To be or not to be? What molecules say about Runcina brenkoae Thompson, 1980 (Gastropoda: Heterobranchia: Runcinida)

1 Departamento de Biología, Facultad de Ciencias del Mar y Ambientales, Campus de Excelencia Internacional del Mar (CEIMAR), Universidad de Cádiz, Avenida República Saharaui s/n, 11510 Puerto Real, Cádiz, Spain. (AKA) (Corresponding author) Email: anakarla.araujo@uca.es. ORCID iD: https://orcid.org/0000-0001-5305-6700 2 Departamento de Biología, Facultad de Ciencias, Universidad Autónoma de Madrid, Campus de Excelencia Internacional UAM + CSIC, C/ Darwin 2, 28049 Madrid, Spain. (MP) E-mail: marta.pola@uam.es. ORCID iD: http://orcid.org/0000-0003-0518-346X 3 Section of Taxonomy and Evolution, Department of Natural History, University Museum of Bergen, University of Bergen, PB7800, 5020-Bergen, Norway. (MAM) E-mail: Manuel.Malaquias@uib.no. ORCID iD: http://orcid.org/0000-0002-9668-945X 4 Instituto Universitario de Investigación Marina (INMAR), Campus de Excelencia Internacional del Mar (CEIMAR), Universidad de Cádiz, Avenida República Saharaui s/n, 11510 Puerto Real, Cádiz, Spain. (JLC) E-mail: lucas.cervera@uca.es. ORCID iD: http://orcid.org/0000-0002-8337-2867


INTRODUCTION
Runcinids are small heterobranch sea slugs with an average size of about 4 mm. The largest species known is Runcinida elioti (Baba, 1937) from Amakusa (Japan) which reaches a maximum length of 8 mm (Burn 1963). These slugs inhabit intertidal and shallow rocky shores and are specialized herbivores, feeding on macrophytic algae (Burn 1963, Thompson and Brodie 1988, Schmekel and Cappellato 2001. They are characterized by having an undivided dorsum, a foot lacking parapodial lobes, and an anus located next to the gill under the right posterior side of the mantle. An external or internal vestigial shell may be present, but it is absent in most species (Thompson 1976, Burn and Thompson 1998, Schmekel and Cappellato 2001. The runcinids have traditionally been included in the order Cephalaspidea based on anatomical features such as nervous and reproductive systems (Ghiselin 1963, Kress 1977, Schmekel 1985. However, Malaquias et al. (2009), based on molecular phylogenetic analyses, demonstrated that runcinids were not part of the Cephalaspidea radiation but warrant their own ordinal assignment, a suggestion first proposed by Odhner (1968) and later corroborated by Jörger et al. (2010), Wägele et al. (2014) and Oskars et al. (2015).
The order Runcinida (Burn 1963) comprises two families, Runcinidae H. Adams and A. Adams, 1854 and Ilbiidae Burn, 1963 with nine and two genera, respectively. Within the family Runcinidae, Runcina is the most species-rich genus, with 38 valid species, of which 29 occur in European waters (Cervera et al. 2004, Schmekel and Cappellato 2002. The small size of these animals and the fact that most species have dark, dull cryptic colour patterns render the runcinids difficult to detect and identify. One of the taxonomically difficult species of the European fauna is Runcina brenkoae, Thompson, 1980, which, together with Runcina adriatica Thompson, 1980 and Runcina zavodniki Thompson, 1980, has been described from the Adriatic Sea. Runcina brenkoae is characterized by an elongated body with a characteristic pattern of anastomosing black blotches, a red-brown ground colour, clusters of chalk-white spots on both sides of the head behind the eyes, and presence of two gills. However, Thompson and Brodie (1988) referred to specimens of R. brenkoae collected near Rovinj (Croatia), the type locality, which depicted several differences in respect to the original description: the presence of a developed crest, a pale fawn ground colour and the absence of white spots. Nevertheless, the specimens possessed key features of the species: the anastomosing black blotches and presence of only two gills. Schmekel and Cappellato (2002) reported the species outside the Adriatic Sea for the first time in Banuyls-sur-Mer (French Mediterranean coast) and Ballesteros et al. (2016) reported R. brenkoae in Catalonia (Spanish northeastern coast).
The use of integrative taxonomic approaches, and in particular of molecular phylogenetics, has revealed the existence of numerous species complexes and con-tributed to the discovery of unknown species among heterobranch sea slugs (Padula et al. 2014, Austin et al. 2018, Krug et al. 2018. The variable chromatic patterns described for R. brenkoae hint at yet another possible example of cryptic diversity masked under a single species name, but to date the taxonomy of this elusive species has only been studied on the basis of morphology.
Here we investigate for the first time the taxonomic status of the taxonomically difficult species Runcina brenkoae following an integrative approach combining multi-locus molecular phylogenetics and morpho-anatomical characters, based on specimens from the central and western Mediterranean Sea and the southern Iberian coastline of Portugal and Spain.

Taxon sampling
Specimens identified as Runcina brenkoae were collected by the authors and colleagues from algae and seagrass or were obtained on loan from the Zoologische Staatssammlung München, Germany (ZSM). Specimens were photographed alive and preserved in 96% EtOH. The newly collected material was deposited at the Museo Nacional de Ciencias Naturales (MNCN), Madrid, Spain.

DNA extraction, amplification and sequencing
Tissue samples were taken from the foot and DNA was extracted using the DNeasy Blood and Tissue Kit (Qiagen, Valencia, CA). Partial sequences of the mitochondrial cytochrome c oxidase subunit I (COI), and 16S rRNA(16S), and nuclear histone H3 (H3) genes were amplified by polymerase chain reaction (PCR) using the universal primers LCO1490 and HCO2198 (Folmer et al. 1994 for COI); 16S ar-L and 16S br-H (Palumbi et al.1991 for 16S); and H3aF and H3aR (Colgan et al. 1998 for H3). PCRs were conducted in a 25 µl reaction volume containing 1 µl of both forward and reverse primers (10 µM), 2.5 µl of dNTP (2 mM), a gene-dependent amount of magnesium chloride (25 mM), 0.25 µl of Qiagen DNA polymerase (5 units/µl), 5 µl of "Q-solution" (5x), 2.5 µl of Qiagen buffer (10x) (Qiagen Taq PCR Core Kit) and 2 µl of genomic DNA. Amplification of COI was performed with an initial denaturation for 5 min at 94°C, followed by 35-36 cycles of 1 min at 94°C, 30s at 45°C (annealing temperature) and 1 min at 72°C, with a final extension of 10 min at 72°C. Amplification of 16S began with an initial denaturation for 5 min at 94°C, followed by 35-36 cycles of 1 min at 94ºC, 30s at 42 and 49°C (annealing temperatures) and 1 min at 72°C, with a final extension of 10 min at 72°C. Amplification of H3 was performed with an initial denaturation for 5 min at 94°C, followed by 35 cycles of 1 min at 94°C, 30s at 52°C (annealing temperature) and 1 min at 72°C, with a final extension of 10 min at 72°C. Successful PCR products were sent to Macrogen, Inc for purification and sequencing on a 3730XL DNA sequencer (Applied Biosystems). All new DNA sequences have been deposited in GenBank (Table 1).

Phylogenetic analyses
Sequences were edited in Genious v10.2.3 (Drummond et al. 2009) and aligned using MAFFT (Katoh et al. 2009) implemented in Geneious v10.2.3 (Drummond et al. 2009) with the default  (Talavera and Castresana 2007). Nevertheless, analyses including and excluding these regions provided similar results. Therefore, final analyses were performed including all bases. Sequences of the COI, 16S and H3 genes were trimmed to 658, 457 and 328 nucleotides, respectively. All three genes were concatenated using Mesquite v3.2 (Maddison and Maddison 2018), resulting in a final dataset of 1443 base pairs. Single gene and concatenated (H3+COI+16S) analyses were performed. Saturation for the first, second and third codon positions of the COI and H3 genes were calculated in MEGA v7.0 (Kumar et al. 2016).
The best-fit evolutionary model for each gene was determined in jModeltest v2.1.6 (Guindon andGascuel 2003, Darriba et al. 2012) under the Akaike information criterion (Akaike 1974). The GTR + G + I model was selected for the COI and H3 genes, and GTR + G for the 16S gene. Bayesian inference (BI) analyses were performed in MrBayes v. 3.2.1 (Ronquist and Huelsenbeck 2003) with a random starting tree and two parallel runs of 10 7 generations. Convergence was checked in TRACER v1.7.1 (Rambaut et al. 2018) with a burn-in of 25%. Nodes with a posterior probability (PP) ≥ 0.95 (Alfaro et al. 2003) were considered well supported and discussed. Maximum likelihood (ML) analysis was executed using RAxML v8 (Stamatakis 2014) and node support was assessed with nonparametric bootstrapping (BS) with 5000 replicates. Nodes with bootstrap values (BS)≥70 (Hillis and Bull 1993) were considered significant and were discussed. Both BI and ML trees were visualized in FigTree v1.4.3 (http://tree.bio. ed.ac.uk/software/figtree/). Minimum and maximum pairwise uncorrected p-distances of COI within and between species were calculated in MEGA v7.0 using all sequences available. (Kumar et al. 2016).

Species delimitation analyses
The Automatic Barcode Gap Discovery (ABGD) (Puillandre et al. 2012) and Bayesian Poisson tree processes (bPTP) (Zhang et al. 2013) were used to aid delimitation of species. For the ABGD we used the alignment from the fast-evolving COI gene with default settings (P min =0.001, P max =0.1, Steps=10, X=1.2, Nb bins=20) under the three models of evolution available, namely Jukes-Cantor (JC69), Kimura (K80) and Simple Distance. The bPTP analysis is an updated version of the original maximum likelihood PTP (modelling speciation in terms of the number of substitutions), which adds Bayesian support values to delimit species. The bPTP analyses were run with the COI and 16S trees using the webserver (https://species.h-its.org/ ptp/) (Zhang et al. 2013).

Morphology
To complete and compare the results obtained by molecular phylogenetics and species delimitation analyses, specimens previously identified as Runcina brenkoae and Runcina sp. from Croatia (Adriatic) (3), Catalonia (Mediterranean, Spain) (6), Cádiz (Atlantic, Spain) (1) and Algarve (Atlantic, Portugal) (5), and one specimen early identified as R. adriatica from Banyuls-sur-Mer (France) were studied for their morpho-anatomy. Animals were dorsally dissected and the buccal bulbs were extracted and dissolved in a solution of 10% sodium hydroxide to expose the radula. The radulae and gizzard plates were then immersed in water, dried and mounted for scanning electron microscopy (SEM) with a Nova NanoSEM 450 available at the University of Cádiz (Cádiz, Spain). The reproductive system was examined and drawn using a dissecting microscope with the aid of a camera lucida.

Phylogenetic analyses
The concatenated (H3+COI+16S) tree provided better resolution than the individual gene analyses (Fig. 1, and Supplementary material Figs S1, S2 and S3). No saturation was observed, even in the third codon position. Both BI and ML analyses supported the monophyly of the genus Runcina (PP=1; BS=100) and showed L. divae to be its sister lineage (PP=0.98; BS=86). The species Ilbia ilbi was rendered sister to the Lapinura + Runcina clade (PP=1; BS=100). In the Runcina clade the species R. ferruginea was rendered sister to a sub-clade containing all remaining species (PP=1; BS=80). The specimens previously identified as R. brenkoae split into three subclades all with maximum support (PP=1; BS=100). The first clade (Group A) includes specimens from Portugal; the second clade (Group B) includes one specimen previously identified as Runcina adriatica from France (Mediterranean) and specimens from Spain (Atlantic and Mediterranean); and the third clade (Group C) includes specimens from Croatia and Spain (Mediterranean) (Fig. 1).

Species delimitation analyses
The ABGD analysis of the COI sequences with all three models of evolution resulted in 11 groups with three of them corresponding to the same R. brenkoae groups, A, B and C, recovered in the BI and ML analyses ( Fig 1A). However, the recursive partition, at lower values of prior intraspecific divergence (P), recovered seven groups for the "R. brenkoae complex", separating specimens from Group A and C into two distinct groups each, and specimens from Group B into three distinct groups (not shown).
Regarding the COI uncorrected p-distances, the minimum distance was 11.7% between Groups A and B; 9.6% between Groups A and C; and 10.4% between Groups B and C. The maximum distance was 0% within specimens of Group A, 4% within Group B, and 4.6% within Group C (Table 2). Between species in the genus Runcina the COI uncorrected pdistances ranged from 9.3% to 15.1%, while between the genera Runcina and Lapinura they ranged from 16.3% to 20.7%. No COI gene sequences from Ilbia ilbi were available for this analysis. The results obtained with the bPTP analysis were congruent with the ABGD output in suggesting the same three groups of Runcina brenkoae (Fig. 1B).
The molecular results support the occurrence of three species under the name Runcina brenkoae, and this hypothesis is backed by morphological differences across specimens from the three R. brenkoae clades (see Systematic description section). Therefore, we present below a redescription of R. brenkoae and we describe two new species.

Family RUNCINIDAE H. Adams and A. Adams, 1854
Genus Runcina Forbes in Forbes and Hanley, 1851 Runcina brenkoae Thompson, 1980 (Figs 2, 5A-C, 6A, D) Runcina brenkoae Thompson 1980: 156, fig. 1C. Thompson and Brodie 1988: 340, fig   External morphology (Fig. 2). Body moderately elongated and tapered. Notum smooth. Foot as wide as notum, showing a developed median pallial crest. Ground colour of body red-brown, sometimes translucent pale fawn bearing a pattern of anastomosing dark blotches on notum, margin and sole of foot. Eyes difficult to discern. Chalk-white spots all over body, more concentrated on margin of tail, both sides of head behind eyes and on metapodium in front of dark band. Some specimens with small red spots on margin of tail and surface of metapodium. The slugs have a longitudinal band of dark brown or wine-red colour on the surface of the metapodium. Two equal-sized translucent gills with white spots bearing pinnules on right posterior side of body. Anal pore situated beneath gills.
Internal anatomy (Figs 5A-C, 6A, D). Radular formulae 20 × 1.1.1 (MNCN 15.05/88086, MNCN 15.05/88088). Rachidian tooth boomerang-shaped with long, smooth lateral wings on each side. Central part of rachidian tooth bilobed; masticatory edge contains a pair of cockle-shaped rounded pads, each pad with 8-10 denticles. Median deep and broad depression is present between the pads; a small denticle may be present (Fig. 5A). Lateral teeth smooth, elongate and curved like a swan neck (Fig. 5B). Triangular jaws present. Four gizzard plates with 5-7 lamellae (Fig. 5C). Shell absent. Reproductive system monaulic. Female gland mass slightly divided into two lobes. Common genital duct connecting the female gland to the exterior on right posterior side of the body. Bursa copulatrix absent. Female gland placed on right posterior side of digestive gland (Fig. 6A). Male copulatory organ opens to the right of the mouth. Short and unarmed penial papilla projects into the atrium. Prostate gland long and cylindrical. Slender seminal vesicle with half size of prostate gland (Fig. 6D). Etymology. Lusitania was the name of a Roman province in the west of the Iberian Peninsula that occupied much of what now is Portugal. External morphology (Fig. 3). Body elongated and moderately broad. Notum smooth. Foot as wide as notum. Posterior part of notum rounded without pallial crest. Ground colour of body brown and translucent yellowish bearing a pattern of anastomosing dark blotches on notum and margin of foot. Some specimens have a large pale fawn patch on the posterior part of head and notum. Eyes not visible. White spots on some specimens. Longitudinal band, sometimes wide, of dark brown colour on surface of metapodium. Two large, yellowish gills with dark spots bearing irregular pinnules on right posterior side of body. Upper gill unipinnate and the most ventral bipinnate. Anal pore situated beneath gills.

Runcina lusitanica
Internal anatomy (Figs 5D-F, 6B, E). Radular formulae 25 × 1.1.1 (MNCN 15.05/88092) and 29 × 1.1.1 (MNCN 15.05/88093). Rachidian tooth boomerang shaped with one long and smooth lateral wing on each side. Central part of rachidian tooth bilobed; masticatory edge contains a pair of flat, comb-shaped pads, each one possessing 10-12 denticles. Median deep and broad depression is present between the pads; a small denticle present (Fig. 5D). Lateral teeth smooth, elongate and curved like a swan neck (Fig.  5E). Triangular jaws present. Four gizzard plates with 10-11 lamellae (Fig. 5F). Shell absent. Reproductive system monaulic. Female gland mass divided into two lobes, located on right side and behind the digestive gland. Bursa copulatrix absent. Common genital duct opening to exterior on right posterior side of body (Fig. 6B). Male copulatory organ comprises a relatively large atrium, which opens on right side next to mouth. Short, unarmed, conical penial papilla projects inside atrium. Long and cylindrical prostate gland. Elongated and convoluted seminal vesicle (Fig. 6E).  Etymology. This species is dedicated to Marcos Martínez Vazquez, husband of the first author, for all his help, enthusiasm and support during the course of this work.
External morphology (Fig. 4). Body moderately elongated. Notum smooth. Foot as wide as notum. Some specimens show developed median pallial crest. Ground colour of body red-brown or translucent pale fawn bearing a pattern of anastomosing dark or reddish blotches on notum, margin of foot and metapodium. Eyes difficult to discern. White spots all over the body. Longitudinal band of dark brown or wine-red colour on surface of metapodium. Two translucent gills bearing regular pinnules on right posterior side of body. Upper gill unipinnate and the most ventral bipinnate. Anal pore situated beneath gills.
Internal anatomy (Figs 5G-I, 6C, F, G). Radular formulae 10 x 1.1.1 (MNCN 15.05/88097) and 13 × 1. 1.1 (MNCN 15.05/88095). Rachidian tooth boomerang-shaped with long and smooth lateral wings on each side. Central part of rachidian tooth bilobed; masticatory edge contains a pair of flat, comb-shaped pads, each one with 10-11 denticles. Median deep and broad depression present between the pads; small denticle absent (Fig. 5G). Lateral teeth smooth, elongate and curved like a swan neck (Fig. 5H). Triangular jaws present. Four gizzard plates with 7-8 lamellae (Fig. 5I). Shell absent. Reproductive system monaulic. Female gland mass placed on right side and behind the diges-tive gland. Divided into two lobes, perhaps albumen and mucous glands. Long common genital duct connects the female gland to exterior on right posterior side of body. Bursa copulatrix absent (Fig. 6C). Elongated and cylindrical male copulatory organ. Atrium opens to right side of mouth. Short and unarmed penial papilla projects into the atrium. Cylindrical prostate gland. Slender seminal vesicle with half size of prostate gland (Fig. 6F, G).

DISCUSSION
Recent molecular studies on heterobranch sea slugs, mostly nudibranchs, have demonstrated the existence of many complexes of cryptic species (Austin et al. 2018, Layton et al. 2018, Korshunova et al. 2019, among many others). Up to now, most studies related to the order Runcinida have focused only on morphological aspects in order to identify and describe new species and genera (Cervera et al. 1991, Scale bars: A, B, E, H=10 µm; C=50 µm; D, I=20 µm; F=100 µm; G=5 µm. Chernyshev 2006, Moro and. Our contribution is the first to use molecular phylogenetics combined with morphology to test the status of taxonomically difficult European runcinids, with a focus on the Runcina brenkoae species complex. Our study recognized three distinct species within this complex, namely R. brenkoae Thompson, 1980 proper and two new species described here as R. marcosi n. sp. and R. lusitanica n. sp. (Table 3). Externally, all species of this complex are similar in colour, but R. marcosi n. sp., despite its chromatic variability, has a characteristic concentration of white spots on the anterior part of the body forming a "necklace". R. brenkoae is the only one among the three species of the complex with both gills unipinnate, whereas R. lusitanica n. sp. and R. marcosi n. sp. have one gill unipinnate and the other bipinnate. R. lusitanica n. sp. reaches comparatively larger sizes (up to 5 mm in length in preserved animals), but overlaps chromatically with R. brenkoae. R. marcosi n. sp. shows a considerable chromatic variation and, in fact, some individuals can be confused with R. adriatica, which has chalk-white spots on the pallial crest and behind the eyes forming a "necklace" (Thompson 1980, Thompson andBrodie 1988). However, R. adriatica has three gills (two bipinnate and one unipinnate) and a higher number of radular rows (21 × 1.1.1) (Thompson 1980). Anatomically these species differ in subtle details of the radula and gizzard plates. The pads of the rachidian tooth are more oval in shape in R. brenkoae, as observed by Schmekel andCappellato (2001, 2002), whereas in R. marcosi n. sp. and R. lusitanica n. sp. these pads are more flattened. In R. lusitanica n. sp. and R. brenkoae, a small denticle is present in the depression between the two pads, but it may be absent in some rows. The gizzard plates of R. brenkoae have 5-6 lamellae, while in R. marcosi n. sp. and R. lusitanica n. sp. they have 7-8 and 10-11 lamellae, respectively.
The male copulatory organ of the runcinids consists of a penial papilla projecting into an atrium, a prostate gland, and a seminal vesicle (Vayssière 1883, Kress 1977, Burn and Thompson 1998. The male copulatory organ does not differ much between R. brenkoae and R. marcosi n. sp. The prostate is more curved in R. brenkoae than in R. marcosi n. sp., and the seminal vesicle in R. brenkoae is more rounded on one of the sides. Thompson (1980) did not mention any aspect of the male organ of R. brenkoae, nor did Thompson and Brodie (1988), and Schmekel and Cappellato (2002) only reported that the copulatory organ of R. brenkoae was similar to that of R. ferruginea, which has the same basic anatomical structure as the species described here. In R. lusitanica n. sp. the penial papilla is larger than in R. brenkoae and R. marcosi and the posterior end of the cylindrical prostate narrows slightly into a very long and twisted seminal vesicle, which is not present in R. brenkoae and R. marcosi n. sp. The female part of the reproductive system in runcinids consists of an albumen and mucous gland opening to the outside through a common genital duct (Vayssière 1883, Kress 1977, Burn and Thompson 1998. However, the presence of an ampulla and bursa copulatrix have been described for the species Runcina macfarlandi (Gosliner, 1991), R. coronate and Ilbia ilbi, among others (Vayssière 1883, Burn 1963, Gosliner 1991. All three species of the R. brenkoae complex have similar female glands and we were unable to recognize an ampulla and bursa copulatrix. In general, the female part of the reproductive system in runcinids is poorly studied and, for example, Thompson (1980), Thompson and Brodie (1988) and Schmekel and Cappellato (2002) never referred to it.
Our study suggests that the geographical distribution of Runcina brenkoae proper is restricted to the Adriatic Sea (Croatia) and to the western Mediterranean (Spain and France), where it overlaps with the species R. marcosi n. sp., at least in northeastern Spain (Mediterranean Sea). Schmekel andCappellato (2001, 2002) referred to its presence in Banyuls-sur-Mer (French Mediterranean coast) but their specimens were initially fixed in formalin (Ronald Janssen, pers. comm., Senckenberg Research Institute and Natural History Museum) and could not be tested for DNA. Thus, under the present taxonomic scenario the iden-tity of these samples remains doubtful. The species R. lusitanica n. sp. is so far only known from the southern coast of Portugal. The distribution of R. marcosi n. sp. is restricted to southwestern Spain (Atlantic) and the western Mediterranean (Spain and France).
The present study is the first to evaluate the taxonomy of European species of runcinids using DNA data and to expose the occurrence of cryptic diversity among previously well-established species. Runcinids are small animals on average less than 5 mm in length, mostly with dull colour patterns, which complicates their identification and taxonomy. Runcinids clearly lack and will benefit from a DNA barcoding and molecular phylogenetics approach that could characterize the species molecularly, establishing a framework for understanding the value of colour patterns and morphological characters and their systematics.  Thompson (1980), Thompson and Brodie (1988), Schmekel and Cappellato (2002) and present study.
Colour pattern Body red-brown, sometimes translucent pale fawn. Anastomosing dark blotches on notum, margin and sole of foot. Chalk-white spots all over body, more concentrated on margin of tail, both sides of head behind eyes and on metapodium in front of the dark band. Longitudinal band of dark brown or wine-red colour on surface of metapodium.
Body brown and translucent yellowish. Anastomosing dark blotches on notum and margin of foot. Some specimens have a large pale fawn patch on posterior part of head and notum. Longitudinal dark brown band, sometimes wide, on surface of metapodium.
Body red-brown or translucent pale fawn. Anastomosing dark or reddish blotches on notum, margin of foot and metapodium. White spots all over body. Longitudinal band of dark brown or wine-red colour on the surface of metapodium.

Gills
Two equal-sized translucent gills with white spots bearing pinnules. Rachidian tooth bilobed. Two flat pads with 10-12 denticles each. Lateral teeth smooth, elongate and curved like a swan's neck.

SUPPLEMENTARY MATERIAL
The following supplementary material is available through the online version of this article and at the following link: http://scimar.icm.csic.es/scimar/supplm/sm04907esm.pdf