Seed Longevity of Six Native Forbs in a Closed Themeda triandra Grassland

1995 ◽  
Vol 43 (5) ◽  
pp. 439 ◽  
Author(s):  
ID Lunt
Keyword(s):  
Soil Seed Bank ◽  
Seed Mass ◽  
Soil Surface ◽  
Seed Longevity ◽  
Short Term ◽  
Themeda Triandra ◽  
Native Grassland ◽  
Buried Seeds ◽  
Small Seed ◽  
Closed Canopy

Seeds of six native forbs̵2Arthropodium strictum R.Br., Burchardia umbellata R.Br., Bulbine bulbosa (R.Br.) Haw., Chrysocephalum apiculatum (Labill.) Steetz, Craspedia variabilis Everett & Doust and Leptorhynchos squamatus (Labill.) Less.-were sown on and below the soil surface in a closed, native grassland dominated by Themeda triandra Forsskal. Replicate seed lots were recovered after 2, 4, 6, 9 and 12 months, and viability was assessed. Less than 7% of sown surface seeds of B. bulbosa, B. umbellata, C. variabilis and L. squamatus, and less than 10% of buried seeds of A. strictum, B. umbellata and C. variabilis remained viable after 12 months. Virtually all losses of Liliaceae seeds were due to germination. Fates of Asteraceae seeds were difficult to assess accurately after 6 months, but germination accounted for most seed losses. Burial significantly promoted longevity of B. bulbosa, C. variabilis and L. squamatus seeds. No obvious relationship existed between seed longevity and taxonomic group (Liliaceae versus Asteraceae) or seed mass, for surface or buried seeds; the response of the large-seeded lily, B. bulbosa, was most similar to that of the small-seeded daisy, L. squamatus. Of the six species, C. apiculatum appears to have the greatest potential to accumulate a soil seed bank beneath a closed grass canopy, owing to its small seed size, inhibition of germination beneath a closed canopy, both on and below the soil surface, and sustained viability of buried seeds. Naturally dispersed seeds of the other five species are likely to form smaller, transient or short-term seed banks.

When is the Best Time to Emerge—II: Seed Mass, Maturation, and Afterripening of Common Waterhemp (Amaranthus tuberculatus) Natural Cohorts

Weed Science ◽  
2015 ◽  
Vol 63 (4) ◽  
pp. 846-854 ◽  
Author(s):  
Chenxi Wu ◽  
Micheal D. K. Owen
Keyword(s):  
Seed Bank ◽  
Soil Seed Bank ◽  
Seed Mass ◽  
Soil Surface ◽  
Life Strategy ◽  
Flower Initiation ◽  
Population Densities ◽  
Common Waterhemp ◽  
Primary Dormancy ◽  
Seed Population

Field studies were conducted to determine the effect of emergence timing on the fitness of the next generation as represented by seed mass, maturation, and afterripening of common waterhemp cohorts. Five natural cohorts were documented both in 2009 and 2010. Different maternal environments resulting from varied cohort emergence timings did not influence seed maturation time and seed mass, but had an inconsistent effect on seed afterripening. Here are our major findings. (1) Waterhemp cohorts needed similar amounts of time to generate viable seeds (20 to 27 d after flower initiation) and the seeds produced were of similar size (2.0 to 2.35 g), and (2) waterhemp has strong primary dormancy that may be released within 4 mo during the afterripening process, depending on the dormancy level. Seeds produced by later cohorts were more sensitive to the afterripening period, suggesting more flexibility in life strategy. Seeds from the 2009 cohorts had similar afterripening patterns; newly harvested seeds had strong primary dormancy (<10% germination), which was gradually released during dry storage and reached the maximum germination (>80%) rate 4 mo after harvest (MAH). However, germination then dropped to 40% 6 and 8 MAH, suggesting the induction of secondary seed dormancy. Strong primary dormancy at harvest for 2010 seeds was sustained in dry afterripening, perhaps because of higher dormancy level, which was the result of less-favorable parental environments brought by 10 to 30 times higher population densities and 2.5 to 5 times higher accumulative precipitation than in 2009 (see Wu and Owen 2014). We also tested the soil seed-bank seed population densities for each waterhemp cohort and found that early cohorts greatly influenced the seed population densities at the soil surface level and the turnover rate of the soil seed bank. Results from this research will provide insights into better management of waterhemp, targeting a better understanding of the seed bank.

Stimulating dormancy release and emergence of annual ryegrass (Lolium rigidum) seeds using short-term hydrated storage in darkness

2004 ◽  
Vol 55 (7) ◽  
pp. 787 ◽  
Author(s):  
Kathryn J. Steadman ◽  
Gavin P. Bignell ◽  
Pippa J. Michael
Keyword(s):  
Effective Means ◽  
Soil Surface ◽  
Dormancy Release ◽  
Annual Ryegrass ◽  
Moist Soil ◽  
Lolium Rigidum ◽  
Short Term ◽  
Water Conditions ◽  
Buried Seeds ◽  
Diurnal Temperatures

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.

Seasonal cycles in germination and seedling emergence of summer and winter populations of catchweed bedstraw (Galium aparine) and wild mustard (Brassica kaber)

Weed Science ◽  
2006 ◽  
Vol 54 (1) ◽  
pp. 114-120 ◽  
Author(s):  
Husrev Mennan ◽  
Mathieu Ngouajio
Keyword(s):  
Soil Depth ◽  
Cropping Systems ◽  
Seedling Emergence ◽  
Seed Mass ◽  
Soil Surface ◽  
Burial Depth ◽  
Galium Aparine ◽  
Wild Mustard ◽  
Seed Population ◽  
Brassica Kaber

Catchweed bedstraw and wild mustard each produce two populations per year: a winter population (WP) in June, and a summer population (SP) in September. Experiments were conducted to determine whether the WP and SP differ in seed mass and seasonal germination. Seeds of both weeds were buried at 0, 5, 10, and 20 cm in cultivated fields, and retrieved at monthly intervals for 24 mo for germination tests in the laboratory. Additionally, seedling emergence from seeds buried at 0, 5, and 10 cm in the field was evaluated for 1 yr. Seeds from the WP were heavier than those from the SP for both species. Germination of exhumed seeds was affected by burial depth and by seed population. It was highest for seeds that remained on the soil surface and declined with increasing depth of burial. The WP of catchweed bedstraw produced two germination peaks per year, whereas the SP and all populations of wild mustard had only one peak. The WP of both weeds germinated earlier than the SP. Seedling emergence for both species in the field was greater for the WP than for the SP. Increasing soil depth reduced seedling emergence of both the WP and SP of wild mustard and affected only the WP of catchweed bedstraw. We conclude that the WP and SP of catchweed bedstraw and wild mustard seeds used in this study differed in seed mass, seasonal germination, and seedling emergence. The ability of a WP to produce large seeds that germinate early and have two germination peaks per year could make these populations a serious problem in cropping systems.

Comparisons of soil seed bank classification systems

2003 ◽  
Vol 13 (2) ◽  
pp. 101-111 ◽  
Author(s):  
Péter Csontos ◽  
Júlia Tamás
Keyword(s):  
Seed Bank ◽  
Soil Seed Bank ◽  
Plant Ecology ◽  
Classification Systems ◽  
Seed Longevity ◽  
Individual Species ◽  
Ecological Knowledge ◽  
Main Factor

AbstractSince 1969, ten soil seed bank classification systems have been published. Among these systems, the number of recognized seed bank categories varies from three to twelve. Seed longevity is the main factor used for distinguishing categories, but dormancy and germination types are also important. Systems considering relatively few seed bank categories have been the most commonly proposed in contemporary plant ecology. In contrast, systems involving high numbers of categories have received limited interest because the detailed ecological knowledge of individual species required for their successful categorization is usually missing. A comprehensive table on the main features of seed bank classification systems is provided.

scholarly journals Crop residues on short-term CO2 emissions in sugarcane production areas

2013 ◽  
Vol 33 (4) ◽  
pp. 699-708 ◽  
Author(s):  
Mariana M. Corradi ◽  
Alan R. Panosso ◽  
Marcílio V. Martins Filho ◽  
Newton La Scala Junior
Keyword(s):  
Co2 Emissions ◽  
Field Experiments ◽  
Crop Residues ◽  
Soil Surface ◽  
Dry Mass ◽  
Agricultural Crop ◽  
Short Term ◽  
Sugarcane Production ◽  
Soil Temperatures ◽  
Production Areas

The proper management of agricultural crop residues could produce benefits in a warmer, more drought-prone world. Field experiments were conducted in sugarcane production areas in the Southern Brazil to assess the influence of crop residues on the soil surface in short-term CO2 emissions. The study was carried out over a period of 50 days after establishing 6 plots with and without crop residues applied to the soil surface. The effects of sugarcane residues on CO2 emissions were immediate; the emissions from residue-covered plots with equivalent densities of 3 (D50) and 6 (D100) t ha-1 (dry mass) were less than those from non-covered plots (D0). Additionally, the covered fields had lower soil temperatures and higher soil moisture for most of the studied days, especially during the periods of drought. Total emissions were as high as 553.62 ± 47.20 g CO2 m-2, and as low as 384.69 ± 31.69 g CO2 m-2 in non-covered (D0) and covered plot with an equivalent density of 3 t ha-1 (D50), respectively. Our results indicate a significant reduction in CO2 emissions, indicating conservation of soil carbon over the short-term period following the application of sugarcane residues to the soil surface.

The seed ecology of Aegilops triuncialis: linking trait variation to growing conditions

2017 ◽  
Vol 27 (3) ◽  
pp. 183-198 ◽  
Author(s):  
Andrew R. Dyer
Keyword(s):  
Seed Mass ◽  
Seed Viability ◽  
Seed Type ◽  
Aegilops Triuncialis ◽  
Trait Variation ◽  
Growing Seasons ◽  
Small Seed ◽  
Annual Grasses ◽  
Growing Conditions ◽  
Plastic Responses

AbstractAdaptive plastic responses in invasive species allow for establishment and persistence despite the lack of genetic matching to new environments. The capacity of annual species to invade habitats to which they are not adapted is likely to be predicated on post-invasion seed trait variation correlated with conditions in the new habitat. To test this, I compared variation in seed traits and germination patterns of Aegilops triuncialis, an invasive annual grass, from 69 sample populations from 24 sites in California (USA) across 13 years. Seed mass, germination fractions, seed viability, and strength of induced dormancy between dimorphic seed pairs were used to investigate plastic variation within and among populations, across two general soil types, and among two widespread maternal genotypes. I found that seed mass variation was constrained although both seed types showed a 3-fold range among populations, 20–25% variation within populations between years, and was positively correlated with longer growing seasons. However, induced seed dormancy in the small seed type was correlated with large seed mass and to late-season precipitation, suggesting that longer growing seasons influence the strength of maternal and sibling chemical signals that induce dormancy in the small seeds. Thus variation in small seed germination fractions varies with the growing conditions experienced by the maternal plant. The greater longevity of the small seed type suggests that plasticity in germination in this species may contribute to seed bank formation, which is atypical of invasive annual grasses in California, and this may contribute to the persistence and spread of A. triuncialis in invaded ranges.

Seed mass and early survivorship of tree species in upland clearings and shelterwoods

1998 ◽  
Vol 28 (9) ◽  
pp. 1307-1316 ◽  
Author(s):  
D F Greene ◽  
E A Johnson
Keyword(s):  
Leaf Litter ◽  
Power Law ◽  
Tree Species ◽  
Picea Glauca ◽  
Mineral Soil ◽  
Seed Mass ◽  
High Survivorship ◽  
Small Seed ◽  
Negative Exponential ◽  
The Relationship

We examined recommended sowing densities of 25 North American tree species (26 observations) to measure the relationship between juvenile survivorship and seed mass in large clearings and shelterwoods. Two models for expressing the relationship (simple power law or a cumulative negative exponential adjusted to account for rodent-repellent application and seedbed type) all showed that survivorship is highly dependent on seed mass. For a small seed, mineral soil and thin humus confer roughly equally high survivorship. Leaf litter is very poor, and undisturbed thick moss appears to be the worst possible organic seedbed on upland sites. An examination of 30 records of Picea glauca (Moench) Voss survivorship (3- to 6-year-old cohorts) on mineral soil revealed substantial intraspecific variation with only 50% of the values within twofold of the predicted value.

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.

scholarly journals The early growth of supermassive black holes in cosmological hydrodynamic simulations with constrained Gaussian realizations

2020 ◽  
Vol 496 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Kuan-Wei Huang ◽  
Yueying Ni ◽  
Yu Feng ◽  
Tiziana Di Matteo
Keyword(s):  
Black Holes ◽  
Large Scale ◽  
Initial Conditions ◽  
Seed Mass ◽  
Early Growth ◽  
Supermassive Black Holes ◽  
Formation Mechanisms ◽  
Density Peak ◽  
Hydrodynamic Simulations ◽  
Small Seed

ABSTRACT The paper examines the early growth of supermassive black holes (SMBHs) in cosmological hydrodynamic simulations with different BH seeding scenarios. Employing the constrained Gaussian realization, we reconstruct the initial conditions in the large-volume bluetides simulation and run them to z = 6 to cross-validate that the method reproduces the first quasars and their environments. Our constrained simulations in a volume of $(15 \, h^{-1} {\rm Mpc})^3$ successfully recover the evolution of large-scale structure and the stellar and BH masses in the vicinity of a ${\sim}10^{12} \, M_{\odot }$ halo which we identified in bluetides at z ∼ 7 hosting a ${\sim}10^9 \, M_{\odot }$ SMBH. Among our constrained simulations, only the ones with a low-tidal field and high-density peak in the initial conditions induce the fastest BH growth required to explain the z &gt; 6 quasars. We run two sets of simulations with different BH seed masses of 5 × 103, 5 × 104, and $5 \times 10^5 \, h^{-1} M_{\odot }$, (i) with the same ratio of halo to BH seed mass and (ii) with the same halo threshold mass. At z = 6, all the SMBHs converge in mass to ${\sim}10^9 \, M_{\odot }$ except for the one with the smallest seed in (ii) undergoing critical BH growth and reaching 108 – $10^9 \, M_{\odot }$, albeit with most of the growth in (ii) delayed compared to set (i). The finding of eight BH mergers in the small-seed scenario (four with masses 104 – $10^6 \, M_{\odot }$ at z &gt; 12), six in the intermediate-seed scenario, and zero in the large-seed scenario suggests that the vast BHs in the small-seed scenario merge frequently during the early phases of the growth of SMBHs. The increased BH merger rate for the low-mass BH seed and halo threshold scenario provides an exciting prospect for discriminating BH formation mechanisms with the advent of multimessenger astrophysics and next-generation gravitational wave facilities.

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