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Journal articles on the topic 'Snapping shrimp'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Lai, K. S., Z. Z. Goh, and S. M. Ghazali. "The effects of temperature and pH change on the snapping sound characteristic of Alpheus edwardsii." Journal of Environmental Biology 42, no. 3(SI) (2021): 832–39. http://dx.doi.org/10.22438/jeb/42/3(si)/jeb-15.

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Aim: The current study undertook manipulative experiments to observe changes in snapping shrimp sound signals in relation to temperature and pH changes. Methodology: Sounds of intertidal snapping shrimp (Alpheus edwardsii) sequentially exposed to different temperature/pH treatments manipulation for a period of 2 week each, were recorded in the laboratory and analysed. The acoustic characteristics of snapping sound signal were examined to relate to the change in temperature, pH and combination of both parameters. Results: Our results showed that there was a significant reduction in the frequenc

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2

Park, Soo Hyun, Jinuk Park, and Jungpyo Hong. "Snapping shrimp noise detection methods based on linear prediction analysis." INTER-NOISE and NOISE-CON Congress and Conference Proceedings 268, no. 3 (2023): 5040–47. http://dx.doi.org/10.3397/in_2023_0716.

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This paper proposes features for detecting snapping shrimp noise based on linear predictive analysis. Snapping shrimps are a species inhabiting the ocean depths and are one of the main sources of underwater noise due to their high-amplitude signals that occur frequently. The proposed features utilize the characteristic of sudden onset and rapid decay of pistol shrimp noise by using linear predictive analysis to accurately detect the noise segments and mitigate the impact of snapping shrimp noise. The large error between the predicted values by linear predictive analysis and the actual measured

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3

Yang, Yuliang, Shimu Qin, Changchun Di, Junqi Qin, Dalin Wu, and Jianxin Zhao. "Research on Claw Motion Characteristics and Cavitation Bubbles of Snapping Shrimp." Applied Bionics and Biomechanics 2020 (September 21, 2020): 1–12. http://dx.doi.org/10.1155/2020/6585729.

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Snapping shrimp produces a high-speed jet through the rapid closure of the snapper claw, which stimulates the formation of cavitation bubbles of various shapes. In order to explore the fast motion characteristics of snapper claw, the formation and change process of cavitation, and the physical principles underlying the biological phenomena, the equivalent model of snapper claw was constructed through CT scanning technology. A high-speed camera was used to capture the claw’s motion characteristics, thereby simulating the production of cavitation bubbles by snapping shrimp. The results show that

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4

Tang, Xin, and David Staack. "Bioinspired mechanical device generates plasma in water via cavitation." Science Advances 5, no. 3 (2019): eaau7765. http://dx.doi.org/10.1126/sciadv.aau7765.

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Nature can generate plasma in liquids more efficiently than human-designed devices using electricity, acoustics, or light. In the animal world, snapping shrimp can induce cavitation that collapses to produce high pressures and temperatures, leading to efficient plasma formation with photon and shock wave emission via energy focusing. Here, we report a bioinspired mechanical device that mimics the plasma generation technique of the snapping shrimp. This device was manufactured using additive manufacturing based on micro–x-ray computed tomography of a snapping shrimp claw molt. A spring fixture

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5

Jeong, Inyong, and Dong-Guk Paeng. "Circadian and Tidal Changes in Snapping Shrimp (Alpheus brevicristatus) Sound Observed by a Moored Hydrophone in the Coastal Sea of Western Jeju." Applied Sciences 12, no. 13 (2022): 6493. http://dx.doi.org/10.3390/app12136493.

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Numerous studies have evaluated the acoustic characteristics of soniferous snapping shrimp, but a few are based on long-term mooring measurements. In this study, underwater ambient noise signals were collected from a hydrophone moored 10 m from the sea bed in the coastal sea of western Jeju, South Korea, from mid-September 2019 for 90 days to analyze the variation in the sound of snapping shrimp. The kernel signal and a threshold value were utilized to identify the snapping shrimp, and the snap rate per minute was computed for quantitative analysis. The results show that the mean and standard

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6

Lohse, Detlef, Barbara Schmitz, and Michel Versluis. "Snapping shrimp make flashing bubbles." Nature 413, no. 6855 (2001): 477–78. http://dx.doi.org/10.1038/35097152.

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7

Lee, Dawoon, Gihoon Byun, and Wookeen Chung. "Adaptive iterative transfer learning for effective snapping shrimp sound detection." Journal of the Acoustical Society of America 156, no. 2 (2024): 865–78. http://dx.doi.org/10.1121/10.0028178.

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This study aims to detect the bioacoustics signal in the underwater soundscape, specifically those produced by snapping shrimp, using adaptive iterative transfer learning. The proposed network is initially trained with pre-classified snapping shrimp sounds and Gaussian noise, then applied to classify and remove snapping-free noise from field data. This separated ambient noise is subsequently used for transfer learning. This process was iterated to distinguish more effectively between ambient noise and snapping shrimp sounds characteristics, resulting in improved classification. Through iterati

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8

Rossi, Tullio, Sean D. Connell, and Ivan Nagelkerken. "Silent oceans: ocean acidification impoverishes natural soundscapes by altering sound production of the world's noisiest marine invertebrate." Proceedings of the Royal Society B: Biological Sciences 283, no. 1826 (2016): 20153046. http://dx.doi.org/10.1098/rspb.2015.3046.

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Soundscapes are multidimensional spaces that carry meaningful information for many species about the location and quality of nearby and distant resources. Because soundscapes are the sum of the acoustic signals produced by individual organisms and their interactions, they can be used as a proxy for the condition of whole ecosystems and their occupants. Ocean acidification resulting from anthropogenic CO 2 emissions is known to have profound effects on marine life. However, despite the increasingly recognized ecological importance of soundscapes, there is no empirical test of whether ocean acid

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9

Versluis, Michel, Anna von der Heydt, Detlef Lohse, and Barbara Schmitz. "On the Sound of Snapping Shrimp." Physics of Fluids 13, no. 9 (2001): S13. http://dx.doi.org/10.1063/1.4739187.

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10

Readhead, Mark L. "Snapping shrimp noise near Gladstone, Queensland." Journal of the Acoustical Society of America 101, no. 3 (1997): 1718–22. http://dx.doi.org/10.1121/1.418153.

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11

Fox, Bradley K., Kelvin D. Gorospe, Roxanne D. Haverkort-Yeh, and Malia Ana J. Rivera. "It’s a Snap! An Inquiry-Based, Snapping Shrimp Bioacoustics Activity." American Biology Teacher 75, no. 7 (2013): 470–75. http://dx.doi.org/10.1525/abt.2013.75.7.5.

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This bioacoustics activity combines concepts in invertebrate taxonomy, animal communication, and acoustical physics while providing a unique opportunity for physics and biology teachers to collaborate and introduce their students to an exciting, interdisciplinary research field. Here, we propose a lab- and field-based activity that uses hydrophones to explore how shrimp snapping behavior changes in response to different stimuli and introduces students to the process of scientific inquiry. Using free software, students use spectrograms to visualize and analyze their experimental data. Furthermo

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12

McQuarrie, Frank, C. Brock Woodson, and Catherine R. Edwards. "A Reef’s High-Frequency Soundscape and the Effect on Telemetry Efforts: A Biotic and Abiotic Balance." Journal of Marine Science and Engineering 13, no. 3 (2025): 517. https://doi.org/10.3390/jmse13030517.

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Acoustic telemetry is a tool for tracking animals, but transmitted signals from tagged animals are not always detected. Detection efficiency declines with increasing background noise, which can have both abiotic and biotic sources. The abiotic noise present in reef environments (waves, bubbles, etc.) is primarily low-frequency, but snapping shrimp create high-frequency noise that can interfere with transmission detections. Prior work in shallow coastal reefs correlated winds with less high-frequency background noise, and hypothesized that it was due to a balance of biotic and/or abiotic factor

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13

Schmitz, Barbara, and Jens Herberholz. "Snapping behaviour in intraspecific agonistic encounters in the snapping shrimp (Alpheus heterochaelis)." Journal of Biosciences 23, no. 5 (1998): 623–32. http://dx.doi.org/10.1007/bf02709175.

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14

Khaled M. Abdelsalam, Khaled M. Abdelsalam. "First Record of Synalpheus africanus Crosnier & Forest, 1965 (Caridea, Alpheidae) in the Egyptian Mediterranean Coast." journal of king abdulaziz university marine science 28, no. 2 (2018): 89–97. http://dx.doi.org/10.4197/mar.28-2.7.

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The snapping shrimp Synalpheus africanus Crosnier & Forest, 1965 is recorded for the first time in the Egyptian Mediterranean coast. During August and September 2018, specimens were accidentally collected from the associated fouling communities of the Eastern Harbor of Alexandria city, Egypt. It is the second species of genus Synalpheus Spence Bate, 1888 to be recorded in the Egyptian Mediterranean waters. A brief re-description with illustrative photos, distribution, and remarks for discrimination from other recorded alpheid shrimps are provided.

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15

Pandit, Aniruddha B., Manisha V. Bagal, and Parag R. Gogate. "What Chemical Engineers Can Learn from Shrimp." Annual Review of Chemical and Biomolecular Engineering 16, no. 1 (2025): 433–53. https://doi.org/10.1146/annurev-chembioeng-082223-102200.

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This review focuses on how the cavitation mechanism in the snapping shrimp can be explored to intensify various chemical engineering applications. Effective bubble collapse can lead to hot spot formation, increased transport coefficients (momentum, heat, and mass), and enhanced interfacial area and also results in the formation of highly reactive radicals. Cavitation's ability to induce rapid micromixing, enhance mass transfer, and facilitate nucleophilic chemical reactions can find applications in various industries. An overview of cavitation applications, reactors used for cavitation, effect

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16

Hess, David, Christoph Brücker, Franziska Hegner, Alexander Balmert, and Horst Bleckmann. "Vortex Formation with a Snapping Shrimp Claw." PLoS ONE 8, no. 11 (2013): e77120. http://dx.doi.org/10.1371/journal.pone.0077120.

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17

Chak, Solomon TC, and Dustin R. Rubenstein. "Social transitions in sponge-dwelling snapping shrimp." Current Opinion in Insect Science 34 (August 2019): 33–39. http://dx.doi.org/10.1016/j.cois.2019.02.006.

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18

Kim, Byoung-Nam, Jooyoung Hahn, Bok Kyoung Choi, and Bong-Chae Kim. "Snapping Shrimp Sound Measured Under Laboratory Conditions." Japanese Journal of Applied Physics 49, no. 7 (2010): 07HG04. http://dx.doi.org/10.1143/jjap.49.07hg04.

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19

Versluis, M. "How Snapping Shrimp Snap: Through Cavitating Bubbles." Science 289, no. 5487 (2000): 2114–17. http://dx.doi.org/10.1126/science.289.5487.2114.

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20

Kingston, Alexandra C. N., Rebecca L. Lucia, Luke T. Havens, Thomas W. Cronin, and Daniel I. Speiser. "Vision in the snapping shrimp Alpheus heterochaelis." Journal of Experimental Biology 222, no. 21 (2019): jeb209015. http://dx.doi.org/10.1242/jeb.209015.

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21

Anker, Arthur. "Alpheus naranjo, a new brightly coloured snapping shrimp from the Caribbean coast of Panama (Malacostraca, Decapoda, Alpheidae)." Zootaxa 4433, no. 3 (2018): 574–82. https://doi.org/10.11646/zootaxa.4433.3.11.

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Anker, Arthur (2018): Alpheus naranjo, a new brightly coloured snapping shrimp from the Caribbean coast of Panama (Malacostraca, Decapoda, Alpheidae). Zootaxa 4433 (3): 574-582, DOI: 10.11646/zootaxa.4433.3.11

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22

Rahman, Nasreen. "SIZE-ASSORTATIVE PAIRING IN THE BIG-CLAWED SNAPPING SHRIMP, ALPHEUS HETEROCHELIS." Behaviour 139, no. 11-12 (2002): 1443–68. http://dx.doi.org/10.1163/15685390260514717.

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AbstractThe big-clawed snapping shrimp, Alpheus heterochelis, is found in size-matched male-female pairs. A common assumption is that a large size advantage in males, an extended pair bond, and a positive correlation between female size and fecundity promotes size-assortative pairing. Since all of these conditions apply to A. heterochelis, we investigated size-assortative pairing in the laboratory by designing experiments in which the pairs were size matched or mismatched using three size categories; large, medium and small. We found that snapping shrimps prefer to pair according to size and t

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23

Anker, Arthur, Tomoyuki Komai, and Ivan N. Marin. "A new echiuran-associated snapping shrimp (Crustacea: Decapoda: Alpheidae) from the Indo-West Pacific." Zootaxa 3914, no. 4 (2015): 441–55. https://doi.org/10.11646/zootaxa.3914.4.4.

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Anker, Arthur, Komai, Tomoyuki, Marin, Ivan N. (2015): A new echiuran-associated snapping shrimp (Crustacea: Decapoda: Alpheidae) from the Indo-West Pacific. Zootaxa 3914 (4): 441-455, DOI: 10.11646/zootaxa.3914.4.4

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24

SCIOLI, JUSTIN A., and ARTHUR ANKER. "Description of Alpheus gallicus, a new deep-water snapping shrimp from Galicia Bank, northeastern Atlantic (Malacostraca, Decapoda, Alpheidae)." Zootaxa 4731, no. 3 (2020): 347–58. http://dx.doi.org/10.11646/zootaxa.4731.3.4.

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A new species of the snapping shrimp genus Alpheus Fabricius, 1798 is described based on material from Galicia Bank, an offshore seamount off northwestern Spain. The type series of Alpheus gallicus n. sp. was collected at a depth of 768–785 m, making it one of the deepest occurring snapping shrimps. The new species belongs to the Alpheus macrocheles species group and is morphologically most similar to several deep-water members of this group, viz. A. lentiginosus Anker & Nizinski, 2011, A. platydactylus Coutière, 1897, A. romensky Burukovsky, 1990, as well as to the shallow-water A. macroc

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25

Anker, Arthur, and Paulo P.G. Pachelle. "Alpheus perlas, sp. nov., a new infaunal snapping shrimp from the Pacific coast of Panama (Malacostraca: Decapoda: Alpheidae)." Zootaxa 4651, no. 1 (2019): 75–84. https://doi.org/10.11646/zootaxa.4651.1.5.

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Anker, Arthur, Pachelle, Paulo P.G. (2019): Alpheus perlas, sp. nov., a new infaunal snapping shrimp from the Pacific coast of Panama (Malacostraca: Decapoda: Alpheidae). Zootaxa 4651 (1): 75-84, DOI: 10.11646/zootaxa.4651.1.5

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Scioli, Justin A., and Arthur Anker. "Description of Alpheus gallicus, a new deep-water snapping shrimp from Galicia Bank, northeastern Atlantic (Malacostraca, Decapoda, Alpheidae)." Zootaxa 4731, no. 3 (2020): 347–58. https://doi.org/10.11646/zootaxa.4731.3.4.

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Scioli, Justin A., Anker, Arthur (2020): Description of Alpheus gallicus, a new deep-water snapping shrimp from Galicia Bank, northeastern Atlantic (Malacostraca, Decapoda, Alpheidae). Zootaxa 4731 (3): 347-358, DOI: 10.11646/zootaxa.4731.3.4

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27

Komai, Tomoyuki, and Jun Ohtomi. "A new deep-sea species of the snapping shrimp genus Alpheus Fabricius, 1798 (Decapoda: Caridea: Alpheidae) from Kagoshima Bay, Japan." Zootaxa 4434, no. 1 (2018): 99–110. https://doi.org/10.11646/zootaxa.4434.1.6.

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Komai, Tomoyuki, Ohtomi, Jun (2018): A new deep-sea species of the snapping shrimp genus Alpheus Fabricius, 1798 (Decapoda: Caridea: Alpheidae) from Kagoshima Bay, Japan. Zootaxa 4434 (1): 99-110, DOI: 10.11646/zootaxa.4434.1.6

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Park, Suhyeon, Jongwon Seok, and Jungpyo Hong. "Snapping Shrimp Noise Detection Based on Statistical Model." Journal of Marine Science and Engineering 12, no. 1 (2023): 42. http://dx.doi.org/10.3390/jmse12010042.

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Snapping Shrimps (SSs) live in a warm ocean except the North and South Poles, and they are characterized by generating strong shock waves underwater using large claws. Shock waves generated by these SSs are used for marine noise research as a signal and as a noise source, because they cause a decrease in the Signal-to-Noise Ratio (SNR), acting as one of the disruptors in fields such as sonar for target detection and underwater communication. A state-of-the-art technique to detect Snapping Shrimp Noise (SSN) is Linear Prediction (LP) analysis. Using the feature where SSN occurs for a very short

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Mueller, C., A. Monczak, J. Soueidan, et al. "Sound characterization and fine-scale spatial mapping of an estuarine soundscape in the southeastern USA." Marine Ecology Progress Series 645 (July 9, 2020): 1–23. http://dx.doi.org/10.3354/meps13373.

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Estuaries are areas known for biological diversity, and their soundscapes reflect the acoustic signals used by organisms to communicate, defend territories, reproduce, and forage in an environment that has limited visibility. These biological sounds may be rhythmic in nature, spatially heterogeneous, and can provide information on habitat quality. The goal of our study was to investigate the temporal and spatial variability of sounds in Chechessee Creek (Stns CC1 and CC2) and an adjacent saltwater impoundment (Great Salt Pond, GSP) in South Carolina, USA, from April to November 2016. Fixed rec

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Yasser, A. Gh., and M. D. Naser. "A New Record Of The Snapping Shrimp, Alpheus Lobidens, From The Iraqi Coast (Malacostraca, Decapoda, Alpheidae)." Zoodiversity 57, no. 5 (2023): 461–64. https://doi.org/10.15407/zoo2023.05.461.

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Yasser, A. Gh., Naser, M. D. (2023): A New Record Of The Snapping Shrimp, Alpheus Lobidens, From The Iraqi Coast (Malacostraca, Decapoda, Alpheidae). Zoodiversity 57 (5): 461-464, DOI: 10.15407/zoo2023.05.461, URL: http://dx.doi.org/10.15407/zoo2023.05.461

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Indeck, Katherine L., Peter Simard, Shannon Gowans, Susan Lowerre-Barbieri, and David A. Mann. "A severe red tide (Tampa Bay, 2005) causes an anomalous decrease in biological sound." Royal Society Open Science 2, no. 9 (2015): 150337. http://dx.doi.org/10.1098/rsos.150337.

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Although harmful algal blooms (HABs) are known to cause morbidity and mortality in marine organisms, their sublethal effects are poorly understood. The purpose of this study was to compare ambient noise levels during a severe HAB event in Tampa Bay, Florida, to those during non-HAB periods. Passive acoustic monitoring was conducted using bottom-mounted autonomous acoustic recorders during a severe HAB in summer 2005, and in summers 2006, 2011 and 2012 (non-severe HAB years). Ambient noise levels were significantly higher during the non-HAB years due to an abundance of snapping shrimp ( Alpheid

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32

Boltaña, S., and M. Thiel. "Associations between two species of snapping shrimp, Alpheus inca and Alpheopsis chilensis (Decapoda: Caridea: Alpheidae)." Journal of the Marine Biological Association of the United Kingdom 81, no. 4 (2001): 633–38. http://dx.doi.org/10.1017/s0025315401004295.

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This study examined the association pattern of two snapping shrimp species that inhabit burrows at exposed rocky shores of the Chilean Pacific coast. The two species Alpheus inca and Alpheopsis chilensis were frequently found to share the same burrows. In most burrows an heterosexual pair of each species was found. A strong positive correlation between the body length of female and male conspecifics cohabiting in a burrow was found both for Alpheus inca and for Alpheopsis chilensis. Similarly, a positive correlation existed between the mean body length of Alpheus inca and that of Alpheopsis ch

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33

Komai, Tomoyuki. "A new species of the snapping shrimp genus Alpheus (Crustacea: Decapoda: Caridea: Alpheidae) from Japan, associated with the innkeeper worm Ikedosoma elegans (Annelida: Echiura: Echiuridae)." Zootaxa 4058, no. 1 (2015): 101–11. https://doi.org/10.11646/zootaxa.4058.1.5.

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Komai, Tomoyuki (2015): A new species of the snapping shrimp genus Alpheus (Crustacea: Decapoda: Caridea: Alpheidae) from Japan, associated with the innkeeper worm Ikedosoma elegans (Annelida: Echiura: Echiuridae). Zootaxa 4058 (1): 101-111, DOI: 10.11646/zootaxa.4058.1.5

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Azofeifa-Solano, Juan C., Jeffrey A. Sibaja-Cordero, and Ingo S. Wehrtmann. "Sexual dimorphism of the major chela and sex ratio as indicators of the mating system in the estuarine snapping shrimp Alpheus colombiensis Wicksten, 1988 (Decapoda: Caridea: Alpheidae)." Journal of Crustacean Biology 40, no. 6 (2020): 649–56. http://dx.doi.org/10.1093/jcbiol/ruaa069.

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Abstract The sexual selection over traits that favor access to mating partners could promote the emergence of sexual dimorphism when the pressure is different between sexes. Monogamous species are considered to have a low degree of sexual dimorphism. The highly diverse snapping shrimps are usually regarded as monogamous, but the mating system has been studied only in few species. We aimed to provide insights into the mating system and sexual dimorphism of Alpheus colombiensisWicksten, 1988. The adult sex ratio was female biased, and solitary ovigerous females were found, suggesting a temporary

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Bracken-Grissom, Heather D., and Darryl L. Felder. "Provisional revision of American snapping shrimp allied to Alpheus floridanus Kingsley, 1878 (Crustacea: Decapoda: Alpheidae) with notes on A. floridanus africanus." Zootaxa 3895, no. 4 (2014): 451–91. https://doi.org/10.11646/zootaxa.3895.4.1.

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Bracken-Grissom, Heather D., Felder, Darryl L. (2014): Provisional revision of American snapping shrimp allied to Alpheus floridanus Kingsley, 1878 (Crustacea: Decapoda: Alpheidae) with notes on A. floridanus africanus. Zootaxa 3895 (4): 451-491, DOI: 10.11646/zootaxa.3895.4.1

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Cunha, Andressa Maria, Mariana Terossi, Fernando L. Mantelatto, and Alexandre O. Almeida. "Delimiting the snapping shrimp Alpheus lobidens De Haan, 1849 (Caridea: Alpheidae) based on morphological and molecular data." Zootaxa 4718, no. 3 (2020): 337–54. https://doi.org/10.11646/zootaxa.4718.3.3.

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Cunha, Andressa Maria, Terossi, Mariana, Mantelatto, Fernando L., Almeida, Alexandre O. (2020): Delimiting the snapping shrimp Alpheus lobidens De Haan, 1849 (Caridea: Alpheidae) based on morphological and molecular data. Zootaxa 4718 (3): 337-354, DOI: 10.11646/zootaxa.4718.3.3

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Almeida, Alexandre O., Arthur Anker, and Fernando L. Mantelatto. "A new snapping species of the shrimp genus Typton Costa, 1844 (Decapoda: Palaemonidae) from the coast of São Paulo, southeastern Brazil." Zootaxa 3835, no. 1 (2014): 110–20. https://doi.org/10.11646/zootaxa.3835.1.6.

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Almeida, Alexandre O., Anker, Arthur, Mantelatto, Fernando L. (2014): A new snapping species of the shrimp genus Typton Costa, 1844 (Decapoda: Palaemonidae) from the coast of São Paulo, southeastern Brazil. Zootaxa 3835 (1): 110-120, DOI: 10.11646/zootaxa.3835.1.6

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WATANABE, Moriyoshi, Masahiko SEKINE, Yoshiyuki HAMADA, and Masao UKITA. "Monitoring of Sea Environment by Using Snapping Shrimp." Doboku Gakkai Ronbunshu, no. 643 (2000): 49–60. http://dx.doi.org/10.2208/jscej.2000.643_49.

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39

Milius, Susan. "Snapping Shrimp Whip up a Riot of Bubbles." Science News 158, no. 13 (2000): 199. http://dx.doi.org/10.2307/3981312.

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40

Au, Whitlow W. L., and Kiara Banks. "The acoustics of snapping shrimp in Kaneohe Bay." Journal of the Acoustical Society of America 99, no. 4 (1996): 2533–74. http://dx.doi.org/10.1121/1.415805.

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41

Jeffery, Nicholas W., Kristin Hultgren, Solomon Tin Chi Chak, T. Ryan Gregory, and Dustin R. Rubenstein. "Patterns of genome size variation in snapping shrimp." Genome 59, no. 6 (2016): 393–402. http://dx.doi.org/10.1139/gen-2015-0206.

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Although crustaceans vary extensively in genome size, little is known about how genome size may affect the ecology and evolution of species in this diverse group, in part due to the lack of large genome size datasets. Here we investigate interspecific, intraspecific, and intracolony variation in genome size in 39 species of Synalpheus shrimps, representing one of the largest genome size datasets for a single genus within crustaceans. We find that genome size ranges approximately 4-fold across Synalpheus with little phylogenetic signal, and is not related to body size. In a subset of these spec

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42

Hee Wai, Tyler, John S. Allen, John Gebbie, and Martin Siderius. "Nonlinear time series analysis of snapping shrimp sounds." Journal of the Acoustical Society of America 134, no. 5 (2013): 4147. http://dx.doi.org/10.1121/1.4831199.

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Mahmood, Ahmed, Mandar Chitre, and Hari Vishnu. "Locally Optimal Inspired Detection in Snapping Shrimp Noise." IEEE Journal of Oceanic Engineering 42, no. 4 (2017): 1049–62. http://dx.doi.org/10.1109/joe.2017.2731058.

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Bohnenstiehl, DelWayne R., Ashlee Lillis, and David B. Eggleston. "The Curious Acoustic Behavior of Estuarine Snapping Shrimp: Temporal Patterns of Snapping Shrimp Sound in Sub-Tidal Oyster Reef Habitat." PLOS ONE 11, no. 1 (2016): e0143691. http://dx.doi.org/10.1371/journal.pone.0143691.

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Lillis, Ashlee, and T. A. Mooney. "The snapping shrimp conundrum: Spatial and temporal complexity of snapping sounds on coral reefs." Journal of the Acoustical Society of America 140, no. 4 (2016): 3071. http://dx.doi.org/10.1121/1.4969566.

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Almeida, Alexandre O., Mariana Terossi, Catarina L. Araújo-Silva, and Fernando L. Mantelatto. "Description of Alpheus buckupi spec. nov., a new amphi-Atlantic snapping shrimp (Caridea: Alpheidae), based on morphological and molecular data." Zootaxa 3652, no. 4 (2013): 437–52. https://doi.org/10.11646/zootaxa.3652.4.3.

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Almeida, Alexandre O., Terossi, Mariana, Araújo-Silva, Catarina L., Mantelatto, Fernando L. (2013): Description of Alpheus buckupi spec. nov., a new amphi-Atlantic snapping shrimp (Caridea: Alpheidae), based on morphological and molecular data. Zootaxa 3652 (4): 437-452, DOI: 10.11646/zootaxa.3652.4.3

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Anker, Arthur, Ivan N. Marin, Paulo P. G. Pachelle, and Tomoyuki Komai. "Redescription of Alpheus vladivostokiensis (Vinogradov, 1950), a large and conspicuous snapping shrimp from the northern Sea of Japan (Decapoda: Caridea: Alpheidae)." Zootaxa 4127, no. 1 (2016): 171–84. https://doi.org/10.11646/zootaxa.4127.1.10.

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Anker, Arthur, Marin, Ivan N., Pachelle, Paulo P. G., Komai, Tomoyuki (2016): Redescription of Alpheus vladivostokiensis (Vinogradov, 1950), a large and conspicuous snapping shrimp from the northern Sea of Japan (Decapoda: Caridea: Alpheidae). Zootaxa 4127 (1): 171-184, DOI: 10.11646/zootaxa.4127.1.10

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Ramos-Tafur, Gabriel E., and Rebeca Franke-Ante. "Synalpheus amintae sp. nov., a new species of sponge-dwelling snapping shrimp (Crustacea: Decapoda: Alpheidae) from Parque Nacional Natural Isla Gorgona, Pacific Coast of Colombia." Zootaxa 4646, no. 1 (2019): 173–88. https://doi.org/10.11646/zootaxa.4646.1.10.

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Ramos-Tafur, Gabriel E., Franke-Ante, Rebeca (2019): Synalpheus amintae sp. nov., a new species of sponge-dwelling snapping shrimp (Crustacea: Decapoda: Alpheidae) from Parque Nacional Natural Isla Gorgona, Pacific Coast of Colombia. Zootaxa 4646 (1): 173-188, DOI: 10.11646/zootaxa.4646.1.10

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Cunha, Andressa Maria, Mariana Terossi, Fernando L. Mantelatto, and Alexandre O. Almeida. "Morphological and molecular analyses support the amphi-Atlantic distribution and taxonomic status of the snapping shrimp Alpheus intrinsecus Spence Bate, 1888 (Crustacea: Decapoda: Alpheidae)." Zootaxa 4303, no. 4 (2017): 573–89. https://doi.org/10.11646/zootaxa.4303.4.8.

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Cunha, Andressa Maria, Terossi, Mariana, Mantelatto, Fernando L., Almeida, Alexandre O. (2017): Morphological and molecular analyses support the amphi-Atlantic distribution and taxonomic status of the snapping shrimp Alpheus intrinsecus Spence Bate, 1888 (Crustacea: Decapoda: Alpheidae). Zootaxa 4303 (4): 573-589, DOI: 10.11646/zootaxa.4303.4.8

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Bochini, Gabriel Lucas, Rodrigo Guéron, Mariana Terossi, and Alexandre Oliveira Almeida. "Extension of the known range of the snapping shrimp Alpheus christofferseni Anker, Hurt and Knowlton, 2007 (Caridea: Alpheidae)." Nauplius 31 (March 27, 2023): 1–7. https://doi.org/10.1590/2358-2936e2023001.

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Bochini, Gabriel Lucas, Guéron, Rodrigo, Terossi, Mariana, Almeida, Alexandre Oliveira (2023): Extension of the known range of the snapping shrimp Alpheus christofferseni Anker, Hurt and Knowlton, 2007 (Caridea: Alpheidae). Nauplius (e2023001) 31: 1-7, DOI: 10.1590/2358-2936e2023001, URL: http://dx.doi.org/10.1590/2358-2936e2023001

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