Next Article in Journal
Application of Basis Functions for Hull Form Surface Modification
Previous Article in Journal
Method for Prediction of Extreme Wave Loads Based on Ship Operability Analysis Using Hindcast Wave Database
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

In Situ Aerobic Bioremediation of Sediments Polluted with Petroleum Hydrocarbons: A Critical Review

by
Efsevia Fragkou
1,
Eleftheria Antoniou
1,
Ioannis Daliakopoulos
2,3,
Thrassyvoulos Manios
2,3,
Marianna Theodorakopoulou
3 and
Nicolas Kalogerakis
1,4,*
1
School of Chemical and Environmental Engineering, Technical University of Crete, 73500 Chania, Greece
2
Department of Agriculture, Hellenic Mediterranean University, 71410 Heraklion, Greece
3
TM Solutions Ltd., 71409 Heraklion, Greece
4
Institute of Petroleum Research, Foundation for Research and Technology Hellas, 73500 Chania, Greece
*
Author to whom correspondence should be addressed.
J. Mar. Sci. Eng. 2021, 9(9), 1003; https://doi.org/10.3390/jmse9091003
Submission received: 25 August 2021 / Accepted: 9 September 2021 / Published: 14 September 2021

Abstract

:
Oil pollution has been a worldwide concern especially in environments where treatment is quite difficult to apply. Marine polluted sediments, in particular, constitute one of the most recalcitrant environments for bioremediation and are often the final repository of petroleum contaminants, as a result of runoff and deposition. Aerobic hydrocarbon degraders present in the sediments are tackling the pollution under oxygen-limited or oxygen-depleted conditions. Research has focused on new ways to enhance bioremediation under anoxic conditions, however aerobic bioremediation is faster, and hence more effort should be made to sustain oxygen concentration levels. In this review, the different bioremediation techniques used for the decontamination of marine sediments are briefly discussed, and focus is primarily given to the different oxygenation methods used for enhancing aerobic bioremediation and the aeration methods that are suitable for in situ application, as well as state of the art technologies that make in situ aeration an appealing approach. Based on the technologies analyzed, suggestions are made for sediment bioremediation techniques in different marine environments.

1. Introduction

With 5.72 million tonnes of oil spilled as a result of oil shipping accidents between 1970 and 2015 [1], and over 1.45 million tonnes of oil spilled due to marine oil rig accidents [2,3], oil spills constitute a major environmental management problem, adversely affecting the marine ecosystem and, consequently, human life. The marine environment has been the receiver of large quantities of hydrocarbon pollutants that ultimately end up on the sea floor and get absorbed by the sediments [4]. To date, different response strategies have evolved to treat petroleum-contaminated environments [5,6], but sediment contamination, which constitutes a serious environmental concern for the deterioration of the ecosystem, is often overlooked.
Bioremediation is a process that utilizes the natural capacity of microorganisms to degrade or detoxify hazardous waste [7]. Engineered bioremediation modifies the environmental conditions (physical, chemical, biochemical, or microbiological) to enhance the degradation capacity of the native microorganisms [8]. It is an ecofriendly approach for restoring contaminated ecosystems without causing additional damage. Sediment bioremediation techniques have been applied over the years in different aquatic environments; however, they are limited to shallow applications due to implementation difficulties in deeper environments. As research progresses, more and more techniques have been developed to overcome these difficulties [9]. The importance of engineered bioremediation and natural attenuation came to the foreground after the Exxon Valdez oil spill, where a storm washed most of the oil to the shorelines [10]. The effectiveness of bioremediation is interchangeably linked to the capacity of the indigenous microorganisms to degrade and detoxify chemical contaminants. Field research after the Deepwater Horizon accident showed that indigenous microbial communities play a pivotal role in oil spill remediation [11]. Exploiting these hydrocarbon-degrading microbes for bioremediation purposes is of great importance. It has been shown that, in the presence of adequate oxygen, biodegradation rates of hydrocarbons are very fast, yet under anaerobic conditions, which is the case for most sediments, bioremediation can be an extremely slow process [12]. Hence, oxygen availability is fundamental for fast hydrocarbon biodegradation and can shape the bioremediation time. This realization raises the need for development of efficient aeration and oxygenation techniques for the sediments to promote and enhance aerobic bioremediation.
Bioremediation techniques are distinguished in two broad categories based on the site of application [5,6,7]. Ex situ techniques involve the excavation of polluted sediments from the site of contamination and their subsequent transfer to another site for treatment. The so-called dredging of sediments comes with a number of considerations since it can be the cause of deeper penetration of the contaminants into the sediments and it can also cause the release of the contaminants to the water column, negatively affecting the surrounding ecosystem. In situ bioremediation, on the other hand, is a highly promising and cost-effective technology for the sustainable remediation of contaminated sites. In situ techniques can be categorized into engineered and intrinsic bioremediation. Intrinsic bioremediation relies solely on the microorganisms to return the environment to its original state prior to contamination, while engineered bioremediation is either based on stimulating the autochthonous microorganisms for faster biodegradation of the pollutants, or on the addition of allochthonous microorganisms specifically targeted to degrade petroleum hydrocarbons with ease [13].
Besides large-scale catastrophic events, lesser but long-lasting pollution hydrocarbon pollution, such as that occurring in ports, has been overlooked. Harbors and marinas are hot spots of contamination dominated by polycyclic aromatic hydrocarbons (PAHs) produced by leaks (petrogenic) or combustion processes (pyrogenic), with the latter being less bioavailable and thus posing additional challenges for bioremediation [14]. While better monitored due to urban area proximity, this type of pollution has been taken more or less for granted. Nevertheless, in the context of Green Ports as part of the global environmental agenda and the sustainable development goals, especially those for life below water and future-proofing infrastructure, ecosystem restoration and environmental sustainability in the port environment has become more relevant. In situ aerobic bioremediation techniques may have additional advantages here as they require limited space, cause minimum disturbance, and can lead to faster removal of recalcitrant compounds.

2. Engineered Bioremediation

2.1. Bioaugmentation

Bioaugmentation involves the implementation of cultured microbial populations into a contaminated zone to promote biodegradation of the contaminants. These microbial populations include pure bacterial strains, consortia, genetically engineered bacteria, and genes transferred to the indigenous microorganisms [15]. The application of microorganisms preadapted to the contamination seems very promising. However, the scientific community is torn between the actual effects of bioaugmentation. The introduction of allochthonous microorganisms in field studies for the bioremediation of oil contaminated sediments has shown little enhancement of biodegradation in some cases [16,17,18], while other research studies support the technique’s effectiveness on hydrocarbon bioremediation [19,20,21,22,23]. Allochthonous microorganisms might be equipped to battle hydrocarbon pollution but there are several factors to be considered for an effective application. Environmental conditions and even competition with the indigenous microorganisms could lead in limited action of the introduced microbes [17,24]. Autochthonous bioaugmentation (ABA) has been developed to overcome such implications [25]. Examining the indigenous microorganisms, classified for hydrocarbon degradation, on their native environment, could be an effective alternative to combat oil pollution. In a bioremediation study simulating an oil spill event, it was shown that the application of ABA coupled with biostimulation is a promising bioremediation strategy [26].

2.2. Biostimulation

Biostimulation of the indigenous microbiome to battle hydrocarbon pollution is a widely used bioremediation technique for aerobic sites, but its use is hindered in oxygen-depleted sediments [27]. There are several factors that can affect the rate of hydrocarbon degradation including environmental factors, the type of sediments, the autochthonous microorganisms, and the type of hydrocarbons and the extent of the pollution. Among the environmental factors are nutrient and oxygen availability, hydrocarbons bioavailability, pH, and temperature [28,29]. Biostimulation is employed to overcome some of these limitations and prolong the biodegradation efficiency of the microorganisms. Besides oxygen and nutrient addition as biostimulation strategies, other techniques can fall into this category, such as the use of chemical dispersants and surfactants to enhance bioavailability of hydrocarbons to the microbes [30], and phytoremediation, as a means of soil aeration in some cases [31].

2.2.1. Nutrients

Nutrients are available in most aquatic systems, however under the stress of petroleum contamination, nutrients can be depleted after a while due to the increased metabolic activity of the microorganisms in their efforts to degrade the contaminants. In most highly hydrocarbon contaminated coastal systems, nutrient availability is the limiting factor for biodegradation [5,32]. The most commonly employed elements in hydrocarbon degradation are carbon, nitrogen, and phosphorous. Typical requirements of these elements for the metabolic activities of the microorganisms are in a C:N:P ratio of 100:10:1 with some studies reporting optimum results for crude oil bioremediation of ratios ~70:3:0.6 [33] and 8:1:0.07 [34]. Nutrients are usually introduced in the form of inorganic salts, urea, anhydrous ammonia, and fertilizers [35,36]. However, direct application can lead to unnecessary losses into the environment due to wash out such as in the case of open seas and intertidal environments. Efforts have been made to develop nutrient delivery systems capable of overcoming these implications. Slow-release fertilizers and oleophilic fertilizers present a better distribution of nutrients into the contaminated system. They were first introduced for bioremediation purposes after the Exxon Valdez oil spill and have been proven an effective biostimulation strategy ever since in a number of in situ applications for sediment bioremediation [37,38,39,40,41,42].

2.2.2. Oxygen

Nutrient addition is not expected to present any significant enhancement in oil biodegradation rates if oxygen is depleted [43,44]. Oxygen is the main electron acceptor in aerobic bioremediation, and, if not present in adequate concentrations, can limit the biodegradation potential of aerobic microorganisms. In the absence of oxygen, anaerobic bioremediation, which has been proven to be a very slow process compared to aerobic bioremediation [12,45], becomes the dominant process. Oxygen demand for sustaining and promoting aerobic bioremediation can be significantly high. In the case of hydrocarbon pollutants, different studies estimate different stoichiometric ratios of oxygen required for complete degradation of the contaminants: 3 M O2 for 1 mole of hydrocarbon [46], 3 kg of oxygen for every kg of petroleum product degraded [47], 8.6 mole oxygen for every mole of diesel fuel degraded [48], and 0.5–1 g oxygen/g hydrocarbon [49]. However, for the variable and dynamic conditions of the marine environment, these requirements can only be roughly estimated and are quite difficult to meet. Different techniques have been developed for the supplement of oxygen in contaminated environments and are further discussed in Section 3.3.

2.2.3. Dispersion of Oil

Chemical dispersants and surfactants consist of a common bioremediation strategy, but their use is controversial and their actual effect on microorganisms has been questioned. Dispersants are chemicals that break down oil into fine droplets to make it more bioavailable for microbial degradation. When applied on surface oil slicks, dispersed oil is mixed with water due to wave activity and enters the water column, becoming prone to microbial degradation. The primary purpose of dispersants use, on oil spills that occur in the sea, is to not reach sensitive shoreline habitats, like marshes and mangroves [50]. Dispersants constitute one of the first response actions in the occurrence of an oil spill, but are applied after careful consideration, since they can have a toxic effect on living organisms. Dispersant toxicity should also be taken into consideration when applied for sediment bioremediation, as it could inhibit microbial metabolic activities. Ferguson et al. [51] examined the dispersant activity on oil biodegradation in subarctic deep-sea sediments, and their results showed that dispersant addition led to significant increase in the rate of degradation at sediments collected from 1000 m deep, but had no effect at 500 m, thus indicating an ambiguous effect of the dispersants and a further need for research studies.
Biosurfactants have gained popularity in the recent years over the respective synthetic surfactants. Biosurfactants are amphiphilic molecules of microbial origin with surface active properties that reduce the surface tension and facilitate the contact between microorganism and pollutants [52]. They present all the benefits of the chemical surfactants with the addition that they are not toxic to microorganisms and provide higher biodegradability [52]. Biosurfactants can also maintain their activity under extreme conditions of pH, salinity, and temperature [53,54]. Their use for oil bioremediation purposes has been highlighted in numerous studies [55,56,57]. Nevertheless, industrialized biosurfactant production remains a financially unviable option compared to chemical surfactants [58].

2.2.4. Phytoremediation

Phytoremediation is considered a biostimulation strategy for the degradation of hydrocarbon pollutants that exploits the natural growth processes of plants and their associated microorganisms. Phytoremediation is an attractive potential for petroleum hydrocarbon cleanup in terrestrial environments [59,60] but has also gained attention for the decontamination of sediments in sensitive aquatic environments such as salt marshes and mangroves [61,62]. Restoration of such ecosystems is very tricky and challenging [63,64]. Salt marshes and mangroves are nursery habitats for a plethora of marine organisms and plants. They serve as a buffer between land and sea, filtering nutrients and absorbing toxic compounds, and providing a shield to coastal areas from natural phenomena and erosion. Phytoremediation is primarily based on the inherent ability of wetland plant species to aerate the soil rhizospheres for the stimulation of aerobic oil biodegradation. Wetland plants might accumulate quantities of oil and release exudates and enzymes that enhance microbial activity. Phytoremediation alone has been shown to significantly enhance microbial degradation of oil in mangrove sediments in regard to natural attenuation [62]. However, when combined with fertilizers for nutrient supplement, phytoremediation may lead to superior results [65].

2.3. Intrinsic Bioremediation

Intrinsic bioremediation, also called natural attenuation, solely relies on the microbial degradation potential [66]. Indigenous microorganisms have adapted to their environment and, if previously exposed to petroleum contamination, might be equipped with defense mechanisms and respond immediately to an oil spill event. Natural attenuation is a cost-effective technique since no intervention is required; however, monitoring is required to determine the sustainability of the process. Prior to application, risk assessments should be conducted to eliminate the risk of human exposure to contaminants. Intrinsic bioremediation is not a very attractive choice for the bioremediation of sediments since it is a very slow process, especially under the prevailing anaerobic conditions of the deeper layers.

3. Aerobic Bioremediation

In general, the applicability and efficiency of bioremediation depend on various factors. The primary criteria are based on the geographical and geological characteristics of the contaminated site (e.g., offshore locations, type of sediment), the nature and amount of contaminants, environmental constraints that may apply, and cost of application [67,68]. Biodegradation rates are also linked to environmental conditions and microbial community characteristics. Environmental conditions such as pH, temperature, availability of nutrients and oxygen, high hydrostatic pressures and the bioavailability of contaminants can significantly shape the bioremediation efficiency [28,31].
Sediment bioremediation is often hindered by some of these environmental conditions such as the prevailing high hydrostatic pressures (e.g., deep-sea polluted sediments) and anoxia. Even though bioelectrochemical approaches have been evolved to enhance anaerobic degradation of contaminants by providing different electron acceptors (microbial fuel cells [69,70,71], snorkels [72,73,74,75], cable bacteria [76,77,78,79,80]), they still fail to meet the biodegradation rates achieved under aerobic conditions. Hence, in this work we focus on aerobic bioremediation applications on shallow sediments.

3.1. Oxygen Profile in Marine Sediments

The oxygen profile in marine sediments strongly depends on the aquatic zone examined. Open seas offer a bigger span in the oxic zone, up to a few decimeters in depth [81], while on continental margins, oxygen penetration depth ranges from mm up to a few centimeters [82]. Coastal sediments on the other hand, typically present oxygen penetration depths of a few millimeters unless they are comprised of very permeable sandy sediments [81]. In general, oxygen penetration can be deeper in areas with low sedimentary respiration [83]. Oxygen concentration in the sediments is dependent upon a lot of factors. Temperature, depth, permeability of the sediments, tidal and wave forces, extent of pollution, redox compounds, and even salinity [84] can affect the dissolved oxygen (DO) concentrations. For instance, for the past half century the increasing temperature of the oceans has led in ~2% DO decline in the seawater [85]. DO has also been shown to diffuse only within the top few millimeters in the sediments even if the overlying waters are saturated with oxygen [86].
Oxygen is the most important electron acceptor for biodegradation processes [87]. Microorganisms under aerobic conditions can easily degrade various pollutants that accumulate on the sediments and pose a threat to sensitive ecosystems. For instance, the presence of hydrocarbon pollution in marine sediments can lead to a quick consumption of oxygen due to the continuous uptake from microorganisms to degrade the contaminants. Oxygen consumption leads to the alternation of aerobic conditions to anoxic and even anaerobic with subsequent alternation in the microbial populations. Besides the oxygen uptake from the microorganisms, oxygen depletion can occur due to abiotic reactions in which oxygen takes place. Therefore, knowing the oxygen profile of sediments that face petroleum contamination is essential to adjust the bioremediation strategies accordingly.

3.2. Microbial Community and Metabolism Affected by Shifts in Sediments’ Oxygenation

The indigenous microbial population of marine sediments is interchangeably linked to the presence of oxygen. Shifts in sediment oxygenation result in shifts in microbial communities as different metabolic pathways prevail. In the oxic layer, aerobic biodegradation is promoted. Since the oxic layer is typically very thin, ranging from mm to cm, but microbial activities are known to be present even at great depths into the sediments, anaerobic metabolism is dominant. Nevertheless, oxygen deficiency in sediments can lead in changes in the microbial populations that could ultimately harm marine ecosystems and lead in alterations in the biogeochemical cycles [88]. A comprehensive study by Broman et al. [89] examined the changes in microbial populations and encoded genes for metabolic processes inflicted by shifts in oxygen levels in coastal oxic, intermediate, and anoxic zones. Their results supported that oxygenation of the sediments had a high impact on microbial communities. From experiments in the oxic-anoxic zone, they showed that anaerobic microorganisms are more likely to adapt in the presence of oxygen rather than the aerobic ones under anoxic conditions. Oxygenating anoxic sediments is likely to limit the release of produced methane to the atmosphere and re-oxygenating anoxic sediments can lead to an approximate 2.5 months of restoration of coastal dead zones [90], indicating that oxygenation is in fact an effective remediation strategy for marine sediments.

3.3. Oxygen Amendments

Providing oxygen is essential for bioremediation processes and can lead to a faster biodegradation of petroleum hydrocarbons, even the persistent heavier and aromatic compounds. An adequate supply of oxygen is of great importance to sustain the aerobic biodegradation of the indigenous microbiome. A number of technologies have been developed to provide oxygen for the enhancement of aerobic bioremediation. The most common techniques are presented below.

3.3.1. Oxygen Releasing Compounds

Oxygen releasing compounds are engineered chemical formulations, mainly designed to enhance in situ aerobic bioremediation of petroleum hydrocarbons in various aquatic environments including marine environments. However, their use can be expanded to sediment applications, when dispersed in a powdered form for the treatment of contaminants. The original Oxygen Releasing Compound (ORC®) is a patented phosphate-intercalated magnesium peroxide [91], which when in contact with water, produces a controlled-release of oxygen (10% w/w of molecular oxygen) [8] with up to a year of activity on a single application. Both the ORC and the produced hydroxide from the water reaction are environmentally benign and can be safely ingested, making this method suitable for direct application in sensitive ecosystems without a particular need for monitoring [92]. Their use is well established since they have been extensively tested over the past 27 years since their first appearance. It is proven that ORCs can accelerate aerobic biodegradation 10 to 100 times compared to the intrinsic rates of biodegradation [91], and accompanied by their long-lasting application, they are considered a highly cost-effective method for enhancing aerobic bioremediation. However, since oxygen can be incorporated into abiotic reactions as well, significant amounts could be consumed rapidly in undesirable reactions. Other types of peroxides such as calcium peroxide have also been employed for the release of oxygen in contaminated sediments [93]. Newly developed technologies of oxygen slow releasing materials (OSRM) [94] have been implemented for the bioremediation of hydrocarbon polluted sites and, by altering the concentration of the embedding medium, oxygen-releasing rates could be adjusted to the requirements of the aquatic environment. However, magnesium peroxide is the usual preference due to its low solubility, and the ability to release oxygen for a longer period [95]. ORCs have also been tested in research studies for the bioremediation of marine sediments as a biostimulation strategy [96]; however, their application in the marine environment has not been addressed in detail [63].

3.3.2. Pure Oxygen Injection

Pure oxygen has been widely used for the ex situ biodegradation of organic pollutants, but its in situ application is also feasible. Pure oxygen injection is another technique designed to promote aerobic bioremediation. Oxygen is introduced in its vapor phase (approximately 95% oxygen) into the saturated zone via vertical injection wells, specifically placed to meet the needs of the contaminated area. Oxygen is stored in a bulk tank, concentrated in a liquid form at ~−155 °C, and then passed through an ambient air vaporizer that adjusts the flowrate. Vapor oxygen is then injected to the site through spargers or other types of diffusers [97]. Compared to air injection, where atmospheric air is introduced to provide oxygen, pure oxygen injection could cause a four to fivefold increase in the dissolved oxygen concentration. To achieve high dissolved oxygen concentrations, oxygen is sparged at a low flow rate to optimize the contact time between oxygen and the contaminated zone which could be further increased by oxygen entrapment in the sediments. Low flow rates also reduce the risk of producing volatile organic vapors and migrating of the organic pollutants [8]. Field demonstrations of the method in polluted river sediments have proven the technique’s effectiveness in stimulating the aerobic biodegradation rates without affecting the overlying water quality [98].

3.3.3. Hydrogen Peroxide Infiltration

Hydrogen peroxide infiltration is a controversial method regarding its true impact on the environment. However, its application is considered to provide one of the highest levels of available oxygen to the contaminated area: half of the amount introduced to the site is stoichiometrically expected to provide molecular oxygen (H2O2 → ½ O2 + H2O). Hydrogen peroxide is introduced to shallow contaminated sediments by a system of pipes or sprinklers, but for deeper applications, injection wells are used [99]. When in contact with water, H2O2 decomposes rapidly, making it difficult to treat target zones and qualifying it as a cost-intensive process. Hydrogen peroxide may also be involved in non-beneficial reactions, both biotic and abiotic, resulting in significant losses in oxygen production [100,101]. Efforts have been made to stabilize H2O2 to prolong its decomposition as an oxygen provider but with little to no success so far [102]. In the presence of an iron catalyst, a concentrated form of hydrogen peroxide is used as a chemical oxidant (Fenton’s reagent) to produce highly toxic hydroxyl free radicals [103,104]. Microorganisms are not capable of withstanding large amounts of hydrogen peroxide. A typical concentration limit is 100–200 ppm [8] after which H2O2 becomes cytotoxic. Hence, the in situ use of hydrogen peroxide should be determined after a number of factors are taken into consideration such as the soil geochemistry, the native biota, and the type of contaminants [105]. The technique has been proven to enhance DO in lakes with positive results in enhancing organic matter removal from the sediments [106]; however, a field study on the bioremediation of organically polluted marine sediments, presented by Thomas et al. [107], showed no enhancement on the degradation of organic pollutants.

3.3.4. Ozone Injection

Ozonation transforms residual organics into available biodegradable products, including organic acids, and releases nitrate and reactive phosphate; hence, it should be able to accelerate the rate of total petroleum hydrocarbons (TPH) reduction during bioremediation, and reduce the need for external addition of nutrients. Thus, ozonation could enhance bioremediation by the removal of heavy petroleum hydrocarbons in the field [108]. Ozone injection, as well as hydrogen peroxide infiltration serves a dual application: ozone is used as a chemical oxidation treatment, while at the same time provides a substantial source of oxygen for the bioremediation processes. As a chemical oxidant, ozone can inhibit microbial activity, but this effect seems to be temporary, since the surviving microorganisms from ozone application are sufficient to sustain bioremediation [109]. Hydrogen peroxide and ozone are two of the most commonly employed chemical oxidants [110], but the in situ application for the bioremediation of organic polluted sediments is often inhibited by the unknown environmental side-effects and the difficulty of direct application on the sediments [111]. Ozone is added in dissolved or gaseous form and can diffuse into soil aggregates promoting aerobic bioremediation. It is 10 times more soluble in water than pure oxygen and when applied in the subsurface, ozone reacts with the organic pollutants and decomposes rapidly into oxygen. So far, no information is available concerning the proper dose of ozone that gives minimal mineralization [108]. A typical application involves injection or sparging of ozone gas at a 5% concentration in the contaminated area [109]. Due to the production of gases, soil vapor extraction wells might also be required.

4. Sediment Aeration

Besides the oxygen amendments, aeration techniques can be used to promote aerobic bioremediation. Sediment aeration is an essential process for enhancing the aerobic biodegradation of hydrocarbon pollutants that end up on the sediments of aquatic environments. Different aeration systems have been developed and can be applied depending on the type of aquatic environment (e.g., lakes, rivers, ponds, shorelines, ports, etc.). Especially in the case of marine environments, where sediments are the ultimate receiver of contaminants and anoxic conditions prevail and inhibit biodegradation processes, it is of great importance to generate new knowledge and solutions for a sustainable sediment aeration system. Sand is a high permeability sediment, hence the use of a form of aeration to provide oxygen could be practical. The most common sediment aeration techniques, including newly developed promising systems, are presented here.

4.1. Aeration Systems

4.1.1. Tilling

Tilling, which is also called mixing or aeration, is a physical method that disturbs the oiled sediment layer and increases the penetration depth of oxygen and nutrient supplements [112]. The goal of this method is to accelerate the natural oil removal process, by exposing the oiled sediments to weathering processes. Additionally, by mixing the sediments, oil is subjected to natural physical degradation, while nutrients, if applied, and oxygen can penetrate deeper into the sediments thus enhancing microbial degradation processes. Field demonstrations of the method on shallow sediments, however, show no significant effect of tilling on biodegradation rates [39,113,114]. The application of tilling is inhibited in sensitive ecosystems, such as salt marshes and wetlands, due to its destructive impact on vegetative growth [115].

4.1.2. Biosparging-Forced Aeration

Biosparging is a technique designed to introduce air for stimulation of the aerobic microbial community. It is applied to contaminated aquifers or sediments. High-pressure air is injected into the sediments, usually combined with the addition of nutrients, increasing the oxygen concentration, and enhancing biodegradation processes. Biosparging is a highly effective [116] and affordable technique, often cheaper among other remedial alternatives [117] due to the inexpensive and low-maintenance equipment that is used. It is not labor-intensive since it can be left unattended for long periods of time. The effectiveness of biosparging depends on the permeability of the sediments and the biodegradability of the contaminants [118]. High permeability sediments, such as sand and gravel, allow air to penetrate deeper and come in contact with remote microorganisms [119]. This capacity makes biosparging an attractive technique for marine sediment bioremediation, however an in situ application faces difficulties due to the dynamic profile of the environment. Biosparging cannot be applied in sites where high concentrations of inorganic salts, heavy metals, or organic compounds are present, as microbial growth is hindered [117].

4.1.3. Coarse and Fine Bubble Diffusers

Diffusers are an ever-evolving technology for providing oxygen for bioremediation purposes in different environmental settings. Depending on the generated bubble size, diffusers can significantly enhance the aeration effectiveness and can come in a wide variety of geometries, sizes, and shapes (tube, disc, plate, dome) to meet specific requirements of a process. Their cost is relatively low compared to other aeration systems. The material of construction shapes the size of the bubbles produced. Membrane (ethylene propylene diene terpolymer, silicone, nitrile rubber, thermoplastic polyurethane, etc.) and ceramic air diffusers for example, can provide significantly smaller air bubbles, even in the scale of nanometers. Each type of diffuser comes with different specifications regarding the service area (m2), the aeration volume (L/min) and the oxygenation capability (kg O2/h), directly linked to the size of the bubbles that are formed and the air flowrate that the system can have during operation. These technical characteristics, however, refer to water or wastewater testing and little is known for the efficiency of air diffusers when they are used for sediment aeration. Out of the different air diffuser configurations, the most suitable to come in contact with sediments and provide oxygen are the tube diffusers, placed on top of the sediments. Diffused-air system aerators use a low-pressure, high-volume air blower to provide air to diffusers. The aeration efficiency of the diffusers is interchangeably linked with depth of application and flow rate of air [120]. As most of the equipment subjected to contact with microorganisms and redox compounds, the diffusers may exhibit erosion, biofouling, clogging of the pores, subsequently resulting in decreased efficiency and additional expenses for maintenance and cleaning. Diffusers can be categorized into two broad categories based on the type of bubbles they create: coarse bubble diffusers and fine bubble diffusers.

Coarse Bubble Diffusers

Coarse bubble diffusers produce bubbles of diameters greater than 10 mm [121]. Due to their size, coarse bubbles are not indicated for aeration purposes rather than mixing actions. Produced bubbles have a very limited time when introduced in water. They tend to coalesce and quickly escape from the water column, providing minimum residency time. For this purpose, coarse bubble diffusers are selected in applications where the medium presents high viscosity, such as the wastewater treatment. In general, coarse bubble diffusers’ operation is cost and energy intensive. A more viable option of fine bubble diffusing systems has emerged and tends to eliminate the use of these diffusers. The only advantage of coarse bubble diffusers over the respective fine bubble ones is that due to larger pores, clogging could be avoided [119].

Fine Bubble Diffusers

Fine bubbles present a higher oxygen transfer efficiency (OTE); hence, they have gained a lot of attention against coarse bubble aeration systems. Their small size, typically less than 2 mm [122], provides a large surface area and enables higher residency time in the water due to less buoyancy forces [123]. Fine bubble diffusers are made of fine porous media such as ceramics, perforated membranes and porous plastics [124]. The advantages of smaller sized bubbles have led to the development of ultrafine pore diffusers which can produce bubbles in the scale of μm and nm. A more comprehensive overview of ultrafine (micro-nano) bubbles, which are nevertheless not produced by diffusers, is presented in Section 4.1.5.

4.1.4. Injectors

Injectors are used to provide air or oxygen into the sediments and aquatic environments. For soil remediation, a typical air injection system consists of an air compressor to create the appropriate pressure drop for sparging, air filters to prevent the compressor from dust particles or produced vapors that include contaminants, control valves to regulate flowrate, and vertical injection wells, 2.5–10 cm in diameter and 30–60 cm deep, in which the appropriate piping is set for injection [125]. This setup constitutes a direct injection method in which the reagents are injected directly into the subsurface [126]. In aquatic environments, injectors are used for the recirculation of water, an injection method in which groundwater is extracted, mixed with air or oxygen and other nutrients and then reinjected from another injection well or from the same well (pull-push method). Direct injection, on the other hand, is only effective at sites with moderate groundwater flow, otherwise good distribution of the air within the plume is not achieved [127]. These methods mix the air with water, providing an oxygen rich jet which can promote efficient horizontal mixing of the aquifer but fails to promote the dissolution of oxygen vertically in the water column. This application is also constrained by the sediment characteristics: large constituents such as gravels or cobbles inhibit the application of this method [127].

4.1.5. Micro-Nano Bubbles Technology

The use of micro and nano bubbles has extended beyond the diffusers. Their special characteristics have made them an attractive choice for use in air sparging as well, for bioremediation purposes [128]. Microbubbles diameter ranges between 10–50 μm and for nanobubbles is less than 200 nm [129]. When both types of bubbles are introduced into a system, their diameter ranges between 0.1–50 μm [130]. Research has shown that nanobubbles in water have a life expectancy that can reach up to weeks and even months in some cases [131]. Bubbles with diameters in the scale of microns offer a large surface area, thus being ideal for enhancing the oxygen transfer efficiency. Nanobubbles offer other advantages as well. They are found to be negatively charged [132], which prevents coalescence between the bubbles due to repulsion forces, resulting in high mass transfer efficiency and promoting self-pressurization dissolution [133]; their high inner pressure leads to fast diffusion of entrapped gases, which leads the bubbles to shrink even further and finally collapse, providing a large number of free radicals [128]. Specially designed generators have been developed over the years to produce tiny bubbles of air that can apply in a wide range of operations; from pharmaceuticals to wastewater treatment and can be categorized into two types. First the gas-water circulation type, where gas is introduced into a water vortex and breaks down into bubbles and second, the pressurized dissolution type, where about 5% of gas is under pressure dissolved in water and upon depressurization, the gas escapes forming nanobubbles [134]. Nanobubbles technology has shown to significantly improve water quality in an urban river, causing an 8-fold increase in the DO concentrations [135].

4.1.6. Mechanical Agitation

Mechanical agitation could be as important as aeration, since it can increase the rate of oxygen transfer from the air bubbles to the water column and also increase the rate of nutrient supply to microorganisms. Wave and tidal forces in the marine environment sometimes offer naturally the proper mechanical agitation needed to replenish oxygen in the water column and sediments. However, these forces are absent in closed aquatic environments, such as lakes, ponds, and ports; hence, it is important to provide some kind of agitation for better oxygen distribution. In this case, pumps and paddle wheels are preferable for aeration but require a great amount of energy for throwing large quantities of water into the air. Aeration systems with a high air or oxygen flowrate could also cause agitation: typical examples are the coarse bubble diffusers and direct-push injection wells.

4.1.7. Active Nautical Depth

First introduced in the port of Emden in Germany in 1990 [136], Active Nautical Depth (AND) is a sediment management technology which evolved as an alternative to dredging for minimizing siltation and maintaining navigable ports and harbors. AND derives from the concept of Passive Nautical Depth (PND), an alternative way to determine the depth of ports using density parameters, by the fact that fluid mud is created in situ by mixing and aerating the mud at the bottom of the water column which makes it navigable and therefore increases the nautical depth. The method uses a low-power submerged dredge pump that fluidizes the mud by breaking the inter-particle bonds and transfers it into a hopper dredger where it is aerated by exposure to the atmosphere and placed back to the bottom of the water body. The resuspension and aeration promote the aerobic growth of microorganisms and the production of extracellular polymeric substances (EPS) which allow particles to be kept in suspension for longer [137] and the fluid remains navigable for weeks. AND has limitations regarding the sediment particle size: it can be applied to muddy substrates with a sand content up to 10% [138]. In cases of higher sand content, the hopper dredger can perform sand extraction. Besides sediment management, AND has recently gained attention as a biostimulation method for the degradation of contaminants found in ports, such as tributyltin, a toxic xenobiotic found in aquatic environments [139]. This is due to the fact that AND changes the physicochemical properties of the sediment while maintaining aerobic conditions. However, sediment resuspension caused by this method, perturbates the aquatic ecosystem, therefore side-effects should be carefully examined prior to application.

4.1.8. Floating Bioreactor

This aeration technique was first presented by Thomas et al. [107] and involves a floating device developed to treat sediments with organic pollutants by airlifting and by resettling the aerated sediments at the same place. The main objective of the process is not to move dredged sediments to an onshore facility for treatment or disposal, but to recycle them at the same place where they have been accumulated. It is a similar method to airlift suspension reactors used for biodegradation processes. An airlift pump lifts the sediments above the water table. Compressed air is introduced right above the inlet of the riser pipe, creating a stream of air bubbles aiding the upwards movement of sediment particles and water. A knockout tank is integrated in the system where volatiles are stripped and treated with granulated activated coal. The lifted and aerated sediment suspension can be treated on-site through conventional separation and dewatering techniques but also reintroduced to the bottom of the water body. The acceleration with oxygen rich air not only stimulates microbiological degradation effects but also strengthens precipitation by flocculation. Since suspension can have a negative impact on the aquatic ecosystem by spreading the contaminants, floating barriers are used to control sediments during extraction and resuspension. Resettling process can be controlled with fixed cone shields and silt curtains to avoid contamination of the water column.

4.1.9. Modular Slurry System (MSS)

A modular slurry system was initially introduced in 2014 [27] in an effort to provide sufficient oxygen for the biodegradation of oil polluted marine sediments avoiding the ex situ practices that could cause contamination of adjacent aquifers. The containment of marine sediments and the introduction of air through a submerged reactor resulted in 98% removal of the total extracted and resolved hydrocarbons and a decrease in toxicity of the contaminants in the area treated, thus indicating an efficient stimulation of the indigenous hydrocarbon degrading microorganisms [27]. A year later, Capello et al. [140] applied the MSS with simultaneous addition of nutrients to sustain aerobic bioremediation, and the results supported the previous findings, suggesting that in situ aeration of contaminated marine sediments after capping could be a feasible approach.

4.1.10. Module for the Decontamination of Units of Sediment (MODUS)

Another novel technology for the aeration of sediments was introduced in 2020 [141]. The so-called module for the decontamination of units of sediment (MODUS) is a bench-scale system designed to aerate the bottom of the water column through a laminar flow directed tangentially to the seabed, without perturbing the top sediment layer. In a different approach, this technology could cause the oxygenation of sinking organic matter to the bottom of the sea or other aquatic ecosystems, resulting in the formation of a bio-oxy layer (bio-ox-capping) which is the development of oxygen-rich sediment layers. Left undisturbed, this layer would promote the aerobic metabolic activities of the indigenous microbiome and would restore the ecosystem prior to contamination toxicity.

5. Aerobic Bioremediation of Sediments—Case Studies

Engineered bioremediation was used extensively for the first time in Alaska shorelines after the Exxon Valdez oil spill in 1989, by means of the application of oleophilic and slow-release fertilizers [142,143,144], enhancing the biodegradation rates of oil. Since then, bioremediation has been applied to treat shallow polluted sediments in a number of situations. Early field demonstrations for sediment bioremediation in coastal environments and shorelines have been previously reviewed by Swannell et al. [145], and in salt marshes by Zhu et al. [146]. Table 1 presents the most recent field applications on aerobic sediment bioremediation from oil contaminants with focus on case studies that involve oxygen amendments and aeration.

6. Conclusions and Perspectives

Site characterization is the primary concern prior to applying any bioremediation technique. Ex situ techniques that involve the dredging of contaminated sediments often come at higher costs, attributed to excavation and transport and present high probability of contaminant spreading during the removal. In situ techniques tend to be less invasive to the environment and cost-effective; nevertheless, their application must be in accordance with a number of factors. Sensitive ecosystems, for example, require a more delicate bioremediation approach.
The main consideration for treating sediments is to apply the most suitable and effective technique for oxygen supply. Oxygen being the limiting factor in sediment treatment often leads to long bioremediation times where the anaerobic metabolism of the indigenous microorganisms is employed. Different approaches have evolved to enhance anaerobic bioremediation; however, the time of the treatment still remains significantly slower than the one under aerobic conditions. Oxygen supply in some form seems to be the most efficient approach for the enhancement of the aerobic bioremediation. The quest for efficient aeration techniques has led in the development of novel technologies to provide alternatives for sediment bioremediation.
Among the sediments, marine sediments pose a real challenge for treatment due to the dynamic environment of the seas, linked with the high hydrostatic pressures of the deep ocean floor, and make any bioremediation implementation difficult. However, it is of great importance to address this matter because it poses great threat for marine ecosystems. Deep sea sediments bioremediation is still under investigation; nonetheless, suggestions can be made for sediment bioremediation in marine shorelines and commercial ports that directly affect human life.
Sediments in shorelines are known to be treated in situ with tilling during low tide, for better penetration of oxygen and nutrients, but other bioremediation techniques can be implemented. Phytoremediation could be the solution for sensitive environments such as salt marshes and mangroves. The use of aeration techniques in inhibited by tidal and wave activities of the shorelines. In the case of commercial ports, microporous aeration operated above the sediment or AND could be implemented for aerobic bioremediation purposes. The application of a MSS has proven the method’s efficiency. Microporous aeration, coupled with specialized injection systems or diffusers, seems to be very promising in providing sufficient quantities of oxygen for enhanced aerobic bioremediation and, thus, could constitute a bioremediation strategy for the intricate environment of marine sediments.

Author Contributions

Conceptualization, T.M. and N.K.; methodology, E.F. and E.A.; resources, N.K.; writing—original draft preparation, E.F.; writing—review and editing, N.K., I.D., T.M., M.T. and E.A.; supervision, N.K.; project administration, I.D.; funding acquisition, T.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research was co-financed by the European Union and Greek national funds through the Operational Program Competitiveness, Entrepreneurship, and Innovation, under the call RESEARCH –CREATE –INNOVATE (Project Code: T1EDK-04256, WAVE2ENERGY: Wave to Energy: Innovative Technology for Direct and Indirect Utilization).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Chen, J.; Zhang, W.; Li, S.; Zhang, F.; Zhu, Y.; Huang, X. Identifying critical factors of oil spill in the tanker shipping industry worldwide. J. Clean. Prod. 2018, 180, 1–10. [Google Scholar] [CrossRef]
  2. Jernelöv, A. The threats from oil spills: Now, then, and in the future. Ambio 2010, 39, 353–366. [Google Scholar] [CrossRef] [Green Version]
  3. On Scene Coordinator Report: Deepwater Horizon Oil Spill. Available online: https://lccn.loc.gov/2012427375 (accessed on 4 July 2021).
  4. Zhang, B.; Matchinski, E.J.; Chen, B.; Ye, X.; Jing, L.; Lee, K. Marine oil spills-Oil pollution, sources and effects. In World Seas: An Environmental Evaluation, 2nd ed.; Sheppard, C., Ed.; Academic Press: Cambridge, MA, USA, 2018; Volume 3, pp. 391–406. [Google Scholar]
  5. Mapelli, F.; Scoma, A.; Michoud, G.; Aulenta, F.; Boon, N.; Borin, S.; Kalogerakis, N.; Daffonchio, D. Biotechnologies for Marine Oil Spill Cleanup: Indissoluble Ties with Microorganisms. Trends Biotechnol. 2017, 35, 860–870. [Google Scholar] [CrossRef]
  6. Hoang, A.T.; Pham, V.V.; Nguyen, D.N. A Report of Oil Spill Recovery Technologies. Int. J. Appl. Eng. Res. 2018, 13, 4915–4928. [Google Scholar]
  7. Milić, J.S.; Beškoski, V.P.; Ilić, M.V.; Ali, S.A.M.; Gojgić-Cvijović, G.D.; Vrvić, M.M. Bioremediation of soil heavily contaminated with crude oil and its products: Composition of the microbial consortium. J. Serb. Chem. Soc. 2009, 74, 455–460. [Google Scholar] [CrossRef]
  8. Introduction to in Situ Bioremediation of Groundwater. Available online: https://www.epa.gov/remedytech/introduction-situ-bioremediation-groundwater (accessed on 2 July 2021).
  9. Paniagua-Michel, J.; Rosales, A. Marine Bioremediation—A Sustainable Biotechnology of Petroleum Hydrocarbons Biodegradation in Coastal and Marine Environments. J. Bioremediat. Biodegrad. 2015, 6, 273. [Google Scholar]
  10. Xia, Y.; Boufadel, M.C. Lessons from the Exxon Valdez Oil Spill Disaster in Alaska. Disaster Adv. 2010, 3, 270–273. [Google Scholar]
  11. Kimes, N.E.; Callaghan, A.V.; Suflita, J.M.; Morris, P.J. Microbial transformation of the Deepwater Horizon oil spill-past, present, and future perspectives. Front. Microbiol. 2014, 5, 603. [Google Scholar] [CrossRef]
  12. Ron, E.Z.; Rosenberg, E. Enhanced bioremediation of oil spills in the sea. Curr. Opin. Biotechnol. 2014, 27, 191–194. [Google Scholar] [CrossRef] [PubMed]
  13. Rocchetti, L.; Beolchini, F.; Ciani, M.; Dell’Anno, A. Improvement of Bioremediation Performance for the Degradation of Petroleum Hydrocarbons in Contaminated Sediments. Appl. Environ. Soil Sci. 2011, 2011, 319657. [Google Scholar] [CrossRef]
  14. Vitali, F.; Mandalakis, M.; Chatzinikolaou, E.; Dialianis, T.; Senatore, G.; Casalone, E.; Mastromei, G.; Sergi, S.; Lussu, R.; Arvanitidis, C.; et al. Benthic prokaryotic community response to polycyclic aromatic hydrocarbon chronic exposure: Importance of emission sources in Mediterranean ports. Front. Mar. Sci. 2019, 6, 1–13. [Google Scholar] [CrossRef]
  15. El Fantroussi, S.; Agathos, S.N. Is bioaugmentation a feasible strategy for pollutant removal and site remediation? Curr. Opin. Microbiol. 2005, 8, 268–275. [Google Scholar] [CrossRef]
  16. Venosa, A.; Suidan, M.; Wrenn, B.; Strohmeier, K.L.; Haines, J.; Eberhart, B.; King, A.; Holder, E. Bioremediation of an Experimental Oil Spill on the Shoreline of Delaware Bay. Environ. Sci. Technol. 1996, 30, 1764–1775. [Google Scholar] [CrossRef]
  17. Lee, V.K.; Levy, E.M. Enhanced biodegradation of a light crude oil in sandy beaches. In Proceedings of the 1987 International Oil Spill Conference, Baltimore, MA, USA, 6–9 April 1987; pp. 411–416. [Google Scholar]
  18. Simon, M.A.; Bonner, J.S.; Page, C.A.; Townsend, R.T.; Mueller, D.C.; Fuller, C.B.; Autenrieth, R.L. Evaluation of two commercial bioaugmentation products for enhanced removal of petroleum from a wetland. Ecol. Eng. 2004, 22, 263–277. [Google Scholar] [CrossRef]
  19. Fodelianakis, S.; Antoniou, E.; Mapelli, F.; Magagnini, M.; Nikolopoulou, M.; Marasco, R.; Barbato, M.; Tsiola, A.; Tsikopoulou, I.; Giaccaglia, L.; et al. Allochthonous bioaugmentation in ex situ treatment of crude oil-polluted sediments in the presence of an effective degrading indigenous microbiome. J. Hazard. Mater. 2015, 287, 78–86. [Google Scholar] [CrossRef] [Green Version]
  20. Mrozik, A.; Piotrowska-Seget, Z. Bioaugmentation as a strategy for cleaning up of soils contaminated with aromatic compounds. Microbiol. Res. 2010, 165, 363–375. [Google Scholar] [CrossRef] [PubMed]
  21. Wang, C.; He, S.; Zou, Y.; Liu, J.; Zhao, R.; Yin, X.; Zhang, H.; Li, Y. Quantitative evaluation of in-situ bioremediation of compound pollution of oil and heavy metal in sediments from the Bohai Sea, China. Mar. Pollut. Bull. 2020, 150, 110787. [Google Scholar] [CrossRef]
  22. Zhao, G.; Sheng, Y.; Wang, C.; Yang, J.; Wang, Q.; Chen, L. In situ microbial remediation of crude oil-soaked marine sediments using zeolite carrier with a polymer coating. Mar. Pollut. Bull. 2018, 129, 172–178. [Google Scholar] [CrossRef]
  23. Gallego, J.R.; Fernández, L.; Fernández, J.R.; Díez-Sanz, F.; Ordóñez, S.; González-Rojas, E.; Pelaez, A.I.; Sánchez, J. On Site Bioremediation and Washing Techniques in a Cobble Beach Affected by Prestige Oil Spill. In Modern Multidisciplinary Applied Microbiology: Exploiting Microbes and Their Interactions; Mendez-Vilas, A., Ed.; John Wiley and Sons: Hoboken, NJ, USA, 2008; pp. 556–560. [Google Scholar]
  24. Dueholm, M.S.; Marques, I.G.; Karst, S.M.; D’Imperio, S.; Tale, V.P.; Lewis, D.; Nielsen, P.H.; Nielsen, J.L. Survival and activity of individual bioaugmentation strains. Bioresour. Technol. 2015, 186, 192–199. [Google Scholar] [CrossRef]
  25. Hosokawa, R.; Nagai, M.; Morikawa, M.; Okuyama, H. Autochthonous bioaugmentation and its possible application to oil spills. World, J. Microbiol. Biotechnol. 2009, 25, 1519–1528. [Google Scholar] [CrossRef] [Green Version]
  26. Nikolopoulou, M.; Pasadakis, N.; Kalogerakis, N. Evaluation of autochthonous bioaugmentation and biostimulation during microcosm-simulated oil spills. Mar. Pollut. Bull. 2013, 72, 165–173. [Google Scholar] [CrossRef] [PubMed]
  27. Genovese, M.; Crisafi, F.; Denaro, R.; Cappello, S.; Russo, D.; Calogero, R.; Santisi, S.; Catalfamo, M.; Modica, A.; Smedile, F.; et al. Effective bioremediation strategy for rapid in situ cleanup of anoxic marine sediments in mesocosm oil spill simulation. Front. Microbiol. 2014, 5, 162. [Google Scholar] [CrossRef] [Green Version]
  28. Andreoni, V.; Gianfreda, L. Bioremediation and monitoring of aromatic-polluted habitats. Appl. Microbiol. Biotechnol. 2007, 76, 287–308. [Google Scholar] [CrossRef]
  29. Prince, R.C. Biostimulation of Marine Crude Oil Spills Using Dispersants. In Hydrocarbon and Lipid Microbiology Protocols, 1st ed.; McGenity, T., Timmis, K., Nogales, B., Eds.; Springer: Berlin/Heidelberg, Germany, 2015; pp. 95–104. [Google Scholar]
  30. Phytoremediation of Contaminated Soil and Ground Water at Hazardous Waste Sites. Available online: https://www.epa.gov/remedytech/phytoremediation-contaminated-soil-and-ground-water-hazardous-waste-sites (accessed on 10 July 2021).
  31. Haritash, A.K.; Kaushik, C.P. Biodegradation aspects of Polycyclic Aromatic Hydrocarbons (PAHs): A review. J. Hazard. Mater. 2009, 169, 1–15. [Google Scholar] [CrossRef] [PubMed]
  32. Roy, A.; Dutta, A.; Pal, S.; Gupta, A.; Sarkar, J.; Chatterjee, A.; Saha, A.; Sarkar, P.; Sar, P.; Kazy, S.K. Biostimulation and bioaugmentation of native microbial community accelerated bioremediation of oil refinery sludge. Bioresour. Technol. 2018, 253, 22–32. [Google Scholar] [CrossRef]
  33. Atlas, R.M. Microbial degradation of petroleum hydrocarbons: An environmental perspective. Microbiol. Rev. 1981, 45, 180–209. [Google Scholar] [CrossRef]
  34. Atlas, R.M.; Bartha, R. Hydrocarbon Biodegradation and Oil Spill Bioremediation. In Advances in Microbial Ecology; Marshall, K.C., Ed.; Springer: Boston, MA, USA, 1992; Volume 12, pp. 287–338. [Google Scholar]
  35. Misselbrook, T.; Bittman, S.; Cordovil, C.M.D.S.; Rees, B.; Sylvester-Bradley, R.; Olesen, J.; Vallejo, A. Field Application of Organic and Inorganic Fertilizers and Manure. Draft Section for a Guidance Document. In Proceedings of the Workshop on Integrated Sustainable Nitrogen Management, Brussels, Belgium, 30 September–2 October 2019. [Google Scholar]
  36. Azubuike, C.C.; Chikere, C.B.; Okpokwasili, G.C. Bioremediation techniques–classification based on site of application: Principles, advantages, limitations and prospects. World J. Microbiol. Biotechnol. 2016, 32, 180. [Google Scholar] [CrossRef] [Green Version]
  37. Xu, R.; Lau, N.L.A.; Ng, K.L.; Obbard, J.P. Application of a slow-release fertilizer for oil bioremediation in beach sediment. J. Environ. Qual. 2004, 33, 1210–1216. [Google Scholar] [CrossRef] [PubMed]
  38. Xu, R.; Lau, A.N.L.; Lim, Y.G.; Obbard, J.P. Bioremediation of oil-contaminated sediments on an inter-tidal shoreline using a slow-release fertilizer and chitosan. Mar. Pollut. Bull. 2005, 51, 1062–1070. [Google Scholar] [CrossRef] [PubMed]
  39. Prince, R.C.; Bare, R.E.; Garrett, R.M.; Grossman, M.J.; Haith, C.E.; Keim, L.G.; Lee, K.; Holtom, G.J.; Lambert, P.; Sergy, G.A.; et al. Bioremediation of stranded oil on an arctic shoreline. Spill Sci. Technol. Bull. 2003, 8, 303–312. [Google Scholar] [CrossRef]
  40. Gallego, J.R.; Fernández, J.R.; Díez-Sanz, F.; Ordóñez, S.; Sastre, H.; González-Rojas, E.; Pelaez, A.I.; Sánchez, J. Bioremediation for shoreline cleanup: In situ vs. on-site treatments. Environ. Eng. Sci. 2007, 24, 493–504. [Google Scholar] [CrossRef]
  41. Jiménez, N.; Viñas, M.; Sabaté, J.; Díez, S.; Bayona, J.M.; Solanas, A.M.; Albaiges, J. The Prestige oil spill. Enhanced biodegradation of a heavy fuel oil under field conditions by the use of an oleophilic fertilizer. Environ. Sci. Technol. 2006, 40, 2578–2585. [Google Scholar] [CrossRef] [PubMed]
  42. Ramsay, M.A.; Swannell, R.P.J.; Shiptonà, W.A.; Duke, N.C.; Hill, R.T. Effect of Bioremediation on the Microbial Community in Oiled Mangrove Sediments. Mar. Pollut. Bull. 2000, 41, 413–419. [Google Scholar] [CrossRef]
  43. Geng, X.; Pan, Z.; Boufadel, M.C.; Ozgokmen, T.; Lee, K.; Zhao, L. Simulation of oil bioremediation in a tidally influenced beach: Spatiotemporal evolution of nutrient and dissolved oxygen. J. Geophys. Res. Ocean. 2016, 121, 2385–2404. [Google Scholar] [CrossRef]
  44. Tate, P.T.; Shin, W.S.; Pardue, J.H.; Jackson, W.A. Bioremediation of an experimental oil spill in a coastal Louisiana salt marsh. Water Air Soil Pollut. 2012, 223, 1115–1123. [Google Scholar] [CrossRef]
  45. Ritzkowski, M.; Heyer, K.U.; Stegmann, R. Fundamental processes and implications during in situ aeration of old landfills. Waste Manag. 2006, 26, 356–372. [Google Scholar] [CrossRef]
  46. Coates, J.D.; Anderson, R.T.; Woodward, J.C.; Phillips, E.J.P.; Lovley, D.R. Anaerobic Hydrocarbon Degradation in Petroleum-Contaminated Harbor Sediments under Sulfate-Reducing and Artificially Imposed Iron-Reducing Conditions. Environ. Sci. Technol. 1996, 30, 2784–2789. [Google Scholar] [CrossRef]
  47. How to Evaluate Alternative Cleanup Technologies for Underground Storage Tank Sites—A Guide for Corrective Action Plan Reviewers, Chapter 5, Landfarming. Available online: https://www.epa.gov/ust/how-evaluate-alternative-cleanup-technologies-underground-storage-tank-sites-guide-corrective (accessed on 11 July 2021).
  48. Fogel, S.; Norris, R.; Crockett, E.; Findlay, M. Enhanced Bioremediation Techniques for In Situ and On-Site Treatment of Petroleum-Contaminated Soils and Groundwater. Dairy Food Environ. Sanit. 1988, 9, 240–244. [Google Scholar]
  49. Goldsmith, C.D.; Balderson, R.K. Biokinetic Constants of a Mixed Microbial Culture with Model Diesel Fuel. Hazard. Waste Hazard. Mater. 1989, 6, 145–154. [Google Scholar] [CrossRef]
  50. Duke, N.C.; Burns, K.A.; Swannell, R.P.J.; Dalhaus, O.; Rupp, R.J. Dispersant Use and a Bioremediation Strategy as Alternate Means of Reducing Impacts of Large Oil Spills on Mangroves: The Gladstone Field Trials. Mar. Pollut. Bull. 2000, 41, 403–412. [Google Scholar] [CrossRef]
  51. Ferguson, R.M.W.; Gontikaki, E.; Anderson, J.A.; Witte, U. The variable influence of dispersant on degradation of oil hydrocarbons in subarctic deep-sea sediments at low temperatures (0–5 °C). Sci. Rep. 2017, 7, 2253. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Jahan, R.; Bodratti, A.M.; Tsianou, M.; Alexandridis, P. Biosurfactants, natural alternatives to synthetic surfactants: Physicochemical properties and applications. Adv. Colloid Interface Sci. 2020, 275, 102061. [Google Scholar] [CrossRef] [PubMed]
  53. Naughton, P.J.; Marchant, R.; Naughton, V.; Banat, I.M. Microbial biosurfactants: Current trends and applications in agricultural and biomedical industries. J. Appl. Microbiol. 2019, 127, 12–28. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Silva R de, C.F.S.; Almeida, D.G.; Rufino, R.D.; Luna, J.M.; Santos, V.A.; Sarubbo, L.A. Applications of biosurfactants in the petroleum industry and the remediation of oil spills. Int. J. Mol. Sci. 2014, 15, 12523–12542. [Google Scholar] [CrossRef]
  55. De Almeida, D.G.; Soares Da Silva, R.C.; Luna, J.M.; Rufino, R.D.; Santos, V.A.; Banat, I.M.; Sarubbo, L.A. Biosurfactants: Promising Molecules for Petroleum Biotechnology Advances. Front. Microbiol. 2016, 7, 1718. [Google Scholar] [CrossRef] [Green Version]
  56. Lee, D.W.; Lee, H.; Kwon, B.O.; Khim, J.S.; Yim, U.H.; Kim, B.S.; Kim, J.J. Biosurfactant-assisted bioremediation of crude oil by indigenous bacteria isolated from Taean beach sediment. Environ. Pollut. 2018, 241, 254–264. [Google Scholar] [CrossRef]
  57. Sáenz-Marta, C.I.; Ballinas-Casarrubias, M.L.; Rivera-Chavira, B.E.; Nevárez-Moorillón, G.V. Biosurfactants as Useful Tools in Bioremediation. In Advances in Bioremediation of Wastewater and Polluted Soil; Shiomi, N., Ed.; IntechOpen: London, UK, 2015. [Google Scholar]
  58. Mandalenaki, A.; Kalogerakis, N.; Antoniou, E. Production of high purity biosurfactants using heavy oil residues as carbon source. Energies 2021, 14, 3557. [Google Scholar] [CrossRef]
  59. Kamath, R.; Rentz, J.A.; Schnoor, J.L.; Alvarez, P.J.J. Phytoremediation of Hydrocarbon-Contaminated Soils: Principles and Applications. Stud. Surf. Sci. Catal. 2004, 151, 447–478. [Google Scholar]
  60. Schnoor, J.L.; Licht, L.A.; McCutcheon, S.C.; Wolfe, N.L.; Carreira, L.H. Phytoremediation of Organic and Nutrient Contaminants. Environ. Sci. Technol. 1995, 29, 318–323. [Google Scholar] [CrossRef] [PubMed]
  61. Ribeiro, H.; Mucha, A.P.; Almeida, C.M.R.; Bordalo, A.A. Potential of phytoremediation for the removal of petroleum hydrocarbons in contaminated salt marsh sediments. J. Environ. Manag. 2014, 137, 10–15. [Google Scholar] [CrossRef]
  62. Moreira, I.T.A.; Oliveira, O.M.C.; Triguis, J.A.; dos Santos, A.M.P.; Queiroz, A.F.S.; Martins, C.M.S.; Silva, C.S.; Jesus, R.S. Phytoremediation using Rizophora mangle L. in mangrove sediments contaminated by persistent total petroleum hydrocarbons (TPH’s). Microchemical 2011, 99, 376–382. [Google Scholar] [CrossRef]
  63. Lee, K.; Merlin, F.X. Bioremediation of oil on shoreline environments: Development of techniques and guidelines. Pure Appl. Chem. 1999, 71, 161–171. [Google Scholar] [CrossRef] [Green Version]
  64. Baker, J.M.; Leonardo, G.M.; Bartlett, P.D.; Little, D.I.; Wilson, M.C. Long-term fate and effects of untreated thick oil deposits on salt marshes. In International Oil Spill Conference Proceedings 1993; pp. 395–399. Available online: https://meridian.allenpress.com/iosc/article/1993/1/395/198706/LONG-TERM-FATE-AND-EFFECTS-OF-UNTREATED-THICK-OIL (accessed on 5 June 2021).
  65. Merkl, N.; Schultze-Kraft, R.; Arias, M. Influence of fertilizer levels on phytoremediation of crude oil-contaminated soils with the tropical pasture grass Brachiaria brizantha (Hochst. ex a. rich.) stapf. Int. J. Phytoremediation 2005, 7, 217–230. [Google Scholar] [CrossRef]
  66. Kumar, G.; Shahi, S.K.; Singh, S. Bioremediation: An Eco-sustainable Approach for Restoration of Contaminated Sites. In Microbial Bioprospecting for Sustainable Development, 1st ed.; Singh, J., Sharma, D., Kumar, G., Sharma, N.R., Eds.; Springer: Singapore, 2018; pp. 115–136. [Google Scholar]
  67. Frutos, F.J.C.; Pérez, R.; Escolano, O.; Rubio, A.; Gimeno, A.; Fernandez, M.D.; Carbonell, G.; Perucha, C.; Laguna, J. Remediation trials for hydrocarbon-contaminated sludge from a soil washing process: Evaluation of bioremediation technologies. J. Hazard. Mater. 2012, 199–200, 262–271. [Google Scholar] [CrossRef] [PubMed]
  68. Smith, E.; Thavamani, P.; Ramadass, K.; Naidu, R.; Srivastava, P.; Megharaj, M. Remediation trials for hydrocarbon-contaminated soils in arid environments: Evaluation of bioslurry and biopiling techniques. Int. Biodeterior. Biodegrad. 2015, 101, 56–65. [Google Scholar] [CrossRef]
  69. Chen, Z.; Huang, Y.C.; Liang, J.H.; Zhao, F.; Zhu, Y.G. A novel sediment microbial fuel cell with a biocathode in the rice rhizosphere. Bioresour. Technol. 2012, 108, 55–59. [Google Scholar] [CrossRef] [PubMed]
  70. Li, W.W.; Yu, H.Q. Stimulating sediment bioremediation with benthic microbial fuel cells. Biotechnol. Adv. 2015, 33, 1–12. [Google Scholar] [CrossRef]
  71. Morris, J.M.; Jin, S. Enhanced biodegradation of hydrocarbon-contaminated sediments using microbial fuel cells. J. Hazard. Mater. 2012, 213–214, 474–477. [Google Scholar] [CrossRef] [PubMed]
  72. Matturro, B.; Viggi, C.C.; Aulenta, F.; Rossetti, S. Cable bacteria and the bioelectrochemical Snorkel: The natural and engineered facets playing a role in hydrocarbons degradation in marine sediments. Front. Microbiol. 2017, 8, 1–13. [Google Scholar] [CrossRef] [Green Version]
  73. Hoareau, M.; Erable, B.; Bergel, A. Microbial electrochemical snorkels (MESs): A budding technology for multiple applications. A mini review. Electrochem. Commun. 2019, 104, 106473. [Google Scholar] [CrossRef]
  74. Viggi, C.C.; Presta, E.; Bellagamba, M.; Kaciulis, S.; Balijepalli, S.K.; Zanaroli, G.; Papini, M.P.; Rossetti, S.; Aulenta, F. The “Oil-Spill Snorkel”: An innovative bioelectrochemical approach to accelerate hydrocarbons biodegradation in marine sediments. Front. Microbiol. 2015, 6, 881. [Google Scholar]
  75. Aulenta, F.; Palma, E.; Marzocchi, U.; Viggi, C.C.; Rossetti, S.; Scoma, A. Enhanced hydrocarbons biodegradation at deep-sea hydrostatic pressure with microbial electrochemical snorkels. Catalysts 2021, 11, 263. [Google Scholar] [CrossRef]
  76. Pfeffer, C.; Larsen, S.; Song, J.; Dong, M.; Besenbacher, F.; Meyer, R.L.; Kjeldsen, K.U.; Schreiber, L.; Gorby, Y.A.; El-Naggar, M.Y.; et al. Filamentous bacteria transport electrons over centimetre distances. Nature 2012, 491, 218–221. [Google Scholar] [CrossRef]
  77. Meysman, F.J.R. Cable Bacteria Take a New Breath Using Long-Distance Electricity. Trends Microbiol. 2018, 26, 411–422. [Google Scholar] [CrossRef]
  78. Liu, F.; Wang, Z.; Wu, B.; Bjerg, J.T.; Hu, W.; Guo, X.; Guo, J.; Nielsen, L.P.; Qiu, R.; Xu, M. Cable bacteria extend the impacts of elevated dissolved oxygen into anoxic sediments. ISME J. 2021, 15, 1551–1563. [Google Scholar] [CrossRef] [PubMed]
  79. Bjerg, J.T.; Boschker, H.T.S.; Larsen, S.; Berry, D.; Schmid, M.; Millo, D.; Tataru, P.; Meysman, F.J.R.; Wagner, M.; Nielsen, L.P.; et al. Long-distance electron transport in individual, living cable bacteria. Proc. Natl. Acad. Sci. USA. 2018, 115, 5786–5791. [Google Scholar] [CrossRef] [Green Version]
  80. Müller, H.; Bosch, J.; Griebler, C.; Damgaard, L.R.; Nielsen, L.P.; Lueders, T.; Meckenstock, R.U. Long-distance electron transfer by cable bacteria in aquifer sediments. ISME J. 2016, 10, 2010–2019. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  81. Cai, W.J.; Sayles, F.L. Oxygen penetration depths and fluxes in marine sediments. Mar. Chem. 1996, 52, 123–131. [Google Scholar] [CrossRef]
  82. Cai, W.J.; Reimers, C.E. Benthic oxygen flux, bottom water oxygen concentration and core top organic carbon content in the deep northeast Pacific Ocean. Deep Sea Res. Part I 1995, 42, 1681–1699. [Google Scholar] [CrossRef]
  83. Orcutt, B.N.; Wheat, C.G.; Rouxel, O.; Hulme, S.; Edwards, K.J.; Bach, W. Oxygen consumption rates in subsea floor basaltic crust derived from a reaction transport model. Nat. Commun. 2013, 4, 1–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Testing Micro-Nanobubble Generating Device at Different Salinities. Available online: https://www.aquaculturealliance.org/advocate/testing-micro-nanobubble-generating-device-at-different-salinities/ (accessed on 8 July 2021).
  85. Schmidtko, S.; Stramma, L.; Visbeck, M. Decline in global oceanic oxygen content during the past five decades. Nature 2017, 542, 335–339. [Google Scholar] [CrossRef]
  86. Brendel, P.J.; Luther, G.W. Development of a Gold Amalgam Voltammetric Microelectrode for the Determination of Dissolved Fe, Mn, O2, and S(-II) in Porewaters of Marine and Freshwater Sediments. Environ. Sci. Technol. 1995, 29, 751–761. [Google Scholar] [CrossRef]
  87. Technology Screening Matrix. Available online: https://frtr.gov/matrix/default.cfm (accessed on 9 July 2021).
  88. Sinkko, H.; Hepolehto, I.; Lyra, C.; Rinta-Kanto, J.M.; Villnäs, A.; Norkko, J.; Norkko, A.; Timonen, S. Increasing oxygen deficiency changes rare and moderately abundant bacterial communities in coastal soft sediments. Sci. Rep. 2019, 9, 1–15. [Google Scholar] [CrossRef] [PubMed]
  89. Broman, E.; Sjöstedt, J.; Pinhassi, J.; Dopson, M. Shifts in coastal sediment oxygenation cause pronounced changes in microbial community composition and associated metabolism. Microbiome 2017, 5, 96. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  90. Conley, D.J. Ecology: Save the Baltic Sea. Nature 2012, 486, 463–464. [Google Scholar] [CrossRef]
  91. Oxygen Release Compound. Available online: https://regenesis.com/en/oxygen-release-compound-orc/ (accessed on 4 July 2021).
  92. Sandefur, C.A.; Koenigsberg, S.S. The use of hydrogen Release Compound for the accelerated bioremediation of anaerobically degradable contaminants: The advent of time-release electron donors. Remediation 1999, 10, 31–53. [Google Scholar] [CrossRef]
  93. Hanh, D.N.; Rajbhandari, B.K.; Annachhatre, A.P. Bioremediation of sediments from intensive aquaculture shrimp farms by using calcium peroxide as slow oxygen release agent. Environ. Technol. 2005, 26, 581–590. [Google Scholar] [CrossRef] [PubMed]
  94. Zhou, Y.; Fang, X.; Zhang, Z.; Hu, Y.; Lu, J. An oxygen slow-releasing material and its application in water remediation as oxygen supplier. Environ. Technol. 2017, 38, 2793–2799. [Google Scholar] [CrossRef]
  95. Abdallah, E.; Goncalves, A.A.; Gagnon, G.A. Oxygen release compound as a chemical treatment for nutrient rich estuary sediments and water. J. Environ. Sci. Health A 2009, 44, 707–713. [Google Scholar] [CrossRef]
  96. Vezzulli, L.; Pruzzo, C.; Fabiano, M. Response of the bacterial community to in situ bioremediation of organic-rich sediments. Mar. Pollut. Bull. 2004, 49, 740–751. [Google Scholar] [CrossRef]
  97. Pure & Enriched: The Advantages of Using Oxygen in Wastewater Treatment Processes. Available online: https://www.airbestpractices.com/industries/wastewater/pure-enriched-advantages-using-oxygen-wastewater-treatment-processes (accessed on 15 July 2021).
  98. Che, L.; Jin, W.; Zhou, X.; Cao, C.; Han, W.; Qin, C.; Tu, R.; Chen, Y.; Feng, X.; Wang, Q. Biological Reduction of Organic Matter in Buji River Sediment (Shenzhen, China) with Artificial Oxygenation. Water 2020, 12, 3592. [Google Scholar] [CrossRef]
  99. A Quick Look at Bioremediation. Available online: https://staff.icar.cnr.it/spezzano/colombo/bioris/cortesto.htm (accessed on 27 July 2021).
  100. Zappi, M.; White, K.; Hwang, H.M.; Bajpai, R.; Qasim, M. The fate of hydrogen peroxide as an oxygen source for bioremediation activities within saturated aquifer systems. J. Air Waste Manag. Assoc. 2000, 50, 1818–1830. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  101. Pardieck, D.L.; Bouwer, E.J.; Stone, A.T. Hydrogen peroxide use to increase oxidant capacity for in situ bioremediation of contaminated soils and aquifers: A review. J. Contam. Hydrol. 1992, 9, 221–242. [Google Scholar] [CrossRef]
  102. Bajpai, R.K.; Zappi, M.E.; Gunnison, D. Additives for Establishment of Biologically Active Zones during in Situ Bioremediation. Ann. N. Y. Acad. Sci. 1994, 721, 450–465. [Google Scholar] [CrossRef]
  103. Talvenmäki, H.; Saartama, N.; Haukka, A.; Lepikkö, K.; Pajunen, V.; Punkari, M.; Yan, G.; Sinkkonen, A.; Piepponen, T.; Silvennoinen, H.; et al. In situ bioremediation of Fenton’s reaction-treated oil spill site, with a soil inoculum, slow release additives, and methyl-β-cyclodextrin. Environ. Sci. Pollut. Res. 2021, 28, 20273–20289. [Google Scholar] [CrossRef] [PubMed]
  104. Mahaseth, T.; Kuzminov, A. Potentiation of hydrogen peroxide toxicity: From catalase inhibition to stable DNA-iron complexes. Mutat. Res. Rev. Mutat. Res. 2017, 773, 274–281. [Google Scholar] [CrossRef]
  105. Sutton, N.B.; Grotenhuis, J.T.C.; Langenhoff, A.A.M.; Rijnaarts, H.H.M. Efforts to improve coupled in situ chemical oxidation with bioremediation: A review of optimization strategies. J. Soils Sediments 2011, 11, 129–140. [Google Scholar] [CrossRef] [Green Version]
  106. Nykänen, A.; Kontio, H.; Klutas, O.; Penttinen, O.P.; Kostia, S.; Mikola, J.; Romantschuk, M. Increasing lake water and sediment oxygen levels using slow release peroxide. Sci. Total Environ. 2012, 429, 317–324. [Google Scholar] [CrossRef]
  107. Thomas, J.; Beitinger, E.; Grosskinsky, H.; Koch, T.; Preuss, V. Innovative in situ treatment options for contaminated sediments. In Proceedings of the 5th International SEDNET Conference, Oslo, Norway, 27–29 May 2008. [Google Scholar]
  108. Chen, T.; Maldonado, J.; Delgado, A.G.; Yavuz, B.M.; Proctor, A.J.; Maldonado, J.; Zuo, Y.; Westerhoff, P.; Krajmalnik-Brown, R.; Rittmann, B.E. Ozone enhances biodegradability of heavy hydrocarbons in soil. J. Environ. Eng. Sci. 2016, 11, 7–17. [Google Scholar] [CrossRef]
  109. How to Evaluate Alternative Cleanup Technologies for Underground Storage Tank Sites: A Guide for Corrective Action Plan Reviewers. Chapter XIII—Chemical Oxidation. Available online: https://www.epa.gov/ust/how-evaluate-alternative-cleanup-technologies-underground-storage-tank-sites-guide-corrective (accessed on 3 June 2021).
  110. Shih, Y.J.; Binh, N.T.; Chen, C.W.; Chen, C.F.; Dong, C.D. Treatability assessment of polycyclic aromatic hydrocarbons contaminated marine sediments using permanganate, persulfate and Fenton oxidation processes. Chemosphere 2016, 150, 294–303. [Google Scholar] [CrossRef]
  111. Lofrano, G.; Libralato, G.; Minetto, D.; De Gisi, S.; Todaro, F.; Conte, B.; Calabrò, D.; Quatraro, L.; Notarnicola, M. In situ remediation of contaminated marine sediment: An overview. Environ. Sci. Pollut. Res. 2017, 24, 5189–5206. [Google Scholar] [CrossRef] [Green Version]
  112. Sergy, G.A. The Svalbard Experimental Oilspill Field Trials. In Proceedings of the 21st Arctic and Marine Oilspill Program (AMOP) Technical Seminar, Edmonton, AB, Canada, 10–12 June 1998. [Google Scholar]
  113. Owens, E.H.; Sergy, G.A.; Guénette, C.C.; Prince, R.C.; Lee, K. The reduction of stranded oil by in situ shoreline treatment options. Spill Sci. Technol. Bull. 2003, 8, 257–272. [Google Scholar] [CrossRef]
  114. Sergy, G.A.; Guénette, C.C.; Owens, E.H.; Prince, R.C.; Lee, K. In-situ treatment of oiled sediment shorelines. Spill Sci. Technol. Bull. 2003, 8, 237–244. [Google Scholar] [CrossRef]
  115. Garcia-Blanco, S.; Venosa, A.D.; Suidan, M.T.; Lee, K.; Cobanli, S.; Haines, J.R. Biostimulation for the treatment of an oil-contaminated coastal salt marsh. Biodegradation 2007, 18, 1–15. [Google Scholar] [CrossRef] [PubMed]
  116. Kao, C.M.; Chen, C.Y.; Chen, S.C.; Chien, H.Y.; Chen, Y.L. Application of in situ biosparging to remediate a petroleum-hydrocarbon spill site: Field and microbial evaluation. Chemosphere 2008, 70, 1492–1499. [Google Scholar] [CrossRef]
  117. Juwarkar, A.A.; Singh, S.K.; Mudhoo, A. A comprehensive overview of elements in bioremediation. Rev. Environ. Sci. Biotechnol. 2010, 9, 215–288. [Google Scholar] [CrossRef]
  118. Philp, J.C.; Atlas, R.M. Bioremediation of Contaminated Soils and Aquifers. In Bioremediation: Applied Microbial Solutions for Real-World Environmental Cleanup; Philp, J.C., Atlas, R.M., Eds.; John Wiley and Sons: Hoboken, NJ, USA, 2005; pp. 139–236. [Google Scholar]
  119. How to Evaluate Alternative Cleanup Technologies for Underground Storage Tank Sites. A Guide for Corrective Action Plan Reviewers. Chapter VIII, Biosparging. Available online: https://www.epa.gov/ust/how-evaluate-alternative-cleanup-technologies-underground-storage-tank-sites-guide-corrective (accessed on 5 June 2021).
  120. Wagner, M.R.; Popel, H.J. Oxygen transfer and aeration efficiency—Influence of diffuser submergence, diffuser density, and blower type. Water Sci. Technol. 1998, 38, 1–6. [Google Scholar] [CrossRef]
  121. Bubble Aeration. Available online: http://www.nzdl.org/cgi-bin/library?e=d-00000–00---off-0aginfo--00–0----0–10–0---0---0direct-10---4-------0–0l--11-en-50---20-about---00–0-1–00–0-0–11----0–0-&a=d&c=aginfo&cl=CL2.14&d=HASH03bf527f36108e1b5ecaf3.8.6.6.1#HASH03bf527f36108e1b5ecaf3.8.6.6.1 (accessed on 4 July 2021).
  122. Fine Bubble Aeration Systems. Available online: https://www.wastewater.com/aerationsystems/fine-bubble-system (accessed on 25 July 2021).
  123. Alkhalidi, A.A.T.; Amano, R.S. Factors affecting fine bubble creation and bubble size for activated sludge. J. Water Environ. Technol. 2015, 29, 105–113. [Google Scholar] [CrossRef]
  124. Ashley, K.I.; Mavinic, D.S.; Hall, K.J. Bench-scale study of oxygen transfer in coarse bubble diffused aeration. Water Res. 1992, 26, 1289–1295. [Google Scholar] [CrossRef]
  125. Rosansky, S.; Condit, W.; Sirabian, R. NFESC Technical Report: Air Sparging Guidance Document; Naval Facilities Engineering Service Center: Washington, DC, USA, 2001; pp. 1–118. [Google Scholar]
  126. Rosansky, S.; Condit, W.; Sirabian, R. NAVFAC Technical Report: Best Practices for Injection and Distribution of Amendments; NAVFAC: Washington, DC, USA, 2013; pp. 93043–94370. [Google Scholar]
  127. He, Y.T.; Su, C. Use of Additives in Bioremediation of Contaminated Groundwater and Soil. In Advances in Bioremediation of Wastewater and Polluted Soil; Shiomi, N., Ed.; IntechOpen: London, UK, 2015. [Google Scholar]
  128. Li, H.; Hu, L.; Song, D.; Lin, F. Characteristics of micro-nano bubbles and potential application in groundwater bioremediation. Water Environ. Res. 2014, 86, 844–851. [Google Scholar] [CrossRef]
  129. Agarwal, A.; Ng, W.J.; Liu, Y. Principle and applications of microbubble and nanobubble technology for water treatment. Chemosphere 2011, 84, 1175–1180. [Google Scholar] [CrossRef] [PubMed]
  130. Chen, Y. Innovative Design for Vortex Micro-Nano Bubble generator Based on TRIZ. In Proceedings of the 2016 3rd International Conference on Mechatronics and Information Technology, Shenzhen, China, 9–10 April 2016; Advances in Computer Science Research. Atlantic Press: New York, NY, USA, 2016; pp. 710–713. [Google Scholar]
  131. Ohgaki, K.; Khanh, N.Q.; Joden, Y.; Tsuji, A.; Nakagawa, T. Physicochemical approach to nanobubble solutions. Chem. Eng. Sci. 2010, 65, 1296–1300. [Google Scholar] [CrossRef]
  132. Ushikubo, F.Y.; Furukawa, T.; Nakagawa, R.; Enaria, M.; Makinoa, Y.; Kawagoea, Y.; Shiinab, T.; Oshitaa, S. Evidence of the existence and the stability of nano-bubbles in water. Colloids Surf. A Physicochem. Eng. Asp. 2010, 361, 31–37. [Google Scholar] [CrossRef]
  133. Takahashi, M.; Kawamura, T.; Yamamoto, Y.; Ohnari, H.; Himuro, S.; Shakutsui, H. Effect of shrinking microbubble on gas hydrate formation. J. Phys. Chem. B 2003, 107, 2171–2173. [Google Scholar] [CrossRef]
  134. Nanobubble Generator. Available online: https://www.acniti.com/tags/nano-bubble-generator/ (accessed on 2 June 2021).
  135. Wu, Y.; Lin, H.; Yin, W.; Shao, S.; Lv, S.; Hu, Y. Water Quality and Microbial Community Changes in an Urban River after Micro-Nano Bubble Technology in Situ Treatment. Water 2019, 11, 66. [Google Scholar] [CrossRef] [Green Version]
  136. Kirby, R. Minimising harbour siltation-findings of PIANC Working Group. Ocean. Dyn. 2011, 61, 233–244. [Google Scholar] [CrossRef]
  137. Pang, Q.X.; Han, P.P.; Zhang, R.B.; Wen, C.P. Delaying Effect of Extracellular Polymer Substances on Fluid Mud Consolidation and Application for Nautical Depth. J. Waterw. Port. Coast. Ocean. Eng. 2018, 144, 04018001. [Google Scholar] [CrossRef]
  138. Wurpts, R.; Torn, P. 15 years experience with fluid mud: Definition of the nautical bottom with rheological parameters. Terra Aqua 2005, 99, 22–32. [Google Scholar]
  139. Polrot, A. Marine Bioremediation of Port Sediment: Investigation of Tributyltin Degradation Using Active Nautical Depth. In Proceedings of the 15th International Conference on Microbial Interactions & Microbial Ecology, Barcelona, Spain, 17–18 August 2020. [Google Scholar]
  140. Cappello, S.; Calogero, R.; Santisi, S.; Genovese, M.; Denaro, R.; Genovese, L.; Giuliano, L.; Mancini, G.; Yakimov, M.M. Bioremediation of oil polluted marine sediments: A bio-engineering treatment. Int. Microbiol. 2015, 18, 127–134. [Google Scholar] [PubMed]
  141. Perin, G.; Romagnoli, F.; Perin, F.; Giacometti, A. Preliminary Study on Mini-Modus Device Designed to Oxygenate Bottom Anoxic Waters without Perturbing Polluted Sediments. Environments 2020, 7, 23. [Google Scholar] [CrossRef] [Green Version]
  142. Bragg, J.R.; Prince, R.C.; Harner, E.J.; Atlas, R.M. Effectiveness of bioremediation for the Exxon Valdez oil spill. Nature 1994, 368, 413–418. [Google Scholar] [CrossRef]
  143. Guidelines for the Bioremediation of Marine Shorelines and Freshwater Wetlands. Available online: https://www.epa.gov/emergency-response/guidelines-bioremediation-marine-shorelines-and-freshwater-wetlands (accessed on 5 June 2021).
  144. Prince, R.C.; Bragg, J.R. Shoreline bioremediation following the Exxon Valdez oil spill in Alaska. Bioremediat. J. 1997, 1, 97–104. [Google Scholar] [CrossRef]
  145. Swannell, R.P.J.; Lee, K.; Mcdonagh, M. Field evaluations of marine oil spill bioremediation. Microbiol. Rev. 1996, 60, 342–365. [Google Scholar] [CrossRef]
  146. Guidelines for The Bioremediation of Oil-Contaminated Salt Marshes. Available online: https://www.epa.gov/emergency-response/guidelines-bioremediation-oil-contaminated-salt-marshes (accessed on 5 June 2021).
  147. Bonardi, M.; Ravagnan, G.; Morucchio, C.; Tosi, L.; Almeida, P.; De Sanctis, S. Environmental Recovery of Coastal Areas: The Bio—Remediation Study Case of the Industrial Harbour of Marghera, Venice, Italy. J. Coast. Res. 2006, 1044–1048. [Google Scholar]
  148. Bonardi, M.; Ravagnan, G.; Stirling, J.; Morucchio, C.; De Sanctis, S. Innovative treatment by bioremediation of contaminated sediments from the Venice Lagoon, Italy: The Arsenale Vecchio case study. J. Coast. Res. 2007, 50, 895–899. Available online: https://www.jstor.org/stable/26481709 (accessed on 5 June 2021).
  149. Delille, D.; Delille, B.; Pelletier, E. Effectiveness of bioremediation of crude oil contaminated subantarctic intertidal sediment: The microbial response. Microb. Ecol. 2002, 44, 118–126. [Google Scholar] [CrossRef] [PubMed]
  150. Kostecki, M.; Mazierski, J. Biodegradation of polycyclic aromatic hydrocarbons in bottom sediments in presence of calcium peroxide. Przem. Chem. 2008, 87, 278–283. [Google Scholar]
  151. Fu, D.; Singh, R.P.; Yang, X.; Ojha, C.S.P.; Surampalli, R.Y.; Kumar, A.J. Sediment in-situ bioremediation by immobilized microbial activated beads: Pilot-scale study. J. Environ. Manag. 2018, 226, 62–69. [Google Scholar] [CrossRef] [PubMed]
  152. Venosa, A.D.; Lee, K.; Suidan, M.T.; Garcia-Blanco, S.; Cobanli, S.; Moteleb, M.; Haines, J.R.; Tremblay, G.; Hazelwood, M. Bioremediation and biorestoration of a crude oil-contaminated freshwater wetland on the St. Lawrence river. Bioremediat. J. 2002, 6, 261–281. [Google Scholar] [CrossRef]
  153. Swannell, R.P.J.; Mitchell, D.; Lethbridge, G.; Jones, D.; Heath, D.; Hagley, M.; Jones, M.; Petch, S.; Milne, R.; Croxford, R.; et al. A field demonstration of the efficacy of bioremediation to treat oiled shorelines following the sea empress incident. Environ. Technol. 1999, 20, 863–873. [Google Scholar] [CrossRef]
  154. Swannell, R.P.J.; Mitchell, D.; Jones, D.M.; Petch, S.; Head, I.M.; Lee, K.; Willis, A.; Lepo, J.E. Bioremediation of oil contaminated fine sediments. In International Oil Spill Conference Proceedings; American Petroleum Institute: Washington, DC, USA, 1999; pp. 751–756. [Google Scholar]
  155. Röling, W.F.; Milner, M.G.; Jones, D.M.; Fratepietro, F.; Swannell, R.P.; Daniel, F.; Head, I.M. Bacterial community dynamics and hydrocarbon degradation during a field-scale evaluation of bioremediation on a mudflat beach contaminated with buried oil. Appl. Environ. Microbiol. 2004, 70, 2603–2613. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  156. Burns, K.A.; Codi, S.; Duke, N.C. Gladstone, Australia field studies: Weathering and degradation of hydrocarbons in oiled mangrove and salt marsh sediments with and without the application of an experimental bioremediation protocol. Mar. Pollut. Bull. 2000, 41, 392–402. [Google Scholar] [CrossRef]
  157. Mills, M.A.; Bonner, J.S.; Page, C.A.; Autenrieth, R.L. Evaluation of bioremediation strategies of a controlled oil release in a wetland. Mar. Pollut. Bull. 2004, 49, 425–435. [Google Scholar] [CrossRef]
  158. Venosa, A.D.; Suidan, M.T.; Lee, K.; Cobanli, S.E.; Garcia-Blanco, S.; Haines, J.R. Bioremediation of oil-contaminated coastal freshwater and saltwater wetlands. J. Environ. Stud. 2002, 8, 139–148. [Google Scholar]
  159. Garcia-Blanco, S.; Moteleb, M.; Suidan, M.T.; Venosa, A.D.; Lee, K.; King, D.W. Restoration of an oil-contaminated St. Lawrence river shoreline: Bioremediation and phytoremediation. In International Oil Spill Conference Proceedings; American Petroleum Institute: Washington, DC, USA, 2001; pp. 303–308. [Google Scholar]
  160. Thomas, J.; Preuss, V.; Wach, A.; Beitinger, E.; Grosskinsky, H. Treatment of organic-rich sediments through combined in situ and on site techniques-Case Study. In Proceedings of the 6th International SEDNET Conference, Hamburg, Germany, 6–8 October 2009. [Google Scholar]
  161. Gallego, J.R.; González-Rojas, E.; Peláez, A.I.; Sánchez, J.; García-Martínez, M.J.; Llamas, J.F. Effectiveness of bioremediation for the prestige fuel spill: A summary of case studies. In Proceedings of the Second IASTED International Conference on Advanced Technology in the Environmental Field, Lanzarote, Spain, 6–8 February 2006; pp. 68–73. [Google Scholar]
  162. Tsutsumi, H.; Kono, M.; Takai, K.; Manabe, T.; Haraguchi, M.; Yamamoto, I.; Oppenheimer, C. Bioremediation on the shore after an oil spill from the Nakhodka in the sea of Japan. III. Field tests of a bioremediation agent with microbiological cultures for the treatment of an oil spill. Mar. Pollut. Bull. 2000, 40, 320–324. [Google Scholar] [CrossRef]
Table 1. Recent field applications on aerobic sediment bioremediation from oil contaminants with focus on case studies that involve oxygen amendments and aeration.
Table 1. Recent field applications on aerobic sediment bioremediation from oil contaminants with focus on case studies that involve oxygen amendments and aeration.
Case StudyLocationAquatic EnvironmentType of Treatment 1AdditivesSediment CharacteristicsApplication PointDuration of ApplicationApplication RateEffectivenessReference/
Year
1Harbor of Marghera, Venice Lagoon, ItalyPortFA+OOxygenQuaternary sediments (unconsolidated sand, silt, clay, peats)50 cm above the sediments28 months12 h/day continuous operationReduction of heavy metal contentBonardi et al. [147],
2006
2Arsenale shipyard, Venice Lagoon, ItalyShipyardFA+OOxygenunconsolidated sand, silt, clay, peatsSea floor6 monthsDuring the nightReduction of heavy metal content. Recovery of the water body above the sedimentsBonardi et al. [148],
2007
3Kerguelen Archipelago, The Grande Terre beachBeachBSSlow-release fertilizer (Inipol EAP-22 or fish composts)sand-3 years-Complete removal of aliphatic hydrocarbons after 6 monthsDelille, Delille and Pelletier [149], 2002
4Rybnik water basin, Poland-BSCalcium peroxide--150 days100 g/m2 and 200 g/m2Effective PAH removalKostecki and Mazierski [150], 2008
5Shedu River, Jiangsu, ChinaRiverBA+BSMicrobial activated beads-On top of the sediments45 days1.77–2.12 kg/m2Good removal efficiency of pollutantsFu et al. [151],
2018
6Fish Farm, 2 nm offshore Porto Palo (Agrigento, Italy) in the Sicily channel (Med Sea)Fish FarmBA
BS
BA + BS
Biovase
Oxygen Releasing Compounds
--5 months0.5 kg/m2 Biovase
1 kg/m2 ORC
Higher bacterial density and enzymatic activityVezzulli, Pruzzo and Fabiano [96],
2004
7Bohai Sea, ChinaSeaBAZeolite carrier with a polymer coating-Ocean floor70 days370 tons of remedy agentsOver 50% oil degradationZhao et al. [22], 2018
8Bohai Sea, ChinaSeaBAZeolite carrier with a polymer coating-Ocean floor 210 days487 tons/km2 of remedy agentsIncreased oil biodegradationWang et al. [21], 2020
9 Inter-tidal foreshore of Pulau Semakau, SingaporeBeachBSSlow-release fertilizer (Osmocote)
Slow-release fertilizer + oil sorbent biopolymer (Chitosan)
75.16% sand, 24.73% silt and 0.11% clayMixed on the top sediments105 days 95 days1.2% Os (w/w) and 0.1% chitosan (ChS)Accelerated PAH degradationXu et al. [37], 2004;
Xu et al. [38],
2005
10St. Lawrence River at Ste. Croix, Quebec, CanadaShoreBS
Ph
Inorganic Fertilizers (ammonium nitrate NH4NO3 and monobasic calcium phosphate Ca(H2PO4)2)-2–3 cm455 days2.85 kg of NH4NO3 or 6.06 kg of NaNO3, and 1.22 kg of Ca(H2PO4)2·H2O per plotNo difference to natural attenuationVenosa et al. [152], 2002
11Bullwell Bay, Milford Haven, UKBeachBSInorganic Fertilizer
(Sodium Nitrate NaNO3 and Potassium phosphate KH2PO4)
Slow-release fertilizer
shingle, pebble, clay<10 mm2 monthsInorganic Fertilizer (1.15 kg NaNO3 and 0.08 kg KH2PO4 in 9 L seawater/plot/week
Pellet slow-release fertilizer single application
Increased heavy fuel oil degradation in both casesSwannell et al. [153],
1999
12Stert Flats, Somerset, United KingdomMudflatBSInorganic fertilizer (fertilizer grade Sodium Nitrate NaNO3 and Potassium phosphate KH2PO4)fine sand15 cm108 daysWeekly for a month, every 2 weeks thereafterSignificant enhancement of light crude oil bioremediationSwannell et al. [154],
1999
13Stert Flats, Somerset, United KingdomMudflatBSSlow-release fertilizer
Liquid inorganic fertilizer
fine sand10 cm~1 yearWeekly application of liquid fertilizerSignificant enhancement of light crude oil bioremediationRöling et al. [155],
2004
14Fisherman’s Landing Wharf, Gladstone AustraliaMangrove
Rhizophora stylosa
Salt Marsh
BS + FA
BS + FA + CD
Aquarium airstones
Osmocote Tropical
Corexit 9527
-2–3 cm270 days100 L/min of air for 4 months
Osmocote Tropical added in the beginning and after 6 months
1 to 2-month lag time
1000-fold increase in alkane degraders
Ramsay et al. [42], 2000;
Duke et al. [50], 2000;
Burns, Codi and Duke [156], 2000
15San Jacinto Wetland Research Facility (SJWRF), San Jacinto River near Houston, TexasWetlandBSInorganic Nutrients (diammonium phosphate (NH4)2(HPO4))
Inorganic Nutrients + Alternative Electron Acceptor (Potassium Nitrate KNO3)
-On top of the sediments140 daysInorganic Nutrients 40 mg N/kg dry sediment weight
Electron Acceptor 100 mg N–NO3−/kg dry sediment weight
bi-weekly broadcast spreading
Enhanced biodegradation ratesMills et al. [157],
2004
16San Jacinto Wetland Research Facility (SJWRF), San Jacinto River near Houston, TexasWetlandBA
BS
Dry, wheat-bran-based powder containing a large consortium of hydrocarbon-degrading bacteria dry, wheat-bran-based (plus non-ionic surfactant) powder containing large numbers of oil-degrading microorganisms
Inorganic fertilizer (diammonium phosphate (NH3)2HPO4)
-On top of the sediments152 daysApplied 5 times (Days 4, 7, 11, 18, 28)
Applied twice (Days 4 and 28)
Broadcast spread prior to microorganisms
No additional response from exogenous microbes
No significant differences to intrinsic bioremediation
Simon et al. [18],
2004
17Pointe au Chien Wildlife Management Area in Terrebonne Parish, LASpartina alterniflora salt marshBS
Ph
Ammonium Nitrate (NH4NO3)
Time-release Urea
-On top of the sediments180 daysAmmonium Nitrate 60 g N/m2
Urea 30 g N/m2
Alkane degradation rates were not enhancedTate et al. [44],
2012
18St. Lawrence River at Ste. Croix, Quebec, Canada
Conrod’s Beach, on the Eastern Shore of Nova Scotia, Canada
Freshwater wetland
Spartina alterniflora salt marsh
Ph
BS + T
Ammonium Nitrate (NH4NO3)
Sodium Nitrate (NaNO3) and Orthophosphate nutrients (Ca(H2PO4)2·H2O)
-2–3 cm65 weeks1 kg-N and 0.3 kg-P per plot applied weekly
1.28 kg and 0.55 kg/plot applied when N concentration <5 mg/L
Inorganic nutrients can accelerate hydrocarbon degradation when oil is present mostly on the surfaceVenosa et al. [158],
2002
19Conrod’s Beach, on the Eastern Shore of Nova Scotia, CanadaSpartina alterniflora salt marshBS
Ph
Ammonium Nitrate (NH4NO3) and Orthophosphate nutrients (Ca(H2PO4)2·H2O)-On top of the sediments20 weeks0.45 kg-N and 0.135 kg-P per plot applied on days 0, 50 and 82Alkane degradation enhancement, no effect on PAH degradationGarcia-Blanco et al. [116],
2007
20St. Lawrence River at Ste. Croix, Quebec, CanadaScirpus pungens freshwater shorelinePh
BS + T
Ammonium Nitrate (NH4NO3)
Sodium Nitrate (NaNO3) and Orthophosphate nutrients (Ca(H2PO4)2·H2O)
sandy loam (58% sand, 32% silt and 10% clay)1–2 cm21 weeks1 kg-N and 0.3 kg-P per plot reapplied when N concentration <5 mg/LNo significant biodegradation enhancementGarcia-Blanco et al. [159],
2001
21Sveagruva, Spitsbergen, Svalbard, NorwayArctic ShorelineBS
T
BS + T
Soluble Fertilizer (ammonium nitrate NH4NO3 and superphosphate Ca(H2PO4)2)
Slow-Release Fertilizer (Inipol SP1)
Ferrous sulfate
Yeast extract
Site 1: 41% pebble, 16% granules, 18% coarse sand, 25% sand/mud (Low energy); Site 2: 53% pebble, 11% granules, 13% coarse sand, 23% mud (moderate energy)
Site 3: 75% pebble, 5% granules, 2% coarse sand, 18% sand/mud (locally high energy)
On top of the sediments
2–3 cm penetration
400 days100 g/m2 ammonium nitrate
10 g/m2 superphosphate
1 g/m2 ferrous sulfate
0.1 g/m2 yeast extract (Day 0)
140 g/m2 Inipol SP1
1 g/m2 ferrous sulfate
0.1 g/m2 yeast extract (Day 7)
100 g/m2 Inipol SP1 (Day 23)
50 g/m2 ammonium nitrate
5 g/m2 superphosphate
1 g/m2 ferrous sulfate
0.1 g/m2 yeast extract
70 g/m2 Inipol SP1 (Day 58)
Tilling did not clearly contribute to the removal of oil within the intertidal sediments
Biostimulation increased the biodegradation rates in the intertidal sediments
Prince et al. [113], 2003;
Owens et al. [114], 2003;
Sergy et al. [115], 2003
22N/AHarborFAAir--12 months5–10 L/hTPH removal up to 60–75%
PAH removal up to 75–85%
Thomas et al. [107],
2008
23Upper Main Harbor, Frankfurt/M. GermanyHarborBSHydrogen Peroxide and Fenton’s reagentsFine-grained (80% clay and silt)Injected at the base of the sediment body-0.16 L/h of 1% peroxide solution (5 g/kg sediment) per screenNo degradation of organic pollutants was observedThomas et al. [107],
2008
24N/AArtificial fish pondsFB-----Under investigationThomas et al. [107], 2008;
Thomas et al. [160], 2009
25Virgen del Mar beach, at the north coast of SpainBeachBSOleophilic fertilizer S-200Large and medium cobble stones overlying a mixed sand and gravel baseOn top of the sediments220 days15.8 g N/m2 and 1.37 g P/m2, according to C:N:P ratio of 120:10:1, applied on Day 0 and Day 20The addition of fertilizer increased the biodegradation rate during the first 60 daysJiménez et al. [41],
2006
26Bahinas beach, coast of Asturias, Northern SpainBeachBS
BA
Ammonium Nitrate (NH4NO3)
Ammonium Phosphate ((NH4)2PO4)
Surfactant
Commercial Bioaugmentation Products
Medium grain-size sand covered by pebbles and cobblesOn top of the sediments45 daysC:N:P ratio 100:10:1
Weekly application
Bioaugmentation had positive effects on the degradation of the saturated fractionsGallego et al. [23], 2008;
Gallego et al. [161], 2007
27Delaware Bay, United StatesShorelineBS
BA
Sodium Nitrate (NaNO3)
Sodium Tripolyphosphate (Na5P3O10)
-On top of the sediments-2 kg of technical grade sodium nitrate (330 g of nitrogen) and 128 g of sodium tripolyphosphate applied everyday
30 L suspended mixed population of hydrocarbon degrading bacteria applied once a week
Biostimulation enhances the intrinsic rates of biodegradation
Bioaugmentation has no significant effect
Venosa et al. [16],
1996
28Kasumi-cho, Kinosaki-gun, Hyogo prefecture, JapanBeachBATerraZyme™RocksOn top of the sediments8 weeks250 kgSignificant enhancement on the biodegradation of heavy crude oilTsutsumi et al. [162],
2000
1 Type of treatment: FA refers to forced aeration, O to oxygenation, BS to biostimulation, BA to bioaugmentation, FB to floating bioreactor, T to tilling, Ph to phytoremediation, and CD to chemical dispersants.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Fragkou, E.; Antoniou, E.; Daliakopoulos, I.; Manios, T.; Theodorakopoulou, M.; Kalogerakis, N. In Situ Aerobic Bioremediation of Sediments Polluted with Petroleum Hydrocarbons: A Critical Review. J. Mar. Sci. Eng. 2021, 9, 1003. https://doi.org/10.3390/jmse9091003

AMA Style

Fragkou E, Antoniou E, Daliakopoulos I, Manios T, Theodorakopoulou M, Kalogerakis N. In Situ Aerobic Bioremediation of Sediments Polluted with Petroleum Hydrocarbons: A Critical Review. Journal of Marine Science and Engineering. 2021; 9(9):1003. https://doi.org/10.3390/jmse9091003

Chicago/Turabian Style

Fragkou, Efsevia, Eleftheria Antoniou, Ioannis Daliakopoulos, Thrassyvoulos Manios, Marianna Theodorakopoulou, and Nicolas Kalogerakis. 2021. "In Situ Aerobic Bioremediation of Sediments Polluted with Petroleum Hydrocarbons: A Critical Review" Journal of Marine Science and Engineering 9, no. 9: 1003. https://doi.org/10.3390/jmse9091003

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop