			Home About us Contact

Larger Seeds (larger + seed)

Distribution by Scientific Domains

Life Sciences	83%

Distribution within Life Sciences

Ecology & Organismal Biology	30%
Plant Science	19%

Selected Abstracts

Seed Dispersal of a High Quality Fruit by Specialized Frugivores: High Quality Dispersal?,

BIOTROPICA, Issue 2 2000
Daniel G. Wenny
ABSTRACT Dispersal quality, as estimated by the cumulative effects of dispersal, germination, seed predation, and seedling survival, was examined for Beilschmiedia pendula (Lauraceae) in Monteverde, Costa Rica. I determined the pattern of dispersal by finding seeds deposited by birds, protected the seeds from seed predators with cages to assess germination and seedling survival, and examined seed predation rates with marked seeds. Seed predation, germination, and seedling survival were compared between seeds naturally dispersed by birds and seeds placed at randomly located sites. Approximately 70 percent of seeds dispersed by birds (N= 244) were deposited <10 m from crown edges of fruiting B. pendula trees, although some seeds were dispersed at least 70 m away. Larger seeds were more likely to be dispersed under or close to the parent trees, and larger seeds produced larger seedlings. Seed size was not correlated directly with seedling survival, but larger seedlings at three months were most likely to survive one year. Seed predation by mammals and insects and seedling mortality due to fungal pathogens were concentrated beneath the crowns of parent trees. Seedlings and saplings were more abundant beneath fruiting B. pendula trees, but individuals farther away were taller on average. Thus, dispersal is beneficial for B. pendula, but such benefits appear most pronounced at a small spatial scale; seeds dispersed >30 m from the crown edges actually had a lower probability of survival than those dispersed 10,20 m. Only 10 percent of B. pendula. seeds received high-quality dispersal in terms of landing in the zone with the highest per seed probability of seedling survival 10,20 m from parental crowns. RESUMEN La calidad de dispersión, estimado del efecto acurnulativo de dispersión, germinación, predación de semillas, y sobrevivencia de plantulas fue examinada por Beikcbmiedia pendula (Lauracea) en Monteverde, Costa Rica. Determinté el partén de disperstón, encontrando semillas defecadas o regurgitadas por aves, protegi semillas de predatores con jaulas para determinar germinación y sobrevivencia de plantulas, y examiné la proporción de predación de semillas con semillas marcadas. Predación de semillas, germinación y sobrevivencia de plantulas fueron comparadas con semillas dispersadas naturalmente por aves y con semillas localizadas en lugares al azar. Aproximadamente 70 porcento de las semillas dispersadas por aves (N = 244) fueron depositadas cerca de 10 mdel horde de la corona de árboles en fruto de B. pendula, aunque algunas semillas fueron dispersadas hasta 70 m mas lejos. Semillas grandes tuvieron la tendencia de ser dispersadas debajo o cerca del Brbol parental, y semillas grandes produjeron plantulas grandes. El tamaño de la semilla no estaba correlacionada directamente con sobrevivencia de plantulas, pero plantulas grandes a 3 mesa tuvieron la tendencia de sobrevivir. Predación de semillas por los roedores y insectos, y mortalitad de plantulas por hongos patogtnicos fueron lo mas comun debajo de la corona de los árboles parentales. Plantulas y arbolillos fueron mós abundantes debajo de drboles en fruto de B. pendula, pero individuos distantes fueron en promedio más altos. Dispersión es favorable para B. pendula, pero estos beneficios aparentan ser más ptonunciados a una escala espacial menot; semillas dispersadas más de 30 m del horde de la corona en realidad tienen una probabilidad menor de sobrevivencia que las que son dispersadas entre 10,20 m. Solamente 10 porcento de las seniillas de B. pendula recibieron despersión de calidad alta en terminos de aterrizar en una zona con la más alta probabilidad de sobrevivencia de plantulas entre 10,20 m de la corona parental. [source]

Effects of search experience in a resource-heterogeneous environment on the oviposition decisions of the seed beetle, Callosobruchus maculatus (F.)

ECOLOGICAL ENTOMOLOGY, Issue 4 2006
ROU-LING YANG
Abstract 1.,This study investigates how female seed beetles, Callosobruchus maculatus, distribute their eggs on various-sized seeds when the size of seed was varied during the egg-laying period. 2.,Beetles were allowed to lay eggs on one of three arrays of 64 adzuki beans (Vigna angularis). Each array contained four size classes of seed, ranging from small (5.0,5.5 mm diameter) to large (6.5,7.0 mm), but differed in how they were distributed within the environment. In the most heterogeneous condition (the 64-patch design), the four sizes were interspersed, while in the least heterogeneous condition (the four-patch design) they were grouped into four separate blocks. Thus, a beetle exploring the 64-patch design would frequently encounter all four seed sizes, whereas a beetle exploring the four-patch design would only rarely encounter a change in bean size. 3.,Beetles experiencing greater seed size heterogeneity were more likely to lay eggs on larger seeds, whereas those in the blocked condition were more likely to oviposit on small seeds. Beetle responses to seed size heterogeneity suggest that the degree of preference for large seeds depends on a female's recent experience. 4.,Female beetles exhibited size discrimination throughout their egg-laying process; however, there was a trade-off between seed size and egg discrimination (i.e. avoiding those seeds already containing developing eggs) in response to the change in fitness gained from either laying on larger seeds or lower egg-load seeds during the egg-laying process. 5.,Our model provides the first evidence that evolving seed size discrimination ability is adaptive for the seed beetle with egg-discrimination ability. [source]

Does a latitudinal gradient in seedling survival favour larger seeds in the tropics?

ECOLOGY LETTERS, Issue 10 2004
Angela T. Moles
Abstract The mean size of seeds produced by plants at the equator is two to three orders of magnitude higher than the mean size of seeds produced by plants at 60°. We compiled data from the literature to assess the possibility that this latitudinal gradient in seed size allows species to cope with more difficult seedling establishment conditions in tropical environments. We found no relationship between latitude and seedling survival through 1 week (P = 0.27, n = 112 species). There was also no evidence that a larger seed mass is required to gain a given level of seedling survival in tropical environments (P = 0.37, n = 112 species), and no relationship between latitude and the duration of the juvenile period (P = 0.57, n = 132 species). Thus, our results are not compatible with the idea that seedling establishment is more difficult in the tropics. [source]

CO2 and nitrogen, but not population density, alter the size and C/N ratio of Phytolacca americana seeds

FUNCTIONAL ECOLOGY, Issue 3 2005
J.-S. HE
Summary 1Plants can provision seeds by optimizing seed size, number and nutrient content to maximize parental fitness. According to the McGinley,Charnov hypothesis, seed size should be determined by the ratio of carbon to nitrogen (C/N) available to the plant, with larger seed size correlating with larger C/N ratios and smaller absolute N content. 2This hypothesis was tested by establishing monocultures of Phytolacca americana L. (Phytolaccaceae) at three population densities under ambient and elevated CO2 environments, with two availabilities of soil N. 3Elevated CO2 reduced both seed size and N concentration while increasing the C/N ratio; high soil N availability produced the opposite result for N concentration and C/N ratio. Higher planting densities reduced plant biomass, but did not alter seed size. 4In accordance with the McGinley,Charnov hypothesis, larger seeds had both larger C/N ratios and smaller N content. However, the increase in C/N ratio caused by elevated CO2 corresponded with smaller seeds overall: elevated CO2 reduced seed size, although the seed size,C/N relationship remained positive. 5These results suggest an alternative mechanism to explain variation in seed size, and suggest that future climate conditions may alter seed quality and plant reproductive behaviour. [source]

The evolution of rewards: seed dispersal, seed size and elaiosome size

JOURNAL OF ECOLOGY, Issue 3 2006
WILL EDWARDS
Summary 1We examine the relationship between the reward offered to ants to disperse seeds (elaiosome size) and seed size, and the possible mechanisms that may generate this relationship in Australian plant species. 2We used seed and elaiosome sizes from our own data set containing 87 Acacia species, supplemented with 22 species from a previously published data set, and 98 ,Other species' from 51 genera in 25 families, also from published data. 3The relationship between ln(elaiosome size) and ln(seed size) was determined using standard major axis (SMA) regression for both data sets. For the Other data set we also determined the relationship among species independent of the differences between genera, among genera independent of the differences between families, among genera and among families. We used SMA to test for differences in slopes between groups. 4We found a significant common slope amongst all subsets of the larger data set. The estimated common slope and the 95% confidence interval for the relationship between ln(elaiosome size) and ln(seed size) across all data sets fell above one (1.24, 95%CI = 1.17,1.32), suggesting positive allometry. Slopes were also significantly positive and strikingly similar between the Acacia species data set and the Other species data sets. Similar positive allometry was shown in the ,other' species data set among genera and families, and among species independent of genus means (,species effects'). 5Significant and consistent relationships between taxonomic levels, independent of relationships at other levels, along with significant relationships at the species level, and similarity of slopes, suggest independent convergence towards an underlying functional relationship that has persisted over long evolutionary periods. Our results therefore suggest that ants have been agents of selection on seed traits. 6Such a functional relationship might result from a trade-off in ant foraging behaviour between the benefit of the reward (elaiosome) and the cost of the dispersal (determined by seed size). Slopes > 1 would then suggest that ants need more than proportionally larger rewards to remove larger seeds. [source]

Seedling survival and seed size: a synthesis of the literature

JOURNAL OF ECOLOGY, Issue 3 2004
ANGELA T. MOLES
Summary 1Large-seeded species have long been known to have higher survivorship during establishment than small-seeded species. Here, we assessed the size of this advantage by compiling published data on survival through seedling emergence, seedling establishment and sapling establishment. 2We found no relationship between seed mass and survival through the transition from viable seed in or on the soil to newly emerged seedlings (P = 0.47, n = 33 species). 3Synthesis of data from experimental studies on the advantages of large-seeded species establishing under particular hazards (such as shade, drought or herbivory) confirmed that seedlings of large-seeded species perform better than those of small-seeded species in most situations. However, the magnitude of this advantage was not sufficient to counterbalance the greater number of seeds produced by small-seeded species m,2 of canopy outline year,1. 4Synthesis of data from field studies of populations under natural conditions also showed that large-seeded species have higher survival through early seedling establishment than small-seeded species (P = 0.006, n = 112 species). However, the magnitude of this advantage would only be sufficient to counterbalance the greater number of seeds produced by small-seeded species m,2 of canopy outline year,1 if mortality continued at the same rate for some time. 5The time required for a species with 10-fold larger seeds to recoup the advantage gained by a smaller-seeded species during seed production ranged from 8.8 weeks for the smallest seeded species in the data set, up to an implausible 4.2 years for the largest-seeded species. Thus, while large-seeded species do have a survival advantage over small-seeded species during seedling establishment, the available evidence suggests that advantages must also accrue during other stages in the life cycle. One possibility is that the greater seed production of small-seeded species (m,2 of canopy outline year,1) is partly offset by larger canopies and longer reproductive life spans in large-seeded species. [source]

Plant traits and functional types in response to reduced disturbance in a semi-natural grassland

JOURNAL OF VEGETATION SCIENCE, Issue 2 2005
F. Louault
Abstract. Question: How do functional types respond to contrasting levels of herbage use in temperate and fertile grasslands? Location: Central France (3°1'E, 45°43'N), 870 m a.s.l. Methods: Community structure and the traits of dominant plant species were evaluated after 12 years of contrasted grazing and mowing regimes in a grazing trial, comparing three levels of herbage use (high, medium and low). Results and Conclusions: Of 22 measured traits (including leaf traits, shoot morphology and composition, phenology), seven were significantly affected by the herbage use treatment. A decline in herbage use reduced individual leaf mass, specific leaf area and shoot digestibility, but increased leaf C and dry matter contents. Plants were taller, produced larger seeds and flowered later under low than high herbage use. Nine plant functional response types were identified by multivariate optimization analysis; they were based on four optimal traits: leaf dry matter content, individual leaf area, mature plant height and time of flowering. In the high-use plots, two short and early flowering types were co-dominant, one competitive, grazing-tolerant and moderately grazing-avoiding, and one grazing-avoiding but not -tolerant. Low-use plots were dominated by one type, neither hardly grazing-avoiding nor grazing-tolerant, but strongly competitive for light. [source]

Temporal trends in species composition and plant traits in natural grasslands of Uruguay

JOURNAL OF VEGETATION SCIENCE, Issue 3 2003
Claudia Rodríguez
Cabrera (1970) Abstract. We report the successional trends of the major life-forms (graminoids and forbs) in natural grasslands of Uruguay over a 9-yr period after the removal of domestic herbivores. For the whole community, species richness and diversity decreased over the successional period. In graminoids we observed clear temporal trajectories in floristic composition; the rate of floristic change decreased with time and was associated with a shift in plant traits. The exclusion of large herbivores promoted erect and tall grasses with narrow leaves and greater seed length, vegetative growth constrained to the cool season and increased frequency of annual species. Forbs did not show a clear temporal trend in species composition, but there was, nevertheless, a plot-specific species turnover of this functional group that was reflected in their attributes. Species spreading by means of rhizomes, with vegetative growth restricted to the warm season. Species with larger seeds increased under grazing exclusion, as did annual and nitrogen-fixing forbs. The floristic changes induced by cattle exclusion occurred early in the succession. This early high rate of change has practical implications for management and conservation programs of the natural grasslands of Uruguay. Additionally, the shift in plant traits may be helpful in devising simple indicators of grazing impact. [source]

Time , size tradeoffs: a phylogenetic comparative study of flowering time, plant height and seed mass in a north-temperate flora

OIKOS, Issue 3 2008
Kjell Bolmgren
Parents face a timing problem as to when they should begin devoting resources from their own growth and survival to mating and offspring development. Seed mass and number, as well as maternal survival via plant size, are dependent on time for development. The time available in the favorable season will also affect the size of the developing juveniles and their survival through the unfavorable season. Flowering time may thus represent the outcome of such a time partitioning problem. We analyzed correlations between flowering onset time, seed mass, and plant height in a north-temperate flora, using both cross-species comparisons and phylogenetic comparative methods. Among perennial herbs, flowering onset time was negatively correlated with seed mass (i.e. plants with larger seeds started flowering earlier) while flowering onset time was positively correlated with plant height. Neither of these correlations was found among woody plants. Among annual plants, flowering onset time was positively correlated with seed mass. Cross-species and phylogenetically informed analyses largely agreed, except that flowering onset time was also positively correlated with plant height among annuals in the cross-species analysis. The different signs of the correlations between flowering onset time and seed mass (compar. gee regression coefficient=,7.8) and flowering onset time and plant height (compar. gee regression coefficient=+30.5) for perennial herbs, indicate that the duration of the growth season may underlie a tradeoff between maternal size and offspring size in perennial herbs, and we discuss how the partitioning of the season between parents and offspring may explain the association between early flowering and larger seed mass among these plants. [source]

Ecological and evolutionary trends in wetlands: Evidence from seeds and seed banks in New South Wales, Australia and New Jersey, USA

PLANT SPECIES BIOLOGY, Issue 2 2000
Mary A. Leck
Abstract Aquatic plants include a variety of life forms and functional groups that are adapted to diverse wetland habitats. Both similarities and differences in seed and seed-bank characteristics were discovered in comparisons of Australian (New South Wales) temporary upland wetlands with a North American (New Jersey) tidal freshwater marsh having both natural and constructed wetlands. In the former, flooding and drying are unpredictable and in the latter water levels vary diurnally and substrate is constantly moist. The hydrologic regimen provides the overriding selective force, with climate an important second factor. Other factors related to water level, such as oxygen availability, temperature and light, vary spatially and temporally, influencing germination processes, germination rates and seedling establishment. Seed and seed-bank characteristics (size, desiccation and inundation tolerance, germination cues and seed-bank longevity and depletion) differ, with the Australian temporary wetland being more similar to the small-seeded persistent seed bank of the constructed wetland site than to the natural tidal freshwater site with its larger seeds, transient seed bank and seasonal spring germination. Some non-spring germination can occur in the tidal constructed wetland if the soil is disturbed. In contrast, seeds in the temporary Australian wetlands germinated in response to wet/dry cycles rather than to season. Functional groups (e.g. submerged, amphibious) are more diverse in the Australian temporary wetlands, where all species tolerate drying. We suggest that the amphibious zone, with its hydrologic gradient, is the site of selection pressure determining establishment of wetland plants from seed. In this zone, multiple selective factors vary spatially and temporally. [source]

Resource distribution and the trade-off between seed number and seed weight: a comparison across crop species

ANNALS OF APPLIED BIOLOGY, Issue 1 2010
B.L. Gambín
In grain crops, total sink capacity is usually analysed in terms of two components, seed number and individual seed weight. Seed number and potential individual seed weight are established at a similar timing, around the flowering period, and seed weight at maturity is highly correlated with the potential established earlier. It is known that, within a species, available resources during the seed set period are distributed between both yield components, resulting in a trade-off between seed number and seed weight. Here we tested if this concept could apply for interspecific comparisons, where combinations of numbers and size across species could be related to the total available resources being either allocated to more seed or larger potential individual seed weight during the seed set period. Based on this, species differences in seed weight should be related to resource availability per seed around the period when seed number is determined. Resource availability per seed was estimated as the rate of increase in aboveground biomass per seed around the period of seed set. Data from 15 crop species differing in plant growth, seed number, seed weight and seed composition were analysed from available literature. Because species differed in seed composition, seed weight was analysed following an energy requirement approach. There was an interspecific trade-off relationship between seed number per unit of land area and seed weight (r = 0.92; F(1, 13) = 32.9; n = 15; P < 0.001). Seed weight of different species was positively correlated (r = 0.90; F(1, 13) = 52.9; n = 15; P < 0.001) with resource availability per seed around the seed set period. This correlation included contrasting species like quinoa (Chenopodium quinoa; ,100000 seeds m,2, ,4 mg equivalent-glucose seed,1) or peanut (Arachis hypogaea; ,800 seeds m,2, ,1000 mg equivalent-glucose seed,1). Seed number and individual seed weight combinations across species were related and could be explained considering resource availability when plants are adjusting their seed number to the growth environment and seeds are establishing their storage capacity. Available resources around the seed set period are proportionally allocated to produce either many small seeds or few larger seeds depending on the particular species. [source]