had lost their preconditioned state. Treatment at 48/15°C was less successful in identifying preconditioned seeds of Santorini and Charano. Rates of imbibition differed markedly between lines. Most soft seeds of GEH72-1A and GRC5045-2-2 imbibed within days, whereas they took weeks in Santorini and an intermediate time in Charano. Seedling age distributions in the 4 lines in June closely reflected the times their soft seeds took to imbibe in the laboratory. Imbibition time can be an important germination regulating mechanism having implications that may be either favourable or unfavourable depending on rainfall distribution around the break of season and the system of management.

Effect of pod burial, light, and temperature on seed softening in yellow serradella

1999 ◽  
Vol 50 (7) ◽  
pp. 1203 ◽  
Author(s):  
G. B. Taylor ◽  
C. K. Revell
Keyword(s):  
Final Stage ◽  
Soil Surface ◽  
Light Level ◽  
Inhibitory Effect ◽  
Temperature Treatment ◽  
Diurnal Temperature ◽  
Light Levels ◽  
Buried Seeds ◽  
Softening Process ◽  
A Site

Studies were made on the preconditioning stage (which produces latent soft seeds) and the final stage of seed softening in newly ripened seeds of the GEH72-1A accession of yellow serradella (Ornithopus compressus L.). Pods grown at Yelbeni, Western Australia, in 1996 were collected in December and placed on the soil surface or buried at a depth of 0.5 cm at a site near Perth. Other pods were subjected to a gradual diurnal temperature fluctuation of 60/15°C in darkness in a laboratory chamber. Pod samples were taken from the field at intervals from January to June in 1997, and over 336 days from the 60/15°C treatment. Pods were broken into segments and the number of soft seeds determined. Numbers of latent soft seeds were then determined by subjecting residual hard seeds to 7 gradual diurnal temperature cycles of 48/15°C in darkness and retesting for permeability. In a second experiment, seeds preconditioned at the soil surface until 3 March were subjected to a range of light levels in the field in March before testing for permeability. The time taken for seeds to precondition under a range of constant temperatures between 30° and 70°C was determined in a third experiment. Preconditioning commenced early in summer in both surface and buried seeds. All buried seeds that preconditioned completed the softening process to produce about 80% soft seeds, with most seeds softening in March when diurnal temperatures fluctuated between maxima of 45–50°C and minima of 10–20°C. Only 15% of the seeds at the soil surface softened so that relatively few preconditioned seeds completed the softening process. Preconditioning occurred more rapidly than did the completion of softening in the 60/15°C treatment, indicating that this temperature regime was above optimum for the final stage of softening. Reversal of the preconditioning process took place in the field as temperatures declined during May. Effects of reduced temperatures in causing this reversion were confirmed in the laboratory on seeds preconditioned at 60/15°C. The final stage of softening was inhibited in some seeds by light levels as low as 0.3% of daylight, and in all seeds at a light level between 5 and 25%. A close negative linear relation was obtained between the log of the time taken for 50% of seeds to precondition and the constant temperature treatment between 30°C and 70°C, with the rate of preconditioning doubling with every 5.2°C rise in temperature within this range. Although many seeds preconditioned at the soil surface, the main constraint to completion of the seed softening process during autumn was the inhibitory effect of light.

Biology of Brassica tournefortii in the northern grains region of Australia

2020 ◽  
Vol 71 (3) ◽  
pp. 268
Author(s):  
Gulshan Mahajan ◽  
Rajandeep Singh ◽  
Bhagirath S. Chauhan
Keyword(s):  
Soil Depth ◽  
Integrated Management ◽  
Management Strategies ◽  
Burial Depth ◽  
Hordeum Vulgare L ◽  
Tillage Systems ◽  
No Till ◽  
Short Period ◽  
Buried Seeds ◽  
Brassica Tournefortii

Brassica tournefortii Gouan. (wild turnip, WT) has become a problematic weed in the no-till production systems of the northern grains region of Australia. Experiments were undertaken using different biotypes of B. tournefortii to examine its phenology, emergence and seedbank persistence. Biotypes were obtained from paddocks of barley (Hordeum vulgare L.) (WT1 and WT9) and chickpea (Cicer arietinum L.) (WT1/17 and WT2/17). Fresh seeds initially had high dormancy rates and persisted for a short period on the surface. Seedbank persistence increased with burial depth, with 39% of seeds remaining for WT1 and 5% for WT9 after 30 months at 2 cm depth. Persistence of buried seeds varied across biotypes; WT1/17 seedlings also emerged in the second growing season from 2 cm depth. Compared with buried seeds, seedlings readily emerged from the surface (in March–June following increased rainfall) within 6 months of planting. Emergence was greatest on the surface and varied between biotypes and tillage systems; the highest rate recorded was ~14%. Multiple cohorts were produced between February and October. No-till systems produced higher emergence rates than conventional tillage systems. Seedlings of B. tournefortii did not emerge from 5 cm soil depth; therefore, diligent tillage practices without seedbank replenishment could rapidly reduce the presence of this weed. A soil-moisture study revealed that at 25% of water-holding capacity, B. tournefortii tended to produce sufficient seeds for reinfestation in the field. Brassica tournefortii is a cross-pollinated species, and its wider emergence time and capacity to produce enough seeds in a dry environment enable it to become widespread in Australia. Early cohorts (March) tended to have vigorous growth and high reproduction potential. This study found B. tournefortii to be a poor competitor of wheat (Triticum aestivum L.), having greater capacity to compete with the slow-growing crop chickpea. Therefore, control of early-season cohorts and use of rotations with a more vigorous crop such as wheat may reduce the seedbank. The information gained in this study will be important in developing better understanding of seed ecology of B. tournefortii for the purpose of developing integrated management strategies.

Seed and seedling studies of three Trifolium subterraneum var. brachycalycinum lines, in a predominantly summer rainfall environment

1995 ◽  
Vol 35 (8) ◽  
pp. 1101
Author(s):  
GM Lodge
Keyword(s):  
Seed Production ◽  
Field Experiments ◽  
Seedling Survival ◽  
Seedling Emergence ◽  
Trifolium Subterraneum ◽  
Summer Rainfall ◽  
Sowing Time ◽  
Buried Seeds ◽  
Initial Seed ◽  
Total Seed

Field experiments were conducted in a predominantly summer rainfall environment to investigate burr burial, seed production, seed characteristics, seedling emergence and survival, and the effects of time of sowing on 3 Trifolium subterraneum var. brachycalycinum lines (cv. Clare and 2 local lines). Each line produced more surface than buried burrs; surface burrs were 59% (range 56-62%) of the total number of burrs recovered and produced 59% of the total seed number. Numbers of seeds per burr were similar for surface and buried burrs, however, buried seeds were 0.97 mg heavier (P<0.05) than surface seeds. Storage for 5 months at 25/60�C decreased hardseed content of surface seed by 50% and buried seed by 70%. Surface and buried seeds stored at 25/25�C for 3 months prior to sowing in trays had a total emergence of <10%, compared with 70% emergence for seeds stored at 25/60�C before sowing. These emergence differences reflected their levels of hardseededness. Numbers of seeds recovered from the soil were not significantly different among lines, declining from about 4200 seeds/m2 after initial seed set to 150 seeds/m2 by the following winter, a 97% decrease. Seed production in the second year increased seed reserves to about 8730 seeds/m2. With no further seed production, levels had declined by 93% in June 1990 and by 99% in May 1991. These data confirm the importance of annual seed production for persistence. Total seedling emergence in summer-autumn accounted for only 10% of the estimated seed production in each year. Seedling survival in summer-autumn 1988-89 was 92.7%, more than double the survival in 1989-90. The effect of sowing time on flowering was always significant, with time to first flower being highest (196 days) for the earliest sowing in March (P<0.05), progressively decreasing (P<0.05) to 108 days for the latest sowing in July. In March, April and May sowings, inflorescence numbers on the first day of flowering were similar at about 120/m2, but increased markedly (P<0.05) for sowing in June or July. However, for the March and July sowings, number of inflorescences at the 9 November 1990 count, were lowest (P<0.05). May or June sowings had the highest number of burrs and seeds (P<0.05), indicating that these may be the best sowing times for maximum seed production in these Trifolium subterraneum var. brachycalycinum lines.

Seasonal Changes in the Germination Responses of Buried Witchgrass (Panicum capillare) Seeds

Weed Science ◽  
1986 ◽  
Vol 34 (1) ◽  
pp. 22-24 ◽  
Author(s):  
Jerry M. Baskin ◽  
Carol C. Baskin
Keyword(s):  
Seasonal Changes ◽  
Late Summer ◽  
Late Spring ◽  
Seasonal Temperature ◽  
Temperature Changes ◽  
Late Autumn ◽  
Buried Seeds ◽  
Autumn And Winter

Buried seeds of witchgrass (Panicum capillare L., # PANCA) exposed to natural seasonal temperature changes in Lexington, KY, for 0 to 35 months exhibited annual dormancy/nondormancy cycles. Seeds were dormant at maturity in early October. During burial in late autumn and winter, fresh seeds and those that had been buried for 1 and 2 years became nondormant. Nondormant seeds germinated from 76 to 100% in light at daily thermoperiods of 15/6, 20/10, 25/15, 30/15, and 35/20 C, while in darkness they germinated from 1 to 24%. In late spring, seeds lost the ability to germinate in darkness, and by late summer 63 to 100% of them had lost the ability to germinate in light. As seeds became nondormant, they germinated (in light) at high (35/20, 30/15 C) and then at lower (25/15, 20/10, and 15/6 C) temperatures. As seeds reentered dormancy, they lost the ability to germinate (in light) at 15/6 C and at higher thermoperiods 2 to 3 months later.

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