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Scorpions and life-history strategies: from evolutionary dynamics toward the scorpionism problem
© The Author(s). 2018
- Received: 12 July 2018
- Accepted: 3 August 2018
- Published: 22 August 2018
This work aims to contribute to the general information on scorpion reproductive patterns in general including species that can be noxious to humans. Scorpions are unusual among terrestrial arthropods in several of their life-history traits since in many aspects their reproductive strategies are more similar to those of superior vertebrates than to those of arthropods in general. This communication focuses mainly on the aspects concerning embryonic and post-embryonic developments since these are quite peculiar in scorpions and can be directly connected to the scorpionism problem. As in previous similar contributions, the content of this communication is addressed mainly to non-specialists whose research embraces scorpions in several fields such as venom toxins and public health. A precise knowledge of reproductive strategies presented by several scorpion groups and, in particular, those of dangerous species may prove to be a useful tool in the interpretation of results dealing with scorpionism, and also lead to a better treatment of the problems caused by infamous scorpions.
- Reproductive strategies
- Postembryonic development
In a series of previous publications addressed to the readers of the Journal of Venomous Animals and Toxins including Tropical Diseases, I attempted to provide some general information about scorpions and scorpionism, broadly addressed to non-specialists whose research embraces scorpions in several fields such as venom toxins and public health [1–6]. Most of the information previously supplied concerned historical aspects of scorpion studies but also several questions on their taxonomy, evolution and geographic distribution [1–6].
It is obvious, however that the scorpionism problem is not only associated with the evolution of toxins in some groups (families and genera) of scorpions, but also has close connections with their life-history strategies. For example, the ecology of a given population can directly influence its presence in nearby human habitations . Similarly, reproductive strategies are globally associated with the dynamics of each scorpion population. General aspects of scorpion ecology and ecophysiology remain incompletely studied but will not be the subject of the present communication. Contrarily, many reproductive aspects of scorpions are presently known and attest to the strong particularities in their mode of reproduction . In many aspects, scorpion reproductive strategies are more similar to those of superior vertebrates than to those of arthropods in general. In this communication, I will focus on the aspects concerning embryonic and post-embryonic developments since these aspects are peculiar to scorpions and have direct connection with scorpionism problems. Furthermore, I will avoid discussing behavioral aspects that are of less interest in relation to the problem of scorpionism. Much information has been published for more than a century on the development of the scorpions, but it is usually available in specialized literature, and is so scattered that it becomes unavailable for non-experts on the subject. Previous syntheses are already old [7, 8]; consequently a new presentation should be welcome to a broad audience.
The synthesis presented in this communication is mainly based on my personal research on scorpion reproductive biology performed during more than 40 years. It must, however be considered incomplete, since our global knowledge on scorpions’ biology still presents numerous gaps. For some extremely poorly studied groups no data are presently available. Nevertheless, the proposal of a more accessible synopsis appears to be valid in relation to the non-expert readers of the journal.
On account of the unusual traits of their life history, many aspects of the reproductive biology of scorpions were poorly understood by pioneering authors, such as the classical “promenade à deux” described by Maccary  and Fabre . Only by the middle of the 1950s, several researchers discovered, independently, that sperm transfer was accomplished by means of a spermatophore. The first reports were those by Angermann  and Alexander .
Nevertheless, long before the middle of the twentieth Century, detailed studies of scorpion embryology were developed by authors such as Laurie [17–20], which were followed by those of Pavlovsky [21, 22] and Pflugfelder . Naturally, all these authors worked mainly through the techniques of comparative morphology based only on preserved specimens. Observations on living specimens started to take place by the 1950–1960s [24–26]. After these pioneering original contributions, much less attention was paid to embryology and only isolated publications provided additional information [27–35].
The first contribution on the post-embryonic development of scorpions was the publication by Schultze . Beginning in the mid-1950s, several accounts of various aspects of the reproductive biology, in some cases of the entire post-embryonic development of scorpions, have been published. These were mainly by biologists such as Alexander [16, 37, 38], Auber [39, 40], Matthiesen [25, 26], Maury [41, 42], Shulov and Amitai , Shulov et al. , Varela  and Williams . More recently other biological cycles of scorpions were studied [11, 47–53]. Several of these works dealt with groups never before observed. Naturally, these citations are certainly not exhaustive; a more complete list of references can be found in Polis and Sissom  and Lourenço .
The mid-1970s saw a renewal of interest in the reproductive biology of scorpions and particularly in their post-embryonic development. Research on this subject was multiplied during the 1980s and continued throughout the 1990s and 2000s. Interestingly, most of the authors of this work were taxonomists who, in addition to obtaining biological information, were investigating the ontogenetic variability of the characters used in taxonomy (see Lourenço  for references). The contributions by Polis and Farley [54, 55] represented an interesting exception since these authors attempted for the first time to explain reproductive traits in the context of evolutionary ecology. However, in more recent years disengagement toward biological studies has been observed since almost all the attention is given to phylogenetic and molecular studies.
A great disparity is evident from the known biological data in relation to the used methodology and the quality of the observations made. In many cases, the information reported may be speculative or even fallacious. I will not, however, discuss these aspects here.
Interpretation of the ecology and geographical distribution patterns of scorpions cannot be achieved without a precise knowledge of the reproductive biology of these animals. Their capacity for a passive dispersion (normally transport by human agency) and possible re-adaptation to different and/or largely modified environments is totally dependent on their reproductive strategies. For this reason, scorpion species are generally divided into two categories: (i) equilibrium species, and (ii) opportunistic species. The reproduction models observed in these two categories are generally in accordance with their ecological requirements. Equilibrium species are totally dependent on stable and predictable environments, whereas opportunistic species have weak ecological requirements and are able to colonize highly modified and unpredictable environments. I will emphasize in the following sections two aspects of scorpion reproduction that are factors related to their definition as equilibrium or opportunistic species, and to their embryonic and post-embryonic developments. For more details on other aspects of scorpion reproduction, the reader can refer to Polis and Sissom  and Lourenço , where these aspects are presented in full detail.
The most complex gradients of embryonic development with well-developed diverticula are exhibited by the best known scorpion families including the Scorpionidae, Diplocentridae, Hormuridae, Hadogenidae, Urodacidae, and most certainly the Hemiscorpiidae and Heteroscorpionidae (Fig. 9). In other families – such as the Buthidae, Bothriuridae, Chactidae, Euscorpiidae, Scorpiopidae, Superstitioniidae, Vaejovidae, Iuridae and Chaerilidae – the gradients range from simple to moderately complex (Figs. 7 and 8). No data are available for poorly known families, such as the Microcharmidae, Troglotayosicidae and Pseudochactidae.
According to the model of embryonic development and also in association with the species’ lineage, the duration times of this development can show some huge variations ranging from 2.5 months for some buthid species to 24 months for some species of the family Hormuridae. Nearly complete tables are available in Polis and Sissom  and Lourenço .
After a single insemination, females of species belonging to these genera are able to give birth to as many as five broods when isolated in laboratory conditions. Isometrus maculatus represents a particular case since the number of broods can reach seven in this species . These observations have a bearing on the interpretation of the reproductive strategies of scorpions. Storage of spermatozoa can greatly increase the reproductive potential of some species and is most significant given that two of the buthid genera concerned (Centruroides and Tityus) contain species of medical importance that are responsible for thousands of incidents in which human beings are stung and not infrequently killed.
Many, if not most, of these small species of buthids and microcharmids show a strongly reduced litter size, in most cases with numbers less than 10 and in others less than 7 juveniles. It is important to note that reduced broods have also been observed in large species of buthids, in which normal values range from 15 to 50. These weak numbers have frequently been reported as standard by several authors ; however, this interpretation is incorrect since this situation can be observed among females of any species arriving at the end of their reproductive life, when the number of follicles starts to decline . These numbers should not be retained as standard average values.
In fact the number of juveniles in a litter is directly related not only to the scorpion lineage but also to the durations of embryonic and post-embryonic development, i.e. the number of molts necessary to reach adulthood. This leads to a number of conclusions: the size of litter size in a given species is independent of ecological factors, since species with similar brood sizes can be humicolous or live in rain forests while others inhabit arid environments and even deserts. In all cases, as already proposed by Francke , litter size is directly proportional to the size of the female and inversely proportional to the size of the young. The large body size of pro-juveniles at birth seems to be associated with a more ‘complete’ embryonic development. This factor may permit a strategy of post-embryonic development with a smaller number of instars. Morphometric growth values presented by pro-juveniles that belong to very small broods are higher than those observed generally in other buthoids. Finally, the sex ratio of most species within a given population is often close to 1:1, but some species have ratios of 3:1 or 4:1 in favor of females.
Post-embryonic development comprises the period after birth until the adult stage has been reached. It can be divided into two phases: pro-juvenile and juvenile. The pro-juvenile phase consists of a single instar that lasts from the moment of birth until the first molt. During this instar the young remain on their mother’s back (Figs. 12, 13 and 14). The first instar young cannot feed or sting. Their tarsi possess suckers instead of the ungues that appear only after the first molt. The duration of the pro-juvenile instar is variable, ranging in general from 5 to 25 days. The first molt takes place simultaneously among all the pro-juveniles in the litter. On average, it takes from 6 to 8 h. The juvenile phase begins after the first molt and comprises a variable number of instars that differ according to the species; a variation in the number of instars can also be observed within the same species [7–9, 59, 61]. The duration of a given instar is variable among juveniles of the same litter. However, in social species such as Opisthacanthus cayaporum (Fig. 15) most if not all the juveniles of the litter will molt within a short period of time, normally during the same night . This behavior suggests a group effect.
In several species, males and females can be distinguished only after the last molt when sexual dimorphism becomes visible. This is the case in several species from the buthid or chactid genera, such as Tityus, Centruroides, Babycurus, Brotheas and Broteochactas, etc. In other buthid or ischnurid species, such as those belonging to the genera Grosphus and Opisthacanthus, sexual dimorphism is apparent from birth and the sexes can easily be recognized after the first juvenile instar (instar 2).
Parthenogenesis (from the Greek παρθενος parthenos = ‘virgin’ + γενεσις genesis = ‘birth’) is a form of reproduction in which the ovum develops without fertilization. This phenomenon in scorpions was previously outlined in previous papers [5, 63]; however, since this last synthesis some more data became available and are herein summarized.
Historically, this very peculiar phenomenon was first described in the Brazilian buthid Tityus serrulatus . Most new findings about this reproduction process in scorpions were confirmed after the 1990s and 2000s, in contrast with the suggestion of Polis and Sissom  to whom this phenomenon would be rare.
Among more than 2200 species of scorpions distributed throughout the world, about 15 are known or at least have been suggested to be parthenogenetic [5, 63, 64, 66]. After the original report by Matthiesen  on Tityus serrulatus, several other species proved to be parthenogenetic. The majority of the reports concern species of the family Buthidae that belong to the genera Tityus, Hottentota, Ananteris, Lychas and Pseudolychas. Other reports are also known for non-buthid species that belong to the genera Liochelis (Hormuridae) and Serradigitus (Vaejovidae).
The parthenogenetic pattern observed in scorpions corresponds in all cases to the model defined by Vandel  as ‘geographic parthenogenesis’, and can be tentatively explained in terms of the life-history strategies of the populations. However, very few studies are available on the comparative dynamics of parthenogenetic vs. sexual populations. The single exception is the comparative study carried out by Lourenço et al.  on the Colombian populations of Tityus columbianus. The authors reported that most ecological parameters have been compared between parthenogenetic and sexual aspects, and demonstrated that the sexual females were significantly larger and had significantly greater relative litter mass than the parthenogenetic ones .
Reproductive strategies are intrinsically associated with the population dynamics of each scorpion species. Consequently, species presenting short life cycles, capacity to store spermatozoa and the potential to reproduce asexually (parthenogenesis) will be preferentially selected in newly created environments generally disturbed by human action. The longer life cycles seem to predominate in older lineages with narrow-ranged species, but variability is also observed in these groups, and may have been the key for the adaptation of so many scorpions in a diversity of habitats on all continents.
When these reproductive parameters are associated with strongly opportunistic species capable of colonizing disturbed and unpredictable environments, one can observe populations ‘explosions’, since in these cases regulations are not of the density-dependent type, but rather of the catastrophic type [59, 69]. This basic model seems to be perfectly applicable to several infamous species of Tityus in South America, Centruroides in North America and Androctonus in North Africa [2–4].
I am most grateful to the staff of JVATiTD for their new invitation to contribute a communication to the journal. To Elise-Anne Leguin (Muséum, Paris) for her assistance in the preparation of several plates. To Eric Ythier, Syntech Research, France, for permission to use some of his scorpion photos and in particular to Lucienne Wilmé of the Missouri Botanical Garden for very useful comments on the initial versions of the text.
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