We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
The Australian SKA Pathfinder (ASKAP) radio telescope has carried out a survey of the entire Southern Sky at 887.5 MHz. The wide area, high angular resolution, and broad bandwidth provided by the low-band Rapid ASKAP Continuum Survey (RACS-low) allow the production of a next-generation rotation measure (RM) grid across the entire Southern Sky. Here we introduce this project as Spectral and Polarisation in Cutouts of Extragalactic sources from RACS (SPICE-RACS). In our first data release, we image 30 RACS-low fields in Stokes I, Q, U at 25$^{\prime\prime}$ angular resolution, across 744–1032 MHz with 1 MHz spectral resolution. Using a bespoke, highly parallelised, software pipeline we are able to rapidly process wide-area spectro-polarimetric ASKAP observations. Notably, we use ‘postage stamp’ cutouts to assess the polarisation properties of 105912 radio components detected in total intensity. We find that our Stokes Q and U images have an rms noise of $\sim$80 $\unicode{x03BC}$Jy PSF$^{-1}$, and our correction for instrumental polarisation leakage allows us to characterise components with $\gtrsim$1% polarisation fraction over most of the field of view. We produce a broadband polarised radio component catalogue that contains 5818 RM measurements over an area of $\sim$1300 deg$^{2}$ with an average error in RM of $1.6^{+1.1}_{-1.0}$ rad m$^{-2}$, and an average linear polarisation fraction $3.4^{+3.0}_{-1.6}$ %. We determine this subset of components using the conditions that the polarised signal-to-noise ratio is $>$8, the polarisation fraction is above our estimated polarised leakage, and the Stokes I spectrum has a reliable model. Our catalogue provides an areal density of $4\pm2$ RMs deg$^{-2}$; an increase of $\sim$4 times over the previous state-of-the-art (Taylor, Stil, Sunstrum 2009, ApJ, 702, 1230). Meaning that, having used just 3% of the RACS-low sky area, we have produced the 3rd largest RM catalogue to date. This catalogue has broad applications for studying astrophysical magnetic fields; notably revealing remarkable structure in the Galactic RM sky. We will explore this Galactic structure in a follow-up paper. We will also apply the techniques described here to produce an all-Southern-sky RM catalogue from RACS observations. Finally, we make our catalogue, spectra, images, and processing pipeline publicly available.
In recent years, a variety of efforts have been made in political science to enable, encourage, or require scholars to be more open and explicit about the bases of their empirical claims and, in turn, make those claims more readily evaluable by others. While qualitative scholars have long taken an interest in making their research open, reflexive, and systematic, the recent push for overarching transparency norms and requirements has provoked serious concern within qualitative research communities and raised fundamental questions about the meaning, value, costs, and intellectual relevance of transparency for qualitative inquiry. In this Perspectives Reflection, we crystallize the central findings of a three-year deliberative process—the Qualitative Transparency Deliberations (QTD)—involving hundreds of political scientists in a broad discussion of these issues. Following an overview of the process and the key insights that emerged, we present summaries of the QTD Working Groups’ final reports. Drawing on a series of public, online conversations that unfolded at www.qualtd.net, the reports unpack transparency’s promise, practicalities, risks, and limitations in relation to different qualitative methodologies, forms of evidence, and research contexts. Taken as a whole, these reports—the full versions of which can be found in the Supplementary Materials—offer practical guidance to scholars designing and implementing qualitative research, and to editors, reviewers, and funders seeking to develop criteria of evaluation that are appropriate—as understood by relevant research communities—to the forms of inquiry being assessed. We dedicate this Reflection to the memory of our coauthor and QTD working group leader Kendra Koivu.1
Vertebrates may be born highly dependent (altricial) or may rapidly gain independence (precocial). Primates are generally considered somatically precocial. However, all are at least initially helpless, and many primates have a prolonged phase of juvenility. In this chapter, we discuss how selection may influence the relative timing of appearance of morphological features (heterochrony). Newborn primate morphology offers unique insights into the roles of prenatal and postnatal growth processes, primarily because metabolic costs for growth commence a transition from the mother to the infant at this point in time. With this in mind, primates vary remarkably at birth in dental eruption and mineralization status as well as limb skeleton ossification (e.g., wrists and ankles). We also discuss evidence, still relatively scant, that at birth primates vary greatly in the degree to which neural organs (e.g., brains, eyes) have achieved adult size and proportions. In preparation for morphological descriptions to follow, the reader is introduced to the concept of modularity of growth: different parts of the skeleton or even parts of regions have different rates of growth and development.
Skeletal Anatomy of the Newborn Primate was written to broaden our knowledge of non-human primates from a comparative and developmental perspective. This chapter explains that the main focus of our book is on the inherently risky neonatal period. The “neonate,” or newborn, is considered here to be a perinatal primate of up to seven days postnatal age. However, there is no simple way to physically identify primate newborns, not in the same many have defined “infants,” based on dental maturity. This is precisely what makes the neonatal stage so interesting: primates, like most other groups of mammals, vary in how rapidly they attain physical maturity. This introductory chapter discusses terminology and methodological challenges in studying newborns.
Feeding ontogeny in primates has three stages. In utero, nutrition is gained maternally. After birth, primates suckle. We know little about functional variation in these stages. The transition to adult feeding – highlighted by weaning – varies across species. Variation is tied to many socioecological and morphological influences across primates. Primate feeding apparatus ontogeny is affected by many factors. Diet exhibits a complex relationship with the clearest signal marked by rapid dental mineralization and eruption in folivorous strepsirrhines. Mineralization varies across primates. Emergence and eruption of postcanine teeth tends to follow size in both suborders with smaller taxa showing earlier emergence, the exception being rapid eruption in some folivores. Compared to teeth, less is known about the musculoskeletal ontogeny of the feeding apparatus. Most studies compare closely related species and link musculoskeletal robustness to challenging diets. Looking forward, better understanding of primate feeding apparatus growth will require improved samples (a challenge for long-lived species) and emphasis on the evolutionary significance of feeding throughout ontogeny.
In this chapter we introduce concepts in dental development, microanatomy of the tooth germ and mineralizing crowns, and terminology relating to dental morphology. Subsequently, tooth morphology in newborn hominoids (apes and humans) is discussed based on the literature, followed by accounts of the extent of crown mineralization at birth in a newly described sample of tarsiers, Old World monkeys, New World monkeys, and strepsirrhines (lemurs and lorises). Morphology of crowns is described in all species in which the crown is completely formed at birth. The chapter ends with a brief discussion of the “perinatal” trajectory of dental development in selected primate species based on a comparison of species at different stages (fetal, neonatal, and older infant), including some at similar known ages.
Life-history theory pertains to the entirety of prenatal and postnatal ontogeny, and therefore morphology of the newborn offers an important perspective on how primates invest in their young. Generally, longer gestations yield larger neonates that are weaned later, become sexually mature later, and have larger brain masses. But can the variations in skeletal maturity are birth explained by life-history traits? Here, we examine new somatic data on 47 species of primates in light of life-history traits and modularity of growth among body regions. “Snout” length is uniformly diminutive in newborns compared to adults, although some scaling differences are already apparent at birth (relatively longer palates in strepsirrhines and tarsiers). Correlations of life-history characteristics indicate gestational length has a significant influence on facial functional matrices, with a positive correlation with permanent tooth and eye size, and a negative correlation with deciduous tooth germ size. We may as yet lack a broad enough perspective on brain size at birth, but some existing observations suggest primates preferentially prioritize prenatal brain growth over general somatic growth.
Primate locomotor development is a protracted process. We summarize the time course of locomotor development in approximately 50 primates distributed across the extant radiation. Despite substantial variance, we identify several broad trends. Primates are somewhat precocial at birth – born with their eyes open and able to strongly grasp. Locomotor onset age generally increases with body mass, although certain taxonomic groups (e.g., lemurids and cercopithecids) develop early for their size whereas others (e.g., indriids and hominids) develop relatively late. Initial locomotor movements are similar across primates and dominated by quadrupedal crawling. Only later do more specialized forms of locomotion emerge (e.g., leaping and brachiation), often in concert with functional changes in musculoskeletal anatomy (e.g., maturation of intermembral indices, center of mass position, and bony muscle leverage). We advocate viewing locomotor development as a fundamental life-history parameter, responding to the same evolutionary pressures shown to be fundamental to other aspects of primate life history (e.g., predation, resource access, body size, encephalization).
In this chapter we discuss the vertebral column, ribs, and sternum from a developmental perspective. The axial skeleton of newborn hominoids (apes and humans) is discussed based on the literature, followed by accounts of osteology in a newly described sample of newborn tarsiers, Old World monkeys, New World monkeys, and strepsirrhines (lemurs and lorises). The neonatal vertebral column is fragmented in skeletonized specimens, because in most vertebrae, actively growing synchondroses connect the right and left neural arches and connect the centrum to the arches. Transverse processes, portions of the articular facets, and the ventral arch of C1 are also cartilaginous in most primates. However, tarsiers and most monkeys have an ossified C1 ventral arch. The chapter ends with a brief discussion of the early postnatal trajectory of axial skeleton ossification in selected primate species based on a comparison of species at different stages (neonatal and older infant), including some at similar known ages.
Birth represents a transitional point in time – a static moment that borders a time of complete dependency and the march toward independence. This chapter reviews some basic concepts of vertebrate development and histology. Of particular relevance are tissue changes that reflect differentiation of mineralized tissues: skeletogenesis and odontogenesis, beginning with changes to the primitive connective tissue (mesenchyme). Viewed by microscopy, mesenchyme condenses prior to differentiation into cartilage, bone or tooth germs. Most mesenchymal condensations for the skeleton form during the embryonic period, but they continue to appear during the fetal period or postnatally for some structures (e.g., successional teeth). Most growth of the skeleton occurs during the fetal and postnatal periods. Mineralized connective tissues have different available growth processes. The contributions of appositional growth (new matrix is added to existing matrix), interstitial growth (cell replication and matrix production within existing tissue), and bone modeling (selective osteoclastic and osteoblastic activity) are discussed according to types of bones and skeletal regions.
In this chapter we discuss the osteology of the primate hindlimb and pelvic girdle of the newborn. This region in newborn hominoids (apes and humans) is discussed based on the literature and illustrated based on museum specimens. Subsequently, the hindlimb skeleton of newborn tarsiers, Old World monkeys, New World monkeys, and strepsirrhines (lemurs and lorises) are described. At birth, the os coxa of all primates is represented by three ossified elements (ilium, pubs, ischium), which are connected at synchondroses centered at the acetabulum. Generally, cercopithecoids, tarsiers, and galagids more frequently have ossified femoral and tibial epiphyses at birth than other primates. In all newborn primates, the talus and calcaneus has commenced ossification. Naviculars have commenced ossification in many strepsirrhines, tarsiers and all known cercopithecoids (but few other anthropoids). Many primate species vary in the number of tarsals ossified at birth. This chapter also includes preliminary histological observations on variations in epiphyseal growth plates of newborn, and on differing rates of early postnatal ossification of the tarsus.
In this chapter we discuss parts of the primate skull (cranium and mandible) according to embryology and the evolutionary history (neurocranium and viscerocranium) and according to their mode of ossification (chondrocranium and dermatocranium). Subsequently, the osteology of the skull in newborn hominoids (apes and humans) is discussed based on the literature, followed by regional accounts of skull anatomy in a newly described sample of tarsiers, Old World monkeys, New World monkeys, and strepsirrhines (lemurs and lorises). The chapter ends with a brief discussion of the early postnatal trajectory of skull ossification and growth in selected primate species based on a comparison of species at similar known ages during infancy.