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020 ▼a 9781088353462
035 ▼a (MiAaPQ)AAI22585421
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 247004
0820 ▼a 631.4
1001 ▼a Sharma, Kriti.
24510 ▼a Illuminating Dark Matter: Light Microscopy and Raman Microspectroscopy Through Transparent Porous Media for Applications in Soil and Sediment Microbial Ecology.
260 ▼a [S.l.]: ▼b The University of North Carolina at Chapel Hill., ▼c 2019.
260 1 ▼a Ann Arbor: ▼b ProQuest Dissertations & Theses, ▼c 2019.
300 ▼a 167 p.
500 ▼a Source: Dissertations Abstracts International, Volume: 81-05, Section: B.
500 ▼a Advisor: Shank, Elizabeth A.
5021 ▼a Thesis (Ph.D.)--The University of North Carolina at Chapel Hill, 2019.
506 ▼a This item must not be sold to any third party vendors.
520 ▼a Soils offer habitats to an unparalleled abundance and diversity of microorganisms, whose activities are critical to agriculture, ecosystem health, and biogeochemical cycling. A major barrier to understanding soil microbes within their habitats is the opacity of natural soils. Despite a long history of endeavors to visualize life in the soil, and promising advancements in this field, non-destructive approaches that allow dynamic insights into microbial life in soils are particularly lacking. Chapter 1 reviews this field and outlines the history and potential of optically transparent porous media as model soil systems amenable to non-destructive imaging of soil microorganisms within three-dimensional soil-like matrices.In Chapter 2, I introduce the utility of single-cell Raman spectroscopy (SCRS) for non-destructive stable isotope probing over time, particularly for monitoring the uptake of 13C by bacteria from complex natural polysaccharides. This spatially resolved and non-destructive approach allows us to ask the question, "Do bacterial biofilms allow bacteria to stick together in numbers large enough to initiate cooperative decomposition of necromass?'In Chapter 3, I assess the polymer Nafion and the crystal cryolite as substrates for optically transparent model soil systems called "transparent soil" (TS) microcosms. I find that both substrates are compatible with optical microscopy and enable growth, maintenance, and visualization of micron-sized bacteria in three-dimensional porous matrices over time. Both substrates are also compatible with SCRS, and enable stable isotope probing (SIP) using deuterium (D2O) as a non-destructive marker of microbial activity in situ, while cryolite-based microcosms also enable measurement of 13C label uptake in bacteria. I use D2O label tracing to show that bacterial cells attached to dead fungal hyphae within a Nafion matrix show more metabolic activity after a dry-wet cycle than cells far away from the fungal hyphae, corroborating the important role of fungi in facilitating survival of bacteria in the fluctuating conditions found in soils.In Chapter 4, I present a method for rapid and inexpensive manufacture of microfluidics devices that were used to construct TS microcosms at the lab bench. Chapter 5 summarizes the dissertation overall and offers suggestions for future research.
590 ▼a School code: 0153.
650 4 ▼a Microbiology.
650 4 ▼a Ecology.
650 4 ▼a Soil sciences.
690 ▼a 0410
690 ▼a 0329
690 ▼a 0481
71020 ▼a The University of North Carolina at Chapel Hill. ▼b Biology.
7730 ▼t Dissertations Abstracts International ▼g 81-05B.
773 ▼t Dissertation Abstract International
790 ▼a 0153
791 ▼a Ph.D.
792 ▼a 2019
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T15492943 ▼n KERIS ▼z 이 자료의 원문은 한국교육학술정보원에서 제공합니다.
980 ▼a 202002 ▼f 2020
990 ▼a ***1008102
991 ▼a E-BOOK