Sponges architecture by colour: new insights into the fibres morphogenesis, skeletal spatial layout and morpho-anatomical traits of a marine horny sponge species (Porifera)

Abstract This paper focuses on the skeletal architecture and morphotraits of the Mediterranean horny sponge Sarcotragus spinosulus (Demospongiae, Keratosa, Dictyoceratida, Irciniidae). This special endoskeletal system consists of a dense, variably complex connective architecture, which extends throughout the entire sponge body and is embedded in an abundant jelly-like extracellular matrix (ECM). To investigate the topographic arrangement and micro-morphotraits of these connective structures in detail and by colour, also during morphogenetic processes, histology techniques using light microscopy are essential. New information is provided on the coordinated morphogenetic processes that characterize the growth and assembly of collagenic prototype structures in the matrix of fibrous skeletal elements and drive skeleton remodelling. Our results also highlight some novelties and some remarkable peculiarities of fibrous, filamentous and fibrillar components at the levels of both composition and structure. The morphofunctional significance of skeletal architecture is suggested in the background of the anatomical complexity of S. spinosulus.


Introduction
In Demospongiae Sollas, 1885, the exclusively organic filamentous and reticular fibrous skeleton represents a key evolutionary novelty in the phylogeny of Keratosa Grant, 1861 (Demospongiae widespread in shallow and deep water in all oceans) of the clade Dictyoceratida Minchin, 1900, known classically as horny sponges or also as tricky tree sponges sensu Erpenbeck et al. (2020). The spatial layout and abundance of filaments, coexisting with the irregular reticulum of anastomosing fibres, is typical of the monophyletic family Irciniidae (Cook & Bergquist 2002;Pronzato & Manconi 2011;Erpenbeck et al. 2020). These predominantly collagen structures play a key role in the skeletal architecture of the Irciniidae Gray, 1867 family and are suggestive of their divergent evolutionary trends (Garrone 1985;Hooper & van Soest 2002;Erpenbeck et al. 2020).
The development of electron microscopy techniques has meant that sponge studies performed by means of light microscopy have been neglected, even though morpho-anatomic traits can be discerned in detail at this latter level of investigation. Although histological and histochemical analyses in the 1950s-70s revealed an outstanding range of structural architectures of sponges (Gross et al. 1956;Cowden 1970;Brien et al. 1973;Garrone et al. 1973;Cowden & Harrison 1976;Garrone 1978Garrone , 1985, there are still knowledge gaps in this field. Bergquist et al. (1998) highlighted the performances of the histological analyses as a key tool to understand the architecture and composition of the horny sponges skeleton.
The aim of the present study was to extend basic knowledge of the skeletal architecture, spatial arrangement and topographic distribution of collagen structures (fibres, filaments and fibrils) to also support applied research on biomaterials of sponges. Our experimental model species is Sarcotragus spinosu Schmidt, 1862, the type species of the genus Sarcotragus Schmidt, 1862 (Demospongiae, Keratosa, Dictyoceratida, Irciniidae). Here, we provide a morpho-anatomical histological analysis of the skeletal pattern of this species and its morphogenetic processes of fibres growth and remodelling.

Experimental design, study area and sampling
Our morpho-anatomical targets were to (a) verify the identity at the species level of samples from in situ farmed clones, and (b) characterize skeletal microstructures by means of differential staining, confocal microscopy and Scanning Electron Microscopy (SEM).
Clones of Sarcotragus spinosulus had been obtained during previous farming experiments on donors from the wild population inhabiting shallow water (0.2-3 m) rocky substrata, intermattes and rhizomes of Posidonia oceanica (L.) Delile, 1813 meadows in Porto Conte Bay (Figure 1, Sardinia, Italy) (see Perez-Lopez et al. 2017;Padiglia et al. 2018;). This is a pristine area in the Capo Caccia -Isola Piana Marine Protected Area (MPA) in the Northern Sardinian Sea (Western Mediterranean).
Mariculture plant is located on special submerged man-made structures in a small marina in Tramariglio Cove (40°35ʹ32.47"N, 8°10ʹ11.50"E); plant modules are anchored to the underwater structure of a pier in shallow water (2-3 m depth), and are partially shaded by the pier (see Perez-Lopez et al. 2017;Padiglia et al. 2018). The cove is sheltered from the north-western wind, but exposed to the east wind and strong gales from the southwest.
Representative fragments of 3 clonal S. spinosulus (n = 12) were collected during cold and warm seasons (2018-2020) by means of a scalpel. Live sponges were photographed in the field (EOS G10, Canon, Japan). To investigate their morphological and histological traits, samples were kept in sea water in refrigerated bags, and transferred to the Zoology Lab, Veterinary Medicine Department, Sassari University, for microscopy analyses.

Diagnostic traits and morpho-anatomical analyses
A few hours (2-4) after collection, unstained samples of the sponges were examined in reflected and transmitted light with a low-magnification stereomicroscope.
For taxonomic analyses in the lab, samples were washed, dried at room temperature, labelled, registered in reference collections (KER-Sassari University, Zoology Lab, Veterinary Medicine Department) and processed. The diagnostic morphotraits considered for identification at the species level were as follows: growth form; dermal membrane (surface unarmed vs. armed with foreign material); conules and oscules (morphometry, shape and topographic distribution); general skeletal architecture; fine texture of fibrous network; primary, secondary and tertiary spongin fibres (topographic distribution and morphometry); collagen filaments (distribution, abundance and morphometry); ornamentation of fibres; and presence of foreign material in the pith of fibres. Thin slices of skeletons were obtained by dissecting samples by hand with scalpels under a Leica Wild M3C stereo-microscope; the slices

238
G. A. Stocchino et al. were then macerated in sea water for a variable time according to the sample size and skeletal texture. After final rinsing and drying in ethanol, skeleton fragments were laid on a slide, under a weight, to be gently plated as flat thin slices; finally, the sections were cleared in Bio Clear (Bio-Optica, Milan) and mounted in Eukitt® under a coverslip. Observations were made by Light Microscopy (LM, Nikon ECLIPSE 80i, Japan) and photographs were taken with a Nikon Digital-Sight DS-FI camera (Japan). To characterize diagnostic microtraits in detail, similar skeletal preparations for scanning electron microscopy (SEM Tescan Vega3, Czech Republic) were glued to a stub and sputter-coated with gold.
To characterize skeletal microstructures, several fragments were fixed at room temperature for 48 h in Bouin's fluid, dehydrated in an ascending ethanol series, cleared in xylene, and embedded in paraffin. Sections were cut at intervals of 4-5 µm and routinely stained with Masson trichrome and Azan-Mallory trichrome to evaluate the presence and distribution of collagen structures, and with Alcian blue stain (pH 2.5) to verify the presence of glycosaminoglycan (GAG)-like molecules. Slides were examined under a Nikon ECLIPSE 80i (Japan) light microscope and photographs were taken with a Nikon Digital-Sight DS-FI camera (Japan).
To obtain details of the collagen network of filaments, other sponge fragments were washed in PBS 1x and in mQ water, frozen at −80°C and then sectioned at 50-100 μm by means of a Leica CM1950 cryostat (medium Killik, Bio-Optica, Milan). Slides were observed and images were acquired by means of a Leica TCS SP 5 confocal microscope (Leica Microsystems, Germany) and processed by means of LAS AF Lite application software developed by Leica Microsystems CMS GmbH for contrast and brightness adjustment.

General morpho-anatomy
The samples of Sarcotragus spinosulus displayed a massive, rounded growth form with variable body size. The surface was brownish in colour, black to dark grey in vivo; the interior was orange to light brown ( Figure 2(A-B)). The body was slightly compressible, tough, and relatively difficult to cut or tear. The body surface was irregularly conulose and entirely covered by a dermal membrane consisting of a smooth, very thin hyaline layer (unarmed by detritus, Figure 2(A)) overlying a pigmented cellular layer of T-shaped exopinacocytes (Figure 3(D)). Conules had pointed apices, 1-2 mm in height and 1-5 mm apart, and an axis made by tips primary of fibres; conules were usually covered by a dermal membrane, sometimes fibre tips protruded from their apices (Figures 2(A), 3(A-C)). Oscules (up to 1 cm in diameter) were variably abundant, irregularly scattered, and had a small laminar collar (Figure 2(A-B)).
The three-dimensional endoskeleton was extended and embedded in the amorphous jelly-like Extracellular Matrix (ECM) of the entire ectosomal and choanosomal regions of the sponge body ( Figure 2(C-D)).

Fibrous skeleton
The skeleton, orange to light brown in colour (in vivo), was made up of a fibrous, reticulate, anisotropic network with irregularly polygonal meshes of main cylindrical fibres (primaries) intersecting with irregularly transverse cylindrical fibres (secondaries) . This network also displayed laminar cribrose plates, which anastomosed the neighbouring main fibres to form quite rare fasciculate fibres . Main fibres (primaries), fascicular along large tracts, were ascending, radial, more or less parallel, and stout. Secondary fibres were thinner and irregularly scattered. Cribrose plates were frequently large and irregularly scattered in the network . Primaries fibres were morphologically heterogeneous along their length, with smooth linear tracts irregularly alternating with thicker nodulous tracts and laminar tracts (Figures 4-5). These tracts are distinguishable on the basis of their structure, composition and maturation phase.
Secondary fibres were entirely smooth and linear and irregularly arise both from primaries and from cribrose plates ( Figure 5). Other, less frequent, partially "free" long fibres (secondaries) were also seen ( Figure 5). Secondary fibres showed the same structural composition as the linear tracts of primaries. The diameter of secondaries and linear tracts of primaries (rounded sections) ranged 44-160 µm. The cribrose plates joining the primary fibres in fascicles displayed scattered meshes of variable number, shape and size (Figures 4(C, E), 5). All fibrous structures were made up of a bark surrounding a non-laminated axial pith ( Figure 6). Moreover, . Body architecture (inner view, cross-section) with spiny brownish surface covered with conules, a dense, orange extracellular matrix with scattered whitish aquiferous canals (arrows) and orange-brownish ascending, more or less radial, primary skeletal fibres (arrowheads). (C-D). General views of ectosomal (ec, outer) and choanosomal regions (ch, inner) with evident canals (ca), primary fibres (pf), cribrose plate (cp), filaments (fi). proto-fibres originating ex novo were observed at different stages of formation and maturation.

Sponge connective system
Linear tracts of primary tracts. The bark was seen to be made up of dense concentric tightly adherent laminae (red with Masson trichrome, colourless with Alcian blue) alternating with layers of amorphous matrix (blue with Masson trichrome, colourless with Alcian blue) ( Figure 6). On staining with Azan-Mallory trichrome, the bark appeared blue. Concentric layers appeared as growth lines. The non-laminated axial pith was amorphous (except when foreign spicules were present, i.e. intermittent core, see Figure 4) as was the matrix (blue) between the red layers of bark. On moving from the periphery to the inner part, the pith appeared blue to light blue to colourless on staining with Masson and Azan-Mallory trichrome (Azan-Mallory not shown). By contrast, Alcian blue tinged the inner pith light blueturquoise ( Figure 6(C-D)). The ECM was also intensively coloured with Alcian blue (Figure 6(D)). Fibres sometimes showed signs of degeneration of the red layers, i.e. irregular scalloped margins (cross and tangential Laminar tracts of primary fibres. These tracts were seen to be composed of cribrose plates with irregular outlines (Figures 7(A-B)) made up of concentric tightly adherent laminae (red with Masson trichrome, colourless with Alcian blue) alternating with layers of amorphous matrix (blue with Masson trichrome, colourless with Alcian blue). On staining with Azan-Mallory trichrome, the bark appeared blue (not shown). On section, these plates (140-680 μm in diameter) had highly variable outlines. They were always endowed with a nonlaminated amorphous pith that was seen to vary in colour from the periphery to the inner part from blue to light blue to colourless with Masson ( Figure 7(A-B)) and Azan-Mallory trichrome (not shown). The inner pith appeared light blueturquoise on staining with Alcian blue (not shown).
Nodular tracts of primary fibres. As revealed by SEM, the fibrous nodular tracts along the primary fibres frequently appeared almost hollow ( Figure 5(A-B)). In LM sections, these nodular tracts had a pith containing resting and active zones of growing fibres, mature fibres, and filaments embedded in an amorphous material surrounded by a well-defined laminated outer bark characterized by clearly disjointed stratification (Figure 7(C-D)). Proto-fibres originating ex novo. Fibres originating ex novo (187 to 433 μm in diameter) were seen to be made up of a well-defined laminated outer bark with clearly disjointed stratification surrounding a central pith. The pith contained thick filaments (see below) embedded in an amorphous material and was characterized by the absence of cells (Figures 8-9). Filaments in the pith of the fibres were frequently associated with endobiotic microorganisms (see below) ( Figure 8(B-D)). The thickness of the bark, which was composed of alternating layers (pink to light blue with Masson trichrome), varied considerably from a single very thin lamina (Figure 8(A-B)) up to multiple layers occupying more than the half of the diameter of the fibre (Figures 8(C-F), 9). In the proto-fibres with the thinnest bark, the outline of the bark was either wavy (Figure 8(A)) or more regular and circular (Figure 8(B)). Thickening of the bark was seen to occur through the inward deposition of multiple layers. Each pink layer of the growing bark was formed by a process of inward apposition of pink granular structures within a light blue matrix, which were arranged in short parallel rows oriented perpendicularly to the inner surface of the bark (Figure 9(B)). During morphogenesis, the amorphous material in the pith of these structures appeared colourless or very light pink in the inner part and mainly colourless in the periphery on staining with Masson's trichrome, while it was light blueturquoise with Alcian blue (Figure 9(C-D)). The amorphous material interposed between the layers was formed by the deposition of light blue filamentous-like material (Figure 9(B)).

Fibres inclusions.
A few monaxial spicules and their fragments were embedded in the fibres, mainly parallel to the fibre axis; other particles of debris were also present ( Figure 4). In all the specimens examined, still unidentified, endobiotic microorganisms were strictly associated to  the layers of the fibres (Figures 8(B, D), 10(E)). These associated microorganisms will be investigated in a companion paper.

Filamentous skeleton
The filamentous component occurred in the entire sponge body as thick filaments, mainly organized in bundles, and single thin filaments.
Thick filaments. Thick filaments (0.6-1.1 μm in diameter) were mainly organized in very abundant bundles, which were scattered singly or assembled in networks with various topographic and steric arrangements (Figures 2(C-D), 3(A-C), 4, 5, 7, 8, 9, 10(A-D), 11, 12(A, C-D)). At the ectosomal level, a sub-dermal network (conular and interconular) oriented parallel to the body surface was composed by bundles of filaments variably oriented to form the net meshes (Figures 10(A-B), 11). In each conule variably oriented bundles of filaments supported the axial fibre (Figure 3(A-C)). In inner body regions, the bundles were scattered and variably oriented.
The filaments appeared blue on staining with Masson trichrome (Figure 10(A-D)) and Azan-Mallory trichrome (not shown). On confocal microscopy, the subdermal filamentous network was evident, and the filaments showed auto-fluorescence with a less fluorescent inner axis (Figure 11(B-C)).
Thin filaments. Scattered, rare single thin filaments (0.2-0.4 μm in diameter) characterized by terminal bulbar knobs were dispersed in the abundant ECM; bulbar knobs (2.6-4 μm in diameter) occur at the end of these filaments although in sections it is not possible to clearly define if knobs can occur at both or at a single end (Figures 4(B), 10(D-J)). In histological sections, these thin filaments showed a wavy course (Figure 10(D-J)) and appeared uniformly coloured, except for the terminal knobs. These latter were drop-shaped, and were all endowed with a rounded lighter core surrounded by a thin, more intensely coloured, layer (Figure 10(D-J)). In some cases, a structure made up of concentric layers was seen within the knobs (Figure 10(F, J)). On staining with  Masson and Azan-Mallory trichrome these filaments appeared blue (Azan-Mallory not shown).

Collagen fibrils
Masson and Azan-Mallory trichrome revealed fibrillar collagen dispersed throughout the abundant ECM, mainly at the level of the ectosome appearing as fine light blue homogeneous material (Figure 12(A, C)), and in the regions surrounding aquiferous canals appearing as a pale blue trabecular network (Figure 12  (B, D)).

Discussion
Porifera evolved the ability to produce prototypes of the ECM and connective structures as organic skeletal system. The evolutionary novelty of exclusively collagenic skeletal structures components is an autapomorphy shared by Keratosa taxa. An autapomorphy exclusive of the family Irciniidae (order Dictyoceratida) is the filamentous skeleton associated to the fibrous one (Minchin 1900;Vacelet 1959;Garrone et al. 1973;Junqua et al. 1974;Cook & Bergquist 2002;Erpenbeck et al. 2020). It is known that Sarcotragus spinosulus is characterized by an irregularly reticulate spongin network of primary fibres lacking inclusions or bearing only rare foreign spicules, connected by secondary fibres and, as all Irciniidae, also by peculiar very thin knobended filaments together with fibrillar collagen dispersed throughout the ECM (Garrone et al. 1973;Bergquist 1978;Simpson 1984;Cook & Bergquist 2002;Gaino 2011;Pronzato & Manconi 2011;Manconi et al. 2013). However, in our samples, we found some remarkable differences from the above-mentioned previous literature, and peculiarities of skeleton components, at the level of both composition and structure, that have never been reported before.

Fibres
Each mature primary fibre displays irregularly alternating linear, nodular, and laminar tracts along its length, all of which share in the bark concentric laminar growth lines alternating with layers of amorphous matrix. The fact that the inner pith appears colourless on staining with Masson and Azan-Mallory trichrome, and turquoise on staining with Alcian blue, indicates the presence of GAG-like molecules in this region. While the amorphous matrix of the fibres could be considered to have the same collagen composition as the thick filaments and knob-ended filaments (Figures 3, 6, 9), the laminar layers of fibres could correspond to peculiar morphs of collagen, i.e. spongin, which is exclusive to Porifera (Figures 3, 6). However, studies are in progress to clarify the nature of these different fibre components and, especially, to determine whether other macromolecules besides collagen are involved in fibre formation.
Interestingly, we found that mature primary and secondary fibres, regardless of their dimensions, together with cribrose plates, are always equipped with a non-laminated amorphous axial pith, and appear to be made up of collagen and, in the inner part, of GAG-like material. We may consider the "fibrillar-like" pith to be the pith that bears filaments in sections of newly formed and growing fibres (Figures 8-9).
Glycosaminoglycan-like were also observed in the ECM (Figures 6(D), 9(D)). The presence of GAG-like molecules has previously been reported in several species of horny sponges (see Formato et al. 2008;Langasco et al. 2017; and references therein). In a preliminary histological study, Manconi et al. (2002Manconi et al. ( ), (2006 observed these macromolecules also in the fibres of S. spinosulus. The nodular tracts of primary fibres bearing resting and active zones of growth (Figure 7(C-D)) appear as morphogenetic regions in which the first stages of the growth process occur in the same way as that of the bark formation of newly formed fibres from which fibre growth and remodelling processes can start ex novo (see below). Sequential phases of growth or remodelling processes occur in the fibres that originate ex novo, as is indicated by the fact that the larger the diameter of the fibres is, the smaller the thickness of its bark (blue) is, owing to compaction of the collagen structure. We found that, as the bark thickness of the fibres increases, the total diameter of the fibres decreases (Figures 8-9).
During fibres morphogenesis it can be hypothesized the following sequence of growth stages: (1) a very thin layer of bark bordering appears in an area of ECM rich in filaments and lacking cells; (2) the bark progressively thickens through the deposition of multiple alternate layers of proto-spongin and non-laminated collagen. This structural shift could be due to chemical and structural modification of the amorphous matrix/filaments and the resulting reduction of the central area of the fibre, which can be considered an axial pith; (3) further biochemical maturation and remodelling of the proto-spongin layers occurs as the pith is filled with amorphous collagen material and GAG-like material (Figures 8, 9).
Thus, in S. spinosulus, the structure of the fibres seems to reach, during morphogenesis, its complex layout without the direct involvement of specialized cells driving the process, but means of modifications and new spatial assembly of pre-existing simpler collagen structures. This process occurs inwardly (i.e. the fibres grow by means of the inward deposition of successive layers) (Figure 9(B)); this is in contrast with the literature, according to which horny sponge fibres are synthesized by discrete groups of specialized cells driving also their assembling. In this regard, it has been reported that spongoblasts, by means of a "cooperative behaviour", first secrete the innermost part of the fibres, and then elongate and slide slowly down the fibre, laying down bark as they move (Vacelet 1971;Bergquist 1978;Simpson 1984;Gaino 2011). Thus, according to this latter hypothesis, bark construction occurs from the inside to the outside of the fibre, as shown by Vacelet (1971, Figure 1) in the case of Aplysina aerophoba (reported as Verongia). However, it has recently been demonstrated that Aplysina (Verongiida) has a skeleton composed in part by chitin (Klinger et al. 2014(Klinger et al. , 2019a(Klinger et al. , 2019b with a composition diverging from that of Sarcotragus (Irciniidae, Keratosa), which is made of collagen. Moreover, according to recent molecular analyses, the Verongomorpha and Keratosa subclasses diverge widely (Erpenbeck et al. 2012). It does not seem incongruous that different processes occur between distant taxa in the production of the skeleton. Other morphogenetic processes, involving the degeneration and resorption of fibres, seem to lead to the remodelling of fibres (Figure 6(E-F)). These processes, together with those of the newly formed fibres and nodular tracts, may be related to the chronic morphogenesis and phenotypic plasticity typical of Porifera (see Gaino et al. 1995).

Filaments
The homogeneous collagen structure of filaments is confirmed by blue staining (Masson and Azan Mallory trichrome) although the terminal knobs bear a core that is sometimes surrounded by concentric lines.
By contrast, on confocal microscopy, the thick filaments appear less homogeneous, showing a less fluorescent internal axis. Using transmission electronic microscopy, Garrone et al. (1973) found that these filaments were made up of three layers: a cuticle-like outermost layer, a soft cylinder, and an axial central thread. Moreover, each filament appeared as bundles of microfibrils twisted in a helical fashion, nearly straight in the axis of the filament and becoming increasingly coiled toward the periphery, while the knob-ends corresponded to a denser, more disordered, spiralized region. Furthermore, Garrone et al. (1973) found that, in S. spinosulus, filaments organized in bundles were separated from one another by collagen trabeculae, which formed a sort of chamber around each filament. However, at the ectosomal level we found that filament bundles formed a more complex spatial structure as a sub-dermal network (Figures 3(A-C), 10(A-B), 11) and in each conule variably oriented bundles of filaments supported the axial fibre (Figure 3(A-C)). In other body regions, the bundles were scattered and variably oriented.
Several authors (Brien et al. 1973;Garrone et al. 1973;Gaino 2011) have claimed that the nature of filaments in the genera Ircinia and Sarcotragus is very similar to that of the spongin fibres. However, Junqua et al. (1974) reported that, in the genus Ircinia (formerly including the present Sarcotragus), fibres and filaments differed in terms of their chemical composition, behaviour in alkali and morphology, suggesting that they may have different mechanisms of biosynthesis and organization. Similarly, our results demonstrated that, in S. spinosulus, the filaments showed a different composition and structure from that of the fibres.
Interestingly, we found that, in S. spinosulus, the number of terminal knobs was much lower than that of the filaments. Knobs were localized at the terminal end of very thin filaments, which were mainly seen scattered in the ECM and were not associated with the typical filament bundles of this species. Moreover, as we never found filaments with two knobs, the occurrence of knobs at both terminal ends in S. spinosulus was not confirmed. Further comparative studies are in progress with the aim of shedding light on these skeleton components.

Fibrillar collagen
Collagen occurring as fibrils is usually dispersed throughout the ECM, and its organization needs electron microscopy investigation (Garrone et al. 1973;Gaino 2011;Ehrlich et al. 2018). However, this component of the ECM can also be revealed by means of some histological stains. Gross et al. (1956) called this collagen material (fine blue staining with Mallory aniline blue or Masson trichrome) "spongin A" and noted that it was distributed throughout the body as a ramifying reticular meshwork of the horny sponge Spongia graminea Hyatt, 1877 (currently Spongia (Spongia) graminea). Similarly, in our study, ECM fibrillar collagen was highlighted as a trabecular network (Figure 12(B, D)), presumably corresponding to the so-called "chondrochyma" reported in other species by some authors (see Minchin 1900;Cowden & Harrison 1976), and also as fine amorphous material (Figure 12(A, C, D)), but mainly at the level of the ectosome and the regions surrounding canals of the aquiferous system.

Morphofunctional aspects
The morphofunctional role of skeletal collagen networks as a supporting structure clarifies some aspects of the evolution of ECM prototypes in the background of the huge morphofunctional plasticity displayed by Porifera. Indeed, our data on Sarcotragus spinosulus indicate a supportive functional role (a) of the tangential subdermal filamentous network, and fibrillar collagen, at the sponge surface, which maintain the dermal membrane; (b) of the variably oriented bundles of filaments in conular areas cooperating with distal portions of the fibres that act as the conular axis; (c) of fibrillar collagen and associated GAGs-like molecules acting as layout to balance water retention in the jelly-like ECM and to water pumping and circulation during the contraction/relaxation phases of the areas surrounding the aquiferous system. The topographic distribution of all these skeletal collagen elements is fundamental to the body plan of the sponge and its physiological performance.

Conclusions
The auto-assembling and remodelling processes occurring in fibres morphogenesis from collagenic structures preexisting in the ECM, as found out in our experimental model, seem to be an evolutionary novelty for the genus Sarcotragus and, more in general, for basal Metazoa. Our results indicate that knowledge on morphogenesis, morpho-anatomical and functional architecture of sponges could be a key tool in the field of applied research for identifying and defining the potentialities of biomaterials in organisms provided with a skeleton rich in collagen. Last but not least, this kind of dataset could contribute to clarify the problematic status of the family Irciniidae from a systematic and phylogenetic point of view.