These authors contributed equally to this work.
Functional rare males in diploid parthenogenetic Artemia
Article first published online: 10 JUL 2013
© 2013 The Authors. Journal of Evolutionary Biology © 2013 European Society For Evolutionary Biology
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Journal of Evolutionary Biology
Volume 26, Issue 9, pages 1934–1948, September 2013
How to Cite
Maccari, M., Gómez, A., Hontoria, F. and Amat, F. (2013), Functional rare males in diploid parthenogenetic Artemia. Journal of Evolutionary Biology, 26: 1934–1948. doi: 10.1111/jeb.12191
- Issue published online: 21 AUG 2013
- Article first published online: 10 JUL 2013
- Manuscript Accepted: 29 APR 2013
- Manuscript Revised: 5 APR 2013
- Manuscript Received: 7 SEP 2012
- Plan Nacional. Grant Number: CGL2008-03277
- National Environment Research Council (NERC). Grant Number: NE/B501298/1
- Artemia ;
- evolution of sex;
- Top of page
- Materials and methods
- Supporting Information
Functional males that are produced occasionally in some asexual taxa – called ‘rare males’ – raise considerable evolutionary interest, as they might be involved in the origin of new parthenogenetic lineages. Diploid parthenogenetic Artemia produce rare males, which may retain the ability to mate with females of related sexual lineages. Here, we (i) describe the frequency of male progeny in populations of diploid parthenogenetic Artemia, (ii) characterize rare males morphologically, (iii) assess their reproductive role, using cross-mating experiments with sexual females of related species from Central Asia and characterize the F1 hybrid offspring viability and (iv) confirm genetically both the identity and functionality of rare males using DNA barcoding and microsatellite loci. Our result suggests that these males may have an evolutionary role through genetic exchange with related sexual species and that diploid parthenogenetic Artemia is a good model system to investigate the evolutionary transitions between sexual species and parthenogenetic strains.
- Top of page
- Materials and methods
- Supporting Information
Parthenogenetic reproduction occurs in one of 10 000 animal species (Lynch et al., 2008). Populations in these species are made of females that reproduce through apomixis (strict asexuality where there is no meiotic division) or automixis, where some of the products of a single meiosis fuse in diverse ways to restore diploidy (Bell, 1982). However, the presence of occasional males in all-female populations is not an uncommon phenomenon (Schön et al., 2009). Some of these species are cyclical parthenogens, where sexual and parthenogenetic phases are regulated environmentally and males and sexual females are part of the life cycle (Bell, 1982; De Meester et al., 2004). Other species are androdioecious, where self-fertilizing hermaphrodites coexist with a small proportion of males, such as the branchiopods Eulimnadia, Limnadia and Triops and the nematode Caenorhabditis elegans (Weeks, 2006; Weeks et al., 2008; Zierold et al., 2009; Anderson et al., 2010). Lineages of sperm-dependent apomictic flatworm Schmidtea polychroa have also been shown to present occasional male function (D'Souza & Michiels, 2010). Female-biased populations can also be due to infection with Wolbachia or other feminizing bacteria, rather than being genetically determined (Plantard et al., 1998; Stouthamer et al., 1999). Research, however, has confirmed the occurrence of rare males in various obligate parthenogens (Blackman, 1972; Butlin et al., 1998; Martens, 1998; Rispe et al., 1999; Simon et al., 1999; Delmotte et al., 2001; Snyder et al., 2006; Engelstädter et al., 2011). These observations of rare males raise important questions, such as their role in the origin and persistence of asexual lineages, the mechanisms involved in replenishing the diversity of such lineages, the avoidance of mutation accumulation and the occurrence of contagious parthenogenesis (Lynch, 1984; Butlin et al., 1998). In addition, functional rare males may challenge assumptions of evolution of sex theory, such as the complete reproductive isolation between sexual and parthenogenetic lineages (Lynch, 1984), or the absence of a ‘cost of males’ in parthenogenetic lineages (Neiman et al., 2012). Despite the importance of this topic, little research has been devoted to characterize their population frequency or to understand their mechanisms of origin. Most rare males found in parthenogenetic species appear to exhibit abnormal spermatogenesis and sterility, although some are functional (Lynch, 1984). Rare males, purportedly, cannot fertilize conspecific females as these females are parthenogenetic, and, given the low frequency of males in these populations, they are often seen as ‘atavisms’ of little consequence with their potential evolutionary impact deemed unimportant (Schön et al., 2009). However, if parthenogenetic lineages retain the ability to produce occasional males on a regular basis, and reproductive isolation between them and their sexual relatives is incomplete, such males may represent a vector for genetic exchange between parthenogenetic and sexual lineages when both coexist (Lynch, 1984; Rispe et al., 1999; Simon et al., 1999; Delmotte et al., 2001; Engelstädter et al., 2011). Indeed, males produced by parthenogenetic females, when mating with sexual females of related species, may transmit the genes conferring parthenogenesis to their offspring (Innes & Hebert, 1988; Lynch et al., 2008; Engelstädter et al., 2011; Eads et al., 2012), a mechanism termed ‘contagious parthenogenesis’ (Simon et al., 2003). This mechanism could (i) increase the fitness of parthenogenetic lineages producing rare males, (ii) boost the genetic diversity of such asexual lineages and (iii) potentially contribute to the ecological success and the evolutionary potential of such asexual lineages.
Brine shrimps of the genus Artemia (Crustacea, Branchiopoda, Anostraca) include gonochoric sexual species with separate males and females, and lineages of obligate parthenogenetic populations of different ploidy levels (Abatzopoulos et al., 2002). Parthenogenetic populations occur only in the Old Word, from the Canary Islands in the west to China in the east, and they have been introduced in Australia (Gajardo et al., 2002; McMaster et al., 2007). These parthenogenetic lineages co-occur with diverse sexual species across their range, including A. salina (Linnaeus 1758) in the Mediterranean region and South Africa (Amat et al., 1995), A. urmiana (Günther 1899) in and around lake Urmia (Iran) and Crimean salt lakes (Abatzopoulos et al., 2009), A. sinica (Cai 1989) in Central and Northern China, A. tibetiana (Abatzopoulos et al., 2002; Van Stappen et al., 2007) in the Tibetan plateau and a yet undescribed sexual species in Kazakhstan (Pilla & Beardmore, 1994; Litvinenko & Boyko, 2008). In Australia, introduced populations of diploid parthenogenetic Artemia may coexist with endemic brine shrimps of the genus Parartemia (McMaster et al., 2007). Parthenogenetic lineages are closely related genetically to Central Asian sexual species (in particular A. urmiana, A. sinica and the undescribed Artemia sp. from Kazakhstan), and they have originated independently several times (Baxevanis et al., 2006; Muñoz et al., 2010; Maniatsi et al., 2011).
Parthenogenetic diploid Artemia populations, which reproduce through automictic parthenogenesis (Abreu-Grobois, 1987), produce males in low numbers, and these are usually referred to as rare males (Stefani, 1964; Bowen et al., 1978; MacDonald & Browne, 1987; Amat et al., 1991; Cai, 1993; Mura & Nagorskaya, 2005). Rare males are produced by a yet unknown cytogenetic mechanism, possibly involving crossing over between sex chromosomes (Stefani, 1964; Abreu-Grobois & Beardmore, 2001). These males have normal and functional reproductive organs and display normal sexual behaviour (MacDonald & Browne, 1987), their sperm being slightly larger than those of sexual males (Stefani, 1964). Rare males have not been shown to fertilize females from their own diploid parthenogenetic lineages (Stefani, 1964; MacDonald & Browne, 1987) or sexual females from A. franciscana, A. persimilis or A. salina (MacDonald & Browne, 1987; but see Bowen et al., 1978). In contrast, rare males can fertilize sexual females of the closely related species A. urmiana (Bowen et al., 1978) and A. sinica (Cai, 1993), thus potentially enabling gene flow among these lineages. The coexistence of parthenogenetic lineages with their close sexual relatives therefore may provide an opportunity for rare males to mate with sexual females and have an evolutionary impact.
The aims of this study were (i) to describe the frequency of male progeny in populations of diploid parthenogenetic Artemia, (ii) to characterize rare males morphologically in the context of the variation in closely related sexual Central Asian Artemia species, (iii) to assess the reproductive role of rare males in cross-mating experiments with sexual females of Central Asian sexual populations and estimate the viability of F1 hybrid offspring and (iv) to confirm genetically both the identity and functionality of rare males. The evolutionary role and functionality of rare males are discussed on the basis of the results obtained.
Materials and methods
- Top of page
- Materials and methods
- Supporting Information
Brine shrimp cyst samples were used to establish laboratory populations of diploid parthenogenetic Artemia (see Table 1). Samples covering most of the known geographical distribution of diploid parthenogenetic Artemia were obtained from the collection of the cyst bank kept in the Instituto de Acuicultura de Torre de la Sal (IATS-CSIC). Most cultured populations of diploid parthenogenetic individuals were obtained from cyst samples of pure parthenogenetic natural populations. In some cases, original cyst samples contained an additional species (see Table 1). Whenever cyst samples containing other Artemia species were obtained, as indicated by the presence of abundant males, diploid parthenogenetic females were carefully isolated from the cultures according to the morphological traits described by Amat (1980). Parthenogenetic females were then allowed to reproduce, and their naupliar or encysted offspring used to obtain pure cultured laboratory parthenogenetic populations.
|Population||Coordinates||Year||Other species||Individuals sexed||Number of males||Males/1000 individuals|
|Odiel, Huelva, Spain||37°15′26″N–06°58′53″W||1987||4n||14 188||14||0.99|
|Rocío, Cádiz, Spaina||36°51′19″N–06°20′14″W||2001||A. salina||12 202||12||0.98|
|Hortales, Cádiz, Spain||36°44′18″N–05°32′06″W||2009||–||2297||0||0.00|
|San Fernando, Cádiz, Spain||36°27′58″N–06°10′41″W||1990||A. salina||12 504||12||0.96|
|Calpe, Alicante, Spain||38°38′37″N–00°03′60″W||1986||–||12 000||12||1.00|
|La Mata, Alicante, Spaina||38°02′08″N–00°42′02″W||1989||–||19 690||51||2.59|
|Bonmatí, Alicante, Spain||38°10′20″N–00°37′16″W||1980||A. salina||7268||19||2.61|
|Bras de Port, Alicante, Spain||38°11′22″N–00°36′36″W||2004||A. salina||3283||1||0.30|
|Rasall, Murcia, Spain||37°38′03″N–00°43′23″W||2011||–||3250||9||2.77|
|Cabo de Gata, Almería, Spain||36°45′48″N–02°13′19″W||1998||–||4040||20||4.95|
|Gerri, Lleida, Spain||42°19′39″N–01°04′04″E||1990||–||12 320||1||0.08|
|Aveiro, Portugal||40°38′01″N–08°40′49″W||1992||–||18 105||36||1.99|
|Rio Maior, Santarem, Portugal||39°21′49″N–08°56′45″W||2004||–||7062||2||0.28|
|Giraud, Camargue, France||43°23′58″N–04°43′37″E||1990||–||348||1||2.87|
|Aigües Mortes, Camargue, Francea||43°33′35″N–04°10′54″E||2003||A. franciscana||1272||5||3.93|
|Margherita Di Savoia, Puglia, Italy||41°22′50″N–16°05′24″E||2004||4n, A. franciscana||12 103||12||0.99|
|Torre Colimena, Puglia, Italy||40°18′13″N–17°44′03″E||2004||–||1993||5||2.51|
|Santa Gilla, Sardinia, Italy||39°13′33″N–09°02′53″E||1988||A. salina||4647||5||1.08|
|Molentargius, Sardinia, Italy||39°13′51″N–09°12′33″E||2004||A. salina||1631||8||4.90|
|Notteri, Sardinia, Italya||39°07′04″N–09°30′55″E||2009||A. salina||5715||16||2.80|
|Koyashskoe, Ukrainea||45°02′57″N–36°11′02″E||2007||A. urmiana||2908||7||2.41|
|Kujalnik, Ukraine||46°38′00″N–30°43′21″E||1991||–||12 656||91||7.19|
|Maloje Jarove Lake, Russia||53°01′35″N–79°08′54″E||1993||–||8031||13||1.62|
|Janubio, Lanzarote, Spain||28°56′16″N–13°49′14″W||1988||–||13 092||0||0.00|
|Tenefé, Gran Canaria, Spain||27°48′51″N–15°25′19″W||2005||–||14 810||0||0.00|
|Guatiza, Lanzarote, Spain||29°03′29″N–13°27′41″W||2010||–||9374||20||2.13|
|El Río, Lanzarote, Spain||29°13′03″N–13°29′41″W||2010||–||2418||0||0.00|
|Relisane, Algeria||35°50′31″N–00°39′10″E||2009||4n, A. salina||9659||34||3.52|
|Bethioua, Algeria||35°42′31″N–00°16′53″W||2009||4n, A. salina||6308||12||1.90|
|Oran, Algeria||35°32′09″N–00°48′00″W||2009||A. salina||5951||3||0.50|
|Ezzemoul, Algeria||35°52′54″N–06°30′14″E||2008||A. salina||2065||11||5.33|
|Wadi Natron, Egypt||30°27′29″N–30°10′15″E||2003||A. salina||4947||5||1.01|
|El Max, Egypt||31°06′54″N–29°50′13″E||2010||–||3931||1||0.25|
|Walvis Bay, Namibia||23°00′17″S–14°25′37″E||1990||–||10 066||10||0.99|
|Bjurliu, Kazakhstan||51°49′00″N–78°00′00″E||1989||–||18 946||181||9.55|
|Aral Sea, Uzbekistan||44°43′41″N–59°34′22″E||2004||–||1497||3||2.00|
|Bagdad, Iraqa||33°17′06″N–44°15′13″E||2004||–||41 568||398||9.57|
|Urmia, Irana||37°36′20″N–45°28′21″E||1988||A. urmiana||4619||78||16.89|
|Korangi Creek, Pakistana||24°47′46″N–67°09′07″E||2005||–||8387||58||6.92|
|Aibi, Xinjiang, Chinaa||44°53′05″N–82°53′55″E||1991||–||2207||19||8.61|
|Gahai, Qinghai, China||37°00′38″N–97°59′04″E||1991||–||1464||13||8.88|
|Dong Fang, Hainan, China||19°05′17″N–108°37′35″E||1992||–||8920||14||1.57|
|Tanggu, Tianjin, China||38°55′55″N–117°37′17″E||1989||A. sinica||1747||8||4.58|
|Luannan, Tianjin, China||39°06′03″N–118°25′55″E||2005||A. sinica, A. franciscana||3904||4||1.02|
|Dagang, Tianjin, China||38°48′50″N–117°32′44″E||2005||A. sinica, A. franciscana||8920||14||1.57|
|Xiaotan, Shandong, Chinaa||36°07′38″N–120°04′36″E||1992||–||16 570||92||5.55|
|Yingkou, Liaoning, China||40°37′15″N–122°08′16″E||1989||–||5920||9||1.52|
|Lagkor Co, Tibet, China||32°01′30″N–84°10′46″E||2005||A. tibetiana||2232||8||3.58|
Hatching was induced by incubating cyst samples under standard conditions, in 35 g L−1 sea water, at 28 °C, with continuous fluorescent lighting and gentle aeration (Vanhaecke & Sorgeloos, 1980). The resulting nauplii were mass-cultured in different volumes according to cyst availability and hatching efficiency. Mass cultures were usually kept in 60-L containers at 80 g L−1 brine salinity, at 20–24 °C, and fed Dunaliella sp. and Tetraselmis sp. (1 : 1) microalgae mixture every other day.
Sex ratio estimates and geographical patterns
Rare male frequencies were estimated for 54 laboratory populations of diploid parthenogenetic Artemia from a wide range of geographical locations (Table 1). Individuals were reared until maturity in mass cultures as detailed above and the sex ratio for each population (males per 1000 sexed individuals) were calculated as soon as most females showed signs of reproductive maturity (first ovulation or first offspring filling the ovisac), to minimize any possible effects of selective mortality. For sexing, animals were placed in Petri dishes with seawater and anaesthetized with a few drops of freshwater saturated with chloroform, and males carefully searched for with a binocular microscope.
To test whether there was a geographical pattern of distribution of the frequency of rare males, we carried out a spatial correlation of rare male frequencies using Moran's Index (Griffith, 1987). Given a set of locations and an associated variable, in this case rare male frequency, Moran's Index estimates whether the pattern is dispersed, random or clustered. For this purpose, we added the coordinates of each sampling site, confirmed in Google Earth, into spatial data using the ArcGIS package v. 10.0 (ESRI Inc., Redlands, CA, USA). In addition, to identify areas where the presence of rare males is highest, we looked for hot spots using the Gi* statistical test of Getis-Ord (Getis & Ord, 2010).
A 709-bp fragment of mitochondrial cytochrome c oxidase subunit I (COI) gene region was amplified and sequenced in 28 rare males from 14 diploid parthenogenetic Artemia populations across its distribution range. This same fragment was also sequenced in 12 females from 9 populations (Table 2) to confirm that these derived from parthenogenetic strains, instead of resulting from culture contamination by a sexual female. Total DNA was extracted from part of the antenna of ethanol-preserved adult males and from the first phyllopod for females, using the HotSHOT protocol optimized for zooplanktonic invertebrate organisms and their diapausing eggs (Montero-Pau et al., 2008). We used the COI primers HCO2198 and LCOI490 (Folmer et al., 1994). PCR was carried out in a total volume of 50 μL containing 5 μL of template DNA, 0.2 mm of each nucleotide, 0.2 μm of each primer, 0.05 U of Taq polymerase (Bioline) and 10 × Bioline buffer (with a MgCl2 final concentration of 2 mm). The cycling profile consisted of one cycle of 3 min at 95 °C, followed by 40 cycles of 15 s at 95 °C, 20 s at 50 °C and 30 s at 72 °C, with a final step of 5 min at 72 °C. PCR products were purified and sequenced in both directions by Macrogen Inc. (Macrogen Europe, Amsterdam, the Netherlands, www.macrogen.com) using an ABI PRISM 3700 DNA analyser.
|Population||Rare male codes (GenBank Acc. Num)||Females codes (GenBank Acc. Num)||Comparison male-female haplotypes|
|Rocío, Cadiz, Spain||rmROC1,2 (KC193640-41)||Not done||–|
|La Mata, Alicante, Spain||rmMATA1,2 (KC193661-62)||MATA1 (KC193677)||5 bp difference|
|Notteri, Sardinia, Italy||rmNOT1,2 (KC193642-43)||Not done||–|
|Margherita di Savoia, Italy||rmMAR1,2 (KC193638-39)||APD02 (7)a||1 bp difference|
|Aigües Mortes, France||rmAIG1,2 (KC193646-47)||AIG1 (KC193670)||Same|
|Atanosovsko, Bulgaria||rmATA1,2 (KC193663-50)||APD02 (5)a, APD07 (1)a, ATA15 (KC193674)||Same|
|Koyashskoe, Ukraine||rmKOY1,2 (KC193648-49)||KOY1 (KC193667)||Same|
|Kujalnik, Ukraine||rmKUJ1,2 (KC193664-65)||APD04 (2)a||11 bp difference|
|Bagdad, Iraq||rmIRAQ1,2 (KC193651-52)||IRAQ2 (KC193666)||Same|
|Urmia Lake, Iran||rmURM1,2 (KC193653-54)||URM4 (KC193671)||Same|
|Korangi Creek, Pakistan||rmPAK1,2 (KC193659-60)||PAK2 (KC193669)||5 bp difference|
|Aibi Lake, Xinjiang, China||rmAIBI1,2 (KC193655-56)||AIBI 1,3,7 (KC193672-73-75)||2 bp difference with AIBI1|
|Xiaotan, Shandong, China||rmXIAO1,2 (KC193657-58)||Not done||–|
|Lagkor Co, Tibet, China||rmLAGK1,2 (KC193644-45)||LAGK1,4 (KC193668-76)||Same|
The electropherograms were checked with eye using CodonCode Aligner v. 3.5 (CodonCode Corporation, Dedham, MA, USA). Sequences obtained here were aligned with published sequences from the same COI fragment from diploid parthenogenetic Artemia populations (DQ426824–DQ426826, GU591380–GU591384) and Central Asian sexual species A. urmiana (DQ119651), A. sinica (DQ119650), A. tibetiana (EF615588) and Artemia sp. from Kazakhstan (DQ119653, GU591385-GU591389), from GenBank, using Clustal in MEGA5 (Tamura et al., 2011). We used A. franciscana (DQ119645) and A. sinica (DQ119650) as outgroups. Phylogenetic reconstructions were carried out using MEGA5. The neighbour-joining (NJ) tree was reconstructed using evolutionary distances computed with the maximum composite likelihood method. The maximum likelihood (ML) tree was obtained using a GTR plus gamma model. The robustness of the branches was assessed with 1000 bootstrap pseudo-replicates. All sequences generated here were deposited in GenBank (Accession Numbers: KC193638–KC193677).
Reproductively mature males were characterized according to specific morphological traits following standard procedures (Hontoria & Amat, 1992) for a total of 11 parthenogenetic populations where 30 rare males were available (see Table 1). For this procedure, males were anaesthetized as described above and measured under a dissecting microscope. The following 12 morphometric characters were measured: total length, abdominal length, abdominal width, head width, distance between the compound eyes, eye diameter, length of the first antenna, furca length, number of setae on the left branch of the furca, number of setae on the right branch of the furca, ratio of abdominal length to total length (×100) and width of the genital segment. Morphometric data of males from the Asian sexual species were taken from the database of the Instituto de Acuicultura de Torre de la Sal (Amat et al., 1994) including two A. urmiana (Urmia and Koyashskoe), one Artemia sp. from Kazakhstan, three A. sinica (Tanggu, Yuncheng and Tonkhil) (Abatzopoulos et al., 2009) and four A. tibetiana (Lagkor Co, Hayan, Gaize, Jingyu) (Van Stappen et al., 2003). The full data matrix was subjected to multivariate discriminant analysis (Hontoria & Amat, 1992) using spss v. 15.0 (SPSS Inc., Chicago, IL, USA). The morphological variables mentioned above were used to establish relationships among the populations (Anderson, 1984) setting the geographical origin of the cyst samples as the separation criterion.
Mating experiments between rare males and females of Asian sexual populations were set up to obtain successful fertilization as evidenced by production of live viable or encysted offspring. The diploid parthenogenetic population from Bagdad (Iraq) was chosen as a source of males due to its high incidence of rare males and good cyst availability. Females used were chosen from sexual Asian populations, A. urmiana from Koyashskoe lake (Ukraine), A. sinica from Yuncheng lake (China), A. tibetiana from Lagkor Co lake (Tibet) and Artemia sp. from Kazakhstan (Artemia Reference Center code – ARC1039, unknown locality). Females used were either virgin (paired when still sexually immature) or kept isolated during the 2 weeks prior to the experiments to ensure that they had not been inseminated. Sperm storage does not occur in Artemia, and each copulation fertilizes the eggs present in the brood pouch (Bowen, 1962; M. Maccari & F. Amat, unpublished results). Isolated size-matched male–female single pairs were kept in small beakers (60 mL) under the culture conditions described above. Quantitative and qualitative reproductive outputs of each pair were monitored every other day during culture medium renewal. The total number of fertilized and unfertilized eggs produced per female in each mating experiment was recorded. Offspring quality was also characterized using the number of live and dead nauplii, as well as the number of abortive embryos (pale yellow-orange colour eggs) in ovoviviparous offspring. The number of normally shelled dormant cysts (pale grainy surface floating in 200 g L−1 brine), as opposed to abortive, abnormally shelled embryos (bright brown colour cyst not floating in 200 g L−1 brine), in oviparous offspring was also monitored. Mating experiments between sexual males and their conspecific females following the same procedure as above were used as controls.
We tested whether the means of the proportion of fertilized and unfertilized eggs and the means of the proportion of offspring quality variables per female were the same in the crosses involving rare males and in the corresponding controls. If the data were normal and homoscedastic, we used t-tests, otherwise Mann–Whitney tests were conducted. Statistical analyses were performed with spss v. 15.0.
Microsatellite analysis of hybrid F1 offspring
To obtain evidence of rare males' functionality regarding their ability to transmit genetic material to their offspring, we screened three microsatellite loci in the rare males, in the sexual females used in the crosses and in their F1 offspring. DNA extractions were obtained as described above. Each microsatellite locus (Apdq02TAIL, Apdq03TAIL and Apd05TAIL) (Muñoz et al., 2009) was amplified separately in PCRs performed in a total volume of 20 μL containing 2 μL of template DNA, 10 μL of 2× QIAGEN® (Qiagen, Hilden, Germany) PCR Master Mix (including 3 mm MgCl2, dNTP Mix and HotStarTaq® Polymerase; Qiagen), 2 μL of 10× Primer Mix (2 μm each primer) and 2 μL of Q solution (QIAGEN). The 5′ end of each reverse primer was labelled with a fluorescent dye (Apdq02TAIL, Apd05TAIL with Cy5 and Apdq03TAIL with Cy5.5, MWG Biotech, Eurofins MWG Operon, Ebersberg, Germany). The following PCR programme was used: 95 °C for 15 min, 35 cycles of 94 °C for 30 s, 53 °C for 90 s, 72 °C for 90 s, followed by 60 °C for 10 min. Diluted PCR products (1 : 20) were combined with a 400-bp size standard and separated on a Beckman-Coulter CEQ™ 8000 analysis system. Alleles were scored using the CEQ Fragment Analysis software (Beckman Coulter™, Fullerton, CA, USA) and checked manually.
- Top of page
- Materials and methods
- Supporting Information
Rare male frequency and geographical patterns
In total, 415 666 diploid parthenogenetic Artemia specimens were sexed in this experiment (see Table 1 for male ratio and population details). The number of specimens sexed for each diploid parthenogenetic population varied depending on its cyst availability, cyst hatching efficiency and nauplii survival rate to maturity and ranged from 348 individuals for Salin de Giraud (France) to 41 568 individuals for Bagdad (Iraq). The presence of rare males was verified in 50 of the 54 populations sampled. Janubio and El Rio (Lanzarote) and Tenefé (Gran Canaria) in the Canary Islands and Hortales (Cádiz) in Spain were the only populations where the presence of rare males could not be confirmed.
The spatial autocorrelation analysis was not significant (Moran's Index, 0.10; z-score, 0.50; P-value: 0.61), indicating that the distribution of the male ratio does not appear to be significantly different than random. Despite that, we found the highest ratios – reaching or surpassing 1% of rare males – in the Central Asian populations: Bagdad saltern (Iraq), Urmia Lake (Iran), Bjurliu Lake (Kazakhstan) and Aibi and Gahai Lakes (Inner China); and the lower ratios in the western, eastern and southern populations (Iberian Peninsula, China, India and Africa). This was confirmed by the Gi* test, which indicated that there are three statistically significant male ratio hot spots, Urmia Lake, Bagdad Saltern and Bjurliu Lake (Fig. 1), where a hot spot is a population with a high male ratio surrounded by other populations with high male ratio.
Cytochrome c oxidase subunit I sequences from 28 rare males from 14 populations (two individuals for each one) and 12 parthenogenetic females from nine populations were obtained (Table 2). After trimming, collapsing identical haplotypes for each population, and adding sequences from GenBank, the alignment had a length of 617 bp and comprised 47 sequences including outgroups. No insertions, deletions or stop codons were present. There was a total of 161 variable sites, 63 of them parsimony informative. Rare male sequences collapsed into eight haplotypes. NJ and ML phylogenetic reconstructions had a virtually identical topology and branch support. The most widespread haplotype in rare males, found in 15 rare males from eight populations, was identical to APD02, the most common haplotype in Mediterranean diploid parthenogenetic Artemia, and was closely related to haplotypes in sexual Artemia sp. from Kazakhstan (Muñoz et al., 2010; Fig. 2). The remaining seven haplotypes were found in single diploid parthenogenetic populations. Four of these haplotypes (rmMAR1-2, rmAIBI1-2, rmXIAO1-2 and rmPAK1-2) were closely related to APD02 and differed from it by 1, 2, 5 and 5 substitutions, respectively. Two haplotypes (rmATA1 and rmMATA1-2) were identical or closely related to haplotypes previously found in the diploid parthenogenetic population of Atanosovsko (APD07), which are closely related to the A. urmiana haplotype. The last haplotype, rmKUJ1-2, was very divergent, forming a sister branch to the remaining parthenogenetic sequences and differing in 10 and 8 substitutions from the APD02 haplotype and from the A. urmiana reference sequence, respectively.
Rare male mtDNA haplotypes in 6 of the 14 populations were identical to those found in parthenogenetic females from the same population (see Table 2 for details). In Margherita di Savoia and Aibi Lake, the rare male haplotype differed in 1 or 2 bp, respectively, from haplotypes in parthenogenetic females from the same population, whereas in Korangi Creek and La Mata, rare male haplotypes differed from the common haplotypes in females from these populations by 5 bp. Although female haplotypes from Rocio and Notteri were not available, rare males displayed the common APD02 haplotype. Sequences from females of Xiaotan were not available and the haplotypes obtained in the rare males from this population had never been reported before, although they differed in 5 bp from APD02. The rare males from Kujalnik differed from the two available sequences from the same population in 11 bp, and this haplotype has not been reported before.
Rare male morphometry
The morphometric multivariate analysis produced twelve discriminant functions. When they were included in the model, all except the last function significantly (P ≤ 0.05) accounted for the variance with the first five discriminant functions accounting for 88.9% of the variation. The ratio of abdominal length to total length, and the length of the furca were highly correlated with the first discriminant function, and the length of the first antenna and the total length made the highest contributions to the second function. Data of the mean values of the morphological traits measured for each population are available upon request.
Discriminant analysis separated morphometrically the males belonging to sexual species A. urmiana and A. tibetiana from the rest (Fig. 3). The morphometry of the parthenogenetic males was very variable, and their population centroids were located within the limits of the sexual populations. However, most rare males were morphologically closer to the males from A. sinica and Artemia sp. from Kazakhstan. No obvious association between the haplotype group that the parthenogenetic rare male mtDNA belonged to and their morphological resemblance to either A. urmiana or Artemia sp. from Kazakhstan was found. For example, rare males from Atanosovsko or La Mata have haplotypes very similar to those of A. urmiana from Koyashskoe, but they do not appear morphologically closer to males of this sexual species.
A total of 30 mating pairs were set up for each combination of sexual species with rare males, and between females of each sexual species with their conspecific males (controls). As some individuals died before mating, the final number of experimental pairs was between 8 and 25 per mating experiment (Table 3). Rare males were observed clasping and copulating with the sexual females of all species tested during the mating trials. Mating trials resulted in a total of 220 fertile hybrid broods and in 558 conspecific broods (controls). The proportion of fertilized eggs was always high (over 70%), and it was slightly higher in two of the four hybrid crosses (rare male × A. urmiana and rare male × A. tibetiana) than its corresponding controls, but in any case, there were no statistically significant differences between rare male crosses and controls (Table 3).
|Cross||Pairs||Broods||Fertilized eggs (%)||P-value|
|rare male × A. urmiana||18||58||77.99||1.000|
|rare male × Kazakhstan sp.||15||61||90.39||0.472|
|rare male × A. sinica||25||102||89.54||0.436|
|rare male × A. tibetiana||18||40||94.03||0.102|
Crosses involving rare males resulted in viable ovoviviparous and oviparous hybrid offspring (Fig. 4). Remarkably, all interspecific crosses between Central Asian sexual females and rare males had a similar or higher F1 offspring quality than controls (intraspecific sexual crosses). There were no statistically significant differences between rare male crosses and controls for most of the features analysed in both in ovoviviparous and oviparous quality traits. The only significant differences occurred in the proportion of dead nauplii obtained from ovoviviparous offspring from the crosses between rare males and A. urmiana or A. sinica females, which were higher in the controls (Fig. 4 and Table S1).
Microsatellite scoring showed that diploid partheno-genetic Artemia rare males underwent meiotic reduction and successfully fertilized sexual Central Asian Artemia females, transferring their alleles to the F1 progeny, and producing diploid hybrid offspring as a result (Table 4). Most males were heterozygotes for all loci (with the exception of male Iraq8 for locus Apd05). In those cases where the male was heterozygous, only one of the alleles was transmitted to each offspring, indicating that rare males produced haploid sperm through meiosis. No evidence for triploid offspring was found. In all the crosses performed, we found evidence of null alleles in the mother for one or more of the analysed loci. In these cases, the allele or alleles present in the father were found in the F1 offspring, demonstrating that the father had transmitted the amplifiable copy to the offspring.
|rare male × A. urmiana||F0 (F-Koy 15)||233-281||207-Ø||170-Ø|
|F0 (M-Iraq 15)||254-233||216-231||115-185|
|rare male × A. urmiana||F0 (F-Koy 16)||248-Ø||208-Ø||90-90|
|F0 (M-Iraq 16)||233-251||216-230||117-189|
|rare male × Artemia sp. Kazakhstan||F0 (F-Kaz 8)||233-233||213-245||Ø-Ø.|
|F0 (M-Iraq 8)||233-242||208-231||115-Ø|
|Rare male × A. sinica||F0 (F-sin 7)||Ø-Ø||Ø-Ø||Ø-Ø|
|F0 (M-Iraq 7)||233-254||216-231||115-180|
In the two crosses between a rare male and a female from A. urmiana, the mother amplified a single allele at Apd03 and Apd05, and for Apd02, the mother was heterozygous in the first cross and only amplified a single allele in the second, whereas the father was heterozygous at all three loci. All F1 hybrid offspring of both crosses amplified one paternal allele, whereas they either amplified one maternal allele or showed evidence of a null allele inherited from her.
In the cross between a rare male and a female from Artemia sp. from Kazakhstan, the mother was hetero-zygous at Apd03 and homozygous at Apd02 and failed to amplify, probably due to null alleles at loci Apd05. The male was heterozygous at Apd02 and Apd03 and homozygous at Apd05. All alleles present at the three loci in the father were detected in the five hybrid offspring screened.
In the crosses between rare males and A. sinica females, none of the three microsatellite loci tested amplified successfully in A. sinica. Despite this, in all hybrids, progeny produced one of the paternal alleles amplified. The lack of amplification of these three microsatellite loci in A. sinica was confirmed by checking additional individuals from this species. Microsatellite scoring in crosses between rare males and A. tibetiana females was problematic in both parents and the resulting hybrid offspring, and therefore, paternity analysis was not carried out.
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The presence of fertile males in otherwise partheno-genetic lineages raises questions about their potential role in genetic exchange with sexual species and in generating new parthenogenetic lineages. Here, we have described the presence, frequency, functionality and reproductive potential of parthenogenetically produced rare males in the genus Artemia.
Our results indicate that most diploid partheno-genetic Artemia populations produce males sporadically with a frequency up to 17 per 1000 individuals. Statistical analysis showed three statistically significant male ratio hot spots, Urmia Lake, Bagdad saltern and Bjurliu Lake. Populations showing a higher ability to produce rare males are therefore found in a geographical region around 40°N between the Mediterranean–Caspian basin and the salt lakes region in Kazakhstan, a region where the coexistence with closely related sexual species is more likely. Phylogenetic and phylogeographical analyses suggest that diploid parthenogenetic lineages may be evolutionarily recent (Holocene), having arisen in a region of Central Asia around Iran and Kazakhstan and subsequently expanded towards the Mediterranean and other regions (Muñoz et al., 2010). Our results indicate that male production is a general feature in diploid parthenogenetic Artemia with the possible exception of the most western populations.
Similarly to the pattern found in the obligate parthenogenetic Daphnia pulex (Innes & Hebert, 1988) where some clones have the ability to produce males, whereas others have lost it, there is also intrapopulational variation in the tendency to generate rare males in diploid parthenogenetic Artemia, which differs between clonal lineages from 0.12% to 0.60% in a population in Salin de Giraud (France) (MacDonald & Browne, 1987), which could explain our results. However, the role of genetic vs. environmental effects in the ability of diploid parthenogenetic Artemia to produce rare males should be the focus of further studies.
DNA barcoding confirmed the identity of the rare males produced by diploid parthenogenetic Artemia populations. The haplotypes of most of the rare males analysed were identical to those of diploid partheno-genetic Artemia females. COI haplotypes of rare males form two main mtDNA clades, the more widespread one is closely related to the sexually reproducing Artemia sp. from Kazakhstan that is awaiting formal description, and the second one is found only in four diploid parthenogenetic populations and is more closely related to A. urmiana. These results agree with previous studies of phylogenetic relationships of diploid parthenogenetic populations, indicating close phylogenetic relationships between diploid parthenogenetic Artemia and both A. urmiana and Artemia sp. from Kazakhstan (Baxevanis et al., 2006; Muñoz et al., 2010; Maniatsi et al., 2011). The haplotypes of some rare males, although related to haplotypes in rare males of other parthenogenetic populations, differed from the common haplotypes in females sequenced from their own population. The intrapopulation variability in the propensity to generate males reported in Artemia (MacDonald & Browne, 1987) mentioned above may explain this discrepancy between the haplotypes of rare males and the common haplotypes in the females of their populations, as this would be expected if, by chance, rarer lineages in the population (bearing rarer mtDNA haplotypes) had a higher propensity to produce males. In addition, as we had no available sequences from Xiaotan population females to compare with their divergent rare male haplotypes, further analyses are needed to understand the genetic diversity held by parthenogenetic Artemia populations, as these haplotypes had never been reported before. Overall however, it is clear that in most populations, rare males have the same haplotype as the parthenogenetic females from their populations, and these haplotypes were identical, or closely related, to haplotypes previously found in diploid parthenogenetic lineages.
Discriminant analysis proved to be a useful tool to separate Artemia rare males into different morphological clusters. Rare males differed morphologically from both A. urmiana and A. tibetiana males, whereas they were more similar to males from Kazakhstan Artemia sp. and from A. sinica. In a previous analysis (Triantaphyllidis et al., 1997), the morphology in Artemia was studied through a discriminant analysis, but the sexual and the parthenogenetic populations were analysed separately and parthenogenetic males were not included in the analysis. In that work, the sexual population from Kazakhstan appears morphologically close to A. sinica, but it is considered a different species (Triantaphyllidis et al., 1997). Possibly, rare males show higher morphological variability than the males from the Asian sexual species, because similar results are obtained when parthenogenetic females were compared with the sexual females (Mura et al., 2006; Amat et al., 2007). This could be explained by the heterogeneous geographical origin of parthenogenetic lineages (from Portugal to the Chinese coast) and the inability for them to interbreed.
The results of cross-mating experiments were used to evaluate the fertility and the reproductive potential of rare males. There are different kinds of isolating mechanisms which determine the degree of divergence among populations: (i) inability of the two populations to live in the same medium (habitat isolation); (ii) failure of the male to clasp the female (ethological isolation); (iii) failure to produce a viable F1 (mechanical isolation, gametic or zygote mortality or hybrid inviability); and (iv) hybrid sterility (absence of an F2 or production of a deficient F2) (Mayr, 1963). Our findings show that rare males from obligate parthenogenetic diploid A. parthenogenetica populations (i) often coexist in the same habitat as sexual Asian species and (ii) show normal pairing behaviour with central Asia sexual females, excluding the first two isolating mechanisms described above. We also showed that (iii) rare males are fully functional and capable of fertilizing eggs from females of sexual Asian species, and hybrid crosses resulted in similar or higher offspring viability than the controls, in both ovoviviparous and oviparous broods. We (iv) obtained live nauplii from ovoviviparous F1 hybrid broods, which, upon culture, were morphologically normal and produced viable hybrid sexual populations (unpublished results).
The paternity analysis using microsatellite markers further shows that rare males from a parthenogenetic population undergo normal meiosis, produce viable haploid sperm and contribute to the genetic material of the hybrid offspring when mated with females from three of four sexual Asian Artemia species (A. urmiana, Artemia sp. from Kazakhstan and A. sinica). Given that this set of microsatellite loci were developed initially for diploid parthenogenetic Artemia (Muñoz et al., 2009), it is not surprising that we found evidence of null alleles in some mothers for some loci, whereas the fathers (rare males of the diploid parthenogenetic lineage) amplified well and show a high degree of heterozygosis. Despite the fact that this set of microsatellites failed to amplify in A. sinica females, the cross gave informative results because the F1 offspring obtained when mating rare males with A. sinica inherited one paternal allele.
In an early pioneering work, Bowen et al. (1978) obtained four rare males – which they called exceptional males – from three diploid parthenogenetic Artemia populations. They documented a transfer of genes from a Yamaguchi (Japan) parthenogenetic population rare male to an A. urmiana female by polymorphism of three genetic markers (one haemoglobin and two esterase isozymes). They also obtained viable offspring mating a rare male from a Madras (India) parthenogenetic population with an A. franciscana female and documented transfer of genes from this male to the hybrid offspring. However, and in agreement with previous results (MacDonald & Browne, 1987), we have been unable to obtain viable offspring when mating A. franciscana females with rare males (unpublished results). Our study has considerably extended these early experiments, as we have produced more than 250 hybrid broods between rare males and Central Asian sexual females.
Artemia is one of the few known examples of parthenogenetic animal species that produce functional males. These rare males can successfully mate with congeneric sexual females, transmitting their genes to their diploid highly viable F1 offspring. Such ability makes the brine shrimp an exceptional model system to study the evolutionary process and to investigate the potential of these rare asexual males in generating new partheno-genetic lineages. In the absence of available coexisting sexual relatives, parthenogenetic lineages producing rare males or investing in male function incur a fitness cost compared with parthenogenetic lineages not producing such males (D'Souza & Michiels, 2010; Neiman et al., 2012). Although the costs of producing rare males might be regarded as very low, the highly competitive conditions in Artemia populations, where rapid reproduction and resource limitation can be important, make it possible that this ability has persisted due to compensating direct or indirect benefits to the parthenogenetic lineage. An indirect benefit can be obtained if male production is linked to an advantageous trait, for example if males were the product of sex chromosome recombination during automixis, and parthenogenetic strains producing more males were benefiting from increased recombination rates generating more diverse offspring or purging deleterious alleles. As our results suggest, in the presence of potential partners such as sexual females of related species, rare male production could also obtain direct benefits as such rare males can produce fertile hybrid offspring as a result of mating with sexual females. In addition, these Artemia diploid parthenogenetic males might be able to transmit the parthenogenesis trait to their offspring (Lynch, 1984; Eads et al., 2012), a topic that will be the subject of a future study. Alternatively, rare male production might persist in populations due to genetic drift, as genetic bottlenecks are likely to occur during colonization and migration between habitats, is likely to be constrained by habitat monopolization (De Meester et al., 2002; Muñoz et al., 2008, 2009). More research is needed into the cytological mechanisms behind rare male production, to understand the genetic basis of the variation in male production rates among and within populations and potential interactions between genetic and environmental effects into rare male production.
The occurrence and potential reproductive role of parthenogenetic Artemia rare males led MacDonald & Browne (1987) and Browne & Bowen (1991) to suggest that cross-fertilizations of sexual females by parthenogenetic males could provide a source of gene flow between the different genotypes. Further, Abreu-Grobois & Beardmore (1982) suggested that fertilization by rare males might result in the generation of polyploid parthenogenetic Artemia lineages. Recent mitochondrial DNA and microsatellite analysis of polyploid parthenogenetic Artemia strains (Maniatsi et al., 2011) suggests that triploid strains might have originated by fertilization of an unreduced ovum by a partheno-genetic rare male. Further research is needed to fully understand the evolutionary role of rare males into the origin of polyploid parthenogenetic Artemia.
Our work demonstrates the functionality of rare males and, given that co-occurrence between these rare males and sexual species is common in Central Asia, suggests an evolutionary role for males of parthenogenetic origin through hybridization and genetic exchange between parthenogenetic and sexual Artemia lineages through hybridization via rare males.
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We thank Anna Badosa and Jennie Brigham for their technical help using the Beckman sequencer. We would like to thank Fernando Pacios for his analyses with the ArcGis program. Authors are especially grateful to all those colleagues and institutions that provided Artemia cyst samples during over three decades. We thank Dave Lunt for constructive comments in previous versions of this manuscript, and the comments of two anonymous reviewers. This study has been funded by the Plan Nacional CGL2008-03277 project, sponsored by Spanish Government MICIN. AG was supported by a National Environment Research Council (NERC) Advanced Fellowship (NE/B501298/1). MM was supported by a fellowship of the JAE Program from CSIC and European Social Fund.
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- Supporting Information
|jeb12191-sup-0001-TableS1.doc||Word document||62K||Table S1 Results of statistical tests on proportions of offspring quality in cross-breeding experiments in ovoviviparous and oviparous broods between Artemia urmiana (URM), Artemia sinica (SIN), Artemia tibetiana (TIB), Kazakhstan sp. (KAZ) and diploid parthenogenetic Artemia rare males (PD) (hybrid crosses) and in conspecific crosses (controls).|
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