Erick Corro

Dr. Erick Corro

orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
11 December 2019 in Ecology
Verified
Journal Article
Open access
PDF file
Wesley DáttiloWesley Dáttilo
Wesley Dáttilo
MVMiguel Vásquez‐Bolaños
Miguel Vásquez‐Bolaños
DADiana A. Ahuatzin
Diana A. Ahuatzin
RAReuber Antoniazzi
Reuber Antoniazzi
ECEdgar Chávez‐González
Edgar Chávez‐González
IMIan MacGregor‐Fors
Ian MacGregor‐Fors
Mexico is one of the most biodiverse countries in the world, with an important proportion of endemism mainly because of the convergence of the Nearctic and Neotropical biogeographic regions, which generate great diversity and species turnover at different spatial scales. However, most of our knowledge of the Mexican ant biota is limited to a few well‐studied taxa, and we lack a comprehensive synthesis of ant biodiversity information. For instance, most of the knowledge available in the literature on Mexican ant fauna refers only to species lists by states, or is focused on only a few regions of the country, which prevents the study of several basic and applied aspects of ants, from diversity and distribution to conservation. Our aims in this data paper are therefore (1) to compile all the information available regarding ants across the Mexican territory, and (2) to identify major patterns in the gathered data set and geographic gaps in order to direct future sampling efforts. All records were obtained from raw data, including both unpublished and published information. After exhaustive filtering and updating information and synonyms, we compiled a total of 21,731 records for 887 ant species distributed throughout Mexico from 1894 to 2018. These records were concentrated mainly in the states of Chiapas (n = 6,902, 32.76%) and Veracruz de Ignacio de la Llave (n = 4,329, 19.92%), which together comprise half the records. The subfamily with the highest number of records was Myrmicinae (n = 10,458 records, 48.12%), followed by Formicinae (n = 3,284, 15.11%) and Ponerinae (n = 1,914, 8.8%). Most ant records were collected in the Neotropical region of the country (n = 12,646, 58.19%), followed by the Mexican transition zone (n = 5,237, 24.09%) and the Nearctic region (n = 3,848, 17.72%). Native species comprised 95.46% of the records (n = 20,745). To the best of our knowledge, this is the most complete data set available to date in the literature for the country. We hope that this compilation will encourage researchers to explore different aspects of the population and community research of ants at different spatial scales, and to aid in the establishment of conservation policies and actions. There are no copyright restrictions. Please cite this data paper when using its data for publications or teaching events.

22 November 2018 in Landscape Ecology
Verified
Journal Article
Closed access
PDF file
ECErick Corro
Erick Corro
DADiana A. Ahuatzin
Diana A. Ahuatzin
AJArmando Aguirre Jaimes
Armando Aguirre Jaimes
MFMario E. Favila
Mario E. Favila
MRMilton Cezar Ribeiro
Milton Cezar Ribeiro
Wesley DáttiloWesley Dáttilo
Wesley Dáttilo

25 February 2020 in Diversity
Verified
Journal Article
Open access
PDF file
PLPedro Luna
Pedro Luna
ECErick Corro
Erick Corro
RAReuber Antoniazzi
Reuber Antoniazzi
Wesley DáttiloWesley Dáttilo
Wesley Dáttilo
Biotic interactions are part of all ecosystem attributes and play an important role in the structure and stability of biological communities. In this study, we give a brief account of how the threads of biotic interactions are linked and how we can measure such complexity by focusing on mutualistic interactions. We start by explaining that although biotic interactions are fundamental ecological processes, they are also a component of biodiversity with a clear α, β and γ diversity structure which can be measured and used to explain how biotic interactions vary over time and space. Specifically, we explain how to estimate the α-diversity by measuring the properties of species interaction networks. We also untangle the components of the β-diversity and how it can be used to make pairwise comparisons between networks. Moreover, we move forward to explain how local ecological networks are a subset of a regional pool of species and potential interactions, γ-diversity, and how this approach allows assessing the spatial and temporal dynamics of ecological networks. Finally, we propose a new framework for studying interactions and the biodiversity–ecosystem function relationship by identifying the unique and common interactions of local networks over space, time or both together.

13 February 2019 in Biodiversity and Conservation
Verified
Journal Article
Closed access
PDF file
DADiana A. Ahuatzin
Diana A. Ahuatzin
ECErick Corro
Erick Corro
AJArmando Aguirre Jaimes
Armando Aguirre Jaimes
JGJorge E. Valenzuela González
Jorge E. Valenzuela González
Rodrigo Machado FeitosaRodrigo Machado Feitosa
Rodrigo Machado Feitosa
Wesley DáttiloWesley Dáttilo
Wesley Dáttilo

1 November 2018 in Acta Oecologica
Verified
Journal Article
Closed access
RFRoberth Fagundes
Roberth Fagundes
DLDenise Lange
Denise Lange
DADiego Anjos
Diego Anjos
FLFilipe Paixão de Lima
Filipe Paixão de Lima
LNLarissa Nahas
Larissa Nahas
Wesley DáttiloWesley Dáttilo
Wesley Dáttilo

31 March 2017 in Parasitology
Verified
Journal Article
Closed access
PDF file
PLPedro Luna
Pedro Luna
ECErick Corro
Erick Corro
DADiana A. Ahuatzin-Flores
Diana A. Ahuatzin-Flores
RAReuber Antoniazzi
Reuber Antoniazzi
NBNathalia Barrozo
Nathalia Barrozo
Wesley DáttiloWesley Dáttilo
Wesley Dáttilo
SUMMARY: In the last years, there were a growing number of studies using the metric H2′ to calculate complementary specialization in host–parasite interaction networks. However, only a few studies have explored the sensitivity of H2′ to network dimensions (i.e. species richness and number of interactions), which consequently could generate studies that are not comparable among them or lead to biased conclusions. In this study, we used the recent published study conducted by Rivera-García et al. in 2016 involving host–bat fly networks as an example to call attention to the risk of using H2′ to calculate specialization for small matrices. After conducting analyses based on both empirical and simulated data, we show that H2′ values are strongly affected by randomly allocation of species interactions to another cell in the matrix for small networks and that therefore the results and conclusions presented in Rivera-García et al. in 2016 are only an artefact of the dataset used. Therefore, we fully recommended taking into account the careful use of small networks to measuring specialization in host–parasite interactions.