From egg to “no-body”: an overview and revision of developmental pathways in the ancient arthropod lineage Pycnogonida
© The Author(s). 2017
Received: 21 October 2016
Accepted: 23 January 2017
Published: 7 February 2017
Arthropod diversity is unparalleled in the animal kingdom. The study of ontogeny is pivotal to understand which developmental processes underlie the incredible morphological disparity of arthropods and thus to eventually unravel evolutionary transformations leading to their success. Work on laboratory model organisms has yielded in-depth data on numerous developmental mechanisms in arthropods. Yet, although the range of studied taxa has increased noticeably since the advent of comparative evolutionary developmental biology (evo-devo), several smaller groups remain understudied. This includes the bizarre Pycnogonida (sea spiders) or “no-bodies”, a taxon occupying a crucial phylogenetic position for the interpretation of arthropod development and evolution.
Pycnogonid development is variable at familial and generic levels and sometimes even congeneric species exhibit different developmental modes. Here, we summarize the available data since the late 19th century. We clarify and resolve terminological issues persisting in the pycnogonid literature and distinguish five developmental pathways, based on (1) type of the hatching stage, (2) developmental-morphological features during postembryonic development and (3) selected life history characteristics. Based on phylogenetic analyses and the fossil record, we discuss plausible plesiomorphic features of pycnogonid development that allow comparison to other arthropods. These features include (1) a holoblastic, irregular cleavage with equal-sized blastomeres, (2) initiation of gastrulation by a single bottle-shaped cell, (3) the lack of a morphologically distinct germ band during embryogenesis, (4) a parasitic free-living protonymphon larva as hatching stage and (5) a hemianamorphic development during the postlarval and juvenile phases. Further, we propose evolutionary developmental trajectories within crown-group Pycnogonida.
A resurgence of studies on pycnogonid postembryonic development has provided various new insights in the last decades. However, the scarcity of modern-day embryonic data – including the virtual lack of gene expression and functional studies – needs to be addressed in future investigations to strengthen comparisons to other arthropods and arthropod outgroups in the framework of evo-devo. Our review may serve as a basis for an informed choice of target species for such studies, which will not only shed light on chelicerate development and evolution but furthermore hold the potential to contribute important insights into the anamorphic development of the arthropod ancestor.
KeywordsSea spider Evolution Arthropoda Embryology Gastrulation Postembryonic development Anamorphic development Evo-devo Protonymphon larva
Arthropod evolution has led to an overwhelming species richness, which goes hand in hand with an extraordinary disparity of morphological forms (e.g., ). When attempting to unravel the evolutionary transformations that underlay the appearance of this multitude of arthropod forms, the study of development can contribute significant insights (e.g., ).
Given the extreme arthropod diversity, it is not surprising that development of many taxa has not been investigated in nearly as much detail as in groups with long-standing laboratory model organisms. Pycnogonida, also known as Pantopoda or sea spiders, is one of these understudied taxa. Although they have since their first description fascinated and puzzled their students – including the Nobel prize-winning founder of Drosophila genetics T.H. Morgan  – investigations of sea spider development remain to this day relatively scarce.
Due to their rather peculiar adult morphology, which features an unusually small and often tube-like body that contrasts starkly to a prominent anterior proboscis and four pairs of long spindly walking legs (Fig. 1a), pycnogonids are occasionally nicknamed the “no-bodies”. However, contrary to the insignificance suggested by this sobriquet, sea spiders are one of the pivotal taxa to take into consideration when reconstructing the evolutionary transformations along the first bifurcations of the arthropod tree of life. Extant pycnogonids are nowadays widely accepted as the descendants of one of the oldest arthropod lineages, which diverged from their next closest surviving relatives in the Cambrian (ca. 500 million years ago, e.g., ). Although their exact phylogenetic position is still not entirely beyond debate (see  for a history of the discussion), recent analyses recover sea spiders within the Chelicerata, as sister group to all remaining extant chelicerate taxa (e.g., [6–8]; see  for review). Accordingly, a better understanding of pycnogonid development has been recognized to hold “great potential to inform on chelicerate evolution and development more generally” .
The last three decades have seen comparably few new investigations on aspects of embryonic development in sea spiders [10–13], which have nonetheless added important new insights to the histological studies from the late 19th and the 20th century [14–18]. By contrast, significantly more studies have investigated postembryonic development (e.g., [19–22]). Differences between the postembryonic development of some pycnogonid lineages were recognized long ago (e.g., [16, 23, 24]) and some more recent works have compiled data and distinguished several developmental pathways (e.g., [19, 25, 26]), with Bain  giving a good overview of the literature on postembryonic development up to the time of publication. However, there are persisting terminological inconsistencies and the need for clarity in the definition of each developmental pathway that has been proposed in earlier summaries and more recently based on new data.
Here, we first summarize key features of sea spider reproduction and embryonic development briefly, before focusing on the postembryonic period. We present a synthesis of previous ideas and propose a more consistent terminology with clearer definitions. The redefined developmental pathways are based on (1) the type and anatomy of the hatching stage, (2) developmental-morphological characteristics during subsequent postembryonic development and (3) selected life history features. Based on these key features and on the current hypotheses on internal phylogenetic relationships, we discuss possible evolutionary developmental trajectories within Pycnogonida.
A primer to pycnogonid biology
With less than 1500 described species, Pycnogonida is a comparably small group by arthropod standards. However, many recent morphological and molecular studies illustrate that the taxonomy of traditional pycnogonid families, genera and even species needs to be critically approached and that actual diversity is hitherto underestimated, with new species being described on a regular basis (e.g., [27–34]). In this review, species names have been updated according to .
Sea spiders are restricted to marine habitats, in which they mostly inhabit the epibenthos, and are encountered at all latitudes and in all depths, including even deep sea hydrothermal vents (e.g., ). Their presence is often not apparent at first glance, since many species are of small size and cryptic in the benthic communities, where they prey on sessile or slow-moving and predominantly soft-bodied invertebrates, often cnidarians but also bryozoans, mollusks, echinoderms or polychaetes [37, 38]. The life cycle of many (but not all) pycnogonids includes different host/prey species during different phases (early postembryonic instars vs. juveniles/adults). This, coupled to the small size of early postembryonic stages and a comparably slow development, renders the establishment of successfully reproducing laboratory cultures challenging and time-consuming. To this day, there are only very few species for which the complete life cycle has been investigated in the laboratory (e.g., Pycnogonum litorale [10, 11, 39–41]; Propallene longiceps [42–44]; Nymphon hirtipes ).
Adult morphology of Pycnogonida
Egg size and egg number
During mating, fertilized eggs are transferred from the female to the ovigers of the male, where they are glued into packages with secretions of cement glands located in the male's femora (see  for review). The egg packages are carried on the ovigers at least until hatching of the first postembryonic instar (Figs. 1b-e and 3a). For some taxa, a polygamous mating system has been documented (e.g., Achelia simplissima ) and males may bear several egg packages stemming from different matings, either separately on each oviger (e.g., Ammotheidae, Endeidae, Nymphonidae, Callipallenidae; Fig. 1c) or with both ovigers together (e.g., some Ascorhynchidae; Fig. 1d). In other groups, only one massive package from a single mating is carried by the male at a time (e.g., Pycnogonidae). While some species are known to reproduce repeatedly over the course of several years (e.g., Pycnogonum litorale ), others have been indicated to die after one reproductive season (e.g., Nymphon hirtipes ).
Range of egg sizes of species belonging to various pycnogonid taxa
Egg diameter [μm]
Brenneis pers. observation
Nymphon gracilipes (“N. fuscum”)
Nymphon macrum (“N. brevicollum”)
(most likely erroneous)
Brenneis pers. observation.
Brenneis pers. observation.
Anoplodactylus jonesi (“A. antillianus”)
(“P. maxillare”, “P. tubulariae”)
Embryonic development of Pycnogonida
By contrast, representatives of some taxa (Callipallenidae, some Nymphonidae, Ammotheidae, Pallenopsidae) have large yolk-rich eggs (diameter ≥ 200 μm, Fig. 2d–f) and unequal cell divisions are observed early on, starting sometimes even with the very first cleavage (e.g., [14, 16, 17]). The resulting blastomere asymmetry could be indicative of an early cell determination, but blastomere arrangements in later stages have not been reported to show a stereotypic pattern. However, rigorous cell lineage studies are pending. The early blastomere asymmetry translates subsequently into an arrangement of small densely packed cells in the prospective ventral embryonic hemisphere (germ disc) and the persistence of slowly dividing, large yolk-rich cells in the other hemisphere (Fig. 2d) [12, 17]. Classical histological studies have characterized the gastrulation as epiboly (e.g., ), detailed observations obtained with modern techniques are lacking. The germ disc develops into a germ band (Fig. 2e, “intermediate germ” according to ), the margins of which continue to extend and overgrow the yolk-rich cells during subsequent embryonic morphogenesis .
Reinvestigations of stomodeum and proboscis formation during embryonic morphogenesis of “small egg species” as well as “large egg species” show that the stomodeum is formed distinctly anterodorsal to the cheliphoral limb buds [10–12]. Only subsequent morphogenetic movements result in the pre-/paroral position of the first limb pair in relation to the outgrowing proboscis. In support of one of the earliest descriptions , proboscis formation does not seem to involve a structure that can be homologized with the labrum (upper lip) of other arthropods [11, 12]. This renders pycnogonids the only arthropod taxon without an identifiable labrum.
With regard to embryonic organogenesis, progress has been made at the level of nervous system development. The cellular processes underlying neurogenesis have been shown to exhibit similarities to different arthropod groups . Among others, the involvement of a neural stem cell type – as indicated in previous histological studies (e.g., [14, 18]) – could be confirmed in advanced stages of neurogenesis. This finding might question the validity of neural stem cells as an apomorphy of hexapods and (some) crustaceans [13, 56]. Importantly, however, gene expression, gene function and cell lineage studies are needed to gain deeper insights not only into these neural stem cells but also into all other aspects of pycnogonid development. As of now, such investigations are almost completely missing (but see [57, 58]).
The protonymphon larva – the most common pycnogonid hatching stage
Postembryonic development of pycnogonids is always indirect, encompassing a series of instars (the term used here to denote developmental stages separated by intermittent molts). More specifically, the great majority of studied pycnogonids show a hemianamorphic postembryonic development (as defined in ), which features an anamorphic phase (=with segment addition per molt) followed by an epimorphic phase (=no further segment addition per molt). The actual molting process has been observed only in a few laboratory cultures (e.g., [39, 44], but see ) and the occurrence of molts is usually inferred from morphological differences between instars.
The larval cheliphore is comprised of three articles: the proximal scape and the two more distal ones, which form a chela (Fig. 3b). The palpal and ovigeral larval limbs are uniramous and three-articled as well, their distalmost article being generally claw-shaped (Fig. 3b–d; exception: Phoxichilidiidae, see below).
Posterior to the ovigeral larval limbs, the hind body is fairly undifferentiated. Internally, it comprises the anlage of the first walking leg segment (in some species even that of the second walking leg segment), as evidenced by the presence of primordia of the segmental ventral ganglia (Fig. 3c; e.g., Achelia borealis , Nymphon brevirostre ). Externally, however, it shows no signs of segmentation and only in some species, a slight elevation of the walking leg 1 primordium may be discernible at the posterior body pole. Dorsal to the developing ventral nerve cord, the midgut represents a blind ending sac – hindgut and anus are not yet developed (Fig. 3c and d). Anteriorly and posteriorly directed midgut extensions may indicate the anlagen of the midgut diverticula of cheliphores and future walking legs 1 (Fig. 3d).
Typically, an attachment gland is located in the cheliphore’s scape (Fig. 3c and d), being connected to a hollow spine on the scape. Thread-like secretions are released through this spine, by means of which the larva either secures attachment to its invertebrate host or remains fixed on the father’s oviger. Correspondingly, the palpal and ovigeral larval limbs may each bear a flexible spine with a pore on the proximal article (Fig. 3b-d; e.g., Ammothella biunguiculata ), being connected to a gland suggested to be serially homologous to the cheliphoral attachment gland [15, 67]. However, the function of these palpal and ovigeral glands is unknown.
In addition, the chela itself often houses another set of glands (Fig. 3c and d) that open to the outside via a pore on each of the chela fingers [15, 19, 61, 67]. An involvement of the chela glands in feeding or defense has been suggested but not yet conclusively proven [16, 68].
The larval, postlarval and juvenile phases of pycnogonid development
Postembryonic development after hatching can be subdivided into three different phases: the larval, postlarval and juvenile phase.
The larval phase
The postlarval phase
In the majority of species, the postlarval phase encompasses the anamorphic molts of the postembryonic development and is always characterized by the formation and further differentiation of the walking leg segments with their substructures. Characteristic larval features are still retained during (parts of) this phase. For instance, the cheliphoral attachment gland and its associated spine often remain functional in the first postlarval instars. Likewise, the structure of three-articled palpal and ovigeral larval limbs may at first stay unchanged, but soon after the anterior walking leg pairs become functional they decrease in size and gradually atrophy (especially the ovigeral larval limbs) (Fig. 4b–e). The timing of walking leg segment development varies between different pycnogonid groups (see below). Most commonly, each walking leg differentiates via three external stages, separated by two intermittent molts. An unarticulated elongate limb bud is followed by an intermediate seven-articled leg (with “femur-tibia 1” and “tarsus-propodus” precursor articles), which then finally transforms into the nine-articled adult leg (e.g., Tanystylum orbiculare ; Nymphon unguiculatum ). Slight deviations from this pattern are documented in some species (see  for an overview).
As in the protonymphon larva, the formation of the ventral segmental ganglia continues to predate limb bud outgrowth in each walking leg segment (e.g., [65, 70]). Thus, the complete number of segmental ganglia is already discernible in instars with an incomplete set of walking leg anlagen (Fig. 4c and d). Addition of new neural cells to the growing ganglia continues during the entire postlarval and also in the subsequent juvenile phase (potentially even still in adults). The regions of neural cell production (“neurogenic niches”) correspond to the “ventral organs” described in classical histological studies [14, 16, 71]. Extant pycnogonids develop one or two additional small ganglia in late postlarval instars, which then fuse with the last walking leg ganglion (Fig. 4d and e; e.g., ).
Soon after walking limb bud outgrowth, the corresponding midgut diverticulum begins to extend into it (Fig. 4). Data on the timing of hindgut and anus formation are scarce. To all appearances, these events are related to the beginning of active feeding, which varies significantly between postembryonic developmental pathways (see below).
Reliable information on the location of the primordial germ cell(s) in the larval stages is missing, but the paired gonad anlagen become recognizable in the early postlarval phase in a dorsal position at the border of walking leg segments 1 and 2 . From that point on, they continue to differentiate and expand through the trunk and into the walking legs [14, 16, 72].
The juvenile phase
The transition from postlarval to juvenile phase is here based on the molt that leads to a “miniature adult” with the full number of functional walking legs (although the last pair might still lack the complete article number) (Fig. 4f). In most known cases, this represents the first epimorphic molt.
In the juvenile phase, the cheliphoral attachment gland and its spine are lacking. The palpal and ovigeral larval limb pairs start to transform into the adult structures, i.e., they grow gradually out into the palps and ovigers (if present in the adult) or are completely atrophied (e.g., Fig. 4f). Also the proboscis and cheliphores attain their definite adult structure, which leads in some taxa to a partial (e.g., Tanystylidae ) or even complete cheliphore reduction (e.g., Colossendeidae: Fig. 1a; Pycnogonidae ). The ocular tubercle has become more prominent and bears by now the final number of eyes (sometimes already during late postlarval phase) (Fig. 4e and f). The complete through-gut is formed and terminates with the functional anus at the distal tip of the anal tubercle, which is found in its definite orientation. Due to ongoing gonad expansion and maturation, distinguishing advanced juvenile instars (sometimes called subadults) from mature adults can be challenging. In this phase, external changes after molts may be minimal and mainly limited to an increase of overall body size. Hence, it has been difficult to determine whether a fixed number of species- and sex-specific juvenile molts occur before sexual maturity. Speaking against this, four independent investigations of the development of Pycnogonum litorale [16, 39–41] indicate that the number of juvenile molts varies, ranging from normally five to seven (for both sexes), to exceptionally eight or even nine. Additionally, low temperature and starvation have been shown to increase the duration of intermolt intervals .
Apart from visible mature oocytes in the gonads of females or the bearing of egg packages by males, the most important morphological indicator of sexual maturity is the presence of gonopores on the second coxae.
From hatching to adult: five pathways of postembryonic development
Type 1: Parasitic development with sequential differentiation of walking legs
The eggs and hatching protonymphon larvae are generally of medium size (roughly 100–200 μm) but exceptions are found, e.g., in Endeidae (Endeis spinosa [17, 60] with an egg diameter of 50–60 μm). The scape of the larval cheliphore bears an elongate attachment gland spine that may project beyond the chela tips. The attachment gland comprises exactly two large secreting cells, which also act as reservoirs for the secretion product. Frequently, the hatching larva abandons the father’s ovigers, but offspring may also stay attached to the oviger for one or two molts and leave as postlarval instars with limb buds of the first walking leg pair (e.g., Achelia borealis [65, 75]). The postlarval instars feed actively as parasites. The great majority of investigated species are ectoparasitic, but some cases of apparent endoparasitic development have been reported (e.g., Achelia alaskensis ). The walking leg segments are formed sequentially during the anamorphic molts along a pronounced anterior-posterior developmental gradient, whereby each leg pair differentiates according to the mentioned three-stage-sequence (see above).
In laboratory cultures of Pycnogonum litorale – the best investigated representative of developmental type 1 – five molts from protonymphon larva to the last postlarval instar have been observed [39, 41]. Development up to this fifth molt took on average 83 days at 15 °C water temperature . Adults of this species were observed to live for up to 9 years in laboratory cultures .
Type 2: Lecithotrophic development with sequential differentiation of walking legs
This type corresponds to type 3 of Dogiel , is included in the “attaching larva” pathway of Bain  and represents the “lecithotrophic protonymphon” mode of Bogomolova and Malakhov  and the “prolonged attaching” mode of Burris .
This developmental mode has been observed only in some representatives of Nymphonidae and Ammotheidae. The eggs and hatching protonymphon larvae are large and exceed 300 μm in all reported cases. The protonymphon larva is equipped with a copious amount of yolk that is contained in the sac-like midgut anlage (e.g., [16, 26]). Hence, the posterior body region is significantly more massive as compared to a larva of developmental type 1. Also the first or even all following postlarval instars are lecithotrophic and remain attached to the father’s ovigers. In nymphonids, attachment to the oviger is secured by the thread-like secretions of the cheliphoral attachment glands, which comprise two or more secreting cells and release the secretions at the tip of an inconspicuous short spine [16, 19, 20, 26]. Furthermore, the larval limbs are actively used to cling to the oviger and egg package remnants. Ammotheid larval and postlarval instars belonging to developmental type 2 lack the cheliphoral attachment gland spine (and presumably also the gland), active grasping being their only means to secure attachment to the male [21, 76–78]. The formation of the walking leg segments is strictly anamorphic and the legs themselves develop in a three-stage-sequence. In nymphonids, the offspring leaves the oviger frequently as late as the last postlarval instar, whereas in ammotheids, the oldest documented stage attached to the oviger is a postlarval instar with only two functional walking leg pairs.
Recently, the first successful laboratory culture of a deep sea representative has been established for Nymphon hirtipes . In this species, embryonic development alone lasts for about 4 months and subsequent postembryonic development up to the last postlarval instar (which is leaving the father’s oviger) takes five additional months. Based on available studies, five to six molts from protonymphon larva to the first juvenile instar can be estimated (e.g., [19, 20]).
Type 3: Ectoparasitic development with synchronous differentiation of walking legs
In comparison to the other postembryonic pathways, this type of development remains poorly documented and, as of now, has been encountered only in Ammotheidae. The newly hatched protonymphon larva has been observed in a single species (Nymphonella tapetis ). It hatches from small eggs of 70 μm diameter. The three-articled cheliphore lacks an attachment gland spine and probably also the attachment gland itself. The few reported representatives have been found to parasitize in the mantle cavity of bivalves [79, 80], on sedentary polychaetes living in tubes , or on nudibranchs . Contra Burris , this developmental mode should be still considered ectoparasitic instead of endoparasitic, since none of the postembryonic instars penetrate into the interior of the host body. The first parasitizing instar bears considerable resemblance to a protonymphon larva, but appears to have lost the external articulation of the limbs, although terminal claws may be still present. In contrast to developmental types 1 and 2, the walking leg segments develop almost synchronously, with only a very slight advance in the more anterior limbs. Accordingly, some molts of the postlarval phase are epimorphic. Also the stepwise differentiation sequence of the legs seems to be missing. Notably, in Nymphonella tapetis, neither the palpal nor the ovigeral larval limbs are atrophied. Rather, the adult palps and ovigers arise directly via gradual elongation and articulation of the larval limbs of the first parasitizing instar.
No published report on a successful laboratory culture is available. The number of molts during postembryonic development is undocumented but the described stages of Ammothella spinifera point to at least six . In Nymphonella tapetis, the number might be lower (see ).
Type 4: Endoparasitic development with partially synchronous differentiation of walking legs
All Phoxichilidiidae belong to this developmental type. They possess the smallest reported eggs and a characteristic protonymphon larva (<100 μm in body size). The larval proboscis is very prominent and the larval cheliphores lack the attachment gland and its spine. The terminal articles of the palpal and ovigeral larval limbs are elongated and filamentous, which may facilitate locomotion (“walking”) over benthic communities and/or floating and dispersal in the pelagic zone, as suggested by larvae of Phoxichilidium femoratum found in plankton samples . They are also used to hold on to the host . Predominantly, hydrozoan polyps are infested, but parasitism of hydromedusae has also been described [84, 85]. The larva molts upon encountering a suitable host, which is then entered by the second instar . In some phoxichilidiids, endoparasitic instars are encysted in the host tissue, but in others they are encountered freely in the gastrovascular cavity (e.g., [38, 86, 87]). Hence, we discourage the use of the terms “encysted”  or “encysting”  to designate this pathway as a whole (see also ). The first endoparasitic stage (= second instar) is characterized by significantly reduced, unarticulated palpal and ovigeral larval limbs, but can still be considered a larval stage due to the undifferentiated posterior body region. During the postlarval phase, the limb buds of walking leg pairs 1–3 arise along a very weak anterior-posterior developmental gradient (e.g., Anoplodactylus eroticus ), but their further elongation and differentiation is synchronized, whereas the anlagen of walking leg pair 4 lag distinctly behind. The last postlarval instar emerges through the body wall of the host (e.g., [16, 87–89]).
Reports of a laboratory culture of a phoxichilidiid species are lacking. In P. femoratum, only four molts are described for the complete development from protonymphon larva to the emerging juvenile, this period lasting in total less than 21 days .
Notably, a single ammotheid has been conclusively shown to follow a similar endoparasitic pathway (Ammothea hilgendorfi ). Interestingly, the protonymphon larva of this species lacks the distinctive features of its phoxichilidiid counterpart and represents basically a larva of developmental type 1 .
Type 5: Postembryonic development with hatching of an advanced postlarva
Hatching stages with advanced development of walking leg segments occur in all investigated Callipallenidae (e.g., [17, 44, 68, 92]) and in some nymphonids (e.g., ; Bogomolova, personal observation) and pallenopsids (Brenneis, personal observation). They hatch from large yolk-rich eggs (diameter ≥ 200 μm, in nymphonids and pallenopsids > 500 μm) and are lecithotrophic with a voluminous yolk-filled midgut anlage. Previously, these stages have been termed “attaching larvae” (e.g., [25, 44, 62, 68]) since they remain attached to the father’s oviger after hatching. However, this behavior is not exclusive to them (see types 1 and especially 2) and hence this name is discouraged. Likewise, the term “walking leg-bearing larva”  is here discouraged, and we adopt the more general name “advanced postlarva”, which acknowledges that the developmental level of the hatching stages corresponds to postlarval instars of other pycnogonids. Obviously, all pycnogonids hatching as advanced postlarva lack the larval phase in their development.
Simultaneously to hatching, the postlarva sheds an embryonic cuticle (e.g., [12, 17, 44]). It features at least the limb buds of walking legs 1 and 2 [44, 63, 68] but in some species, elongate unarticulated walking legs 1–3 plus a small limb bud of walking leg 4 are already present [14, 22, 23]. This latter case, as found, for instance, in all investigated species of the genus Callipallene, represents thus an exception to the hemianamorphic theme – all postembryonic molts are epimorphic. The hatching postlarva lacks fully pigmented eyes and an open anus and remains attached to the father’s oviger for at least one additional molt. Attachment is achieved via strong threads of the cheliphoral attachment gland that comprises three or more secreting cells [24, 26, 65]. Hatching postlarvae of pallenopsids possess small but fully developed palpal and ovigeral larval limbs (Fig. 9e), but nymphonid representatives feature only a limb bud at the position of the palpal larval limb, and callipallenids lack distinct buds of larval limbs completely. If posterior body segments are still missing at hatching, they form sequentially and their walking legs follow the typical three-stage-development [22, 44, 68]. The earliest stage known to abandon the father is a postlarval instar with two functional walking leg pairs (Propallene longiceps ), but in other species it may be only the last postlarval or even a juvenile instar that leaves the oviger (e.g., Callipallene brevirostris, C. emaciata [14, 18]).
In a laboratory culture of P. longiceps, five molts (including shedding of embryonic cuticle) were observed from hatching to the first juvenile instar. Up to the mature adult, a total of nine molts occur, the entire development from fertilized egg to adult lasting about 5 months .
The evolution of the different developmental pathways in Pycnogonida
Fossils, phylogenies and the ancestral mode of pycnogonid development
From a comparative developmental perspective, the five postembryonic pathways share notable correspondences, representing variations of a common hemianamorphic theme, in which mainly the relative timing of events relating to the forming walking leg segments is modified. Type 5 with its more pronounced embryonization of development deviates most from the others due to the complete lack of the protonymphon larva, but shares nonetheless many similarities with regard to the developmental sequence of segmental substructures (e.g., early development of segmental ganglia, pattern of walking leg segmentation). This leaves still the open question, which of the five pathways has retained most plesiomorphic features of the development of the pycnogonid stem species.
In general agreement with this notion, the oldest allegedly pycnogonid fossil – the Cambrian Cambropycnogon klausmuelleri  – has been described as a postlarval instar with three anterior limb pairs (presumably homologous to cheliphores plus palpal and ovigeral larval limbs) and just a single pair of elongate limb buds (presumably anlagen of first walking legs). Also the body length (~270 μm) corresponds well to a comparable postlarval instar of extant representatives of developmental type 1 (e.g., Pycnogonum litorale: 260 μm ). Thus, the discovery of Cambropycnogon seems to support an anamorphic postembryonic development as an ancient pycnogonid feature. However, it has to be cautioned that all described fossil specimens belong to a single instar only, and neither an earlier protonymphon-like larva, nor further advanced postlarval or juvenile instars are known. Accordingly, direct fossil evidence for a protonymphon-like larva without walking leg anlagen – dating back to the Cambrian or any later geological age – is still missing.
Yet, not only the fossil record but also extant sea spiders leave us with some persisting gaps of knowledge: For the three pycnogonid taxa Austrodecidae, Colossendeidae and Rhynchothoracidae neither mating behavior, nor embryonic or early postembryonic development have ever been documented. This is especially astounding in the case of the large-sized colossendeids – which are cosmopolitan, relatively diverse and frequently collected – and leads to the suspicion that this group may exhibit a deviating mode of reproduction and development that completely lacks paternal brood care [25, 37, 93]. Coincidentally, the two hitherto most comprehensive phylogenetic analyses [96, 97] indicate that Austrodecidae and Colossendeidae might have diverged relatively close to the base of the pycnogonid crown-group (if not even at the base itself, see Fig. 10). Additionally, a basal position of colossendeids within pycnogonids has also received some support from the analysis of the mitochondrial genome  (but only a very limited number of taxa are included). In light of this, the lack of developmental data in these taxa needs to be borne in mind when drawing conclusions regarding ancestral developmental patterns of Pycnogonida.
As of now, developmental type 1 remains uncontested as most plausible ancestral pathway of pycnogonid development (Fig. 10). However, with new data and a more reliable pycnogonid phylogeny, some of the features currently considered plesiomorphic for sea spider development may yet turn out to have evolved only within the pycnogonid crown-group.
Multiple transitions from parasitic to lecithotrophic protonymphon larvae during pycnogonid evolution
To date, developmental type 2 with a lecithotrophic protonymphon larva has been described only in some nymphonids and ammotheids, both taxa also containing species following developmental type 1. Apart from the yolk-related size increase of the protonymphon larva and the correlated prolonged lecithotrophic nutrition, type 2 is closest to type 1, with no major changes in the sequence or timing of developmental events (apart from the nutrition-related differentiation of the hindgut and anus). It seems therefore plausible that an evolutionary switch from type 1 to type 2 may have occurred independently within both pycnogonid taxa (Fig. 10). Interestingly enough, some representatives described as type 1 show the “beginning” of lecithotrophic nutrition in the first postembryonic instars (e.g., Achelia borealis [65, 75]); thus, type 1 and type 2 might well represent the extremes of a more continuous distribution.
Notably, developmental type 2 is documented predominantly in species living in cold waters as opposed to species of temperate or tropical latitudes. Accordingly, the switch to a more pronounced K-strategy via lecithotrophic nutrition and prolonged attachment of the offspring has been suggested to be an adaptation to low temperature habitats [25, 94, 99]. Yet, since type 1 representatives coexist in the same environments, lecithotrophic nutrition may well be a favorable but not an indispensable life history feature for pycnogonid survival in the cold.
Without a reliable internal phylogeny for nymphonids or ammotheids, independent type 1-to-type 2 transitions within each group remain a possibility. However, as of now, reports of lecithotrophic protonymphon larvae in ammotheids remain restricted to Antarctic species of the genus Ammothea. Further, all of these Ammothea species lack the characteristic cheliphoral attachment gland spine and most likely also the corresponding gland itself. This indicates a single evolutionary switch to lecithotrophic developmental type 2 in the genus Ammothea, coupled to an apomorphic loss of the attachment gland and spine in the larva.
Endoparasitic development is apomorphic for Phoxichilidiidae and a derived trait in the pycnogonid tree
The endoparasitic developmental type 4 is encountered in all phoxichilidiids. It can be unequivocally characterized by the unique – and therefore likely apomorphic – morphology of the protonymphon larva, the short duration of the development and the low number of molts. Phoxichilidiidae has been repeatedly recovered well-nested in the pycnogonid tree, as sister group to Endeidae [96, 97, 100]. Both taxa encompass pronounced r-strategists with extremely small eggs and hatching larvae. Since endeids – as unequivocally shown for Endeis spinosa [16, 17] – include representatives of developmental type 1, this mode seems a likely starting point for the evolution of the endoparasitic phoxichilidiid development (Fig. 10). The comparatively fast course of the latter might be an evolutionary adaptation that facilitates exploitation of hosts with distinct yearly growth periods in habitats governed by significant seasonal variations .
In light of the available phylogenetic studies (e.g., [96, 97]), the occurrence of a similar endoparasitic development in the ammotheid Ammothea hilgendorfi has to be interpreted as an independent evolutionary event. It is intriguing that this species seems to show a corresponding partially synchronized differentiation of the walking leg segments and reinvestigation of the encysting postlarval instars would be desirable, in order to assess similarities and differences to phoxichilidiids in more detail.
Multiple gains of embryonized development during pycnogonid evolution
Large yolk-rich eggs and the hatching of an advanced postlarva (type 5) are characteristic of all Callipallenidae, but are also found in some nymphonids (e.g., ; Bogomolova, personal observation) and members of the Pallenopsidae (Brenneis, personal observation).
Callipallenids and nymphonids have been recovered together in a clade [96, 97, 100, 101]. Yet, callipallenids have been recovered as a paraphyletic group due to the nested position of Nymphonidae (Fig. 10). If this controversial finding should receive further corroboration in future studies, one possible evolutionary scenario advocates the embryonization of development as a derived feature of the callipallenid-nymphonid clade, leading to a postlarva as an apomorphic hatching stage (Fig. 10). However, a reversal of this process must then have led to the re-occurrence of the protonymphon larvae of developmental types 1 and 2 within nymphonids (for discussion see ).
Regardless of the prevailing interpretation in the callipallenid-nymphonid case, the presence of developmental type 5 in some Antarctic Pallenopsis reveals at least one parallel event of embryonization of pycnogonid development (Fig. 10). The relationship of the genus Pallenopsis to other pycnogonid taxa has been matter of recurrent debate, having traditionally been considered a “transitional genus” between Callipallenidae and Phoxichilidiidae [47, 101–104]. In contrast to this, available phylogenetic studies generally suggest closer affinities to ammotheids and Endeidae + Phoxichilidiidae (albeit with weak support) [96, 97, 100]. Due to this and the presence of developmental type 1 in some Pallenopsis species, we must assume that a separate evolutionary transition from type 1 to type 5 within the genus Pallenopsis has taken place. A remarkable feature of pallenopsid hatching postlarvae is the presence of functional palpal and ovigeral larval limbs (Fig. 9e) as opposed to their absence or undifferentiated state in callipallenids or nymphonids, respectively. This morphological feature thus distinguishes pallenopsids from the other two pycnogonid groups with embryonized development.
Outlook – the no-body’s contribution to arthropod evolution
The last two decades witnessed a resurgence of studies on pycnogonid postembryonic development, which provided new data and insights into the diversity of developmental types in crown-group pycnogonids. We considered it pertinent to review the data available and to resolve current inconsistencies by clarifying the terminology and delineating the different postembryonic pathways known so far. It is conceivable that new data, especially on some of the enigmatic pycnogonid groups (such as Austrodecidae and Colossendeidae) may render the re-evaluation of this scheme necessary at some point in the future. In particular the recent success of the laboratory husbandry of a deep sea nymphonid  holds promise for more revelations regarding the life cycle of some of the largely unstudied deep sea preferring taxa.
With no established laboratory model organism found among sea spiders, our understanding of many developmental processes at the cellular level and in terms of the underlying genetic mechanisms is still in its infancy. Clearly, additional studies are overdue and future investigations could address, among others, (1) the early embryonic development in “large egg species”, (2) the gastrulation in “large egg species” and the exact relationship of the mesodermal and entodermal cell lineages in pycnogonids in general, (3) the identification and localization of the germ line precursors during embryology, and the (4) understanding of axial growth and segmentation processes in the different developmental types. Ideally, such studies would include modern live imaging techniques, and their underpinning with gene expression and gene function data is needed. Although previous attempts to address the latter two issues have faced several challenges, first progress in the optimization of protocols has been made (e.g., [57, 86, 105]) and the by now straightforward generation of RNA seq data (or even genomes) for non-model organisms has removed several of the formerly cumbersome obstacles.
In terms of species choice for such studies, Pycnogonum litorale is without doubt the most promising candidate of the putatively plesiomorphic developmental type 1. Not only have successfully reproducing populations of this long-lived species been kept in the laboratory for several years (e.g., [39, 40]), but also the general course of embryonic and postembryonic development is best understood due to a series of relatively recent studies (e.g., [10, 11, 41]). By contrast, however, representatives of the further derived type 5 have the great advantage of developing part (or all) of the body segments and legs during the embryonic phase, which facilitates many investigations considerably, since embryos of different developmental stages are easily located on the males’ ovigers (as opposed to free-living postembryonic instars in type 1). Hence, a long-term laboratory culture of a type 5 species – as at least partially achieved for Propallene longiceps some decades ago [42–44] – would be highly desirable for pycnogonid research. Ideally, a combination of studies on both developmental types will enable the elucidation of general developmental mechanisms of crown-group sea spiders at the level of gene expression and gene function and thus pave the way for detailed comparison with available data on other arthropods and arthropod outgroups.
It is noteworthy that Pycnogonida is the only extant chelicerate taxon that shares with many crustaceans a life cycle that includes a minute marine larva with only three limb-bearing segments [e.g., ). The correspondence between the protonymphon larva and crustacean nauplius larva has been noted early on (see ) and traditionally some authors have even used it as an argument in support of a sister group relationship of both arthropod groups (e.g., [15, 16]). Even though today’s countless phylogenetic studies render this close relationship untenable (see  for review), it remains plausible that protonymphon and nauplius larvae have a common origin in a segment-poor larva in the life cycle of the marine arthropod ancestor [55, 107, 108]. Seen from this perspective, a renewed interest in the development of the arthropod “no-bodies” might not only shed more light on chelicerate evolution and development . Beyond that – and in combination with further studies on crustaceans with nauplius larva and with new fossil evidence (e.g., ) – it has the potential to yield insights into the anamorphic development of the ancestor of today’s most diverse and successful animal lineage.
Attachment gland spine
Ovigeral larval limb
Palpal larval limb
Ventral nerve cord
Walking leg ganglion
Darwin Devidas Ramteke and Baban Ingole are thanked for providing the postlarvae of Propallene kempi. The help of Katsumi Miyazaki and Koichiro Nakamura in identifying Ascorhynchus ramipes is gratefully acknowledged. We are indebted to Amy Maxmen for permitting us to use images of Anoplodactylus eroticus. We thank two anonymous reviewers for their comments and suggestions which helped to improve the manuscript.
GB is funded by a postdoctoral fellowship of the Deutsche Forschungsgemeinschaft (BR 5039/1-1). CPA would like to thank the Australian Biological Resources Study (ABRS) (Grant No. 204–61) and the Australian Antarctic Science Grants (AA3010).
Availability of data and material
The great majority of the discussed data were extracted from the literature. Images showing previously unpublished material were taken from material in the care of the first author (GB).
GB drafted the manuscript and designed the figures, including some hitherto unpublished images of adults and developmental stages. EVB, CPA and FK intensively discussed data with GB and contributed significantly to the structuring and rewriting of the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
The studied animals are non-regulated invertebrates. Therefore no ethics approval is needed.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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