nutrient addition
Recently Published Documents


TOTAL DOCUMENTS

415
(FIVE YEARS 111)

H-INDEX

45
(FIVE YEARS 5)

PLoS ONE ◽  
2021 ◽  
Vol 16 (12) ◽  
pp. e0259937
Author(s):  
Matthew J. Peterson ◽  
Pubudu P. Handakumbura ◽  
Allison M. Thompson ◽  
Zachary R. Russell ◽  
Young-Mo Kim ◽  
...  

The microbial and molecular characterization of the ectorhizosphere is an important step towards developing a more complete understanding of how the cultivation of biofuel crops can be undertaken in nutrient poor environments. The ectorhizosphere of Setaria is of particular interest because the plant component of this plant-microbe system is an important agricultural grain crop and a model for biofuel grasses. Importantly, Setaria lends itself to high throughput molecular studies. As such, we have identified important intra- and interspecific microbial and molecular differences in the ectorhizospheres of three geographically distant Setaria italica accessions and their wild ancestor S. viridis. All were grown in a nutrient-poor soil with and without nutrient addition. To assess the contrasting impact of nutrient deficiency observed for two S. italica accessions, we quantitatively evaluated differences in soil organic matter, microbial community, and metabolite profiles. Together, these measurements suggest that rhizosphere priming differs with Setaria accession, which comes from alterations in microbial community abundances, specifically Actinobacteria and Proteobacteria populations. When globally comparing the metabolomic response of Setaria to nutrient addition, plants produced distinctly different metabolic profiles in the leaves and roots. With nutrient addition, increases of nitrogen containing metabolites were significantly higher in plant leaves and roots along with significant increases in tyrosine derived alkaloids, serotonin, and synephrine. Glycerol was also found to be significantly increased in the leaves as well as the ectorhizosphere. These differences provide insight into how C4 grasses adapt to changing nutrient availability in soils or with contrasting fertilization schemas. Gained knowledge could then be utilized in plant enhancement and bioengineering efforts to produce plants with superior traits when grown in nutrient poor soils.


2021 ◽  
Vol 918 (1) ◽  
pp. 012030
Author(s):  
E Novriyanti ◽  
M Watanabe ◽  
Q Mao ◽  
K Takayoshi

Abstract Acacia and Eucalypt are important species in the global forest plantations. The resilience of those species under the changing environment would define their significance in the dynamic of forest plantation. This study was aimed to provide information on the growth performance of two acacias and two eucalypts seedlings under elevated CO2 concentrations. The seedlings of A. auriculiformis, A. mangium, E. camadulensis, and E. urophylla were subjected to two levels of CO2 and two levels of nutrient supply in the FACE system in Sapporo Experimental Forest, Japan. The eucalypts showed significantly higher growth performance than the acacias. The nutrient addition significantly increased the growth, yet the CO2 and interaction between CO2 and nutrients were not significantly different. LMA was not significantly affected by the elevated CO2 and nutrient addition. Although nutrients significantly affected the C/N in the eucalypts, they showed no different effect on the acacias. As expected, Nmass and Narea were higher in the acacia than those in the eucalypts, although no significant responses were shown to elevated CO2 and nutrient addition. The tested acacia and eucalypts showed relatively insensitivity to elevated CO2. Thus they might possess resilience capacity under the keep increasing level of the atmospheric CO2 concentration.


2021 ◽  
Vol 910 (1) ◽  
pp. 012074
Author(s):  
Ihab A.J. Awadh ◽  
Bushra S.R. Zangana

Abstract The aim of this study was conducted to add low levels of Astaxanthin to the feed on some physical and chemical traits of broiler carcasses raised at 42 days of age. 240 unsexed chicks, one day age, used the ROSS 308 strain, which was distributed randomly into five treatments by 48 chicks/treatment, and each treatment was divided into three replicates (16 chicks/replicate). The chicks were fed on three diets that included the initiator, growth, and final (23, 21.5, and 19.44% crude protein), respectively. Representative energy has amounted to 3000.5, 3100.7, and 3199.25 kcal/kg feed, respectively. Astaxanthin powder was added to the diet at levels 0, 10, 20, 30, and 40 mg/Kg of feed (T1, T2, T3, T4, and T5 treatments group), respectively. The results show the following: The treatments with Astaxanthin has recorded a significant improvement (P <0.01) in the percentages of liquids loss during cooking, drip and thawing loss, a significant increase in water holding capacity and pH in favor of the nutrient addition treatments compared to the control group. It, also, showed a significant improvement in the chemical traits of the Myoglobin and cholesterol concentration of minced chicken meat for the Astaxanthin treatments compared to the control group. It is concluded from the present study that the addition of low levels of Astaxanthin to broiler feed during the 42-day rearing period gave the best results in the physical and chemical traits of the carcass.


Oecologia ◽  
2021 ◽  
Author(s):  
Chhaya M. Werner ◽  
Maria Tuomi ◽  
Anu Eskelinen

AbstractPlant communities worldwide show varied responses to nutrient enrichment—including shifts in species identity, decreased diversity, and changes in functional trait composition—but the factors determining community recovery after the cessation of nutrient addition remain uncertain. We manipulated nutrient levels in a tundra community for 6 years of nutrient addition followed by 8 years of recovery. We examined how community recovery was mediated by traits related to plant resource-use strategy and plant ability to modify their environment. Overall, we observed persistent effects of fertilization on plant communities. We found that plants with fast-growing traits, including higher specific leaf area, taller stature and lower foliar C:N, were more likely to show a persistent increase in fertilized plots than control plots, maintaining significantly higher cover in fertilized plots 8 years after cessation of fertilization. Additionally, although graminoids responded most strongly to the initial fertilization treatment, forb species were more vulnerable to fertilization effects in the long-term, showing persistent decline and no recovery in 8 years. Finally, these persistent fertilization effects were accompanied by modified environmental conditions, including persistent increases in litter depth and soil phosphorous and lower soil C:N. Our results demonstrate the potential for lasting effects of nutrient enrichment in nutrient-limited systems and identify species traits related to rapid growth and nutrient-use efficiency as the main predictors of the persistence of nutrient enrichment effects. These findings highlight the usefulness of trait-based approach for understanding the persistent feedbacks of nutrient enrichment, plant dynamics, and niche construction via litter and nutrient build-up.


2021 ◽  
Vol 95 (1) ◽  
Author(s):  
Bahman Shafii ◽  
G. Wayne Minshall ◽  
Charles E. Holderman ◽  
Paul J. Anders ◽  
William J. Price

Author(s):  
Jennifer Margaret Gardner ◽  
Michelle Elisabeth Walker ◽  
Paul Kenneth Boss ◽  
Vladimir Jiranek

2021 ◽  
Author(s):  
Volker H.W. Rudolf

While there is mounting evidence indicating that the relative timing of predator and prey phenologies shapes the outcome of trophic interactions, we still lack a comprehensive understanding of how important the environmental context (e.g. abiotic conditions) is for shaping this relationship. Environmental conditions not only frequently drive shifts in phenologies, but they can also affect the very same processes that mediate the effects of phenological shifts on species interactions. Thus, identifying how environmental conditions shape the effects of phenological shifts is key to predict community dynamics across a heterogenous landscape and how they will change with ongoing climate change in the future. Here I tested how environmental conditions shape effects of phenological shifts by experimentally manipulating temperature, nutrient availability, and relative phenologies in two predator-prey freshwater systems (mole salamander- bronze frog vs dragonfly larvae-leopard frog). This allowed me to (1) isolate the effect of phenological shifts and different environmental conditions, (2) determine how they interact, and (3) how consistent these patterns are across different species and environments. I found that delaying prey arrival dramatically increased predation rates, but these effects were contingent on environmental conditions and predator system. While both nutrient addition and warming significantly enhanced the effect of arrival time, their effect was qualitatively different: Nutrient addition enhanced the positive effect of early arrival while warming enhanced the negative effect of arriving late. Predator responses varied qualitatively across predator-prey systems. Only in the system with strong gape-limitation were predators (salamanders) significantly affected by prey arrival time and this effect varied with environmental context. Correlations between predator and prey demographic rates suggest that this was driven by shifts in initial predator-prey size ratios and a positive feedback between size-specific predation rates and predator growth rates. These results highlight the importance of accounting for temporal and spatial correlation of local environmental conditions and gape-limitation in predator-prey systems when predicting the effects of phenological shifts and climate change on predator-prey systems.


Author(s):  
Nolan J. T. Pearce ◽  
James H. Larson ◽  
Mary Anne Evans ◽  
Paul C. Frost ◽  
Marguerite A. Xenopoulos

Author(s):  
Shu Ying Wee ◽  
Virginia P. Edgcomb ◽  
David Beaudoin ◽  
Shari Yvon-Lewis ◽  
Jason B. Sylvan

International Ocean Discovery Program Expedition 360 drilled Hole U1473A at Atlantis Bank, an oceanic core complex on the Southwest Indian Ridge, with the aim of recovering representative samples of the lower oceanic crust. Recovered cores were primarily gabbro and olivine gabbro. These mineralogies may host serpentinization reactions that have the potential to support microbial life within the recovered rocks or at greater depths beneath Atlantis Bank. We quantified prokaryotic cells and analyzed microbial community composition for rock samples obtained from Hole U1473A, and conducted nutrient addition experiments to assess if nutrient supply influences the composition of microbial communities. Microbial abundance was low (≤10 4 cells cm −3 ) but positively correlated to the presence of veins in rocks within some depth ranges. Due to the heterogeneous nature of the rocks downhole (alternating stretches of relatively unaltered gabbros and more significantly altered and fractured rocks), the strength of the positive correlations between rock characteristics and microbial abundances was weaker when all depths were considered. Microbial community diversity varied at each depth analyzed. Surprisingly, addition of simple organic acids, ammonium, phosphate, or ammonium plus phosphate in nutrient addition experiments did not affect microbial diversity or methane production in nutrient addition incubation cultures over 60 weeks. The work presented here from Site U1473A, which is representative of basement rock samples at ultraslow spreading ridges and the usually inaccessible lower oceanic crust, increases our understanding of microbial life present in this rarely studied environment and provides an analog for basement below ocean world systems such as Enceladus. IMPORTANCE The lower oceanic crust below the seafloor is one of the most poorly-explored habitats on Earth. The rocks from the Southwest Indian Ridge (SWIR) are similar to rock environments on other ocean-bearing planets and moons. Studying this environment helps us increase our understanding of life in other subsurface rocky environments in our solar system that we do not yet have the capability to access. During an expedition to the SWIR, we drilled 780 meters into lower oceanic crust and collected over 50 rock samples to count the number of resident microbes and determine who they are. We also selected some of these rocks for an experiment where we provided them with different nutrients to explore energy and carbon sources preferred for growth. We found that the number of resident microbes and community structure varied with depth. Additionally, added nutrients did not shape the microbial diversity in a predictable manner.


Sign in / Sign up

Export Citation Format

Share Document