The environment experienced by a plant before and after reproduction can have a profound effect on the behaviour of the progeny after shedding. Maternal environmental effects on seeds are important for phenology and fitness in plants, especially for bet-hedging reproductive strategies. Maternal tissues that disperse with seeds are important for dormancy in many species, particularly those with coat-imposed dormancy and those that disperse in indehiscent fruits. Maternal nitrogen status, temperature and photoperiod modify maternal tissues and also influence the developing zygote. During seed development on the mother, the progeny may acquire environmental information directly, but there is also evidence for maternal–filial signalling and the epigenetic inheritance of environmental information through the germline.

Growth data on Jersey crossbred calves, maintained at ICAR-National Dairy Research Institute, Eastern Regional Station, Kalyani, Nadia, West Bengal, India, were collected and analysed to assess the influence of maternal effects on growth traits of calves. Traits considered for this study were birth weight (BW) and weights at 3 months (W3M), 6 months (W6M), 9 months (W9M) and 12 months (W12M) of age. Least-squares analyses were employed to obtain the effects of non-genetic factors on the traits of interest. Determination of influence of maternal effects on growth traits was estimated by fitting three univariate animal models (including or excluding maternal effects) using Bayesian approach. The most appropriate model for each trait was selected based on Deviance Information Criterion. Direct heritability (h2) estimates for BW, W3M, W6M, W9M and W12M were 0.31 ± 0.08, 0.26 ± 0.10, 0.48 ± 0.10, 0.44 ± 0.11 and 0.39 ± 0.14, respectively, under the best model. Permanent environmental maternal effects (c2) varied from 0.04 to 0.12 for all traits. Existence of maternal effects for all ages reflects the importance of maternal components for these traits. Moderate to high heritability estimates for growth traits indicate the possibility of modest genetic progress for these traits through selection under prevalent management system.

This study investigates the genetic and phenotypic aspects of early growth performance in the Murciano-Granadina goat breed, using data collected between 2016 and 2022 from a private dairy farm in Ghale-Ganj city, located in the southern area of Kerman province, Iran. Pedigree and data information were collected on several early body weight traits, including birth weight (BW), weaning weight (WW), average daily gain (ADG), Kleiber ratio (KR) and growth efficiency from birth to weaning (GE). Nine univariate animal models included direct additive genetic effects and different combinations of maternal effects were compared by using Akaike information criterion (AIC). Among the tested models, the best genetic analysis model for BW, included direct additive, maternal additive, maternal permanent and maternal temporary environmental effects. The best model for ADG, KR and GE included direct additive, maternal permanent and litter effects. For WW, the best model was determined to be one that included direct additive and maternal additive genetic effects. The estimated direct heritabilities were low values of 0.04, 0.07, 0.08, 0.05 and 0.07 for BW, ADG, KR, GE and WW, respectively. The estimates of genetic correlations among the studied traits were positive and low to high in magnitude which ranged from 0.11 for BW-KR to 0.91 for BW-GE. The phenotypic correlations ranged from 0.03 for KR-WW to 0.87 for ADG-KR. The positive correlations observed among the studied growth traits of the Murciano-Granadina goat breed indicate no negative genetic or phenotypic changes associated with selection for these traits.

The goal was to study imprinting effects on birth weight (BW), weaning weight (WW), six months weight (W6), pre- and post-weaning growth rate (GRa and GRb), and pre- and post-weaning Kleiber ratio (KRa and KRb) in Baluchi and Makuie sheep breeds. Analyses were done in a two steps process. In the first step, each trait was analysed with a series of 12 univariate animal models, including different combinations of direct and maternal effects and the best model was selected by the AIC criterion. In the second step, three new models were fitted by adding either maternal imprinting effect, paternal imprinting effect, or both of them, respectively, to the best model already selected in the first step, and changes in AIC were monitored. (Co)variances between traits were estimated using bivariate analyses. In Baluchi sheep, for BW, WW and W6, estimates of maternal imprinting heritability (${\boldsymbol h}_{{\boldsymbol mi}}^2$) were 0.12 ± 0.02, 0.08 ± 0.01 and 0.09 ± 0.01, respectively. In Makuie sheep, paternal imprinting heritability (${\boldsymbol h}_{{\boldsymbol pi}}^2$) for BW, WW, W6, GRb and KRb were 0.17 ± 0.05, 0.8 ± 0.05, 0.38 ± 0.10, 0.71 ± 0.15 and 0.65 ± 0.13, respectively. In Baluchi sheep, strong maternal imprinting correlations were observed between BW and WW (0.93 ± 0.05), BW and W6 (0.80 ± 0.07) and WW and W6 (0.91 ± 0.02). In Makuie sheep, paternal imprinting correlations ranged from −0.97 ± 0.33 (BW-GRb) to 0.99 ± 0.47 (GRb-KRb). It was concluded that imprinting effects need to be included in the statistical model to increase the accuracy of genetic evaluation. However, to have accurate and reliable estimates of imprinting effects, the availability of large data sets and deep pedigrees are necessary.

The present work evaluated animal models comprising direct and maternal effects to estimate (co)variance components and genetic parameters of growth rates and Kleiber ratio in Harnali sheep. The information on pedigree and targeted traits of 1862 lambs born to 144 sires and 591 dams was collected for the period from 1998 to 2018. The traits studied were average daily gain from birth to 3 months of age (ADG1), 3 months to 6 months of age (ADG2), and 6 months to 12 months of age (ADG3) and their corresponding Kleiber ratios as KR1, KR2 and KR3, respectively. The statistical methods included the general linear model for analyzing the effects of fixed factors and animal models for deriving variance components for targeted traits. According to best model evaluated on the basis of likelihood ratio test, the estimated direct heritability was low in magnitude and ranged from 0.04 to 0.14. Direct heritability estimates for ADG1, ADG2, ADG3, KR1, KR2 and KR3 were 0.06, 0.14, 0.05, 0.04, 0.11 and 0.05, respectively. The maternal genetic effects contributed (4–7%) significantly for ADG1, KR1 and KR2 traits. The genetic correlations ranged from −0.35 ± 0.11 (ADG1-KR2) to 0.98 ± 0.01 (ADG2-KR2 and ADG3-KR3) and phenotypic correlations ranged from −0.36 ± 0.02 to 0.98 ± 0.01 for ADG1-KR2 and ADG2-KR2, respectively. The significant maternal effects along with low levels of direct effects for average daily gain and Kleiber ratio at different age group should be considered while setting selection and managerial strategies to achieve anticipated growth rates in Harnali sheep.

Aphids parasitized in later instars can give birth to several nymphs before their reproduction is curtailed by the developing parasitoid. We examined the life histories of Aphis fabae Scopoli born to mothers parasitized by Lysiphlebus fabarum Marshall, and their suitability as subsequent hosts, to test the ‘fecundity compensation’ hypothesis. Maternal parasitism negatively impacted life history parameters, resulting in reduced estimates of population increase (rm, R0, and λ), and increased generation time (GT) and doubling time (DT). These impacts were greater when the larva developing in the mother turned out to be female rather than male, and greater still when mothers were superparasitized. Maternal parasitism produced aphids with shorter hind tibia (HTL), at birth and at maturity, but their developmental time was unaffected. Although female L. fabarum readily accepted such aphids for oviposition, rates of mummification and wasp emergence were lower, and more so when the maternal parasitoid was female. The resulting parasitoids took longer to develop than progeny from control wasps, had shorter HTLs, lower egg loads, smaller eggs, and produced fewer mummies with lower rates of adult emergence, all differences that were more pronounced when the maternal parasitoid was female. The progeny of these wasps exhibited similar impairments to these biological parameters as their parents, demonstrating that the negative impacts of development in maternally parasitized hosts extended for at least two generations. Thus, our results do not support fecundity compensation, but suggest that any benefits of post-parasitism reproduction will be offset by reduced fitness in both aphid progeny and the parasitoids that develop in them.

Crop–weed interactions are affected by environmental alterations resulting from a crop’s presence, such as modifications in temperature, light quality and quantity, and moisture conditions that could modify weed performance. The objectives of this work were to study (1) how soybean [Glycine max (L.) Merr.] crop structure modifies the environment under the canopy and large crabgrass [Digitaria sanguinalis (L.) Scop.] plant structure, biomass, and seed production and dormancy; and (2) the relative importance of these environmental changes on the weed’s characteristics. A field experiment in a completely randomized block design with five replicates was performed to evaluate narrow and wide interrow spacing and soybean maturity groups 3 and 4. Measured variables were intercepted solar radiation (RAD); red–far red (R-FR) ratio; humidity; minimum, maximum, and alternating temperatures; and weed biomass, tillers per plant, height, and seed dormancy. Crop canopy reduced solar radiation, R-FR ratio, and daily average maximum and alternating temperatures. Soybean presence reduced the weed biomass, tillers and seeds per plant, and seed dormancy. High solar radiation intercepted by the crop during the reproductive phase was the main environmental variable related to reductions in weed biomass, tillers per plant, and fecundity. The combination of low temperature and solar radiation received by developing seeds was more related to seed dormancy than the rest of the variables. Crop management decisions focused on the fact that keeping the crop canopy alive for a longer time at the end of the season would not only reduce the weed growth but also seed dormancy.

Body size is a trait with many potential impacts on fitness. Adult body size can affect the strength of condition-dependent parental effects that determine offspring phenotypes, with potentially important transgenerational consequences. In a preliminary experiment, larval food deprivation (30 min daily access) created Harmonia axyridis Pallas (Coleoptera: Coccinellidae) females that weighed <50% of controls reared on ad libitum food (eggs of Ephestia kuehniella Zeller). Although only 1/3 of larvae survived to adulthood in the 30 min treatment, adult pairs produced eggs that were not significantly different in size from those of pairs fed ad libitum as larvae. Less extreme larval food deprivation (4 h daily access) was used to create a cohort of H. axyridis that weighed <60% of controls reared on ad libitum food. Small couples had lower 20-day fecundities and reduced egg fertility relative to large couples. Both egg and pupal periods were shortest when both parents were small, and longest when both parents were large, with reciprocal crosses intermediate. There were no consistent effects of parental body size on larval development time, but the progeny of small females mated to large males pupated later than other treatments. Progeny of large pairs had the heaviest adult weights at emergence, and progeny of small pairs, the lightest, with the progeny of reciprocal crosses intermediate. Small females produced the lightest female offspring, whereas small males sired the lightest male offspring, suggesting stronger responses to epigenetic signals from parents of the same sex. These results indicate that H. axyridis cohorts maturing with abundant food will produce progeny with larger potential body size and fitness, whereas those experiencing food limitation will confer size and fitness limitations to the subsequent generation, with potentially important implications for short-term population dynamics.

Distillers dried grains with solubles (DDGS) are highly susceptible to lipid oxidation because DDGS contain about 10% crude fat, which is largely composed of polyunsaturated fatty acids. l-carnitine serves an important function in fatty acids β-oxidation, and also has antioxidant properties. The objective of this study was to examine the effects of l-carnitine in the DDGS diet of gestating and lactating sows on reproductive performance, milk composition and antioxidant status of sows and their offspring. One hundred and twenty sows (Landrace×Large white, mean parity 4.2, initial BW 230 kg) were randomly allotted to 1 of 4 dietary treatments (n=30 sows/treatment). Treatments were arranged as a 2×2 factorial with two levels of dietary DDGS (0 v. 250 g/kg in gestating diets and 400 g/kg in lactating diets) and two levels of dietary l-carnitine (0 v. 100 mg/kg in gestating diets and 0 v. 200 mg/kg in lactating diets). Distillers dried grains with solubles had no significant effect on litter size but significantly reduced the birth weights and weaning weights of piglets (P<0.05). Distillers dried grains with solubles reduced the antioxidant enzyme activities (P<0.05) and increased the malondialdehyde level in the plasma of sows on day 60 of gestation (P=0.004) and day 14 of lactation (P=0.008). The compositions of colostrum and milk were not affected by inclusion of DDGS and dietary l-carnitine (P>0.05). Supplementing the diets with l-carnitine had no significant effect of total litter size (P>0.05) but increased the number of piglets born alive and piglets weaned, birth weight and weaning weight of piglets and litter weight at birth and weaning (P<0.05). l-carnitine supplementation also increased the concentration of l-carnitine in milk and l-carnitine status of piglets (P<0.05). The antioxidant enzyme activities of new born and weaning piglets were increased (P<0.05) by maternal dietary l-carnitine but this did not extend to finishing pigs. In conclusion, including DDGS in the sows diet could induce oxidative stress, which may be associated with the reduced individual birth and weaning weight of piglets. Dietary l-carnitine supplementation improved the antioxidant and l-carnitine status of sows, which may be associated with the improved reproduction and piglet performance and the antioxidant status of piglets at birth and weaning. There were no interactions between DDGS and l-carnitine.

A study was conducted to estimate the genetic relationship between weaning weight and milk yield in Nguni cattle. Milk yield data (n=125) were collected from 116 Nguni cows from Mara Research Station located in Limpopo Province and Loskop South Farm located in Mpumalanga Province using the weigh-suckle-weigh technique. Weaning weight data (n=19 065) were obtained from stud Nguni cattle from 146 herds distributed throughout South Africa. Estimates of (co)variance components for milk yield and weaning weight were calculated using PEST and VCE softwares. The average weaning weight, age of the calf at weaning and 24-h milk yield was 158.94 kg, 210 days and 5.25 kg/day, respectively. Heritability estimates for milk yield, direct and maternal weaning weight were 0.22±0.238, 0.47±0.039 and 0.25±0.029, respectively. Estimates of genetic correlations for milk yield and maternal weaning weight, milk yield and direct weaning weight, direct and maternal weaning weight were 0.97±0.063, −0.71±0.416 and −0.56±0.247, respectively. The results indicate that maternal weaning weight is genetically highly predictive of milk yield in Nguni cattle. Maternal breeding values for weaning weight could therefore be used as a selection criterion to improve milk yield in Nguni cattle.

The germination behavior of giant foxtail and shattercane seed was investigated to determine whether environment in which maternal plants grow and progeny seed develop affects seed dormancy. Giant foxtail and shattercane seed was collected in 1985, 1991, and 1992. Plants from this seed were grown to maturity in the field and the greenhouse in 1993 and 1994. Experiments were conducted using mature progeny seed collected from these plants to determine the influence of environment of maternal growth on seed germination. Greenhouse-raised giant foxtail seed was more dormant than field-raised seed. Progeny of the 1991 giant foxtail collection had the most dormant seed, whereas progeny of the 1992 collection had the least dormant seed. Field-raised shattercane seed was more dormant than greenhouse-raised seed, but this dormancy was easily overcome by placing them in fluctuating temperatures. Moist stratification of giant foxtail seed increased its overall germination and reduced the differences in germination between individual collections and between field- and greenhouse-raised seed lots. Moist stratification of shattercane seed resulted in increased variability in germination within and among seed lots. Subjecting shattercane seed to freezing and thawing was most detrimental and caused an 89% reduction in germination due to seed death. These data indicate that before overwintering, giant foxtail seed differed in germination percentage, but overwintering reduced these differences. Shattercane seed produced in different environments had similar germination percentage. This suggests that successful overwintering depends on its ability to survive freezing and thawing conditions.

A study was conducted to quantify the magnitude and sources of variation in common waterhemp temporal patterns of emergence over 1 yr. In 2008 and 2010, emergence patterns in the absence of soil disturbance were determined for replicated samples of maternal families (progeny from one individual) separately harvested during the previous year from four plants within each of four agricultural fields (16 maternal families yr−1) at a university research farm near Urbana, IL. Combining data across years, variance partitioning indicated that seed sample within maternal family explained 48% of total variation in the percentage of viable, buried seeds that produced seedlings. Differences within, rather than among, maternal families also accounted for large fractions (60 to 99%) of total variation in cumulative percentage emergence at specific points during the growing season. Within years, seed samples characterized by delayed or accelerated emergence patterns did not originate from specific maternal plants. These results indicate that common waterhemp seed populations are without strong maternal plant effects that limit emergence to narrow intervals within the overall emergence period. Thus, results of this study support the use of contemporary approaches for modeling herbicide resistance evolution in common waterhemp, which assume seedling cohorts contain offspring from all individuals occurring within the maternal population.

The environment in which a plant grows (maternal environment) can affect seed viability, germination, and dormancy. We assessed the effects of maternal environment on wild oat seed viability, germination, dormancy, and pathogen infection by collecting and analyzing wild oat seed from above and below a barley canopy at three field sites in Montana. The viability of wild oat seed collected below a crop canopy was consistently less than it was for seed from the overstory but varied among sites and years. Reductions in viability because of relative canopy position ranged from 10% to 30%. Effects of position relative to crop canopy on weed seed germination/dormancy rates varied by site and suggest that the direction and magnitude of the effects of maternal environment on dormancy depend on environmental conditions. These effects may be driven by crop competition or by changes in seed pathogen pressure or both. Seven species each of fungi and bacteria were isolated from wild oat seeds. The only fungi causing reductions in seed viability (15%) was isolated from understory seeds, and several bacteria from both overstory and understory sources reduced seed germination. Results suggest that, in addition to the known weed-suppressive effects of using taller or earlier emerging varieties of crops, such crops can reduce weed spread through effects on weed seed demography because weeds growing beneath the crop canopy produce a reduced amount of viable seed that is less likely to germinate in the following year.

Integrated management techniques for several U.S. winter wheat production regions have been proposed for jointed goatgrass control. These strategies may be improved by a greater understanding of the genetic and environmental influences on seed production and germination. Plants from six jointed goatgrass collections were grown in common garden nurseries at two Oregon locations over two growing seasons. Unbroken spikes from each collection were used to evaluate seed dormancy and quantify seed production by inflorescence position. Germination tests were conducted over 14 d using spikelets of dormant and after-ripened samples in growth chambers set to 25/15 C day/night temperatures and a 12-h photoperiod. Spikelet position on the spike affected germination of the secondary seed in dormant samples of jointed goatgrass Collections D and G. In contrast, spikelet position did not affect secondary seed germination in dormant samples of Collection B. Spikelet position did not influence secondary seed germination in nondormant samples of all three collections. Spikelet position affected germination of the primary positioned seed in dormant samples of Collection B, and in nondormant samples of Collections B, E, and H. Unbroken spikes from jointed goatgrass Collections B and D were used to quantify seed production per spikelet position on the spike and per floret position within the spikelet. Seed production by floret position depended on spikelet position on the spike. This relationship varied for spikes of different lengths and for samples from the two collections. Efforts to model the life history of jointed goatgrass and predict germination should be adjusted to account for floret position within the spikelet, spikelet position within the spike, and source population. We suggest that future dormancy and germination research include sampling seed from several weed populations and efforts be made to standardize germination tests according to seed position on the inflorescence.

The historic maternal environment; the identity of competing, neighboring plants; and biotic stresses, such as fungal disease and herbivory, interact to influence the competitive ability, reproductive output, and plasticity of weed populations. A weed capable of altering its phenotype in response to environmental factors is better able to compete for resources in agroecosystems, thereby reducing crop yields and contributing more seeds to the seed bank. Velvetleaf is a highly competitive annual weed in many North American cropping systems, exhibiting a high degree of phenotypic plasticity in response to biotic and abiotic factors. We examined the effects of seed size (small and large), competitive environment (with and without soybean), and stress level (none = no treatment, moderate = pathogen inoculation, high = pathogen plus herbicide) on velvetleaf allometry and reproductive output during three field seasons. Only under the high-stress treatment was velvetleaf biomass, height, and reproductive output compromised (> 15% each), and these traits were further reduced with soybean competition. Soybean competition alone reduced velvetleaf biomass (> 50%), height (25%), and seed output (50%), but effects of competition varied with stress level. Velvetleaf plants that originated from large seeds (≥ 10 mg) generally outperformed plants originating from small seeds (< 10 mg) except under the high-stress treatment. These findings suggest that velvetleaf life-history traits and reproductive output in the current generation are a function of both present and historic factors. Management strategies for this species should involve tactics that not only reduce its competitive ability (e.g., biomass, height) but also decrease its seed production via synergistic stressors such as increased crop competitiveness, reduced-rate herbicide applications, and pathogen infection.

Species with physically dormant (PY) seeds make up over 25% of plant species in a number of ecologically important ecosystems around the globe, such as savannah and Mediterranean shrublands. Many of these ecosystems are subject to temporally stochastic events, such as fire and drought; but are in areas projected to experience some of the most extreme climatic changes in the future. Given the importance of PY in controlling germination timing for successful recruitment, we ask how plastic the PY trait is, and if changes to the maternal environment from climate change could alter recruitment. This review focuses on: (1) the evidence for inter- and intraspecific variation in PY; (2) the genetic, maternal and environmental controls involved; and (3) the ecological consequences of (1) and (2) above. Evidence for (within-community) interspecific variation in conditions required to break PY is strong, but for intraspecific variation evidence is contradictory and limited by a paucity of studies. Identifying controllers of variation in PY is complex, there is some suggestion that conditions of the maternal environment may be important, but no consensus on the nature of effects. The implications of PY plasticity for the persistence of seed banks, species and communities under climate change are discussed. We highlight a number of key knowledge gaps, such as a lack of research estimating the components of variation in non-agricultural species, and identify a suite of seed attributes relevant to understanding the potential impacts of climate change on the population dynamics of PY species in the future.

Seed dormancy can prevent germination under unfavourable conditions that reduce the chances of seedling survival. Freshly harvested seeds often have strong primary dormancy that depends on the temperature experienced by the maternal plant and which is gradually released through afterripening. However, seeds can be induced into secondary dormancy if they experience conditions or cues of future unfavourable conditions. Whether this secondary dormancy induction is influenced by seed-maturation conditions and primary dormancy has not been explored in depth. In this study, we examined secondary dormancy induction in seeds of Arabidopsis thaliana matured under different temperatures and with different levels of afterripening. We found that low water potential and a range of temperatures, from 8°C to 35°C, induced secondary dormancy. Secondary dormancy induction was affected by the state of primary dormancy of the seeds. Specifically, afterripening had a non-monotonic effect on the ability to be induced into secondary dormancy by stratification; first increasing in sensitivity as afterripening proceeded, then declining in sensitivity after 5 months of afterripening, finally increasing again by 18 months of afterripening. Seed-maturation temperature sometimes had effects that were independent of expressed primary dormancy, such that seeds that had matured at low temperature, but which had comparable germination proportions as seeds matured at warmer temperatures, were more easily induced into secondary dormancy. Because seed-maturation temperature is a cue of when seeds were matured and dispersed, these results suggest that the interaction of seed-maturation temperature, afterripening and post-dispersal conditions all combine to regulate the time of year of seed germination.

Changes in host phenotype are often attributed to manipulation that enables parasites to complete trophic transmission cycles. We characterized changes in host phenotype in a colonial host–endoparasite system that lacks trophic transmission (the freshwater bryozoan Fredericella sultana and myxozoan parasite Tetracapsuloides bryosalmonae). We show that parasitism exerts opposing phenotypic effects at the colony and module levels. Thus, overt infection (the development of infectious spores in the host body cavity) was linked to a reduction in colony size and growth rate, while colony modules exhibited a form of gigantism. Larger modules may support larger parasite sacs and increase metabolite availability to the parasite. Host metabolic rates were lower in overtly infected relative to uninfected hosts that were not investing in propagule production. This suggests a role for direct resource competition and active parasite manipulation (castration) in driving the expression of the infected phenotype. The malformed offspring (statoblasts) of infected colonies had greatly reduced hatching success. Coupled with the severe reduction in statoblast production this suggests that vertical transmission is rare in overtly infected modules. We show that although the parasite can occasionally infect statoblasts during overt infections, no infections were detected in the surviving mature offspring, suggesting that during overt infections, horizontal transmission incurs a trade-off with vertical transmission.