Cited by 110Microbial bioremediation and biosurfactantsEnvironmental Toxicology and EcotoxicologyEnvironmental Chemistry and Analysis

Get Rid of Marine Pollution: Bioremediation an Innovative, Attractive, and Successful Cleaning Strategy

Open access
Aliko, Valbona, Multisanti, Cristiana Roberta, Turani, Blerta, Faggio, Caterina·2022·Sustainability

Abstract

Aquatic environmental pollution is a rather worrying and increasingly topical problem that requires the development and promotion of innovative and ecofriendly technologies. Pollutants in water include many common substances that can reach aquatic ecosystems through several pathways including wastewater, the atmosphere, ship discharges, and many other sources. Most of these toxic compounds are internalized by aquatic organisms, leading to bioaccumulation in tissues and reaching any level of the food chain through the biomagnification process. These mechanisms can develop into adverse effects on the physiology of organisms and biochemical processes of natural ecosystems, thus affecting animals, environments, and indirectly, human health. Innovative technologies to tackle marine pollution include bioremediation: a suitable, biological, and ecological approach that enhances the ability of micro-organisms to transform waste and toxic substances into forms that can be used by other organisms. In this context, micro-organisms appear to be essential for the detoxification of aquatic systems due to their metabolic activity. This review provides a careful analysis of the characteristics of the main pollutants that affect aquatic ecosystems, with a focus on their effects on organisms and environments. It also offers clear guidance on innovative biological strategies that can be employed to prevent, limit, and remediate anthropogenic influences on aquatic environments.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3390/su141811784

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Bioremediation offers numerous benefits over other cleanup methods, including avoiding human interference and minimizing disturbance to nearby communities.

    “Bioremediation offers numerous benefits over other cleanup methods, including avoiding human interference and minimizing disturbance to nearby communities [15].”

    From Harnessing bacterial consortia for effective bioremediation: targeted removal of heavy metals, hydrocarbons, and persistent pollutants (2025) · cites this paper as [15]

    Section 4 describes bioremediation as efficient and reliable, supporting the general claim that it has benefits. It does not say that bioremediation minimizes disturbance to nearby communities; it also says that larger oil spills require human intervention, so avoiding human interference is not a general benefit established by this source. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • Bacillus subtilis strains produce β-lactamases that degrade β-lactam antibiotics such as amoxicillin and cephalexin, achieving degradation rates up to 25% under optimal conditions.

    “Bacillus subtilis strains, for example, produce β-lactamases that can degrade β-lactam antibiotics such as amoxicillin and cephalexin, achieving degradation rates of up to 25% under optimal conditions [14,15].”

    From Harnessing bacterial consortia for effective bioremediation: targeted removal of heavy metals, hydrocarbons, and persistent pollutants (2025) · cites this paper as [15]

    Section 5.1 discusses bacterial degradation of hydrocarbons, and the References list a Bacillus subtilis study about crude oil and phenanthrene. Searches for β-lactamases, amoxicillin, cephalexin, and a 25% degradation rate found no passage in our copy addressing the attributed claim. (LLM, conf=0.76)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 91

  1. Trček, B.; Žigon, D.; Zidar, V.K.; Auersperger, P. The fate of benzotriazole pollutants in an urban oxic intergranular aquifer. Water Res. 2018, 131, 264-273. [CrossRef] [PubMed] · DOI
  2. Rocha, A.C.; Camacho, C.; Eljarrat, E.; Peris, A.; Aminot, Y.; Readman, J.W.; Boti, V.; Nannou, C.; Marques, A.; Nunes, M.L.; et al. Bioaccumulation of persistent and emerging pollutants in wild sea urchin Paracentrotus lividus. Environ. Res. 2018, 161, 354-363. [CrossRef] [PubMed] · DOI
  3. Zicarelli, G.; Multisanti, C.R.; Falco, F.; Faggio, C. Evaluation of toxicity of Personal Care Products (PCPs) in freshwaters: Zebrafish as a model. Environ. Toxicol. Pharmacol. 2022, 94, 103923. [CrossRef] · DOI
  4. Porretti, M.; Arrigo, F.; Di Bella, G.; Faggio, C. Impact of pharmaceutical products on zebrafish: An effective tool to assess aquatic pollution. Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2022, 261, 109439. [CrossRef] [PubMed] · DOI
  5. Boscolo, C.N.P.; Pereira, T.S.B.; Batalhão, I.G.; Dourado, P.L.R.; Schlenk, D.; de Almeida, E.A. Diuron metabolites act as endocrine disruptors and alter aggressive behaviour in Nile tilapia (Oreochromis niloticus). Chemosphere 2018, 191, 832-838. [CrossRef] · DOI
  6. Santos, D.; Luzio, A.; Coimbra, A.M. Zebrafish sex differentiation and gonad development: A review on the impact of environ- mental factors. Aquat. Toxicol. 2017, 191, 141-163. [CrossRef] · DOI
  7. Alam, M.W.; Xiangmin, X.; Ahamed, R. Protecting the marine and coastal water from land-based sources of pollution in the northern Bay of Bengal: A legal analysis for implementing a national comprehensive act. Environ. Chall. 2021, 4, 100154. [CrossRef] · DOI
  8. Pagano, M.; Vazzana, I.; Gentile, A.; Caracappa, G.; Faggio, C. Hematological and biochemical parameters in Sea turtles (Caretta caretta) after stranding. Reg. Stud. Mar. Sci. 2019, 32, 100832. [CrossRef] · DOI
  9. Aliko, V.; Korriku, R.S.; Pagano, M.; Faggio, C. Double-edged sword: Fluoxetine and ibuprofen as development jeopardizers and apoptosis' inducers in common toad, Bufo bufo, tadpoles. Sci. Total Environ. 2021, 776, 145945. [CrossRef] · DOI
  10. Catsiki, V.A.; Florou, H. Study on the behavior of the heavy metals Cu, Cr, Ni, Zn, Fe, Mn and 137Cs in an estuarine ecosystem using Mytilus galloprovincialis as a bioindicator species: The case of Thermaikos gulf, Greece. J. Environ. Radioact. 2006, 86, 31-44. [CrossRef] · DOI
  11. Wen, B.; Zhang, N.; Jin, S.R.; Chen, Z.Z.; Gao, J.Z.; Liu, Y.; Liu, H.P.; Xu, Z. Microplastics have a more profound impact than elevated temperatures on the predatory performance, digestion, and energy metabolism of an Amazonian cichlid. Aquat. Toxicol. 2018, 195, 67-76. [CrossRef] [PubMed] · DOI
  12. Torre, A.; Trischitta, F.; Corsaro, C.; Mallamace, D.; Faggio, C. Digestive cells from Mytilus galloprovincialis show a partial regulatory volume decrease following acute hypotonic stress through mechanisms involving inorganic ions. Cell Biochem. Funct. 2013, 31, 489-495. [CrossRef] [PubMed] · DOI
  13. Cajaraville, M.P.; Bebianno, M.J.; Blasco, J.; Porte, C.; Sarasquete, C.; Viarengo, A. The use of biomarkers to assess the impact of pollution in coastal environments of the Iberian Peninsula: A practical approach. Sci. Total Environ. 2000, 247, 295-311. [CrossRef] · DOI
  14. Leblebici, Z.; Aksoy, A.; Duman, F. Influence of salinity on the growth and heavy metal accumulation capacity of Spirodela polyrrhiza (Lemnaceae). Turk. J. Biol. 2011, 35, 215-220. [CrossRef] · DOI
  15. Pagano, M.; Porcino, C.; Briglia, M.; Fiorino, E.; Vazzana, M.; Silvestro, S.; Faggio, C. The influence of exposure of cadmium chloride and zinc chloride on haemolymph and digestive gland cells from Mytilus galloprovincialis. Int. J. Environ. Res. 2017, 11, 207-216. [CrossRef] · DOI
  16. Aliko, V.; Qirjo, M.; Sula, E.; Morina, V.; Faggio, C. Antioxidant defence system, immune response and erythron profile modulation in goldfish, Carassius auratus, after acute manganese treatment. Fish Shellfish Immunol. 2018, 76, 101-109. [CrossRef] · DOI
  17. Sula, E.; Aliko, V.; Marku, E.; Nuro, A.; Faggio, C. Evaluation of kidney histopathological alterations in Crucian Carp, Carassius carassius, from a pesticide and PCB-contaminated freshwater ecosystem, using light microscopy and organ index mathematical model. Int. J. Aquat. Biol. 2020, 8, 154-165.
  18. Kemp, M.; Wepener, V.; De Kock, K.N.; Wolmarans, C.T. Metallothionein induction as indicator of low level metal exposure to aquatic macroinvertebrates from a relatively unimpacted river system in South Africa. Bull. Environ. Contam. Toxicol. 2017, 99, 662-667. [CrossRef] · DOI
  19. Singh, R.; Gautam, N.; Mishra, A.; Gupta, R. Heavy metals and living systems: An overview. Indian J. Pharmacol. 2011, 43, 246. [CrossRef] · DOI
  20. Torre, A.; Trischitta, F.; Faggio, C. Effect of CdCl 2 on Regulatory Volume Decrease (RVD) in Mytilus galloprovincialis digestive cells. Toxicol. In Vitr. 2013, 27, 1260-1266. [CrossRef] · DOI
  21. Matozzo, V.; Ballarin, L.; Pampanin, D.M.; Marin, M.G. Effects of copper and cadmium exposure on functional responses of hemocytes in the clam, Tapes philippinarum. Arch. Environ. Contam. Toxicol. 2001, 41, 163-170. [CrossRef] [PubMed] · DOI
  22. Balbus, J.M.; Boxall, A.B.; Fenske, R.A.; McKone, T.E.; Zeise, L. Implications of global climate change for the assessment and management of human health risks of chemicals in the natural environment. Environ. Toxicol. Chem. 2013, 32, 62-78. [CrossRef] [PubMed] · DOI
  23. Chromcova, L.; Blahova, J.; Zivna, D.; Plhalova, L.; Di Tocco, F.C.; Divisoval, L.; Prokes, M.; Faggio, C.; Tichy, F.; Svobodova, Z. NeemAzal T/S-toxicity to early-life stages of common carp (Cyprinus carpio L.). Veterinární Med. 2015, 60, 23-30. [CrossRef] · DOI
  24. Bartoskova, M.; Dobsikova, R.; Stancova, V.; Zivna, D.; Blahova, J.; Marsalek, P.; Zelníckova, L.; Bartos, M.; Di Tocco, F.C.; Faggio, C. Evaluation of ibuprofen toxicity for zebrafish (Danio rerio) targeting on selected biomarkers of oxidative stress. Neuro Endocrinol. Lett. 2013, 34, 102-108. [PubMed]
  25. Messina, C.M.; Faggio, C.; Laudicella, A.V.; Sanfilippo, M.; Trischitta, F.; Santulli, A. Effect of sodium dodecyl sulfate (SDS) on stress response in the Mediterranean mussel (Mytilus galloprovincialis): Regulatory volume decrease (RVD) and modulation of biochemical markers related to oxidative stress. Aquat. Toxicol. 2014, 157, 94-100. [CrossRef] [PubMed] · DOI
  26. Authman, M.M.; Zaki, M.S.; Khallaf, E.A.; Abbas, H.H. Use of fish as bio-indicator of the effects of heavy metals pollution. J. Aquac. Res. Dev. 2015, 6, 4. [CrossRef] · DOI
  27. Shahjahan, M.; Taslima, K.; Rahman, M.S.; Al-Emran, M.; Alam, S.I.; Faggio, C. Effects of heavy metals on fish physiology-A review. Chemosphere 2022, 300, 134519. [CrossRef] · DOI
  28. Gobi, N.; Vaseeharan, B.; Rekha, R.; Vijayakumar, S.; Faggio, C. Bioaccumulation, cytotoxicity and oxidative stress of the acute exposure selenium in Oreochromis mossambicus. Ecotoxicol. Environ. Saf. 2018, 162, 147-159. [CrossRef] · DOI
  29. Curpan, A.S.; Impellitteri, F.; Plavan, G.; Ciobica, A.; Faggio, C. Mytilus galloprovincialis: An essential, low-cost model organism for the impact of xenobiotics on oxidative stress and public health. Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2022, 256, 109302. [CrossRef] · DOI
  30. LI, W.C.; Tse, H.F.; Fok, L. Plastic waste in the marine environment: A review of sources, occurrence and effects. Sci. Total Environ. 2016, 566, 333-349. [CrossRef] · DOI
  31. Chia, R.W.; Lee, J.Y.; Kim, H.; Jang, J. Microplastic pollution in soil and groundwater: A review. Environ. Chem. Lett. 2021, 19, 4211-4224. [CrossRef] · DOI · Paper page
  32. Alimba, C.G.; Faggio, C.; Sivanesan, S.; Ogunkanmi, A.L.; Krishnamurthi, K. Micro (nano)-plastics in the environment and risk of carcinogenesis: Insight into possible mechanisms. J. Hazard. Mater. 2021, 416, 126143. [CrossRef] · DOI
  33. Sussarellu, R.; Suquet, M.; Thomas, Y.; Lambert, C.; Fabioux, C.; Pernet, M.E.J.; Le Goic, N.; Epelboin, Y.; Corporeau, C.; Guyomarch, J.; et al. Oyster reproduction is affected by exposure to polystyrene microplastics. Proc. Natl. Acad. Sci. USA 2016, 113, 2430-2435. [CrossRef] [PubMed] · DOI
  34. Tosetto, L.; Brown, C.; Williamson, J.E. Microplastics on beaches: Ingestion and behavioural consequences for beachhoppers. Mar. Biol. 2016, 163, 199. [CrossRef] · DOI
  35. Mishra, S.; charan Rath, C.; Das, A.P. Marine microfiber pollution: A review on present status and future challenges. Mar. Pollut. Bull. 2019, 140, 188-197. [CrossRef] [PubMed] · DOI
  36. Prokić, M.D.; Gavrilović, B.R.; Radovanović, T.B.; Gavrić, J.P.; Petrović, T.G.; Despotović, S.G.; Faggio, C. Studying microplastics: Lessons from evaluated literature on animal model organisms and experimental approaches. J. Hazard. Mater. 2021, 414, 125476. [CrossRef] · DOI
  37. Sula, E.; Aliko, V.; Barceló, D.; Faggio, C. Combined Effects of Moderate Hypoxia, Pesticide and PCBs Upon Crucian Carp Fish, Carassius carassius, From a Freshwater Lake-In situ Ecophysiological Approach. Aquat. Toxicol. 2020, 228, 105644. [CrossRef] · DOI
  38. Yalsuyi, A.M.; Vajargah, M.F.; Hajimoradloo, A.; Galangash, M.M.; Prokić, M.D.; Faggio, C. Evaluation of behavioural changes and tissue damages in common carp (Cyprinus carpio) after exposure to the herbicide glyphosate. Vet. Sci. 2021, 8, 218. [CrossRef] · DOI
  39. Ayoola, S.O. Toxicity of glyphosate herbicide on Nile tilapia (Oreochromis niloticus) juvenile. Afr. J. Agric. Res. 2008, 3, 825-834.
  40. Fiorino, E.; Sehonova, P.; Plhalova, L.; Blahova, J.; Svobodova, Z.; Faggio, C. Effects of glyphosate on early life stages: Comparison between Cyprinus carpio and Danio rerio. Environ. Sci. Pollut. Res. 2018, 25, 8542-8549. [CrossRef] [PubMed] · DOI
  41. Matozzo, V.; Fabrello, J.; Masiero, L.; Ferraccioli, F.; Finos, L.; Pastore, P.; Di Gangi, I.M.; Bogialli, S. Ecotoxicological risk assessment for the herbicide glyphosate to non-target aquatic species: A case study with the mussel Mytilus galloprovincialis. Environ. Pollut. 2018, 233, 623-632. [CrossRef] [PubMed] · DOI
  42. Stehle, S.; Schulz, R. Insecticide contamination of global surface waters. Proc. Natl. Acad. Sci. USA 2015, 112, 5750-5755. [CrossRef] [PubMed] · DOI · Paper page
  43. Stara, A.; Pagano, M.; Albano, M.; Savoca, S.; Di Bella, G.; Albergamo, A.; Zuskova, E.; Sandova, M.; Velisek, J.; Fabrello, J.; et al. Effects of long-term exposure of Mytilus galloprovincialis to thiacloprid: A multi-biomarker approach. Environ. Pollut. 2021, 289, 117892. [CrossRef] [PubMed] · DOI
  44. Barathinivas, A.; Ramya, S.; Neethirajan, K.; Jayakumararaj, R.; Pothiraj, C.; Balaji, P.; Faggio, C. Ecotoxicological Effects of Pesticides on Hematological Parameters and Oxidative Enzymes in Freshwater Catfish, Mystus keletius. Sustainability 2022, 14, 9529. [CrossRef] · DOI
  45. Faggio, C.; Pagano, M.; Alampi, R.; Vazzana, I.; Felice, M.R. Cytotoxicity, haemolymphatic parameters, and oxidative stress following exposure to sub-lethal concentrations of quaternium-15 in Mytilus galloprovincialis. Aquat. Toxicol. 2016, 180, 258-265. [CrossRef] · DOI
  46. Machado, M.D.; Soares, E.V. Toxicological effects induced by the biocide triclosan on Pseudokirchneriella subcapitata. Aquat. Toxicol. 2021, 230, 105706. [CrossRef] · DOI
  47. Huang, Y.Q.; Liang, C.H.; He, L.; Tian, J.; Liang, C.S.; Chen, X.; Liu, Z.Y. Development and validation of a radiomics nomogram for preoperative prediction of lymph node metastasis in colorectal cancer. J. Clin. Oncol. 2016, 34, 2157-2164. [CrossRef] · DOI
  48. Meador, J.P.; Yeh, A.; Gallagher, E.P. Adverse metabolic effects in fish exposed to contaminants of emerging concern in the field and laboratory. Environ. Pollut. 2018, 236, 850-861. [CrossRef] · DOI
  49. Dar, O.I.; Aslam, R.; Sharma, S.; Jia, A.Q.; Kaur, A.; Faggio, C. Biomolecular alterations in the early life stages of four food fish following acute exposure of Triclosan. Environ. Toxicol. Pharmacol. 2022, 91, 103820. [CrossRef] · DOI
  50. Sharma, S.; Iqbal Dar, O.; Andotra, M.; Sharma, S.; Kaur, A.; Faggio, C. Environmentally relevant concentrations of Triclosan induce cyto-genotoxicity and biochemical alterations in the hatchlings of Labeo rohita. Appl. Sci. 2021, 11, 10478. [CrossRef] · DOI
  51. Pernoncini, K.V.; Montagnini, B.G.; de Góes, M.L.M.; Garcia, P.C.; Gerardin, D.C.C. Evaluation of reproductive toxicity in rats treated with triclosan. Reprod. Toxicol. 2018, 75, 65-72. [CrossRef] [PubMed] · DOI
  52. Tao, J.; Bai, C.; Chen, Y.; Zhou, H.; Liu, Y.; Shi, Q.; Pan, W.; Dong, H.; Li, L.; Xu, H.; et al. Environmental relevant concentrations of benzophenone-3 induced developmental neurotoxicity in zebrafish. Sci. Total Environ. 2020, 721, 137686. [CrossRef] [PubMed] · DOI
  53. Houghton, J.; Holt, M.M.; Giles, D.A.; Hanson, M.B.; Emmons, C.K.; Hogan, J.T.; Branch, T.A.; VanBlaricom, G.R. The Relationship between Vessel Traffic and Noise Levels Received by Killer Whales (Orcinus orca). PLoS ONE 2015, 10, e0140119. [CrossRef] · DOI
  54. Piwetz, S.; Lundquist, D.; Wuersig, B. Humpback dolphin (genus Sousa) behavioural responses to human activities. In Advances in Marine Biology; Academic Press: Cambridge, MA, USA, 2015; Volume 72, pp. 17-45.
  55. Boudjema, K.; Badis, A.; Moulai-Mostefa, N. Study of heavy metal bioaccumulation in Mytilus galloprovincialis (Lamark 1819) from heavy metal mixture using the CCF design. Environ. Technol. Innov. 2022, 25, 102202. [CrossRef] · DOI
  56. Landis, W.G.; Sofield, R.M.; Yu, M.H. Introduction to Environmental Toxicology: Molecular Substructures to Ecological Landscapes; CRC Press: Boca Raton, FL, USA, 2017.
  57. Gobas, F.A.P.C.; Morrison, H.A. Bioconcentration and biomagnification in the aquatic environment. In Handbook of Property Estimation Methods for Chemicals; Springer: Dordrecht, The Netherlands, 2000; pp. 189-231.
  58. Hemond, H.F.; Fechner, E.J. Chemical Fate and Transport in the Environment; Academic Press: Cambridge, MA, USA, 2022.
  59. Matozzo, V.; Rova, S.; Marin, M.G. The nonsteroidal anti-inflammatory drug, ibuprofen, affects the immune parameters in the clam Ruditapes philippinarum. Mar. Environ. Res. 2012, 79, 116-121. [CrossRef] · DOI
  60. Qyli, M.; Aliko, V. The effect of thermal stress exposure on the hemolymph glucose level in crabs (Carcinus estuaris). Int. J. Ecosyst. Ecol. Sci. IJEES 2015, 5, 537-540.
  61. Aliko, V.; Hajdaraj, G.; Caci, A.; Faggio, C. Copper induced lysosomal membrane destabilisation in haemolymph cells of Mediterranean Green Crab (Carcinus aestuarii, Nardo, 1847) from the Narta Lagoon (Albania). Braz. Arch. Biol. Technol. 2015, 58, 750-756. [CrossRef] · DOI
  62. Sehonova, P.; Plhalova, L.; Blahova, J.; Berankova, P.; Doubkova, V.; Prokes, M.; Tichy, F.; Vecerek, V.; Svobodova, Z. The effect of tramadol hydrochloride on early life stages of fish. Environ. Toxicol. Pharmacol. 2016, 44, 151-157. [CrossRef] · DOI
  63. Burgos-Aceves, M.A.; Cohen, A.; Smith, Y.; Faggio, C. Estrogen regulation of gene expression in the teleost fish immune system. Fish Shellfish. Immunol. 2016, 58, 42-49. [CrossRef] [PubMed] · DOI
  64. Faggio, C.; Fedele, G.; Arfuso, F.; Panzera, M.; Fazio, F. Haematological and biochemical response of Mugil cephalus after acclimation to captivity. Cah. Biol. Mar. 2014, 55, 31-36.
  65. Pramanik, A.; Basak, P.; Sengupta, S.; Bhattacharyya, M. Marine Microbial Diversity: Potential Functions to Degrade Xenobiotics; Biodegradation and Bioremediation of the Series "Environmental Science and Engineering; Studium Press LLC: Houston, TX, USA, 2015; Volume 8.
  66. Dash, H.R.; Mangwani, N.; Chakraborty, J.; Kumari, S.; Das, S. Marine bacteria: Potential candidates for enhanced bioremediation. Appl. Microbiol. Biotechnol. 2013, 97, 561-571. [CrossRef] [PubMed] · DOI
  67. Paniagua-Michel, J.; Rosales, A. Marine bioremediation-A sustainable biotechnology of petroleum hydrocarbons biodegradation in coastal and marine environments. J. Bioremediat. Biodegrad. 2015, 6, 1.
  68. Stephenson, D. Review of Effective Microorganisms (EM) and Bioaugmentation Factors for Wastewater Biosolids Treatment; Environmental Services Limited: Mandan, ND, USA, 2012.
  69. Jones, R.J.; Megarrity, R.G. Successful transfer of DHP-degrading bacteria from Hawaiian goats to Australian ruminants to overcome the toxicity of Leucaena. Aust. Vet. J. 1986, 63, 259-262. [CrossRef] · DOI
  70. Jahangeer and Vikram Kumar An Overview on Microbial Degradation of Petroleum Hydrocarbon Contaminants. Int. J. Eng. Tech. Res. IJETR 2013, 1, 34-37.
  71. Viesser, J.A.; Sugai-Guerios, M.H.; Malucelli, L.C.; Pincerati, M.R.; Karp, S.G.; Maranho, L.T. Petroleum-tolerant rhizospheric bacteria: Isolation, characterization and bioremediation potential. Sci. Rep. 2020, 10, 2060. [CrossRef] · DOI
  72. Oyetibo, G.O.; Chien, M.F.; Ikeda-Ohtsubo, W.; Suzuki, H.; Obayori, O.S.; Adebusoye, S.A.; Ilory, M.O.; Amund, O.O.; Endo, G. Biodegradation of crude oil and phenanthrene by heavy metal resistant Bacillus subtilis isolated from a multi-polluted industrial wastewater creek. Int. Biodeterior. Biodegrad. 2017, 120, 143-151. [CrossRef] · DOI
  73. Lee, S.; Kim, Y.; Kim, J.M.; Chu, B.; Joa, J.H.; Sang, M.K.; Song, J.; Weon, H.Y. A preliminary examination of bacterial, archaeal, and fungal communities inhabiting different rhizocompartments of tomato plants under real-world environments. Sci. Rep. 2019, 9, 9300. [CrossRef] · DOI
  74. Harayama, S.; Kasai, Y.; Hara, A. Microbial communities in oil-contaminated seawater. Curr. Opin. Biotechnol. 2004, 15, 205-214. [CrossRef] · DOI
  75. Lyu, Y.; Zheng, W.; Zheng, T.; Tian, Y. Biodegradation of polycyclic aromatic hydrocarbons by Novosphingobium pentaromativorans US6-1. PLoS ONE 2014, 9, e11131942. [CrossRef] [PubMed] · DOI
  76. Jeyavani, J.; Sibiya, A.; Shanthini, S.; Ravi, C.; Vijayakumar, S.; Rajan, D.K.; Vaseeharan, B. A review on aquatic impacts of microplastics and its bioremediation aspects. Curr. Pollut. Rep. 2021, 7, 286-299. [CrossRef] · DOI
  77. Shah, A.A.; Hasan, F.; Hameed, A.; Ahmed, S. Biological degradation of plastics: A comprehensive review. Biotechnol. Adv. 2008, 26, 246-265. [CrossRef] · DOI · Paper page
  78. Nie, J.; Sun, Y.; Zhou, Y.; Kumar, M.; Usman, M.; Li, J.; Shao, J.; Wang, L.; Tsang, D.C. Bioremediation of water containing pesticides by microalgae: Mechanisms, methods, and prospects for future research. Sci. Total Environ. 2020, 707, 136080. [CrossRef] [PubMed] · DOI
  79. Bilal, M.; Iqbal, H.M.; Barceló, D. Persistence of pesticides-based contaminants in the environment and their effective degradation using laccase-assisted biocatalytic systems. Sci. Total Environ. 2019, 695, 133896. [CrossRef] [PubMed] · DOI
  80. Fomina, M.; Gadd, G.M. Biosorption: Current perspectives on concept, definition and application. Bioresour. Technol. 2014, 160, 3-14. [CrossRef] · DOI
  81. Ungureanu, G.; Santos, S.; Boaventura, R.; Botelho, C. Arsenic and antimony in water and wastewater: Overview of removal techniques with special reference to latest advances in adsorption. J. Environ. Manag. 2015, 151, 326-342. [CrossRef] · DOI
  82. Hussein, M.H.; Abdullah, A.M.; Badr El-Din, N.I.; Mishaqa, E.S.I. Biosorption potential of the microchlorophyte Chlorella vulgaris for some pesticides. J. Fertil. Pestic. 2017, 8, 177. [CrossRef] · DOI
  83. Jin, B.; Xie, L.; Guo, Y.; Pang, G. Multi-residue detection of pesticides in juice and fruit wine: A review of extraction and detection methods. Food Res. Int. 2012, 46, 399-409. [CrossRef] · DOI
  84. Pérez-Legaspi, I.A.; Ortega-Clemente, L.A.; Moha-León, J.D.; Ríos-Leal, E.; Gutiérrez, S.C.R.; Rubio-Franchini, I. Effect of the pesticide lindane on the biomass of the microalgae Nannochloris oculata. J. Environ. Sci. Health 2016, 51, 103-106. [CrossRef] · DOI
  85. Kanekar, N.; Briggs, F.H. 21-cm absorption studies with the Square Kilometer Array. New Astron. Rev. 2004, 48, 1259-1270. [CrossRef] · DOI
  86. Pieper, D.H.; Reineke, W. Engineering bacteria for bioremediation. Curr. Opin. Biotechnol. 2000, 11, 262-270. [CrossRef] · DOI
  87. Cecchin, I.; Reddy, K.R.; Thomé, A.; Tessaro, E.F.; Schnaid, F. Nanobioremediation: Integration of nanoparticles and bioremediation for sustainable remediation of chlorinated organic contaminants in soils. Int. Biodeterior. Biodegrad. 2017, 119, 419-428. [CrossRef] · DOI
  88. Rashidian, G.; Lazado, C.C.; Mahboub, H.H.; Mohammadi-Aloucheh, R.; Prokić, M.D.; Nada, H.S.; Faggio, C. Chemically and green synthesized ZnO nanoparticles alter key immunological molecules in common carp (Cyprinus carpio) skin mucus. Int. J. Mol. Sci. 2021, 22, 3270. [CrossRef] [PubMed] · DOI
  89. Yadav, J.S.; Tiwari, S.K. Effect of waste rubber fibres on the geotechnical properties of clay stabilized with cement. Appl. Clay Sci. 2017, 149, 97-110. [CrossRef] · DOI
  90. Cappello, S.; Mancini, G. Use of nanomaterials for marine bioremediation: A perspective. Ann. Mater. Sci. Eng. 2019, 4, 1035.
  91. Ball, A.S.; Patil, S.; Soni, S. Introduction into nanotechnology and microbiology. In Methods in Microbiology; Academic Press: Cambridge, MA, USA, 2019; Volume 46, pp. 1-18.

Authors
Aliko, V., Multisanti, C. R., Turani, B., & Faggio, C.
Affiliations
  • University of Tirana (AL)
  • University of Messina (IT)
  • Kolegji Universitar Qiriazi (AL)
Corresponding author
Faggio, Caterina
Venue
Sustainability
Publisher
MDPI AG
Published
2022-09-19
Volume
14
Issue
18
Pages
11784
ISSN
2071-1050 (ISSN-L)
OpenAlex
W4297906638
Cited by
110
References
2
Citations by year
2026: 10 · 2025: 28 · 2024: 34 · 2023: 34 · 2022: 4
FWCI
5.87
Type
journal article
Language
en
Open access
Locations
  • Sustainability (publishedVersion, cc-by)
  • RePEc: Research Papers in Economics (submittedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Physical Sciences › Environmental Science › Pollution › Microbial bioremediation and biosurfactants
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Environmental Toxicology and Ecotoxicology
  • Physical Sciences › Environmental Science › Environmental Chemistry › Environmental Chemistry and Analysis
Keywords
marine pollution, bioremediation, aquatic contaminants, bioaccumulation, biomagnification, microorganisms, wastewater, ship discharges, toxic substances, detoxification, anthropogenic impacts on aquatic ecosystems, human health

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review