W. Christopher Long

1.9k total citations
60 papers, 1.4k citations indexed

About

W. Christopher Long is a scholar working on Ecology, Oceanography and Global and Planetary Change. According to data from OpenAlex, W. Christopher Long has authored 60 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Ecology, 33 papers in Oceanography and 33 papers in Global and Planetary Change. Recurrent topics in W. Christopher Long's work include Marine and fisheries research (23 papers), Ocean Acidification Effects and Responses (22 papers) and Crustacean biology and ecology (20 papers). W. Christopher Long is often cited by papers focused on Marine and fisheries research (23 papers), Ocean Acidification Effects and Responses (22 papers) and Crustacean biology and ecology (20 papers). W. Christopher Long collaborates with scholars based in United States, United Kingdom and Australia. W. Christopher Long's co-authors include Katherine M. Swiney, Robert J. Foy, Rochelle D. Seitz, Benjamin Daly, Heather N. Page, P. Raj Pokkuluri, Daniel M. Dauer, M. Schiffer, Yuri Y. Londer and Roberto J. Llansó and has published in prestigious journals such as PLoS ONE, Biochemistry and Conservation Biology.

In The Last Decade

W. Christopher Long

57 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
W. Christopher Long United States 24 870 856 813 118 113 60 1.4k
Robert J. Foy United States 20 608 0.7× 670 0.8× 692 0.9× 208 1.8× 41 0.4× 56 1.1k
Haruko Kurihara Japan 21 2.3k 2.7× 1.4k 1.6× 1.8k 2.2× 45 0.4× 76 0.7× 57 2.7k
Jun Kita Japan 20 693 0.8× 601 0.7× 466 0.6× 153 1.3× 122 1.1× 47 1.2k
M. Langenbuch Germany 10 1.9k 2.2× 1.3k 1.5× 1.4k 1.8× 70 0.6× 60 0.5× 10 2.1k
Kennedy Wolfe Australia 18 823 0.9× 896 1.0× 631 0.8× 48 0.4× 27 0.2× 49 1.2k
Helen S. Findlay United Kingdom 27 1.7k 2.0× 993 1.2× 1.0k 1.2× 81 0.7× 42 0.4× 61 2.0k
Maria Ching Villanueva France 19 166 0.2× 522 0.6× 559 0.7× 257 2.2× 57 0.5× 41 1.2k
Laura Ramajo Chile 17 2.8k 3.2× 1.4k 1.6× 1.8k 2.2× 38 0.3× 67 0.6× 29 3.2k
Alison M. Jones Australia 18 718 0.8× 1.1k 1.3× 432 0.5× 90 0.8× 20 0.2× 34 1.4k
Christopher E. Cornwall New Zealand 33 3.1k 3.6× 2.0k 2.4× 1.1k 1.4× 62 0.5× 23 0.2× 72 3.5k

Countries citing papers authored by W. Christopher Long

Since Specialization
Citations

This map shows the geographic impact of W. Christopher Long's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by W. Christopher Long with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W. Christopher Long more than expected).

Fields of papers citing papers by W. Christopher Long

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by W. Christopher Long. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by W. Christopher Long. The network helps show where W. Christopher Long may publish in the future.

Co-authorship network of co-authors of W. Christopher Long

This figure shows the co-authorship network connecting the top 25 collaborators of W. Christopher Long. A scholar is included among the top collaborators of W. Christopher Long based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with W. Christopher Long. W. Christopher Long is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Small, Hamish J., et al.. (2025). Bitter crab disease dynamics in eastern Bering Sea Tanner and snow crab: An underestimated and emergent stressor. Fisheries Research. 283. 107307–107307.
2.
3.
Litzow, Michael A., et al.. (2025). Ocean acidification may contribute to recruitment failure of Bering Sea red king crab. Canadian Journal of Fisheries and Aquatic Sciences. 82. 1–7. 1 indexed citations
4.
Long, W. Christopher, et al.. (2024). Red king crab larval survival and development are resilient to ocean acidification. Journal of Experimental Marine Biology and Ecology. 577. 152028–152028. 2 indexed citations
5.
Long, W. Christopher, et al.. (2024). Optimizing release strategies for red king crab stock enhancement: Effects of release timing. Fisheries Research. 274. 106975–106975. 3 indexed citations
6.
Long, W. Christopher, et al.. (2024). Narrowed gene functions and enhanced transposon activity are associated with high tolerance to ocean acidification in a juvenile subarctic crustacean. PLOS Climate. 3(3). e0000319–e0000319. 1 indexed citations
7.
Long, W. Christopher, Katherine M. Swiney, Robert J. Foy, et al.. (2023). Adult snow crab, Chionoecetes opilio, display body-wide exoskeletal resistance to the effects of long-term ocean acidification. Marine Biology. 170(5). 6 indexed citations
8.
Long, W. Christopher, Katherine M. Swiney, & Robert J. Foy. (2023). Direct, carryover, and maternal effects of ocean acidification on snow crab embryos and larvae. PLoS ONE. 18(10). e0276360–e0276360. 7 indexed citations
9.
Dickinson, Gary H., W. Christopher Long, Katherine M. Swiney, et al.. (2021). Ocean acidification alters properties of the exoskeleton in adult Tanner crabs, Chionoecetes bairdi. Journal of Experimental Biology. 224(3). 23 indexed citations
10.
Long, W. Christopher, et al.. (2020). Mechanical Resistance in Decapod Claw Denticles: Contribution of Structure and Composition. Acta Biomaterialia. 110. 196–207. 18 indexed citations
11.
Monacci, Natalie, et al.. (2019). Ocean Acidification in Alaska: Chemistry, Clams, Cod, and Crabs. AGU Fall Meeting Abstracts. 2019. 1 indexed citations
12.
Long, W. Christopher, et al.. (2017). Ocean acidification leads to altered micromechanical properties of the mineralized cuticle in juvenile red and blue king crabs. Journal of Experimental Marine Biology and Ecology. 495. 1–12. 33 indexed citations
13.
Swiney, Katherine M., W. Christopher Long, & Robert J. Foy. (2016). Decreased pH and increased temperatures affect young-of-the-year red king crab (Paralithodes camtschaticus). ICES Journal of Marine Science. 74(4). 1191–1200. 21 indexed citations
14.
Salisbury, J., Joan M. Bernhard, Wei‐Jun Cai, et al.. (2015). And on Top of All That… Coping with Ocean Acidification in the Midst of Many Stressors. Oceanography. 25(2). 48–61. 140 indexed citations
15.
16.
Swiney, Katherine M. & W. Christopher Long. (2015). Primiparous Red King CrabParalithodes camtschaticusare Less Fecund than Multiparous Crab. Journal of Shellfish Research. 34(2). 493–498. 11 indexed citations
17.
18.
Long, W. Christopher, et al.. (2014). Effects of ghost fishing on the population of red king crab (Paralithodes camtschaticus) in Womens Bay, Kodiak Island, Alaska. Fishery Bulletin. 112(2-3). 101–111. 3 indexed citations
19.
Long, W. Christopher, Katherine M. Swiney, & Robert J. Foy. (2013). Effects of ocean acidification on the embryos and larvae of red king crab, Paralithodes camtschaticus. Marine Pollution Bulletin. 69(1-2). 38–47. 85 indexed citations
20.
Seitz, Rochelle D., et al.. (2008). Stock Enhancement and Carrying Capacity of Blue Crab Nursery Habitats in Chesapeake Bay. Reviews in Fisheries Science. 16(1-3). 329–337. 26 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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