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  • American Chemical Society  (2,084,048)
  • Cell Press  (242,170)
  • American Chemical Society (ACS)
Collection
Publisher
Years
  • 1
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.2000 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1525-7797
    Electronic ISSN: 1526-4602
    Topics: Chemistry and Pharmacology
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  • 2
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    American Chemical Society (ACS)
    Online: 94.2016 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0009-2347
    Electronic ISSN: 1520-605X , 2474-7408
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 3
    Journal cover
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    Cell Press | Elsevier
    Online: 80(1).1995 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 0092-8674
    Electronic ISSN: 1097-4172
    Topics: Biology , Medicine
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  • 4
    Journal cover
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    Cell Press | Elsevier
    Online: 23.2016 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Electronic ISSN: 2451-9456
    Topics: Biology , Chemistry and Pharmacology
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  • 5
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    Cell Press | Elsevier
    Online: 1(1).2015 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 2405-4712
    Electronic ISSN: 2405-4720
    Topics: Biology
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  • 6
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    Cell Press
    Online: 1(1).2016 – (older than 12 months)
    Publisher: Cell Press
    Print ISSN: 2451-9308
    Electronic ISSN: 2451-9294
    Topics: Chemistry and Pharmacology
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  • 7
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    Cell Press | Elsevier
    Online: 2(1).1995 – 22.2015
    Publisher: Cell Press , Elsevier
    Print ISSN: 1074-5521
    Electronic ISSN: 1879-1301
    Topics: Biology , Chemistry and Pharmacology
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  • 8
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    American Chemical Society (ACS)
    Online: 1.2009 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1944-8244
    Electronic ISSN: 1944-8252
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 9
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    American Chemical Society (ACS)
    Online: 1(1).2015 –
    Publisher: American Chemical Society (ACS)
    Electronic ISSN: 2374-7951
    Topics: Chemistry and Pharmacology
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  • 10
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.2006 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1554-8929
    Electronic ISSN: 1554-8937
    Topics: Biology , Chemistry and Pharmacology
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  • 11
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.2016 –
    Publisher: American Chemical Society (ACS)
    Electronic ISSN: 2380-8195
    Topics: Energy, Environment Protection, Nuclear Power Engineering
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  • 12
    Journal cover
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    American Chemical Society (ACS)
    Online: 1(1).2016 –
    Publisher: American Chemical Society (ACS)
    Electronic ISSN: 2470-1343
    Topics: Chemistry and Pharmacology
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  • 13
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.2018 –
    Publisher: American Chemical Society (ACS)
    Electronic ISSN: 2575-9108
    Topics: Chemistry and Pharmacology , Medicine
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  • 14
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    American Chemical Society (ACS)
    Online: 1.1929 –
    Formerly as: Industrial and Engineering Chemistry / Analytical Edition  (1929–1946)
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0003-2700 , 0096-4484
    Electronic ISSN: 1520-6882
    Topics: Chemistry and Pharmacology
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  • 15
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    American Chemical Society (ACS)
    Online: 1.1962 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0006-2960
    Electronic ISSN: 1520-4995
    Topics: Biology , Chemistry and Pharmacology
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  • 16
    Journal cover
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    Cell Press | Elsevier
    Online: 1(1).1994 – 22(12).2015
    Publisher: Cell Press , Elsevier
    Print ISSN: 1074-5521
    Electronic ISSN: 1879-1301
    Topics: Biology , Chemistry and Pharmacology
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  • 17
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.1989 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0897-4756
    Electronic ISSN: 1520-5002
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 18
    Journal cover
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    American Chemical Society (ACS)
    Online: 1(1).2016 –
    Publisher: American Chemical Society (ACS)
    Electronic ISSN: 2379-3694
    Topics: Biology , Chemistry and Pharmacology
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  • 19
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    American Chemical Society (ACS)
    Online: 1.2012 –
    Publisher: American Chemical Society (ACS)
    Electronic ISSN: 2161-5063
    Topics: Biology , Chemistry and Pharmacology
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  • 20
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    Cell Press | Elsevier | American Society of Human Genetics | früher University of Chicago Press | PubMed Central
    Online: 1.1949 – (older than 6 months)
    Publisher: Cell Press , Elsevier , American Society of Human Genetics , früher University of Chicago Press , PubMed Central
    Corporation: American Society of Human Genetics
    Print ISSN: 0002-9297
    Electronic ISSN: 1537-6605
    Topics: Biology , Medicine
    Parallel titles: The American Journal of Human Genetics
    Acronym: AJHG
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  • 21
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    American Chemical Society (ACS)
    Online: 3(8).2000 – 7(12).2004
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1099-8209
    Electronic ISSN: 1532-4486
    Topics: Chemistry and Pharmacology
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  • 22
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    American Chemical Society (ACS)
    Online: 1.1990 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1043-1802
    Electronic ISSN: 1520-4812
    Topics: Chemistry and Pharmacology
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  • 23
    Journal cover
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    Cell Press | Elsevier
    Online: 1.1960 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 0006-3495
    Electronic ISSN: 1542-0086
    Topics: Biology , Physics
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  • 24
    Journal cover
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    Cell Press | Elsevier | Biophysical Society, PubMed Central, Highwire Press
    Online: 1.1960 – (older than 12 months)
    Publisher: Cell Press , Elsevier , Biophysical Society, PubMed Central, Highwire Press
    Print ISSN: 0006-3495
    Electronic ISSN: 1542-0086
    Topics: Biology , Physics
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  • 25
    Journal cover
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    Cell Press | Elsevier
    Online: 1.2012 –
    Publisher: Cell Press , Elsevier
    Electronic ISSN: 2211-1247
    Topics: Biology
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  • 26
    Journal cover
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    Cell Press | Elsevier
    Online: 1.2007 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Electronic ISSN: 1931-3128 , 1934-6069
    Topics: Biology
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  • 27
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    American Chemical Society (ACS)
    Online: 30(9).2000 – 31(12).2001
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1531-5339
    Electronic ISSN: 1527-4799
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 28
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.1924 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0009-2665
    Electronic ISSN: 1520-6890
    Topics: Chemistry and Pharmacology
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  • 29
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    Elsevier | Cell Press
    Online: 1.2018 –
    Publisher: Elsevier , Cell Press
    Electronic ISSN: 2589-0042
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Natural Sciences in General , Physics
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  • 30
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    American Chemical Society | ACS Publications
    Online: 1(1).2021 –
    Publisher: American Chemical Society , ACS Publications
    Electronic ISSN: 2691-3704
    Topics: Chemistry and Pharmacology
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  • 31
    Formerly as: Journal of Chemical Documentation; Journal of Chemical Information and Computer Sciences  (1961–2004)
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0021-9576 , 0095-2338 , 1549-9596
    Electronic ISSN: 1520-5142 , 1549-960X
    Topics: Chemistry and Pharmacology
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  • 32
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    American Chemical Society (ACS)
    Online: 1.1959 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0022-2623 , 0095-9065
    Electronic ISSN: 1520-4804 , 1943-2992
    Topics: Chemistry and Pharmacology , Medicine
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  • 33
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    Cell Press
    Online: 1(1).2020 –
    Publisher: Cell Press
    Electronic ISSN: 2666-2477
    Topics: Biology , Medicine
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  • 34
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    Elsevier | Cell Press
    Online: 1(1).2020 –
    Publisher: Elsevier , Cell Press
    Electronic ISSN: 2666-6758
    Topics: Natural Sciences in General
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  • 35
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    Cell Press | Elsevier
    Online: 1.1974 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 0092-8674
    Electronic ISSN: 1097-4172
    Topics: Biology , Medicine
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  • 36
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    Cell Press | Elsevier
    Online: 1(1).2007 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 1934-5909
    Electronic ISSN: 1875-9777
    Topics: Biology
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  • 37
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    American Chemical Society (ACS)
    Online: 1.2002 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1535-3893
    Electronic ISSN: 1535-3907
    Topics: Chemistry and Pharmacology
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  • 38
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    American Chemical Society (ACS)
    Online: 1.1968 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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  • 39
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    American Chemical Society (ACS)
    Online: 1.1967 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0013-936X
    Electronic ISSN: 1520-5851
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
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  • 40
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    American Chemical Society (ACS)
    Online: 1.2014 –
    Publisher: American Chemical Society (ACS)
    Electronic ISSN: 2328-8930
    Topics: Energy, Environment Protection, Nuclear Power Engineering
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  • 41
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    American Chemical Society (ACS)
    Online: 1.1953 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0021-8561
    Electronic ISSN: 1520-5118
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
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  • 42
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    American Chemical Society (ACS)
    Online: 1.2005 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1549-9618
    Electronic ISSN: 1549-9626
    Topics: Chemistry and Pharmacology
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  • 43
    Journal cover
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    American Chemical Society (ACS)
    Online: 101.1997 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1089-5639
    Electronic ISSN: 1520-5215
    Topics: Chemistry and Pharmacology , Physics
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  • 44
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    American Chemical Society (ACS)
    Online: 101(1).1997 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1089-5647 , 1520-6106
    Electronic ISSN: 1520-5207
    Topics: Chemistry and Pharmacology , Physics
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  • 45
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.2010 –
    Publisher: American Chemical Society (ACS)
    Electronic ISSN: 1948-7185
    Topics: Chemistry and Pharmacology , Physics
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  • 46
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    American Chemical Society (ACS)
    Online: 111.2007 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1932-7447
    Electronic ISSN: 1932-7455
    Topics: Chemistry and Pharmacology
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  • 47
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    American Chemical Society (ACS)
    Online: 1.1896 – 39.1935
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0022-3654
    Electronic ISSN: 1541-5740
    Topics: Chemistry and Pharmacology , Physics
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  • 48
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    American Chemical Society (ACS)
    Online: 1.1896 – 100.1996
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0022-3654 , 0092-7023 , 0092-7325
    Electronic ISSN: 1541-5740 , 1943-300X , 1943-3018
    Topics: Chemistry and Pharmacology , Physics
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  • 49
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    American Chemical Society (ACS)
    Online: 1(1).1961 – 14(4).1974
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0021-9576
    Electronic ISSN: 1541-5732
    Topics: Chemistry and Pharmacology
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  • 50
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.1956 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0021-9568 , 0095-9146
    Electronic ISSN: 1520-5134
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 51
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    American Chemical Society (ACS)
    Online: 1.1936 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0022-3263
    Electronic ISSN: 1520-6904
    Topics: Chemistry and Pharmacology
    Parallel titles: The Journal of Organic Chemistry
    Acronym: JOC
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  • 52
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    American Chemical Society (ACS)
    Online: 1.1962 – 25.1986
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0196-4313
    Electronic ISSN: 1541-4833
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 53
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0091-1968 , 0196-4321 , 0536-1079
    Electronic ISSN: 1541-4841 , 1943-2976 , 1943-3026
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 54
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    Cell Press | Elsevier
    Online: 5(1).1995 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 0960-9822
    Electronic ISSN: 1879-0445
    Topics: Biology
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  • 55
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    Cell Press | Elsevier
    Online: 1(1).2001 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 1534-5807
    Electronic ISSN: 1878-1551
    Topics: Biology , Medicine
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  • 56
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    American Chemical Society (ACS)
    Online: 1.1987 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0887-0624
    Electronic ISSN: 1520-5029
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Process Engineering, Biotechnology, Nutrition Technology
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  • 57
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    Cell Press | Elsevier
    Online: 1.1988 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 0896-6273
    Electronic ISSN: 1097-4199
    Topics: Biology , Medicine
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  • 58
    Journal cover
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    Cell Press | Elsevier
    Online: 14(1).1995 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 0896-6273
    Electronic ISSN: 1097-4199
    Topics: Biology , Medicine
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  • 59
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.2001 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1528-7483
    Electronic ISSN: 1528-7505
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 60
    Journal cover
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    American Chemical Society (ACS)
    Online: 1.1909 – 62.1970
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0019-7866 , 0095-9014
    Electronic ISSN: 1541-5724 , 1943-2968
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 61
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    American Chemical Society (ACS)
    Online: 1.1962 – 25.1986
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0196-4305
    Electronic ISSN: 1541-5716
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 62
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    American Chemical Society (ACS)
    Online: 1.1962 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0020-1669
    Electronic ISSN: 1520-510X
    Topics: Chemistry and Pharmacology
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  • 63
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    American Chemical Society | ACS Publications
    Online: 1.1879 –
    Publisher: American Chemical Society , ACS Publications
    Print ISSN: 0002-7863
    Electronic ISSN: 1520-5126
    Topics: Chemistry and Pharmacology
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  • 64
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    American Chemical Society (ACS)
    Online: 1.2001 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1530-6984
    Electronic ISSN: 1530-6992
    Topics: Chemistry and Pharmacology , Physics
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  • 65
    Journal cover
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    Cell Press | Elsevier
    Online: 1.2019 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Electronic ISSN: 2590-3322
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
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  • 66
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    American Chemical Society (ACS)
    Online: 1.1982 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0276-7333
    Electronic ISSN: 1520-6041
    Topics: Chemistry and Pharmacology
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  • 67
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    American Chemical Society (ACS)
    Online: 26.1987 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0888-5885
    Electronic ISSN: 1520-5045
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 68
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    American Chemical Society (ACS)
    Online: 1.1999 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1523-7060
    Electronic ISSN: 1523-7052
    Topics: Chemistry and Pharmacology
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  • 69
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    American Chemical Society (ACS)
    Online: 1.1985 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 0743-7463
    Electronic ISSN: 1520-5827
    Topics: Chemistry and Pharmacology
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  • 70
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    Cell Press | Elsevier
    Online: 1(1).1997 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 1097-2765
    Topics: Biology , Medicine
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  • 71
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    American Chemical Society (ACS)
    Online: 1.2004 –
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1543-8384
    Electronic ISSN: 1543-8392
    Topics: Chemistry and Pharmacology
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  • 72
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    Cell Press | Elsevier
    Online: 1.1993 – (older than 1 year)
    Publisher: Cell Press , Elsevier
    Print ISSN: 0969-2126
    Electronic ISSN: 1878-4186
    Topics: Biology , Medicine
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  • 73
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    Cell Press | Elsevier
    Online: 3(1).1995 – (older than 12 months)
    Publisher: Cell Press , Elsevier
    Print ISSN: 0969-2126
    Electronic ISSN: 1878-4186
    Topics: Biology , Medicine
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  • 74
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    Cell Press | Elsevier
    Online: 1(1).2020 –
    Publisher: Cell Press , Elsevier
    Electronic ISSN: 2666-1667
    Topics: Biology , Medicine
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  • 75
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    American Chemical Society (ACS)
    Online: 9(11).2000 – 13(12).2004
    Publisher: American Chemical Society (ACS)
    Print ISSN: 1062-094X
    Electronic ISSN: 1532-4494
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  • 76
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    American Chemical Society
    In:  EPIC3Environmental Science and Technology, American Chemical Society, 48, pp. 13451-13458, ISSN: 0013-936X
    Publication Date: 2014-11-21
    Description: Plastic pollution is an emerging global threat for marine wildlife. Many species of birds, reptiles and fishes are directly impaired by plastics as they can get entangled in ropes and drown or they can ingest plastic fragments which, in turn, may clog their stomachs and guts. Microplastics of less than 1 mm can be ingested by small invertebrates but their fate in the digestive organs and their effects on the animals are yet not well understood. We embedded fluorescent microplastics in artificial agarose-based food and offered the food to marine isopods, Idotea emarginata. The isopods did not distinguish between food with and food without microplastics. Upon ingestion, the microplastics were present in the stomach and in the gut but not in the tubules of the midgut gland which is the principal organ of enzyme-secretion and nutrient resorption. The feces contained the same concentration of micro-plastics as the food which indicates that no accumulation of microplastics happens during the gut passage. Long-term bioassays of six weeks showed no distinct effects of continu¬ous micro-plastic consumption on mortality, growth, and intermolt duration. I. emarginata are able to prevent intrusion of particles even smaller than 1 µm into the midgut gland which is facilitated by the complex structure of the stomach including a fine filter system. It separates the midgut gland tubules from the stomach and allows only the passage of fluids and chyme. Our results indicate that micro¬plastics, as administered in the experi¬ments, do not clog the digestive organs of isopods and do not have adverse effects on their life history parameters.
    Repository Name: EPIC Alfred Wegener Institut
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  • 77
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    American Chemical Society
    In:  EPIC3Environmental Science & Technology, American Chemical Society, 52(22), pp. 13279-13288
    Publication Date: 2019-03-13
    Repository Name: EPIC Alfred Wegener Institut
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  • 78
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    American Chemical Society
    In:  EPIC3Environmental Science & Technology, American Chemical Society, 54(24), pp. 15893-15903, ISSN: 0013-936X
    Publication Date: 2021-04-08
    Repository Name: EPIC Alfred Wegener Institut
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  • 79
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    American Chemical Society
    In:  EPIC3Environmental Science & Technology, American Chemical Society, 53, pp. 8747-8756, ISSN: 1520-5851
    Publication Date: 2020-06-04
    Description: Recent studies pointed to a high ice nucleating activity (INA) in the Arctic sea surface microlayer (SML). However, related chemical information is still sparse. In the present study, INA and free glucose concentrations were quantified in Arctic SML and bulk water samples from the marginal ice zone, the ice-free ocean, melt ponds, and open waters within the ice pack. T50 (defining INA) ranged from −17.4 to −26.8 °C. Glucose concentrations varied from 0.6 to 51 μg/L with highest values in the SML from the marginal ice zone and melt ponds (median 16.3 and 13.5 μg/L) and lower values in the SML from the ice pack and the ice-free ocean (median 3.9 and 4.0 μg/L). Enrichment factors between the SML and the bulk ranged from 0.4 to 17. A positive correlation was observed between free glucose concentration and INA in Arctic water samples (T50(°C) = (−25.6 ± 0.6) + (0.15 ± 0.04)·Glucose(μg/L), RP = 0.66, n = 74). Clustering water samples based on phytoplankton pigment composition resulted in robust but different correlations within the four clusters (RP between 0.67 and 0.96), indicating a strong link to phytoplankton-related processes. Since glucose did not show significant INA itself, free glucose may serve as a potential tracer for INA in Arctic water samples.
    Repository Name: EPIC Alfred Wegener Institut
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  • 80
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    American Chemical Society
    In:  EPIC3Environmental Science and Technology, American Chemical Society, 50(13), pp. 7066-7073, ISSN: 0013936X
    Publication Date: 2016-10-12
    Description: Atmospheric nuclear weapons testing (NWT) resulted in the injection of plutonium (Pu) into the atmosphere and subsequent global deposition. We present a new method for continuous semiquantitative measurement of 239Pu in ice cores, which was used to develop annual records of fallout from NWT in ten ice cores from Greenland and Antarctica. The 239Pu was measured directly using an inductively coupled plasma-sector field mass spectrometer, thereby reducing analysis time and increasing depth-resolution with respect to previous methods. To validate this method, we compared our one year averaged results to published 239Pu records and other records of NWT. The 239Pu profiles from the Arctic ice cores reflected global trends in NWT and were in agreement with discrete Pu profiles from lower latitude ice cores. The 239Pu measurements in the Antarctic ice cores tracked low latitude NWT, consistent with previously published discrete records from Antarctica. Advantages of the continuous 239Pu measurement method are (1) reduced sample preparation and analysis time; (2) no requirement for additional ice samples for NWT fallout determinations; (3) measurements are exactly coregistered with all other chemical, elemental, isotopic, and gas measurements from the continuous analytical system; and (4) the long half-life means the 239Pu record is stable through time.
    Repository Name: EPIC Alfred Wegener Institut
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  • 81
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    American Chemical Society
    In:  EPIC3Crystal Growth & Design, American Chemical Society, 18, pp. 2563-2571
    Publication Date: 2018-04-23
    Description: The morphology and growth kinetics of ice single crystals in aqueous solutions of type III antifreeze protein (AFP-III) have been studied in detail over a range of AFP-III concentrations and supercoolings. In pure water, the shape of ice crystals changes from the circular disklike to planar dendritic with increasing supercooling. In AFP-III solutions, ice crystals in the form of faceted plates, irregular dendrites with polygonized tips, and needles appear with increasing supercooling and AFP-III concentration. The growth rate of ice crystals in the crystallographic a direction is 2 orders of magnitude higher than that in the c direction. AFP-III molecules cause the stoppage of the growth of the prismatic and basal faces at low supercoolings. When supercooling exceeds the critical value, AFP-III favors the acceleration of the growth in both a and c directions. The observed behavior of AFP-III is explained in terms of the Cabrera-Vermilyea pinning model and the specificity of the dissipation of latent heat from the growing crystals with different shapes.
    Repository Name: EPIC Alfred Wegener Institut
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  • 82
    Publication Date: 2017-04-04
    Description: Red Pompeian paintings, very famous for their deep intensity, are currently suffering from darkening. The origins of this darkening degradation are not clearly identified yet and remain a major issue for curators. In the specific case of cinnabar (HgS)-based red pigment, a photoinduced conversion into black metacinnabar is usually suspected. This work is focused on the blackening of red cinnabar paintings coated on a sparry calcite mortar. Different samples exhibiting different levels of degradation were selected upon visual observations and analyzed by synchrotron-based microanalytical techniques. Atomic and molecular compositions of the different debased regions revealed two possible degradation mechanisms. On one hand, micro X-ray fluorescence elemental maps show peculiar distributions of chlorine and sulfur. On the other hand, X-ray absorption spectroscopy performed at both Cl and S K-edges confirms the presence of characteristic degradation products: (i) Hg- Cl compounds (e.g., corderoite, calomel, and terlinguaite), which may result from the reaction with exogenous NaCl, in gray areas; (ii) gypsum, produced by the calcite sulfation, in black coatings. Metacinnabar is never detected. Finally, a cross section was analyzed to map the in-depth alteration gradient. Reduced and oxidized sulfur distributions reveal that the sulfated black coating consists of a 5-ím-thick layer covering intact cinnabar.
    Description: Published
    Description: 7484-7492
    Description: reserved
    Keywords: Microspectroscopy Analysis ; 05. General::05.09. Miscellaneous::05.09.99. General or miscellaneous
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
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  • 83
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    American Chemical Society
    In:  EPIC3Environ. Sci. Technol., American Chemical Society, 46, pp. 11327-11335
    Publication Date: 2019-07-17
    Description: In this study, we investigated if industrial high-density polyethylene (HDPE) particles, a model microplastic free of additives, ranging 〉 0− 80 μm are ingested and taken up into the cells and tissue of the blue mussel Mytilus edulis L. The effects of exposure (up to 96 h) and plastic ingestion were observed at the cellular and subcellular level. Microplastic uptake into the gills and digestive gland was analyzed by a new method using polarized light microscopy. Mussel health status was investigated incorporating histological assessment and cytochemical biomarkers of toxic effects and early warning. In addition to being drawn into the gills, HDPE particles were taken up into the stomach and transported into the digestive gland where they accumulated in the lysosomal system after 3 h of exposure. Our results show notable histological changes upon uptake and a strong inflammatory response demonstrated by the formation of granulocytomas after 6 h and lysosomal membrane destabilization, which significantly increased with longer exposure times. We provide proof of principle that microplastics are taken up into cells and cause significant effects on the tissue and cellular level, which can be assessed with standard cytochemical biomarkers and polarized light microscopy for microplastic tracking in tissue.
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  • 84
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    Cell Press
    In:  EPIC3Current Biology, Cell Press, 23(14), pp. 1330-1334, ISSN: 09609822
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
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  • 85
    Publication Date: 2022-05-25
    Description: © The Author(s), 2015. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Cell Reports 11 (2015): 1-12, doi:10.1016/j.celrep.2015.03.049.
    Description: Although recent research revealed an impact of westernization on diversity and composition of the human gut microbiota, the exact consequences on metacommunity characteristics are insufficiently understood, and the underlying ecological mechanisms have not been elucidated. Here, we have compared the fecal microbiota of adults from two non-industrialized regions in Papua New Guinea (PNG) with that of United States (US) residents. Papua New Guineans harbor communities with greater bacterial diversity, lower inter-individual variation, vastly different abundance profiles, and bacterial lineages undetectable in US residents. A quantification of the ecological processes that govern community assembly identified bacterial dispersal as the dominant process that shapes the microbiome in PNG but not in the US. These findings suggest that the microbiome alterations detected in industrialized societies might arise from modern lifestyle factors limiting bacterial dispersal, which has implications for human health and the development of strategies aimed to redress the impact of westernization.
    Description: This study was partly funded by BioGaia AB. BioGaia had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. A portion of this research is part of the Microbiomes in Transition Initiative at Pacific Northwest National Laboratory (PNNL). This research was conducted under the Laboratory Directed Research and Development Program at PNNL, a multi-program national laboratory operated by Battelle for the US Department of Energy under contract DE-AC05-76RL01830.
    Repository Name: Woods Hole Open Access Server
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  • 86
    Publication Date: 2022-05-25
    Description: © The Author(s), 2012. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Cell Reports 2 (2012): 242–248, doi:10.1016/j.celrep.2012.06.016.
    Description: Ion selectivity of metazoan voltage-gated Na+ channels is critical for neuronal signaling and has long been attributed to a ring of four conserved amino acids that constitute the ion selectivity filter (SF) at the channel pore. Yet, in addition to channels with a preference for Ca2+ ions, the expression and characterization of Na+ channel homologs from the sea anemone Nematostella vectensis, a member of the early-branching metazoan phylum Cnidaria, revealed a sodium-selective channel bearing a noncanonical SF. Mutagenesis and physiological assays suggest that pore elements additional to the SF determine the preference for Na+ in this channel. Phylogenetic analysis assigns the Nematostella Na+-selective channel to a channel group unique to Cnidaria, which diverged 〉540 million years ago from Ca2+-conducting Na+ channel homologs. The identification of Cnidarian Na+-selective ion channels distinct from the channels of bilaterian animals indicates that selectivity for Na+ in neuronal signaling emerged independently in these two animal lineages.
    Description: This study was supported by a research grant from the Austrian National Science Foundation (FWF P 21108-B17) to U.T., and by a United States-Israel Binational Agricultural Research and Development Grant (IS-4313-10) and an Israeli Science Foundation grant (107/08) to M.G.
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  • 87
    Publication Date: 2022-05-25
    Description: © American Chemical Society, 2015. This article is posted here by permission of American Chemical Society; copying and redistribution for non-commercial research and education purposes only. The definitive version was published in ACS Nano 10 (2016): 6-37, doi:10.1021/acsnano.5b07826.
    Description: The microbiome presents great opportunities for understanding and improving the world around us and elucidating the interactions that compose it. The microbiome also poses tremendous challenges for mapping and manipulating the entangled networks of interactions among myriad diverse organisms. Here, we describe the opportunities, technical needs, and potential approaches to address these challenges, based on recent and upcoming advances in measurement and control at the nanoscale and beyond. These technical needs will provide the basis for advancing the largely descriptive studies of the microbiome to the theoretical and mechanistic understandings that will underpin the discipline of microbiome engineering. We anticipate that the new tools and methods developed will also be more broadly useful in environmental monitoring, medicine, forensics, and other areas.
    Description: This research was supported by the Office of Naval Research Grant #N000141410051 (P.S.W., G.C.L.W., and T.Y.), the Genomic Science Program of the U.S. DOE-OBER,
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  • 88
    Publication Date: 2022-05-25
    Description: Author Posting. © American Chemical Society, 2018. This is an open access article published under an ACS AuthorChoice License. The definitive version was published in Environmental Science and Technology Letters 5 (2018): 226–231, doi:10.1021/acs.estlett.8b00084.
    Description: Chemical dispersants are one of many tools used to mitigate the overall environmental impact of oil spills. In principle, dispersants break up floating oil into small droplets that disperse into the water column where they are subject to multiple fate and transport processes. The effectiveness of dispersants typically decreases as oil weathers in the environment. This decrease in effectiveness is often attributed to evaporation and emulsification, with the contribution of photochemical weathering assumed to be negligible. Here, we aim to test this assumption using Macondo well oil released during the Deepwater Horizon spill as a case study. Our results indicate that the effects of photochemical weathering on Deepwater Horizon oil properties and dispersant effectiveness can greatly outweigh the effects of evaporative weathering. The decrease in dispersant effectiveness after light exposure was principally driven by the decreased solubility of photo-oxidized crude oil residues in the solvent system that comprises COREXIT EC9500A. Kinetic modeling combined with geospatial analysis demonstrated that a considerable fraction of aerial applications targeting Deepwater Horizon surface oil had low dispersant effectiveness. Collectively, the results of this study challenge the paradigm that photochemical weathering has a negligible impact on the effectiveness of oil spill response and provide critical insights into the “window of opportunity” to apply chemical dispersants in response to oil spills in sunlit waters.
    Description: This work was supported, in part, by National Science Foundation Grant OCE-1333148, Gulf of Mexico Research Initiative Grants 015, SA 16-30, the DEEP-C consortium, and the Clark Family Foundation, Inc. EPA funding was provided to R.N.C. from the Oil Spill Liability Trust Fund.
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  • 89
    Publication Date: 2022-05-25
    Description: © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in iScience 1 (2018): 24-34, doi:10.1016/j.isci.2018.01.001.
    Description: The color and pattern changing abilities of octopus, squid, and cuttlefish via chromatophore neuro-muscular organs are unparalleled. Cuttlefish and octopuses also have a unique muscular hydrostat system in their skin. When this system is expressed, dermal bumps called papillae disrupt body shape and imitate the fine texture of surrounding objects, yet the control system is unknown. Here we report for papillae: (1) the motoneurons and the neurotransmitters that control activation and relaxation, (2) a physiologically fast expression and retraction system, and (3) a complex of smooth and striated muscles that enables long-term expression of papillae through sustained tension in the absence of neural input. The neural circuits controlling acute shape-shifting skin papillae in cuttlefish show homology to the iridescence circuits in squids. The sustained tension in papillary muscles for long-term camouflage utilizes muscle heterogeneity and points toward the existence of a “catch-like” mechanism that would reduce the necessary energy expenditure.
    Description: This work was funded by an AFOSR grant no. FA9550-14-1-0134, Isaac Newton Trust/Wellcome Trust ISSF/University of Cambridge Joint Research Grant (097814/Z/11/Z) to P.T.G-B., and a Biotechnology and Biological Sciences Research Council David Phillips Fellowship (BBSRC, BB/L024667/1) to T.J.W.
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  • 90
    Publication Date: 2022-05-25
    Description: © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Cell Reports 25 (2018): 1281–1291, doi:10.1016/j.celrep.2018.10.005.
    Description: Morphogenesis and mechanoelectrical transduction of the hair cell mechanoreceptor depend on the correct assembly of Usher syndrome (USH) proteins into highly organized macromolecular complexes. Defects in these proteins lead to deafness and vestibular areflexia in USH patients. Mutations in a non-USH protein, glutaredoxin domain-containing cysteine-rich 1 (GRXCR1), cause non-syndromic sensorineural deafness. To understand the deglutathionylating enzyme function of GRXCR1 in deafness, we generated two grxcr1 zebrafish mutant alleles. We found that hair bundles are thinner in homozygous grxcr1 mutants, similar to the USH1 mutants ush1c (Harmonin) and ush1ga (Sans). In vitro assays showed that glutathionylation promotes the interaction between Ush1c and Ush1ga and that Grxcr1 regulates mechanoreceptor development by preventing physical interaction between these proteins without affecting the assembly of another USH1 protein complex, the Ush1c- Cadherin23-Myosin7aa tripartite complex. By elucidating the molecular mechanism through which Grxcr1 functions, we also identify a mechanism that dynamically regulates the formation of Usher protein complexes.
    Description: This work was supported by grants from the NIH (DC004186, OD011195, and HD22486).
    Keywords: Grxcr1 ; Usher syndrome ; Hair cell ; Stereocilia ; Glutathionylation ; Harmonin ; Sans
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  • 91
    Publication Date: 2019-07-17
    Description: The low temperatures of polar regions and high-altitude environments, especially icy habitats, present challenges for many microorganisms. Their ability to live under subfreezing conditions implies the production of compounds conferring cryotolerance. Colwellia psychrerythraea 34H, a γ-proteobacterium isolated from subzero Arctic marine sediments, provides a model for the study of life in cold environments. We report here the identification and detailed molecular primary and secondary structures of capsular polysaccharide from C. psychrerythraea 34H cells. The polymer was isolated in the water layer when cells were extracted by phenol/water and characterized by one- and two-dimensional NMR spectroscopy together with chemical analysis. Molecular mechanics and dynamics calculations were also performed. The polysaccharide consists of a tetrasaccharidic repeating unit containing two amino sugars and two uronic acids bearing threonine as substituent. The structural features of this unique polysaccharide resemble those present in antifreeze proteins and glycoproteins. These results suggest a possible correlation between the capsule structure and the ability of C. psychrerythraea to colonize subfreezing marine environments.
    Repository Name: EPIC Alfred Wegener Institut
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  • 92
    Publication Date: 2022-01-07
    Description: Microplastic (MP) pollution has been found in the Southern Ocean surrounding Antarctica, but many local regions within this vast area remain uninvestigated. The remote Weddell Sea contributes to the global thermohaline circulation, and one of the two Antarctic gyres is located in that region. In the present study, we evaluate MP (〉300 μm) concentration and composition in surface (n = 34) and subsurface water samples (n = 79, ∼11.2 m depth) of the Weddell Sea. All putative MP were analyzed by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. MP was found in 65% of surface and 11.4% of subsurface samples, with mean (±standard deviation (SD)) concentrations of 0.01 (±0.01 SD) MP m–3 and 0.04 (±0.1 SD) MP m–3, respectively, being within the range of previously reported values for regions south of the Polar Front. Additionally, we aimed to determine whether identified paint fragments (n = 394) derive from the research vessel. Environmentally sampled fragments (n = 101) with similar ATR-FTIR spectra to reference paints from the research vessel and fresh paint references generated in the laboratory were further subjected to micro-X-ray fluorescence spectroscopy (μXRF) to compare their elemental composition. This revealed that 45.5% of all recovered MP derived from vessel-induced contamination. However, 11% of the measured fragments could be distinguished from the reference paints via their elemental composition. This study demonstrates that differentiation based purely on visual characteristics and FTIR spectroscopy might not be sufficient for accurately determining sample contamination sources.
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  • 93
    Publication Date: 2022-05-26
    Description: Author Posting. © American Chemical Society, 2014. This article is posted here by permission of American Chemical Society for personal use, not for redistribution. The definitive version was published in Environmental Science and Technology 38 (2014): 4732–4738, doi:10.1021/es4053076.
    Description: We present an extensive survey of floating plastic debris in the eastern North and South Pacific Oceans from more than 2500 plankton net tows conducted between 2001 and 2012. From these data we defined an accumulation zone (25 to 41°N, 130 to 180°W) in the North Pacific subtropical gyre that closely corresponds to centers of accumulation resulting from the convergence of ocean surface currents predicted by several oceanographic numerical models. Maximum plastic concentrations from individual surface net tows exceeded 106 pieces km–2, with concentrations decreasing with increasing distance from the predicted center of accumulation. Outside the North Pacific subtropical gyre the median plastic concentration was 0 pieces km–2. We were unable to detect a robust temporal trend in the data set, perhaps because of confounded spatial and temporal variability. Large spatiotemporal variability in plastic concentration causes order of magnitude differences in summary statistics calculated over short time periods or in limited geographic areas. Utilizing all available plankton net data collected in the eastern Pacific Ocean (17.4°S to 61.0°N; 85.0 to 180.0°W) since 1999, we estimated a minimum of 21 290 t of floating microplastic.
    Description: This work was supported by Sea Education Association, NFWF-NOAA Marine Debris Program (Nos. 2009-0062-002, NA10OAR4320148, Amend. 71), and NSF (Nos. OCE-0087528, OCE-1155379, OCE-1260403, OCE-1352422).
    Repository Name: Woods Hole Open Access Server
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  • 94
    Publication Date: 2022-05-26
    Description: © The American Chemical Society, 2016. This is an open access article published under an ACS AuthorChoice License. The definitive version was published in Analytical Chemistry 88 (2016): 7154–7162, doi:10.1021/acs.analchem.6b01260.
    Description: Discovery and identification of molecular biomarkers in large LC/MS data sets requires significant automation without loss of accuracy in the compound screening and annotation process. Here, we describe a lipidomics workflow and open-source software package for high-throughput annotation and putative identification of lipid, oxidized lipid, and oxylipin biomarkers in high-mass-accuracy HPLC-MS data. Lipid and oxylipin biomarker screening through adduct hierarchy sequences, or LOBSTAHS, uses orthogonal screening criteria based on adduct ion formation patterns and other properties to identify thousands of compounds while providing the user with a confidence score for each assignment. Assignments are made from one of two customizable databases; the default databases contain 14 068 unique entries. To demonstrate the software’s functionality, we screened more than 340 000 mass spectral features from an experiment in which hydrogen peroxide was used to induce oxidative stress in the marine diatom Phaeodactylum tricornutum. LOBSTAHS putatively identified 1969 unique parent compounds in 21 869 features that survived the multistage screening process. While P. tricornutum maintained more than 92% of its core lipidome under oxidative stress, patterns in biomarker distribution and abundance indicated remodeling was both subtle and pervasive. Treatment with 150 μM H2O2 promoted statistically significant carbon-chain elongation across lipid classes, with the strongest elongation accompanying oxidation in moieties of monogalactosyldiacylglycerol, a lipid typically localized to the chloroplast. Oxidative stress also induced a pronounced reallocation of lipidome peak area to triacylglycerols. LOBSTAHS can be used with environmental or experimental data from a variety of systems and is freely available at https://github.com/vanmooylipidomics/LOBSTAHS.
    Description: This research was supported by the Gordon and Betty Moore Foundation through Grant GBMF3301 to B.A.S.V.M. This research was also funded in part by a grant to B.A.S.V.M. from the Simons Foundation and is a contribution of the Simons Collaboration on Ocean Processes and Ecology (SCOPE). J.R.C. acknowledges support from a U.S. Environmental Protection Agency (EPA) STAR Graduate Fellowship (Fellowship Assistance Agreement No. FP-91744301-0).
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  • 95
    Publication Date: 2022-10-27
    Description: © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Meaders, J. L., de Matos, S. N., & Burgess, D. R. A pushing mechanism for microtubule aster positioning in a large cell type. Cell Reports, 33(1), (2020): 108213, doi:10.1016/j.celrep.2020.108213.
    Description: After fertilization, microtubule (MT) sperm asters undergo long-range migration to accurately position pronuclei. Due to the large sizes of zygotes, the forces driving aster migration are considered to be from pulling on the astral MTs by dynein, with no significant contribution from pushing forces. Here, we re-investigate the forces responsible for sperm aster centration in sea urchin zygotes. Our quantifications of aster geometry and MT density preclude a pulling mechanism. Manipulation of aster radial lengths and growth rates, combined with quantitative tracking of aster migration dynamics, indicates that aster migration is equal to the length of rear aster radii, supporting a pushing model for centration. We find that dynein inhibition causes an increase in aster migration rates. Finally, ablation of rear astral MTs halts migration, whereas front and side ablations do not. Collectively, our data indicate that a pushing mechanism can drive the migration of asters in a large cell type.
    Description: We would like to thank Dr. Jesse Gatlin for sending us the Tau-mCherry fusion protein for imaging live MTs. We would also like to thank Dr. Timothy Mitchison, Dr. Christine Field, and Dr. James Pelletier for supplying us with CA4, p150-CC1, and EB1-GFP peptides, as well as for fruitful discussions. Finally, we would like to thank Dr. Charles Shuster and Leslie Toledo-Jacobo for constructive feedback when preparing the manuscript. We thank Bret Judson and the Boston College Imaging Core for infrastructure and support. This material is based upon work supported by NSF grant no. 124425 to D.R.B.
    Keywords: Dynein ; Aster ; Microtubule ; Centrosome ; Pronucleus ; Fertilization ; Aster position
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  • 96
    Publication Date: 2022-10-27
    Description: © The Author(s), 2022. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Stolp, Z. D., Kulkarni, M., Liu, Y., Zhu, C., Jalisi, A., Lin, S., Casadevall, A., Cunningham, K. W., Pineda, F. J., Teng, X., & Hardwick, J. M. Yeast cell death pathway requiring AP-3 vesicle trafficking leads to vacuole/lysosome membrane permeabilization. Cell Reports, 39(2), (2022): 110647, https://doi.org/10.1016/j.celrep.2022.110647.
    Description: Unicellular eukaryotes have been suggested as undergoing self-inflicted destruction. However, molecular details are sparse compared with the mechanisms of programmed/regulated cell death known for human cells and animal models. Here, we report a molecular cell death pathway in Saccharomyces cerevisiae leading to vacuole/lysosome membrane permeabilization. Following a transient cell death stimulus, yeast cells die slowly over several hours, consistent with an ongoing molecular dying process. A genome-wide screen for death-promoting factors identified all subunits of the AP-3 complex, a vesicle trafficking adapter known to transport and install newly synthesized proteins on the vacuole/lysosome membrane. To promote cell death, AP-3 requires its Arf1-GTPase-dependent vesicle trafficking function and the kinase Yck3, which is selectively transported to the vacuole membrane by AP-3. Video microscopy revealed a sequence of events where vacuole permeability precedes the loss of plasma membrane integrity. AP-3-dependent death appears to be conserved in the human pathogenic yeast Cryptococcus neoformans.
    Description: Funding sources: National Institutes of Health, United States grants AI144373 and NS127076 (J.M.H.), AI115016 and AI153414 (K.W.C.), and AI052733, AI152078, and HL059842 (A.C.); National Natural Science Foundation of China 31970550; and the Priority Academic Program Development of the Jiangsu Higher Education Institutes (X.T.).
    Keywords: Yeast ; Programmed cell death ; Vesicle trafficking ; AP-3 ; Vacuole ; Cryptococcus ; Yck3 ; Regulated cell death ; Lysosome ; Vacuolar membrane permeabilization
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  • 97
    Publication Date: 2022-10-26
    Description: © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Walsh, A. N., Reddy, C. M., Niles, S. F., McKenna, A. M., Hansel, C. M., & Ward, C. P. Plastic formulation is an emerging control of its photochemical fate in the ocean. Environmental Science & Technology, 55(18), (2021): 12383–12392, https://doi.org/10.1021/acs.est.1c02272.
    Description: Sunlight exposure is a control of long-term plastic fate in the environment that converts plastic into oxygenated products spanning the polymer, dissolved, and gas phases. However, our understanding of how plastic formulation influences the amount and composition of these photoproducts remains incomplete. Here, we characterized the initial formulations and resulting dissolved photoproducts of four single-use consumer polyethylene (PE) bags from major retailers and one pure PE film. Consumer PE bags contained 15–36% inorganic additives, primarily calcium carbonate (13–34%) and titanium dioxide (TiO2; 1–2%). Sunlight exposure consistently increased production of dissolved organic carbon (DOC) relative to leaching in the dark (3- to 80-fold). All consumer PE bags produced more DOC during sunlight exposure than the pure PE (1.2- to 2.0-fold). The DOC leached after sunlight exposure increasingly reflected the 13C and 14C isotopic composition of the plastic. Ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry revealed that sunlight exposure substantially increased the number of DOC formulas detected (1.1- to 50-fold). TiO2-containing bags photochemically degraded into the most compositionally similar DOC, with 68–94% of photoproduced formulas in common with at least one other TiO2-containing bag. Conversely, only 28% of photoproduced formulas from the pure PE were detected in photoproduced DOC from the consumer PE. Overall, these findings suggest that plastic formulation, especially TiO2, plays a determining role in the amount and composition of DOC generated by sunlight. Consequently, studies on pure, unweathered polymers may not accurately represent the fates and impacts of the plastics entering the ocean.
    Description: Funding was provided by the Seaver Institute, the Gerstner Family Foundation, Woods Hole Oceanographic Institution, and the National Science Foundation Graduate Research Fellowship Program (A.N.W.). The Ion Cyclotron Resonance user facility at the National High Magnetic Field Laboratory is supported by the National Science Foundation Division of Chemistry and Division of Materials Research through DMR-1644779 and the State of Florida.
    Keywords: Plastic pollution ; Marine debris ; Additives ; Dissolved organic carbon ; Photochemical oxidation ; FT-ICR-MS ; Titanium dioxide
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 98
    Publication Date: 2022-05-27
    Description: © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Gosselin, K. M., Nelson, R. K., Spivak, A. C., Sylva, S. P., Van Mooy, B. A. S., Aeppli, C., Sharpless, C. M., O’Neil, G. W., Arrington, E. C., Reddy, C. M., & Valentine, D. L. Production of two highly abundant 2-methyl-branched fatty acids by blooms of the globally significant marine cyanobacteria Trichodesmium erythraeum. ACS Omega, 6(35), (2021): 22803–22810, https://doi.org/10.1021/acsomega.1c03196.
    Description: The bloom-forming cyanobacteria Trichodesmium contribute up to 30% to the total fixed nitrogen in the global oceans and thereby drive substantial productivity. On an expedition in the Gulf of Mexico, we observed and sampled surface slicks, some of which included dense blooms of Trichodesmium erythraeum. These bloom samples contained abundant and atypical free fatty acids, identified here as 2-methyldecanoic acid and 2-methyldodecanoic acid. The high abundance and unusual branching pattern of these compounds suggest that they may play a specific role in this globally important organism.
    Description: This work was funded with grants from the National Science Foundation grants OCE-1333148, OCE-1333162, and OCE-1756254 and the Woods Hole Oceanographic Institution (IR&D). GCxGC analysis made possible by WHOI’s Investment in Science Fund.
    Keywords: Lipids ; Alkyls ; Bacteria ; Genetics ; Chromatography
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 99
    Publication Date: 2022-05-27
    Description: © The Author(s), 2022. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Mazzotta, M. G., Reddy, C. M., & Ward, C. P. Rapid degradation of cellulose diacetate by marine microbes. Environmental Science & Technology Letters, 9(1), (2022): 37-41. https://doi.org/10.1021/acs.estlett.1c00843.
    Description: The persistence of cellulose diacetate (CDA), a biobased plastic used in textiles and single-use consumer products, in the ocean is currently unknown. Here, we probe the disintegration and degradation of CDA-based materials (25 μm films, 510 μm foam, and 97 g/m2 fabric) by marine microbes in a continuous flow seawater mesocosm. Photographic evidence and mass loss measurements demonstrate that CDA-based materials disintegrate in months. Disintegration is marked by the increasing esterase and cellulase activity of the biofilm community, suggesting that marine microbes degrade CDA. The natural abundance stable (13C) and radiocarbon (14C) isotopic signature of carbon dioxide respired during short-term bottle incubations confirms the rapid degradation of both acetyl and cellulosic components of CDA by seawater microbial communities. These findings challenge the paradigm set by governmental agencies and advocacy groups that CDA-based materials persist in the ocean for decades, and represent a positive step toward identifying high-utility, biobased plastics with low environmental persistence.
    Description: M.G.M., C.M.R., and C.P.W. thank Eastman Chemical Co. and Woods Hole Oceanographic Institution (WHOI) for scientific and financial support.
    Repository Name: Woods Hole Open Access Server
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  • 100
    Publication Date: 2022-05-27
    Description: © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Xie, L., Liu, X., Caratenuto, A., Tian, Y., Chen, F., DeGiorgis, J. A., Wan, Y., & Zheng, Y. Environmentally friendly and efficient hornet nest envelope-based photothermal absorbers. Acs Omega, 6(50), (2021): 34555–34562, https://doi.org/10.1021/acsomega.1c04851.
    Description: Water shortage is a critical global issue that threatens human health, environmental sustainability, and the preservation of Earth’s climate. Desalination from seawater and sewage is a promising avenue for alleviating this stress. In this work, we use the hornet nest envelope material to fabricate a biomass-based photothermal absorber as part of a desalination isolation system. This system realizes an evaporation rate of 3.98 kg m–2 h–1 under one-sun illumination, with prolonged evaporation rates all above 4 kg m–2 h–1. This system demonstrates a strong performance of 3.86 kg m–2 h–1 in 3.5 wt % saltwater, illustrating its effectiveness in evaporation seawater. Thus, with its excellent evaporation rate, great salt rejection ability, and easy fabrication approach, the hornet nest envelope constitutes a promising natural material for solar water treatment applications.
    Description: The authors acknowledge the support from the National Science Foundation, USA, through grant number CBET-1941743 and the National Science Foundation under EPSCoR Cooperation Agreement OIA-1655221.
    Repository Name: Woods Hole Open Access Server
    Type: Article
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