Publications

Peer-reviewed scientific journals:

[25] Perez Castro S*, Peredo EL*…. Z Cardon. Vegetated salt marsh sediments reveal the uncultivated diversity of sulfur-cycling bacteria (Submission expected Fall 2022)

[24] Schön I, Fontaneto D, Peredo EL. Microbiomes of aquatic animals. Hydrobiologia (2023): 1-3. https://link.springer.com/article/10.1007/s10750-023-05328-x

[23] Cardon Z., Peredo EL, Enloe C, Oakey J, Wu S-Z, Bezanilla M. (2022) Slip slidin’ away: bristle-driven gliding by Tetradesmus deserticola (Chlorophyta) in microfluidic chambers. J Phycol. 58: 626–630 https://onlinelibrary.wiley.com/doi/epdf/10.1111/jpy.13271

[22] Peredo EL, Cardon Z. (2020) Shared upregulation and contrasting downregulation of gene expression distinguish desiccation tolerant from intolerant green algae. PNAS 117: 17438-17445 https://www.pnas.org/content/117/29/17438

Work highlighted in the National Science Foundation website; Eureka news; Phys Org; Environmental Network; ScienMag.

[21] Stark J, Cardon Z, Peredo EL. (2020) Extraction of high-quality, high molecular-weight DNA depends heavily on cell homogenization methods in green microalgae. Apps in Plant Sci, 8: e11333. https://bsapubs.onlinelibrary.wiley.com/doi/full/10.1002/aps3.11333

[20] Bono L, RJ Orton, EL Peredo, HG Morrison, M Sistrom, SL Simmons, PE Turner. (2019) Spatiotemporal dynamics of RNA viruses associated with white clover (Trifolium repens L.) bioRxiv https://doi.org/10.1101/772475

[19] Cardon Z, EL Peredo, Dohnalkova AC, H Gershone, M Bezanilla. (2018) A model suite of green algae within the Scenedesmaceae for investigating contrasting desiccation tolerance and morphology. Journal of Cell Biology 131 pii: jcs212233. https://doi.org/10.1242/jcs.212233

Article selected for the JCS highlights and as cover image. Work highlighted in Nikon’s Microscopy U.

[18] Peredo EL, SL Simmons. (2018) Leaf-FISH: Microscale imaging of microbial communities on phyllosphere. Frontiers of Microbiology 8: 1–14. https://doi.org/10.3389/fmicb.2017.02669

Work highlighted in microBEnet; Microbiome Digest ; IDEA Bio-Medial.

[17] Les DH, EL Peredo, N Tippery, L Benoit, H Razifard, U King, H Na, H Choi, L Chen, R Shannon, S Sheldon, (2015b) Najas minor (Hydrocharitaceae) in North America: a reappraisal. Aquatic Bot 126:60–72. https://doi.org/10.1016/j.aquabot.2015.06.005

[16] Tippery NP, DH Les, EL Peredo. (2015) Nymphoides grayana (Menyanthaceae) in Florida verified by DNA and morphological data. J Torrey Bot Soc 142:325-330. https://doi.org/10.3159/TORREY-D-15-00008.1

[15] Les DH, AM Les, EL Peredo. (2015) Najas flexilis (Hydrocharitaceae) in Alaska: a reassessment. Rhodora 117:354–370. https://doi.org/10.3119/15-03

[14] Les DH, EL Peredo, U King, L Benoit, NP Tippery, C Ball, R Shannon. (2015a) Through thick and thin: cryptic sympatric speciation in the submersed genus Najas (Hydrocharitaceae). Mol Phylog and Evol 82: 15-30. https://doi.org/10.1016/j.ympev.2014.09.022

[13] Peredo EL, U King, D Les. (2013) The plastid genome Najas flexilis: adaptation to submerged environments lead to the complete loss of the ndh complex in an aquatic angiosperms. Plos One 8: e68591 https://doi.org/10.1371/journal.pone.0068591

[12] Les DH, EL Peredo, L Benoit, N Tippery, U King, S Sheldon. (2013) Phytogeography of Najas gracillima (Hydrocharitaceae) in North America and its cryptic introduction to California. Am J of Bot 100:1905-15 https://doi.org/10.3732/ajb.1300005

[11] Peredo EL, Mendez-Couz M, Revilla MA (2013) Mating system in Blechnum spicant and Dryopteris affinis ssp. affinis correlates with genetic variability. American Fern J 103:27–39. https://doi.org/10.1640/0002-8444-103.1.27

[10] Peredo EL, D Les, U King, L Benoit. (2012) Extreme conservation of the psaA/psaB intercistronic spacer reveals a translational motif coincident with the evolution of land plants. J Mol Evol 75:184–197. https://doi.org/10.1007/s00239-012-9526-z

[9] Peredo EL, A Revilla, B Reed, B Javornik, R Arroyo-García (2010) The influence of the European and American wild germplasm in hop cultivars. Gen Res Crop Evol, 57: 575–586. https://doi.org/10.1007/s10722-009-9495-2

[8] Cires E, C Cuesta, EL Peredo, A Revilla, JA Fernández Prieto. (2010) Genome size variation and morphological differentiation within Ranunculus parnassifolius group (Ranunculaceae) from calcareous screes in the Northwest of Spain. Plant Sys Evol, 281: 193–208 https://doi.org/10.1007/s00606-009-0201-9

[7] Peredo EL, A Revilla, B Jiménez-Alfaro, A Bueno, J Fernández Prieto, R Abbott (2009) Historical biogeography of a disjunctly distributed, Spanish alpine plant, Senecio boissieri (Asteraceae). Taxon, 58: 883–892.

[6] Peredo EL, R Arroyo-García, A Revilla. (2009) Epigenetic changes detected in micropropagated hop plants. J Plant Physiol, 166: 1101–1111. https://doi.org/10.1016/j.jplph.2008.12.015

[5] Peredo EL, Revilla MA, Jimenez-Alfaro B, Bueno A, Cires E, Fernandez Prieto JA, Abbott R (2009) Applications of molecular markers prior conservation actions on the Spanish endemic Senecio boissieri. Cryoletters 30: 382–97. Pp 391.

[4] Peredo EL, R Arroyo-García, B Reed, A Revilla. (2008) Genetic and epigenetic stability of cryopreserved and cold-stored hops (Humulus lupulus L.) Cryobiology 57:234–241. https://doi.org/10.1016/j.cryobiol.2008.09.002

[3] Folgado R, Y Enai, EL Peredo, H Fernández, A Revilla (2007) Genetic stability of in vitro conserved germplasm of Humulus lupulus L. Cryoletters 29: 73–88. Pp 87.

[2] Peredo EL, A Revilla, R Arroyo-García (2006) Assessment of genetic and epigenetic variation in hop plants regenerated from sequential subcultures of organogenic calli. J Plant Physiol 163: 1071–1079. https://doi.org/10.1016/j.jplph.2005.09.010

[1] Peredo EL, R Arroyo-Garcia, JM Martínez-Zapater, A Revilla (2005) Evaluation of microsatellite detection using autoradiography and capillary electrophoresis in hops. J Am Soc Brew Chem 63: 57–62.

Book chapters:

[4] Peredo EL, SL Simmons (2021) Leaf-FISH: in situ hybridization method for visualizing bacterial taxa on plant surfaces. In 'An overview of FISH concepts and protocols for microbial cells', N. Azevedo and C. Almeida eds. Methods in Molecular Biology, (Springer Nature) https://experiments.springernature.com/articles/10.1007/978-1-0716-1115-9_8

[3] King U, DH Les, EL Peredo, L Benoit (2017) Adaptive evolution of the chloroplast genome in the submersed Monocotyledon Najas (Hydrocharitaceae). In: Lisa Campbell, Davis JI, Meerow AW, Robert F. C. Naczi, Stevenson DW, Thomas WW, eds. Diversity and Phylogeny of the Monocotyledons: Contributions from Monocots V (Memoirs of The New York Botanical Garden Volume 118). NYBG Press, 52-68.

[2] Peredo EL, A Revilla, M Méndez, V Menéndez, H Fernández. Diversity in natural fern populations: dominant markers as a genetic tool. Chapter 16 in book, Working with ferns: Issues and Applications. Editors: Kumar A & H Fernández, 2010, XXII, 386 p.

[1] Menéndez V, A Revilla, EL Peredo, A Revilla, H Fernández. Sexual reproduction in ferns. Chapter 4 in book, Working with ferns: Issues and Applications. Eds: Kumar A & H Fernández, 2010, XXII, 386 p.