Species‐specific size vulnerabilities in a competitive arena: Nutrient heterogeneity and soil fertility alter plant competitive size asymmetries

2019 ◽  
Vol 33 (8) ◽  
pp. 1491-1503 ◽  
Author(s):  
Charlotte Brown ◽  
Kenneth J. Oppon ◽  
James F. Cahill
2021 ◽  
Author(s):  
Alyssa Laney Smith ◽  
Daniel Z Atwater ◽  
Wonjae Kim ◽  
David C Haak ◽  
Jacob N Barney

Abstract Aims Within-species genetic and phenotypic variations have well-known effects on evolutionary processes, but less is known about how within species variation may influence community-level processes. Ecologically meaningful intraspecific variation might be particularly important in the context of anthropogenic impacts on natural systems, such as agriculture and species invasion, because human actions can cause strong selection pressures. Methods In a greenhouse study, we explored intraspecific (30 accessions) and ecotypic variation (representing agricultural and non-agricultural habitats) in biomass and rhizome production in response to inter- and intra-specific competition and soil fertility of Johnsongrass (Sorghum halepense), a widespread invasive species and agricultural weed. Important findings Contrary to our expectations and previous results, we did not find variation in biomass production among Johnsongrass ecotypes at this early life stage. However, we did find that Johnsongrass biomass varied substantially depending on competitor identity, soil fertility treatments, and among accessions. Rhizomes were 11% larger in the agricultural ecotype and up to 3-fold larger in fertilized treatment; while rhizome biomass increased by ~50% when fertilized, but did not differ among ecotypes. Interestingly, in competition, Johnsongrass produced 32% less biomass and 20% less rhizome mass with a conspecific than when competing interspecifically with corn. Our results indicate species-specific competitive responses and changes in rhizome allocation in response to neighbor identity; suggesting the possibility of adaptation by Johnsongrass to shift allocation under competition.


Author(s):  
Linda Sicko-Goad

Although the use of electron microscopy and its varied methodologies is not usually associated with ecological studies, the types of species specific information that can be generated by these techniques are often quite useful in predicting long-term ecosystem effects. The utility of these techniques is especially apparent when one considers both the size range of particles found in the aquatic environment and the complexity of the phytoplankton assemblages.The size range and character of organisms found in the aquatic environment are dependent upon a variety of physical parameters that include sampling depth, location, and time of year. In the winter months, all the Laurentian Great Lakes are uniformly mixed and homothermous in the range of 1.1 to 1.7°C. During this time phytoplankton productivity is quite low.


2005 ◽  
Vol 173 (4S) ◽  
pp. 18-18
Author(s):  
Joseph C. Liao ◽  
Mitra Mastali ◽  
David A. Haake ◽  
Bernard M. Churchill

1960 ◽  
Vol 15 (10) ◽  
pp. 665-665
Author(s):  
George S. Grosser
Keyword(s):  

1996 ◽  
Vol 76 (06) ◽  
pp. 1090-1095 ◽  
Author(s):  
C Ravanat ◽  
M Freund ◽  
S Schuhler ◽  
P Grunert ◽  
L Meyer ◽  
...  

SummaryThe purpose of this study was to develop specific and sensitive immunoassays to detect early indices of hypercoagulability in the rat. Rat platelet factor 4 (rPF4) and rat fibrinopeptide A (rFPA) assays, tools for the detection of activation of platelets and coagulation respectively, were designed using antibodies raised against purified rPF4 and against synthetic rFPA. The relevance of these new assays and of the commercially available ELISA kit for thrombin-antithrombin III (TAT) complexes was demonstrated in a rat model of a prethrombotic state induced by intravenous infusion of varying doses of thromboplastin (90 to 2400 μl/kg/h). In this model, the immunoassays allowed simultaneous detection of low levels of rFPA and rPF4 which were correlated with fibrinogen and platelet consumption and TAT generation and further proved to be of higher sensitivity than the classical methods of platelet count or measurement of fibrinogen levels. Plasma concentrations of rFPA, rPF4 and TAT were dependent on infusion time and thromboplastin dose, while hirudin (1 mg/kg) prevented their appearance. Thus the new specific immunoassays for rPF4 and rFPA and the commercial human TAT assay represent useful tools for pathophysiological studies or the screening of antithrombotic drugs in rats.


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