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Does dinocyst wall composition really reflect trophic affinity? New evidence from ATR micro‐FTIR spectroscopy measurements
Attenuated total reflection (ATR) microscope Fourier transform infrared (micro‐FTIR) spectroscopy was used to investigate the dinosporin composition in the walls of modern, organic‐walled dinoflagellate resting cysts (dinocysts). Variable cyst wall compositions were observed, which led to the erection of four spectrochemical groups, some with striking similarities to other resistant biomacromolecules such as sporopollenin and algaenan. Furthermore, possible proxies derivable from the spectrochemical composition of modern and fossil dinocysts were discussed. The color of the dinocyst walls was reflected in the spectral data. When comparing that color with a standard and the results of a series of bleaching experiments with oxidative agents, eumelanin was assigned as a likely pigment contributing to the observed color. Following this assignment, the role of eumelanin as an ultraviolet sunscreen in colored dinocysts was hypothesized, and its implications on the autofluorescence and morphological preservation of dinocysts were further discussed. Unlike what had previously been assumed, it was shown that micro‐FTIR data from dinocysts cannot be used to unambiguously infer trophic affinities of their associated cells. Finally, using methods with high spatial resolutions (synchrotron transmission micro‐FTIR and optical photothermal infrared spectroscopy), it was shown that dinocyst wall layers are chemically homogenous at the probed scales. This study fills a large knowledge gap in our understanding of the chemical nature of dinocyst walls and has nuanced certain assumptions and interpretations made in the past.
Keyword(s)
attenuated total reflection micro-Fourier transform infrared spectroscopy, bleaching, dinosporin composition, optical photothermal infrared spectroscopy, organic-walled dinocysts, pigments, spectrochemical methods, sunscreen, synchrotron radiation, trophic affinity
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Publisher's official version | 21 | 12 Mo | ||
Figure S1.The effects of UVA bleaching on the morphology of an initially colored (Archaeperidinium minutum) and initially transparent (Pentapharsodinium dalei) cyst. | - | 652 Ko | ||
Figure S2. The presence of small protrusions (red arrows) of the resistant and transparent inner wall layer of a UVA bleached cyst of Archaeperidinium minutum which are located at the locations ... | - | 678 Ko | ||
Figure S3. The areas analyzed with O-PTIR spectroscopy from the cyst specimens presented in Figure 4c (each blue or red square represents a measurement point). The corresponding spectral data is ... | - | 1 Mo | ||
Plate S1. Selection of modern dinocysts isolated from surface sediments, analyzed ... | - | 14 Mo | ||
Plate S2. Selection of modern dinocysts isolated from surface sediments, analyzed via ATR micro-FTIR spectroscopy and assigned to spectrochemical group 2.... | - | 12 Mo | ||
Plate S3. Selection of modern dinocysts isolated from surface sediments, analyzed via ATR micro-FTIR spectroscopy and assigned to spectrochemical groups 2.... | - | 15 Mo | ||
Table S1. Overview and additional information of all surface sediment and rock samples used in this study. | - | 12 Ko | ||
Table S2. Complete ATR micro-FTIR dataset used and presented in this study (Figures 1–3). This table is in a format directly loadable into the Quasar software package (see Materials and Methods... | - | 6 Mo | ||
Table S3. Metadata, counts and spectrochemical group assignments of all specimens and standards analyzed via ATR micro-FTIR spectroscopy in this study. | - | 17 Ko | ||
Table S4. The synchrotron transmission micro-FTIR dataset corresponding to the specimen presented in Figure 4a–b. This table is in a format directly loadable into the Quasar software package ... | - | 4 Mo | ||
Table S5. The O-PTIR dataset corresponding to the specimens presented Figure 4c. This table is in a format directly loadable into the Quasar software package (see Materials and Methods section). | - | 583 Ko | ||
Video S1. Bleaching of a cyst of Gymnodinium catenatum under UVA (385–330 nm) exposure. Captured at 1000× using 1 frame⋅s−1. Playback speed is 8× (8 frames⋅s−1). | - | 15 Mo | ||
Video S2. Bleaching of a cyst of Pentapharsodinium dalei under UVA (385–330 nm) exposure. Captured at 1000× using 1 frame⋅s−1. Playback speed is 8× (8 frames⋅s−1). | - | 16 Mo | ||
Video S3. Bleaching of a cyst of Archaeperidinium minutum under UVA (385–330 nm) exposure. Captured at 1000× using 1 frame⋅s−1. Playback speed is 8× (8 frames⋅s−1). | - | 4 Mo | ||
Video S4. Bleaching of a cyst of Dubridinium sp. under UVA (385–330 nm) exposure. Captured at 1000× using 1 frame⋅s−1. Playback speed is 8× (8 frames⋅s−1). | - | 34 Mo | ||
Author's final draft | 50 | 888 Ko |