scholarly journals Phosphorus Retention in Lakes: A Critical Reassessment of Hypotheses and Static Models

2021 ◽  
Author(s):  
Hamed Khorasani ◽  
Zhenduo Zhu

Various hypotheses and models for phosphorus (P) retention in lakes are reviewed and 39 predictive models are assessed in three categories, namely mechanistic, semi-mechanistic, and strictly-empirical models. A large database consisting of 738 data points is gathered for the analyses. Assessing four pairs of competing hypotheses used in mechanistic models, we found that (i) simulating lakes as mixed-flow reactor is superior to plug-flow reactor hypothesis; (ii) modeling P loss as a second-order reaction outperforms the first-order reaction; (iii) P loss is better explained as a removal process throughout the lake volume than as a settling process across the sediments; and (iv) considering a fraction of P loading is associated with fast settling particles enhances lake total phosphorus (TP) predictions. Due to the systematic approach used for combining the hypotheses, some models are for the first time developed and assessed. For instance, the preeminent mechanistic model combines, for the first time, the second-order reaction hypothesis with the hypothesis that a specific proportion of P loading settles rapidly at the lake entrance. Results also showed that semi-mechanistic models outperform both mechanistic and strictly-empirical models since they take the form of a mechanistic model based on the physical representation of the lakes and utilize statistically acquired equations for unknown parameters. The best-fit model is a semi-mechanistic model that adopts the mixed-flow reactor hypothesis with a second-order volumetric reaction rate that is calculated as a non-linear function of inflow TP concentration, lake average depth, and water retention time. This model predicts 77.8% of the variability of log10-transformed lake TP concentration, which is 4.2% higher than the best mechanistic model and 0.8% higher than the best strictly-empirical model. The findings of this study not only shed light on the understanding of P retention in lakes but also can be useful for assessment of data-limited lakes and large-scale hydrological models to simulate the P cycle.

1985 ◽  
Vol 50 (7) ◽  
pp. 1594-1601 ◽  
Author(s):  
Jiří Klíma ◽  
Larisa Baumane ◽  
Janis Stradinš ◽  
Jiří Volke ◽  
Romualds Gavars

It has been found that the decay in dimethylformamide and dimethylformamide-water mixtures of radical anions in five of the investigated 5-nitrofurans is governed by a second-order reaction. Only the decay of the radical anion generated from 5-nitro-2-furfural III may be described by an equation including parallel first- and second-order reactions; this behaviour is evidently caused by the relatively high stability of the corresponding dianion, this being an intermediate in the reaction path. The presence of a larger conjugated system in the substituent in position 2 results in a decrease of the unpaired electron density in the nitro group and, consequently, an increase in the stability of the corresponding radical anions.


1983 ◽  
Vol 48 (11) ◽  
pp. 3279-3286
Author(s):  
Slavko Hudeček ◽  
Miloslav Bohdanecký ◽  
Ivana Hudečková ◽  
Pavel Špaček ◽  
Pavel Čefelín

The reaction between hexamethylenediisocyanate and 1-pentanol in toluene was studied by means of reversed-phase liquid chromatography. By employing this method, it was possible to determine all components of the reaction mixture including both products, i.e. N-(6-isocyanate hexyl)pentylcarbamate and N,N'-bis(pentyloxycarbonyl)hexamethylenediamine. Relations for the calculation of kinetic constants were derived assuming a competitive consecutive second-order reaction. It was demonstrated that the reaction involved in this case is indeed a second-order reaction, and the rate constants of the first and second consecutive reactions were determined.


2003 ◽  
Vol 35 (6) ◽  
pp. 246-251
Author(s):  
A. E. Croce ◽  
L. V. Mogni ◽  
C. Vicente Irrazábal

1973 ◽  
Vol 135 (3) ◽  
pp. 573-576 ◽  
Author(s):  
Bryan D. Young ◽  
John Paul

Certain features of RNA–DNA hybridization can be accounted for in terms of second-order-reaction theory. These include the use of annealing kinetics to estimate RNA complexity and the occurrence of approximately linear double-reciprocal plots.


1995 ◽  
Vol 33 (3) ◽  
pp. 363-367 ◽  
Author(s):  
L. Ratke ◽  
D. Uffelmann ◽  
W. Bender ◽  
P.W. Voorhees

Sign in / Sign up

Export Citation Format

Share Document