Histologic, metabolomic, and transcriptomic differences in fir trees from a peri‐urban forest under chronic ozone exposure

Author:

Reyes‐Galindo Verónica12ORCID,Jaramillo‐Correa Juan P.1,Shishkova Svetlana3ORCID,Sandoval‐Zapotitla Estela4ORCID,Flores‐Ortiz César Mateo5ORCID,Piñero Daniel1ORCID,Spurgin Lewis G.6ORCID,Martin Claudia A.67ORCID,Torres‐Jardón Ricardo8ORCID,Zamora‐Callejas Claudio9,Mastretta‐Yanes Alicia1011ORCID

Affiliation:

1. Departamento de Ecología Evolutiva Instituto de Ecología, Universidad Nacional Autónoma de México Mexico City Mexico

2. Programa de Maestría en Ciencias Biológicas Universidad Nacional Autónoma de México Mexico City Mexico

3. Departamento de Biología Molecular de Plantas, Instituto de Biotecnología Universidad Nacional Autónoma de México Cuernavaca Morelos Mexico

4. Jardín Botánico, Instituto de Biología Universidad Nacional Autónoma de México Mexico City Mexico

5. Unidad de Biotecnología y Prototipos, Facultad de Estudios Superiores Iztacala Universidad Nacional Autónoma de México Tlalnepantla Estado de México Mexico

6. School of Biological Sciences University of East Anglia Norwich Research Park Norfolk United Kingdom

7. School of Biological Sciences The University of Edinburgh Edinburgh United Kingdom

8. Departamento de Ciencias Ambientales Instituto de Ciencias de la Atmósfera y Cambio Climático, Universidad Nacional Autónoma de México Mexico City Mexico

9. Bienes Comunales Santa Rosa Xochiac Mexico City Mexico

10. Consejo Nacional de Humanidades, Ciencias y Tecnologías Mexico City Mexico

11. Departamento de Ecología de la Biodiversidad Instituto de Ecología, Universidad Nacional Autónoma de México Mexico City Mexico

Abstract

AbstractUrbanization modifies ecosystem conditions and evolutionary processes. This includes air pollution, mostly as tropospheric ozone (O3), which contributes to the decline of urban and peri‐urban forests. A notable case are fir (Abies religiosa) forests in the peripheral mountains southwest of Mexico City, which have been severely affected by O3 pollution since the 1970s. Interestingly, some young individuals exhibiting minimal O3—related damage have been observed within a zone of significant O3 exposure. Using this setting as a natural experiment, we compared asymptomatic and symptomatic individuals of similar age (≤15 years old; n = 10) using histologic, metabolomic, and transcriptomic approaches. Plants were sampled during days of high (170 ppb) and moderate (87 ppb) O3 concentration. Given that there have been reforestation efforts in the region, with plants from different source populations, we first confirmed that all analyzed individuals clustered within the local genetic group when compared to a species‐wide panel (Admixture analysis with ~1.5K SNPs). We observed thicker epidermis and more collapsed cells in the palisade parenchyma of needles from symptomatic individuals than from their asymptomatic counterparts, with differences increasing with needle age. Furthermore, symptomatic individuals exhibited lower concentrations of various terpenes (ß‐pinene, ß‐caryophylene oxide, α‐caryophylene, and ß‐α‐cubebene) than asymptomatic trees, as evidenced through GC–MS. Finally, transcriptomic analyses revealed differential expression for 13 genes related to carbohydrate metabolism, plant defense, and gene regulation. Our results indicate a rapid and contrasting phenotypic response among trees, likely influenced by standing genetic variation and/or plastic mechanisms. They open the door to future evolutionary studies for understanding how O3 tolerance develops in urban environments, and how this knowledge could contribute to forest restoration.

Funder

Universidad Nacional Autónoma de México

Consejo Nacional de Ciencia y Tecnología

Publisher

Wiley

Reference94 articles.

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