Marcin Daniel Syczewski

Dr. Marcin Daniel Syczewski

Faculty of Geology, University of Warsaw
orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 September 2022 in Chemosphere
Verified
Journal Article
Open access
Agnieszka DąbrowskaAgnieszka Dąbrowska
Agnieszka Dąbrowska
MMMaria Mielańczuk
Maria Mielańczuk
MSMarcin Daniel Syczewski
Marcin Daniel Syczewski
The increasing amount of marine microplastics and nanoplastics is due to primary (P-MPs) and secondary sources (S-MPs). Among small P-MPs and fibres from textiles, nurdles or industrial dust, the microbeads from cosmetics (peelings, scrubs) are dominant. The polyethylene and polypropylene debris, already <5 mm, enlarge Plastisphere and have a complex influence on environmental processes. Fortunately, the situation has changed with the limitation of synthetic materials in scrubs in recent years. This paper summarizes the six years of studies (2015-2021) on microplastics in cosmetics available on the Polish market. It focuses on those still available and presents the potential of Raman spectroscopy for the efficient qualitative and quantitative characterization of those materials. Finally, surface morphology's vital role in microplastics' general behaviour is underlined. The SEM/EDX and numerical modelling enables a more detailed description of particles.

1 April 2021 in Ore Geology Reviews
Verified
Journal Article
Closed access
XLXifeng Liu
Xifeng Liu
GGGrzegorz Gil
Grzegorz Gil
YLYan Liu
Yan Liu
XHXuemei He
Xuemei He
MSMarcin Daniel Syczewski
Marcin Daniel Syczewski
XSXiaochao Shu
Xiaochao Shu

1 November 2018 in Ecotoxicology and Environmental Safety
Verified
Journal Article
Closed access
ABAndrzej Borkowski
Andrzej Borkowski
ŁGŁukasz Gutowski
Łukasz Gutowski
MSMarcin Daniel Syczewski
Marcin Daniel Syczewski
TCTomasz Cłapa
Tomasz Cłapa
GCGrzegorz Czerwonka
Grzegorz Czerwonka

2 January 2019 in Biofouling
Verified
Journal Article
Closed access
GCGrzegorz Czerwonka
Grzegorz Czerwonka
DGDawid Gmiter
Dawid Gmiter
AGAnna Guzy
Anna Guzy
PRPatrycja Rogala
Patrycja Rogala
AJAgnieszka Jabłońska-Wawrzycka
Agnieszka Jabłońska-Wawrzycka
WKWiesław Kaca
Wiesław Kaca
Pseudomonas aeruginosa biofilm-associated infections are a serious medical problem, and new compounds and therapies acting through novel mechanisms are much needed. Herein, the authors report a ruthenium(IV) complex that reduces P. aeruginosa PAO1 biofilm formation by 84%, and alters biofilm morphology and the living-to-dead cell ratio at 1 mM concentration. Including the compound in the culture medium altered the pigments secreted by PAO1, and fluorescence spectra revealed a decrease in pyoverdine. Scanning electron microscopy showed that the ruthenium complex did not penetrate the bacterial cell wall, but accumulated on external cell structures. Fluorescence quenching experiments indicated strong binding of the ruthenium complex to both plasmid DNA and bovine serum albumin. Formamidopyrimidine DNA N-glycosylase (Fpg) protein digestion of plasmid DNA isolated after ruthenium(IV) complex treatment revealed the generation of oxidative stress, which was further proved by the observed upregulation of catalase and superoxide dismutase gene expression.

9 April 2021 in Biology
Verified
Journal Article
Open access
PDF file
Nataliia KhomutovskaNataliia Khomutovska
Nataliia Khomutovska
AMAsuncion de los Ríos Murillo
Asuncion de los Ríos Murillo
MSMarcin Daniel Syczewski
Marcin Daniel Syczewski
IJIwona Jasser
Iwona Jasser
Microbial communities found in arid environments are commonly represented by biological soil crusts (BSCs) and endolithic assemblages. There is still limited knowledge concerning endoliths and BSCs occurring in the cold mountain desert of Pamir. The aim of the study was to investigate the composition and structure of endolithic bacterial communities in comparison to surrounding BSCs in three subregions of the Eastern Pamir (Tajikistan). The endolithic and BSC communities were studied using culture-independent and culture-dependent techniques. The structure of the endolithic bacterial communities can be characterized as Actinobacteria–Proteobacteria–Bacteroidetes–Chloroflexi–Cyanobacteria, while the BSCs’ can be described as Proteobacteria–Actinobacteria–Bacteroidetes–Cyanobacteria assemblages with low representation of other bacteria. The endolithic cyanobacterial communities were characterized by the high percentage of Chroococcidiopsaceae, Nodosilineaceae, Nostocaceae and Thermosynechococcaceae, while in the BSCs were dominated by Nodosilineaceae, Phormidiaceae and Nostocaceae. The analysis of 16S rRNA genes of the cyanobacterial cultures revealed the presence of possibly novel species of Chroococcidiopsis, Gloeocapsopsis and Wilmottia. Despite the niches’ specificity, which is related to the influence of microenvironment factors on the composition and structure of endolithic communities, our results illustrate the interrelation between the endoliths and the surrounding BSCs in some regions. The structure of cyanobacterial communities from BSC was the only one to demonstrate some subregional differences.

1 February 2018 in Carbon
Verified
Journal Article
Closed access
WKWojciech Kicinski
Wojciech Kicinski
MSMateusz Szala
Mateusz Szala
TCTomasz Cłapa
Tomasz Cłapa
MSMarcin Daniel Syczewski
Marcin Daniel Syczewski
ABAndrzej Borkowski
Andrzej Borkowski