Abstract
The ring nematode genus Xenocriconemella De Grisse and Loof, 1965 comprises only one nominal species, Xenocriconemella macrodora (Taylor, 1936) De Grisse and Loof, 1965. The initial objective of the present study was to investigate the morphological–morphometric and molecular diversity of 28 X. macrodora populations in the Iberian Peninsula associated with tree forests (mainly Quercus spp.). However, a detailed integrative taxonomic analysis (morphological–morphometric and molecular data) from each population and analysis of this data using principal component analysis (PCA) for morphometric data (including these 28 populations and other 25 X. macrodora populations around the world) and molecular and phylogenetic species delimitation methods revealed that X. macrodora forms a species complex. This species complex is composed by species that are morphometricly and morphologically similar, but clearly different at the molecular level. Three new species are described applying integrative taxonomy, namely as Xenocriconemella iberica sp. nov., Xenocriconemella paraiberica sp. nov. and Xenocriconemella pradense sp. nov. However, the molecular diversity of this species in USA and Italy confirmed that additional species are likely present in this species complex, and the diversity of this group may be higher than expected. The study of X. macrodora topotypes can clarify the position of this species using molecular markers under an integrative approach.
Similar content being viewed by others
Introduction
The ring nematode genus Xenocriconemella De Grisse and Loof, 1965 [1] comprises obligate ectoparasite nematodes included under subfamily Discocriconemellinae Geraert, 2010 [2] and is characterized by a body length ca. 250–300 µm, a long and flexible stylet (ca. 100–140 µm and up to 40% of body length), lip region annulated but lacking submedian lobes or pseudolips, body annuli smooth without anastomosis, vulva closed, and juveniles similar to females [2]. Xenocriconemella macrodora (Taylor, 1936) De Grisse and Loof, 1965 [1, 3] is the only nominal species within the genus.
A world review of X. macrodora indicated that this species occurs in association with woodland forests [4, 5]. This species is distributed worldwide (Fig. 1), with a widespread presence in USA [5] and several European countries, particularly in Spain [4, 6]. Owing to its large morphological diversity, some taxonomic studies have challenged the possibility that the genus Xenocriconemella is monospecific. Lϋbbers and Zell [7] morphologically studied several populations of X. macrodora from Germany and concluded that German populations differed morphologically from those of the USA and several European countries in a higher number of annuli (R = 147 vs R = 99-120), concluding that these populations belong to a new species, X. degrissei Lϋbbers and Zell, 1989. Later on, Ganguly et al. [8] also studied X. macrodora populations from peach and blue pine in India and concluded that these populations belong to two new species, X. pruni Ganguly et al. 2008 and X. pini Ganguly et al. 2008. However, Sturhan [9] compared the morphometry of all three species and concluded that all three species overlap with populations of X. macrodora, disallowing the existence of these proposed new taxa, but no molecular markers were provided to confirm this action. Only ribosomal and mitochondrial sequences are available in NCBI from the USA [5, 10] and Italy [11], despite its being a cosmopolitan species, which may be recognized as a major gap in nematode biodiversity knowledge. Molecular taxonomy and DNA barcoding can provide definitively accurate and useful tools for assessing populations and species boundaries in the genus Xenocriconemella only through integrative-based taxonomy studies (combination of morphology-morphometry with molecular data) as in other Criconematidae spp. [5, 10,11,12,13,14,15].
The initial objective of the present study was to investigate the morphological–morphometric and molecular diversity of X. macrodora populations in the Iberian Peninsula associated with tree forests (mainly Quercus spp.) (Fig. 1), and compared with the available molecular cytochrome c oxidase subunit 1 (COI) barcodes of X. macrodora from the USA [5] and ribosomal sequences from Italy [11]. However, the scarce similarity values detected among mitochondrial and ribosomal sequences from the Iberian Peninsula populations and the available accessions from USA and Italy populations prompted us to carry out detailed morphological, morphometric and molecular studies on these populations to clarify the taxonomic status of these ring nematode populations, thus determining whether it is a new case of cryptic species complex within the genus Xenocriconemella, such as those recently described in the genera Mesocriconema [16], Criconemoides [17], or Criconema [15, 18]. Notably, we will follow the classification proposed by Geraert [2], representing the widely accepted classification of this group of nematodes [14] and separating Criconemoides from Xenocriconemella. Hence, the main objectives of this study were to (i) accurately identify with morphological and morphometric approaches several populations of Xenocriconemella detected in an extensive nematode survey in natural habitats in the Iberian Peninsula, (ii) discover the diversity of Xenocriconemella populations through integrative taxonomy, combining morphological analysis and a species delineation approach based on multivariate analysis of morphometric data and genetic methods; (iii) describe three new species of the genus Xenocriconemella belonging to the X. macrodora species complex; (iv) provide molecular characterization of these Xenocriconemella populations using ribosomal (D2-D3 expansion segments of 28S rRNA, ITS region, partial 18S rRNA) and COI markers; and (v) study phylogenetic relationships within Criconematidae spp. and these species of the X. macrodora species complex.
Materials and methods
Sampling
A nematological survey was conducted in the principal areas and sampling sites where X. macrodora had been reported in the Iberian Peninsula [4, 6, 19], as well as new areas not previously sampled in Spain and Portugal. Since X. macrodora has been associated with oak forests [4, 5], most of the sampling program was concentrated on Quercus spp. forests (including Quercus canariensis Willd., Quercus faginea Lam., Quercus ilex L., Quercus pyrenaica Willd., Quercus pubescens Willd., Quercus suber L.), as well as Castanea sativa Mill. and Fagus sylvatica L., covering the majority of the area of the potential distribution of X. macrodora in the Iberian Peninsula from south to north (Table 1, Fig. 1). A total of 28 sites showed the presence of specimens of putative X. macrodora. An additional soil sample was collected in the type locality of the ring nematode Criconemoides rosmarini (Castillo, Siddiqi and Gómez-Barcina, 1988) [20] Siddiqi, 2000 to molecularly characterize and check the phylogenetic relationships with Xenocriconemella. Soil samples for nematode analysis were collected with a shovel from two randomly selected trees and mixed to constitute a soil sample from each sampling site; samples came from the upper 5–40 cm depth of soil. Nematodes were extracted by centrifugal flotation from a 500 cm3 soil subsample [21].
Morphology
Nematode identification was completed using an integrative approach, combining morphological and morphometric evaluation with molecular techniques. Morphological and morphometric analyses were conducted using fixed individuals mounted on permanent slides. To prepare the fixed material, specimens of Xenocriconemella specimens were killed at 70–75 °C and fixed in an aqueous solution of 4% formaldehyde + 1% glycerol, dehydrated using an alcohol-saturated chamber and processed to pure glycerin using Seinhorst’s method [22] as modified by De Grisse [23]. A total of 185 individuals, including 183 females and two males were used for morphological and morphometric analyses. Fixed, mounted individuals were then examined, and measurements of each nematode population were performed using a Leica DM6 compound microscope with a Leica DFC7000 T digital camera. Morphological terminologies follow Archidona-Yuste et al. [18]. Measurements and ratios included: n, number of specimens studied; L, (total body length); a = body length/maximal body width; b = body length/pharyngeal length; c = body length/tail length; c’ = tail length/body width at anus; O = distance between stylet base and orifice of dorsal pharyngeal gland as percentage of stylet length; R = total number of body annuli; Roes = number of annuli in pharyngeal region; Rex = number of annuli between anterior end of body and excretory pore; Rst = number of body annuli between labial disc and stylet knobs; RV = number of annuli between posterior end of body and vulva; Rvan = number of annuli between vulva and anus; Ran = number of annuli on tail; V = (distance from anterior end to vulva/body length) × 100; VL/VB = distance between vulva and posterior end of body divided by body width at vulva; T = (distance from cloacal aperture to anterior end of testis/body length) × 100 [18].
Females of each species mounted in glycerin were selected for SEM observations. The nematodes were hydrated in distilled water, dehydrated in a graded ethanol-acetone series, critical point-dried, coated with gold, and observed with a Zeiss Merlin scanning electron microscope (5 kV) (Zeiss, Oberkochen, Germany) [24].
DNA extraction, PCR and Sequencing
For molecular analyses, and to avoid mistakes in the case of mixed populations in the same sample, single nematodes were pre-mounted in a drop of NaCl and used for molecular identification after recording morphological data. Genomic DNA extraction from single specimens was conducted as described by Archidona-Yuste et al. [18]. Briefly, an individual nematode was cut using a scalpel in a drop of PCR buffer (ThermoPol®, Biolabs, New England, USA) (20 μL), and 2 μL proteinase K (600 μg/mL) was added. Tubes were frozen at −80°C (15 min) and then incubated at 65°C (1 h) and 95°C (10 min) consecutively. Tubes were centrifuged (1 min, 16,000 × g) and kept at −20°C until use in PCR; more importantly, all three molecular markers for each population of Xenocriconemella were extracted from the same single individual in each PCR tube without any exception. In addition, male conspecificity was confirmed by single DNA extraction of males.
The D2-D3 expansion domains of the 28S rRNA were amplified using the D2A (5′-ACAAGTACCGTGAGGGAAAGTTG-3′) and D3B (5′-TCGGAAGGAACCAGCTACTA-3′) primers [25]. The ITS region was amplified by using forward primer TW81 (5′-GTTTCCGTAGGTGAACCTGC-3′) and reverse primer AB28 (5′-ATATGCTTAAGTTCAGCGGGT-3′) [26]. The partial 18S rRNA was amplified using the primers 988 (5′-CTCAAAGATTAAGCCATGC-3′), 1912R (5′-TTTACGGTCAGAACTAGGG-3′), 1813F (5´- CTGCGTGAGAGGTGAAAT -3´), and 2646R (5´- GCTACCTTGTTACGACTTTT -3´) [27]. The COI gene was amplified using the primers JB3 (5´- TTTTTTGGGCATCCTGAGGTTTAT-3`) and JB5 (5’- AGCACCTAAACTTAAAACATAATGAAAATG -3´) [28, 29]. The PCR cycling conditions for the 28S rRNA, ITS and 18S rRNA were as follows: 95°C for 15 min, followed by 35 cycles of 94°C for 30 s, an annealing temperature of 55°C for 45 s, and 72°C for 1 min, and one final cycle of 72°C for 10 min. The PCR cycling for COI primers was as follows: 95°C for 15 min, 39 cycles at 94°C for 30 s, 53°C for 30 s, and 68°C for 1 min, followed by a final extension at 72°C for 7 min. The PCR volumes were adapted to 20 μL for each reaction, and primer concentrations were as described in De Ley et al. [25], Subbotin et al. [11], Holterman et al. [27] and Powers et al. [30]. We used 5x HOT FIREpol Blend Master Mix (Solis Biodyne, Tartu, Estonia) in all PCRs. The PCR products were purified using ExoSAP-IT (Affimetrix, USB products, Kandel, Germany) and used for direct sequencing in both directions with the corresponding primers. The resulting products were analysed in a DNA multi-capillary sequencer (Model 3130XL Genetic Analyzer; Applied Biosystems, Foster City, CA, USA), using the BigDye Terminator Sequencing Kit v.3.1 (Applied Bio-systems) at the Stab Vida sequencing facility (Caparica, Portugal). The sequence chromatograms of the four markers (18S rRNA, ITS, COI and D2-D3 expansion segments of 28S rRNA) were analysed using DNASTAR LASERGENE SeqMan v. 7.1.0. The Basic Local Alignment Search Tool (BLAST) at the National Center for Biotechnology Information (NCBI) was used to confirm the species identity of the DNA sequences obtained in this study [31]. The newly obtained sequences were deposited in the GenBank database under accession numbers indicated on the phylogenetic trees and in Table 1.
Species delimitation within the Xenocriconemella macrodora species complex
Two independent strategies of species delimitation were used to determine species boundaries within the X. macrodora species complex including morphometric and molecular data.
Species delineation using morphometry was conducted using principal component analysis (PCA) [32]. We established the species delimitation among these morphometrically similar new unresolved populations of Xenocriconemella found in the Iberian Peninsula, and we further assessed the relationships between these new populations with those already described as X. macrodora. PCA was based upon the following morphological characters: L, stylet length, R, Rst, Roes, Rex, RV, Rvan, Ran, and the ratios a, b, c, V, VL/VB [18]. Depending on data availability, we selected 25 X. macrodora populations previously reported from several countries for comparison with the 28 new Iberian populations of X. macrodora studied under an integrative taxonomical approach (Table 1 and S1). In the previously reported data, we used the average values of the morphological characters mentioned above in each population. Diagnostic characters were previously standardized and tested for collinearity [33]. We used the collinearity test based on the values of the variance inflation factor (VIF) method that iteratively excludes numeric covariates showing VIF values > 10 as suggested by Montgomery et al. [34]. PCA was performed using the PCA function implemented in the software package ‘FactoMineR’ [35]. All data analyses were done with the R version 4.2.2 (R Core Team, 2022; https://www.R-project.org).
Species delineation based on molecular data was performed using the species delimitation plugin [36] from the program Geneious Prime v2022.1.1. (Geneious, Auckland, New Zealand), and was used to calculate intra- and inter-species variation by means of the P ID liberal and Rosenberg’s PAB value. The intra- and inter-species molecular variation was determined by calculating the ratio between the average genetic distance between individuals within a species and the average genetic distance between individuals belonging to the sister species [36]. The P ID (Liberal) value [37] represents the probability that a correct species identification would be made using the best sequence alignment (BLAST), closest genetic distance or placement on a tree (falling within or being sister to a monophyletic species clade). Species with P ID (Liberal) ≥ 0.93 were considered to be adequately delimited [38]. Rosenberg’s PAB represents the probability that the monophyly of a group of sequences is the result of random branching [39].
Phylogenetic analyses
The D2-D3 expansion segments of the 28S rRNA, ITS rRNA, 18S rRNA, and COI mtDNA sequences of the 28 populations of Xenocriconemella were obtained in this study. These sequences and other sequences of Criconematidae spp. from GenBank were used for phylogenetic analyses. The selection of outgroup taxa for each dataset was based on previously published studies [13, 14, 40]. Multiple sequence alignments of the different genes were completed using the FFT-NS-2 algorithm of MAFFT V.7.450 [41]. The BioEdit program V. 7.2.5 [42] was used for sequence alignment visualization and manually edited and trimmed of the poorly aligned positions using a light filtering strategy (up to 20% of alignment positions), which has little impact on tree accuracy and may save computation time, as suggested by Tan et al. [43], since methods for automated filtering of multiple sequence alignments frequently worsen single-gene phylogenetic inference [43]. Phylogenetic analyses of the sequence datasets were based on Bayesian inference (BI) using MrBayes 3.1.2 [44]. The best-fit model of DNA evolution was achieved using JModelTest V.2.1.7 [45] with the Akaike information criterion (AIC). The best-fit model, the base frequency, the proportion of invariable sites, and the gamma distribution shape parameters and substitution rates in the AIC were then used in MrBayes for phylogenetic analyses. The general time-reversible model with invariable sites and a gamma-shaped distribution (GTR + I + G) for the D2-D3 segments of 28S rRNA, the transversion model with invariable sites and a gamma-shaped distribution (TVM + I + G) for the ITS rRNA region, and the transition models with invariable sites and a gamma-shaped distribution (TIM2ef + I + G, TIM3 + I + G) for the partial 18S rRNA gene and COI gene were run with four chains for 4 × 106 generations. A combined analysis of the three ribosomal genes was not undertaken because some sequences were not available for all species. The sampling for Markov chains was conducted at intervals of 100 generations. For each analysis, two runs were conducted. After discarding burn-in samples of 30% and evaluating convergence, the remaining samples were retained for more in-depth analyses. The topologies were used to generate a 50% majority-rule consensus tree. For each appropriate clade, posterior probabilities (PP) were given. FigTree software version v.1.4.3 [46] was used for visualizing trees from all analyses.
The alignment for COI sequences was used to determine haplotypes of the COI gene using DnaSP5 software [47], while the haplotype network map of all haplotypes of the COI gene for each species was constructed using the TCS network of PopART V. 1. 7. (Population Analysis with Reticulate Trees) software (http://popart.otago.ac.nz) [48].
Results
The 28 ring nematode populations clearly resembling Xenocriconemella macrodora were mainly associated with Quercus spp., but also with Castanea sativa and Fagus sylvatica from several natural environments in the Iberian Peninsula (Portugal and Spain) (Table 1). Nematode populations showed a mean density of 361 nematodes/500 cm3 of soil, but ranged from very low (three nematodes/500 cm3 of soil) to very high (2310 nematodes/500 cm3 of soil) soil nematode densities in a sample from cork oak in northern Portugal and a sample from cork oak in southern Spain (Table 1). All these populations were identified herein using integrative taxonomical approaches (morphometric and molecular) and a new species complex within the morphospecies X. macrodora was described herein separating three new species of Xenocriconemella. These 28 populations were separated into 13 populations of X. iberica sp. nov., 12 populations of X. paraiberica sp. nov., and 3 populations of X. pradense sp. nov. based on different approaches explained below.
Species delimitation using morphometry
In PCA results, the first three components (sum of squares (SS) loadings>1) accounted for 68% of the total variance in the morphometric characteristics when considering new and described taxa within the genus Xenocriconemella. Notably, our results showed significant results when the dimensional reductions were plotted (Fig. 2). First, we observed a wide intraspecific variation among the specimens in each Xenocriconemella spp. based on the wide morphometric variation in stylet and body length and width (i.e. L, a and Stylet), body annuli feature (i.e. R, Rv, Roes and Rex) and the distance between vulva and posterior end of body divided by body width at vulva position (VL/VB) (see contributions in Fig. 2). As expected, our findings supported the notable morphological diversity exhibited by X. macrodora (Table S1). PCA clearly separated almost all specimens of X. pradense sp. nov from those belonging to X. iberica sp. nov. and X. paraiberica sp. nov. However, it should be noted that this spatial separation was to a lesser extent between X. pradense sp. nov and X. iberica sp. nov., where several specimens were located close to each other (Fig. 2). This species separation was mostly observed along the dimension (Dim 1; 42.7% of the total variance). Considering that the eigenvalues for each character were used to identify the key morphological characters for this species delimitation (see the quality of representation of the variables in Fig. 2), the Dim 1 was mainly dominated by the body annuli feature (i.e. R, Rv, Roes and Rex) and subsequently by stylet length, V and VL/VB. We mainly detected that species separations were based in the number of annuli in body (R), in the in pharyngeal region (Roes), and between posterior end of body and vulva (Rv). More specifically, specimens with higher values in R, Roes and Rv were located on the right (i.e. X. pradense sp. nov.), and those with lower values for these traits on the left side of the dimension 1 (i.e. X. paraiberica sp. nov.). On the contrary, most of the specimens of X. iberica sp. nov. and X. paraiberica sp. nov. were found overlapping each other because they showed similar values for characters associated with Dim 1 (Fig. 2; see species description section). This therefore implied that both species are closely related morphologically. PCA showed a similar pattern in the spatial distribution of specimens (i.e., mean values of populations) of X. macrodora. In this case, the populations of the species already described were located throughout the spatial projection occupied by each of the new species given the wide morphometric variation that describes the populations of X. macrodora (Fig. 2, Table S1). This result supports the idea that this already described and the new species (X. pradense sp. nov., X. paraiberica sp. nov. and X. iberica sp. nov.) comprise a new complex of cryptic species (i.e. X. macrodora species complex) in which morphologically and morphometrically indistinguishable taxa appear within this genus of nematodes.
Principal component on Xenocriconemella macrodora species complex. Projections of species on the plane of dimensions 1 and 2, 1 and 3, 2 and 3. Correlation plot between dimensions and qualities of representation of the morphometric characters (“square cosine” (cos2)). Barplot showing the standardized contribution (%) of morphometric variables for the three dimensions retained by the PCA (only dimensions with sum of squares (SS) loadings > 1 were extracted). A reference soil (red) line is also shown on the barplot. This reference line corresponds to the expected value if the contribution where uniform. For a given dimension, any row/column with a contribution above the reference line can be considered important in contributing to the dimension
Species separation based on ribosomal and mitochondrial DNA
Species separation using molecular markers demonstrated that X. iberica sp. nov., X. paraiberica sp. nov., and X. pradense sp. nov., were clearly separated among them and from X. macrodora from the USA and Italy. The ratio between intra- and inter-species molecular variation for D2-D3 expansion segments of 28S rRNA and ITS region of all three Spanish species was very low (0.01–0.05), whereas COI was higher in X. macrodora (0.25), X. iberica sp. nov. (0.12), and X. iberica sp. nov. (0.11) (Table 2), confirming that COI is highly diversified in USA populations. However, for all three new species, the D2D3 and ITS genes clearly showed intra- and inter-species molecular variation (Table 2), suggesting that the probability of species separation with these loci was high [37]. Likewise, the P ID (Liberal) values for all four species and loci were ≥ 0.95, suggesting that species can be adequately separated [37, 38]. The P ID (Liberal) value [37] represents the probability that a correct species identification would be made using best sequence alignment (BLAST), closest genetic distance, or placement on a tree (falling within or being sister to a monophyletic species clade). Species with P ID (Liberal) ≥ 0.93 were considered to be adequately delimited [38]. Additionally, all clade supports for the three loci were well-supported (PP = 1.00), except for X. iberica sp. nov. in COI marker (PP = 0.89) and Rosenberg’s PAB values also supported the monophyly (P < 0.05) of each of the four species separately [39].
Ribosomal and mitochondrial diversity within the Xenocriconemella species complex
Amplification of the D2-D3 expansion segments of 28S rRNA, 18S rRNA, ITS rRNA, and partial COI regions from the three new Xenocriconemella species and Criconemoides rosmarini yielded single fragments of approximately 900, 1000, and 400 bp, respectively, based on gel electrophoresis. Forty-five, 51 and 16 sequences from the D2-D3 region of the 28S rRNA were generated from 13 populations of X. iberica sp. nov. (OR880107-OR880151), 12 populations of X. paraiberica sp. nov. (OR880152-OR880202) and from three populations of X. pradense sp. nov. (OR880203-OR880218), respectively, showing very low intraspecific variation for this region. Only three variable positions for X. iberica sp. nov., two variable positions for X. paraiberica sp. nov., and no variable positions were detected in X. pradense sp. nov.
D2-D3 expansion segments of 28S rRNA sequences from the three new Xenocriconemella species are related but clearly dissimilar, with the unique accession available in GenBank for this genus, X. macrodora (AY780960, Italy) showing similarity values of 95% (differing by 28 nucleotides and four indels) with X. pradense sp. nov., 94% with X. iberica sp. nov. (32 nucleotides and four indels) and 90% with X. paraiberica sp. nov. (53 nucleotides and four indels). The species closest to X. iberica sp. nov. (OR880107-OR880151) was X. pradense sp. nov. (OR880203-OR880218), being 94% similar for the D2-D3 region (differing by 43–46 nucleotides and no indels). In the case of X. paraiberica sp. nov. (OR880152-OR880202), the closest species was X. iberica sp. nov., being 92% similar among them (differing by 56–58 nucleotides and no indels). Finally, X. pradense sp. nov. (OR880203-OR880218) showed the highest similarity values when compared with X. macrodora from Italy (AY780960), 95% similarity (differing by 28 nucleotides and four indels).
Intraspecific variation in the ITS rRNA gene detected among the three studied populations of X. paraiberica sp. nov. (OR878338-OR878349) varied from none to three nucleotides (99% similarity and no indels). However, no intraspecific variation for this region was detected between the studied populations of X. iberica sp. nov (OR878332-OR878337) and X. pradense sp. nov. (OR878350-OR878355) ITS rRNA aligned sequences of Xenocriconemella species from the Iberian Peninsula were dissimilar in a wide range from 139 to 204 nucleotides (15–18%). This range increases when including the sequence of X. macrodora from the USA (JQ708139), up to 25% (101–115 nucleotides and 40–45 indels).
The 18S rRNA from the three new Xenocriconemella spp. (OR878356- OR878361) described here showed high similarity values (98.4–99% similarity, from 10 to 30 nucleotides and four indels) among them, and with all accessions from X. macrodora deposited in GenBank, including one accession most probably misidentified as X. macrodora from Portugal (MT229843, , differing by 8–11 bp). Unfortunately, no more molecular data were available in GenBank from this population and further studies will be needed for clarifying this identification. No intraspecific variability was detected for this marker in any populations included in the present study.
Ninety-seven new COI sequences were obtained in this study, 50 from X. iberica sp. nov. (OR885933-OR885982), 37 from X. paraiberica sp. nov. (OR885983-OR886019), and 10 from X. pradense sp. nov. (OR886020-OR886029). These partial COI sequences were clearly different from the COI sequences of X. macrodora from the USA deposited in GenBank [5], being from 88 to 92% similar (from 26 to 32 nucleotides in difference), including the accessions from specimens collected near the type locality MN711389, MF094906–MF094907 (Long Branch Stream Valley Park, Accotink Watershed, Fairfax County, Virginia). Intraspecific variation for the partial COI region within the Iberian Xenocriconemella species was higher than that for the D2-D3 region but, in any case, not more than 1%. fifty aligned sequences from 13 populations of X. iberica sp. nov. (OR885933-OR885982) showed 13 variable positions, resulting in 10 different haplotypes (Fig. 3). HAPi1 was the most common and prevalent, grouping 20 sequences from four populations located in four different provinces at northern, central and southern Spain, including Lleida (PIR17), Albacete (COT22), Ciudad Real (FCQ02) and Huelva (HUC01). The 11 sequences from Portugal generated 2 haplotypes, HAPi2 and HAPi3 with eight and three sequences, respectively, both of which were detected in the northern and central regions (provinces of Tras-os-Montes and Estremadura, respectively). HAPi4 corresponds to the unique sequences from X. iberica sp. nov. detected in Cáceres Province (GUR05). HAPi5 and HAPi6 grouped seven sequences from the two populations from Guadalajara Province (XN48B and XN56B). Finally, populations from Santander Province (HCANT and RCANT) were the most variable, with four haplotypes, HAPi7 and HAPi8 with six and two sequences from both populations, and HAPi9 and HAPi10 with two and one sequences from the Gismana (RCANT) population. Intraspecific variability observed in the 37 sequences from X. paraiberica sp. nov. (OR885983-OR886019) was similar to X. iberica sp. nov., 15 variable positions were detected in the partial COI sequences included in this study. These variations were grouped into 12 different haplotypes (Fig. 3). However, any haplotype was predominant in the sampled populations and each haplotype had its own specific province (Fig. 3). HAPpi1 corresponds to the sequences from the type locality, Casares, Málaga province, (CAS22), and HAPpi2 includes the two sequences belonging to the Córdoba population (COA01). HAPpi3 and HAPpi4 grouped three sequences from one population from Cádiz Province (CAC01). The five sequences from the two Granada populations (BUQ1 and CNR01) comprise the haplotype HAPpi5. Sequences from two populations from Huelva Province (HUE00 and HUA03) gave rise in two different haplotypes, HAPpi6 and HAPpi7, formed by 3 and 1 sequences, respectively. Populations from Jaén (CZQ05) and Guadalajara (XN43B and XN55A) provinces yield only one haplotype each, HAPpi8 and HAPpi12, respectively. Last, sequences from Caceres Province (GUR03 and GUR04) were grouped into three different haplotypes, HAPpi9, three sequences from sample GUR04, HAPpi10 two sequences from sample GUR04, and HAPpi11, four sequences from sample GUR03.
TCS network analysis of partial mitochondrial COI haplotypes of the Xenocriconemella macrodora species complex. a Xenocriconemella iberica sp. nov. COI haplotypes; (b) Xenocriconemella paraiberica sp. nov. COI haplotypes; (c) Xenocriconemella pradense sp. nov. COI haplotypes. Coloured circles embody haplotypes for each geographic sampling region, and their diameter is proportionate to the number of individuals sharing the same haplotype. Black short lines on the branches specify the numbers of mutated nucleotides in the alignment that separate each haplotype
Finally, the ten sequences from X. pradense sp. nov. (OR886020-OR886029) showed an intraspecific variability of only two nucleotides, which grouped into two haplotypes, one of them (HAPpr1) with the six sequences from the type population (GRQ01) and the other (HAPr2) with the four sequences from populations GRQ02 and GRQ05.
Molecular data from Criconemoides rosmarini were obtained for the first time in the present study. Specifically, two new sequences from the D2-D3 expansion segments of 28S rRNA (OR880219-OR880220) and one sequence from the partial COI region (OR886030) were identified. The closest species to C. rosmarini was Discocriconemella limitanea (MZ262311-MZ262314, MT159832), being 90% similar and varying from 67 to 69 nucleotides and one indel for the D2-D3 expansion segments of 28S rRNA and 85% similar, from 104 to 101 nucleotides and 8 indels, for the partial COI. D2-D3 expansion segments of 28S rRNA and COI sequences from C. rosmarini differed significantly from those of the Xenocriconemella species complex, showing similarity values of 83% for the D2-D3 expansion segments of 28S rRNA (117-119 nucleotides and no indels), and from 79 to 81% (57-60 nucleotides and five indels) for the partial COI.
Phylogeny
A total of 158 sequences from the D2-D3 domains of the 28S rRNA gene alignment (697 bp long) were included. Three outgroup species (Paratylenchus bukowinensis (MN088372), Paratylenchus enigmaticus (MZ265080), and Paratylenchus parastraeleni (MZ265065)) were included in the analysis. The Bayesian 50% majority rule consensus tree inferred from the D2-D3 alignment is given in Fig. 4. For this region, all species that belong to the X. macrodora species complex clustered together in a well-supported (PP = 1.00) clade, which was subdivided into two subclades, one of them (PP = 1.00) formed by X. paraiberica sp. nov. (OR880152-OR880202) and the other one (PP = 1.00) by X. iberica sp. nov (OR880107-OR880151), X. pradense sp. nov (OR880203-OR880218) and X. macrodora from Italy (AY780960). In this analysis, X. pradense sp. nov (OR880203-OR880218) and X. macrodora (AY780960) clustered together, although clearly separated, in a well-supported subclade (PP = 1.00). Criconemoides rosmarini (OR880219–OR880220) appears to occupy a basal position in a well-supported clade (PP = 1.00) with Discocriconemella limitanea (MZ262311) and these two species are included in a not well-supported subclade with Criconemoides obtusicaudatus (JQ231186).
Phylogenetic relationships within the genus Xenocriconemella. Bayesian 50% majority rule consensus tree as inferred from D2-D3 expansion domains of the 28S rRNA sequence alignment under the general time-reversible model with invariable sites and a gamma-shaped distribution (GTR + I + G). Posterior probabilities of more than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. The scale bar indicates expected changes per site, and the coloured boxes indicate the clade association of the Xenocriconemella macrodora species complex
The phylogenetic position of X. iberica sp. nov., X. paraiberica sp. nov. and X. pradense sp. nov. in the ITS region tree is given in Fig. 5. The phylogenetic tree based on ITS Criconematidae spp. sequences resolved a well-supported major clade (PP = 1.00), including a subclade not well-supported with Hemicriconemoides spp., some Criconema spp., and Ogma decalineatus (MF683235), and a well-supported subclade (PP = 0.99) including Xenocriconemella spp. together with Discocriconemella hengsungica (MK253544), Criconema mutabile (JQ708132) and Criconema sp. Livingston4 (FN435300). Xenocriconemella iberica sp. nov. (OR878332-OR878337), X. paraiberica sp. nov. (OR878338-OR878349) and X. pradense sp. nov. (OR878350-OR878355) clustered together in a well-supported clade (PP = 1.00) and these species clustered with Discocriconemella hengsungica (MK253544) in a well-supported clade (PP=1.00), but were clearly separated from the unique ITS of X. macrodora from the USA (JQ708139).
Phylogenetic relationships within the genus Xenocriconemella. Bayesian 50% majority rule consensus tree as inferred from ITS rRNA sequence alignment under the transversion model with invariable sites and a gamma-shaped distribution (TVM + I + G). Posterior probabilities of more than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. The scale bar indicates expected changes per site, and the coloured boxes indicate the clade association of the Xenocriconemella macrodora species complex
The 18S rRNA gene alignment (1660 bp long) included six new sequences: two sequences from X. iberica sp. nov. (OR878356-OR878357), two sequences from X. paraiberica sp. nov. (OR878358-OR878359), and two sequences from X. pradense sp. nov. (OR878360-OR878361) see Fig. 6. Accessions from the three new species and X. macrodora from the USA and Portugal clustered together in a moderately-supported clade (PP= 0.98). However, the different branches in which these subclades are not well-supported.
Phylogenetic relationships within the genus Xenocriconemella. Bayesian 50% majority rule consensus tree as inferred from 18S rRNA sequence alignment under the transition model with invariable sites and a gamma-shaped distribution (TIM2ef + I + G). Posterior probabilities of more than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. The scale bar indicates expected changes per site, and the coloured boxes indicate the clade association of the Xenocriconemella macrodora species complex
The COI gene alignment (323 bp long) included 106 new sequences: 50 sequences from X. iberica sp. nov. (OR885933-OR885982), 37 sequences from X. paraiberica sp. nov. (OR885983-OR886019), 10 sequences from X. pradense sp. nov. (OR886020-OR886029) and one sequence from C. rosmarini (OR886030). Finally, Paratylenchus baldaccii (MZ262220), Paratylenchus hamatus (MW797016) and Paratylenchus indalus (MW797005) were used as outgroups. The Bayesian 50% majority rule consensus tree inferred from the COI sequence alignment is given in Fig. 7. For COI, Xenocriconemella spp. clustered together in a well-supported clade (PP= 1.00), with the difference that for this marker, X. iberica sp. nov. is the only species that appears alone in a weakly supported subclade (PP= 0.89) while X. pradense and X. macrodora from the USA clustered together in a well-supported subclade (PP = 0.99), but the phylogenetic relationship of these species with X. pradense sp. nov. is not well-defined and remains unresolved. However, each species is well-separated in its own clade (PP = 1.00). Once again, C. rosmarini (OR886030) appears in a well-supported clade (PP = 0.99) with Discocriconemella limitanea (MZ820007-MZ820008).
Phylogenetic relationships within the genus Xenocriconemella. Bayesian 50% majority rule consensus tree as inferred from cytochrome c oxidase subunit 1 (COI) sequence alignment under the transition model with invariable sites and a gamma-shaped distribution (TIM3 + I + G). Posterior probabilities of more than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. The scale bar indicates expected changes per site, and the coloured boxes indicate the clade association of the Xenocriconemella macrodora species complex
Taxonomic account
Xenocriconemella iberica sp. nov. (Figs. 8, 9, 10 and 11; Tables 3, 4)
Zoobank
urn:lsid:zoobank.org:act:18F75622-A236-4448-AC13-EA2E3777072A Figs. 8, 9, 10 and 11; Tables 3, 4.
Light micrographs of Xenocriconemella iberica sp. nov. male. a, whole body, showing spicules (arrow); (b, c), anterior region showing absence of stylet and undifferentiated pharynx; (d), detail of excretory pore (arrow); (e-g), male tail showing spicules, gubernaculum and bursa (arrow). Abbreviations: b = bursa; ep = excretory pore; g = gubernaculum; sp = spicules. Scale bars: (a) = 50 µm; (b) = 20 µm; (c–g) = 10 µm
SEM micrographs of Xenocriconemella iberica sp. nov. female. a anterior region; (b, c) lip region showing 1st and 2nd body annuli; (d) en face view showing oral aperture (arrow); (e) posterior region in frontal view showing vulva and anus (arrow). Abbreviations: a = anus; oa = oral aperture; V = vulva; 1st, 2nd = first- and second-body annuli. Scale bars: (a, b) = 5 µm; (c) = 2 µm; (d) = 1 µm; (e) = 5 µm
Holotype
Adult female collected from a soil sample from the rhizosphere of Pyrenean oak (Quercus pyrenaica Willd.) at Cotillas, Albacete province, southern Spain (38°24′24.15″N, 2°28′36.72″W, 1533 m above sea level) by P. Castillo, mounted in pure glycerine, and deposited in the Nematode Collection of the Institute for Sustainable Agriculture, CSIC, Córdoba, Spain (slide number Xen_cot_01).
Paratypes
Eighteen female paratypes were collected at the same time as the holotype from the type locality by P. Castillo, mounted in pure glycerine and deposited in the Nematode Collection of the Institute for Sustainable Agriculture, CSIC, Córdoba, Spain (slides numbers Xen_cot_02-Xen_cot_9), and two females were deposited at the USDA Nematode Collection (slide T-8025p).
Etymology
The specific epithet is named for the wide distribution of the species in the Iberian peninsula.
Diagnosis and relationships
Xenocriconemella iberica sp. nov. is characterized by the following measurements and ratios (considering all the studied populations, Tables 3, 4): a short-sized female body 246-350 µm, stylet = 80.0-103.0 µm long, V = 87.5–91.9, a = 6.4–11.9, b = 2.0–2.7, c = 12.1–27.3, c’ = 0.6–1.1, R = 97-119, RV = 11–16, Ran = 7–12, VL/VB = 0.7–1.4. Morphologically and morphometrically, X. iberica sp. nov. resembles members of the X. macrodora species complex (including X. macrodora, X. paraiberica sp. nov. and X. pradense sp. nov.) from which it is very difficult to separate; in particular, it is almost undistinguishable phenotypically from X. macrodora and X. paraiberica sp. nov. (Tables 3, 4, 5, 6 and 7, Table S1). From X. pradense sp. nov. slightly differs in some main diagnostic characters, including a slightly shorter body length 294 (246–350) µm vs 333 (249–383) µm, a slightly shorter stylet length 93.1 (80.0–103.0) µm vs 101.1 (92.5–110.0) µm, a slightly lower number of body annuli (R) 104 (97–119) vs 122 (112–128), a slightly lower VL/VB ratio 1.2 (0.7–1.4) vs 1.4 (1.1–1.5), a slightly shorter tail length 16.4 (11.0–24.5) µm vs 20.2 (15.5–25.0) µm, a slightly higher c ratio 18.3 (12.1–27.3) vs 16.6 (13.7–21.3), and a slightly lower c’ ratio 0.8 (0.6–1.1) vs 0.9 (0.8–1.2). In any case, these minor differences are within the range of the X. macrodora species complex, and all four species need to be considered as a complex of cryptic species (see above morphometric study).
Description
Female. Nematodes ventrally arcuate, slightly tapering anteriorly and posteriorly. Body annuli smooth and retrorse 2.7 (2.5–3.0) µm wide, without anastomosis. Lip region with two annuli, not offset, not separated from body annuli, first lip annulus partially covering the second lip annulus (Fig. 9b), second lip annulus retrorse and slightly wider than first annulus (8.1 ± 0.7 (7.0–9.0) vs (6.8 ± 0.5 (6.0–8.0)) µm wide. SEM images (Fig. 11) showed a labial plate low, with oral aperture oval, pseudolips not visible, and submedian lobes absent. Stylet thin, long and flexible, occupying 32.5 (28.1–35.6) % of the body length, with short basal portion (6.1 (5.0–7.5)) µm long, and knobs slightly rounded (4.5 (3.5–5.0)) µm wide. Pharynx typical criconematoid, with a cylindroid procorpus widening to a large muscular oval median bulb containing well developed valves (7.0–8.5 µm long), isthmus slender and amalgamated with basal bulb. Excretory pore from one annulus posterior to three annuli anterior of level of stylet knobs, at 92 (82–106) µm from anterior end. Nerve ring located at level of isthmus, 100 (91–113) µm from anterior end. SEM showed a vulva closed as a simple slit, directed out of the contour of the body (Fig. 11e), with the anterior vulval lip nonoverlapping. Vagina slightly ventrally curved (11–14 µm long). Female genital tract monodelphic, prodelphic, outstretched and occupying 46.1 (38.8–58.6) % of the body length, spermatheca rounded, some females (ca. 30%) containing round sperm (1.0-1.5 µm wide). Anus located at 8.6 (7–9) annuli from the terminus. Tail conoid and bluntly rounded terminus, annuli decreasing in diameter and thickness, the last 2–3 annuli merging and difficult to count.
Male. Nematodes extremely rare, with only two specimens detected in a sample from Aracena, Huelva Province, southern Spain, out of 4527 female and juvenile specimens counted within the 13 populations studied (Table 1). Both male specimens were sequenced for ribosomal and mitochondrial genes, confirming their species identity. Body slightly curved ventrally, narrowing to the tail region (Fig. 10). The lip region was conoid-rounded, the stylet was absent, the pharynx was undistinguishable and not functional, lateral fields with three incisures observed. The testis was straight and it was 38.8, 68.1% of the total body length. Tail conoid with a widely rounded terminus. Bursa small (28–29 µm) extending from the posterior third of spicules to the terminus. Spicules slender and ventrally curved, gubernaculum rod-shaped and slightly curved ventrally (Fig. 10).
Juveniles. Body similar to females, including tail shape, but shorter. Edge of body annuli without appendages, marked with delicate irregular punctations.
Additional material studied. Additional populations of this species were collected from several localities in Portugal and Spain from the rhizosphere of Castanea sativa L., Fagus sylvatica L., Quercus canariensis Willd., Quercus faginea Lam., Quercus ilex L., Quercus pubescens Willd., Quercus pyrenaica Willd., Quercus suber L. (Table 1).
Xenocriconemella paraiberica sp. nov. (Figs. 12, 13 and 14; Tables 5, 6)
Zoobank
urn:lsid:zoobank.org:act:F05DD1CA-662B-46E6-BEB9-377D70788A6C Figs. 12, 13 and 14; Tables 5, 6.
Light micrographs of Xenocriconemella paraiberica sp. nov. females. a, whole body, flexible stylet arrowed; (b), pharyngeal region showing flexible stylet and excretory pore (arrowed); (c) lip region showing details of 1st and 2nd body annuli (arrowed); (d) posterior region showing spermatheca (arrowed); (e-k) posterior region showing an egg, vulva and anus (arrowed); (l) ventral view of female posterior region showing vulva and anus (arrowed). Abbreviations: a = anus; e = egg; ep = excretory pore; spm = spermatheca, st = stylet; V = vulva; 1st, 2nd = first- and second-body annuli. Scale bars: (a) = 50 µm; (b–k) = 20 µm; (c, l) = 10 µm
SEM micrographs of Xenocriconemella paraiberica sp. nov. female. (a) anterior region; (b, c) lip region with detail of 1st and 2nd body annuli and stylet (arrowed); (d) en face view showing oral aperture (arrowed); (e, f) posterior region in frontal view showing vulva and anus (arrowed). Abbreviations: a = anus; oa = oral aperture; st = stylet; V = vulva; 1st, 2nd = first- and second-body annuli. Scale bars: (a) = 10 µm; (b) = 2 µm; (c, f) = 3 µm; (d) = 1 µm; (e) = 5 µm
Holotype
Adult female collected from a soil sample from the rhizosphere of cork oak (Quercus suber L.) at Casares, Málaga Province, southern Spain (36°26′46.21″N, 5°14′57.00″W, 348 m above sea level) by G. Leon Ropero and J. Martin Barbarroja (IAS-CSIC), mounted in pure glycerine and deposited in the Nematode Collection of the Institute for Sustainable Agriculture, CSIC, Córdoba, Spain (slide number Xen_cas_01).
Paratypes
Eighteen female paratypes were collected at the same time as the holotype from the type locality by G. Leon Ropero and J. Martin Barbarroja (IAS-CSIC), mounted in pure glycerine and deposited in the Nematode Collection of the Institute for Sustainable Agriculture, CSIC, Córdoba, Spain (slides numbers Xen_cas_02-Xen_cas_11), and two females were deposited at the USDA Nematode Collection (slide T-8026p).
Etymology
The specific epithet refers to Gr. prep. para, alongside of, resembling; N.L. fem. n. iberica, because of its close resemblance to Xenocriconemella iberica sp. nov.
Diagnosis and relationships
Xenocriconemella paraiberica sp. nov. is characterized by the following measurements and ratios (considering all the studied populations, Tables 5 and 6): a short-sized female body 221–386 µm, stylet = 80.0–100.0 µm long, V = 84.6–91.7, a = 7.4–12.8, b = 2.1–3.1, c = 13.0–28.6, c’ = 0.6–1.0, R = 95–116, RV = 11–14, Ran = 7–10, VL/VB = 0.7–1.5. Morphologically and morphometrically, X. paraiberica sp. nov. resembles members of the X. macrodora species complex (including X. macrodora, X. iberica sp. nov. and X. pradense sp. nov.) from which it is very difficult to separate it; in particular, it is almost undistinguishable phenotypically from X. macrodora and X. iberica sp. nov. (Tables 3, 4, 5, 6 and 7, Table S1). From X. pradense sp. nov. slightly differs in some main diagnostic characters, including a slightly shorter body length 298 (221–386) µm vs 333 (249–383) µm, a slightly shorter stylet length 89.6 (80.0–100.0) µm vs 101.1 (92.0–110.0) µm, a slightly lower number of body annuli (R) 104 (95–116) vs 122 (112–128), a slightly lower VL/VB ratio 1.1 (0.7–1.5) vs 1.4 (1.1–1.5), a slightly shorter tail length 15.1 (10.0–21.0) µm vs 20.2 (15.5–25.0) µm, a slightly higher c ratio 20.2 (13.0–28.6) vs 16.6 (13.7–21.3), and a slightly lower c’ ratio 0.8 (0.6–1.0) vs 0.9 (0.8–1.2). In any case, these minor differences are within the range of the X. macrodora species complex, and all four species need to be considered as a complex of cryptic species (see above morphometric study).
Description
Female. Nematodes ventrally arcuate, slightly tapering anteriorly and posteriorly. Body annuli smooth and retrorse 2.9 (2.5–3.5) µm wide, without anastomosis. Lip region similar to X. iberica sp. nov., second lip annulus retrorse and slightly wider than the first annulus (9.1 ± 0.6 (8.0–10.0) vs (7.8 ± 0.4 (7.0–8.5)) µm wide. SEM images showed a labial plate low, without pseudolips or submedian lobes (Fig. 14). Stylet thin, long and flexible, occupying 30.1 (27.4–33.1) % of the body length, with short basal portion (6.3 (5.5–10.0)) µm long, and knobs slightly rounded (4.8 (4.0–5.0)) µm wide. Pharynx with a cylindroid procorpus widening to a large muscular oval median bulb containing well-developed valves (8.0–9.0 µm long), istmus slender and amalgamated with basal bulb. Excretory pore from one annulus posterior to the level of stylet knobs, 90 (76–99) µm from the anterior end. Nerve ring located at the level of isthmus, 98 (85–110) µm from the anterior end. Vulva closed as a simple slit, directed out of the contour of the body (Fig. 14e,f), and the anterior vulval lip non-overlapping. Vagina slightly ventrally curved (10–13 µm long). Female genital tract monodelphic, prodelphic, outstretched and occupying 48.8 (32.5–63.7) % of the body length, spermatheca rounded, some females (ca. 30%) containing round sperm (1.0–1.5 µm wide). Anus located at 7.6 (7–9) annuli from the terminus. Tail conoid and bluntly rounded terminus, annuli decreasing in diameter and thickness, in some specimens the last 2–3 annuli merging and difficult to count.
Male. Not detected in 4046 female and juvenile specimens counted within the 12 populations studied (Table 1).
Juveniles. Body similar to females, including tail shape, but shorter. Edge of body annuli without appendages, marked with delicate irregular punctations.
Additional material examined. Additional populations of this species were collected from several localities in Spain from the rhizosphere of Quercus canariensis Willd., Quercus faginea Lam., Quercus ilex L., Quercus pyrenaica Willd., Quercus suber L. (Table 1).
Xenocriconemella pradense sp. nov. (Figs. 15, 16, 17 and 18; Table 7)
Zoobank
urn:lsid:zoobank.org:act:82EF28F3-3C22-4E8A-9A68-8A63A483F141 Figs. 15, 16, 17 and 18; Table 7.
Light micrographs of Xenocriconemella pradense sp. nov. females. (a–g) whole body; (h-n) anterior region showing flexible stylet (arrowed); (o-x) posterior region showing anus, vulva, and some anastomosis (arrowed). Abbreviations: a = anus; an = anastomosis; st = stylet; V = vulva. Scale bars: (a–g) = 50 µm; (h–x) = 20 µm
SEM micrographs of Xenocriconemella pradense sp. nov. female. a whole body; (b) detail of 1st and 2nd body annuli; (c) en face view showing oral aperture (arrowed); (d) posterior region showing vulva and anus (arrowed). Abbreviations: a = anus; oa = oral aperture; V = vulva; 1st, 2nd = first- and second-body annuli. Scale bars: (a) = 25 µm; (b, c) = 2 µm; (d) = 5 µm
SEM micrographs of Xenocriconemella pradense sp. nov. juvenile. a anterior region showing ornamented annuli; (b) detail of ornamented annuli ant mid-body; (c) detail of 1st and 2nd body annuli; (d) posterior region showing ornamented annuli. Abbreviations: 1st, 2nd = first- and second-body annuli. Scale bars: (a) = 10 µm; (b, d) = 2 µm; (c) = 1 µm
Holotype
Adult female collected from a soil sample from the rhizosphere of Portuguese oak (Quercus faginea L.) at Prado del Rey, Cadiz Province, southern Spain (36°45′08.48″N, 5°24′11.18″W, 950 m above sea level) by A. Archidona-Yuste, mounted in pure glycerine and deposited in the Nematode Collection of the Institute for Sustainable Agriculture, CSIC, Córdoba, Spain (slide number Xen_cho_01).
Paratypes
Eighteen female paratypes were collected at the same time as the holotype from the type locality by A. Archidona-Yuste, mounted in pure glycerine and deposited in the Nematode Collection of the Institute for Sustainable Agriculture, CSIC, Córdoba, Spain (slides numbers Xen_cho_02-Xen_cho_12), and two females were deposited at the USDA Nematode Collection (slide T-8027p).
Etymology
The specific epithet, pradense, refers to the demonym of inhabitants of the type locality, Prado del Rey.
Diagnosis and relationships
Xenocriconemella pradense sp. nov. is characterized by the following measurements and ratios (considering all the studied populations, Table 7): a short-sized female body 249-383 µm, stylet = 92.5–110.0 µm long, V = 85.7–90.2, a = 7.5–12.8, b = 1.8–2.7, c = 13.7–21.3, c’ = 0.8–1.1, R = 112–128, RV = 14–18, Ran = 10–13, VL/VB = 1.1–1.5. Morphologically and morphometrically, X. pradense sp. nov. resembles members of the X. macrodora species complex (including X. macrodora, X. iberica sp. nov. and X. paraiberica sp. nov.) from which it is very difficult to separate (Tables 3, 4, 5, 6 and 7, Table S1). From X. iberica sp. nov. slightly differs in some main diagnostic characters, including a slightly larger body length 333 (249-383) µm vs 294 (246-350) µm, a slightly larger stylet length 101.1 (92.5–110.0) µm vs 93.1 (80.0–103.0) µm, a slightly higher number of body annuli (R) 122 (112–128) vs 104 (97–119), a slightly higher VL/VB ratio 1.4 (1.1–1.5) vs 1.2 (0.7–1.4), a slightly larger tail length 20.2 (15.5–25.0) µm vs 16.4 (11.0–24.5) µm, a slightly lower c ratio 16.6 (13.7–21.3) vs 18.3 (12.1–27.3), and a slightly higher c’ ratio0.9 (0.8–1.1) vs 0.8 (0.6–1.1). In any case, these minor differences are within the range of the X. macrodora species complex, and all four species need to be considered as a complex of cryptic species (see above morphometric study).
Description
Female. Nematodes slightly ventrally arcuate, slightly tapering posteriorly. Body annuli smooth and retrorse 2.6 (2.5–3.0) µm wide, without anastomosis. Lip region with two annuli, not offset, not separated from body annuli, first lip annulus partially covering the second lip annulus (Fig. 16), second lip annulus retrorse and slightly wider than first lip annulus (7.9 ± 0.5 (7.0–9.0) vs 8.9 ± 0.5 (8.0–10.0)) µm wide. SEM images showed a labial plate low, pseudolips not visible, and submedian lobes absent (Fig. 17c). Stylet thin, long and flexible, occupying 30.6 (26.3–39.0) % of the body length, with short basal portion (8.2 (6.0–11.0)) µm long, and knobs slightly rounded (4.7 (4.0–5.0)) µm wide. Pharynx typical criconematoid, with a cylindroid procorpus widening to a large muscular oval median bulb containing well developed valves (7.5–8.5 µm long), isthmus slender and amalgamated with basal bulb. Excretory pore from one annulus posterior to three annuli anterior of level of stylet knobs, at 101 (80–115) µm from anterior end. Nerve ring located at the level of isthmus, 118 (108–138) µm from the anterior end. Vulva closed as a simple slit, directed out of the contour of the body (Fig. 17d), and the anterior vulval lip non-overlapping. Vagina slightly ventrally curved (12–14 µm long). Female genital tract monodelphic, prodelphic, outstretched and occupying 48.2 (39.4–58.6) % of the body length, spermatheca round-oval (8–9 x 10-11 µm), some females (ca. 10%) with round sperm (1.0 µm wide). Anus located at 11.6 (11–13) annuli from the terminus. Tail conoid and bluntly rounded terminus, annuli decreasing in diameter and thickness, the last 2-3 annuli usually merging with terminus into a small projection oriented dorsally (Fig. 16o-x).
Male. Not detected in 975 female and juvenile specimens counted within the three populations studied (Table 1).
Juveniles. Body similar to females, including tail shape, but shorter. Edge of body annuli without appendages, marked with delicate irregular punctations (Fig. 18).
Additional material examined. Two additional populations of this species were collected from other places in the type locality in the rhizosphere Portuguese oak (Table 1).
SEM remarks on Criconemoides rosmarini and the Xenocriconemella species complex
SEM studies on female and juvenile topotypes of Criconemoides rosmarini (Fig. S1) presented body annuli with margins showing a fringe of small blunt spine-like processes formed by deep incision or crenation, and numerous anastomoses. These crenate processes were also detected in juveniles, which lack spines or scales. First lip annulus forwardly directed, oral plate without submedian lobes, and vulva open type with rounded lips (Fig. S1).
Additionally, in the three Xenocriconemella species studied under light microscopy and that on X. pradense sp. nov. also with SEM (Fig. 18), the margin of body annuli appeared marked with delicate irregular punctations, except for annuli near the lip region (Fig. 18c), which showed a similar pattern as adult females.
Discussion
Asystematic review of X. macrodora indicated that this species is distributed worldwide and occurs in association with woodland forests [4, 5]. It has been reported widely in USA, and to a lesser extent in Canada and Mexico [5, 10, 49], several European countries (viz. Belgium, Bulgaria, Czech Republic, France, Germany, Italy, Netherlands, Norway, Poland, Portugal, Romania, Russia, Slovak Republic, Spain, Ukraine, and United Kingdom) [4, 6, 50,51,52,53], South Africa and Malawi [54, 55], several Asian countries including India, Iran, Korea, and Vietnam [14, 56,57,58], and Australia [59] (Fig. 1). Based on morphological, morphometric and molecular evidence, we found a new cryptic species complex from the nominal species X. macrodora in the Iberian peninsula, USA, and probably Italy (this one only based on a ribosomal molecular marker and this can be another different species, but additional studies are needed for confirming this hypothesis). Xenocriconemella macrodora species complex is defined here with the additional description of three new species (X. iberica sp. nov., X. paraiberica sp. nov., and X. pradense sp. nov.) applying a broad taxonomic framework on 28 nematode populations (Fig. 1). Our study claimed that the X. macrodora species complex is an example of cryptic species, since most of its members can only be recognized using molecular data [60]. More specifically, species delimitation by morphometry showed an overlap between some populations of the new species of X. macrodora described here. species complex(viz. X. iberica sp. nov., X. paraiberica sp. nov., and X. pradense sp. nov.) (Fig. 2). However, we certainly support the validity of multivariate analyses in providing a useful tool for species delimitation within cryptic species complex in soil nematodes [15, 18, 61, 62]. Focusing on the three new species, PCA allowed us to discriminate species seemingly undistinguishable morphologically by their morphometric features (i.e. X. pradense sp. nov. from the other new species by the body annuli features (R, Rv, Roes and Rex; Fig. 2). In addition, PCA also showed that the populations of these new species are morphometrically described by a rather extensive intraspecific variation (Fig. 2). This study confirms that males are extremely rare within these nematodes (only two specimens were detected in one population of X. iberica sp. nov.). Nevertheless, the presence of sperm in the spermatheca of some specimens confirms that parthenogenesis and amphimictic reproduction in these species is highly probable. Apart from their shortage, the difficulty in finding males can also be related to the lack of feeding (stylet absent) and their very short life span. Sturhan [9] found also the presence of filled spermatheca and the males in some X. macrodora populations. In our case, these males of X. iberica sp. nov are confirmed molecularly as conspecific. This data confirms that males could be produced in some populations, maybe induced in low numbers by environmental cues.
Ribosomal- and mitochondrial-based phylogenies clearly separate the X. macrodora species complex into four separate species, which was confirmed by morphometric and molecular species delimitation analyses. All the molecular markers used in the present study match our identified species, clearly separating them from the only species of this genus described to date, X. macrodora, giving evidence that they could help in the identification process for the majority of the populations belonging to this genus. As already documented for other ring nematodes [15, 18], the sequence divergence of COI within the X. macrodora species complex was higher than that for the D2-D3 and ITS loci, most likely because mtDNA accumulated nucleotide substitutions at a much higher rate of substitutions than D2-D3 and ITS [18]. These COI haplotypes seem to be related to geographical origin, especially in the case of X. paraiberica sp. nov., where each geographical population gave rise to a different haplotype, even more than one, as in the case of the Cantabria population (northern Spain). Nevertheless, the variability detected for these species was considerably lower than that detected in X. macrodora from the USA, where the variability found was up to 5%. Unfortunately, no information is available about other ribosomal markers for these American populations of X. macrodora [5, 10]. Molecular analyses of this study clearly supported the separation of the genera Criconemoides and Xenocriconemella, since well-separated lineages in the phylogenetic tree of ribosomal (28S rRNA) and mitochondrial (COI) loci were demonstrated (Figs. 4, 5, 6 and 7). In 28S rRNA, ITS region (except for JQ708139-X. macrodora from the USA, which need additional molecular confirmation with additional markers) and COI trees, the Xenocriconemella species complex clustered together in a single cluster (suggesting monophyly) and was clearly separated from Criconemoides spp., including C. rosmarini, which clustered in no resolved lineages with Discocriconemella limitanea, Criconemoides annulatus and Lobocriconema iranense. Our results on juvenile annuli ornamentation and molecular (ribosomal and mitochondrial loci) analysis showed that Xenocriconemella is a valid and separate genus from other genera within Criconematidae, and these results supported the hypothesis of several authors considering Xenocriconemella as a valid genus [2, 63]. In addition, since ornamented annuli are also a shared trait by a few species within the genus Criconemoides, including C. ihlathum, C. lizarbus, C. ornativulvatus, C. silvicola, and C. tiaraensis [2], further studies are needed to confirm the taxonomical status of these groups and their phylogenetic relationships.
This study gave molecular markers for the first time for Criconemoides rosmarini, two D2-D3 expansion segments of 28S rRNA and one partial COI sequence, which showed rather low similarity values with the accessions available in GenBank, with Discocriconemella limitanea being the most similar, with a value of 90%. Phylogenetic analyses based on the D2-D3, ITS, 18S and partial COI genes using BI resulted in a consistent position for the newly described species of the Xenocriconemella species complex from Spain, and X. macrodora from several geographical origins. The position of C. rosmarini within the D2-D3 and partial COI trees showed that the phylogenetic relationship with the species belonging to the Xenocriconemella species complex is quite distant. These results showed the monophyly of the genus Xenocriconemella by ribosomal and mitochondrial loci but also confirmed that the genus Criconemoides is polyphyletic, as already reported by other researchers [14].
Conclusion
This study confirms that the globally distributed nominal Xenocriconemella macrodora species is a species complex composed of species that are morphometrically and morphologically similar, but clearly different at the molecular level. In this study, three new species (X. iberica sp. nov., X. paraiberica sp. nov., and X. pradense sp. nov.) are described by the application of integrative taxonomy. However, the molecular diversity of this species in USA and Italy confirmed that additional species are likely present in this species complex, and the diversity of this group may be higher than expected. The study of X. macrodora topotypes can clarify the position of this species using molecular markers under an integrative approach.
Availability of data and materials
All data generated or analysed during this study are included in this published article. Sequences are deposited in GenBank, NCBI. This article has been registered at Zoobank (urn:lsid:zoobank.org:pub:B4A7D5EC-511D-4F75-A257-29745B56F363).
References
De Grisse A, Loof PAA. Revision of the genus Criconemoides (Nematoda). Meded Landb Opzoekstns Staat Gent. 1965;30:577–603.
Geraert E. The Criconematidae of the world. Identification of the Family Criconematidae (Nematoda). Ghent: Academia Press; 2010.
Taylor AL. The genera and species of the Criconematinae, a subfamily of the Anguillulinidae (Nematoda). Trans Amer Micr Soc. 1936;55:391–421.
Bello A, Topham PB, Alphey TJW, Ibañez JJ. Geographical distribution of Xenocriconemella macrodora. Nematol Medit. 1986;14:223–9.
Powers TO, Harris TS, Higgins RS, Mullin PG, Powers KS. Nematode biodiversity assessments need vouchered databases: A BOLD reference library for plant-parasitic nematodes in the superfamily Criconematoidea. Genome. 2021;64:232–41.
Escuer M, Lara MP, Bello A. Distribution of the Criconematidae in Peninsular Spain and Balearic Islands. Int J Nematol. 1999;9:47–67.
Lübbers A, Zell H. Criconemella macrodora (Taylor, 1936) (Nematoda: Criconematidae) - eine Artengruppe. Zool Anz. 1989;222:99–109.
Ganguly S, Singh M, Lal M, Rathour KS. Two new species of Xenocriconemella De Grisse and Loof, 1965 (Tylenchida: Criconematoidea). Ind J Nematol. 2008;38:94–7.
Sturhan D. Notes on Xenocriconemella macrodora (Taylor, 1936) and its synonyms (Tylenchida: Criconematidae). Nematology. 2013;15:505–6.
Cordero MA, Robbins RT, Szalanski AL. Taxonomic and molecular identification of Bakernema, Criconema, Hemicriconemoides, Ogma and Xenocriconemella species (Nematoda: Criconematidae). J Nematol. 2012;44:427–46.
Subbotin SA, Vovlas N, Crozzoli R, Sturhan D, Lamberti F, Moens M, Baldwin J. Phylogeny of Criconematina Siddiqi, 1980 (Nematoda: Tylenchida) based on morphology and D2–D3 expansion segments of the 28S-rRNA gene sequences with application of a secondary structure model. Nematology. 2005;7:927–44.
Powers TO, Harris TS, Higgins RS, Mullin PG, Powers KS. An 18S rDNA perspective on the classification of Criconematoidea. J Nematol. 2017;49:236–44.
Etongwe CM, Singh PR, Bert W, Subbotin SA. Molecular characterisation of some plant-parasitic nematodes (Nematoda: Tylenchida) from Belgium. Russ J Nematol. 2020;28:1–28.
Nguyen HT, Nguyen TD, Le TML, Trinh QP, Bert W. Remarks on phylogeny and molecular variations of criconematid species (Nematoda: Criconematidae) with case studies from Vietnam. Sci Re. 2022;12:14832. https://doi.org/10.1038/s41598-022-18004-2.
Clavero-Camacho, I., Palomares-Rius, J.E., Cantalapiedra-Navarrete, C., Castillo, P., Liébanas, G., Archidona-Yuste, A. A proposed new species complex within the cosmopolitan ring nematode Criconema annuliferum (de Man, 1921) Micoletzky, 1925. Plants 2022;11,1977. https://doi.org/10.3390/plants11151977.
Olson M, Harris T, Higgins R, Mullin P, Powers K, Olson S, Powers TO. Species delimitation and description of Mesocriconema nebraskense n. sp. (Nematoda: Criconematidae), a morphologically cryptic, parthenogenetic species from North American grasslands. J Nematol. 2017;49:42–66.
Maria M, Miao W, Cai R, Tian Z, Castillo P, Zheng J. Species diversity of ring nematodes of the genus Criconemoides (Nematoda: Criconematidae) based on three new species from China, using integrative taxonomy. Eur J Plant Pathol. 2020;157:119–39.
Archidona-Yuste A, Palomares-Rius JE, Clavero-Camacho I, Cantalapiedra-Navarrete C, Liébanas G, Castillo P. A blind-identification test on Criconema annuliferum (de Man, 1921) Micoletzky, 1925 species complex corroborate the hyper-cryptic species diversity using integrative taxonomy. Plants. 2023;12:1044. https://doi.org/10.3390/plants12051044.
Gómez-Barcina A, Castillo P, González-País MA. Nematodos fitoparásitos de la subfamilia Criconematinae Taylor, 1936 en la Sierra de Cazorla. Rev Iber Parasitol. 1989;49:241–55.
Castillo P, Siddiqi MR, Gómez-Barcina A. Criconemella rosmarini sp. n. (Criconematidae, Tylenchida) from Spain. Nematol Medit. 1988;16:19–23.
Coolen, W.A. Methods for extraction of Meloidogyne spp. and other nematodes from roots and soil. In Root-Knot Nematodes (Meloidogyne Species). Systematics, Biology and Control; Lamberti, F., Taylor, C.E., Eds.; Academic Press: NY, USA, 1979; pp. 317–329.
Seinhorst JW. Killing nematodes for taxonomic study with hot F.A. 4:1. Nematologica. 1966;12:178.
De Grisse AT. Redescription ou modifications de quelques techniques utilisées dans l’étude de nématodes phytoparasitaires. Meded Rijksfac Landbouwwet Gent. 1969;34:315–59.
Abolafia J. A low-cost technique to manufacture a container to process meiofauna for scanning electron microscopy. Microsc Res Tech. 2015;78:771–6.
De Ley P, Felix MA, Frisse L, Nadler S, Sternberg P, Thomas WK. Molecular and morphological characterisation of two reproductively isolated species with mirror-image anatomy (Nematoda: Cephalobidae). Nematology. 1999;1:591–612.
Subbotin SA, Vierstraete A, De Ley P, Rowe J, Waeyenberge L, Moens M, Vanfleteren JR. Phylogenetic relationships within the cyst-forming nematodes (Nematoda, Heteroderidae) based on analysis of sequences from the ITS regions of ribosomal DNA. Mol Phylogenet Evol. 2001;21:1–16.
Holterman M, Van der Wurff A, Van den Elsen S, Van Megen H, Bongers T, Holovachov O, Bakker J, Helder J. Phylum wide analysis of SSU rDNA reveals deep phylogenetic relationships among nematodes and accelerated evolution toward crown clades. Mol Biol Evol. 2006;23:1792–800.
Hu M, Chilton NB, Gasser RB. Single-stranded conformation polymorphism- based analysis of mitochondrial cytochrome c oxidase subunit 1 reveals significant substructuring in hookworm populations. Electrophoresis. 2002;23:27–34.
Derycke S, Remerie T, Vierstraete A, Backeljau T, Vanfleteren J, Vincx M, Moens T. Mitochondrial DNA variation and cryptic speciation within the free-living marine nematode Pellioditis marina. Mar Ecol Prog Ser. 2005;300:91–103.
Powers TO, Bernard EC, Harris T, Higgins R, Olson M, Lodema M, Mullin P, Sutton L, Powers KS. COI haplotype groups in Mesocriconema (Nematoda: Criconematidae) and their morphospecies associations. Zootaxa. 2014;3827:101–46.
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990;215:403–10.
Legendre, P., Legendre, L. Numerical ecology. 3th ed.; Elsevier Science: Amsterdam. 2012; 990.
Zuur AF, Ieno EN, Elphick CS. A protocol for data exploration to avoid common statistical problems. Methods Ecol Evol. 2010;1:3–14.
Montgomery DC, Peck EA, Vining GG. Introduction to Linear Regression Analysis. New York: Wiley; 2012.
Le, S., Josse, J., Husson, F. FactoMineR: An R Package for Multivariate Analysis. Journal of Statistical Software 2008;25,1–18. https://doi.org/10.18637/jss.v025.i01.
Masters BC, Fan V, Ross HA. Species delimitation a Geneious plugin for the exploration of species boundaries. Mol Ecol Resour. 2011;11:154–7.
Ross HA, Murugan S, Li WLS. Testing the reliability of genetic methods of species identification via simulation. Syst Biol. 2008;57:216–30.
Hamilton CA, Hendrixson BE, Brewer MS, Bond JE. An evaluation of sampling effects on multiple DNA barcoding methods leads to an integrative approach for delimiting species: A case study of the North American tarantula genus Aphonopelma (Araneae, Mygalomorphae, Theraphosidae). Mol Phylogen Evol. 2014;71:79–93.
Rosenberg NA. Statistical tests for taxonomic distinctiveness from observations of monophyly. Evolution. 2007;61:317–23.
Munawar M, Powers TO, Tian Z, Harris T, Higgins R, Zheng J. Description and distribution of three criconematid nematodes from Hangzhou, Zhejiang Province China. J Nematol. 2017;50:183–206.
Katoh K, Rozewicki J, Yamada KD. MAFFT online service: Multiple sequence alignment, interactive sequence choice. Brief Bioinform. 2019;20:1160–6.
Hall TA. BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 1999;41:95–8.
Tan G, Muffato M, Ledergerber C, Herrero J, Goldman N, Gil M, Dessimoz C. Current methods for automated filtering of multiple sequence alignments frequently worsen single-gene phylogenetic inference. Syst Biol. 2015;64:778–91.
Ronquist F, Huelsenbeck JP. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003;19:1572–4.
Darriba D, Taboada GL, Doallo R, Posada D. jModelTest 2: More models, new heuristics and parallel computing. Nat Methods. 2012;9:772.
Rambaut, A. FigTree v.1.4.3, A Graphical Viewer of Phylogenetic Trees. 2016. Available online: http://tree.bio.ed.ac.uk/software/figtree/. Accessed 27 Nov 2023.
Librado P, Rozas J. DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009;25:1451–2.
Clement, M., Snell, Q., Walker, P., Posada, D., Crandall, K. TCS: Estimating Gene Genealogies. In Proceedings of the 6th International Parallel and Distributed Processing Symposium, Fort Lauderdale, FL, USA, 15–19 April 2002; IEEE Computer Society: Fort Lauderdale. 2002; 184.
Cid del Prado VI. Contribución al conocimiento morfológico de Criconemella macrodora (Taylor 1936) Luc & Raski, 1981. Rev Mex Fitopatol. 1988;6:224–47.
De Grisse AT. Morphological observations on Criconemoides, with a description of four new species found in Belgium. (Nematoda) Meded Landb Hogesch Opzoekstns Gent. 1964;29,734–761.
Kozlovskyi, M.P., Kramerets, V.O., Maciakh, I.P. Phytohelminths of the wood seed plots of Ukrainian Beskyds. VI International Scientific Conference on Zoocenosis 2011;183–184.
Peneva V, Neilson R, Boag B, Brown DJF. Criconematidae (Nematoda) from oak forest in two natural reserves in Russia. Syst Parasitol. 2000;49:191–201.
Lišková M, Vovlas N, Sasanelli N. Criconematidae (Nematoda) in the Slovak Republic. Helminthologia. 2004;41:161–70.
Corbett DCM. The occurrence of Criconemoides macrodorum Taylor, 1936 in Central Africa. Nematologica. 1962;8:176.
Heyns, J. South African Criconematidae. Part I. Genera Nothocriconema, Lobocriconema, Criconemella, Xenocriconemella and Discocriconemella (Nematoda). Phytophylactica. 1970;2,49–56.
Edward JC, Misra SL. Criconemoides magnoliae n. sp. and C juniperi n. sp. (Nematoda: Criconematidae) from Kumaon region, Uttar Pradesh India. Nematologica. 1964;10:95–100.
Eskandari A, Karegar A, Pourjam E, Alizadeh A. Three new records of Criconematidae (Nematoda: Tylenchida) from Iran Iran. J Plant Pathol. 2006;42:134–57.
Choi YE, Geraert E. Criconematids from Korea with the description of eight new species (Nematoda: Tylenchida). Nematologica. 1975;21(21):35–52.
McLeod, R., Reay, F., Smyth. J. Plant Nematodes of Australia listed by plant and by genus. RIRDC 1994;20.
Bickford D, Lohman DJ, Sodhi NS, Ng PKL, Meier R, Winker K, Ingram KK, Das I. Cryptic species as a window on diversity and conservation. Trends Ecol Evol. 2007;22:148–55. https://doi.org/10.1016/j.tree.2006.11.004.
Archidona-Yuste A, Cai R, Cantalapiedra-Navarrete C, Carreira JA, Rey A, Viñegla B, Liébanas G, Palomares-Rius JE, Castillo P. Morphostatic speciation within the dagger nematode Xiphinema hispanum-complex species (Nematoda: Longidoridae). Plants. 2020;9:1649. https://doi.org/10.3390/plants9121649.
Cai R, Archidona-Yuste A, Cantalapiedra-Navarrete C, Palomares-Rius JE, Castillo P. New evidence of cryptic speciation in the family Longidoridae (Nematoda: Dorylaimida). J Zool Syst Evol Res. 2020;58:869–99. https://doi.org/10.1111/jzs.12393.
Siddiqi, M.R. Tylenchida: Parasites of Plants and Insects, 2nd ed.; CAB International: Wallingford, UK, 2000;848 pp.
Acknowledgements
A. Archidona-Yuste is funded by the Ramón y Cajal program (RYC2021-031108-I), funded by MCIN/AEI/https://doi.org/10.13039/501100011033 and UE “Next Generation EU/PRTR”. Spanish authors acknowledge grant PRE2019-090206 funded by MCIN and European Social Fund (ESF) “Investing in your future” for I. Clavero-Camacho. A.N. Ruiz-Cuenca is a recipient of a postdoctoral grant for the requalification of the Spanish University System 2021-2023 (modality ‘Margarita Salas’), financed by Next Generation EU (NGEU) funding through the Spanish Ministry of Universities. The authors thank J. Martin Barbarroja (IAS-CSIC), G. León-Ropero (IASCSIC) for their excellent technical assistance, and Manuel Cuestas (Senderos-Córdoba) and Navara Gutierrez for helping in some of the surveys. Scanning electron microscopic pictures were obtained with the assistance of technical staff at the Centro de Instrumentación Científico-Técnica (CICT) of the University of Jaén. We also acknowledge support of the publication fee by the CSIC Open Access Publication Support Initiative through its Unit of Information Resources for Research (URICI). The first author would like to thank Mr. Antonio Archidona-Garrido and Mrs. Francisca Yuste-Sánchez for their tremendous effort and dedication for sampling in some areas.
Funding
Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. This research was supported by grant 201740E042, “Análisis de diversidad molecular, barcoding, y relaciones filogenéticas de nematodos fitoparásitos en cultivos mediterráneos” from the Spanish National Research Council (CSIC), grant RYC2021-031108-I, funded by MCIN/AEI/https://doi.org/10.13039/501100011033 and UE “Next Generation EU/PRTR”.
Author information
Authors and Affiliations
Contributions
AAY, PC and JEPR conceptualized and designed the study. AAY, ICC, ANRC, CCN, GL, PC and JEPR conducted the field surveys. AAY, ICC, ANRC, CCN, GL, PC and JEPR collected and analysed morphological and molecular data, prepared figures, and drafted the manuscript. All authors contributed to the final discussion data and have read and agreed to the published version of the manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Additional file 1:
Table S1. Measurements of several populations of Xenocriconemella macrodora De Grisse and Loof, 1965 from several countries.
Additional file 2:
Fig. S1. SEM micrographs of Criconemoides rosmarini (Castillo, Siddiqi and Gómez-Barcina, 1988) Siddiqi, 2000 female and juvenile. (a, b) female anterior region showing crenate annuli; (c, d) female lip region; (e, f) female en face view showing oral aperture; (g) female posterior region showing vulva and anus (arrowed); (h) juvenile tail. Abbreviations: a = anus; V = vulva. Scale bars: (a) = 10 µm; (b, h, g) = 5 µm; (d, e, f) = 1 µm; (c) = 2 µm.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Archidona-Yuste, A., Clavero-Camacho, I., Ruiz-Cuenca, A.N. et al. The more we search, the more we find: discovering and expanding the biodiversity in the ring nematode genus Xenocriconemella De Grisse and Loof, 1965 (Nematoda: Criconematidae). Zoological Lett 10, 8 (2024). https://doi.org/10.1186/s40851-024-00230-3
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s40851-024-00230-3