Madagascar: an unexpected hotspot of social Anelosimus spider diversity (Araneae: Theridiidae)

Abstract. The spider genus Anelosimus Simon, 1891 (Theridiidae) currently contains over forty described species, found worldwide in tropical to warm temperate areas. American Anelosimus are all social, a rare trait among spiders, but social behaviour has not been reported for Anelosimus species elsewhere. Old World Anelosimus are poorly known, both behaviourally and taxonomically, and no Anelosimus species have yet been described from sub-Saharan Africa or Madagascar. Based on a preliminary phylogenetic analysis we predicted sociality in an undescribed Madagascar species because it grouped among social New World species. An expedition to Madagascar then found no less than five undescribed periodic-social (subsocial) Anelosimus species in Périnet reserve. A sixth species from the same locality is known from museum specimens and the Anelosimus diversity of Périnet is comparable with the most diverse single locality in the Americas. Subsocial species play a key role in understanding the evolution of permanent sociality (quasisociality). This increased pool of available subsocial study species demonstrates the utility of phylogenies as predictors of traits in species thus far unstudied. Here, A. andasibe sp.n. , A. may Agnarsson sp.n. , A. nazariani sp.n. , A. sallee sp.n. , A. salut sp.n. and A. vondrona sp.n. are described. Anelosimus locketi Roberts, 1977 from Aldabra Atoll is a junior synonym of A. decaryi ( Fage, 1930 ) comb.n. from Madagascar. Preliminary data on the behaviour of the new species are given, indicating a level of sociality similar to the American A.‘arizona’¹. The phylogenetic analysis supports the monophyly of the Madagascar group and places it as sister to a clade containing the eximius lineage from the Americas, and a pair of undescribed Tanzanian species.     

Revision and phylogenetic analysis of American ethicus and rupununi groups of Anelosimus (Araneae, Theridiidae)

Two species groups of the social spider genus Anelosimus are revised. The ethicus group contains six species found in South America, in an area ranging from the Guianas to southern Brazil and Argentina. Of these, A. rabus Levi, 1963, A. ethicus ( Keyserling, 1884 ), and A. nigrescens ( Keyserling, 1884 ) are redescribed, while A. nigrescens is removed from synonymy with A. ethicus . Three new species are described: A. misiones sp. nov., A. sumisolena sp. nov. and A. inhandava sp. nov. Anelosimus ethicus is reportedly either subsocial or solitary, while the behaviour of the other species in the group is unknown. The rupununi group contains two quasisocial species, A. rupununi Levi, 1956 and A. lorenzo Fowler & Levi, 1979, from the Caribbean and tropical South America. Both are redescribed here. A parsimony analysis of morphological characters provides support for the monophyly of both groups. In the phylogeny, subsociality optimizes to the base of Anelosimus , indicating that the common ancestor of the ethicus group was subsocial. Its members can thus be predicted to be subsocial, or secondarily solitary. Quasisociality arose de novo in the rupununi group, representing one of 6−7 independent origins in theridiids. Study of the biology of Anelosimus is important to advance our understanding of the evolution of sociality in spiders.     

Shifting continents, not behaviours: independent colonization of solitary and subsocial Anelosimus spider lineages on Madagascar (Araneae, Theridiidae)

Agnarsson, I., Kuntner, M., Coddington, J. A. & Blackledge, T. A. (2009). Shifting continents, not behaviours: independent colonization of solitary and subsocial Anelosimus spider lineages on Madagascar (Araneae, Theridiidae). —Zoologica Scripta, 39, 75–87. Madagascar is a biodiversity hotspot, thought to be colonized mostly via Cenozoic dispersal from Africa, followed by endemic radiation of multiple lineages. Anelosimus spiders are diverse in Madagascar, and, like their congeners in the Americas, are most diverse in wet montane forests. Most Anelosimus species are social in that they cooperate in web building and prey capture either during a part of their life cycles (subsocial), including hitherto studied Malagasy species, or permanently (quasisocial). One Central American coastal species, Anelosimus pacificus, has secondarily switched to solitary living, and available evidence suggests that its closest relatives from S. America and Europe are likely also solitary. Here, we show that the only known coastal Anelosimus species in Madagascar and Comoros –Anelosimus decaryi and Anelosimus amelie sp. n. – are also solitary. Using a phylogenetic approach, we test two competing hypotheses: (i) that Malagasy Anelosimus are monophyletic and thus represent a second example of reversal to solitary living in a littoral habitat or (ii) that solitary and subsocial lineages independently colonized Madagascar. We find that solitary Malagasy Anelosimus are closely related to their solitary counterparts from Europe and the Americas, while subsocial Malagasy species nest sister to Anelosimus nelsoni from S. Africa. This finding suggests that (i) the two Anelosimus lineages colonized Madagascar independently and (ii) a reversal to solitary behaviour has occurred only once in Anelosimus. Thus, solitary littoral Malagasy species did not descend from Malagasy mountains, but arrived from much further afar. African and possibly American origin of the two lineages is implied by our findings. To restore natural classification of Anelosimus, Seycellocesa Koçak & Kemal is synonymized with it.     

Molecular phylogenetics and evolution of Orchidinae and selected Habenariinae (Orchidaceae)

Internal transcribed spacer (ITS nuclear rDNA) data have been obtained from 190 terrestrial orchid species, encompassing all genera and the great majority of the widely recognized species of Orchidinae, a heterogeneous selection of species of Habenariinae, and single species of Satyriinae and Disinae (the latter serving as outgroup). The resulting parsimony‐based phylogeny reveals 12 well‐resolved clades within the Orchidinae, based on Anacamptis s.l., Serapias, Ophrys, Steveniella–Himantoglossum s.l. (including ‘Comperia’ and ‘Barlia’, most species being 2n = 36), Neotinea s.l., Traunsteinera–Chamorchis, Orchis s.s., Pseudorchis–Amerorchis–Galearis–Neolindleya–Platanthera s.l. (most 2n = 42), Dactylorhiza s.l., Gymnadenia s.l. (most 2n = 40, 80), Ponerorchis s.l.–Hemipilia s.l.–Amitostigma–Neottianthe, and Brachycorythis (most 2n = 42). Relationships are less clearly resolved among these 12 clades, as are those within Habenariinae; the subtribe appears either weakly supported as monophyletic or as paraphyletic under maximum parsimony, and the species‐rich genus Habenaria is clearly highly polyphyletic. The triphyly of Orchis as previously delimited is confirmed, and the improved sampling allows further generic transfers to Anacamptis s.l. and Neotinea s.l. In addition, justifications are given for: (1) establishing Steveniella as the basally divergent member of an appreciably expanded Himantoglossum that incorporates the former genera ‘Barlia’ and ‘Comperia’, (2) reuniting ‘Piperia’ with a broadly defined Platanthera as section Piperia, necessitating ten new combinations, (3) broadening Ponerorchis to include Chusua, and Hemipilia to include single ‘orphan’ species of Ponerorchis and Habenaria, and (4) recognizing ‘Gymnadenia’camtschatica as the monotypic Neolindleya camtschatica within the Pseudorchis～Platanthera clade. Few further generic transfers are likely in Orchidinae s.s., but they are anticipated among habenariid genera, on acquisition of additional morphological and molecular evidence; one probable outcome is expansion of Herminium. Species‐level relationships are also satisfactorily resolved within most of the major clades of Orchidinae, with the notable exceptions of Serapias, the derived sections of Ophrys, Himantoglossum s.s., some sections within Dactylorhiza, the former genus ‘Nigritella’ (now tentatively placed within Gymnadenia s.l.), Hemipilia s.l., and possibly Ponerorchis s.s. Relationships among the 12 major clades broadly accord with bona fide records of intergeneric hybridization. Current evidence supports the recently recognized 2n = 36 clade; it also indicates a 2n = 40 clade that is further diagnosed by digitate root‐tubers, and is derived relative to the recently recognized clade of exclusively Asian genera (Ponerorchis s.l.–Hemipilia s.l.–Amitostigma–Neottianthe). This in turn appears derived relative to the Afro‐Asiatic Brachycorythis group; together, these two clades identify the plesiomorphic chromosome number as 2n = 42. If the African genus Stenogolottis is correctly placed as basally divergent within a monophyletic Habenariinae, the tribe Orchideae and subtribes Orchidinae and Habenariinae could all have originated in Africa, though in contrast the Asiatic focus of the basally divergent members of most major clades of Orchidinae suggests an Asiatic radiation of the subtribe. Morphological characters informally ‘mapped’ across the molecular phylogeny and showing appreciable levels of homoplasy include floral and vegetative pigmentation, flower shape, leaf posture, gynostemium features, and various pollinator attractants. Qualitative comparison of, and reciprocal illumination between, degrees of sequence and morphological divergence suggests a nested set of radiations of progressively decreasing phenotypic magnitude. Brief scenarios, both adaptive and non‐adaptive, are outlined for specific evolutionary transitions. Recommendations are made for further species sampling, concentrating on Asian Orchidinae (together with the Afro‐Asiatic Brachycorythis group) and both Asian and Southern Hemisphere Habenariinae, and adding plastid sequence data. Taxonomic changes listed are: Anacamptis robusta (T.Stephenson) R.M.Bateman, comb. nov. , A. fragrans (Pollini) R.M.Bateman, comb. nov. , A. picta (Loiseleur) R.M.Bateman, comb. nov. , Neotinea commutata (Todari) R.M.Bateman, comb. nov. , N. conica (Willdenow) R.M.Bateman, comb. nov. , Platanthera elegans Lindley ssp. maritima (Rydberg) R.M.Bateman, comb. nov. , P. elegans Lindley ssp. decurtata (R.Morgan & Glicenstein) R.M.Bateman, comb. nov. , P. elongata (Rydberg) R.M.Bateman, comb. nov. , P. michaelii (Greene) R.M.Bateman, comb. nov. , P. leptopetala (Rydberg) R.M.Bateman, comb. nov. , P. transversa (Suksdorf) R.M.Bateman, comb. nov. , P. cooperi (S.Watson) R.M.Bateman, comb. nov. , P. colemanii (R.Morgan & Glicenstein) R.M.Bateman, comb. nov. , P. candida (R.Morgan & Ackerman) R.M.Bateman, comb. nov. and P. yadonii (R.Morgan & Ackerman) R.M.Bateman, comb. nov. © 2003 The Linnean Society of London, Botanical Journal of the Linnean Society, 2003, 142 , 1–40.     

MOLECULAR PHYLOGENY OF THE UPRIGHT ERYTHROPELTIDALES (COMPSOPOGONOPHYCEAE,RHODOPHYTA): MULTIPLE CRYPTIC LINEAGES OF ERYTHROTRICHIA CARNEA1

The phylogeny of morphologically simple algae is problematic due to insufficient morphological characters to aid in distinguishing species and relationships. The problem is further compounded because multiple evolutionary lineages of morphologically similar species occur in most well‐sampled biogeographic locations; therefore, location cannot be used as a proxy for species. The phylogeny of the upright members of the Erythropeltidales is partially clarified by combining molecular data, unialgal culture observations, and worldwide sampling. Our results show that there are several well‐supported lineages within the Erythropeltidales with only two morphologically recognizable taxa at present. The first is the genus Porphyrostromium, with a well‐developed basal crust, which includes two Erythrotrichia species (Porphyrostromium ligulatum comb. nov. and Porphyrostromium pulvinatum comb. nov.). The second is the branched species Erythrotrichia welwitschii (Rupr.) Batters. There are also six strongly supported Erythrotrichia carnea–like lineages. While not completely satisfactory, we propose that one lineage (lineage 2) with samples close to the type locality be designated as E. carnea with a specific isolate as an epitype. The lack of morphology to differentiate the other lineages leads to a taxonomy based solely on gene sequencing and molecular phylogeny, with rbcL sequences differentiating the lineages proposed. We hold off on proposing more species and genera until more data and samples can be gathered.     

Synonymy of Etiennea Matile-Ferrero with Hemilecanium Newstead (Hemiptera: Coccidae), based on morphology of adult females, adult males and first-instar nymphs, and description of a new potential pest species from the Ryukyu Archipelago, Japan

The genus Etiennea Matile‐Ferrero is synonymized with Hemilecanium Newstead (Hemiptera: Coccidae). We base this decision on a morphological comparative study of adult females, adult males and first‐instar nymphs (crawlers), including a phylogenetic analysis. We recovered a sister group relationship between the type species of the two genera, Etiennea villiersi Matile‐Ferrero and Hemilecanium theobromae Newstead; that is, each was more closely related to the other than either was to other species in their respective genera. All species hitherto included in Etiennea are transferred to Hemilecanium: H. bursera (Hodgson & Kondo) comb. nov., H. cacao (Hodgson) comb. nov., H. candelabra (Hodgson) comb. nov., H. capensis (Hodgson) comb. nov., H. carpenteri (Newstead) comb. nov., H. cephalomeatus (Hodgson) comb. nov., H. combreti (Hodgson) comb. nov., H. ferina (De Lotto) comb. nov., H. ferox (Newstead) comb. nov., H. gouligouli (Hodgson) comb. nov., H. halli (Hodgson) comb. nov., H. kellyi (Brain) comb. nov., H. madagascariensis (Hodgson) comb. nov., H. montrichardiae (Newstead) comb. nov., H. multituberculum (Hodgson) comb. nov., H. petasus (Hodgson) comb. nov., H. sinetuberculum (Hodgson) comb. nov., H. tafoensis (Hodgson) comb. nov., H. ulcusculum (Hodgson) comb. nov., and H. villiersi (Matile‐Ferrero) comb. nov. Keys to the adult females of all 26 species and known adult males and first‐instar nymphs are provided. The adult males and first‐instar nymphs of H. theobromae Newstead and E. villiersi Matile‐Ferrero are for the first time fully described and illustrated. One new potential pest species of Hemilecanium, H. uesatoi Kondo & Hardy sp. nov., which was collected on three islands of the Ryukyu Archipelago, Japan, is described and illustrated based on the adult female, adult male and first‐instar nymph. We discuss evidence that H. uesatoi is a new introduction to the Ryukyu Archipelago. The first‐instar nymphs of Hemilecanium can be divided into two distinct morphological groups, the petasus group and the theobromae group.     

Description of a new diatom genus Dorofeyukea gen. nov. with remarks on phylogeny of the family Stauroneidaceae

Type material of Navicula kotschyi was studied, and this species was transferred to Dorofeyukea gen. nov. as D. kotschyi comb. nov. Dorofeyukea was described on the basis of DNA sequence and morphological data. Additional species assigned to this genus that were previously included in Navicula include: D. ancisa comb. nov., D. grimmei comb. nov., D. ivatoensis comb. nov., D. orangiana comb. nov., D. rostellata comb. nov. & stat. nov., D. savannahiana comb. nov., D. tenuipunctata comb. nov., and D. texana comb. nov. All Dorofeyukea species share the same morphological features, including having a narrow stauroid fascia surrounded by 1–3 irregularly shortened striae, uniseriate, and weakly radiate striae, circular, or rectangular puncta in the striae that are covered internally by dome‐shaped hymenes, presence of a pseudoseptum at each apex and absence of septa. Partial DNA sequences of SSU and rbcL loci show Dorofeuykae belongs to the clade of stauroneioid diatoms together with Stauroneis, Prestauroneis, Craticula, Karayevia, Madinithidium, Fistulifera, Parlibellus, and, possibly, Schizostauron. A new species from the monoraphid genus Madinithidium, M. vietnamica sp. nov., was described based on valve and chloroplast morphology as well as DNA sequence data.     

A Molecular Phylogenetic Study of the Tribe Corallineae (Corallinales,Rhodophyta) with an Assessment of Genus‐Level Taxonomic Features and Descriptions of Novel Genera

A multigene phylogeny using COI‐5P (mitochondrial cytochrome c oxidase subunit 1), psbA (PSII reaction center protein D1), and EF2 (elongation factor 2) sequence data for members of the tribe Corallineae was constructed to assess generic boundaries. We determined that traditional reliance on conceptacle position as an indicator of generic affinities in the Corallineae is not supported and taxonomic changes are required. We found that species currently assigned to Pseudolithophyllum muricatum resolved within the Corallineae in all analyses. This is the first record of crustose members in the subfamily Corallinoideae. Further‐more, the genus Serraticardia was polyphyletic; we propose to synonomize Serraticardia with Corallina, transfer the type species S. maxima to Corallina (C. maxima (Yendo) comb. nov.), and describe the new genus Johansenia for S. macmillanii (J. macmillanii (Yendo) comb. nov.). Our molecular data also indicate that species in the genus Marginisporum have evolutionary affinities among species of Corallina and these genera should also be synonymized. This necessitates the combinations C. aberrans (Yendo) comb. nov. for M. aberrans (Yendo) Johansen & Chihara, C. crassissima (Yendo) comb. nov. for M. crassissimum (Yendo) Ganesan, and C. declinata (Yendo) comb. nov. for M. declinata (Yendo) Ganesan. Corallina elongata was divergent from all other members of Corallina and is transferred to a new genus, Ellisolandia (E. elongata (J. Ellis & Solander) comb. nov). In addition, COI‐5P and internal transcribed spacer (ITS) data combined with morphological characters were used to establish that rather than the four Corallina species recognized in Canada, there are nine.     

Aphis (Hemiptera: Aphididae) species groups found in the Midwestern United States and their contribution to the phylogenetic knowledge of the genus

A phylogeny of the genus Aphis Linnaeus, 1 758 was built primarily from specimens collected in the Midwest of the United States. A data matrix was constructed with 68 species and 41 morphological characters with respective character states of alate and apterous viviparous females. Dendrogram topologies of analyses performed using UPGMA (Unweighted Pair Group Method with Arithmetic Mean), Maximum Parsimony and Bayesian analysis of Cytochrome Oxidase I, Elongation Factor 1‐α and primary endosymbiont Buchnera aphidicola 16S sequences were not congruent. Bayesian analysis strongly supported most terminal nodes of the phylogenetic trees. The phylogeny was strongly supported by EF1‐α, and analysis of COI and EF1‐α molecular data combined with morphological characters. It was not supported by single analysis of COI or Buchnera aphidicola 16S. Results from the Bayesian phylogeny show 4 main species groups: asclepiadis, fabae, gossypii, and middletonii. Results place Aphis and species of the genera Protaphis Börner, 1952, Toxoptera Koch, 1856 and Xerobion Nevsky, 1928 in a monophyletic clade. Morphological characters support this monophyly as well. The phylogeny shows that the monophyletic clade of the North American middletonii species group belong to the genus Protaphis: P. debilicornis (Gillette & Palmer, 1929 ), comb. nov., P. echinaceae (Lagos and Voegtlin, 2009 ), comb. nov., and P. middletonii (Thomas, 1879 ). The genus Toxoptera should be considered a subgenus of Aphis (stat. nov.). The analysis also indicates that the current genus Iowana Frison, 1954 should be considered a subgenus of Aphis (stat. nov.).     

Molecular phylogeny of the bee genus Hoplitis (Megachilidae: Osmiini) – how does nesting biology affect biogeography?

The genus Hoplitis (Megachilidae: Osmiini) comprises about 360 described species and occurs on all continents except Australia, South America, and Antarctica. Using five genes, we inferred the phylogeny of Hoplitis including 23 out of the 27 currently recognized subgenera, applying both Bayesian and maximum likelihood methods. Compared to the current morphology‐based classification, our phylogeny resulted in three classificatory changes: first, the subgenera Alcidamea, Cyrtosmia, Dasyosmia, Megalosmia, Monumetha, and Prionohoplitis are merged into one large subgenus Alcidamea Cresson, 1864, comb. nov. ; second, the subgenera Annosmia, Bytinskia, Coloplitis, and Hoplitis are merged into one large subgenus Hoplitis Klug, 1807, comb. nov. ; third, the subgenera Acrosmia, Hoplitina, Penteriades, and Proteriades are merged into one large subgenus Proteriades Titus, 1904, comb. nov. We provide evidence that the genus Hoplitis has a Palaearctic origin and that colonization events to southern Africa and to the Nearctic, as well as recolonization events from the Nearctic to the Palaearctic occurred. The species of the genus Hoplitis exhibit an extraordinary diversity in nesting behaviour, comprising both below and above ground nesting. Parsimony mapping revealed that ground nesting in excavated burrows is the ancestral state amongst Hoplitis bees. We hypothesize that nesting biology strongly affected both range expansion and long‐distance dispersal in Hoplitis. © 2012 The Linnean Society of London     

The turtles of the Purbeck Limestone Group of Dorset, southern England

The turtles from the Purbeck Limestone are revised and it is concluded that there are four shell‐based cryptodire species present, namely Pleurosternon bullockii, ‘Glyptops’typocardium comb. nov., Helochelydra anglica comb. nov.,Hylaeochelys latiscutata. There is also one skull‐based species, Dorsetochelys delairi, which may prove to be the skull of ‘Glyptops’, Hylaeochelys or an unknown shell‐type. All other taxa are junior synonyms except ‘Chelone’obovata Owen, 1842 and Tretosternon punctatum Owen, 1842 which are nomina dubia, the material being unfigured and either lost or incorrectly associated. Other taxonomic conclusions are that (1) because Tretosternon is a nomen dubium, the next senior name for this Purbeck–Wealden genus is Helochelydra Nopcsa, 1928; (2) ‘Pleurosternon’typocardium and ‘Glyptops’ruetimeyeri are synonymous, the senior combination being ‘Glyptops’typocardium; (3) the Purbeck ‘Tretosternon’ material is combined with the holotype and only specimen of Platychelys? anglica as Helochelydra anglica comb. nov.; (4) Hylaeochelys emarginata and H. sollasi are junior synonyms of Hylaeochelys latiscutata; (5) one of Owen's ‘lost’ syntypes of ‘Tretosternon punctatum’ has been recognised and is a plastron of Hylaeochelys latiscutata.     

Phylogenetic relationships of corallinaceae (Corallinales,Rhodophyta): taxonomic implications for reef‐building corallines

A new, more complete, five‐marker (SSU, LSU, psbA, COI, 23S) molecular phylogeny of the family Corallinaceae, order Corallinales, shows a paraphyletic grouping of seven well‐supported monophyletic clades. The taxonomic implications included the amendment of two subfamilies, Neogoniolithoideae and Metagoniolithoideae, and the rejection of Porolithoideae as an independent subfamily. Metagoniolithoideae contained Harveylithon gen. nov., with H. rupestre comb. nov. as the generitype, and H. canariense stat. nov., H. munitum comb. nov., and H. samoënse comb. nov. Spongites and Pneophyllum belonged to separate clades. The subfamily Neogoniolithoideae included the generitype of Spongites, S. fruticulosus, for which an epitype was designated. Pneophyllum requires reassesment. The generitype of Hydrolithon, H. reinboldii, was a younger heterotypic synonym of H. boergesenii. The evolutionary novelty of the subfamilies Hydrolithoideae, Metagoniolithoideae, and Lithophylloideae was the development of tetra/bisporangial conceptacle roofs by filaments surrounding and interspersed among the sporangial initials.     

Systematic revision of Hoggicosa Roewer, 1960, the Australian ‘bicolor’ group of wolf spiders (Araneae: Lycosidae)

The Australian wolf spider genus Hoggicosa Roewer, 1960 with the type species Hoggicosa errans (Hogg, 1905) is revised to include ten species: Hoggicosa alfi sp. nov. ; Hoggicosa castanea (Hogg, 1905) comb. nov. (= Lycosa errans Hogg, 1905 syn. nov. ; = Lycosa perinflata Pulleine, 1922 syn. nov. ; = Lycosa skeeti Pulleine, 1922 syn. nov. ); Hoggicosa bicolor (McKay, 1973) comb. nov. ; Hoggicosa brennani sp. nov. ; Hoggicosa duracki (McKay, 1975) comb. nov. ; Hoggicosa forresti (McKay, 1973) comb. nov. ; Hoggicosa natashae sp. nov. ; Hoggicosa snelli (McKay, 1975) comb. nov. ; Hoggicosa storri (McKay, 1973) comb. nov. ; and Hoggicosa wolodymyri sp. nov. The Namibian Hoggicosa exigua Roewer, 1960 is transferred to Hogna, Hogna exigua (Roewer, 1960) comb. nov. A phylogenetic analysis including nine Hoggicosa species, 11 lycosine species from Australia and four from overseas, with Arctosa cinerea Fabricius, 1777 as outgroup, supported the monophyly of Hoggicosa, with a larger distance between the epigynum anterior pockets compared to the width of the posterior transverse part. The analysis found that an unusual sexual dimorphism for wolf spiders (females more colourful than males), evident in four species of Hoggicosa, has evolved multiple times. Hoggicosa are burrowing lycosids, several constructing doors from sand or debris, and are predominantly found in semi‐arid to arid regions of Australia. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 158 , 83–123.     

MOLECULAR PHYLOGENY,ULTRASTRUCTURE, AND TAXONOMIC REVISION OF CHLOROGONIUM (CHLOROPHYTA): EMENDATION OF CHLOROGONIUM AND DESCRIPTION OF GUNGNIR GEN. NOV. AND RUSALKA GEN. NOV.1

We examined the molecular phylogeny and ultrastructure of Chlorogonium and related species to establish the natural taxonomy at the generic level. Phylogenetic analyses of 18S rRNA and RUBISCO LSU (rbcL) gene sequences revealed two separate clades of Chlorogonium from which Chlorogonium (Cg.) fusiforme Matv. was robustly separated. One clade comprised Cg. neglectum Pascher and Cg. kasakii Nozaki, whereas the other clade included the type species Cg. euchlorum (Ehrenb.) Ehrenb., Cg. elongatum (P. A. Dang.) Francé, and Cg. capillatum Nozaki, M. Watanabe et Aizawa. On the basis of unique ultrastructural characteristics, we described Gungnir Nakada gen. nov. comprising three species: G. neglectum (Pascher) Nakada comb. nov., G. mantoniae (H. Ettl) Nakada comb. nov., and G. kasakii (Nozaki) Nakada comb. nov. We also emended Chlorogonium as a monophyletic genus composed of Cg. euchlorum, Cg. elongatum, and Cg. capillatum. Because Cg. fusiforme was distinguished from the redefined Chlorogonium and Gungnir by the structure of its starch plate, which is associated with pyrenoids, we reclassified this species as Rusalka fusiformis (Matv.) Nakada gen. et comb. nov.     

Temperature Mediates Shifts in Individual Aggressiveness,Activity Level,and Social Behavior in a Spider

Although in recent years behavioral syndromes have received a wealth of attention, how traits within syndromes respond to changing environments is not well resolved. Here, we test the effects of temperature on a suite of behavioral traits in the spider Anelosimus studiosus to determine (1) whether there are shifts in individuals’ social tendency, activity level, and foraging behavior in response to temperature, (2) if these traits shift are in the direction predicted by within‐population axes of trait covariance, and (3) whether the effects of temperature differ among individuals. In previous work, we documented a behavioral syndrome in A. studiosus where increased tolerance of conspecifics is correlated with decreased activity level and aggressiveness toward prey. Furthermore, there are distinct among‐population differences in behavior, where individuals from warm sites tend to be more aggressive and active than individuals from cold sites. Our data here reveal that at warmer temperatures A. studiosus exhibit diminished tolerance of conspecifics, increased activity levels, shorter latencies of attack, and increased tendencies to attack multiple prey items. Furthermore, we found that individual differences in behavior were consistent across temperature regimes for the majority of behavioral traits considered here: social tendency, activity level, and latency of attack. These findings are consistent with the hypothesis that these behaviors are linked together by shared genetic underpinnings (e.g., metabolic differences) and shift non‐independently in response to contemporary abiotic environment (i.e., temperature). Furthermore, our data suggest that temperature itself could be responsible for the among‐population variation in social structure in A. studiosus.     

Loss of genetic variability in social spiders: genetic and phylogenetic consequences of population subdivision and inbreeding

The consequences of population subdivision and inbreeding have been studied in many organisms, particularly in plants. However, most studies focus on the short‐term consequences, such as inbreeding depression. To investigate the consequences of both population fragmentation and inbreeding for genetic variability in the longer term, we here make use of a natural inbreeding experiment in spiders, where sociality and accompanying population subdivision and inbreeding have evolved repeatedly. We use mitochondrial and nuclear data to infer phylogenetic relationships among 170 individuals of Anelosimus spiders representing 23 species. We then compare relative mitochondrial and nuclear genetic variability of the inbred social species and their outbred relatives. We focus on four independently derived social species and four subsocial species, including two outbred–inbred sister species pairs. We find that social species have 50% reduced mitochondrial sequence divergence. As inbreeding is not expected to reduce genetic variability in the maternally inherited mitochondrial genome, this suggests the loss of variation due to strong population subdivision, founder effects, small effective population sizes (colonies as individuals) and lineage turnover. Social species have < 10% of the nuclear genetic variability of the outbred species, also suggesting the loss of genetic variability through founder effects and/or inbreeding. Inbred sociality hence may result in reduction in variability through various processes. Sociality in most Anelosimus species probably arose relatively recently (0.1–2 mya), with even the oldest social lineages having failed to diversify. This is consistent with the hypothesis that inbred spider sociality represents an evolutionary dead end. Heterosis underlies a species potential to respond to environmental change and/or disease. Inbreeding and loss of genetic variability may thus limit diversification in social Anelosimus lineages and similarly pose a threat to many wild populations subject to habitat fragmentation or reduced population sizes.     

Non‐Conceptive Sexual Behavior in Spiders: A Form of Play Associated with Body Condition,Personality Type,and Male Intrasexual Selection

In the socially polymorphic spider Anelosimus studiosus, males mature early in the reproductive season and recruit to the webs of juvenile females and guard them until they mature. During the period before females mature, males and females engage in repeated bouts of non‐conceptive (play) sexual behavior, where the pair courts and engages in mock copulation; both males and females gain performance‐enhancing experience via these encounters. In this study, we examined the factors that underlie individual variation in the tendency to engage in non‐conceptive mating and determine whether it impacts male–male competition for females. We found that docile females, being less resistant to mating in general, are more likely to accept male courtship and non‐conceptive copulation as juveniles. Personality type influenced the exhibition of non‐conceptive sexual behavior in males as well. High body condition males of the aggressive phenotype were more likely to engage in non‐conceptive sexual behavior than males with lower body condition. Body condition did not influence docile males’ propensity to engage in non‐conceptive sexual behavior, but female size did. Docile males engaged in more non‐conceptive sexual displays with larger females. Engaging in non‐conceptive sexual displays negatively impacted male performance in staged male–male contests for access to females. This cost was greatest for males of the aggressive phenotype, which are otherwise favored in male–male contests. Our findings indicate expression of non‐conceptive sexual displays is linked to personality and results in reproductive performance trade‐offs for male A. studiosus.