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A diverse sense of place: citizen science as a tool to connect underrepresented students to science and the national parks

Science and underrepresented

Bowser G, Halliwell P.
GSID: PCcrUaveGsAJ
P Halliwell, G Bowser - Mountain Views, 2019 - fs.fed.us

… Citizen science offers great potential to welcome diverse contributions to science on public … highlights the Rocky Mountain Sustainability and Science Network as an organization that …

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Halliwell, P., & Bowser, G. (2019). A diverse sense of place: citizen science as a tool to connect underrepresented students to science and the national parks. Mountain Views, 4, 4-8.
Halliwell, Philip, and Gillian Bowser. "A diverse sense of place: citizen science as a tool to connect underrepresented students to science and the national parks." Mountain Views 4 (2019): 4-8.
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Learning to love protected areas: Citizen science projects inspire place attachment for diverse students in United States National Parks

Geoscience Opportunities for Leadership in Diversity AND Program Evaluation

Bowser G, Halliwell P, Whipple S.
GSID: 4tphgVulXUgJ
P Halliwell, S Whipple, G Bowser - Journal of Geoscience …, 2022 - Taylor & Francis

Citizen science, an emerging research tool employed worldwide, can encourage nonprofessionals to engage in scientific exploration. Additionally, the research strategy presents great potential to serve as a learning platform for students, supporting diverse contributions to science on public lands....

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Halliwell, P., Whipple, S., & Bowser, G. (2022). Learning to love protected areas: Citizen science projects inspire place attachment for diverse students in United States National Parks. Journal of Geoscience Education, 70(3), 412-420.
Halliwell, Philip, Sarah Whipple, and Gillian Bowser. "Learning to love protected areas: Citizen science projects inspire place attachment for diverse students in United States National Parks." Journal of Geoscience Education 70.3 (2022): 412-420.
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Image editing for pathologists.

Histopathology

Helliwell TR.
PMID: 28425135
Histopathology. 2017 Sep;71(3):496-497. doi: 10.1111/his.13241. Epub 2017 Jun 23.

No abstract available.

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Helliwell TR. Image editing for pathologists. Histopathology. 2017;71(3):496-497doi: 10.1111/his.13241.
Helliwell, T. R. (2017). Image editing for pathologists. Histopathology, 71(3), 496-497. https://doi.org/10.1111/his.13241
Helliwell, Timothy R. "Image editing for pathologists." Histopathology vol. 71,3 (2017): 496-497. doi: https://doi.org/10.1111/his.13241
Helliwell TR. Image editing for pathologists. Histopathology. 2017 Sep;71(3):496-497. doi: 10.1111/his.13241. Epub 2017 Jun 23. PMID: 28425135.
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The science is in the data.

IUCrJ

Helliwell JR, McMahon B, Guss JM, Kroon-Batenburg LMJ.
PMID: 29123672
IUCrJ. 2017 Oct 06;4:714-722. doi: 10.1107/S2052252517013690. eCollection 2017 Nov 01.

Understanding published research results should be through one's own eyes and include the opportunity to work with raw diffraction data to check the various decisions made in the analyses by the original authors. Today, preserving raw diffraction data is...

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Helliwell JR, McMahon B, Guss JM, et al. The science is in the data. IUCrJ. 2017;4:714-722doi: 10.1107/S2052252517013690.
Helliwell, J. R., McMahon, B., Guss, J. M., & Kroon-Batenburg, L. M. J. (2017). The science is in the data. IUCrJ, 4714-722. https://doi.org/10.1107/S2052252517013690
Helliwell, John R, et al. "The science is in the data." IUCrJ vol. 4 (2017): 714-722. doi: https://doi.org/10.1107/S2052252517013690
Helliwell JR, McMahon B, Guss JM, Kroon-Batenburg LMJ. The science is in the data. IUCrJ. 2017 Oct 06;4:714-722. doi: 10.1107/S2052252517013690. eCollection 2017 Nov 01. PMID: 29123672; PMCID: PMC5668855.
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Reply to Tagliabue.

EMBO reports

Pearce W, Hartley S, Helliwell R, O'Neill L.
PMID: 29514864
EMBO Rep. 2018 Apr;19(4). doi: 10.15252/embr.201845954. Epub 2018 Mar 07.

No abstract available.

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Pearce W, Hartley S, Helliwell R, et al. Reply to Tagliabue. EMBO Rep. 2018;19(4)doi: 10.15252/embr.201845954.
Pearce, W., Hartley, S., Helliwell, R., & O'Neill, L. (2018). Reply to Tagliabue. EMBO reports, 19(4), . https://doi.org/10.15252/embr.201845954
Pearce, Warren, et al. "Reply to Tagliabue." EMBO reports vol. 19,4 (2018). doi: https://doi.org/10.15252/embr.201845954
Pearce W, Hartley S, Helliwell R, O'Neill L. Reply to Tagliabue. EMBO Rep. 2018 Apr;19(4). doi: 10.15252/embr.201845954. Epub 2018 Mar 07. PMID: 29514864; PMCID: PMC5891398.
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Algae as nutritional and functional food sources: revisiting our understanding.

Journal of applied phycology

Wells ML, Potin P, Craigie JS, Raven JA, Merchant SS, Helliwell KE, Smith AG, Camire ME, Brawley SH.
PMID: 28458464
J Appl Phycol. 2017;29(2):949-982. doi: 10.1007/s10811-016-0974-5. Epub 2016 Nov 21.

Global demand for macroalgal and microalgal foods is growing, and algae are increasingly being consumed for functional benefits beyond the traditional considerations of nutrition and health. There is substantial evidence for the health benefits of algal-derived food products, but...

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Wells ML, Potin P, Craigie JS, et al. Algae as nutritional and functional food sources: revisiting our understanding. J Appl Phycol. 2016;29(2):949-982doi: 10.1007/s10811-016-0974-5.
Wells, M. L., Potin, P., Craigie, J. S., Raven, J. A., Merchant, S. S., Helliwell, K. E., Smith, A. G., Camire, M. E., & Brawley, S. H. (2017). Algae as nutritional and functional food sources: revisiting our understanding. Journal of applied phycology, 29(2), 949-982. https://doi.org/10.1007/s10811-016-0974-5
Wells, Mark L, et al. "Algae as nutritional and functional food sources: revisiting our understanding." Journal of applied phycology vol. 29,2 (2017): 949-982. doi: https://doi.org/10.1007/s10811-016-0974-5
Wells ML, Potin P, Craigie JS, Raven JA, Merchant SS, Helliwell KE, Smith AG, Camire ME, Brawley SH. Algae as nutritional and functional food sources: revisiting our understanding. J Appl Phycol. 2017;29(2):949-982. doi: 10.1007/s10811-016-0974-5. Epub 2016 Nov 21. PMID: 28458464; PMCID: PMC5387034.
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Re-refinement of 4xan: hen egg-white lysozyme with carboplatin in sodium bromide solution.

Acta crystallographica. Section F, Structural biology communications

Tanley SW, Schreurs AM, Kroon-Batenburg LM, Helliwell JR.
PMID: 26919531
Acta Crystallogr F Struct Biol Commun. 2016 Mar;72:251-2. doi: 10.1107/S2053230X16000777. Epub 2016 Feb 19.

A re-refinement of 4xan, hen egg-white lysozyme (HEWL) with carboplatin crystallized in NaBr solution, has been made and is published here as an addendum to Tanley et al. [(2014), Acta Cryst. F70, 1135-1142]. This follows a previous re-refinement and...

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Tanley SW, Schreurs AM, Kroon-Batenburg LM, et al. Re-refinement of 4xan: hen egg-white lysozyme with carboplatin in sodium bromide solution. Acta Crystallogr F Struct Biol Commun. 2016;72:251-2doi: 10.1107/S2053230X16000777.
Tanley, S. W., Schreurs, A. M., Kroon-Batenburg, L. M., & Helliwell, J. R. (2016). Re-refinement of 4xan: hen egg-white lysozyme with carboplatin in sodium bromide solution. Acta crystallographica. Section F, Structural biology communications, 72251-2. https://doi.org/10.1107/S2053230X16000777
Tanley, Simon W M, et al. "Re-refinement of 4xan: hen egg-white lysozyme with carboplatin in sodium bromide solution." Acta crystallographica. Section F, Structural biology communications vol. 72 (2016): 251-2. doi: https://doi.org/10.1107/S2053230X16000777
Tanley SW, Schreurs AM, Kroon-Batenburg LM, Helliwell JR. Re-refinement of 4xan: hen egg-white lysozyme with carboplatin in sodium bromide solution. Acta Crystallogr F Struct Biol Commun. 2016 Mar;72:251-2. doi: 10.1107/S2053230X16000777. Epub 2016 Feb 19. PMID: 26919531; PMCID: PMC4774886.
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Determination of the site of incorporation of cobalt in CoZnPO-CZP by multiple-wavelength anomalous-dispersion crystallography.

Acta crystallographica. Section B, Structural science

Helliwell M, Helliwell JR, Kaucic V, Zabukovec Logar N, Barba L, Busetto E, Lausi A.
PMID: 10927374
Acta Crystallogr B. 1999 Jun 01;55:327-332. doi: 10.1107/s0108768198014414.

Data were collected from a crystal of CoZnPO-CZP {sodium cobalt-zinc phosphate hydrate, Na(6)[Co(0.2)Zn(0.8)PO(4)](6).6H(2)O} using synchrotron radiation at ELETTRA at the inflection point and 'white line' for both the cobalt and zinc K edges, and at 1.45 Å, a wavelength...

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Helliwell M, Helliwell JR, Kaucic V, et al. Determination of the site of incorporation of cobalt in CoZnPO-CZP by multiple-wavelength anomalous-dispersion crystallography. Acta Crystallogr B. 1999;55:327-332doi: 10.1107/s0108768198014414.
Helliwell, M., Helliwell, J. R., Kaucic, V., Zabukovec Logar N, Barba, L., Busetto, E., & Lausi, A. (1999). Determination of the site of incorporation of cobalt in CoZnPO-CZP by multiple-wavelength anomalous-dispersion crystallography. Acta crystallographica. Section B, Structural science, 55327-332. https://doi.org/10.1107/s0108768198014414
Helliwell, et al. "Determination of the site of incorporation of cobalt in CoZnPO-CZP by multiple-wavelength anomalous-dispersion crystallography." Acta crystallographica. Section B, Structural science vol. 55 (1999): 327-332. doi: https://doi.org/10.1107/s0108768198014414
Helliwell M, Helliwell JR, Kaucic V, Zabukovec Logar N, Barba L, Busetto E, Lausi A. Determination of the site of incorporation of cobalt in CoZnPO-CZP by multiple-wavelength anomalous-dispersion crystallography. Acta Crystallogr B. 1999 Jun 01;55:327-332. doi: 10.1107/s0108768198014414. PMID: 10927374.
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Synthesis and characterization of uranyl compounds with iminodiacetate and oxydiacetate displaying variable denticity.

Inorganic chemistry

Jiang J, Sarsfield MJ, Renshaw JC, Livens FR, Collison D, Charnock JM, Helliwell M, Eccles H.
PMID: 12005506
Inorg Chem. 2002 May 20;41(10):2799-806. doi: 10.1021/ic020121v.

Eight uranyl compounds containing the dicarboxylate ligands iminodiacetate (IDA) or oxydiacetate (ODA) have been characterized in the solid state. The published polymeric structures for [UO(2)(C(4)H(6)NO(4))(2)] and [UO(2)(C(4)H(4)O(5))](n) have been confirmed, while Ba[UO(2)(C(4)H(5)NO(4))(2)] x 3H(2)O, [(CH(3))(2)NH(CH(2))(2)NH(CH(3))(2)][UO(2)(C(4)H(4)O(5))(2)] [orthorhombic space group Pnma,...

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Jiang J, Sarsfield MJ, Renshaw JC, et al. Synthesis and characterization of uranyl compounds with iminodiacetate and oxydiacetate displaying variable denticity. Inorg Chem. 2002;41(10):2799-806doi: 10.1021/ic020121v.
Jiang, J., Sarsfield, M. J., Renshaw, J. C., Livens, F. R., Collison, D., Charnock, J. M., Helliwell, M., & Eccles, H. (2002). Synthesis and characterization of uranyl compounds with iminodiacetate and oxydiacetate displaying variable denticity. Inorganic chemistry, 41(10), 2799-806. https://doi.org/10.1021/ic020121v
Jiang, J, et al. "Synthesis and characterization of uranyl compounds with iminodiacetate and oxydiacetate displaying variable denticity." Inorganic chemistry vol. 41,10 (2002): 2799-806. doi: https://doi.org/10.1021/ic020121v
Jiang J, Sarsfield MJ, Renshaw JC, Livens FR, Collison D, Charnock JM, Helliwell M, Eccles H. Synthesis and characterization of uranyl compounds with iminodiacetate and oxydiacetate displaying variable denticity. Inorg Chem. 2002 May 20;41(10):2799-806. doi: 10.1021/ic020121v. PMID: 12005506.
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Dearomatizing cyclization of arylsulfonylalkoxymethyl lithiums: a route to the podophyllotoxin skeleton.

Organic letters

Clayden J, Kenworthy MN, Helliwell M.
PMID: 12633083
Org Lett. 2003 Mar 20;5(6):831-4. doi: 10.1021/ol0340585.

[reaction: see text] The phenylsulfonyl group promotes the dearomatizing cyclization of tethered organolithiums onto aromatic rings. With an ether tether, the cyclizations create a new tetrahydrofuran ring, and both cyclization and subsequent electrophilic quenches proceed with high levels of...

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Clayden J, Kenworthy MN, Helliwell M. Dearomatizing cyclization of arylsulfonylalkoxymethyl lithiums: a route to the podophyllotoxin skeleton. Org Lett. 2003;5(6):831-4doi: 10.1021/ol0340585.
Clayden, J., Kenworthy, M. N., & Helliwell, M. (2003). Dearomatizing cyclization of arylsulfonylalkoxymethyl lithiums: a route to the podophyllotoxin skeleton. Organic letters, 5(6), 831-4. https://doi.org/10.1021/ol0340585
Clayden, Jonathan, et al. "Dearomatizing cyclization of arylsulfonylalkoxymethyl lithiums: a route to the podophyllotoxin skeleton." Organic letters vol. 5,6 (2003): 831-4. doi: https://doi.org/10.1021/ol0340585
Clayden J, Kenworthy MN, Helliwell M. Dearomatizing cyclization of arylsulfonylalkoxymethyl lithiums: a route to the podophyllotoxin skeleton. Org Lett. 2003 Mar 20;5(6):831-4. doi: 10.1021/ol0340585. PMID: 12633083.
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The regioselective aminohydroxylation of allylic carbamates.

Chemical communications (Cambridge, England)

Donohoe TJ, Johnson PD, Helliwell M, Keenan M.
PMID: 12240171
Chem Commun (Camb). 2001 Oct 21;(20):2078-9. doi: 10.1039/b107253f.

The synthesis and aminohydroxylation of a series of acyclic allylic carbamates is described: the formation of a putative O=Os=NR linkage between the transition metal and substrate is proposed to account for the high levels of regioselectivity that were observed;...

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Donohoe TJ, Johnson PD, Helliwell M, et al. The regioselective aminohydroxylation of allylic carbamates. Chem Commun (Camb). 2001;(20):2078-9doi: 10.1039/b107253f.
Donohoe, T. J., Johnson, P. D., Helliwell, M., & Keenan, M. (2001). The regioselective aminohydroxylation of allylic carbamates. Chemical communications (Cambridge, England), (20), 2078-9. https://doi.org/10.1039/b107253f
Donohoe, T J, et al. "The regioselective aminohydroxylation of allylic carbamates." Chemical communications (Cambridge, England) vol. ,20 (2001): 2078-9. doi: https://doi.org/10.1039/b107253f
Donohoe TJ, Johnson PD, Helliwell M, Keenan M. The regioselective aminohydroxylation of allylic carbamates. Chem Commun (Camb). 2001 Oct 21;(20):2078-9. doi: 10.1039/b107253f. PMID: 12240171.
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Directed dihydroxylation of cyclic allylic alcohols and trichloroacetamides using OsO4/TMEDA.

The Journal of organic chemistry

Donohoe TJ, Blades K, Moore PR, Waring MJ, Winter JJ, Helliwell M, Newcombe NJ, Stemp G.
PMID: 12423122
J Org Chem. 2002 Nov 15;67(23):7946-56. doi: 10.1021/jo026161y.

The oxidation of a range of cyclic allylic alcohols and amides with OsO4/TMEDA is presented. Under these conditions, hydrogen bonding control leads to the (contrasteric) formation of the syn isomer in almost every example that was examined. Evidence for...

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Donohoe TJ, Blades K, Moore PR, et al. Directed dihydroxylation of cyclic allylic alcohols and trichloroacetamides using OsO4/TMEDA. J Org Chem. 2002;67(23):7946-56doi: 10.1021/jo026161y.
Donohoe, T. J., Blades, K., Moore, P. R., Waring, M. J., Winter, J. J., Helliwell, M., Newcombe, N. J., & Stemp, G. (2002). Directed dihydroxylation of cyclic allylic alcohols and trichloroacetamides using OsO4/TMEDA. The Journal of organic chemistry, 67(23), 7946-56. https://doi.org/10.1021/jo026161y
Donohoe, Timothy J, et al. "Directed dihydroxylation of cyclic allylic alcohols and trichloroacetamides using OsO4/TMEDA." The Journal of organic chemistry vol. 67,23 (2002): 7946-56. doi: https://doi.org/10.1021/jo026161y
Donohoe TJ, Blades K, Moore PR, Waring MJ, Winter JJ, Helliwell M, Newcombe NJ, Stemp G. Directed dihydroxylation of cyclic allylic alcohols and trichloroacetamides using OsO4/TMEDA. J Org Chem. 2002 Nov 15;67(23):7946-56. doi: 10.1021/jo026161y. PMID: 12423122.
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Showing 1 to 12 of 296 entries