Articles | Volume 10, issue 6
https://doi.org/10.5194/esurf-10-1273-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/esurf-10-1273-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
22 Dec 2022
Research article |
| 22 Dec 2022
| 22 Dec 2022
Higher sediment redistribution rates related to burrowing animals than previously assumed as revealed by time-of-flight-based monitoring
Paulina Grigusova
CORRESPONDING AUTHOR
Laboratory for Climatology and Remote Sensing, Department of
Geography, University of Marburg, 35037 Marburg, Germany
Annegret Larsen
Soil Geography and Landscape, Department of Environmental Sciences,
Wageningen University & Research, 6700 AA Wageningen, the Netherlands
Sebastian Achilles
Laboratory for Climatology and Remote Sensing, Department of
Geography, University of Marburg, 35037 Marburg, Germany
Roland Brandl
Animal Ecology, Department of Biology, University of Marburg, 35032
Marburg, Germany
Camilo del Río
Facultad de Historia, Geografía y Ciencia Política,
Instituto de Geografía, Pontificia Universidad Católica de Chile,
782-0436 Santiago, Chile
Centro UC Desierto de Atacama, Pontificia Universidad Católica de
Chile, 782-0436 Santiago, Chile
Nina Farwig
Conservation Ecology, Department of Biology, University of Marburg,
35047 Marburg, Germany
Diana Kraus
Conservation Ecology, Department of Biology, University of Marburg,
35047 Marburg, Germany
Leandro Paulino
Facultad de Agronomía, Universidad de Concepción, 378-0000
Chillán, Chile
Patricio Pliscoff
Facultad de Historia, Geografía y Ciencia Política,
Instituto de Geografía, Pontificia Universidad Católica de Chile,
782-0436 Santiago, Chile
Facultad de Ciencias Biológicas, Departamento de Ecología,
Pontificia Universidad Católica de Chile, 833-1150 Santiago, Chile
Center of Applied Ecology and Sustainability (CAPES), Pontificia
Universidad Católica de Chile, 833-1150 Santiago, Chile
Kirstin Übernickel
Earth System Dynamics, Department of Geosciences, University of
Tübingen, 72076 Tübingen, Germany
Jörg Bendix
Laboratory for Climatology and Remote Sensing, Department of
Geography, University of Marburg, 35037 Marburg, Germany
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Cited articles
Afana, A., Solé-Benet, A., and Pérez, J. L.: Determination of Soil
Erosion Using Laser Scanners, https://www.iuss.org/19th WCSS/Symposium/pdf/1317.pdf last access: 22 December 2021.
Andersen, D. C.: Geomys Bursarius Burrowing Patterns: Influence of Season
and Food Patch Structure, Ecology, 68, 1306–1318, https://doi.org/10.2307/1939215,
1987.
Ashcroft, M. B., Gollan, J. R., and Ramp, D.: Creating vegetation density
profiles for a diverse range of ecological habitats using terrestrial laser
scanning, Meth. Ecol. Evol., 5, 263–272, https://doi.org/10.1111/2041-210X.12157, 2014.
Bancroft, W. J., Hill, D., and Roberts, J. D.: A new method for calculating
volume of excavated burrows: the geomorphic impact of Wedge-Tailed
Shearwater burrows on Rottnest Island, Funct. Ecol., 18, 752–759,
https://doi.org/10.1111/j.0269-8463.2004.00898.x, 2004.
Bernhard, N., Moskwa, L.-M., Schmidt, K., Oeser, R. A., Aburto, F., Bader,
M. Y., Baumann, K., Blanckenburg, F. von, Boy, J., van den Brink, L.,
Brucker, E., Büdel, B., Canessa, R., Dippold, M. A., Ehlers, T. A.,
Fuentes, J. P., Godoy, R., Jung, P., Karsten, U., Köster, M., Kuzyakov,
Y., Leinweber, P., Neidhardt, H., Matus, F., Mueller, C. W., Oelmann, Y.,
Oses, R., Osses, P., Paulino, L., Samolov, E., Schaller, M., Schmid, M.,
Spielvogel, S., Spohn, M., Stock, S., Stroncik, N., Tielbörger, K.,
Übernickel, K., Scholten, T., Seguel, O., Wagner, D., and Kühn, P.:
Pedogenic and microbial interrelations to regional climate and local
topography: New insights from a climate gradient (arid to humid) along the
Coastal Cordillera of Chile, CATENA, 170, 335–355,
https://doi.org/10.1016/j.catena.2018.06.018, 2018.
Black, T. A. and Montgomery, D. R.: Sediment transport by burrowing mammals,
Marin County, California, Earth Surf. Proc. Land., 16, 163–172,
https://doi.org/10.1002/esp.3290160207, 1991.
Blanch, X., Eltner, A., Guinau, M., and Abellan, A.: Multi-Epoch and
Multi-Imagery (MEMI) Photogrammetric Workflow for Enhanced Change Detection
Using Time-Lapse Cameras, Remote Sensing, 13, 1460, https://doi.org/10.3390/rs13081460,
2021.
Castner, J. L. and Fowler, H. G.: Distribution of Mole Crickets (Orthoptera:
Gryllotalpidae: Scapteriscus) and the Mole Cricket Parasitoid Larra bicolor
(Hymenoptera: Sphecidae) in Puerto Rico, Fla. Entomol., 67, 481,
https://doi.org/10.2307/3494730, 1984.
Cerqueira, R.: The Distribution of Didelphis in South America (Polyprotodontia, Didelphidae), J. Biogeogr., 12, 135, https://doi.org/10.2307/2844837, 1985.
Chen, M., Ma, L., Shao, M.'a., Wei, X., Jia, Y., Sun, S., Zhang, Q., Li, T.,
Yang, X., and Gan, M.: Chinese zokor (Myospalax fontanierii) excavating
activities lessen runoff but facilitate soil erosion – A simulation
experiment, CATENA, 202, 105248, https://doi.org/10.1016/j.catena.2021.105248, 2021.
Coombes, M. A.: Biogeomorphology: diverse, integrative and useful, Earth
Surf. Proc. Land., 41, 2296–2300, https://doi.org/10.1002/esp.4055, 2016.
Corenblit, D., Corbara, B., and Steiger, J.: Biogeomorphological
eco-evolutionary feedback between life and geomorphology: a theoretical
framework using fossorial mammals, Die Naturwissenschaften, 108, 55,
https://doi.org/10.1007/s00114-021-01760-y, 2021.
Eccard, J. A. and Herde, A.: Seasonal variation in the behaviour of a
short-lived rodent, BMC Ecol., 13, 43, https://doi.org/10.1186/1472-6785-13-43, 2013.
Eitel, J. U.H., Williams, C. J., Vierling, L. A., Al-Hamdan, O. Z., and
Pierson, F. B.: Suitability of terrestrial laser scanning for studying
surface roughness effects on concentrated flow erosion processes in
rangelands, CATENA, 87, 398–407, https://doi.org/10.1016/j.catena.2011.07.009, 2011.
Eltner, A., Mulsow, C., and Maas, H.-G.: QUANTITATIVE MEASUREMENT OF SOIL EROSION FROM TLS AND UAV DATA, Int. Arch. Photogramm. Remote Sens. Spatial Inf. Sci., XL-1/W2, 119–124, https://doi.org/10.5194/isprsarchives-XL-1-W2-119-2013, 2013.
Eltner, A., Kaiser, A., Castillo, C., Rock, G., Neugirg, F., and Abellán, A.: Image-based surface reconstruction in geomorphometry – merits, limits and developments, Earth Surf. Dynam., 4, 359–389, https://doi.org/10.5194/esurf-4-359-2016, 2016a.
Eltner, A., Schneider, D., and Maas, H.-G.: INTEGRATED PROCESSING OF HIGH RESOLUTION TOPOGRAPHIC DATA FOR SOIL EROSION ASSESSMENT CONSIDERING DATA ACQUISITION SCHEMES AND SURFACE PROPERTIES, Int. Arch. Photogramm. Remote Sens. Spatial Inf. Sci., XLI-B5, 813–819, https://doi.org/10.5194/isprs-archives-XLI-B5-813-2016, 2016b.
Eltner, A., Kaiser, A., Abellan, A., and Schindewolf, M.: Time lapse
structure-from-motion photogrammetry for continuous geomorphic monitoring,
Earth Surf. Proc. Land., 42, 2240–2253, https://doi.org/10.1002/esp.4178, 2017.
Gabet, E. J., Reichman, O. J., and Seabloom, E. W.: The Effects of
Bioturbation on Soil Processes and Sediment Transport, Annu. Rev. Earth
Planet. Sci., 31, 249–273, https://doi.org/10.1146/annurev.earth.31.100901.141314,
2003.
Galland, O., Bertelsen, H. S., Guldstrand, F., Girod, L., Johannessen, R.
F., Bjugger, F., Burchardt, S., and Mair, K.: Application of open-source
photogrammetric software MicMac for monitoring surface deformation in
laboratory models, J. Geophys. Res.-Sol. Ea., 121, 2852–2872,
https://doi.org/10.1002/2015JB012564, 2016.
Garreaud, R., Rutllant, J., and Fuenzalida, H.: Coastal Lows along the
Subtropical West Coast of South America: Mean Structure and Evolution, Mon.
Weather Rev., 130, 75–88, https://doi.org/10.1175/1520-0493(2002)130<0075:CLATSW>2.0.CO;2, 2002.
Grigusova, P., Larsen, A., Achilles, S., Klug, A., Fischer, R., Kraus, D.,
Übernickel, K., Paulino, L., Pliscoff, P., Brandl, R., Farwig, N., and
Bendix, J.: Area-Wide Prediction of Vertebrate and Invertebrate Hole Density
and Depth across a Climate Gradient in Chile Based on UAV and Machine
Learning, Drones, 5, 86, https://doi.org/10.3390/drones5030086, 2021.
Hakonson, T. E.: The Effects of Pocket Gopher Burrowing on Water Balance and
Erosion from Landfill Covers, J. Environ. Qual., 28, 659–665,
https://doi.org/10.2134/jeq1999.00472425002800020033x, 1999.
Hall, K., Boelhouwers, J., and Driscoll, K.: Animals as Erosion Agents in
the Alpine Zone: Some Data and Observations from Canada, Lesotho, and Tibet,
Arct. Antarct. Alp. Res., 31, 436–446,
https://doi.org/10.1080/15230430.1999.12003328, 1999.
Hancock, G. and Lowry, J.: Quantifying the influence of rainfall, vegetation
and animals on soil erosion and hillslope connectivity in the monsoonal
tropics of northern Australia, Earth Surf. Proc. Land., 46,
2110–2123, https://doi.org/10.1002/esp.5147, 2021.
Hänsel, P., Schindewolf, M., Eltner, A., Kaiser, A., and Schmidt, J.:
Feasibility of High-Resolution Soil Erosion Measurements by Means of
Rainfall Simulations and SfM Photogrammetry, Hydrology, 3, 38,
https://doi.org/10.3390/hydrology3040038, 2016.
Hazelhoff, L., van Hoof, P., Imeson, A. C., and Kwaad, F. J. P. M.: The
exposure of forest soil to erosion by earthworms, Earth Surf. Proc.
Land., 6, 235–250, https://doi.org/10.1002/esp.3290060305, 1981.
Herbst, M. and Bennett, N. C.: Burrow architecture and burrowing dynamics of
the endangered Namaqua dune mole rat (Bathyergus janetta ) (Rodentia:
Bathyergidae), J. Zool., 270, 420–428,
https://doi.org/10.1111/j.1469-7998.2006.00151.x, 2006.
Horn, B. K. P.: Hill shading and the reflectance map, P. IEEE, 69, 14–47,
https://doi.org/10.1109/PROC.1981.11918, 1981.
Imeson, A. C.: Splash erosion, animal activity and sediment supply in a
small forested Luxembourg catchment, Earth Surf. Proc. Land., 2,
153–160, https://doi.org/10.1002/esp.3290020207, 1977.
Imeson, A. C. and Kwaad, F. J. P. M.: Some Effects of Burrowing Animals on
Slope Processes in the Luxembourg Ardennes, Geogr. Ann. A, 58, 317–328, https://doi.org/10.1080/04353676.1976.11879941, 1976.
Iserloh, T., Ries, J. B., Arnáez, J., Boix-Fayos, C., Butzen, V.,
Cerdà, A., Echeverría, M. T., Fernández-Gálvez, J., Fister,
W., Geißler, C., Gómez, J. A., Gómez-Macpherson, H., Kuhn, N.
J., Lázaro, R., León, F. J., Martínez-Mena, M.,
Martínez-Murillo, J. F., Marzen, M., Mingorance, M. D., Ortigosa, L.,
Peters, P., Regüés, D., Ruiz-Sinoga, J. D., Scholten, T., Seeger,
M., Solé-Benet, A., Wengel, R., and Wirtz, S.: European small portable
rainfall simulators: A comparison of rainfall characteristics, CATENA, 110,
100–112, https://doi.org/10.1016/j.catena.2013.05.013, 2013.
James, M. R. and Robson, S.: Sequential digital elevation models of active
lava flows from ground-based stereo time-lapse imagery, ISPRS J.
Photogramm., 97, 160–170,
https://doi.org/10.1016/j.isprsjprs.2014.08.011, 2014.
Jimenez, J. E., Feinsinger, P., and Jaksi, F. M.: Spatiotemporal Patterns of
an Irruption and Decline of Small Mammals in Northcentral Chile, J.
Mammal., 73, 356–364, https://doi.org/10.2307/1382070, 1992.
Jones, C. G., Gutiérrez, J. L., Byers, J. E., Crooks, J. A., Lambrinos,
J. G., and Talley, T. S.: A framework for understanding physical ecosystem
engineering by organisms, Oikos, 119, 1862–1869,
https://doi.org/10.1111/j.1600-0706.2010.18782.x, 2010.
Kaiser, A., Neugirg, F., Rock, G., Müller, C., Haas, F., Ries, J., and
Schmidt, J.: Small-Scale Surface Reconstruction and Volume Calculation of
Soil Erosion in Complex Moroccan Gully Morphology Using Structure from
Motion, Remote Sensing, 6, 7050–7080, https://doi.org/10.3390/rs6087050, 2014.
Katzman, E. A., Zaytseva, E. A., Feoktistova, N. Y., Tovpinetz, N. N.,
Bogomolov, P. L., Potashnikova, E. V., and Surov, A. V.: Seasonal Changes in
Burrowing of the Common Hamster (Cricetus cricetus L., 1758) (Rodentia:
Cricetidae) in the City, Povolzhskiy Journal of Ecology, 17, 251–258,
https://doi.org/10.18500/1684-7318-2018-3-251-258, 2018.
Kinlaw, A. and Grasmueck, M.: Evidence for and geomorphologic consequences
of a reptilian ecosystem engineer: The burrowing cascade initiated by the
Gopher Tortoise, Geomorphology, 157–158, 108–121,
https://doi.org/10.1016/j.geomorph.2011.06.030, 2012.
Kromer, R., Walton, G., Gray, B., Lato, M., and Group, R.: Development and
Optimization of an Automated Fixed-Location Time Lapse Photogrammetric Rock
Slope Monitoring System, Remote Sensing, 11, 1890, https://doi.org/10.3390/rs11161890,
2019.
Kukko, A. and Hyyppä, J.: Small-footprint Laser Scanning Simulator for
System Validation, Error Assessment, and Algorithm Development, Photogramm.
Eng. Rem. S., 75, 1177–1189, https://doi.org/10.14358/PERS.75.10.1177, 2009.
Larsen, A., Nardin, W., Lageweg, W. I., and Bätz, N.: Biogeomorphology,
quo vadis? On processes, time, and space in biogeomorphology, Earth Surf.
Proc. Land., 46, 12–23, https://doi.org/10.1002/esp.5016, 2021.
Le Hir, P., Monbet, Y., and Orvain, F.: Sediment erodability in sediment
transport modelling: Can we account for biota effects?, Cont. Shelf
Res., 27, 1116–1142, https://doi.org/10.1016/j.csr.2005.11.016, 2007.
Lehnert, L. W., Thies, B., Trachte, K., Achilles, S., Osses, P., Baumann,
K., Bendix, J., Schmidt, J., Samolov, E., Jung, P., Leinweber, P., Karsten,
U., and Büdel, B.: A Case Study on Fog/Low Stratus Occurrence at Las
Lomitas, Atacama Desert (Chile) as a Water Source for Biological Soil
Crusts, Aerosol Air Qual. Res., 18, 254–269, https://doi.org/10.4209/aaqr.2017.01.0021,
2018.
Li, G., Li, X., Li, J., Chen, W., Zhu, H., Zhao, J., and Hu, X.: Influences
of Plateau Zokor Burrowing on Soil Erosion and Nutrient Loss in Alpine
Meadows in the Yellow River Source Zone of West China, Water, 11, 2258,
https://doi.org/10.3390/w11112258, 2019.
Li, L.: Time-of-Flight Camera – An Introduction, Technical White Paper,
https://www.ti.com/lit/wp/sloa190b/sloa190b.pdf (last access: 22 December 2021), 2014.
Li, T., Shao, M.'a., Jia, Y., Jia, X., and Huang, L.: Small-scale
observation on the effects of the burrowing activities of mole crickets on
soil erosion and hydrologic processes, Agr. Ecosyst.
Environ., 261, 136–143, https://doi.org/10.1016/j.agee.2018.04.010, 2018.
Li, T., Jia, Y., Shao, M.'a., and Shen, N.: Camponotus japonicus burrowing
activities exacerbate soil erosion on bare slopes, Geoderma, 348, 158–167,
https://doi.org/10.1016/j.geoderma.2019.04.035, 2019.
Li, T. C., Shao, M. A., Jia, Y. H., Jia, X. X., Huang, L. M., and Gan, M.:
Small-scale observation on the effects of burrowing activities of ants on
soil hydraulic processes, Eur. J. Soil Sci., 70, 236–244,
https://doi.org/10.1111/ejss.12748, 2019.
Longoni, L., Papini, M., Brambilla, D., Barazzetti, L., Roncoroni, F.,
Scaioni, M., and Ivanov, V.: Monitoring Riverbank Erosion in Mountain
Catchments Using Terrestrial Laser Scanning, Remote Sensing, 8, 241,
https://doi.org/10.3390/rs8030241, 2016.
Malizia, A. I.: Population dynamics of the fossorial rodent Ctenomys talarum
(Rodentia: Octodontidae), J. Zool., 244, 545–551,
https://doi.org/10.1111/j.1469-7998.1998.tb00059.x, 1998.
Mallalieu, J., Carrivick, J. L., Quincey, D. J., Smith, M. W., and William,
H. M.: An integrated Structure-from-Motion and time-lapse technique for
quantifying ice-margin dynamics, J. Glaciol., 63, 937–949,
https://doi.org/10.1017/jog.2017.48, 2017.
Meysman, F. J. R., Boudreau, B. P., and Middelburg, J. J.: Relations between
local, nonlocal, discrete and continuous models of bioturbation, J.
Mar. Res., 61, 391–410, https://doi.org/10.1357/002224003322201241, 2003.
Monteverde, M. J. and Piudo, L.: Activity Patterns of the Culpeo Fox
(Lycalopex Culpaeus Magellanica ) in a Non-Hunting Area of Northwestern
Patagonia, Argentina, Mamm. Study, 36, 119–125, https://doi.org/10.3106/041.036.0301,
2011.
Morris, R. H., Buckman, S., Connelly, P., Dragovich, D., Ostendorf, B., and
and Bradstock, R. A.: The dirt on assessing post-fire erosion in the Mount
Lofty Ranges: comparing methods, Proceedings of Bushfire CRC & AFAC 2011 Conference Science Day, 1 September 2011, Sydney Australia, Bushfire CRC, 152–169, 2011.
Muñoz-Pedreros, A., Yáñez, J., Norambuena, H. V., and Zúñiga, A.: Diet, dietary selectivity and density of South American grey fox, Lycalopex griseus, in Central Chile, Integr. Zool., 13, 46–57, https://doi.org/10.1111/1749-4877.12260, 2018.
Nasermoaddeli, M. B. and Pasche, E.: Application of terrestrial 3D scanner
in quantification of the riverbank erosion and deposition,
https://www.tuhh.de/t3resources/wb/Publikationen/MA-Veroeffentlichungen/nasermoaddelli/riverflow2008.pdf (last access: 22 December 2021), 2008.
Pang, X. P. and Guo, Z. G.: Plateau pika disturbances alter plant
productivity and soil nutrients in alpine meadows of the Qinghai-Tibetan
Plateau, China, Rangel. J., 39, 133, https://doi.org/10.1071/RJ16093, 2017.
Reichman, O. J. and Seabloom, E. W.: The role of pocket gophers as
subterranean ecosystem engineers, Trends Ecol. Evol., 17,
44–49, https://doi.org/10.1016/S0169-5347(01)02329-1, 2002.
Richards, P. J. and Humphreys, G. S.: Burial and turbulent transport by
bioturbation: a 27-year experiment in southeast Australia, Earth Surf.
Proc. Land., 21, 856–862, https://doi.org/10.1002/esp.2007, 2010.
Ridd, P. V.: Flow Through Animal Burrows in Mangrove Creeks, Estuar.
Coast. Shelf S., 43, 617–625, https://doi.org/10.1006/ecss.1996.0091, 1996.
Romañach, S. S., Reichman, O. J., and Seabloom, E. W.: Seasonal
influences on burrowing activity of a subterranean rodent, Thomomys bottae,
J. Zool., 266, 319–325, https://doi.org/10.1017/S0952836905006941, 2005.
Rutin, J.: The burrowing activity of scorpions (Scorpio maurus palmatus) and
their potential contribution to the erosion of Hamra soils in Karkur,
central Israel, Geomorphology, 15, 159–168,
https://doi.org/10.1016/0169-555X(95)00120-T, 1996.
Sarbolandi, H., Plack, M., and Kolb, A.: Pulse Based Time-of-Flight Range
Sensing, Sensors (Basel, Switzerland), 18, 6, https://doi.org/10.3390/s18061679, 2018.
Schiffers, K., Teal, L. R., Travis, J. M. J., and Solan, M.: An open source
simulation model for soil and sediment bioturbation, PloS one, 6, e28028,
https://doi.org/10.1371/journal.pone.0028028, 2011.
Sharon, D.: The distribution of hydrologically effective rainfall incident
on sloping ground, J. Hydrol., 46, 165–188,
https://doi.org/10.1016/0022-1694(80)90041-4, 1980.
Thomsen, L. M., Baartman, J. E. M., Barneveld, R. J., Starkloff, T., and Stolte, J.: Soil surface roughness: comparing old and new measuring methods and application in a soil erosion model, SOIL, 1, 399–410, https://doi.org/10.5194/soil-1-399-2015, 2015.
Übernickel, K., Ehlers, T. A., Paulino, L., and Fuentes Espoz, J.-P.:
Time series of meteorological stations on an elevational gradient in
National Park La Campana, Chile, [data set], https://doi.org/10.5880/fidgeo.2021.010, 2021a.
Übernickel, K., Pizarro-Araya, J., Bhagavathula, S., Paulino, L., and Ehlers, T. A.: Reviews and syntheses: Composition and characteristics of burrowing animals along a climate and ecological gradient, Chile, Biogeosciences, 18, 5573–5594, https://doi.org/10.5194/bg-18-5573-2021, 2021b.
Valdés-Pineda, R., Valdés, J. B., Diaz, H. F., and Pizarro-Tapia,
R.: Analysis of spatio-temporal changes in annual and seasonal precipitation
variability in South America-Chile and related ocean-atmosphere circulation
patterns, Int. J. Climatol., 36, 2979–3001, https://doi.org/10.1002/joc.4532, 2016.
Voiculescu, M., Ianăş, A.-N., and Germain, D.: Exploring the impact
of snow vole (Chionomys nivalis) burrowing activity in the Făgăra?
Mountains, Southern Carpathians (Romania): Geomorphic characteristics and
sediment budget, CATENA, 181, 104070, https://doi.org/10.1016/j.catena.2019.05.016,
2019.
Wei, X., Li, S., Yang, P., and Cheng, H.: Soil erosion and vegetation
succession in alpine Kobresia steppe meadow caused by plateau pika – A case
study of Nagqu County, Tibet, Chinese Geogr. Sci., 17, 75–81,
https://doi.org/10.1007/s11769-007-0075-0, 2007.
Wilcox, A. C., Escauriaza, C., Agredano, R., Mignot, E., Zuazo, V.,
Otárola, S., Castro, L., Gironás, J., Cienfuegos, R., and Mao, L.:
An integrated analysis of the March 2015 Atacama floods, Geophys. Res.
Lett., 43, 8035–8043, https://doi.org/10.1002/2016GL069751, 2016.
Wilkinson, M. T., Richards, P. J., and Humphreys, G. S.: Breaking ground:
Pedological, geological, and ecological implications of soil bioturbation,
Earth-Sci. Rev., 97, 257–272, https://doi.org/10.1016/j.earscirev.2009.09.005,
2009.
Yair, A.: Short and long term effects of bioturbation on soil erosion, water
resources and soil development in an arid environment, Geomorphology, 13,
87–99, https://doi.org/10.1016/0169-555X(95)00025-Z, 1995.
Yáñez, E., Barbieri, M.A., Silva, C., Nieto, K., and Espıìndola,
F.: Climate variability and pelagic fisheries in northern Chile, Prog.
Oceanogr., 49, 581–596, https://doi.org/10.1016/S0079-6611(01)00042-8, 2001.
Yoo, K., Amundson, R., Heimsath, A. M., and Dietrich, W. E.: Process-based
model linking pocket gopher (Thomomys bottae) activity to sediment transport
and soil thickness, Earth Surf. Proc. Land., 33, 917,
https://doi.org/10.1130/G21831.1, 2005.
Short summary
In our study, we developed, tested, and applied a cost-effective time-of-flight camera to autonomously monitor rainfall-driven and animal-driven sediment redistribution in areas affected by burrowing animals with high temporal (four times a day) and spatial (6 mm) resolution. We estimated the sediment redistribution rates on a burrow scale and then upscaled the redistribution rates to entire hillslopes. Our findings can be implemented into long-term soil erosion models.
In our study, we developed, tested, and applied a cost-effective time-of-flight camera to...
