Effects of Operational Parameters on Decolorization of C. I. Acid Red 88 by UV/H2O2 Process: Evaluation of Electrical Energy Consumption

In the present study, effects of operational parameters on the electrical energy consumption for photooxidative process (UV/H₂O₂) for the decolorization of C. I. Acid Red 88 (AR88) have been investigated. In a series of experiments, 20 mg L^?1 of AR88 solution were irradiated in the presence of different concentrations of H₂O₂ (to find out optimum amount of H₂O₂) by UV light intensity of 30 W m^?2 for certain irradiation times. The decolorization of the dye followed pseudo first‐order kinetics, and hence, the figure‐of‐merit electrical energy per order (E_EO) is appropriate for estimating the electrical energy efficiency. The electrical energy consumption was determined during the variation of some parameters such as initial H₂O₂ concentration, initial dye concentration, UV light intensity, pH, and the gap size of solution. Results showed that electrical energy could be reduced by optimizing operational parameters.     

Response Surface Analysis and Statistical Modeling of Sulfide Generation from Municipal Wastewater

In this study, the interactive effects of four independent variables (initial chemical oxygen demand (COD) concentration, rotational velocity, temperature, and retention time) on the sulfide generation process in municipal wastewater were investigated. The process was modeled and analyzed with the variables in a series batch experiments. Experiments were conducted based on a central composite face‐centered design and analyzed using response surface methodology. The region of exploration for the process was taken as the area enclosed by COD (250 and 650 mg/L), rotational velocity (40 and 200 rpm), temperature (16 and 28°C), and retention time (2 and 40 h) boundaries. Eleven dependent parameters were either directly measured or calculated as response. The most influential variable on H₂S (g) production was found to be retention time. The results showed that simultaneous increase in temperature and rotational velocity caused an increasing trend in the amount of H₂S (g) emitted. Total sulfide was decreased by increasing rotational velocity due to more H₂S (g) secretion resulting from increased mixing rate. The present study provides valuable information about interrelations of quality and process parameters at different values of the studied variables.     

Study of simulation experiments on the TSR system and its effect on the natural gas destruction

In recent years, much work on the natural gas de- struction in carbonate reservoirs has been carried out at home and abroad. The classification of source rocks, the estimation of natural gas resource and the explora-tion of gas reservoirs can be related to the determina-tion of the geochemical depth limit for natural gas. On the basis of reaction kinetics and lab simulation ex- periments, the kerogen decomposition proceeds, sub-stantially, to completion at more than 5% vitrinite re-flectance[1…     

Quantification of the Mass Flux of H2O Gas (Steam) at Three Active Volcanoes Using Thermal Infrared Imagery

We apply a measurement technique that utilizes thermal video of vapor-dominated volcanic plumes to estimate the H₂O gas flux at three degassing volcanoes. Results are compared with H₂O flux measurements obtained using other methods to verify the thermal camera-derived values. Our estimation of the H₂O emission rate is based on the mass and energy conservation equations. H₂O flux is quantified by extracting the temperature and width of the gas plume from the thermal images, calculating the transit velocity of the gas plume from the thermal video, and combining these results with atmospheric parameters measured on-site. These data are then input into the equations for conservation of mass and energy. Selected volcanoes for this study were Villarrica in Chile, Stromboli in Italy, and Santa Ana in El Salvador. H₂O fluxes estimated from the thermal imagery were 38–250?kg?s^?1 at Villarrica, 4.5–14?kg?s^?1 for Stromboli’s Central Crater, and 168–219?kg?s^?1 at Santa Ana. These compare with H₂O flux values estimated by other methods of 73–220, 3–70 and 266?kg?s^?1, at the three volcanoes, respectively. The good agreement between thermal image-derived results and those estimated by other methods seem to validate this method.     

Performance of A Combination Process of UV/H2O2/Micro‐Aeration for Oxidation of Dichloroacetic Acid in Drinking Water

The decomposition of dichloroacetic acid (DCAA) in water using a UV/H₂O₂/micro‐aeration process was investigated in this paper. DCAA cannot be removed by UV radiation, H₂O₂ oxidation or micro‐aeration alone, while UV/H₂O₂/micro‐aeration combination processes have proved effective and can degrade this compound completely. With initial concentrations of about 110 μg/L, more than 95.1% of DCAA can be removed in 180 min under UV intensity of 1048.7 μW/cm², H₂O₂ dosage of 30 mg/L and micro‐aeration flow rate of 2 L/min. However, more than 30 μg/L of DCAA was left after 180 min by UV/H₂O₂ combination process without micro‐aeration with the same UV intensity and H₂O₂ dosage. The effects of applied UV radiation intensity, H₂O₂ dose, initial DCAA concentration and pH on the degradation of DCAA have been examined in this study. Degradation mechanisms of DCAA with hydroxyl radical oxidation have been discussed. The removal rate of DCAA was sensitive to operational parameters. There was a linear relationship between rate constant k and UV intensity and initial H₂O₂ concentration, which indicated that a higher removal capacity can be achieved by improvement of both factors. A newly found nitrogenous disinfection by‐product (N‐DBP)‐DCAcAm, which has the potential to form DCAA, was easier to remove than DCAA by UV/H₂O₂ and UV/H₂O₂/micro‐aeration processes. Finally, a preliminary cost comparison revealed that the UV/H₂O₂/micro‐aeration process was more cost‐effective than the UV/H₂O₂ process in the removal of DCAA from drinking water.     

Kinetics of Methyldiethanolamine Mineralization by Using UV/H2O2 Process

The UV/H₂O₂ is one of the popular techniques in the advanced oxidation processes (AOPs) and has been applied in the wastewater treatment during recent two decades. UV exposure on the H₂O₂ generate highly reactive hydroxyl radicals (OH^?), which are used to degrade organic contaminants through oxidation processes in wastewater. This present study involves the estimation of hydroxyl radical rate constants of methyldiethanolamine (MDEA) mineralization at different temperatures by using UV/H₂O₂ in aqueous solution. Laboratory experiments have been conducted and the profile of MDEA mineralization has been established. The hydroxyl radical rate constants and the activation energy of mineralization process have been calculated. The estimated hydroxyl rate constants and the activation energy are in good agreement with those reported in the literature.     

Orographic distillation and spatio‐temporal variations of stable isotopes in precipitation in the North Atlantic

Little is known about the spatial and temporal variability of the stable isotopic composition of precipitation in the North Atlantic and its relationship to the North Atlantic Oscillation (NAO) and anthropogenic climate change. The islands of the Azores archipelago are uniquely positioned in the middle of the North Atlantic Ocean to address this knowledge gap. A survey of spatial and temporal variability of the stable isotope composition of precipitation in Azores is discussed using newly presented analyses along with Global Network of Isotopes in Precipitation data. The collected precipitation samples yield a new local meteoric water line (δ²H = 7.1 * δ¹⁸O + 8.46) for the Azores region and the North Atlantic Ocean. The annual isotopic mean of precipitation shows a small range for the unweighted and precipitation mass‐weighted δ¹⁸O‐H₂O values. Results show an inverse relation between the monthly δ¹⁸O‐H₂O and the amount of precipitation, which increases in elevation and into the interior of the island. Higher amounts of precipitation (from convective storm systems) do not correspond to the most depleted values of stable isotopes in precipitation. Precipitation shows an orographic effect with depleted δ¹⁸O‐H₂O values related to the Rayleigh effect. Monthly δ¹⁸O‐H₂O values for individual precipitation sampling stations show little relationship to air temperature. Results show a local source of moisture during the summer with the characteristics of the first vapour condensate. The stable isotope composition of precipitation is strongly correlated to the NAO index, and δ¹⁸O‐H₂O values show a statistically significantly trend towards enrichment since 1962 coincident with the increased air temperature and relative humidity due to climate change. Results are in line with observations of increasing sea surface temperature and relative humidity.     

Control of Hydrogen Sulfide by a Wire‐Tube Dielectric Barrier Discharge AC Plasma Reactor

Destruction of hydrogen sulfide by a wire‐tube dielectric barrier discharge (DBD) AC plasma reactor was carried out at atmospheric pressure and room temperature. Six aspects, effect of applied voltage, initial H₂S concentration, gas flow rate, pellets in the reactor, DBD reactor materials, and DBD dielectric thickness on H₂S removal efficiency were investigated. Furthermore, specific energy density (SED), absolute removal amount (ARA), and energy yield (EY) during the discharge process were investigated at the same time. In addition, ozone generation during the decomposition of H₂S was also studied. Experimental results demonstrated the application of DBD AC plasma was an effective technology for odor elimination.     

新疆呼图壁地下储气库断层气体地球化学特征研究

Rn、CO₂、Hg、H₂等断层气体被广泛应用于断层活动性以及断层结构特征的研究。当前，研究介质中压力变化与断层气间的关系是断层气映震研究的主要技术方法之一。新疆呼图壁地下储气库自建成以来，每年以周期性循环“注入/采出”模式运行，该运行模式带来的储气库气压变化会影响周围地区的地震活动。同时，这一定期加压存储与减压释放气体的过程为研究应力变化引起的断层气变化提供了天然的实验场。通过对呼图壁储气库开展断层气定期流动测量以及定点连续观测，获取反复加载、卸载气体过程中储气库及周边区域断层气体Rn、CO₂、Hg、H₂浓度的变化特征，在储气库区域内观测到明显的Hg、H₂浓度高值现象，其最大值分别为190ng/m³和725.40ppm，且其空间分布特征表现为在储气库加压存储过程中，储气库区域内注采井附近的气体浓度高于储气库区域外；此外，长期连续观测结果表明，断层气H₂与储气库的压力变化存在一定的关系，H₂对储气库内压力变化的响应更为灵敏。对呼图壁储气库应力变化引起的断层气变化特征进行分析，可以认识不同应力状态下断层气变化特征，为地震台站勘选与建设、震情跟踪以及异常落实等提供地球化学科技支撑。     

Equilibrium calculations in volcanic gaseous systems

Equilibria calculations of high-temperature volcanic gases from lava lakes are carried out on the basis of best volcanic gas samples. The equilibrium gas composition at temperatures from 800° to 1400°K and pressures up to 25 kilobars (in ideal gas system) was calculated using the free energy minimization model as well as the Newton-Raphson methods. It is shown that the juvenile «magmatic gas » of basaltic magma consists of three components: H₂O, SO₂, CO₂; the water vapor being about 60%. The increase of temperature under constant pressure results in the increase of the SO₂ concentration and in the simultaneous decrease of H₂S. Under the same conditions the ratios CO/CO₂ and H₂/H₂O are found to increase. Methane cannot be a component of «magmatic gas» corresponding to the elemental composition of basaltic lava gases. The calculated values of \(P_{O_2 } \) are in good agreement with the experimental data obtained from direct measurements of \(P_{O_2 } \) in lava lakes and experiments with basaltic melts.     

Mechanism of energy transfer in the lava lake of Niragongo (Zaire), 1959–1977

Heat and mass transfer rates were studied at the Niragongo lava lake during two expeditions directed by H. Tazieff in 1959 and 1972. The results of this study are as follows:Heat is transferred to the surface of the lake by the movement of lava; gas discharge is a result and not the cause of convection. The chemical composition of the gases and magma has changed very little between 1959 and 1972, whereas the mass and energy outputs differ by an order of magnitude. In 1977 a catastrophic explosion seems to have been caused by tectonic factors, stopping the slow convection of magma under the volcano and hence reducing surface manifestations in the form of the lava lake and escaping fumarolic and magmatic gases. The gas discharge was, in tons day⁻¹, 5000 for H₂O, 11,000 for CO₂, 1000 for SO₂ in 1959, and in 1972 7700 for H₂O, 180,000 for CO₂ and 23,000 for SO₂. These values correspond to an energy transfer of 0.9 × 10⁹ W in 1959 and 16 × 10⁹ W in 1972.     

Basical characteristics of fluid geologic process of interlayer oxidation zone sandstone-type uranium deposit

This paper reveals the physicochemical properties such as component, formulation, genesis, tem-perature, pH, Eh, salinity and pressure of all main alteration fluid of interlayer oxidation zone sand-stone-type uranium deposits after studying the geologic process and geochemistry of internal typical sandstone-type uranium deposits such as Shihongtan deposit in the Turpan-Hami basin, 512 deposit in the Yili basin, Dongsheng deposit in the Ordos basin. The composition of fluid can be divided into two parts based on the analysis of inclusion: one can be affirmed as atmospheric water with ordinary temperature epigenesist according to the character of hydrogen and oxygen isotope of inclusion, the other is natural gas containing gaseous hydrocarbon like CH₄, and CO₂ as well as a little H₂S, CO, H₂, N₂ and so on, it always contains a small quantity of hydrocarbon liquid in petroliferous basins. The fluid property of oxidation alteration zone is always oxidation alkaline, and neutrality or weak acid-weak alkaline and reducibility during the metallizing process, but at secondary reduction or deoxidization zone it becomes strong reduction alkaline. Oxygenic groundwater in the fluid is the activate and mig-ratory medium of uranium element, but the gaseous hydrocarbon like CH₄ as well as H₂, H₂S, CO from natural gas is the important sedimentary reducer of uranium mineral; the transformation of pH,Eh in fluid environment is the main reason for the formation of uranium metallization.     

Diffuse volcanic degassing and thermal energy release from Hengill volcanic system, Iceland

We report the first detailed study of spatial variations on the diffuse emission of carbon dioxide (CO₂) and hydrogen sulfide (H₂S) from Hengill volcanic system, Iceland. Soil CO₂ and H₂S efflux measurements were performed at 752 sampling sites and ranged from nondetectable to 17,666 and 722?g?m^?2?day^?1, respectively. The soil temperature was measured at each sampling site and used to evaluate the heat flow. The chemical composition of soil gases sampled at selected sampling sites during this study shows they result from a mixing process between deep volcanic/hydrothermal component and air. Most of the diffuse CO₂ degassing is observed close to areas where active thermal manifestations occur, northeast flank of the Hengill central volcano close to the Nesjavellir power plant, suggesting a diffuse degassing structure with a SSW?CNNE trend, overlapping main fissure zone and indicating a structural control of the degassing process. On the other hand, H₂S efflux values are in general very low or negligible along the study area, except those observed at the northeast flank of the Hengill central volcano, where anomalously high CO₂ efflux and soil temperatures were also measured. The total diffuse CO₂ emission estimated for this volcanic system was about 1,526?±?160?t?day^?1 of which 453?t?day^?1 (29.7?%) are of volcanic/hydrothermal origin. To calculate the steam discharge associated with the volcanic/hydrothermal CO₂ output, we used the average H₂O/CO₂ mass ratio from 12 fumarole samples equal to 88.6 (range, 9.4?C240.2) as a representative value of the H₂O/CO₂ mass ratios for Hengill fumarole steam. The resulting estimate of the steam flow associated with the gas flux is equal to 40,154?t?day^?1. The condensation of this steam results in thermal energy release for Helgill volcanic system of 1.07?×?10¹⁴?J?day^?1 or to a total heat flow of 1,237?MW_t.     

Geochemistry of the Submarine Gaseous Emissions of Panarea (Aeolian Islands, Southern Italy): Magmatic vs. Hydrothermal Origin and Implications for Volcanic Surveillance

The marine sector surrounding Panarea Island (Aeolian Islands, South Italy) is affected by widespread submarine emissions of CO₂ -rich gases and thermal water discharges which have been known since the Roman Age. On November 3^rd, 2002 an anomalous degassing event affected the area, probably in response to a submarine explosion. The concentrations of minor reactive gases (CO, CH₄ and H₂) of samples collected in November and December, 2002 show drastic compositional changes when compared to previous samples collected from the same area in the 1980s. In particular the samples collected after the November 3^rd phenomenon display relative increases in H₂ and CO and a strong decrease in the CH₄ contents, while other gas species show no significant change. The interaction of the original gas with seawater explains the variable contents of CO₂, H₂S, N₂, Ar and He which characterize the different samples, but cannot explain the large variations of CO, CH₄ and H₂ which are instead compatible with changes in the redox, temperature and pressure conditions of the system. Two models, both implying an increasing input of magmatic fluids are compatible with the observed variations of minor reactive species. In the first one, the input of magmatic fluids drives the hydrothermal system towards atypical (more oxidizing) redox conditions, slowly pressurizing the system up to a critical state. In the second one, the hydrothermal system is flashed by the rising high-T volcanic fluid, suddenly released by a magmatic body at depth. The two models have different implications for volcanic surveillance and risk assessment: In the first case, the November 3^rd event may represent both the culmination of a relatively slow process which caused the overpressurization of the hydrothermal system and the beginning of a new phase of quiescence. The possible evolution of the second model is unforeseeable because it is mainly related to the thermal, baric and compositional state of the deep magmatic system that is poorly known.     

三峡水库支流甲烷排放研究进展

甲烷(CH₄)对全球温室效应有着较大的贡献。三峡水库自2003年蓄水以来,其CH₄排放问题已受到广泛关注。但三峡水库反季节的运行方式,使支流库湾CH₄的产生和传输过程受到多方面的影响,进而导致其CH₄排放效应尚不十分明确。本文综述了三峡水库支流CH₄排放的研究进展,典型支流的CH₄排放通量普遍高于干流,位于三峡水库库尾的部分支流CH₄排放通量高于三峡水库库首及库中支流。大多数典型支流的CH₄通量在夏季均达到全年峰值,而在冬季高水位运行期均处于相对较低的水平。同时本文主要从水环境条件、水动力条件、人类活动及气象条件4个方面阐述了三峡水库支流CH₄排放的影响因素。1)水环境条件:支流水华后藻类衰亡分解过程会驱动CH₄释放,且藻类的演替过程会加剧CH₄的产生;温度可以直接影响CH₄的生成速率和消耗速率,也能通过促进藻的生长间接影响CH₄排放;支流相对较低的甲烷氧化菌丰度是其CH₄通量较高的原因之一。2)水动力条件:蓄水期CH₄主要以扩散的方式进行释放,支流较低的流速促进了悬浮物的沉积,上游沉积物中的CH₄含量高于下游;泄水期CH₄主要以冒泡的方式进行释放,下游沉积物中TOC急剧增加,但干流的入侵会削弱支流的温度分层,破坏藻类生长环境,间接影响CH₄通量。3)人类活动:农业耕作使支流水体中的营养物浓度增加,甲烷氧化菌的丰富度降低,细菌群落的营养相关代谢增强;建设用地扩大、支流筑坝增加抑制了有机物的传输,增加了水体中的产CH₄底物,促进了CH₄的产生。4)气象条件:降雨会携带更多营养物质进入支流,同时会增加水体浊度、破坏水体的温度分层,从而对CH₄的产生和传输过程造成影响。最后对未来的研究热点进行了展望,以期为三峡水库CH₄排放的控制和管理提供参考。     

Color Removal from Synthetic Textile Wastewater by Sono‐Fenton Process

In this study, the oxidative decolorization of C.I. reactive yellow 145 (RY 145) from synthetic textile wastewater including RY 145 and polyvinyl alcohol by Fenton and sono‐Fenton processes which are the combination of Fenton process with ultrasound has been carried out. The effects of some operating parameters which are the initial pH of the solution, the initial concentration of Fe²⁺, H₂O₂, and the dye, temperature, and agitation speed on the color and chemical oxygen demand (COD) removals have been investigated. The optimum conditions have been found as [Fe²⁺] = 20 mg/L, [H₂O₂] = 20 mg/L, pH 3 for Fenton process and [Fe²⁺] = 20 mg/L, [H₂O₂] = 15 mg/L, pH 3 for sono‐Fenton process by indirectly sonication at 35 kHz ultrasonic frequency and 80 W ultrasonic power. The color and COD removal efficiencies have been obtained as 91 and 47% by Fenton process, and 95 and 51% by sono‐Fenton processes, respectively. Kinetic studies have been performed for the decolorization of RY 145 under optimum conditions at room temperature. It has been determined that the decolorization has occurred rapidly by sono‐Fenton process, compared to Fenton process.     

Volcanic gases and sublimates from Showashinzan

Volcanic gases from Showashinzan are qualitatively the same as those liberated from igneous rocks when they are heated in vacuum. Their main components are H₂O, CO₂, and H₂. Then follow HCl, HF, N₂, SO₂, H₂S, S, CH₄, CO, Ar, Si, B, Mg, Na, K, Ca, Al, Fe, P, Br, NH₃, As, Zn, Sr, Ba, Cu, Pb, Sn, Sb, Bi, Ge, Ag, Cr, Ni, Mo, Rn, Ra, etc. They come through fumaroles of high temperature (～750°C.). Metallic compounds deposit as sublimates around the outlet of fumaroles. They are fractionated there according to their thermodynamic properties. When the temperature of gases falls, heavy metal elements deposit before reaching the surface of the earth. Ra is among them. Owing to the contribution of Ra thus depositted, Rn content of vapor is larger in low temperature fumaroles than in high temperature ones. Chemical compounds of H, C, N, O, and S vary their composition according to the condition of temperature and pressure. Sulfur exists as SO₂ more than H₂S. As the temperature of gases falls, SO₂ and H₂ decrease and H₂S increases. Mutual relation among them is ruled by the chemical equilibrium: SO₂+3H₂=H₂S+2H₂O. The structure of Showashinzan is not simple. Some deviations from the general rule are explained in connection with ground water.     

Isotopic evidence of TSR origin for natural gas bearing high H<Subscript>2</Subscript>S contents within the Feixianguan Formation of the northeastern Sichuan Basin,southwestern China

The northeastern area of Sichuan Basin, southwestern China, is the area with the maximal reserve of natural gas containing higher hydrogen sulphide (H₂S) that has been found among the petroliferous basins of China, with the proven and controlled gas reserve of more than 200 billion cubic meters. These gas pools, with higher H₂S contents averaging 9%, some 17%, are mainly distributed on structural belts of Dukouhe, Tieshanpo, Luojiazhai, Puguang, etc., while the oolitic-shoal dolomite of the Triassic Feixianguan Fm. (T₁f) is the reservoir. Although many scholars regard the plentiful accumulation of H₂S within the deep carbonate reservoir as the result of Thermochemical Sulfate Reduction (TSR), however, the process of TSR as well as its residual geological and geochemical evidence is still not quite clear. Based on the carbon isotopic analysis of carbonate strata and secondary calcite, etc., together with the analysis of sulfur isotopes within H₂S, sulphur, gypsum, iron pyrites, etc., as well as other aspects including the natural gas composition, carbon isotopes of hydrocarbons reservoir petrology, etc., it has been proved that the above natural gas is a product of TSR. The H₂S, sulphur and calcite result from the participation of TSR reactions by hydrocarbon gas. During the process for hydrocarbons being consumed due to TSR, the carbons within the hydrocarbon gas participate in the reactions and finally are transferred into the secondary calcite, and become the carbon source of secondary calcite, consequently causing the carbon isotopes of the secondary calcite to be lower (−18.2‰). As for both the intermediate product of TSR, i.e. sulfur, and its final products, i.e. H₂S and iron pyrites, their sulfur elements are all sourced from the sulfate within the Feixianguan Fm. During the fractional processes of sulfur isotopes, the bond energy leads to the ³²S being released firstly, and the earlier it is released, the lower δ ³⁴S values for the generated sulphide (H₂S) or sulfur will be. However, for the anhydrite that participates in reactions, the higher the reaction degree, the more ³²S is released, while the less ³²S remains and the more δ ³⁴S is increased. The testing results have proved the process of the dynamic fractionation of sulfur isotopes.     

Etude de la phase gazeuse occluse dans les laves de «l’Ardoukôba», volcan éphémère d’une dorsale émergée (Afar)

Gases trapped in lavas of three main flows of the Ardoukôba eruption (8 to 15 November, 1978) have been analysed by mass spectrometry. These analyses concern both plagioclase phenocrysts and microcrystalline mesostasis. Fluids are released between 500°C and 1200°C, and consist of H₂O, CO₂, CO, N₂, SO₂, HCl, H₂, CH₄ with traces of hydrocarbons and H₂S. The total content is less than 0.3–0.4 wt. % of samples with about 0.1–0.15 wt % of H₂O. No significant variation among the three flows is observed. Plagioclase phenocrysts are less abundant in fluids than the mesostasis (～2/3). The gases trapped in these phenocrysts are richer in CO and organic compounds, whereas mesostasis contain more H₂O, CO₂ and SO₂. CO is likely produced by reduction of CO₂ and H₂O with carbon during either analyses or eruption itself, or is of primary origin. In the latter case, gas composition suggests an entrapment temperature of about 1200°C ± 75°C. Kinetic study of the water and carbon dioxide release allows to calculate the diffusion characteristics of these fluids. Water and carbon dioxide behave rather similarly. Plagioclase gives a single activation energy value (8 Kcal/mole), while mesostasis gives two values (8 Kcal/mole, 15 Kcal/mole). Diffusion coefficients at 20°C are estimated to fall in the range 10^?13 · 10^?12 cm² · sec^?1.     

Laws,place, history and the interpretation of landforms

The state of an Earth surface system (ESS) is determined by three sets of factors: laws, place, and history. Laws ( L = L₁, L₂, . . . , L_n) are the n general principles applicable to any such system at any time. Place factors ( P = P_1, P_2, . . . , P_m) are the m relevant characteristics of the local or regional environment. History factors ( H = H₁ , H₂, . . . , H_q) include the previous evolutionary pathway of the ESS, its stage of development, past disturbance, and initial conditions. Geoscience investigation may focus on laws, place, or history, but ultimately all three are necessary to understand and explain ESS. The LPH triad is useful as a pedagogical device, illustrated here via application to explaining the world's longest cave (Mammoth Cave, KY). Beyond providing a useful checklist, the LPH framework provides analytical traction to some difficult research problems. For example, studies of the avulsions of three southeast Texas rivers showed substantial differences in avulsion regimes and resulting alluvial morphology, despite the proximity and superficial similarity of the systems. Avulsions are governed by the same laws in all cases [ L (A) = L (B) = L (C)], and the three rivers have undergone the same sea‐level, climate, and tectonic histories, as well as the same general anthropic impacts [ H (A) ≈ H (B) ≈ H (C)]. Though regional environmental controls are similar, local details such as the location of the modern main channel relative to Pleistocene meander channels differ, and thus these place factors explain the differences between the rivers. The LPH framework, or similar types of reasoning, is implicit in many types of geoscience analysis. Explicit attention to the triad can help solve or address many specific problems and remind us of the importance of all three sets of factors. Copyright © 2016 John Wiley & Sons, Ltd.