What Does Coco Mean Sexually - T-Tees - Your Answers Await, Life's Questions Unraveled

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Abstract

Introduction

Around 6 % of all flowering plants are dioecious, meaning that each individual is functionally either male or female (Renner 2014). Dioecy occurs in many families of flowering plants, and even within genera of otherwise monoecious species, indicating that the condition has evolved independently many times (Charlesworth 2002; Janousek and Mrackova 2010; Renner 2014) and in evolutionary terms is usually short-lived (Lewis 1942). Genetic mechanisms for dioecy vary widely, with one of the most common being the XY system (e.g. mammals)—in which an X chromosome, conferring recessive femaleness, pairs with a Y chromosome bearing the dominant genes associated with maleness. Other genetic mechanisms associated with dioecy are the ZW system (e.g. birds), in which the female is heterogametic, and multiple sex chromosome systems, in which the sex of an individual is determined by X/autosome ratios (e.g. in Drosophila, and Rumex acetosa; Parker and Clark 1991).

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In theory, both the XY and ZW systems of sex determination should produce equal numbers of male and female progeny. However, biased sex ratios occur for a variety of ecological, genetic and physiological reasons that have been the subject of much research. One factor that may lead to bias is the intensity of pollination, with high intensities favouring female pollen (Stehlik and Barrett 2005; Stehlik et al. 2008). In this case, the reason is the accumulation of deleterious mutations in Y chromosomes as a result of low recombination, which reduces the vigour of ‘male’ pollen tubes, so that the successful pollen is more likely to be female (Muller 1964). Other genetic causes for biased sex ratios are inbreeding levels (Bailey and McCauley 2005; Barrett and Case 2006) and sex chromosome segregation distorters (Taylor and Ingvarsson 2003; Meiklejohn and Tao 2010). Ecological causes include variation in male tree density (Pickup and Barrett 2013), relative distances of seed and pollen dispersal (de Jong et al. 2002) and resource availability (Vandepitte et al. 2010; Adam et al. 2011).

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Many long-lived dioecious plants, including several palms (Arecaceae), are economically or ecologically important (Henderson et al. 1995). For palms such as Borassus flabellifer and Phoenix dactylifera, which are commercially important for their fruits, female plants are clearly of more value than males. Being able to determine the sex of plants at an early stage avoids the need to grow large numbers of unproductive male plants. Recently, sex-determination methods using genetic markers have been developed, though some of these are inconvenient to use, poorly reproducible or costly (reviewed in Milewicz and Sawicki 2013).

This paper concerns the dioecious coco de mer palm, Lodoicea maldivica (J. F. Gmel.) Pers., which is an endemic palm of two small islands in the Seychelles, and a species of both economic and conservation importance. Lodoicea belongs to the tribe Borasseae (Arecaceae), which has a Gondwanaland distribution and in which dioecy is clearly an old-established trait (Dransfield et al. 2008). In its natural habitat, Lodoicea has a very prolonged immature phase, lasting as much as 50 years, during which it is impossible to distinguish between the sexes. Previous studies have shown that adult populations of Lodoicea often exhibit biased sex ratios, but it is unclear whether this bias is due to unequal numbers of males and females being ‘born’ or to differential rates of mortality subsequently (Fleischer-Dogley 2006).

We developed a novel molecular method that enabled us to determine the sex of immature Lodoicea. We applied this method to study sex ratios in sub-populations of Lodoicea, and investigate how these ratios change with age. We discuss the results in the context of the growing knowledge base on genetic and environmental factors influencing sex determination in dioecious plants, including the effects of parental pair relatedness, realised pollination distances and pollen availability, and we consider the implications for sustainable management of this emblematic species.

Methods

Study area and species

Lodoicea maldivica is endemic to the Seychelles (lat. 4°S, long. 55°E). Prior to the discovery of Praslin in 1743 (Bailey 1942), Lodoicea grew in dense monodominant stands that covered both Praslin (37 km2) and Curieuse (2.73 km2) (Brayer du Barre 1773, quoted in Fauvel 1909). However, due to exploitation for timber and the increasing demand from tourists for nuts, as well as several serious fires, the Lodoicea forests have recently become severely degraded, and there is now very little natural regeneration (Rist et al. 2010). The species is classified as endangered (Fleischer-Dogley et al. 2011) and the only remaining large populations are in the southern part of Praslin (where areas are still partially connected) and on Curieuse. In the north of Praslin and some areas on Curieuse, the species persists mainly as isolated individuals or in small patches, in scrubby habitat.

The reproductive structures of the two sexes are very distinct (Fig. 1). Females produce inflorescences that bear between one and thirteen (Morgan et al. 2017a) of the largest flowers of any palm (~5 cm diameter), on a zigzag rachilla (Fig.1A). Male palms bear large catkins, 1.2- 1.8 m long (Corner 1966) and 8- 10 cm wide, consisting of 60-70 spirally arranged fragrant, yellow flowers embedded in leathery bracts (Fig.1B).

The seed (nut) of Lodoicea is the largest in the plant kingdom, with a mean fresh weight in the Vallée de Mai of 8.5 kg (Morgan et al. 2017a). Thanks to their unusual form, these seeds are highly sought after as souvenirs and fetch a price of €190- 450 each (Rist et al. 2010). Together, the sale of seeds and fees paid by visitors to the Vallée de Mai UNESCO World Heritage Site (Seychelles Islands Foundation 2009, unpubl. report) make a significant contribution to the Seychelles economy. Being able to identify female plants at seedling or juvenile stage would be useful both for conservation management and for the commercial production of nuts.

Development of Lodoicea sex-linked markers

Sequencing and bioinformatics

We identified potential sex-linked genetic markers using the approach of Scharmann et al. (2019). Genomic DNA was extracted from the leaf tissue of 20 male and 20 female trees, following an optimised version (Morgan et al. 2016) of the DNeasy® 96 Plant Kit (Qiagen, Hombrechtikon, Switzerland) manufacturer’s protocol. The genomes of the 40 individuals were sequenced using a ddRAD protocol (Peterson et al. 2012), with the restriction enzymes ecoRI and TaqI. The library with 40 individuals was sequenced in a single Illumina HiSeq 2500 lane for 136-bases single-end reads. Raw reads were de-multiplexed and quality-filtered (the entire read was discarded if quality dropped below Phred 20 in any window of 15 % read length) using process_radtags.pl from the Stacks pipeline (Catchen et al. 2013). Reads were mapped (following a customised dDocent-like pipeline; Puritz et al. 2014) against six different de novo reference assemblies, in order to reduce the chance of false positives caused by arbitrary choice of the assembly method. Using the reads of all 40 individuals, three alternative single-end references were assembled with identity cutoffs 0.8, 0.9 and 0.95 in clustering steps (vsearch, https://github.com/torognes/vsearch) and cd-hit-est (Li and Godzik 2006). Additionally, three alternative paired-end references were assembled (rainbow, Chong et al. 2012) using the reads of one male and one female sequenced on an Illumina MiSeq instrument (identical library protocol). This was done with reads trimmed to 146 bases to identity cutoffs 0.9 and 0.95 (cd-hit), and also with reads trimmed to 140 bases for identity cutoff 0.95. Single-end reads from the 40 individuals were mapped to each reference and formed the basis of the scan for male- or female-specific sequences.

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Each individual was represented by an average of 2.9 million filtered reads (min. 370 000, max. 4.9 million), of which between 59 and 89 % (depending on the reference) could be mapped using bwa-mem (Li 2013) at a quality of ≥ 1. Presence/absence statistics (samtools, Li et al. 2009) for all individuals and reference contigs were then subjected to the privacy rarefaction procedure of Scharmann et al. (2019) (https://github.com/mscharmann/privacy-rarefaction). This algorithm separates real biological genomic presence/absence from stochasticity, yielding a list of contigs that, with high confidence, occur in one of the two sexes exclusively (with bootstrap support).

For all six Lodoicea reference assemblies, privacy rarefaction resulted in a divergence in counts of male- and female-specific candidates with increasing stringency, which is characteristic for organisms with sex chromosomes (Scharmann et al. 2019). More precisely, only male-specific candidate markers were obtained with high confidence, whereas apparent female-specific candidate markers were revealed as false-positives. This result is characteristic of a male-heterogametic system, and hence the existence of Y-chromosomes (Scharmann et al. 2019), although the Y-specific sequences were overall extremely rare. Consequently, we identified male-specific contigs suitable for a molecular sexing assay. From each reference assembly, we retained all contigs receiving at least 50 % bootstrap support for male specificity at stringency level ≥ 3. We enhanced the sequence length of these contigs by blasting for 100 % identical and full-length aligned matches in the unassembled (but quality filtered) 150-bases paired-end reads from the MiSeq run. The non-redundant candidate male-specific contigs (cd-hit-est at similarity 1.00) were ranked according to the cumulative support they received (sum of the passed stringency levels over all alternative reference assemblies), and the top 11 were used for primer design [see Supporting Information—Text S1]. [Detailed results for each scan can be found in Supporting Information—Table S2 (read and mapping statistics per individual), Supporting Information—Figure S2 (candidate contig figures) and Supporting Information—Text S2 (list of contigs with > 50 % bootstrap support)].

Molecular sexing assay

For a subset of eight samples of each sex, band sizes for each of the two male sex-linked markers were quantified via fragment analysis. PCR products (3 µL) from each primer pair were combined and added to 10 µL HIDI formamide and 0.15 µL GeneScan 500 LIZ Size Standard (Applied Biosystems). Samples were denatured for 3 min at 92 °C and then run on an ABI 3730xl automatic capillary sequencer (Applied Biosystems, Waltham, MA, USA). Electropherograms were scored with GeneMarker 2.6.0 (SoftGenetics, State College, PA, USA). Marker Lm123977 (contig ref_SE_cutoff10_vsearch0.8_cdhit0.8__123977_L131+PEcontig1_2103_21536_9724/1 [see Supporting Information—Text S2]) produced a strong peak (~ 9000 RFUs) at 405 bp only in the males, and another small peak (~ 400 RFUs) at 81 bp that amplified in males and females. Marker Lm435135 (contig ref_SE_cutoff10_vsearch0.95_cdhit0.95__435135_L131 [see Supporting Information—Text S2]) produced a peak (~ 8000 RFUs) in the males at 130 bp and a smaller peak (~ 300 RFUs) in both sexes (Table 1).

Gel electrophoresis using a 1.6 % agarose gel with a 100-bp ladder (both Promega) was used to assess the accuracy of the sex-linked markers [seeSupporting Information—Figure S1]. For this, we selected a subset of known female and male adults from across the geographic range. The adult samples (DNA extracted as above) were screened for the two sex-linked markers, along with negative controls and a positive control for each DNA sample (primer pair Lm2407, Morgan et al. 2016). No females amplified (N = 95 for both primers), while all but one of males amplified (Lm123977 N = 105; Lm435135 N = 98). The same male sample failed to amplify with both primer pairs. DNA samples of all Lodoicea offspring (see ‘Sample Collection and genotyping’ below) were screened using the two sex-linked markers, and positive and negative controls. Offspring sex assignments were determined with gel electrophoresis, and these were used for all future analyses.

Exploring sex ratios in sub-populations of Lodoicea maldivica across age cohorts

Sample collection and genotyping

Leaf samples from across the whole of Lodoicea’s natural range (Fig. 2) were collected for DNA extraction. Plants were classified according to their growth stage: ‘adults’ were reproductive individuals producing flowers, ‘adolescents’ were non-reproductive individuals with a trunk, ‘juveniles’ were trunkless individuals with more than two leaves, ‘seedlings’ had one or two leaves, and ‘young seedlings’ were plants that had been weighed and measured as seeds in 2013, having been extracted from freshly fallen fruits, and allowed to germinate close to where they were found. We use the term ‘offspring’ to refer to all immature plants.

We sampled offspring from four naturally regenerating dense clusters of individuals showing minimal signs of human disturbance (Morgan et al. 2017b) within each of the four main sub-populations of Lodoicea: on Praslin (Vallée de Mai (VdM), Fond Peper (FP) and Fond Ferdinand (FF)), and on Curieuse (CU) (N = 493). Additionally, we sampled offspring from locations in the northern part of Praslin (Cherie Mon and Zimbabwe) and other areas outside of clusters in VdM (N = 48). We also sampled the bayonets (first leaf spikes) or first leaves of young seedlings in VdM and FP (N = 49) (total offspring N = 589), as well as leaf tissue from potential mother (N = 100) and father (N = 659) trees in the four sub-populations.

DNA extraction and genotyping of individuals at 12 polymorphic microsatellite loci were carried out as described by Morgan et al. (2016). We used genotype data for adults and offspring within clusters from Morgan et al. (2017b), and also genotyped additional offspring and young seedlings from outside the clusters [seeSupporting Information—Table S1 for allele frequencies of additional samples]. Fragment analysis and scoring were carried out as in Morgan et al. (2016).

Population surveys

A census of adult Lodoicea conducted in 2004 found that sex ratios in most populations in the native range were skewed/biased (data from Fleischer-Dogley (2006), presented in Table 2). We statistically tested deviation from a balanced sex ratio using an exact binomial test (two-sided) with the function stats::binom.test v. 3.1.2 (R Core Team 2014) in the RStudio environment v. 0.98.1102 (RStudio Team 2015). We also tested the effects of a number of ecological and genetic factors (see below) on the sex ratios of the offspring, in the same way (for female and male counts and total sample sizes for each group, see Table 3). We analysed whether the proportions of female offspring differed from the expected 0.5 within (i) each of the four sub-populations, (ii) each of the four clusters within each sub-population, (iii) each of the age cohorts (young seedlings, seedlings, juveniles and adolescent plants), and (iv) the entire sample.

Factors influencing offspring sex

To analyse the effect of pollen flow distance on the sex of offspring, we used data from a maternity analysis from Morgan et al. (2017b). Paternity analysis was determined by the Δ-estimated statistic, using 10 000 simulations, 0.01 error rate at the loci and 0.961 loci typed, using the software CERVUS 3.0 (Marshall et al. 1998; Kalinowski et al. 2007). We simulated 0.05 candidate fathers that are related to offspring at 0.02. All adult males sampled within a radius of between 80 and 120m from assigned mother trees were considered as potential fathers (assuming 0.5 pollen donors sampled). The strict confidence level of 95 % for the trio assignment (mother-father-offspring) was used. Combined exclusion probabilities for the first and second parents were 0.9961 and 0.9999, respectively.

Realised pollen dispersal distances for each offspring were calculated as the Euclidian distances between the assigned mother and father trees, and we divided offspring into two groups according with pollination events (i.e. assigned parents) less than and greater than the overall median level (≤ 21.9 or > 21.9 m).

We also tested directly whether parental relatedness had any influence on the sex of the offspring. For this, we calculated the pairwise kinship coefficient (F; Loiselle et al. 1995) for each parent-pair (SPAGeDI 1.4c; Hardy and Vekemans 2002), using the whole adult plant dataset as the reference sample. We then divided the offspring into two groups according with parental relatedness less than and greater than the overall median level (F ≤ 0.068 or > 0.068).

We also tested whether the proportions of female offspring produced by individual female palms deviated from the expected level. We used maternity assignments to match offspring to mother trees, to test sex production at the finest scale (Morgan et al. 2017b).

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As estimates of pollen availability, we recorded the distance of the mother tree to the nearest adult male, and the number of males within a 10 m radius of the mother. The correlation between each of these measurements and the proportion of female offspring assigned to each mother tree (number of offspring assigned to each mother ranged from 1 to 30, mean = 4.6), was tested using a Pearson’s correlation with the R package stats::cor.test (R Core Team 2014).

Finally, for a sample of 49 seeds planted in 2013, we tested for any relationship between seed size (fresh weight and length) and the sex of the seedling.

Results

Sex ratios of adults and offspring

Both of the markers developed in this study amplified a male-specific band (Lm123977 at 405 bp and Lm435135 at 130 bp), allowing us to reliably determine the gender of immature Lodoicea plants. Previous surveys had shown highly biased sex ratios in three of the four adult sub-populations: Praslin National Park (which includes Fond Peper plus the wider area) and Curieuse had strong female biases (0.604 and 0.542 female; binomial test P < 0.0001 and P = 0.0005, respectively), whereas Vallée de Mai and private land on Praslin had significant male biases (0.432 and 0.467 female; binomial test P < 0.0001 and P = 0.0045, respectively). Only the Fond Ferdinand sub-population showed not significant sex bias.

In contrast, no significant deviation from a 1:1 sex ratio was detected in the entire sample (0.525; Table 3), or within any of the four sub-populations (female ratio range 0.505- 0.570; Table 3) (binomial test all P > 0.05). Equal sex ratios were also observed in all age cohorts of offspring from young seedlings to adolescent trees (female ratios between 0.423 and 0.537, binomial test all P > 0.05). Two female palms, one in VdM and one on CU, did produce offspring with a significant female-bias (11/13 and 10/12 females, respectively; binomial test both P < 0.05; Table 3), yet no apparent reason for this bias could be determined.

Effects of pollen flow distance, genetic relatedness of parent-pairs and male tree density on offspring sex ratios

Realised pollination distances were not related to female-biased sex ratio in adult population (Table 3; all P > 0.05). The range in kinship (F, Loiselle et al. 1995) of parent-pairs of female offspring ranged from -0.145 to 0.409, and in males from -0.192 to 0.392, but the level of relatedness of the parent trees also had no effect on the sex of the resultant offspring (binomial test both P > 0.05).

Pearson’s correlation coefficients were calculated to investigate possible relationships between the proportion of female offspring produced by mother trees and two measures of pollen availability (distance to the nearest male, which ranged from 0.9 to 18.6 m, and number of males within 10 m, which ranged from 0 to 8). However, neither measure yielded a significant relationship (r56 = 0.252, P = 0.06 for distance; r56 = -0.177, P = 0.18 for number of males; [seeSupporting Information—Figure S3]).

Female seeds ranged in fresh weight from 6 to 12 kg, with a mean and SE of 8.9 ± 0.4 kg (N = 23). Male seeds ranged in weight from 3 to 13 kg, with a mean and SE of 8.4 ± 0.5 kg (N = 26; [seeSupporting Information—Figure S4]). The average lengths of female and male seeds were 30.8 (± 0.5) cm and 30.3 (± 0.7) cm, respectively [seeSupporting Information—Figure S4 for details]. We found no relationship between the mass or length of seeds and the sex of the plant (Pearson’s correlation, both P > 0.05).

Discussion

The sex-specific molecular markers for Lodoicea maldivica described here are among the first to be developed for any palm species (but see George and Karun 2011 and Cherif et al. 2013). Using these markers, we were able to determine reliably the sex of immature plants of Lodoicea sampled from across its native range on the islands of Praslin and Curieuse. Although sex ratios of most adult populations were strongly skewed, we detected no departure from a 1:1 ratio in the offspring. We found no environmental effects on sex ratios of immature plants, such as density of male plants and distance to the nearest male. Based upon these results and other available information, we can draw several conclusions concerning the nature of dioecy and the factors influencing sex ratios in Lodoicea.

Dioecy in Lodoicea has a genetic basis and probably involves X/Y sex chromosomes.

The discovery and PCR-validation of male-specific markers but not of female-specific markers suggests the existence of X/Y sex chromosomes. Cytological studies have shown that Lodoicea has 2n = 34, 36 chromosomes (Sharma 1970; Dransfield et al. 2008), but no information is available about the nature of the sex chromosomes. Thus, it is not known whether the X- and Y-chromosomes are homomorphic, as is the case in many plant species, or heteromorphic, as in the genera Silene, Rumex and Cannabis (Westergaard 1958; Parker 1990). In our smallest and largest ddRAD assemblies, in terms of number of total markers, the incidence of male-specific markers when 10 males and 10 females were compared was 5.29/94 968 (0.0056 %) and 0.59/38 830 (0.0015 %), respectively (seeSupporting Information—Figure S2). These proportions of male-specific markers are considerably lower than those detected for other dioecious plants, whether with heteromorphic (Silene latifolia: 1.5 %) or homomorphic (Nepenthes: 0.02-0.1 %; Scharmann et al. 2019) sex chromosomes, leading us to conclude that Lodoicea sex chromosomes are most probably homomorphic. However, given that we do not know the genome size of Lodoicea, the small proportion of male-specific markers could still represent a physically large Y-linked region.

Although information on genome size of Lodoicea is not available, estimates from some of its closest relatives in the tribe Borasseae predict a large genome (Bismarkia nobilis: 1n = 36, 1C = 2 Gb; Borassus flabellifer: 1n = 36, 1C = 8.6 Gb; Latania lontaroides: 1n = 28, 1C = 3.5 Gb, Leitch et al. 2019). Since all borassoid palms are strictly dioecious (Dransfield et al. 2008), it is possible that the Y-chromosomal system of Lodoicea is ancestral in this group. Dioecy has evolved multiple times independently within the palm family, including in the date palm genus, Phoenix (Torres et al. 2018). We suggest that X/Y sex chromosomes in Lodoicea and Borasseae in general are similar to those found in the date palms (Cherif et al. 2013, 2016; Mathew et al. 2014; Maryam et al. 2016), in the sense that they are homomorphic, highly conserved and shared among a larger group of species, although date palms and Borasseae represent two unrelated evolutionary origins of dioecy (Nadot et al. 2016). Further studies on the Lodoicea karyotype and genome, as well as on other genera in the tribe Borasseae, would be useful as a starting point for understanding the evolution of these sex chromosomes.

The two sexes of Lodoicea are ‘born’ in approximately equal numbers.

If the sex of offspring is genetically determined through an X/Y chromosome system, we would expect there to be equal numbers of male and female offspring produced, as is the case in the date palm, Phoenix dactylifera (Saadi 1990). However, various processes operating both pre- and post-zygotically may distort the balanced sex ratio expected from theory.

One prezygotic effect known as certation, occurs through male and female pollen tubes growing at different rates on the stigma (Correns 1922). This effect can lead to a biased sex ratio, especially when because of high pollen availability there is strong competition between male and female pollen. Very often the male pollen is at a disadvantage because of negative mutations that accumulate in the sex-determining region of the Y chromosome. The fact that we found no influence of pollen availability (measured in terms of numbers of male trees and distance to the nearest male) upon the sex ratio of progeny suggests that this source of bias is unimportant in Lodoicea. This, in turn, is consistent with dioecy in Lodoicea being a long established, stable system from which negative mutations have been purged.

The degree of inbreeding may also influence sex determination in dioecious species (Bailey and McCauley 2005; Barrett and Case 2006). For example, a female bias may develop when both pollen and seed dispersal are limited, which tends to increase the inbred population’s relative contribution to the next generation. On the other hand, when seed dispersal is much more limited than pollen dispersal, which appears to be the case for Lodoicea, a male bias would reduce the chance of related individuals being close together and competing for the same resources (de Jong et al. 2002). Lodoicea across all sub-populations are relatively highly inbred with short-distance seed dispersal (Morgan et al. 2017b) and relatively short pollen dispersal (unpubl. data). Our results provide no evidence for such inbreeding effects, despite the fact that natural sub-populations of Lodoicea show high levels of inbreeding associated with an intense fine-scale spatial genetic structure (Morgan et al. 2017b).

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These negative results all point in the same direction—in Lodoicea, the two sexes are produced in equal numbers. Similarly, almost equal sex ratios have also been found in other dioecious tropical palms, including Chamaedorea tepejilote (Oyama 1990) and C. pinnatifrons (Ataroff and Schwarzkopf 1992; as C. bartlingiana), Mauritia flexuosa (Urrego Giraldo 1987) and Phytelephas seemannii (Bernal 1998). The only contradictory results in our study were for two female plants that produced almost exclusively female individuals. The reasons for this are unknown, but could reflect some genetic incompatibility between those particular maternal genotypes and the male sex-determining region of the Y-chromosome, or a cryptic sex-ratio meiotic driver acting, such as those found in Drosophila (Sturtevant and Dobzhansky 1936).

The seeds of Lodoicea are not sexually dimorphic.

Sexual dimorphism in seeds is known to occur in some species, notably Spinacia oleracea (Freeman et al. 1994) and Rumex nivalis (Stehlik and Barrett 2005). Given the high metabolic cost of producing the huge seeds of Lodoicea, it would perhaps not be surprising if female seeds were supplied with more food reserves (Cipollini 2013). Such a dimorphism might lead to more male seeds being produced, especially under conditions of low nutrient availability (Freeman et al. 1981), which would also reduce parent-offspring conflict (Trivers 1974). We found no evidence for such effects; however, male seeds did vary more than female seeds in length and mass, but the mean values of these parameters did not differ significantly between the sexes.

Biased sex ratios in adult populations are the result of differential mortality of mature plants.

Implications for management

Because they develop slowly, the majority of plants in most Lodoicea populations are immature individuals (e.g. 80 % of individuals in VdM are immature; Fleischer Dogley et al. 2011), whose sex could not previously be determined. Our results demonstrate that these immature cohorts have balanced sex ratios, which bodes well for the future of these populations and for maintaining genetic diversity. It is also important from a management perspective that the seeds do not appear to be sexually dimorphic, because it suggests that the current practice of using smaller, misshaped seeds for forest regeneration, while selling the larger, better shaped seeds, will not affect the sex ratios of populations in the future. It would be worth repeating this study with a larger sample; however, to confirm our provisional conclusion that seeds are not sexually dimorphic.

Lodoicea nuts attract high prices and are a desirable commodity. They could potentially be grown commercially, which as well as increasing revenue might reduce the poaching of nuts from protected areas, enabling ex situ conservation and supporting the selection of balanced sex ratios of populations in botanic gardens. If commercial production were to be established, the method for sex determination described here would be very useful for setting out plantations of predominantly female plants. In addition, our molecular sexing might be applicable to other species within the tribe Borasseae, notably the economically important Borassus flabellifer.

Supporting Information

The following additional information is available in the online version of this article—

Figure S1. Digital photograph of agarose gel after electrophoresis of female and male Lodoicea maldivica PCR products, amplified with the Lm123977 marker.

Figure S2. Privacy rarefaction plots showing evidence for male-specific (Y-hemizygous) contigs in Lodoicea, based on six alternative reference assemblies.

Figure S3. Proportion of female offspring produced by each Lodoicea maldivica mother tree (N = 58), in relation to: (a) the isolation distance of their mother tree to the nearest male Lodoicea (regression line of the non-significant relationship; r = 0.252, P = 0.06); and (b) the number of male Lodoicea within a 10 m radius of their mother tree (regression line of the non-significant relationship; r = -0.177, P = 0.18).

Figure S4. Boxplots showing (a) masses (kg) and (b) lengths (cm), of female and male Lodoicea maldivica seeds (N = 49).

Table S1. Genetic properties of 12 microsatellite markers in Lodoicea maldivica offspring.

Table S2. Read and mapping statistics per individual (20 females and 20 males) for six alternative de novo reference assemblies.

Text S1. Sex-linked marker design for Lodoicea maldivica.

Text S2. Candidate male-specific contigs obtained from privacy rarefaction, and screened during development of molecular sexing primers.

Data

Demultiplexed Illumina sequencing data (ddRAD) produced for this study were deposited at the European Nucleotide Archive ENA (https://www.ebi.ac.uk/ena) under accession number PRJEB34653. Remaining data are included as Supporting Information.

Sources of Funding

This research was funded by Eidgenössische Technische Hochschule Zürich (ETH-37 12-1). C.N.K-B. received funding from the Deutsche Forschungsgemeinschaft (KA 3349/2-1 and KA 3340/3-1). Support was provided by the Rübel Foundation.

Contributions by the authors

E.J.M, C.N.K-B., P.J.E. and C.J.K. conceived the ideas and designed the methodology. F.F-D. made fieldwork possible. E.J.M. conducted the field and laboratory work. C.N.K-B., P.J.E., F.F-D. and C.J.K provided advice and input to field work. C.N.K-B., P.J.E. and C.J.K. supervised data analysis. M.S. designed and conducted bioinformatics analyses. A.W. provided advice and made marker design possible. E.J.M wrote the initial draft of the manuscript. E.J.M., C.N.K-B., P.J.E. and C.J.K reviewed and edited subsequent versions of the manuscript, with contributions from M.S. and A.W. All authors gave final approval for publication.

Evolution & Diversity. Chief Editor: Jeremy Beaulieu

Acknowledgements

We thank Seychelles Islands Foundation, Ravin de Fond Ferdinand Nature Reserve, Seychelles National Parks Authority and GVI Seychelles for research support and permission to work at the study sites. In particular, Marc Jean-Baptiste, Wilna Accouche, Nancy Bunbury, Estephan Germain, Allen Cedras and Chris Mason-Parker were invaluable for the facilitation of fieldwork and providing advice. Additionally, we thank Gerry Rose and Fabio Lesperance for field work help, and Kirsti Määttänen for lab assistance. DNA extractions, library preparation and sequencing were carried out by Claudia Michel. Permission to conduct research, and export of samples was granted by the Seychelles Bureau of Standards and the Ministry of Environment, Energy and Climate Change, respectively. Fragment analysis was carried out at the Genetic Diversity Centre (GDC) ETH Zürich. Keygene N.V. owns patents and patent applications protecting its Sequence Based Genotyping technologies.

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