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The common ancestor of spiders likely used silk to line burrows or make simple webs, with specialized spinning organs and aerial webs originating with the evolution of the megadiverse “true spiders” (Araneomorphae). The base of the araneomorph tree also concentrates the greatest number of changes in respiratory structures, a character system whose evolution is still poorly understood, and that might be related to the evolution of silk glands. Emphasizing a densesampling of multiple araneomorph lineages where tracheal systems likely originated, we gathered genomic-scale data and reconstructed a phylogeny of true spiders. This robust phylogenomic framework was used to conduct maximum likelihood and Bayesian character evolution analyses for respiratory systems, silk glands, and aerial webs, based on a combination of original and published data. Our results indicate that in true spiders, posterior book lungs were transformed into morphologically similar tracheal systems six times independently, after the evolution of novel silk gland systems and the origin of aerial webs. From these comparative data, we put forth a novel hypothesis that early-diverging web-building spiders were faced with new energetic demands for spinning, which prompted the evolution of similar tracheal systems via convergence; we also propose tests of predictions derived from this hypothesis.

Spiders (Order Araneae) are massively abundant generalist arthropod predators that are found in nearly every ecosystem on the planet and have persisted for over 380 million years. Spiders have long served as evolutionary models for studying complex mating and web spinning behaviors, key innovation and adaptive radiation hypotheses, and have been inspiration for important theories like sexual selection by female choice. Unfortunately, past major attempts to reconstruct spider phylogeny typically employing the “usual suspect” genes have been unable to produce a well-supported phylogenetic framework for the entire order. To further resolve spider evolutionary relationships we have assembled a transcriptome-based data set comprising 70 ingroup spider taxa. Using maximum likelihood and shortcut coalescence-based approaches, we analyze eight data sets, the largest of which contains 3,398 gene regions and 696,652 amino acid sites forming the largest phylogenomic analysis of spider relationships produced to date. Contrary to long held beliefs that the orb web is the crowning achievement of spider evolution, ancestral state reconstructions of web type support a phylogenetically ancient origin of the orb web, and diversification analyses show that the mostly ground-dwelling, web-less RTA clade diversified faster than orb weavers. Consistent with molecular dating estimates we report herein, this may reflect a major increase in biomass of non-flying insects during the Cretaceous Terrestrial Revolution 125–90 million years ago favoring diversification of spiders that feed on cursorial rather than flying prey. Our results also have major implications for our understanding of spider systematics. Phylogenomic analyses corroborate several well-accepted high level groupings: Opisthothele, Mygalomorphae, Atypoidina, Avicularoidea, Theraphosoidina, Araneomorphae, Entelegynae, Araneoidea, the RTA clade, Dionycha and the Lycosoidea. Alternatively, our results challenge the monophyly of Eresoidea, Orbiculariae, and Deinopoidea. The composition of the major paleocribellate and neocribellate clades, the basal divisions of Araneomorphae, appear to be falsified. Traditional Haplogynae is in need of revision, as our findings appear to support the newly conceived concept of Synspermiata. The sister pairing of filistatids with hypochilids implies that some peculiar features of each family may in fact be synapomorphic for the pair. Leptonetids now are seen as a possible sister group to the Entelegynae, illustrating possible intermediates in the evolution of the more complex entelegyne genitalic condition, spinning organs and respiratory organs.

The atypoid mygalomorphs include spiders from three described families that build a diverse array of entrance web constructs, including funnel-and-sheet webs, purse webs, trapdoors, turrets and silken collars. Molecular phylogenetic analyses have generally supported the monophyly of Atypoidea, but prior studies have not sampled all relevant taxa. Here we generated a dataset of ultraconserved element loci for all described atypoid genera, including taxa ( Mecicobothrium and Hexurella) key to understanding familial monophyly, divergence times, and patterns of entrance web evolution. We show that the conserved regions of the arachnid UCE probe set target exons, such that it should be possible to combine UCE and transcriptome datasets in arachnids. We also show that different UCE probes sometimes target the same protein, and under the matching parameters used here show that UCE alignments sometimes include non-orthologs. Using multiple curated phylogenomic matrices we recover a monophyletic Atypoidea, and reveal that the family Mecicobothriidae comprises four separate and divergent lineages. Fossil-calibrated divergence time analyses suggest ancient Triassic (or older) origins for several relictual atypoid lineages, with late Cretaceous/early Tertiary divergences within some genera indicating a high potential for cryptic species diversity. The ancestral entrance web construct for atypoids, and all mygalomorphs, is reconstructed as a funnel-and-sheet web.

In order to study the tempo and the mode of spider orb web evolution and diversification, we conducted a phylogenetic analysis using six genetic markers along with a comprehensive taxon sample. The present analyses are the first to recover the monophyly of orb-weaving spiders based solely on DNA sequence data and an extensive taxon sample. We present the first dated orb weaver phylogeny. Our results suggest that orb weavers appeared by the Middle Triassic and underwent a rapid diversification during the end of the Triassic and Early Jurassic. By the second half of the Jurassic, most of the extant orb-weaving families and web designs were already present. The processes that may have given origin to this diversification of lineages and web architectures are discussed. A combination of biotic factors, such as key innovations in web design and silk composition, as well as abiotic environmental changes, may have played important roles in the diversification of orb weavers. Our analyses also show that increased taxon sampling density in both ingroups and outgroups greatly improves phylogenetic accuracy even when extensive data are missing. This effect is particularly important when addition of character data improves gene overlap.

Web designs have long been used to characterize spider taxa and to deduce the relations between them; but systematic documentation of the amount of variation in webs within and between taxonomic groups is rare. This study, based on previously published observations and new observations of 15 species in the family Uloboridae, including two genera, OctonobaOpell, 1979 and SiratobaOpell, 1979, whose webs were previously undocumented, reviews the taxonomic distribution and variation in 22 orb web traits in at least 43 species in 11 genera in uloborids. These traits appear to occur in all orb-weaving genera in which reasonable samples are available, though only small samples are available for many species. Larger samples of the webs of three species of Uloborus Latreille, 1806, two of Hyptiotes Walckenaer, 1837, and one each of Zosis Walckenaer, 1841, Siratoba, Octonoba, WaitkeraOpell, 1979 and Philoponella Mello-Leitão, 1917, revealed greater intra-specific consistencies in some traits than others. Hub traits were especially consistent. Variations in three traits may represent adjustments to the size of the space in which the orb is built. “Primary” webs, which combine orb and sheet-web traits, are built by spiderlings newly emerged from the egg sac and by adult males in at least five genera of orb-weaving uloborids and may be unique to this family. Preliminary comparisons between uloborid and araneoid orbs suggest that uloborid orbs may also differ from araneoid orbs in combining several other traits.

“Primary” webs of uloborids have large numbers of very fine lines and usually lack sticky cribellum silk. This paper reviews their taxonomic distribution (19 species in 5 genera) and the ontogenetic stages in which primary webs are built (spiderlings newly emerged from the egg sac, older juveniles, mature males, and normal and senile females), expands the knowledge of construction behavior, and describes several previously unnoticed design details. Primary webs differ from typical uloborid orbs in several ways: large numbers of fine radial and non-radial lines; facultative hub removal and replacement; usually closely spaced temporary spiral loops; and lines beyond the frame lines. Construction of supplemental radii in primary webs is distinctive in several respects: break and reel construction; tendencies to lay successive radii either on opposite sides of the web or close together in the same sector; high frequencies of aborted trips from the hub to the frame; production of multiple lines during a single trip from the hub to the frame and back; long pauses during the production of single radii; and variation in the sequences in which radial lines are added to a given sector. Some aspects of primary web construction resemble araneoid rather than typical uloborid behavior. The relation between primary webs and the evolution of orb webs, and the mechanism that spiders use to produce abundant non-radial lines despite making only radial movements during web construction remain uncertain. We speculate that primary webs are favored when spiders are unable to afford the costs of producing cribellate silk for a typical orb.

1. The replacement of dry, fuzzy cribellar prey capture thread by viscous, adhesive capture thread was a major event in the evolution of orb-weaving spiders. Over 95% of all orb-weaving species now produce adhesive threads. 2. Adhesive thread achieves its stickiness with a much greater material economy than does cribellar thread. 3. Transformational analyses show that, relative to spider mass, adhesive orb-weavers invest less material per mm of capture thread and produce stickier capture threads than do cribellate orb-weavers. 4. The total cost of producing an orb-web that contains cribellar thread is reduced by 32% when a spider recycles its silk and another 34% when these capture threads are replaced by adhesive threads of equal stickiness. 5. The increased economy with which adhesive capture thread achieves its stickiness may have been an important factor that favoured the origin and success of modern orb-weaving spiders that produce adhesive capture threads.

We use computer simulations in order to study the interplay between biodiversity and ecosystem functioning (BEF) both during the formation and during the ongoing evolution of large food webs. A species in our model is characterized by its own body mass, its preferred prey body mass, and the width of its potential prey body mass spectrum. On an ecological time scale, population dynamics determines which species are viable and which ones go extinct. On an evolutionary time scale, new species emerge as modications of existing ones. The network structure thus emerges and evolves in a self-organized manner. We analyse the relation between the functional diversity and ve community level measures of ecosystem functioning. These are the metabolic loss of the predator community, the total biomasses of the basal and the predator community and the consumption rates on the basal community and within the predator community. Clear BEF relations are observed during the initial build-up of the networks or when parameters are varied, causing bottom-up or top-down eects. However, ecosystem functioning measures uctuate only very little during long-term evolution under constant environmental conditions, despite changes in the functional diversity. This result supports the hypothesis that trophic cascades are weaker in more complex food webs.

Funnel webs are common and widespread taxonomically, but little is known about how they are built or details of their structure. Aglaoctenus castaneus (Mello-Leitão, 1942) (Lycosidae) builds horizontal, densely meshed funnel webs of non-adhesive silk, with a tangle of lines above. Web construction behavior was unique in that the spider frequently laid swaths of lines rather than simple drag lines, both to float bands of fine lines on the breeze as bridges to distant objects and to fill in the sheet. Spiders utilized special spinneret movements to widen the swaths of lines that they laid on sheets. These movements have not been seen in web construction by other araneomorphs, but are were similar to and perhaps evolutionarily derived from those used during prey wrapping by many other species. Observations, made with a compound microscope, of the construction behavior of the agelenid Melpomene sp. O.P. Cambridge 1898, and of lines and attachments in sheets of these species and another funnel web spider, the zoropsid Tengella radiata (Kulczyński, 1909) demonstrated the possibly general nature of including obstacles in the web. This probably disadvantageous behavior may be related to constraints in selecting web sites imposed by the need for sheltered retreats, or to the spider's inability to remove preliminary lines. The observation also showed the importance of further improvements in the discriminations made between “sheet” and “brushed” webs in recent discussions of spider web evolution.

The paper aims to cover the main contributors to the development of Web 3.0 and to explore their different views on the evolution of the World Wide Web by creating a comprising image on the key theories, models, and frameworks in the evolution of Web 3.0. We used a qualitative research method, more precisely we conducted a literature review to identify the main characteristics of Web 3.0. Based on the selected papers we revealed the evolution of Web 3.0 by investigating a large variety of dimensions. Findings unfold to reveal the chronological publication of studies, main journals, and research methodology used in studies, along with future research directions. Furthermore, we performed an in-depth analysis to of the selected paper to discover a taxonomy of studies by key theories, models, and frameworks, features, technologies, main theories on the evolution of Web 3.0. As this is still a nascent topic, future research directions must focus on both qualitative and quantitative studies covering a wide spectrum of Web 3.0 stakeholders. The originality of the research derives not only from stating the evolution of Web 3.0 but also from the comparison between Web 1.0, Web 2.0, Web 3.0, and Web 4.0 we performed in order to hint towards the promise of the future in terms of opportunities and strengths.