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Functional chloroplasts in metazoan cells - a unique evolutionary strategy in animal life
Frontiers in Zoology volume 6, Article number: 28 (2009)
Among metazoans, retention of functional diet-derived chloroplasts (kleptoplasty) is known only from the sea slug taxon Sacoglossa (Gastropoda: Opisthobranchia). Intracellular maintenance of plastids in the slug's digestive epithelium has long attracted interest given its implications for understanding the evolution of endosymbiosis. However, photosynthetic ability varies widely among sacoglossans; some species have no plastid retention while others survive for months solely on photosynthesis. We present a molecular phylogenetic hypothesis for the Sacoglossa and a survey of kleptoplasty from representatives of all major clades. We sought to quantify variation in photosynthetic ability among lineages, identify phylogenetic origins of plastid retention, and assess whether kleptoplasty was a key character in the radiation of the Sacoglossa.
Three levels of photosynthetic activity were detected: (1) no functional retention; (2) short-term retention lasting about one week; and (3) long-term retention for over a month. Phylogenetic analysis of one nuclear and two mitochondrial loci revealed reciprocal monophyly of the shelled Oxynoacea and shell-less Plakobranchacea, the latter comprising a monophyletic Plakobranchoidea and paraphyletic Limapontioidea. Only species in the Plakobranchoidea expressed short- or long-term kleptoplasty, most belonging to a speciose clade of slugs bearing parapodia (lateral flaps covering the dorsum). Bayesian ancestral character state reconstructions indicated that functional short-term retention arose once in the last common ancestor of Plakobranchoidea, and independently evolved into long-term retention in four derived species.
We propose a sequential progression from short- to long-term kleptoplasty, with different adaptations involved in each step. Short-term kleptoplasty likely arose as a deficiency in plastid digestion, yielding additional energy via the release of fixed carbon. Functional short-term retention was an apomorphy of the Plakobranchoidea, but the subsequent evolution of parapodia enabled slugs to protect kleptoplasts against high irradiance and further prolong plastid survival. We conclude that functional short-term retention was necessary but not sufficient for an adaptive radiation in the Plakobranchoidea, especially in the genus Elysia which comprises a third of all sacoglossan species. The adaptations necessary for long-term chloroplast survival arose independently in species feeding on different algal hosts, providing a valuable study system for examining the parallel evolution of this unique trophic strategy.
Coevolution of host organisms and their specialized consumers, such as small-bodied herbivores or parasites, has been a major driver of speciation in terrestrial ecosystems [1–5]. For instance, tolerance of plant chemistry has facilitated shifts among chemically similar hosts by phytophagous insect lineages; novel hosts then act as distinct selective environments, fuelling the rapid evolution of host races and adaptive diversification of insects [6–11]. Characters associated with host exploitation, such as feeding or detoxification of secondary metabolites, therefore warrant special attention as evolutionary innovations that contribute to biodiversity [12–15]. Such traits have rarely been studied in aquatic systems, however, where the role of ecological associations in speciation remains poorly understood [16–20].
A rare adaptation that rests somewhere between endosymbiosis and predation is the retention of functional chloroplasts within the bodies of herbivores. Termed kleptoplasty, this phenomenon is documented in several marine protists including foraminifers , dinoflagellates  and ciliates . However, chloroplast retention in the Metazoa is known only in the gastropod taxon Sacoglossa, a group of herbivorous sea slugs that feed mainly on green algae in the Ulvophyceae sensu Floyd and O'Kelly [24–32]. Taylor  mentioned kleptoplasts in the digestive system of another metazoan species, the rotifer Ascomorpha ecaudis. Subsequent investigations identified these "organelles" as whole algal organisms, usually called zoochlorellae .
Kleptoplasty may facilitate crypsis because plastids impart the host's color to the slug (Figures 1 and 2). However, the chief adaptive value is likely the nutritional benefit of photosynthetic assimilates released from chloroplasts into the slug cells [35–39]. This additional energy provided by the plastids may enhance slug survival during times of algal scarcity, when calcification impedes feeding, or when slugs migrate off of hosts in search of mates, new habitat patches or sites for oviposition [40, 29, 41, 42].
Past studies indicated that sacoglossans vary widely in their capacity for photosynthesis [43, 38]. However, the range of methods used to quantify plastid activity impedes generalization across studies. Using a Pulse Amplitude Modulated (PAM) Fluorometer, Wägele and Johnsen  demonstrated photosynthetic activity in Plakobranchus ocellatus, Elysia expansa and Thuridilla gracilis (as T. ratna), but detected no activity in Cyerce nigricans (Figure 1). Using the same methods over a longer time period, Evertsen et al.  demonstrated long-term retention of chloroplasts in Plakobranchus ocellatus and E. timida, whereas other Elysia spp. and T. hopei lost photosynthetic activity within a few days (Figures 1 and 2). The record for chloroplast retention is 14 months for E. chlorotica.
Wägele  postulated that functional kleptoplasty was a key character in the Sacoglossa, enhancing speciation by opening new adaptive zones. Although different efficiencies in chloroplasts' retention are known now for several decades, neither any attempt has been made to understand evolutionary history of this unique phenomenon within a metazoan group, nor the assumption of being a key character has ever been tested. We hypothesize that: 1. kleptoplasty is a key character promoting adaptive radiation in this group, 2. different stages in the evolution of kleptoplasty occurred and derived species are able to uphold photosynthetic activity better and longer, 3. a correlation of photosynthetic activity and sequestered food items exists. Testing these hypotheses requires a robust phylogeny. We therefore developed a phylogenetic hypothesis for the Sacoglossa based on molecular data.
We present data on photosynthetic rates for 29 species (186 specimens) representing all major groups within the Sacoglossa, including three of the four species known for high photosynthetic activity - Plakobranchus ocellatus (Indo-Pacific Ocean), E. timida (Mediterranean Sea) and E. crispata (Caribbean Sea) (Figure 1). Bayesian methods were used to infer phylogenetic relationships among extant taxa from nuclear and mitochondrial gene sequences, and to model the evolution of kleptoplasty based on new plastid retention data.
Molecular phylogeny of Sacoglossa
A molecular phylogenetic analysis of the Sacoglossa was undertaken to test conventional systematic groupings based on morphology (Table 1) , and to enable comparative analyses of trait evolution. Cylindrobulla beauii was designated as the outgroup for the analyses of Sacoglossa (see ).
Sequences for a given species were generated in either Bonn, Germany or Los Angeles, California, U.S.A. For phylogenetic analysis, a concatenated dataset was generated from partial sequences of the mitochondrial 16S rDNA and coxI genes, and a partial sequence of the nuclear 28S rDNA gene. Loci were sequenced for at least two specimens of each species if specimens were available to confirm results for that taxon. In Bonn, some of the new 28S and coxI sequences were amplified from DNA extracts of the same specimens used previously by Händeler and Wägele  from which 16S sequences were obtained. All coxI, 16S and 28S sequences generated in Los Angeles were from a single specimen of each species. The final data set consisted of 72 sequences representing 63 nominal species (additional file 1).
DNA was extracted from alcohol-preserved specimens by means of NucleoSpin® Tissue-Kit by Machery-Nagel or Dneasy® Blood and Tissue Kit by Qiagen, following manufacturer's recommendations. Sequences were downloaded from Genbank or were generated using the following protocols and primer sequences given in Table 2.
A portion of the coxI gene was amplified and sequenced in Bonn/Germany using primers LCO1490 and HCO2198. Amplification reactions (50 μl) consisted of 39.15 μl ddH2O, 5 μl 10× PCR Buffer without MgCl2 (Fermentas), 4 μl MgCl2 (25 mM), 0.15 μl Taq-Polymerase (5 U/μl), 0.4 μl of each Primer (10 pmol/μl) and 0.5 μl DNA. The PCR was carried out in the Gene Amp PCR System 9600 by Perkin Elmer® under following conditions: 95°C for 240 s, followed by 9 Touch-down-cycles of 45 s at 94°C, 45 s at 56(-1)°C, 90 s at 72°C, followed by 25 amplification-cycles of 45 s at 94°C, 45 s at 48°C, 90 s at 72°C and a final extension at 72°C for 10 min followed by cooling down to 4°C. Amplicons were purified by means of NucleoSpin® Extract II by Machery-Nagel, guided by the enclosed protocol. The mass of the amplicons was estimated by comparing ethidium bromide staining intensity of 5 μl of each purified reaction. Cycle sequencing reactions (Cycle Sequencing Kit BigDye® Terminator v1.1 by Applied Biosystems) were carried out in the Gene Amp PCR System 9600 by Perkin Elmer® under following conditions: 96°C for 120 s followed by 15 cycles of 10 s at 96°C, 5 s at 50°C, 150 s at 60°C followed by cooling down to 4°C.
Partial sequences of the nuclear 28S rDNA gene were produced in Bonn/Germany by amplifying with primers 28SC1 and 28SD3. Amplification reactions (50 μl) consisted of 39.15 μl ddH2O, 5 μl 10× PCR Buffer without MgCl2 (Fermentas), 4 μl MgCl2 (25 mM), 0.15 μl Taq-Polymerase (5 U/μl), 0.4 μl of each Primer (10 pmol/μl) and 0.5 μl DNA. The PCR was carried out in the Gene Amp PCR System 9600 by Perkin Elmer® under following conditions: 95°C for 240 s, followed by 38 amplification-cycles of 30 s at 94°C, 30 s at 52.5°C, 150 s at 72°C and a final extension at 72°C for 10 min followed by cooling down to 4°C. Amplicons were purified by means of NucleoSpin® Extract II by Machery-Nagel, guided by the enclosed protocol. The mass of the amplicons was estimated by comparing ethidium bromide staining intensity of 5 μl of each purified reaction. Cycle sequencing reactions (Cycle Sequencing Kit BigDye® Terminator v1.1 by Applied Biosystems) were carried out in the Gene Amp PCR System 9600 by Perkin Elmer® under following conditions: 96°C for 120 s followed by 15 cycles of 10 s at 96°C, 5 s at 50°C, 150 s at 60°C followed by cooling down to 4°C. Internal primers 28SC2F(C2')*, 28SD2F, 28SD2R and 28SC2R(C2)* were used if necessary to gain both strains. Reaction products were sequenced using an ABI PrismTM 377 DNA Sequencer by Applied Biosystems or with service of Macrogen inc, Korea.
Partial sequences of the coxI and 16S genes were produced in Los Angeles, California, U.S.A. as described in Ellingson and Krug . Partial 28S sequences were generated as described in Krug et al. .
Sequences were aligned using the web server of MAFFT [51, 52]. Because different primers were used by our respective labs to amplify 28S, sequences produced in Los Angeles were cut to end with sequences produced with primers 28S1 and 28SD3. The coxI data showed evidence of mutational saturation at the 3rd codon position, thus only the 1st and 2nd codon positions were included in phylogenetic analysis. Final length of aligned and concatenated sequences was 2117 bp: 28S rDNA gene, positions 1-1220, 16S rDNA gene, positions 1221-1679, and coxI (1st and 2nd position), positions 1680-2117.
Phylogenetic analysis by Bayesian Inference was performed using Metropolis-Coupled Markov-Chain Monte Carlo methods as implemented in the program BayesPhylogenies . This program uses a mixture model to accommodate among-site heterogeneity in patterns of sequence evolution. Parameters are estimated for a user-defined number of general time reversible (GTR) models of sequence evolution, and the most likely model is assigned to each position in the alignment. Mixture models should equal or out-perform analyses that assign one model to all sites in a given gene or codon partition. Our analyses used three GTR models, each estimating base composition separately and including a parameter for gamma-distributed rate heterogeneity (4 rate classes). Four chains (three heated and one cooled) were run for 2,65 million generations, sampling trees every 1000 iterations of the Markov chain. Based on inspection of log-likelihood scores, the first 1,650 trees were discarded as burn-in. From the retained tree sample, a 50% majority-rule consensus phylogram was constructed with mean branch lengths in the program BayesTrees, and posterior probabilities calculated to estimate nodal support.
The additional file 2 provides details of the specimens and species used in the present study for analysing retention of chloroplasts. Analyses of photosynthetic activity were performed with a Pulse Amplitude Modulated Fluorometer (DIVING PAM, Walz, Germany) by measuring the maximum quantum yield of chlorophyll a fluorescence in photosystem II usually within the first day after collection of animals from their food algae (with the exception of Plakobranchus and Thuridilla species, where food source is not known). The fiber optics from the PAM were usually placed five mm above the animal. Measurements were taken with chloroplasts acclimated to darkness, thus with all reaction centres open and a minimal fluorescence emission. While measuring, an actinic light probe is emitted which induces closure of reaction centres and yields maximum emission of fluorescence. For further details of the methods see Wägele and Johnsen  and Burghardt and Wägele .
In general three or more measurements per animal per day were taken at intervals of over 15 minutes to ensure regeneration of reaction centres and acclimation of chloroplasts to darkness again. Usually animals were kept in small aquaria with a running through water system (25°C to 28°C) or water was changed on a daily base. They were exposed to natural day-night rhythm, but not directly to the sun. Shading was given by plastic roofs or plastic sheaths, which reduced irradiance of the sun (up to 400 μmol quanta per square meter and second), but did not filter certain spectra of the light [pers. comm. Eva McClure, Brisbane]. Animals kept in closed rooms were exposed to sunlight through windows, or light-dark rhythms were imitated by artificial light sources.
When multiple specimens were available, all specimens were measured for initial documentation on photosynthesis, but on long term, only the bigger animals were chosen for analyses, since body sizes below 5 mm yield less reliable measurements. Mean values were calculated from daily measurements taken for each specimen. These values (for individuals) were then pooled to yield a mean and standard deviation for each species (additional file 3). Best-fit trendlines were calculated with Microsoft Office Excel to examine changes in photosynthetic activity over time. For some species only an initial yield value was obtained because insufficient specimens were available for extended measurements.
Reconstruction of ancestral character state
Ancestral character state reconstruction was used to infer when short-term plastid retention evolved in the Sacoglossa, and how many independent origins were likely. Pagel et al.  provide a Bayesian method for estimating ancestral states of discrete traits , combining the probability that a node exists with the probability of a particular state at that node. Continuous-time Markov models of trait evolution were fit to the data with the program BayesMultistate using the MCMC sample of phylogenetic trees generated as described above. This method incorporates phylogenetic uncertainty, as the frequency of a given node in the tree sample limits the statistical confidence in character state reconstructions for that hypothetical ancestor [57, 55]. Each taxon for which PAM data were available was coded as having one of three character states: non-functional chloroplast retention, short-term retention (inability to digest chloroplasts), and long-term retention. Other taxa were coded as missing data if PAM measurements were not available.
A Markov chain was used to estimate posterior probabilities of distributions of the six transition rates between the three alternative character states, and to estimate the ancestral state at each node. A reversible-jump model was used to obtain priors, with an exponential prior seeded from a uniform hyperprior on the interval 0 to 30. The ratedev parameter, which determines the magnitude of changes proposed to rate coefficients, was set to 20 based on pilot runs. These values gave acceptance rates for model parameters of about 20%. After a burn-in period of 105 iterations, chains were sampled for rate coefficients and their associated trees (every 500 generations) to yield 40,000 sampled parameter sets. The posterior probability distribution of character states was estimated for the node representing the last common ancestor of the Plakobranchoidea using the "most recent common ancestor" (MRCA) technique in BayesMultistate. The character state of this node was then fixed as each of the possible states in separate runs using the "fossil" command, and a Markov chain run for 20 million generations as described above, sampling every 500 generations after the burn-in period. These procedures were repeated for the last common ancestor of Elysia chlorotica and E. crispata, to determine if these species represent independent origins of long-term retention or if there was one origin in the ancestor of the clade to which both Elysia spp. belong.
The log of the harmonic mean of the likelihood scores for successive iterations of the chain was calculated for each model. Log-Bayes factor (BF) tests were then used to compare the likelihood of models where the ancestral state was fixed as short-term retention against models where the ancestral state was fixed as non-retention or long-term retention. The BF test statistic is twice the difference in the log-likelihood scores of two models; BF values from 2-5 are taken as positive evidence, while a BF >5 is strong evidence favoring the more likely model .
Molecular phylogeny of Sacoglossa
Phylogenetic analysis of three gene regions strongly support monophyly for the two major sacoglossan lineages: the Oxynoacea, comprising all shelled Sacoglossa, and the shell-less Plakobranchacea, comprising Plakobranchoidea and Limapontioidea (Figure 3). Within the Plakobranchacea, the group Plakobranchoidea is well resolved and strongly supported with a posterior probability (PP) of 0.99. The monotypic family Boselliidae, containing only the genus Bosellia (Figure 2E), was sister taxon to the well-supported family Plakobranchidae which includes the species with parapodia, lateral flaps of the body wall that cover the dorsum. Each of the three genera in the Plakobranchidae (Elysia, Thuridilla and Plakobranchus) was monophyletic.
Relationships of the main subgroups of the Limapontioidea were not resolved. Limapontiidae (PP = 0.90) and the monotypic Costasiellidae (PP = 0.87) were monophyletic (Figure 3). Only one traditional family, the Polybranchiidae, was not monophyletic in our analysis, due to the exclusion of the genus Cyerce. The sister taxon of this "reduced" family was Hermaeidae (Hermaea + Aplysiopsis). The resulting monophylum was sister taxon to the Plakobranchoidea (PP = 0.72).
Comparing all available measurements of yield values throughout the Sacoglossa, three distinct levels of photosynthetic activity were distinguished: 1. No functional retention, with disintegration of chloroplasts within few hours, resulting in yield values lower than 0.2 on the very first day of collecting. 2. Short-term functional retention, with initial yield values above 0.5. These values last for one or two days, and then drop within seven to 14 days. 3. Long-term functional retention, with yield values of more than 0.4 even after 20 days.
Members of the shelled group Oxynoacea exhibited no yield values (Table 3), although ground fluorescence was high in some cases. High ground fluorescence with no yield indicates the presence of chlorophyll a, but a loss of plastid functionality. No species of all four sampled limapontioidean families exhibited photosynthetic activity, indicating no functional retention of chloroplasts in Limapontioidea. One potential exception was Costasiella cf. kuroshimae which had a starting yield value of 0.35, decreasing to < 0.2 within eleven days (Figure 4). Yield values, standard deviation and a corresponding trendline (black line) is shown in comparison to yield values, standard deviation and trendline of Plakobranchus ocellatus (green line) representing the slug with the highest and longest photosynthetic activity in this study.
In contrast, all members of Plakobranchoidea had initial yield values from 0.5 to 0.8 (Figure 5 and 6). Members of the genus Thuridilla had short-term retention with initial yield values above 0.5, but their yield decreased to ~0.2 within a few days. Two specimens of T. kathae had equivalent initial yield values but decline in yield varied markedly between individuals (additional file 3). The lowest initial yield value was obtained for T. hopei (0.4), but its decline was similar to that of the other Thuridilla spp. Bosellia mimetica had short-term retention, initial yield value was 0.56, but yield decreased to less than 0.1 within nine days. Figure 5 compares the trendlines of the species of the genus Thuridilla and Bosellia mimetica (blue lines) with Plakobranchus ocellatus (green line) as reference. Details are listed in the additional file 3. Species of Elysia varied greatly in their photosynthetic ability. Many species (E. bennettae, E. ornata, E. pusilla, E. cornigera, E. tomentosa, E. viridis and Elysia spec. 1) started with yield values of 0.5-0.7 immediately after collection, but yields decreased to <0.4 within one to two weeks. In contrast to most Elysia spp., E. subornata and E. zuleicae exhibited very low values directly after collection - 0.24, and 0.38, respectively.
Three species - E. crispata, E. timida and Plakobranchus ocellatus - exhibited greatly prolonged retention of chloroplast activity (Figure 6). Significant yield values of E. crispata persisted for 40 days, at which point they had dropped to 0.22. Yield values of E. timida remained >0.52 after 35 days. Maximum retention was measured in P. ocellatus, which had a mean initial value 0.78 decreasing to 0.59 over 74 days. Figure 6 compares trendlines of members of Elysia with P. ocellatus as reference. Trendline of E. subornata and initial yield value of E. zuleicae are black indicating no functional retention for the measured specimens. Trendlines of species that had short-term retention (E. bennettae, E. ornata, E. pusilla, E. cornigera, E. tomentosa, E. viridis and Elysia spec. 1) are blue. Trendlines of E. crispata, E. timida and P. ocellatus with long-term retention are green. Details are listed in the additional file 3.
The photosynthetic activity for each species was classified as either no functional retention, short-term retention or long-term retention. Character states were mapped on a simplified cladogram (Figure 7).
Reconstruction of ancestral character state
For character state reconstruction, taxa were grouped into three categories of photosynthetic activity as outlined above (Figure 7). For a few species like Thuridilla kathae and Elysia tomentosa, only initial yield values were available but these were comparable to values for species that maintained photosynthetic ability for about a week; we therefore scored such species as having short-term retention, pending additional study.
Ancestral character state reconstructions statistically supported one origin of short-term chloroplast retention, in the most recent common ancestor (MRCA) of the Plakobranchoidea (Table 4; Figure 7). The posterior probability that the MRCA had short-term retention was estimated as 89.1% ± 18.0% SD. Models of trait evolution in which the MRCA was fixed as having short-term retention were strongly favoured over models in which the MRCA had no retention (BF test = 7.31), and positively supported over models in which the MRCA had long-term retention (BF = 3.92). There were two independent losses of short-term retention (Elysia zuleicae, E. subornata) (Figure 7).
The closely related Elysia chlorotica and E. crispata both express long-term chloroplast retention, but feed on very different host algae. We therefore tested whether long-term kleptoplasty was present in their MRCA or evolved independently in each species. The posterior probability of short-term chloroplast retention was slightly higher than that of long-term retention for the MRCA of E. chlorotica and E. crispata, and models in which their MRCA was fixed as having short-term retention were supported over models in which their ancestor had long-term retention (BF test = 4.24) (Table 4). This result supports independent origins of long-term functionality in E. crispata and E. chlorotica.
Molecular phylogeny of Sacoglossa
Bayesian analysis of three gene sequence regions revealed two monophyletic groups within the Sacoglossa, Oxynoacea and Plakobranchacea, confirming the morphological analysis by Jensen . In the present study, improved taxon sampling and addition of nuclear gene sequence data led to the recovery of a monophyletic Oxynoacea, in contrast to prior molecular analyses based on fewer species and mtDNA alone . Within the Plakobranchacea, Plakobranchoidea was strongly supported as monophyletic, with the monotypic family Boselliidae as sister taxon to the Plakobranchidae. Contrary to Jensen , but concordant with Gosliner  and Bass and Karl , Plakobranchus and Thuridilla were sister taxa.
Monophyly of the cerata-bearing sacoglossans, usually united as Limapontioidea, was not supported in our study, instead major limapontioidean groups formed a polytomy; improved taxon sampling and sequence data from additional loci may solve this problem. The traditional inclusion of Cyerce in the Polybranchiidae was challenged by our finding of a well supported sister taxon relationship between Hermaeidae and part of the Polybranchiidae (Polybranchia +Caliphylla +Mourgona); this merits further attention. The traditional Hermaeidae (Hermaea and Aplysiopsis) was recovered. Costasiella did not show affinity for the other genera classified in the Limapontiidae (Alderia, Ercolania and Placida), but has also been previously placed in its own family.
Our phylogenetic results indicate that the Caribbean "Bosellia marcusi" described by Marcus  is a derived species of Elysia. Morphological examination indicates that the parapodia of "B. marcusi" have secondarily fused over the dorsum, producing a superficial similarity with Bosellia [P. Krug, unpublished data].
Evolution of functional chloroplast retention
Based on our phylogeny and character state reconstructions, there was one probable origin of short-term chloroplast retention in the last common ancestor of the Plakobranchoidea, and four independent origins of long-term retention. No species in the Oxynoacea and Limapontioidea were able to maintain photosynthetic activity, based on PAM measurements. Functional chloroplast retention was not detected in five oxynoacean species representing the basal shelled sacoglossans (Table 3). In species with no functional retention, chloroplasts are phagocytosed by digestive glandular cells and rapidly disintegrate [62, 63]. Clark and Busacca  concluded that Oxynoe retains chloroplasts because they were able to isolate chlorophyll from slugs, but they did not detect net fixation of CO2. We measured high ground fluorescence in oxynoaceans but very low yield values, indicating free chlorophyll but no functional chloroplasts.
Similarly, all limapontioidean species except Costasiella cf. kuroshimae had yield values <0.2, indicating no chloroplast retention. This confirms studies on Placida dendritica[62, 63] and Aplysiopsis enteromorphae (= Hermaeina smithi) . We detected initial yield values of 0.3-0.4 for C. cf. kuroshimae 6-8 hr after collection, whereas the host alga Avrainvillea gave yield values >0.6, leading to the conclusion that chloroplasts are quickly degraded in C. cf. kuroshimae. A former study based, amongst others, on ultrastructural analyses reported intact chloroplasts and carbon-fixation for about 10 days in a specimen of the congener C. ocellifera starved for two weeks , so additional PAM studies on Costasiella spp. are warranted.
No specimens of Hermaea, a genus of red algae feeders, were available for PAM measurements. Short-term retention of functional chloroplasts from the rhodophyte Griffithsia flosculosa was reported for H. bifida, based on O2 production and 14C incorporation in slug tissue [67, 68], but experimental methods were not adequately described . Further studies are therefore needed to assess the fate of chloroplasts within Limapontioidea.
Short- and long-term functional retention were only found in the Plakobranchoidea. Chloroplast function was not detected in Elysia subornata and E. zuleicae from the Caribbean. Based on ancestral character state reconstruction, these lineages represent independent losses of short-term retention, which arose once in the plakobranchoidean ancestor. However, an absence of functional chloroplasts may result from several causes (see discussion of method below), therefore these species should be reinvestigated. Long-term retention was documented for E. crispata, E. timida and Plakobranchus ocellatus. Our study shows for the first time that functional retention in E. crispata lasts up to 40 days, expanding prior studies based on oxygen production [69, 70, 37]. We confirmed stable long-term retention in E. timida, also described by Evertsen et al. . Kleptoplasty may be an ecologically necessity for E. timida as an energy source when algal hosts are heavily calcified or in short supply . The highest rates of photosynthesis occurred in P. ocellatus, lasting over a month with remarkable stability. This is a large species by sacoglossan standards (up to five cm long), and the subject of prior studies on chloroplast retention [, as P. ianthobapsus, , as P. ianthobapsus, [27, 45]]. E. chlorotica, a species best known for its long-term retention, was not available for PAM measurements but its photosynthetic ability is well documented [46, 73–77].
Given that short-term retention was an apomorphy of the Plakobranchoidea, there were likely at least four independent gains of long-term function in the derived species noted above. Ancestral character state reconstructions returned mild support for two independent origins in E. chlorotica and E. crispata. The related species E. viridis feeds on six genera of host algae [C. Trowbridge, pers. comm.] and may be capable of long-term chloroplast retention from a subset of those hosts, which warrants future study. However, when ancestral character state analyses were rerun coding E. viridis as having long-term chloroplast functionality, the results were unchanged with respect to independent origins in E. chlorotica and E. crispata.
We propose that functional chloroplast retention evolved in two sequential steps. The first step was loss of the ability to rapidly digest dietary plastids after phagocytosis by digestive cells. A pre-adaptation for prolonged chloroplast retention, this step produces short-term functionality because undigested chloroplasts perform photosynthesis without support from the (digested) algal nucleus, for as long as the chloroplasts survive. Many sacoglossan host algae are large-celled and coenocytic, including numerous Chlorophyta and the heterokontophyte Vaucheria. Coenocytic algae may require resilient chloroplasts for cytoplasmic streaming or thallus wound-plug formation (giant-celled and coenocytic Chlorophyta: , Vaucheria: ). The toughness of chloroplasts may in turn have facilitated the evolutionary transition to short-term retention in the ancestral plakobranchoidean.
The second requirement for long-term retention is to prolong chloroplast survival by supplying essential proteins such as components of the light-harvesting complex, enzymes involved in chlorophyll biosynthesis, etc. The encoding genes are normally found in the algal nucleus, but in at least Elysia chlorotica have entered the slug's genome by horizontal gene transfer [80, 81]. This strategy is distinct from the reliance on transcriptionally active nuclei, as occurs in ciliates that incorporate plastids from cryptophytes . Future research should determine whether horizontal gene transfer happened once in the plakobranchoidean ancestor, or if gene transfer happened independently in each lineage capable of long-term retention. If gene transfer happened early, then the relevant genes were transcriptionally activated or "switched on" independently in each of the four species capable of prolonged photosynthetic activity. Genetic analysis of selected sacoglossan taxa are planned to resolve this issue, which has fundamental implications for understanding endosymbiosis and the evolution of chimeric genomes .
A second question is whether short- versus and long-term retention is dependant on the type of chloroplasts in the host algae or on some properties of the slugs' digestive cells that affect how the cells deal with sequestered chloroplasts. To explore possible correlations between mode of retention and algal type, available data on host use were mapped onto the cladogram (Figure 7). All members of the Oxynoacea feed on the genus Caulerpa (Caulerpales) and seem to digest them directly. Several derived species like E. subornata, E. tomentosa and E. crispata also feed on Caulerpa and retention of chloroplasts vary within these species. Feeding experiments with Elysia crispata by offering different algal speciesresulted in an increased activity after consumption of Caulerpa verticillata, whereas consumption of Halimeda opuntia did not contribute to photosynthetic activity [Grzymbowski & Wägele, unpublished data]. Although E. timida switches from hosts in the Cladophorales to algae in the Dasycladales during its life cycle, the chloroplasts inducing long-term photosynthetic activity apparently originate only from the dasycladalean Acetabularia acetabulum[41, 42]. Newly hatched juveniles retain chloroplasts from Cladophora dalmatica, but quality of retention has never been investigated.
Long term retention in Elysia chlorotica is based on incorporation of chloroplasts from the heterokontophyte Vaucheria. Although E. crispata has been reported to consume both Vaucheria and a member of the Dasycladales, this species feeds principally on a variety of udoteacean green algae, and the origin of the chloroplasts responsible for long term photosynthetic activity is presently unknown . The food of Plakobranchus ocellatus is unclear [65, 72]; DNA barcoding is currently being used to identify the source of chloroplasts involved in long-term photosynthesis [Händeler et al., unpublished data].
Measuring plastid functionality - methodological considerations
Use of PAM to quantify fluorescence of chlorophyll a in photosystem II reliably indicates whether chloroplasts are intact and functional within metazoan tissues. This method is non-invasive, can be easily applied in the field, and preserves the subjects for further genetic or histological analyses, including DNA barcoding studies to identify the source of sequestered chloroplasts. Direct assessment of chloroplast activity using a standardized method is an advance over prior work in which alternative methods were used to study different taxa, and plastid functionality was often assumed rather than demonstrated. For instance, Hinde and Smith  reported that chloroplast retention in E. viridis is functional for at least three months, based on a lone surviving slug (out of 39 specimens) which lost 96% of its body mass over the experimental period. Also, extrapolation of possible survival of slugs by analysing trendlines should be done with caution . We do not adhere to previous classifications of photosynthetic activity into six  or even eight  different (artificial) levels, as the distinction between many of those proposed levels seems arbitrary according to our results in the present work.
We emphasize that although our data show trends for species, more detailed studies under standardized conditions are needed to resolve some remaining methodological issues. For instance, even when slugs are freshly collected from their food item, it is unknown how recently they consumed algal cytoplasm without direct observation of feeding; thus, only a minimum age can be determined for sequestered chloroplasts from field-caught specimens. In some species, photosynthetic activity may vary seasonally [85, 41], geographically , or over the course of the life cycle [86, 42]. Investigation of different ontogenetic states under starving conditions is thus warranted for species like Elysia subornata and E. zuleicae, to confirm whether the lack of chloroplast retention is limited to adult stages. Importantly, it remains to be determined whether chloroplasts of alternative host algae are retained for different periods of time by sacoglossans such as Elysia crispata, E. viridis and E. timida[87, 25, 83, 86, 88]. PAM studies on slugs that have fed on different algae are needed to rule out long-term retention of chloroplasts from a subset of potential hosts, before firm species-level conclusions can be drawn.
Additional work is also needed to assess how chloroplast retention is affected by abiotic factors such as light intensity and temperature [89–91]. Some sacoglossans exhibit behaviors that minimize exposure to high solar irradiance, which may prolong the activity of functional chloroplasts [91–93]. Parapodia, the lateral body flaps that cover the dorsum of species in the Plakobranchoidea, may have initially been an adaptation for shielding chloroplasts to reduce photosynthesis and, in consequence, production of toxic levels of intracellular oxygen. This resulted in an effective shielding of chloroplasts from destructive irradiance, hence prolonging the time of functional photosynthesis within the slugs. Finally slugs may even exert fine control over the light intensity to which chloroplasts are exposed by adjusting how far their parapodia are held open. Plakobranchus ocellatus was observed to roll its body and lie on the side to further reduce irradiance in bright sunlight [unpublished data of first and senior author]. Thus, anatomical and behavioral traits may together enhance the performance and survival of chloroplasts in different light regimes, and hence optimize the energy budget of slugs.
Demonstrating that a key character promoted an adaptive radiation requires evidence of (1) a rapid burst of speciation, (2) the common ancestry of putative descendant species, and (3) the phenotype-environment correlation or trait utility, meaning the performance or fitness advantage of trait values in their corresponding environments . Short-term retention of functional chloroplasts is a candidate key character that evolved once in the stemline of the Plakobranchoidea as has been shown here by comparative analyses. When not immediately digested, incorporated chloroplasts stay functional, hence provide fixed carbon, even if they degrade gradually over several days. This spares the slug from the energetic demands of feeding, when food availability decreases due to various ecological reasons (calcification of algae, migration in search for adequate mating partners, etc.) Kleptoplasty therefore likely contributed to the evolutionary success of the Plakobranchoidea. This success is evident both in the number of recognized species in the Plakobranchoidea, and in the ecological diversity of the group. Plakobranchoidea include more than 130 species and has five times more species than its putative sister taxon (family Hermaeidae and a part of the Polybranchiidae, see Figure 7) with about 25 species. Nevertheless, a robust estimate of the relative rate of speciation in the Plakobranchoidea will require additional data. Relationship of the Limapontioidea has to be clarified, and sister taxa relation of Plakobranchoidea needs confirmation. Furthermore, to apply statistical approaches as lineages-through-time plots a complete tree comprising all known species is necessary. More complete taxon sampling will be necessary to provide a robust estimate of relative rates of cladogenesis in different groups, permitting a statistical test of the key character hypothesis.
Ample studies demonstrate the trait utility of supplemental energy from kleptoplastids (see background). Evolution of parapodia typical only for Plakobranchoidea enables the slugs to keep chloroplasts alive and protect them against destructive irradiance. These structures even allow the selected exposure to different light intensities. Here we find anatomical as well as behavioral traits that optimize survival of chloroplasts in different light regimes and hence optimize energy budget and survival of slugs. We do not know at the moment how far this also affected switch to other host organisms and incorporation of "better" chloroplasts. It is evident that Plakobranchoidea, especially the species rich genus Elysia (> 80 species), have a broad range of food algae which they exploit (Figure 7). Future studies comprising the identification of the algal origin of incorporated functional chloroplasts will reveal any correlation between host organisms and photosynthetic activity of the slugs.
A second step in kleptoplastid evolution is the prolonged survival and photosynthetic activity of chloroplasts incorporated into the digestive cells of a slug. According to the phylogenetic hypothesis we present, this improvement in plastid retention occurred independently three times in Elysia and once in Plakobranchus. Although Plakobranchus is currently a monotypic genus, recent genetic studies indicate that it in fact comprises a clade of at least eight recently diverged cryptic species [P. Krug, A. Rodriguez, and C. Trowbridge, unpublished data] for which photosynthetic abilities have not been investigated so far.
Short-term retention may thus have been necessary to promote an adaptive radiation of the Plakobranchoidea. Other characters (e.g. host switch) or interactions between slug and host (e.g. usage of secondary metabolites) [95, 96] may have additionally influenced speciation in Sacoglossa, and in particular adaptive radiation of the Plakobranchoidea (see also ).
After Jensen's [48, 29] important first phylogenetic analysis and interpretations based on morphological data, we contribute here the next steps (molecular phylogeny and evolution of kleptoplasty). Nevertheless, only additional studies will clarify what trait combinations drove diversification within the Sacoglossa, and how the relationship between slugs and their host algae affected the evolution of this enigmatic opisthobranch taxon.
most recent common ancestor
Bascompte J, Jordano P: Plant-Animal mutualistic networks: The architecture of biodiversity. Annu Rev Ecol Evol Syst. 2007, 38: 567-593. 10.1146/annurev.ecolsys.38.091206.095818.
Forbes AA, Powel THQ, Stelinski LL, Smith JJ, Feder JL: Sequential sympatric speciation across trophic levels. Science. 2009, 323: 776-779. 10.1126/science.1166981.
Hoberg EP, Brooks DR: A macroevolutionary mosaic: episodic host-switching, geographical colonization and diversification in complex host-parasite systems. J Biogeogr. 2008, 35: 1533-1550. 10.1111/j.1365-2699.2008.01951.x.
Summers K, McKeon S, Sellars J, Keusenkothen M, Morris J, Gloeckner D, Pressley C, Price B, Snow H: Parasitic exploitation as an engine of diversity. Biol Rev Camb Philos Soc. 2003, 78: 639-675. 10.1017/S146479310300616X.
Thompson JN: The coevolving web of life. Am Nat. 2009, 173: 125-140. 10.1086/595752.
Becerra JX: Insects on plants: Macroevolutionary chemical trends in host use. Science. 1997, 276: 253-256. 10.1126/science.276.5310.253.
Caillaud MC, Via S: Specialized feeding behavior influences both ecological specialization and assortative mating in sympatric host races of pea aphids. Am Nat. 2000, 156: 606-621. 10.1086/316991.
Farrell BD: "Inordinate fondness" explained: Why are there so many beetles?. Science. 1998, 281: 555-559. 10.1126/science.281.5376.555.
Feder JL, Opp SB, Wlazlo B, Reynolds K, Go W, Spisak S: Host fidelity is an effective premating barrier between sympatric races of the apple maggot fly. Proc Natl Acad Sci USA. 1994, 91: 7990-7994. 10.1073/pnas.91.17.7990.
Filchak KE, Roethele JB, Feder JL: Natural selection and sympatric divergence in the apple maggot Rhagoletis pomonella. Nature. 2000, 407: 739-742. 10.1038/35037578.
Leschen RAB, Buckley TR: Multistate characters and diet shifts: Evolution of Erotylidae (Coleoptera). Syst Biol. 2007, 56: 97-112. 10.1080/10635150701211844.
Frey JE, Bush GL: Rhagoletis sibling species and host races differ in host odor recognition. Entomol Exp Appl. 1990, 57: 123-131. 10.1007/BF00343500.
Matzkin LM, Watts TD, Bitler BG, Machado CA, Markow TA: Functional genomics of cactus host shifts in Drosophila mojavensis. Mol Ecol. 2006, 15: 4635-3643. 10.1111/j.1365-294X.2006.03102.x.
Rice WR: Speciation via habitat specialization: the evolution of reproductive isolation as a correlated character. Evol Ecol. 1987, 1: 301-314. 10.1007/BF02071555.
Wheat CW, Vogel H, Wittstock U, Braby MF, Underwood D, Mitchell-Olds T: The genetic basis of a plant-insect coevolutionary key innovation. Proc Natl Acad Sci USA. 2007, 104: 20427-20431. 10.1073/pnas.0706229104.
Faucci A, Toonen RJ, Hadfield MG: Host shift and speciation in a coral-feeding nudibranch. Proc R Soc Lond B Biol Sci. 2007, 274: 111-119. 10.1098/rspb.2006.3685.
May RM, Godfrey J: Biological diversity: differences between land and sea. Philos Trans R Soc Lond B Biol Sci. 1994, 343: 105-111. 10.1098/rstb.1994.0014.
Poore AGB, Hill NA, Sotka EE: Phylogenetic and geographic variation in host breadth and composition by herbivorous amphipods in the family Ampithoidae. Evolution. 2008, 62: 21-38.
Sotka EE: Local adaptation in host use among marine invertebrates. Ecol Lett. 2005, 8: 448-459. 10.1111/j.1461-0248.2004.00719.x.
Trowbridge CD, Todd CD: Host-plant change in marine specialist herbivores: Ascoglossan sea slugs on introduced macroalgae. Ecol Monogr. 2001, 71: 219-243.
Lee JJ: Algal symbiosis in larger foraminifera. Symbiosis. 2006, 42: 63-75. [http://0-md1.csa.com.brum.beds.ac.uk/partners/viewrecord.php?requester=gs&collection=ENV&recid=7722815&q=&uid=788713481&setcookie=yes]
Gast RJ, Moran DM, Dennett MR, Caron DA: Kleptoplasty in an Antarctic dinoflagellate: caught in evolutionary transition?. Environ Microbiol. 2007, 9: 39-45. 10.1111/j.1462-2920.2006.01109.x.
Johnson MD, Oldach D, Delwiche CF, Stoecker DK: Retention of transcriptionally active cryptophyte nuclei by the ciliate Myrionecta rubra. Nature. 2007, 445: 426-428. 10.1038/nature05496.
Floyd GL, O'Kelly CJ: Phylum Chlorophyta, Class Ulvophyceae. Handbook of Protoctista. Edited by: Margulis L, Corliss JO, Melkonian M, Chapman D. 1990, Boston: Jones and Bartlett Publishers, 617-635.
Curtis NE, Massey SE, Schwartz JA, Maugel TK, Pierce SK: The intracellular, functional chloroplasts in adult sea slugs (Elysia crispata) come from several algal species, and are also different from those in juvenile slugs. Microsc Microanal. 2005, 11: 1194-1195. 10.1017/S1431927605505774.
Händeler K, Wägele H: Preliminary study on molecular phylogeny of Sacoglossa and a compilation of their food organisms. Bonn Zool Beitr. 2007, 55: 231-254. [http://www.zfmk.de/BZB/BzB_55_3_06_Haendeler.pdf]
Hirose M: Digestive System of the Sacoglossan Plakobranchus ocellatus (Gastropoda: Opisthobranchia): Light- and Electron-Microscopic Observations with Remarks on Chloroplast Retention. Zool Sci. 2005, 22: 905-916. 10.2108/zsj.22.905.
Jensen KR: A review of sacoglossan diets, with comparative notes on radular and buccal anatomy. Malacol Rev. 1980, 13: 55-77.
Jensen KR: Evolution of the Sacoglossa (Mollusca, Opisthobranchia) and the ecological associations with their food plants. Evol Ecol. 1997, 11: 301-335. 10.1023/A:1018468420368.
Kawaguti S, Yamasu T: Electron microscopy on the symbiosis between an elysioid gastropod and chloroplasts of a green alga. Biol J Okayama Univ. 1965, 11: 57-65.
Taylor DL: Chloroplasts as symbiotic organelles in the digestive gland of Elysia viridis (Gastropoda: Opisthobranchia). J Mar Biol Assoc UK. 1968, 48: 1-15. 10.1017/S0025315400032380.
Williams SI, Walker DI: Mesoherbivore-macroalgal interactions: feeding ecology of sacoglossan sea slugs (Mollusca, Opisthobranchia) and their effects on their food algae. Oceanogr Mar Biol Ann Rev. 1999, 37: 87-128.
Taylor DL: Chloroplasts as symbiotic organelles. Int Rev Cytol. 1970, 27: 29-64.
de Manuel Barrabin J: The rotifers of spanish reservoirs: ecological, systematical and zoogeographical remarks. Limnetica. 2000, 19: 91-167. [http://www.limnetica.net/Limnetica/Limne19/L19_091_Rotifers_spanish_reservoirs.pdf]
Greene RW: Symbiosis in sacoglossan Opisthobranchs: Translocation of photosynthetic products from chloroplast to host tissue. Malacologia. 1970, 10: 369-380.
Hinde R, Smith DC: "Chloroplast symbiosis" and the extant to which it occurs in Sacoglossa (Gastropoda: Mollusca). Biol J Linn Soc Lond. 1974, 6: 349-356. 10.1111/j.1095-8312.1974.tb00729.x.
Taylor DL: Photosynthesis of symbiotic chloroplasts in Tridachia crispata (Bergh). Comp Biochem Physiol. 1971, 38A: 233-236. 10.1016/0300-9629(71)90111-3.
Trench RK: Of "leaves that crawl": functional chloroplasts in animal cells. Symp Soc Exp Biol. 1975, 29: 229-265.
Trench RK, Trench ME, Muscatine L: Symbiotic chloroplasts; their photosynthetic products and contribution to mucus synthesis in two marine slugs. Biol Bull. 1972, 142: 335-349. 10.2307/1540236.
Giménez-Casalduero F, Muniain C: The role of kleptoplasts in the survival rates of Elysia timida (Risso, 1818): (Sacoglossa: Opisthobranchia) during periods of food shortage. J Exp Mar Bio Ecol. 2008, 357: 181-187. 10.1016/j.jembe.2008.01.020.
Marín A, Ros J: Dynamics of a peculiar plant-herbivore relationship: the photosynthetic ascoglossan Elysia timida and the chlorophycean Acetabularia acetabulum. Mar Biol. 1992, 112: 667-682. 10.1007/BF00346186.
Marín A, Ros J: Ultrastructural and ecological aspects of the development of chloroplast retention in the sacoglossan gastropod Elysia timida. J Moll Stud. 1993, 59: 95-104. 10.1093/mollus/59.1.95.
Clark KB, Jensen KR, Stirts HM: Survey for functional kleptoplasty among West Atlantic Ascoglossa (= Sacoglossa) (Mollusca: Opisthobranchia). Veliger. 1990, 33: 339-345.
Wägele H, Johnsen G: Observations on the histology and photosynthetic performance of "solar-powered" opisthobranchs (Mollusca, Gastropoda, Opisthobranchia) containinig symbiotic chloroplasts or zooxanthellae. Org Divers Evol. 2001, 1: 193-210. 10.1078/1439-6092-00016.
Evertsen J, Burghardt I, Johnsen G, Wägele H: Retention of functional chloroplasts in some sacoglossans from the Indo-Pacific and Mediterranean. Mar Biol. 2007, 151: 2159-2166. 10.1007/s00227-007-0648-6.
Rumpho ME, Dastoor FP, Manhart JR, Lee J: The Kleptoplast. The Structure and Function of plastids. 2006, 23: 451-473.
Wägele H: Potential key characters in Opisthobranchia (Gastropoda, Mollusca) enhancing adaptive radiation. Org Divers Evol. 2004, 4: 175-188. 10.1016/j.ode.2004.03.002.
Jensen KR: Phylogenetic systematics and classification of the Sacoglossa (Mollusca, Gastropoda, Opisthobranchia). Philos Trans R Soc Lond B Biol Sci. 1996, 351: 91-122. 10.1098/rstb.1996.0006.
Ellingson RA, Krug PJ: Evolution of poecilogony from planktotrophy: cryptic speciation, phylogeography, and larval development in the gastropod genus Alderia. Evolution. 2006, 60: 2293-2310.
Krug PJ, Morley MS, Asif J, Hellyar L, Blom WM: Molecular confirmation of species status for the rare cephalaspidean Melanochlamys lorrainae (Rudman, 1968), and comparison with its sister species M. cylindrica Cheeseman, 1881. J Moll Stud. 2008, 74: 267-276. 10.1093/mollus/eyn018.
Katoh K, Misawa K, Kuma K, Miyata T: MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res. 2002, 30: 3059-3066. 10.1093/nar/gkf436.
Katoh K, Toh H: Recent developments in the MAFFTmultiple sequence alignment program. Brief Bioinform. 2008, 9: 286-298. 10.1093/bib/bbn013.
Pagel M, Meade A: A Phylogenetic Mixture Model for Detecting Pattern-Heterogeneity in Gene Sequence or Character-State Data. Syst Biol. 2004, 53: 571-581. 10.1080/10635150490522232.
Burghardt I, Wägele H: Interspecific differences in the efficiency and photosynthetic characteristics of the symbiosis of "solarpowered" Nudibranchia (Mollusca: Gastropoda) with zooxanthellae. Rec West Austr Mus Suppl. 2006, 69: 1-9.
Pagel M, Meade A, Barker D: Bayesian estimation of ancestral character states on phylogenies. Syst Biol. 2004, 53: 673-684. 10.1080/10635150490522232.
Reading Evolutionary Biology Group. [http://www.evolution.rdg.ac.uk]
Pagel M: The maximum likelihood approach to reconstructing ancestral character states of discrete characters on phylogenies. Syst Biol. 1999, 48: 612-622. 10.1080/106351599260184.
Rafferty AA: Hypothesis testing and model selection. Markov Chain Monte Carlo in practice. Edited by: Gilks WR, Richardson S, Spiegelhalter DJ. 1996, London: Chapman and Hall, 163-188.
Gosliner TM: The genus Thuridilla (Opisthobranchia: Elysiidae) from the tropical Indo-Pacific, with a revision of the phylogeny and systematics of the Elysiidae. Proc Calif Acad Sci. 1995, 49: 1-54.
Bass AL, Karl SA: Molecular phylogenetic analysis of genera in the family Plakobranchidae (Mollusca: Opisthobranchia: Sacoglossa). Rec West Austr Mus Suppl. 2006, 69: 61-68.
Marcus EDBR: On some opisthobranchs from Florida. Bull Mar Sci. 1972, 22: 284-308. [http://0-www.ingentaconnect.com.brum.beds.ac.uk/content/umrsmas/bullmar/1972/00000022/00000002/art00002]
McLean N: Phagocytosis of chloroplasts in Placida dendritica (Gastropoda: Sacoglossa). J Exp Zool. 1976, 197: 321-329. 10.1002/jez.1401970304.
Evertsen J, Johnsen G: In vivo and in vitro differences in chloroplast functionality in the two north Atlantic sacoglossans (Gastropoda, Opisthobranchia) Placida dendritica and Elysia viridis. Mar Biol. 2009, 156: 847-859. 10.1007/s00227-009-1128-y.
Clark KB, Busacca M: Feeding specifity and chloroplast retention in four tropical Ascoglossa, with a discussion of the extent of chloroplast symbiosis and the evolution of the order. J Moll Stud. 1978, 44: 272-282.
Greene RW: Symbiosis in sacoglossan opisthobranchs:Symbiosis with algal chloroplasts. Malacologia. 1970, 10: 357-368.
Clark KB, Jensen KR, Stirts HM, Fermini C: Chloroplast symbiosis in a non-elysiid mollusc, Costasiella lilianae Marcus (Hermaeidae: Ascoglossa) (= Sacoglossa): effects of temeperature, light intensity, and starvation on carbon fixation rate. Biol Bull. 1981, 160: 43-54. 10.2307/1540899.
Kremer BP: Rotalgen-Chloroplasten als funktionelle Endosymbionten in einem marinen Opisthobranchier. Naturwissenschaften. 1977, 64: 147-148. 10.1007/BF00450579.
Taylor DL: Symbiosis between the chloroplasts of Griffithsia flosculosa (Rhodophyta) and Hermaea bifida (Gastropoda: Opisthobranchia). Pubbl Staz Zool Napoli. 1971, 39: 116-120.
Trench RK: Chloroplasts as functional endosymbionts in the mollusc Tridachia crispata (Bergh), (Opisthobranchia, Sacoglossa). Nature. 1969, 222: 1071-1072. 10.1038/2221071a0.
Trench RK, Greene RW, Bystrom BG: Chloroplasts as functional organelles in animal tissue. J Cell Biol. 1969, 42: 404-417. 10.1083/jcb.42.2.404.
Greene RW: Symbiosis in sacoglossan opisthobranchs: functional capacity of symbiotic chloroplasts. Mar Biol. 1970, 7: 138-142. 10.1007/BF00354917.
Kawaguti S, Yamamoto T, Kamishima Y: Electron microscopy on the symbiosis between blue-green algae and an opisthobranch, Placobranchus. Proc Jpn Acad. 1965, 41: 614-617. [http://www.journalarchive.jst.go.jp/english/jnlabstract_en.php?cdjournal=pjab1945&cdvol=41&noissue=7&startpage=614]
Green BJ, Li W-Y, Manhart JR, Fox TC, Summer EJ, Kennedy RA, Pierce SK, Rumpho ME: Mollusc-Algal Chloroplast Endosymbiosis. Photosynthesis, Thylakoid Protein Maintenance, and Chloroplast Gene Expression Continue for Many Months in the Absence of the Algal Nucleus. Plant Physiol. 2000, 124: 331-342. 10.1104/pp.124.1.331.
Mujer CV, Andrews DL, Manhart JR, Pierce SK, Rumpho ME: Chloroplast genes are expressed during intracellular symbiotic association of Vaucheria litorea plastids with the sea slug Elysia chlorotica. Proc Natl Acad Sci USA. 1996, 93: 12333-12338. 10.1073/pnas.93.22.12333.
Pierce SK, Biron RW, Rumpho ME: Endosymbiotic chloroplast in molluscan cells contain proteins synthesized after plastid capture. J Exp Biol. 1996, 199: 2323-2330.
West HH: Chloroplast symbiosis and development in Elysia chlorotica [abstract]. Am Zool. 1977, 17: 968-
West HH: Photosynthetic oxygen evolution by symbiotic chloroplasts in molluscan host [abstract]. Am Zool. 1980, 20: 798-
Grant BR, Borowitzka MA: The chloroplasts of giant-celled and coenocytic algae: Biochemistry and structure. Bot Rev. 1984, 50: 267-307. 10.1007/BF02862634.
Green BJ, Fox TC, Rumpho ME: Stability of isolated algal chloroplasts that participate in a unique mollusc/kleptoplast association. Symbiosis. 2005, 40: 31-40. [http://cat.inist.fr/?aModele=afficheN&cpsidt=17338138]
Pierce SK, Curtis NE, Hanten JJ, Boerner SL, Schwartz JA: Transfer, integration and expression of functional nuclear genes between multicellular species. Symbiosis. 2007, 43: 57-64.
Rumpho ME, Worful JM, Lee J, Kannan K, Tyler MS, Bhattacharya D, Moustafa A, Manhart JR: Horizontal gene transfer of the algal nuclear gene psbO to the photosynthetic sea slug Elysia chlorotica. Proc Natl Acad Sci USA. 2008, 105: 17867-17871. 10.1073/pnas.0804968105.
Palmer JD, Delwiche CF: Second-hand chloroplasts and the case of the disappearing nucleus. Proc Natl Acad Sci USA. 1996, 93: 7432-7435. 10.1073/pnas.93.15.7432.
Curtis NE, Massey SE, Pierce SK: The symbiotic chloroplasts in the sacoglossan Elysia clarki are from several algal species. Invertebr Biol. 2006, 125: 336-345. 10.1111/j.1744-7410.2006.00065.x.
Hinde R, Smith DC: Persistence of functional chloroplasts in Elysia viridis (Opisthobranchia, Sacoglossa). Nat New Biol. 1972, 239: 30-31. 10.1038/239041a0.
Waugh GR, Clark KB: Seasonal and geographic variation in chlorophyll level of Elysia tuca (Ascoglossa: Opisthobranchia). Mar Biol. 1986, 92: 483-487. 10.1007/BF00392508.
Curtis NE, Pierce SK, Massey SE, Schwartz JA, Maugel TK: Newly metamorphosed Elysia clarki juveniles feed on and sequester chloroplasts from algal species different from those utilized by adult slugs. Mar Biol. 2007, 150: 797-806. 10.1007/s00227-006-0398-x.
Brandley BK: Aspects of the ecology and physiology of Elysia cf. furvacauda (Mollusca: Sacoglossa). Bull Mar Sci. 1984, 34: 207-219. [http://0-www.ingentaconnect.com.brum.beds.ac.uk/content/umrsmas/bullmar/1984/00000034/00000002/art00004]
Jensen KR: Influence of filament diameter on food preference and growth in Oxynoe azuropunctata Jensen, 1980 and Elysia cauze Marcus, 1957 (Opisthobranchia, Sacoglossa). Ophelia. 1981, 20: 127-135.
Hawes CR, Cobb AH: The effects of starvation on the symbiotic chloroplasts in Elysia viridis: A fine structural study. New Phytol. 1980, 84: 375-379. 10.1111/j.1469-8137.1980.tb04437.x.
Marín A, Ros J: The chloroplast-animal association in four Iberian sacoglossan opisthobranchs: Elysia timida, Elysia translucens, Thuridilla hopei and Bosellia mimetica. Sci Mar. 1989, 53: 429-440. [http://dialnet.unirioja.es/servlet/articulo?codigo=2187369]
Vieira S, Calado R, Coelho H, Serôdio J: Effects of light exposure on the retention of kleptoplastic photosynthetic activity in the sacoglossan Elysia viridis. Mar Biol. 2009, 156: 1007-1020. 10.1007/s00227-009-1144-y.
Gallop A, Bartrop J, Smith DC: The biology of chloroplast acquisition by Elysia viridis. Proc R Soc Lond B Biol Sci. 1980, 207: 335-349. 10.1098/rspb.1980.0027.
Weaver S, Clark KB: Light intensity preference of five ascoglossan (= sacoglossan) molluscs (Gastropoda: Opisthobranchia): a comparison of chloroplast-symbiotic and aposymbiotic species. Mar Fresh Behav Phys. 1981, 7: 297-306. 10.1080/10236248109386991.
Schluter D: The ecology of adaptive radiation. 2000, Oxford: Oxford University Press
Cimino G, Ghiselin MT: Chemical defense and evolutionary trends in biosynthetic capacity among dorid nudibranchs (Mollusca: Gastropoda: Opisthobranchia). Chemoecology. 1999, 9: 187-207. 10.1007/s000490050052.
Wägele H, Ballesteros M, Avila C: Defensive glandular structures in opisthobranch molluscs - from histology to ecology. Oceanogr Mar Biol Ann Rev. 2006, 44: 197-276.
Skelton PW: Adaptive radiation: definition and diagnostic tests. Evolutionary patterns and processes. Edited by: Lees DE, Edwards D. 1993, London: Academic Press, 45-58.
Teugels B, Bouillon S, Veuger B, Middelburg JJ, Koedman N: Kleptoplasts mediate nitrogen acquisition in the sea slug Elysia viridis. Aquat Biol. 2008, 4: 15-21. 10.3354/ab00092.
Trowbridge CD: Life at the edge: population dynamics and salinity tolerance of a high intertidal, pool-dwelling sacoglossan opisthobranch on New Zealand rocky shores. J Exp Mar Biol Ecol. 1994, 182: 65-84. 10.1016/0022-0981(94)90211-9.
Krug PJ, Ellingson RA, Burton R, Valdes A: A new poecilogonous species of sea slug (Opisthobranchia: Sacoglossa) from California: comparison with the planktotrophic congener Alderia modesta (Lovén, 1844). J Moll Stud. 2007, 73: 29-38. 10.1093/mollus/eyl025.
Palumbi S: Nucleic acids II: The polymerase chain reaction. Molecular systematics. Edited by: Hillis D, Moritz C, Mable B. 1996, Sunderland: Sinauer Associates, 205-247.
Vonnemann V, Schrödl M, Klussmann-Kolb A, Wägele H: Reconstruction of the phylogeny of the Opisthobranchia (Mollusca: Gastropoda) by means of 18S and 28S rRNA gene sequences. J Moll Stud. 2005, 71: 113-125. 10.1093/mollus/eyi014.
Morgan JAT, DeJong RJ, Jung Y, Khallaayoune K, Kock S, Mkoji GM, Loker ES: A phylogeny of planorbid snails, with implications for the evolution of Schistosoma parasites. Mol Phylogenet Evol. 2002, 25: 477-488. 10.1016/S1055-7903(02)00280-4.
We thank Bill Martin and Konrad Bachmann for initiating "Schwerpunktprogramm" SPP 1127, in which this project was funded by the German Science Foundation (Wa 618/8-3) to HW. PJK was supported by grants from the U.S. National Science Foundation program in Systematics and Biodiversity Inventories (DEB 08-17084), Biological Oceanography (OCE 06-48606) and the Human Resources Division (HRD 03-17772). We thank all colleagues who helped to collect material: Richard Allen, Ingo Burghardt, Annette Klussmann-Kolb, Wolfgang Loch, Skip Pierce, Tane Sinclair, Kristina Stemmer, Cynthia Trowbridge, Carmen Zinßmeister, and the directors of the Lizard Island Research Station, Anne Hoggett and Lyle Vail. We thank Nikola Schmidt who helped in preparing figures 1 and 2 and Hans-Volker Thiel for proof-reading. We thank the governments of Australia, the Bahamas, Bermuda, Curaçao, Jamaica, and the states of California and Florida for permission to collect in their territorial waters. Material was collected in Australia in accordance to GRMP.
The authors declare that they have no competing interests.
KH and PK generated sequence data and performed phylogenetic analyses. KH, YG and HW produced PAM measurements. KH analyzed PAM measurements. PK carried out character state reconstructions. KH, PK and HW wrote the manuscript. HW initiated and oversaw the project. All authors read and approved the final manuscript.
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Additional file 3: Yield values for each specimen, mean values and standard deviation for species. There is one table for each species. Full species name can be found in first line. All specimens of one species are listed with internal numbers. For single specimens collection date, date of first yield measurement, collection place and size are given in the table. Yield values are given for every specimen, mean value of yield values from every specimen per day of starvation after capture and standard deviation for one species are given. Mean values are plotted against days of starvation in figures 4 to 6. Standard deviation is plotted for species in figure 4 but not in figures 5 and 6 for better clearity. (XLS 122 KB)
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Händeler, K., Grzymbowski, Y.P., Krug, P.J. et al. Functional chloroplasts in metazoan cells - a unique evolutionary strategy in animal life. Front Zool 6, 28 (2009) doi:10.1186/1742-9994-6-28
- Photosynthetic Activity
- Sister Taxon
- Much Recent Common Ancestor
- Pulse Amplitude Modulate
- Ancestral Character State