Location-dependent marine biodegradability of aliphatic polyesters under simulated seawater conditions

• Lab-controlled marine conditions were established using seawater from 12 Japanese sites. • PHBV exhibited consistently high mineralization regardless of the sampling location. • In contrast, PBSA degradation was highly site-dependent, showing mass loss at only one site. • PHBV plastisphere was dominated by Alteromonadaceae, Colwelliaceae , and Oceanospirillaceae . • The variability in PBSA degradability indicates its sensitivity to local microbial communities. Biodegradable plastics can help reduce marine plastic pollution. However, most studies have tested biodegradability at only one site; therefore, distinguishing material effects from seawater conditions is difficult. In this study, we evaluated the location-dependent marine biodegradability of two representative aliphatic polyesters, poly(3-hydroxybutyrate- co -3-hydroxyvalerate) (PHBV) and poly(butylene succinate- co -adipate) (PBSA), under identical laboratory conditions using seawater collected from 12 coastal sites in Japan. Film mass loss, biochemical oxygen demand (BOD) -based mineralization (BOD/theoretical oxygen demand, ThOD), and plastisphere composition were assessed, with polyethylene serving as a non-biodegradable reference. PHBV degraded in all seawater samples, and achieving substantial BOD-based mineralization (52-86%). In contrast, PBSA degraded only in seawater from Isumi, Chiba (CI), Japan, and no measurable mineralization was detected. Amplicon sequencing indicated that PHBV formed a consistent material-specific plastisphere containing members of Alteromonadaceae, Colwelliaceae , and Oceanospirillaceae , independent of the sampling location. PBSA plastispheres varied among sites. Although genera previously linked to polyester degradation (e.g., Pseudomonas, Halopseudomonas, Alcanivorax ) were detected, their involvement in the biofilm community observed at CI remains speculative. Collectively, these findings demonstrate that PHBV biodegradability is robust across locations, whereas PBSA degradation is site-dependent under the same laboratory conditions.

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Publication Details

Journal
Polymer Degradation and Stability
Published
2026-01-30
DOI
https://doi.org/10.1016/j.polymdegradstab.2026.111975
Citations
1
Primary Topic
biodegradable polymer synthesis and properties
Type
article
Field-Weighted Citation Impact
22.64
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article

Location-dependent marine biodegradability of aliphatic polyesters under simulated seawater conditions

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article

Location-dependent marine biodegradability of aliphatic polyesters under simulated seawater conditions

Yuya Tachibana, Hiroyuki Kashima, Miwa Suzuki, Shun Tsuboi, Phouvilay Soulenthone, Ken-ichi Kasuya, Keiji Numata, Hidetaka Nomaki, Noriyuki Isobe, Tomoya Suzuki, Masaaki Yoshida, Shun’ichi Ishii, Moeka Noguchi
article en
1 citations

Abstract

• Lab-controlled marine conditions were established using seawater from 12 Japanese sites. • PHBV exhibited consistently high mineralization regardless of the sampling location. • In contrast, PBSA degradation was highly site-dependent, showing mass loss at only one site. • PHBV plastisphere was dominated by Alteromonadaceae, Colwelliaceae , and Oceanospirillaceae . • The variability in PBSA degradability indicates its sensitivity to local microbial communities. Biodegradable plastics can help reduce marine plastic pollution. However, most studies have tested biodegradability at only one site; therefore, distinguishing material effects from seawater conditions is difficult. In this study, we evaluated the location-dependent marine biodegradability of two representative aliphatic polyesters, poly(3-hydroxybutyrate- co -3-hydroxyvalerate) (PHBV) and poly(butylene succinate- co -adipate) (PBSA), under identical laboratory conditions using seawater collected from 12 coastal sites in Japan. Film mass loss, biochemical oxygen demand (BOD) -based mineralization (BOD/theoretical oxygen demand, ThOD), and plastisphere composition were assessed, with polyethylene serving as a non-biodegradable reference. PHBV degraded in all seawater samples, and achieving substantial BOD-based mineralization (52-86%). In contrast, PBSA degraded only in seawater from Isumi, Chiba (CI), Japan, and no measurable mineralization was detected. Amplicon sequencing indicated that PHBV formed a consistent material-specific plastisphere containing members of Alteromonadaceae, Colwelliaceae , and Oceanospirillaceae , independent of the sampling location. PBSA plastispheres varied among sites. Although genera previously linked to polyester degradation (e.g., Pseudomonas, Halopseudomonas, Alcanivorax ) were detected, their involvement in the biofilm community observed at CI remains speculative. Collectively, these findings demonstrate that PHBV biodegradability is robust across locations, whereas PBSA degradation is site-dependent under the same laboratory conditions.

Polymer Degradation and StabilityVol. 247
Japan Agency for Marine-Earth Science and Technology (JP), Gunma University (JP), Shimane University (JP), National Institute of Technology and Evaluation (JP), Kyoto University (JP)
Life below water
Openalex Percentile: Top 1%
biodegradable polymer synthesis and properties
22.64
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