Postnatal development in a marsupial model, the fat-tailed dunnart (Sminthopsis crassicaudata; Dasyuromorphia: Dasyuridae) | Communications Biology – Nature.com

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.
Advertisement
Communications Biology volume 4, Article number: 1028 (2021)
938 Accesses
41 Altmetric
Metrics details
Marsupials exhibit unique biological features that provide fascinating insights into many aspects of mammalian development. These include their distinctive mode of reproduction, altricial stage at birth, and the associated heterochrony that is required for their crawl to the pouch and teat attachment. Marsupials are also an invaluable resource for mammalian comparative biology, forming a distinct lineage from the extant placental and egg-laying monotreme mammals. Despite their unique biology, marsupial resources are lagging behind those available for placentals. The fat-tailed dunnart (Sminthopsis crassicaudata) is a laboratory based marsupial model, with simple and robust husbandry requirements and a short reproductive cycle making it amenable to experimental manipulations. Here we present a detailed staging series for the fat-tailed dunnart, focusing on their accelerated development of the forelimbs and jaws. This study provides the first skeletal developmental series on S. crassicaudata and provides a fundamental resource for future studies exploring mammalian diversification, development and evolution.
Marsupials (Metatheria) represent a distinct viviparous lineage within extant Mammalia that have been evolving independently from their sister group placental mammals (Eutheria) for over 160 million years1,2. This evolutionary distance has made them exceptionally powerful in comparative biology for understanding mammalian evolution on both a genetic and developmental level. In addition to their use for comparative studies, marsupials also exhibit unique biological features, chief among them is their unusual mode of reproduction. Eutherian mammals (hereafter referred to as placentals) typically give birth to well-developed young after a prolonged period of gestation with a large maternal contribution to the development of the offspring in utero. In contrast, marsupials give birth to highly altricial young (Fig. 1b) after a short gestation with only a minimal maternal investment during pregnancy via a short-lived, simple placenta3. Instead, marsupials have a large maternal contribution post-birth where the young are dependent on maternal milk through an extended lactation period3,4. Newborn marsupials crawl to the mother’s teat, typically located within her pouch, where they undergo the majority of their development, ex utero4,5,6. To facilitate the crawl to the teat, marsupials have well-developed forelimbs and shoulder girdles, but comparatively delayed development of the hindlimbs7,8,9,10,11,12. Similarly, craniofacial structures such as the nasal cavity, tongue, oral bones and musculature are accelerated relative to the development of the posterior end of the body13,14,15. Chondrification and ossification of the facial skeleton, forelimbs and shoulder girdle are significantly accelerated in marsupials compared to placentals13,14,16. This heterochrony is suggested to underpin developmental constraints in the marsupial clade that have restricted their overall morphological diversity within the limb and facial skeleton compared with placental mammals17,18, though this remains controversial19,20. Defining the mechanisms that control these unique developmental events can therefore provide insights into the processes underlying limb and craniofacial patterning across mammals.
a Adult fat-tailed dunnart (S. crassicaudata). Image: Alan Henderson—Minibeast Wildlife. b Schematic comparing extent of development of the fat-tailed dunnart and mouse (M. musculus) neonates on the day of birth.
Traditionally, the marsupial models, Macropus eugenii (tammar wallaby) and Monodelphis domestica (opossum), have been studied in regard to diverse biological phenomena, including sex determination21,22,23,24,25,26,27,28, reproduction29,30,31,32,33,34, genomic imprinting35,36,37,38,39 and other aspects of development40,41,42,43,44,45,46. Given their ease of captive breeding and experimental manipulation, M. domestica has been used in research across North America, for example to model craniofacial phenotypes observed in children treated with thalidomide47, and to reconstruct the evolution of the mammalian middle ear48. However, the 80-million-year divergence between Australian and North American marsupials49 means that an Australian laboratory-based marsupial model with similarly easy husbandry, year-round breeding and experimental manipulation is still needed for a more complete understanding of mammalian biology. The fat-tailed dunnart (Sminthopsis crassicaudata; hereafter referred to as the dunnart) is an established marsupial model that has been used successfully for studies of brain development, fertilisation, reproduction, respiration, nutrition, thermoregulation, vision and immunology50,51,52,53,54,55,56. In this context, expansion of the developmental and genetics resources available for the dunnart would further its value as a model for investigating mammalian biology and evolution.
Fat-tailed dunnarts are small, carnivorous Australian marsupials from the family Dasyuridae that contains about 70 other living species (Fig. 1a). Dunnarts have a short gestation of 13.5 days and represent one of the most altricial mammals known8 (Figs. 1b and 2). They typically give birth to supernumerary young57 and can suckle up to 10 young (equal to the number of teats). Juvenile dunnarts are weaned after ~65–70 days postpartum (D)50,58, with males reaching sexual maturity at approximately D200 and females entering their first oestrus at approximately D8558. The dunnart can breed all year round, which allows for efficient expansion and maintenance of colony numbers and derivation of staged foetuses and pouch young for experimental studies. As such, the dunnart provides an excellent opportunity to study and manipulate early mammalian development, which occurs almost entirely ex utero.
Numbers below pouch young refer to the day postpartum.
Detailed staging series are imperative resources for facilitating the study of any model species, but are especially interesting in marsupials owing to their unique developmental biology. There are currently no published data on the development of the skeleton of the fat-tailed dunnart, and studies on other related marsupials are often from whole-mount bone and cartilage staining on limited stages59,60,61,62, or X-ray computed tomography (CT) scanning of museum specimens where absolute age is typically unknown63,64,65,66. Previous histological studies of ossification patterns in marsupials have suggested that in highly altricial species, ossification occurs after birth60,61,62. If ossification of the dunnart skeleton also occurs post-birth, observations and manipulations of early skeletal patterning and development can be made postnatally in the pouch, further supporting its use as a model organism. However, a detailed description and staging of these events in the dunnart has yet to be established.
Here, we establish a complete postnatal ontogenetic series of the dunnart, emphasizing critical stages underlying the onset and early ossification of the cranial and postcranial skeleton. We provide quantitative developmental comparisons of craniofacial and limb heterochrony and development compared to the established placental mouse model, Mus musculus. This developmental series lays the foundation for further studies into the molecular and genetic control of the many unique aspects of marsupial development including mechanisms underlying extreme skeletal heterochrony. Our findings complement the ongoing development of additional S. crassicaudata resources as a marsupial laboratory model, including gold standard genetic resources, such as a chromosome level genome, inbred laboratory strains, and induced pluripotent cell lines.
Newborn dunnarts (D0) had an average head length of 2 mm and average weight of 12 mg (Supplementary Table 2). They were bright pink at birth and had highly vascularised, translucent skin with the developing lungs, heart and bladder clearly visible through the skin. Newborns lacked a definitive neck and had a pronounced cervical swelling under the head between the forelimbs, which disappeared by D4. At birth there were no ear primordia, and very faint retina pigmentation was visible indicating the location of the future eyes (Fig. 2, Supplementary Fig. 1a). At birth the dorsal side of the neurocranium was flat and did not begin to round until 24 h after birth. The mandibular and maxillary swellings were visible along with the hyoid/secondary arch. The medial nasal swelling was the dominant feature of the face and contributed to a large prominent nostril (Supplementary Fig. 2). This stage in the development of the facial prominences is comparable to the mouse on embryonic day (E) 11.5–1267 (Supplementary Fig. 2). On the day of birth, the oral region was completely fused except for a small round opening for attachment to the teat. By D15 the mouth began to delaminate and was fully separated by D30, coinciding with tooth eruption (Supplementary Fig. 3a). Dunnart limb heterochrony was distinct, where on D0 forelimbs were well developed (including cartilaginous skeletal elements and musculature) with interdigital separation and claws present, while the hindlimbs were rudimentary and paddle-like with faint digital grooves. The proximal region of the hindlimb remained fused with the base of the tail until approximately D9. There were no cartilaginous condensations in the dunnart hindlimb at D0 or D1 (Fig. 3c, d), comparable to the E11.5 mouse hindlimb68. The newborn fat-tailed dunnart forelimbs appear similar to those of the E14–E15 mouse with regards to digit development68. However, in the mouse forelimb this coincides with the presence of forelimb ossification centres69, which are not present in dunnart newborns. Unlike diprotodontian marsupials (marsupials with forward facing pouches, order Diprotodontia) which display strong climbing motion of the forelimbs at birth4,6,70,71,72, on D0 the dunnart appeared to have a weaker climbing motion after being removed from the pouch (Supplementary Movie 1).
a D0 head sections stained with haematoxylin and eosin Y (purple = nuclei, pink = cytoplasm), alcian blue (cartilage), alizarin red (mineralised bone) and Masson’s trichrome (blue = collagen, red = muscles, cytoplasm, and keratin). Representative images of D0 at higher magnification (×60) show ossification had begun with collagen present in the maxillary and mandible prominences. b D1 head sections stained with haematoxylin and eosin Y (purple = nuclei, pink = cytoplasm), alcian blue (cartilage), and alizarin red (mineralised bone). Wholemount, c D0 and d D1 fat-tailed dunnart specimens cleared and stained with alcian blue (cartilage) and alizarin red (bone). bv = blood vessel, cc = cartilago cupularis, ma = mandible, mc = Merkel’s cartilage, mx = maxillary, ob = osteoblast, oc = oral cavity, pl = palatine process, ton = tongue.
At birth marsupials display sexual dimorphisms which precede gonad development and are under the control of the X chromosome. The appearance of the pouch and scrotum are determined by the number of X chromosomes present, with one X chromosome determining the development of a scrotum and two X chromosomes leading to the development of a pouch73. Female dunnart pouch young display visible mammary primordia from D2 while the scrotal bulges in males are not easily distinguished until D4. Figure 2 shows the gross morphology from D0 to D30. A table of features for staging young is presented in Table 1.
Iodine-stained pouch young allow the visualisation of soft tissues using microCT scanning. For the early stages (<D10) the pouch young tissue is very lean, so the internal resolution at these stages is less clear than older specimens. Nevertheless, details of the developing organs can be observed. The major phase of organogenesis in the dunnart occurs almost entirely in the postnatal period, captured here in high resolution (Supplementary Movies 23456 and 7). These movies span the major differentiation events for all major organs. The lungs of the neonates were characteristic of primitive airways with few tubular-like structures and limited branching (Supplementary Fig. 1b). Air bubbles under the skin were visible (Supplementary Fig. 1a), consistent with gas exchange occurring via the skin at this early stage. The lung increased in complexity between D30 and D35, with the saccules becoming smaller and increasing the surface area for gas exchange (Supplementary Fig. 3, Supplementary Movies 3 and 4). A large mesonephros was present in the peritoneal cavity at birth (Supplementary Fig. 1b, Supplementary Movie 2). The mesonephros is the functional kidney in most neonatal marsupials74,75. By D3 the metanephros (definitive kidney) was visible and by D10, displayed a distinguished renal cortex and medulla. By D20 the mesonephros appeared to have regressed.
Marsupials are one of the few mammals to undergo testicular descent and inguinal closure31,76. In our developmental series we were able to capture the process of testicular descent through the inguinal canal and into the scrotum. On D40 the testes had migrated to the base of the abdomen and were ready to begin the inguinoscrotal phase of testicular descent (Supplementary Fig. 4a, Supplementary Movie 5). At D50 the testes were visible in the body wall (Supplementary Fig. 4b, Supplementary Movie 6), transitioning the inguinal canal and by D60 they were situated in the scrotum (Supplementary Fig. 4c, Supplementary Movie 7).
At birth, pouch young lack an ossified skeleton, showing a cartilaginous postcranial skeleton and chondrocranium (Fig. 3a). Positive alizarin red staining, which stains mineralised bone, was observed in the maxillary and dentary in D1 frontal sections but not at D0 (Fig. 3a, c). However, when stained with Masson’s trichrome stain, collagen deposits (blue) typical of osteoid matrix and bone were present in the maxillary and dentary tissue (Fig. 3a) suggesting that ossification had started in the newborn pouch young. Within 24 h of birth, ossified bones of the facial and postcranial skeleton were present as observed with wholemount alizarin red staining (Fig. 3d) and microCT scanning (Fig. 4a).
The right lateral side of the skeleton is shown in (a), (d) and (g), the dorsal view of the skull in (b), (e) and (h), and the ventral view of the skull in (c), (f) and (i). Pouch young one day after birth (D1) are shown in (a), (b) and (c). Pouch young six days (D6) after birth are shown in (d), (e) and (f). Pouch young 15 days after birth (D15) are shown in (g), (h) and (i). as = alisphenoid, at = atlas, bo = basioccipital, bs = basisphenoid, cl = clavicle, de = dentary, eo = exooccipital, et = ectotympanic, fd = forelimb digits, fe = femur, fi = fibula, fr = frontal, hu = humerus, hy = hyoid, in = incus, il = ilium, ip = interparietal, is = ischium, ju = jugal, la = acrimal, mc = metacarpals, ml = malleus, mt = metatarsals, mx = maxilla, na = nasal, pa = parietal, pl = palatine process, pm = premaxilla, pt = pterygoid, ra = radius, ri = ribs, sc = scapula, so = supraoccipital, sq = squamosal, st = sternum, ti = tibia, ul = ulna, ve = vertebrae.
On D1, ossification centres were evident in the premaxilla, maxilla, palatine process and exoccipital bones (Fig. 4a–c). The pterygoid and basioccipital bones were observed on D3. The first ossification centre of the zygomatic arch began in the jugal on D4, along with the basisphenoid and frontal bones of the skull. By D5, ossification centres in the supraoccipital, squamosal, nasal, lacrimal, ectotympanic, goniale and parietal were present. Ossification of the alisphenoid was evident on D6 and the malleus on D7 (Fig. 4d–f). Ossification centres of the incus and interparietal were present on D15 (Fig. 4g–i). The petrosal bone of the inner ear was the last cranial bone to begin ossification and was clearly observable on D20.
At birth, the lower jaw consists entirely of a thin rod of cartilage, known as Meckel’s cartilage (Fig. 3a, c). By D1 ossification of the dentary bone (mandible) surrounding the Meckel’s cartilage had begun. The coronoid, condylar and angular processes that form as part of the dentary were visible on D4. The oral bones were the first to ossify in both the dunnart and the mouse77,78,79 (Fig. 5). However, the onset of cranial ossification was more uniform in the mouse with bones of the cranium ossifying alongside the oral bones (Fig. 5). In contrast, ossification in the bones of the fat-tailed dunnart cranium occur long after ossification of the oral bones was initiated (Fig. 5).
We also compared the relative timing of the onset of ossification in the fat-tailed dunnart to two other Dasyuridae species, Dasyurus viverrinus (Eastern quoll)13,80 and Sminthopsis macroura (the stripe-faced dunnart), as well as the reconstructed Marsupialia ancestor64. S. crassicaudata (this study) similarly had early ossification of the maxilla, premaxilla and dentary but greater variation in onset of ossification for other bones of the skull with the exception of the petrosal bone (Supplementary Fig. 5b). Aside from the petrosal bone, there was no overlap in the timing of the onset of ossification in the other cranial bones with another dunnart species, the striped-faced dunnart (S. macroura).
The bones surrounding the oral cavity connected early relative to the bones of the cranium, with the maxilla-palatine bone contact event on D8, lacrimal-maxilla and premaxilla-maxilla on D10, premaxilla-nasal on D15, and maxilla-nasal on D25. On D20 the secondary jaw joint (temporomandibular joint) is present with a mortar-shaped condylar head and a concave-shaped glenoid fossa (Fig. 6a, b). Other early connecting bones include the goniale-ectotympanoid (D5) and goniale-malleus (D10) (Supplementary Figs. 6 and 7). On D30, bone contacts in the cranium had begun with the supraoccipital-interparietal, parietal-frontal, frontal-nasal, frontal-lacrimal and alisphenoid-frontal (Fig. 7a–c; Supplementary Fig. 6). The latest bone contacts observed in this cranial series were the supraoccipital-petrosal, supraoccipital-squamosal, and basioccipital-basisphenoid which had just begun to make contact at weaning (D70; Fig. 7g–i, Supplementary Fig. 6). The onset of bone-contacts observed in the fat-tailed dunnart showed a similar pattern to both the Eastern quoll13,80 and the reconstructed Marsupialia ancestor64 with the exception of the supraoccipital-squamosal bone contact (relative timing Marsupialia = 0.17 and S. crassicaudata = 1.0), maxilla-jugal (Marsupialia = 0.20, D. viverrinus = 0.14, dunnart = 0.67), supraoccipital-interparietal (Marsupialia = 0.29, D. viverrinus = 0.14, S. crassicaudata = 0.67), jugal-squamosal (Marsupialia = 0.39, D. viverrinus = 0.50, S. crassicaudata = 0.78; Supplementary Fig. 5a).
Specimens were ranked in order of bone onset or bone contact timing and relative ranks were normalised for comparison between species. M. musculus is shown with pink circles and S. crassicaudata is shown with green triangles, highlighting the early onset of ossification of the oral region in both species.
a Ventral view of the secondary jaw joint with inset white box showing entire skull. b Posterior to anterior view of the secondary jaw joint. c = condyle (orange), et = ectotympanic ring (purple), gf = glenoid fossa (light green), in = incus (yellow), ml = malleus (blue) and sq = squamosal (dark green). Scale bar = 1 mm.
The right lateral side of the skeleton is shown in (a), (d) and (g), the dorsal view of the skull in (b), (e) and (h), and the ventral view of the skull in (c), (f) and (i). Pouch young on D35 are shown in (a), (b) and (c). Pouch young on D50 are shown in (d), (e) and (f). Pouch young on D70 are shown in (g), (h) and (i).
On D1, ossification centres of thoracic and cervical vertebrae were present either side of the neural arch (Fig. 4a). The atlas had begun to ossify by D2 and ossification centres of the lumbar vertebrae were present on D3. The caudal vertebrae did not begin ossification until two days later on D5, coinciding with the onset of ossification of the first bone of the pelvic girdle, the ilium (Fig. 4d). The ischium ossifies later and was evident on D15 (Fig. 4g). The ossification centre of the distal section of the epipubic bone was present on D20. Ossification centres were present in the scapula, clavicle and the body of the first six rib pairs on D1 (Fig. 4a). By D4 the body of the true, false and floating ribs were all undergoing ossification. The capitulum of each rib had an ossification centre on D7. The first ossification centres of the sternum were evident on D15 in the xiphoid process, manubrium and the first three anterior sternebrae of the body (Fig. 4g). The fourth sternebrae began ossification later and was evident on D25.
Cartilage was present in the forelimb but there was no cartilage present in the hindlimb on the day of birth or D1 (Fig. 3c, d). One day after birth, ossification centres in the humerus, radius and ulna were evident (Fig. 4a; Table 2). On D5 the bones of the hindlimbs began to ossify, with the femur, tibia and fibula present (Fig. 4a). Ossification centres were present on D6 in the forelimb phalanges but not until D15 in the hindlimb phalanges (Fig. 4d; Table 2). The metacarpals of the forelimbs had begun ossification on D10 and the metatarsals of the hindlimbs by D15 (Fig. 4g; Table 2). Ossification centres of the carpals and tarsals were the last to ossify and were evident on D40 (Fig. 7d; Table 2).
Pouch young display heterochrony of the limb bones from day one to approximately day 50 (Fig. 8). Individual bones of the dunnart limbs also displayed pronounced differences in allometric scaling during growth (Fig. 8). Following birth, pouch young possess well-developed forelimbs, showing ossification of the humerus, radius and tibia, but possess underdeveloped, paddle-like hindlimbs lacking any bone. By D5, the hindlimbs show their first signs of extension and development, emphasizing the strong developmental heterochrony. The autopod of the forelimb (carpus) and hindlimb (tarsus) are roughly the same length from D15 to D30 (Fig. 8). After D30 the autopod of the hindlimb overtakes the carpus and this difference in length continues to expand until the weaned juvenile stage.
Relative lengths of forelimb and hindlimb elements throughout development, shown as shaded grey bars (n = 1). Limbs are divided into proximal and distal segments: the stylopod (humerus and femur), zeugopod (ulna/radius and tibia/fibula) and autopod (carpals, metacarpals, tarsal, metatarsals and digits).
Here, we present a high-resolution, digital reconstruction of the complete postnatal ontogeny of S. crassicaudata. Our study focused on characterizing early skeletal development in the fat-tailed dunnart to establish it as a comparative laboratory-based model for mammalian skeletal osteogenesis. Our description of postnatal gross morphology including head length, weight and crown-to-rump length provides a staging tool for future studies using this marsupial model. This expands upon a previous staging series54 to include detailed skeletal descriptions and a general overview of some interesting aspects of organ development.
Newborn dunnarts have large heads (almost 50% of the total body length) and well-developed forelimbs compared to hindlimbs that are required to facilitate movement to the pouch and teat attachment. They lack an ossified skeleton, showing a cartilaginous postcranial skeleton and chondrocranium. The chondrocranium is a transitory, embryonic structure critical in the developing mammalian head81,82. In fat-tailed dunnarts, the newborn young display large medial nasal swellings. This is consistent with descriptions of the chondrocranium in Sminthopsis virginiae (the red-cheeked dunnart), which has the most extensive cartilago cupularis (the rostral part of the nasal cartilage) of any marsupial examined83. Previous studies have shown that variation in the cupula nasi anterior (the anterior portion of the cartilaginous nasal capsule) reflects the animal’s life history83. The nasal capsule morphology in marsupials is more uniform across the group than observed in placentals and this is thought to be related to the extended fixation of pouch young to the mother’s teat during lactation83. It has also been proposed that there is a relationship between the innervation of the area proximal to the cupla nasi anterior and the sensory requirements of marsupials at birth84,85,86. An in vitro study in M. domestica newborn young found that when pressure was applied to the innervated snout this induced electromyographic responses from the triceps muscle in both forelimbs87. The forelimb responses were absent when the facial skin was removed, suggesting that the journey to the pouch may be aided by the influence of facial mechanosensation on forelimb movement87. Dunnart neonates lack a distinct neck and any skeletal elements to support the head and the journey to the pouch is instead aided by a large cervical swelling which supports the head until D4. The cervical swelling is also thought to assist with teat attachment88. Cervical swellings have been reported in two other Dasyuridae species: the Tasmanian devil, Sarcophilus harrisii and Eastern quoll, Dasyurus viverrinus8,88 and are correlated with the altricial nature of the pouch young. Marsupials with more precocious newborns, such as macropods (e.g., kangaroos, wallabies), lack cervical swellings and have full head movement at birth8,33.
The microCT scans provide an excellent resource for studying the development of internal organs, particularly in the older stages where the scans are clearer. We have briefly described aspects of lung, gonad and kidney development but make these data publicly available for additional studies of organ development in more detail. The lungs of dunnart newborns were characteristic of primitive airways with large tubular-like structures. On the day of birth, dunnart lungs are similar to that of eutherian lungs during the canicular stage of embryonic development89. At birth, in the fat-tailed dunnart, the skin is responsible for almost all gas exchange with pulmonary ventilation unable to satisfy the demand for oxygen until between D23 and D3589. Interestingly, this is when we observe the rapid increase in lung complexity between D30 and D35. It has been suggested that the short gestation time of dunnarts provides insufficient time for development of a complex respiratory system and therefore relies on transcutaneous gas exchange89.
Remarkably, we were able to capture the process of testicular descent through the inguinal canal into the scrotum. On D40, the testes had migrated through the abdomen and were ready to begin the inguinoscrotal phase of testicular descent. At D50, the testes were visible at the neck of the scrotum and by D60 were situated in the base of the scrotum. It has previously been suggested that the time taken for completion of testicular descent in marsupials may be associated with postnatal growth rate90 given the shorter period (3–4 weeks) for testicular descent in the bandicoot (Perameles gunni)91 compared to kangaroos, wallabies and possums (10–11 weeks)74,92,93,94. However, in our study we find that although dunnarts represent one of the most altricial neonates (Grade 18), the process of testicular descent occurs at almost exactly the same postnatal stage as in other more precocial marsupials74,92,93,94. Our results are also supported by a study in Antechinus stuartii (family Dasyuridae), which found that after one month the testes were situated in the inguinal canal and after two months were present at the base on the scrotum95.
Using a combination of microCT scanning and histological techniques we confirmed that on the day of birth (<24-h old), no ossified bones were present in the dunnart. Mineralized bone was observed one day after birth and was limited to bones in the oral region, forelimbs and vertebrae. We observed osteoid matrix in the maxillary and dentary of D0 pouch young head sections showing that ossification had begun. This suggests that microCT is useful for assessing when ossified bone arises, however, histology is still required for investigating the onset of ossification prior to mineralization.
Previous studies of skeletal development in marsupials have similarly shown that the maxilla, premaxilla and dentary are the first bones to ossify59,61,62,63,64. However, there appears to be some differences in the timing of onset of ossification in different marsupials. In Monodelphis domestica and Macropus eugenii these bones have already begun ossification prior to birth59. In contrast, in Isoodon macrourus62, Trichosurus vulpecula62, Didelphis albiventris60 and Sminthopsis macroura61 ossification begins after birth. Although marsupials show inter- and intraspecies variation in the timing of the onset of ossification in bones of the skull, the relative timing of bone contacts in the oral region, middle ear and late occipital region are highly conserved64. Similar to Spiekman and Werneburg64, we observed the first bone contacts occurred in bones surrounding the mouth cavity (maxilla-palatine) and middle ear bones (ectotympanic-goniale and goniale-malleus). In mammals the middle ear bones form as part of the mandible and separate after the secondary jaw joint has formed48,96. However, due to the altriciality of newborns, marsupials and monotremes are born before the jaw joint forms and use their middle ear bones to articulate the lower jaw with the head to allow for feeding82,97,98,99,100. In the dunnart the secondary jaw joint is formed by D20, which is comparable with the opossum (D14–D2082,96,101). The last bones to make contact were the those that form the back of the cranium, particularly in those that connect the occipital bones. As previously observed in marsupials64, the connections within the occipital region occurred around the time of weaning, suggesting that the region is not required for cervical support during suckling64.
Developmental comparisons to the well-known placental model, the laboratory mouse (Mus musculus), are useful for studying the evolution of skeletal elements, particularly given the heterochrony with in marsupials. Most ossification centres in placentals are present at birth, with ossification in mice beginning on embryonic days 12–13102,103,104, while in the dunnart all ossification occurs postnatally. Similar to the dunnart, the bones of the oral region (premaxilla, maxilla, dentary, palatine and pterygoid) are the first to ossify in the mouse, presumably in preparation for feeding, as in marsupials. However, unlike in the dunnart and other marsupials, the mouse cranium (basioccipital, frontal, parietal and sphenoid) ossifies at a similar stage of development as the oral bones. The developmental timing of the facial morphology appears to be less disparate across marsupials than placental mammals, but displays equal variation in the neurocranial morphology105. This difference in cranial developmental timing between marsupials and placentals is thought to be driven by the early functional requirements of the oral apparatus for continuous suckling in marsupials105. However, the bones of the oral regions (premaxilla, maxilla, dentary and palatine) are also the first to ossify in the reconstructed ancestral ossification sequence of Mammalia63 and often in non-mammalian amniotes suggesting prioritized development of the oral apparatus is the ancestral state in amniotes63,64,106,107,108,109. The short gestation time and altricial stage of the marsupial neonate at birth is likely to have driven a more extreme shift in the developmental timing of this event, relative to the rest of the body. This is supported by the extremely high integration of the oral bones in early marsupial postnatal ontogeny in comparison to other cranial regions where levels of integration are similar to placentals17. In particular, cranial bones arising from the migratory neural crest cell population of the first pharyngeal arch have been shown to be constrained between marsupials to facilitate early functional demands66.
Early ossification of the craniofacial bones in Monodelphis domestica (grey short-tailed opossum) is thought to occur through accelerated migration, proliferation and differentiation of the cranial neural crest cells that pattern the facial prominences and skeletal elements110,111. A marsupial-specific region within a Sox9 enhancer was found to drive early and broad expression of Sox9 in pre-migratory neural crest cell domains contributing to early migration of cranial neural crest cells relative to the mouse112,113. The spatio-temporal expression of downstream key ossification genes such as Runx2 and Osx have not been studied and in comparison to placentals, little is known of the molecular and genetic control of craniofacial development in marsupials96,97,114. Recently, Smith (2020) presented previously unpublished work of J.P. Hill and Katherine Watson on the development of neural crest in other marsupial taxa115. They confirmed that early migration of the neural crest occurs in multiple marsupial taxa, particularly for the neural crest cells that end up in the facial and first arch regions115. Interestingly, dasyurids differed from other marsupials with considerable accumulation of neural crest before somitogenesis had begun, along with far earlier migration of the ectomesenchyme into the craniofacial region115. Smith (2020) suggested that the shorter the period of gestation in marsupials the earlier the accumulation and migration of neural crest will be. Being one of the most altricial marsupials in existence, the dunnart provides an ideal model in which to study the molecular drivers of heterochrony in craniofacial ossification in marsupials.
Based on the facial processes present in the newborn dunnart and the lack of ossification centres, we propose that at D0 dunnart craniofacial development corresponds to that of the E11.5–E12 mouse embryo. This suggests that at birth in the dunnart, neural crest cells are still proliferating and differentiating. Given this new developmental information, the dunnart therefore presents a new and exciting mammalian model to expand craniofacial research as facial primordia can be manipulated ex utero and the role of key genes underlying osteogenesis can be directly observed.
The ossification sequence of the dunnart postcranial skeleton follows a similar pattern to that previously described in marsupials59,61,62,65. Like all marsupials, dunnart pouch young display heterochrony in the development of the limb bones with the forelimbs being longer than the hindlimbs from D1 to ~D50. After D50, the limbs undergo a heterochronic shift in their length and the hindlimbs overtake the length of the forelimbs. This corresponds with the pouch young no longer being permanently attached to the teat in the lead up to weaning58. The bones of the carpals and tarsals were the last to ossify in the limbs. The ossification of the metacarpals, metatarsals and digits before the carpals and tarsals is consistent with ossification patterns in S. macroura61, Trichosurus vulpecula62, Thylacinus cynocephalus65 and Didelphis alviventris60. Embryological and molecular studies suggest that marsupial limb heterochrony is driven by both an acceleration in the development of the forelimb buds and a delay in the development of the hindlimb buds7,9,10,116,117,118. In addition to the heterochrony between the fore- and hindlimbs in marsupials, heterochrony is also observed in the timing of the onset of marsupial forelimb and hindlimb development relative to placentals. Dunnart forelimb development is accelerated compared to the hindlimb, and compared to that in the mouse119, where both limb buds begin to differentiate and grow at a similar stage of development119,120. On the day of birth, the dunnart forelimb has well-developed musculature, and digits with claws to facilitate its crawl to pouch. However, the D0 dunnart lacks ossified forelimb bones, suggesting that it does not require fully formed skeletal elements to complete the crawl to the mother’s pouch. Conversely, the hindlimb has no cartilage or bone and is a paddle-like bud with digital condensations beginning to form. Generally, mammalian forelimbs develop ahead of hindlimbs, with the timing relatively close in placentals, while in marsupials the difference in the rate of forelimb and hindlimb development is extreme6,121. The dunnart represents one of the most altricial neonates8, and so is an extreme example of this heterochronic shift in forelimb and hindlimb development. The heterochrony in marsupial limb development involves the early specification and initiation of patterning in the forelimb bud relative to foetal development122. In the opossum (M. domestica), the early initiation of the forelimb field is initiated during the early stages of somitogenesis through accelerated expression of the necessary forelimb transcription factor TBX5, and limb outgrowth and patterning genes FGF10, FGF8 and SHH, and greater myocyte (forming the later limb musculature) allocation42,122. SHH is also expressed early in the forelimbs of tammar wallaby (Macropus eugenii) embryos relative to hindlimb bud expression123.
Research into marsupial limb development is currently limited by the inability to perform in vivo transgenic experiments42,44,122,123,124,125,126,127. Although limb organ cultures have been successfully used in the opossum to investigate the molecular control of limb heterochrony124, limb development has predominantly been studied in the chick and mouse given the ease of observing and manipulating limb patterning in these species. Electroporation technologies previously used in chick128, xenopus129 and mice130 have recently been successfully applied to manipulating dunnart brain development55. This technology provides a tangible system for the manipulation of gene expression in the fat-tailed dunnart in vivo.
The public availability of precisely staged microCT scans for the fat-tailed dunnart as presented here provides a valuable resource for future studies in mammalian development. The highly altricial state of the newborn dunnart allows for precise, tissue-specific manipulation of skeletal development ex utero, prior to the onset of ossification and over an extended period of time. Such manipulations are challenging to perform in placental mammals where ossification is established in utero. The dunnart provides access to key ossification stages in an easily manipulable mammalian model. A staging series of the fat-tailed dunnart therefore presents a fundamental resource that will underpin future work into marsupial development, in particular defining the molecular control of craniofacial and limb heterochrony.
All animal procedures, including laboratory breeding, were conducted in accordance with the current Australian Code for the Care and Use of Animals for Scientific Purposes131 and were approved by The University of Melbourne Animal Ethics Committee (AEC: 1513686.2) and with the appropriate Wildlife Permit (number 10008652) from the Department of Environment, Land, Water and Planning. Animals were housed in a breeding colony in the School of BioSciences, The University of Melbourne. Animals are bred using the Poiley outbreeding system to limit inbreeding132 and breeding boxes were set up with a male:female ratio of 1:2 or 1:3. Animals were kept in cages with water and vitamin supplements (Pentavite; 1 mL into 100 mL water) changed three times a week. All cages had nest boxes with shredded newspaper, empty toilet rolls, drinking bottle, food bowl and native tree branches. Animals were fed each day a diet consisting of live food (2 crickets and 3 mealworms) and wet mince mixture of 51% beef mince (Whiskas), 36% beef and lamb flavoured biscuits (Whiskas), 12.7% wombaroo and 0.3% calcium carbonate. Dunnart were kept on a 16:8-h light:dark cycle and temperature between 21 and 25 C. Females were monitored to track oestrus cycle133. Body weight fluctuations in female animals and daily examination of urine samples under light microscopy were used to determine whether ovulation had occurred. A decrease in body weight and the presence of cornified epithelial cells in the urine is associated with the day of ovulation133. The presence of sperm in the urine of females confirmed that insemination had occurred. Pregnancy is timed with the detection of ovulation or the appearance of sperm set as day 0 of pregnancy133. Female pouches were checked every day for births by gently holding the animal with one hand and opening the pouch with the thumb and index finger of the other hand. On the day of birth, the mothers often have a small amount of blood in the urine and the pouch young will be pink and highly vascularised. Pouch young were removed by gently holding the female on her back with one hand and using the thumb and index finger of the other hand to gently but quickly slide the young from the teat. Pouch young under D15 were placed on ice for 15 min as an anaesthetic followed by immersion-fixation in 4% paraformaldehyde (PFA) in phosphate-buffered saline (PBS). Pouch young from D15 to D45 were anaesthetised on ice for 15 min, followed by intraperitoneal (IP) injections of 4% PFA in PBS. Pouch young D50 and older were anaesthetised via an intramuscular injection of 10 mg kg−1 Zoletil (1:1 tiletamine HCl, zolazepam HCl), then killed with an 0.05–0.1 mL volume intraperitoneal injection of 150 mg kg−1 pentobarbital sodium (made up to 60 mg ml−1 in sterile saline) After fixation specimens were washed twice with PBS for 1 h and then dehydrated in increasing ethanol solutions before storing in 70% ethanol. Pouch young were photographed using a Nikon Digital Sight DS-U3 (Nikon, Tokyo, Japan) and all images were processed through NIS Elements Analysis D v.4.300.00 64-bit software (Nikon).
Specimens were collected every day from D0 to D10, then every 5 days from D10 to D50, then every 10 days from D50 to D70. Specimens were scanned using X-ray micro-computed tomography (microCT) at the TrACEES platform, School of Earth Sciences, University of Melbourne. One specimen from each stage was stained with 1% iodine in 100% ethanol in order to visualise soft tissue in the microCT images. Specimens under D40 were stained for 24 h and specimens over D40 were stained for 72 h. Specimens were rinsed in 100% EtOH once before scanning. Specimens were either mounted in 200–1000 μL pipette tips (Axygen) suspended in ethanol or suspended dry with cotton wool spacers between specimens. Larger specimens were wrapped in standard bubble wrap and scanned in either a 15 or 50 mL Falcon tube (Sigma). MicroCT scanning was performed in a Phoenix Nanotom m (GE Sensing & Inspection Technologies GmbH) operated using xs control and Phoenix datos—x acquisition and reconstruction software (GE Sensing & Inspection Technologies). Samples were scanned for 10 minutes at varying resolutions ranging from 4.75 to 26.18 μm pixel size (Supplementary Data 1). The X-ray energy varied from 40 to 55 kV and 300 to 250 μA depending upon the size of the specimen and whether it was stained with iodine (Supplementary Data 1). A Diamond target was used and 1199 2D X-ray projections were collected over a 360° rotation of the specimens. Skeletal reconstructions were performed in VGStudio MAX 3.0 (Volume Graphics, Heidelberg, Germany). Left and right-side limb bones were measured for one individual per sampled age and averaged using polyline length tool in VGStudio MAX 3.0 (Volume Graphics, Heidelberg, Germany). First appearance of skeletal elements and cranial bone contacts were observed in VGStudio MAX 3.0 for one specimen from each precisely staged age and recorded (Volume Graphics, Heidelberg, Germany). To compare to previously published datasets from other mammalian species, specimens were ranked in order of bone onset timing or bone contact timing, and relative ranks were distributed between 0 and 1 as described in Koyabu et al.63. Original and relative ranks are listed in Supplementary Table 1 and Supplementary Data 2 and 3.
Pouch young were collected (see the ‘Collection of pouch young’ section) on D0 and D1 either fixed in 4% paraformaldehyde for serial sectioning or fixed in 95% ethanol for whole-mount staining. Samples for serial sectioning were processed through a series of ethanol and xylene washes (15-min steps; Tissue-Tek VIP, School of BioSciences), embedded into paraffin wax (Leica) and 7-μm sections cut with a microtome (Zeiss, Sydney, Australia) and transferred to superfrost slides (Platinum Pro, Grale). For D0 (n = 1) and D1 (n = 1), sections were either stained with Harris’ Haematoxylin (Australian Biostain) and Eosin Y (Australian Biostain), Alizarin Red (ProSciTech, Australia) or Alician Blue (ProSciTech, Australia) according to standard methods134, or a modified Masson’s trichrome stain135,136. Sections were imaged on an Olympus BX51 Microscope with an Olympus DP70 Camera (Olympus, Sydney, Australia). Bone and cartilage wholemount staining was performed according to the described protocol for mouse embryos137. Briefly, pouch young skin (D0, n = 2; D1, n = 2) was removed with forceps, stained in 0.05% alcian blue stain solution overnight then washed for 8 h in 70% ethanol. Specimens were cleared with 1% potassium hydroxide for 2 h and counterstained with alizarin red stain solution (0.005% (w/v) alizarin red in 1% potassium hydroxide) overnight. Specimens were cleared in 1% potassium hydroxide/20% glycerol for 2 days and stored in glycerol:ethanol (1:1). Stained pouch young were photographed using a Nikon Digital Sight DS-U3 (Nikon, Tokyo, Japan) and all images were processed through NIS Elements Analysis D v.4.300.00 64-bit software (Nikon).
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
All X-ray and reconstructed microCT data shown are publicly available through a MorphoSource repository (www.morphosource.org, Project P1150)138. Histology slide images are available through a Figshare repository (www.figshare.com, Project 111930)139. For comparison of ossification patterns between species, timing and ranks were obtained from two previous publication datasets by Koyabu et al.63 and Spiekman et al.64.
Bininda-Emonds, O. R. et al. The delayed rise of present-day mammals. Nature 446, 507–12 (2007).
CAS  PubMed  Article  Google Scholar 
Luo, Z.-X., Yuan, C.-X., Meng, Q.-J. & Ji, Q. A Jurassic eutherian mammal and divergence of marsupials and placentals. Nature 476, 442–445 (2011).
CAS  PubMed  Article  Google Scholar 
Renfree, M. B. Review: Marsupials: placental mammals with a difference. Placenta 31 Suppl, S21–6 (2010).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Tyndale-Biscoe, H. & Renfree, M. Reproductive physiology of marsupials (Cambridge Univ. Press, Cambridge, 1987).
Book  Google Scholar 
Tyndale-Biscoe, C. H. Life of Marsupials (CSIRO Publishing, Collingwood, Victoria, 2005).
Book  Google Scholar 
Gemmell, R. T., Veitch, C. & Nelson, J. Birth in marsupials. Comp. Biochem. Physiol. B. Biochem. Mol. Biol. 131, 621–30 (2002).
PubMed  Article  PubMed Central  Google Scholar 
Bininda-Emonds, O. R. et al. Forelimb-hindlimb developmental timing changes across tetrapod phylogeny. BMC Evol. Biol. 7, 182 (2007).
PubMed  PubMed Central  Article  Google Scholar 
Hughes, R. L. & Hall, L. S. In The Developing Marsupial: Models for Biomedical Research (eds Tyndale-Biscoe, C. H. & Janssens, P. A.) 8–27 (Springer, Berlin, Heidelberg, 1988).
Sears, K. E. Differences in the timing of prechondrogenic limb development in mammals: the marsupial-placental dichotomy resolved. Evolution 63, 2193–200 (2009).
PubMed  Article  PubMed Central  Google Scholar 
Weisbecker, V., Goswami, A., Wroe, S. & Sanchez-Villagra, M. R. Ossification heterochrony in the therian postcranial skeleton and the marsupial-placental dichotomy. Evolution 62, 2027–2041 (2008).
PubMed  Article  PubMed Central  Google Scholar 
Klima, M. Early development of the shoulder girdle and sternum in marsupials (Mammalia: Metatheria). Adv. Anat. Embryol. Cell Biol. 109, 1–91 (1987).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Sanchez-Villagra, M. R. & Maier, W. Ontogenesis of the scapula in marsupial mammals, with special emphasis on perinatal stages of didelphids and remarks on the origin of the therian scapula. J. Morphol. 258, 115–29 (2003).
PubMed  Article  PubMed Central  Google Scholar 
Nunn, C. L. & Smith, K. K. Statistical analyses of developmental sequences: the craniofacial region in marsupial and placental mammals. Am. Nat. 152, 82–101 (1998).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Smith, K. K. Craniofacial development in marsupial mammals: developmental origins of evolutionary change. Dev. Dyn. 235, 1181–93 (2006).
PubMed  Article  PubMed Central  Google Scholar 
Smith, K. K. The evolution of mammalian development. Bull. Mus. Comp. Zool. 156, 119–135 (2001).
Google Scholar 
Smith, K. K. Comparative patterns of craniofacial development in eutherian and metatherian mammals. Evolution 51, 1663–1678 (1997).
PubMed  Article  PubMed Central  Google Scholar 
Goswami, A. et al. Do developmental constraints and high integration limit the evolution of the marsupial oral apparatus? Integr. Comp. 56, 404–415 (2016).
Article  Google Scholar 
Sears, K. E. Constraints on the morphological evolution of marsupial shoulder girdles. Evolution 58, 2353–70 (2004).
PubMed  PubMed Central  Google Scholar 
Martín-Serra, A. & Benson, R. B. J. Developmental constraints do not influence long-term phenotypic evolution of marsupial forelimbs as revealed by interspecific disparity and integration patterns. Am. Nat. 195, 547–560 (2020).
Article  Google Scholar 
Sánchez-Villagra, M. R. Why are there fewer marsupials than placentals? On the relevance of geography and physiology to evolutionary patterns of mammalian diversity and disparity. J. Mamm. Evol. 20, 279–290 (2013).
Article  Google Scholar 
Foster, J. W. et al. Evolution of sex determination and the Y chromosome: SRY-related sequences in marsupials. Nature 359, 531–533 (1992).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Hornecker, J. L., Samollow, P. B., Robinson, E. S., VandeBerg, J. L. & McCarrey, J. R. Meiotic sex chromosome inactivation in the marsupial Monodelphis domestica. Genesis 45, 696–708 (2007).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Pask, A. & Graves, J. A. M. In Genes and Mechanisms in Vertebrate Sex Determination. 71–95 (Birkhäuser, Basel, 2001).
Pask, A., Renfree, M. B. & Graves, J. A. M. The human sex-reversing ATRX gene has a homologue on the marsupial Y chromosome, ATRY: Implications for the evolution of mammalian sex determination. PNAS 97, 13198–13202 (2000).
CAS  PubMed  PubMed Central  Article  Google Scholar 
Pask, A., Toder, R., Wilcox, S. A., Camerino, G. & Graves, J. A. M. The candidate sex-reversing DAX1 gene is autosomal in marsupials: implications for the evolution of sex determination in mammals. Genomics 41, 422–426 (1997).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Pask, A. J., Harry, J. L., Renfree, M. B. & Graves, J. A. M. Absence of SOX3 in the developing marsupial gonad is not consistent with a conserved role in mammalian sex determination. Genesis 27, 145–152 (2000).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Renfree, M. B., Pask, A. J. & Shaw, G. Sex down under: the differentiation of sexual dimorphisms during marsupial development. Reprod. Fertil. Dev. 13, 679–90 (2001).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Moore, H. D. M. & Thurstan, S. M. Sexual differentiation in the grey short-tailed opossum, Monodelphis domestica, and the effect of oestradiol benzoate on development in the male. J. Zool. 221, 639–658 (1990).
Article  Google Scholar 
Bergallo, H. G. & Cerqueira, R. Reproduction and growth of the opossum Monodelphis domestica (Mammalia: Didelphidae) in northeastern Brazil. J. Zool. 232, 551–563 (1994).
Article  Google Scholar 
Chen, Y. et al. Hormone-responsive genes in the SHH and WNT/β-catenin signaling pathways influence urethral closure and phallus growth. Biol. Reprod. 99, 806–816 (2018).
PubMed  Article  PubMed Central  Google Scholar 
Coveney, D., Shaw, G., Hutson, J. M. & Renfree, M. B. Effect of an anti-androgen on testicular descent and inguinal closure in a marsupial, the tammar wallaby (Macropus eugenii). Reproduction 124, 865–874 (2002).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Harder, J. D. & Jackson, L. M. Chemical communication and reproduction in the gray short-tailed opossum (Monodelphis domestica). Vitam. Horm. 83, 373–399 (2010).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Pask, A. J. & Renfree, M. In Marsupial Genetics and Genomics. 285–316 (Springer, Dordrecht, 2010).
Williamson, P., Fletcher, T. P. & Renfree, M. B. Testicular development and maturation of the hypothalamic-pituitary-testicular axis in the male tammar, Macropus eugenii. Reproduction 88, 549–557 (1990).
CAS  Article  Google Scholar 
Das, R. et al. Convergent and divergent evolution of genomic imprinting in the marsupial Monodelphis domestica. BMC Genomics 13, 394 (2012).
CAS  PubMed  PubMed Central  Article  Google Scholar 
Pask, A. In Genomic Imprinting: Methods in Molecular Biology (ed. Engel, N.) 263–75 (Humana Press, Totowa, NJ, 2012).
Wang, X., Douglas, K. C., Vandeberg, J. L., Clark, A. G. & Samollow, P. B. Chromosome-wide profiling of X-chromosome inactivation and epigenetic states in fetal brain and placenta of the opossum, Monodelphis domestica. Genome Res. 24, 70–83 (2014).
CAS  PubMed  PubMed Central  Article  Google Scholar 
Ishihara, T., Hickford, D., Shaw, G., Pask, A. J. & Renfree, M. B. DNA methylation dynamics in the germline of the marsupial tammar wallaby, Macropus eugenii. DNA Res. 26, 85–94 (2019).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Whitworth, D. J. & Pask, A. J. The X factor: X chromosome dosage compensation in the evolutionarily divergent monotremes and marsupials. Semin. Cell Dev. Biol. 56, 117–121 (2016).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Beiriger, A. & Sears, K. E. Cellular basis of differential limb growth in postnatal gray short-tailed opossums (Monodelphis domestica). Exp. Zool. B Mol. Dev. Evol. 322, 221–229 (2014).
Article  Google Scholar 
Vengamanaidu, M. et al. Gene expression profiling of postnatal lung development in the marsupial gray short-tailed opossum (Monodelphis domestica) highlights conserved developmental pathways and specific characteristics during lung organogenesis. BMC Genomics 19, 1–14 (2018).
Article  CAS  Google Scholar 
Keyte, A. & Smith, K. K. Heterochrony in somitogenesis rate in a model marsupial, Monodelphis domestica. Evol. Dev. 14, 93–103 (2012).
PubMed  Article  PubMed Central  Google Scholar 
Doroba, C. K. & Sears, K. E. The divergent development of the apical ectodermal ridge in the marsupial Monodelphis domestica. Anat. Rec. 293, 1325–1332 (2010).
Article  Google Scholar 
Chew, K. Y., Yu, H. S., Pask, A. J., Shaw, G. & Renfree, M. B. HOXA13 and HOXD13 expression during development of the syndactylous digits in the marsupial Macropus eugenii. BMC Dev. Biol. 12, 2 (2012).
CAS  PubMed  PubMed Central  Article  Google Scholar 
Carr, O. P., Glendining, K. A., Leamey, C. A. & Marotte, L. R. Retinal overexpression of Ten-m3 alters ipsilateral retinogeniculate projections in the wallaby (Macropus eugenii). Neurosci. Lett. 566, 167–171 (2014).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Nasrullah, Q., Renfree, M. B. & Evans, A. R. Three-dimensional mammalian tooth development using diceCT. Arch. Oral Biol. 85, 183–191 (2018).
PubMed  Article  PubMed Central  Google Scholar 
Sorensen, D. et al. A new mammalian model system for thalidomide teratogenesis: Monodelphis domestica. Reprod. Toxicol. 70, 126–132 (2017).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Anthwal, N., Urban, D. J., Luo, Z.-X., Sears, K. E. & Tucker, A. S. Meckel’s cartilage breakdown offers clues to mammalian middle ear evolution. Nat. Ecol. Evol. 1, 1–6 (2017).
Article  Google Scholar 
Nilsson, M. A., Arnason, U., Spencer, P. B. S. & Janke, A. Marsupial relationships and a timeline for marsupial radiation in South Gondwana. Gene 340, 189–196 (2004).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Selwood, L. Embryonic development in culture of two dasyurid marsupials, Sminthopsis crassicaudata (Gould) and Sminthopsis macroura (Spencer), during cleavage and blastocyst formation. Gamete Res. 16, 355–71 (1987).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Breed, W. G., Leigh, C. M. & Bennett, J. H. Sperm morphology and storage in the female reproductive tract of the fat-tailed dunnart, Sminthopsis crassicaudata (Marsupialia: Dasyuridae). Gamete Res. 23, 61–75 (1989).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Pires, S. S. et al. Isolation and characterization of melanopsin (Opn4) from the Australian marsupial Sminthopsis crassicaudata (fat-tailed dunnart). Proc. R. Soc. B 274, 2791–9 (2007).
CAS  PubMed  PubMed Central  Article  Google Scholar 
Rehorek, S. J., Hillenius, W. J., Leigh, C. & Firth, B. T. Is it or isn’t it? A reexamination of the anterior orbital glands of the fat-tailed dunnart Sminthopsis crassicaudata (Dasyuridae: Marsupiala) and a reevaluation of definitions for the Harderian gland. Anat. Rec. 293, 1449–54 (2010).
CAS  Article  Google Scholar 
Suarez, R. et al. Development of body, head and brain features in the Australian fat-tailed dunnart (Sminthopsis crassicaudata; Marsupialia: Dasyuridae); a postnatal model of forebrain formation. PLoS ONE 12, e0184450 (2017).
PubMed  PubMed Central  Article  CAS  Google Scholar 
Paolino, A., Fenlon, L. R., Kozulin, P., Richards, L. J. & Suárez, R. Multiple events of gene manipulation via in pouch electroporation in a marsupial model of mammalian forebrain development. J. Neurosci. Methods 293, 45–52 (2018).
CAS  PubMed  Article  Google Scholar 
Paolino, A. et al. Differential timing of a conserved transcriptional network underlies divergent cortical projection routes across mammalian brain evolution. PNAS 117, 10554–10564 (2020).
CAS  PubMed  PubMed Central  Article  Google Scholar 
Godfrey, G. K. & Crowcroft, P. Breeding the fat-tailed marsupial mouse in captivity. Int. Zoo Yearb. 11, 33–38 (1971).
Article  Google Scholar 
Bennett, J. H., Breed, W. G., Hayman, D. L. & Hope, R. M. Reproductive and genetic-studies with a laboratory colony of the dasyurid marsupial Sminthopsis crassicaudata. Aust. J. Zool. 37, 207–222 (1990).
Article  Google Scholar 
Clark, C. T. & Smith, K. K. Cranial osteogenesis in Monodelphis domestica (Didelphidae) and Macropus eugenii (Macropodidae). J. Morphol. 215, 119–49 (1993).
CAS  PubMed  Article  PubMed Central  Google Scholar 
de Oliveira, C. A., Nogueira, J. C. & Mahecha, G. A. B. Sequential order of appearance of ossification centers in the opossum Didelphis albiventris (Didelphidae) skeleton during development in the Marsupium. Ann. Anat. 180, 113–121 (1998).
PubMed  Article  PubMed Central  Google Scholar 
Frigo, L. & Woolley, P. A. Development of the skeleton of the stripe-faced dunnart, Sminthopsis macroura (Marsupialia: Dasyuridae). Aust. J. Zool. 44, 155–164 (1996).
Article  Google Scholar 
Gemmell, R. T., Johnston, G. & Bryden, M. M. Osteogenesis in two marsupial species, the bandicoot Isoodon macrourus and the possum Trichosurus vulpecula. J. Anat. 159, 155–64 (1988).
CAS  PubMed  PubMed Central  Google Scholar 
Koyabu, D. et al. Mammalian skull heterochrony reveals modular evolution and a link between cranial development and brain size. Nat. Commun. 5, 3625 (2014).
PubMed  Article  CAS  PubMed Central  Google Scholar 
Spiekman, S. N. F. & Werneburg, I. Patterns in the bony skull development of marsupials: high variation in onset of ossification and conserved regions of bone contact. Sci. Rep. 7, 11 (2017).
Article  CAS  Google Scholar 
Newton, A. H. et al. Letting the ‘cat’ out of the bag: pouch young development of the extinct Tasmanian tiger revealed by X-ray computed tomography. R. Soc. Open Sci. 5, 171914 (2018).
PubMed  PubMed Central  Article  Google Scholar 
Newton, A. H., Weisbecker, V., Pask, A. J. & Hipsley, C. A. Ontogenetic origins of cranial convergence between the extinct marsupial thylacine and placental gray wolf. Commun. Biol. 4, 1–9 (2021).
Article  CAS  Google Scholar 
Brinkley, J. F. et al. The FaceBase Consortium: a comprehensive resource for craniofacial researchers. Development 143, 2677–2688 (2016).
CAS  PubMed  PubMed Central  Google Scholar 
Wanek, N., Muneoka, K., Holler-Dinsmore, G., Burton, R. & Bryant, S. V. A staging system for mouse limb development. J. Exp. Zool. 249, 41–49 (1989).
CAS  Article  Google Scholar 
Fasel, N. & Schowing, J. Embryonic development of NMRI mice: relationship between the weight, age and ossification of embryos. Lab. Anim. 14, 243–246 (1980).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Lyne, A. G., Pilton, P. E. & Sharman, G. B. Estrous cycle, gestation period and parturition in the marsupial Trichosurus vulpecula. Nature 183, 622–623 (1959).
Article  Google Scholar 
Renfree, M. B. et al. In Kangaroos, Wallabies and Rat-kangaroos (eds Jarman, P., Hume, I.D. & Grigg, G.) Vol. 1, 323–337 (Surrey Beatty and Sons Pty. Ltd., 1989).
Veitch, C. E., Nelson, J. & Gemmell, R. T. Birth in the brushtail possum, Trichosurus vulpecula (Marsupialia: Phalangeridae). Aust. J. Zool. 48, 691–700 (2000).
Article  Google Scholar 
O, W. S., Short, R. V., Renfree, M. B. & Shaw, G. Primary genetic control of somatic sexual differentiation in a mammal. Nature 331, 716–717 (1988).
CAS  PubMed  Article  Google Scholar 
Renfree, M. B., O, W. S., Short, R. V. & Shaw, G. Sexual differentiation of the urogenital system of the fetal and neonatal tammar wallaby, Macropus eugenii. Anat. Embryol. 194, 111–134 (1996).
CAS  Article  Google Scholar 
Wilkes, G. E. & Janssens, P. A. In The Developing Marsupial: Models for Biomedical Research (eds Tyndale-Biscoe, C.H. & Janssens, P.A.) 176–189 (Springer, Berlin, 1988).
Coveney, D., Shaw, G., Hutson, J. M. & Renfree, M. B. The development of the gubernaculum and inguinal closure in the marsupial Macropus eugenii. J. Anat. 201, 239–256 (2002).
PubMed  PubMed Central  Article  Google Scholar 
Johnson, M. L. The time and order of appearance of ossification centers in the albino mouse. J. Anat. 52, 241–271 (1933).
Article  Google Scholar 
Kaufman, M. H. The Atlas of Mouse Development (Academic press, 1992).
Google Scholar 
Theiler, K. The House Mouse: Development and Normal Stages from Fertilization to 4 Weeks of Age (Springer-Verlag, 1972).
Google Scholar 
Fawcett, E. The primordial cranium of Erinaceus europaeus. J. Anat. 52, 211–250.45 (1918).
PubMed  PubMed Central  Google Scholar 
Kaucka, M. & Adameyko, I. Evolution and development of the cartilaginous skull: From a lancelet towards a human face. Semin. Cell Dev. Biol. 91, 2–12 (2019).
PubMed  Article  PubMed Central  Google Scholar 
Maier, W. The angular process of Monodelphis domestica (Didelphidae, Marsupialia) and its relation to the middle ear: an ontogenetic and evolutionary morphologic study. Gegenbaurs Morphol. Jahrb. 133, 123–161 (1987).
CAS  PubMed  PubMed Central  Google Scholar 
Hüppi, E., Sánchez-Villagra, M. R., Tzika, A. C. & Werneburg, I. Ontogeny and phylogeny of the mammalian chondrocranium: the cupula nasi anterior and associated structures of the anterior head region. Zoological Lett. 4, 29 (2018).
PubMed  PubMed Central  Article  Google Scholar 
Gemmell, R. & Nelson, J. Ultrastructure of the olfactory system of three newborn marsupial species. Anat. Rec. 225, 203–208 (1989).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Jones, T. E. & Munger, B. L. Early differentiation of the afferent nervous system in glabrous snout skin of the opossum (Monodelphis domesticus). Somatosens. Res. 3, 169–184 (1985).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Sánchez-Villagra, M. R. & Forasiepi, A. M. On the development of the chondrocranium and the histological anatomy of the head in perinatal stages of marsupial mammals. Zoological Lett. 3, 632 (2017).
Article  Google Scholar 
Desmarais, M., Beauregard, F., Cabana, T. & Pflieger, J. Facial mechanosensory influence on forelimb movement in newborn opossums, Monodelphis domestica. PLoS ONE 11, e0148352 (2016).
PubMed  PubMed Central  Article  CAS  Google Scholar 
Hill, J. P. & Hill, W. O. The growth-stages of the pouch-young of the native cat (Dasyurus viverrinus) together with observations on the anatomy of the new-born young. Trans. Zool. Soc. London. 28, 349–352 (1955).
Article  Google Scholar 
Simpson, S. J. et al. Structural and functional development of the respiratory system in a newborn marsupial with cutaneous gas exchange. Physiol. Biochem. Zool. 84, 634–649 (2011).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Turnbull, K. E., Mattner, P. E. & Hughes, R. L. Testicular descent in the marsupial Trichosurus vulpecula (Kerr). Aust. J. Zool. 29, 189–198 (1981).
Article  Google Scholar 
Heinsohn, G. E. Ecology and reproduction of the Tasmanian bandicoots, Perameles gunni and Isoodon obesulus v. 80 (Univ. of California Press, California, 1966).
Ealey, E. H. M. Ecology of the euro, Macropus robustus (Gould), in North Western Australia—I. The environment and changes in euro and sheep populations. Wildl. Res. 12, 9–25 (1967).
Article  Google Scholar 
Finkel, M. P. The relation of sex hormones to pigmentation and to testis descent in the opossum and ground squirrel. J. Anat. 76, 93–151 (1945).
Article  Google Scholar 
Maynes, G. M. Reproduction in the parma wallaby, Macropus parma Waterhouse. Aust. J. Zool. 21, 331–351 (1973).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Taggart, D. A., Johnson, J. & Temple-Smith, P. D. Testicular and epididymal development in the brown marsupial mouse, Antechinus stuartii (Dasyuridae, Marsupialia). Anat. Embryol. 188, 87–100 (1993).
CAS  Article  Google Scholar 
Urban, D. J. et al. A new developmental mechanism for the separation of the mammalian middle ear ossicles from the jaw. Proc. Royal Soc. B 284, 20162416 (2017).
Article  CAS  Google Scholar 
Anthwal, N., Fenelon, J. C., Johnston, S. D., Renfree, M. B. & Tucker, A. S. Transient role of the middle ear as a lower jaw support across mammals. eLife 9, e57860 (2020).
CAS  PubMed  PubMed Central  Article  Google Scholar 
Crompton, A. W. & Parker, P. Evolution of the mammalian masticatory apparatus: the fossil record shows how mammals evolved both complex chewing mechanisms and an effective middle ear, two structures that distinguish them from reptiles. Am. Sci. 66, 192–201 (1978).
CAS  PubMed  PubMed Central  Google Scholar 
Sánchez-Villagra, M. R., Gemballa, S., Nummela, S., Smith, K. K. & Maier, W. Ontogenetic and phylogenetic transformations of the ear ossicles in marsupial mammals. J. Morphol. 251, 219–238 (2002).
PubMed  Article  PubMed Central  Google Scholar 
Zeller, U. In Mammal Phylogeny: Mesozoic Differentiation, Multituberculates, Monotremes, Early Therians, and Marsupials (eds Szalay, F.S., Novacek, M.J. & McKenna, M.C.) 95–107 (Springer, New York, 1993).
Filan, S. L. Development of the middle ear region in Monodelphis domestica (Marsupialia, Didelphidae): marsupial solutions to an early birth. J. Zool. 225, 577–588 (1991).
Article  Google Scholar 
Wirtschafter, Z. T. The Genesis of the Mouse Skeleton, a Laboratory Atlas (Thomas, Springfield, IL, 1960).
Google Scholar 
Flaherty, K. & Richtsmeier, J. T. It’s about time: ossification center formation in C57BL/6 mice from E12-E16. J. Dev. Biol. 6, https://doi.org/10.3390/jdb6040031 (2018).
Fritz, H. & Hess, R. Ossification of the rat and mouse skeleton in the perinatal period. Teratology 3, 331–8 (1970).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Bennett, C. V. & Goswami, A. Statistical support for the hypothesis of developmental constraint in marsupial skull evolution. BMC Biol. 11, 52 (2013).
PubMed  PubMed Central  Article  Google Scholar 
Maxwell, E. E. & Harrison, L. B. Ossification sequence of the common tern (Sterna hirundo) and its implications for the interrelationships of the Lari (Aves, Charadriiformes). J. Morphol. 269, 1056–1072 (2008).
PubMed  Article  PubMed Central  Google Scholar 
Maxwell, E. E. Comparative embryonic development of the skeleton of the domestic turkey (Meleagris gallopavo) and other galliform birds. Zoology 111, 242–257 (2008).
PubMed  Article  PubMed Central  Google Scholar 
Mitgutsch, C., Wimmer, C., Sánchez-Villagra, M. R., Hahnloser, R. & Schneider, R. A. Timing of ossification in duck, quail, and zebra finch: intraspecific variation, heterochronies, and life history evolution. Zool. Sci. 28, 491–500 (2011).
Article  Google Scholar 
Ollonen, J., Da Silva, F. O., Mahlow, K. & Di-Poi, N. Skull development, ossification pattern, and adult shape in the emerging lizard model organism Pogona vitticeps: a comparative analysis with other squamates. Front. Physiol. 9, 278 (2018).
PubMed  PubMed Central  Article  Google Scholar 
Smith, K. K. Early development of the neural plate, neural crest and facial region of marsupials. J. Anat. 199, 121–131 (2001).
CAS  PubMed  PubMed Central  Article  Google Scholar 
Vaglia, J. L. & Smith, K. K. Early differentiation and migration of cranial neural crest in the opossum, Monodelphis domestica. Evol. Dev. 5, 121–135 (2003).
PubMed  Article  Google Scholar 
Wakamatsu, Y. & Suzuki, K. Sequence alteration in the enhancer contributes to the heterochronic Sox9 expression in marsupial cranial neural crest. Dev. Biol. 456, 31–39 (2019).
CAS  PubMed  Article  Google Scholar 
Wakamatsu, Y., Nomura, T., Osumi, N. & Suzuki, K. Comparative gene expression analyses reveal heterochrony for Sox9 expression in the cranial neural crest during marsupial development. Evol. Dev. 16, 197–206 (2014).
CAS  PubMed  Article  Google Scholar 
Newton, A. H., Feigin, C. Y. & Pask, A. J. RUNX2 repeat variation does not drive craniofacial diversity in marsupials. BMC Evol. Biol. 17, 110 (2017).
PubMed  PubMed Central  Article  CAS  Google Scholar 
Smith, K. K. J. P. Hill and Katherine Watson’s studies of the neural crest in marsupials. J. Morphol. 281, 1567–1587 (2020).
PubMed  Article  PubMed Central  Google Scholar 
Bininda-Emonds, O. R., Jeffery, J. E. & Richardson, M. K. Inverting the hourglass: quantitative evidence against the phylotypic stage in vertebrate development. Proc. Royal Soc. B 270, 341–6 (2003).
Article  Google Scholar 
Weisbecker, V. & Sanchez-Villagra, M. Postcranial sequence heterochrony and the marsupial-placental dichotomy. J. Vertebr. Paleontol. 27, 164A–164A (2007).
Google Scholar 
Harrison, L. B. & Larsson, H. C. Estimating evolution of temporal sequence changes: a practical approach to inferring ancestral developmental sequences and sequence heterochrony. Syst. Biol. 57, 378–87 (2008).
PubMed  Article  Google Scholar 
Martin, P. Tissue patterning in the developing mouse limb. Int. J. Dev. Biol. 34, 323–36 (1990).
CAS  PubMed  Google Scholar 
Fernandez-Teran, M. A., Hinchliffe, J. R. & Ros, M. A. Birth and death of cells in limb development: a mapping study. Dev. Dyn, 235, 2521–37 (2006).
CAS  Article  Google Scholar 
Mate, K. E., Robinson, E. S., Vandeberg, J. L. & Pedersen, R. A. Timetable of in vivo embryonic development in the grey short-tailed opossum (Monodelphis domestica). Mol. Reprod. Dev. 39, 365–74 (1994).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Keyte, A. L. & Smith, K. K. Developmental origins of precocial forelimbs in marsupial neonates. Development 137, 4283–4294 (2010).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Chew, K. Y., Shaw, G., Yu, H. S., Pask, A. J. & Renfree, M. B. Heterochrony in the regulation of the developing marsupial limb. Dev. Dyn. 243, 324–338 (2014).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Dowling, A. et al. Cellular and molecular drivers of differential organ growth: insights from the limbs of Monodelphis domestica. Dev. Genes Evol. 226, 235–43 (2016).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Weisbecker, V. & Nilsson, M. Integration, heterochrony, and adaptation in pedal digits of syndactylous marsupials. BMC Evol. Biol. 8, 160 (2008).
PubMed  PubMed Central  Article  Google Scholar 
Sears, K. E. et al. The relationship between gene network structure and expression variation among individuals and species. PLoS Genet. 11, e1005398 (2015).
PubMed  PubMed Central  Article  CAS  Google Scholar 
Keyte, A. L., Imam, T. & Smith, K. K. Limb heterochrony in the marsupial Monodelphis domestica. J. Morphol. 268, 1092–1092 (2007).
Google Scholar 
Nakamura, H. & Funahashi, J. Introduction of DNA into chick embryos by in ovo electroporation. Methods 24, 43–8 (2001).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Eide, F. F., Eisenberg, S. R. & Sanders, T. A. Electroporation-mediated gene transfer in free-swimming embryonic Xenopus laevis. FEBS Lett. 486, 29–32 (2000).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Matsui, A., Yoshida, A. C., Kubota, M., Ogawa, M. & Shimogori, T. Mouse in utero electroporation: controlled spatiotemporal gene transfection. J. Vis. Exp. https://doi.org/10.3791/3024 (2011).
National Health and Medical Research Council (NHMRC). Australian code for the care and use of animals for scientific purposes (Tech. Rep., National Health and Medical Research Council, Canberra, 2013).
Google Scholar 
Poiley, S. M. A systematic method of breeder rotation for non-inbred laboratory animal colonies. Proc. Anim. Care Panel 10, 159–166 (1960).
Google Scholar 
Selwood, L. & Hickford, D. in Cell Lineage and Fate Determination 505–519 (Academic Press, 1999).
Bancroft, J. D. & Gamble, M. Theory and Practice of Histological Techniques (Elsevier Health Sciences, 2008).
Google Scholar 
Masson, P. Some histological methods. Trichrome stainings and their preliminary technique. J. Tech. Meth. 12, 75–90 (1929).
Google Scholar 
Elbadawi, A. Hexachrome modification of Movat’s stain. Stain Technol. 51, 249–253 (1976).
CAS  PubMed  Article  PubMed Central  Google Scholar 
Ovchinnikov, D. Alcian blue/alizarin red staining of cartilage and bone in mouse. Cold Spring Harb. Protoc. 2009, 5170 (2009).
Article  Google Scholar 
Cook, L. E., Newton, A. H., Hipsley, C. A. & Pask, A. J. Postnatal development in a marsupial model, the fat-tailed dunnart (Sminthopsis crassicaudata; Dasyuromorphia: Dasuryidae). Morphosource Repository. https://www.morphosource.org/projects/0000C1150 (2021).
Cook, L. E., Newton, A. H., Hipsley, C. A. & Pask, A. J. Postnatal development in a marsupial model, the fat-tailed dunnart (Sminthopsis crassicaudata; Dasyuromorphia: Dasuryidae). FigShare Digital Repository. https://doi.org/10.6084/m9.figshare.14445666 (2021).
Download references
The authors thanks Eva Suric, Tania Long and Darren Cipolla for their technical contributions and help with animal husbandry. We would like to acknowledge the technical support by Dr. Jay Black and the Melbourne TrACEES Platform (Trace Analysis for Chemical, Earth and Environmental Sciences) for access to the GE Phoenix Nanotom m micro-CT scanner. This work was supported by Discovery Project funding (DP160103683) from the Australian Research Council to A.J.P. and a Discovery Early Career Award (DE180100629) to C.A.H.
School of Biosciences, University of Melbourne, Parkville, VIC, Australia
Laura E. Cook, Christy A. Hipsley & Andrew J. Pask
Department of Anatomy and Developmental Biology, Monash University, Clayton, VIC, Australia
Axel H. Newton
Department of Biology, University of Copenhagen, Copenhagen, Denmark
Christy A. Hipsley
Department of Sciences, Museums Victoria, Carlton, VIC, Australia
Christy A. Hipsley & Andrew J. Pask
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
A.J.P., L.E.C., C.A.H. and A.H.N. designed and conceived the study. A.J.P. and C.A.H. supervised the study. L.E.C. collected the specimens, described the stages, performed the histological experiments, analysed the data and wrote the manuscript. C.A.H. generated the scan videos. A.H.N. reconstructed the microCT scans and measured the limb stages. All authors reviewed and revised the manuscript and gave final approval for publication.
Correspondence to Andrew J. Pask.
The authors declare no competing interests.
Peer review information Communications Biology thanks the anonymous reviewers for their contribution to the peer review of this work. Primary Handling Editor: Luke R. Grinham. Peer reviewer reports are available.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Reprints and Permissions
Cook, L.E., Newton, A.H., Hipsley, C.A. et al. Postnatal development in a marsupial model, the fat-tailed dunnart (Sminthopsis crassicaudata; Dasyuromorphia: Dasyuridae). Commun Biol 4, 1028 (2021). https://doi.org/10.1038/s42003-021-02506-2
Download citation
Received: 02 February 2021
Accepted: 29 July 2021
Published: 02 September 2021
DOI: https://doi.org/10.1038/s42003-021-02506-2
Anyone you share the following link with will be able to read this content:
Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.
Advertisement
Advanced search
Communications Biology (Commun Biol) ISSN 2399-3642 (online)
© 2021 Springer Nature Limited
Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

source