Dental anomalies in wild and domestic<Emphasis Type="Italic">Sus scrofa</Emphasis> in Illinois

The cleaned skulls of 39 wild and 30 domestic pigs from southern Illinois (USA) were assessed for dental anomalies including polydonty, oligodonty, misalignment, and rotation. Dental anomalies occurred in 16 wild and 15 domestic pigs. Oligodonty (either bilateral or unilateral) was the most common anomaly, occurring in 9 wild (23.1% of the sample) and 15 (50%) domestic pigs. In 22 of the 24 individuals exhibiting oligodonty, this anomaly involved the lower first premolar (P₁). Given the placement of P₁, oligodonty may reflect a trend toward reduction of the dental arcade from the primitive eutherian number. Domesticated species are reported to have more anomalies than wild counterparts because of inbreeding. We found no difference in the number of dental anomalies between domestic and wild pigs.     

Congenital anomalies in the baboon (Papio spp.)

Background A comprehensive survey of the prevalence of congenital anomalies in baboons has not been previously reported. We report the congenital anomalies observed over a 26‐year period in a large captive baboon colony. Methods A computer search was performed for all baboon congenital anomalies identified at necropsy and recorded on necropsy submissions. Results We identified 198 congenital anomalies in 166 baboons from 9972 necropsies (1.66% of total necropsies). The nervous, urogenital, musculoskeletal, and cardiovascular systems were most commonly affected. The most common organs affected were the brain, bone, heart, testicle, kidney, penis, aorta, and skeletal muscle. The most frequent congenital anomalies were blindness, seizures, and hydrocephalus. Conclusions The baboon has an overall frequency of congenital anomalies similar to humans and other non‐human primates. Although the most frequently affected systems are similar, congenital anomalies involving the digestive system appear to be less common in the baboon.     

Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation.

Congenital anomalies have complex etiologies involving both genetic and nongenetic components. Many are sporadic, without obvious evidence for heritability. An important model for these anomalies is a mutation in laboratory mice that is called "disorganization" (Ds), which functions as a variable autosomal dominant and leads to a wide variety of congenital anomalies involving many developmental processes and systems. Variable expressivity, asymmetrical manifestations, and low penetrance suggest that somatic events determine the location and nature of these anomalies. A statistical analysis suggests that occurrence of anomalies in mice with the Ds mutation follows a Poisson distribution. These results suggest that congenital anomalies in mice with the Ds mutation occur independently of each other. We propose that Ds causes a heritable predisposition to congenital anomalies and that Ds and appropriate somatic events combine to compromise normal development. We also propose that some sporadic, nonheritable congenital anomalies involve somatic mutations at Ds-like loci. Ds may therefore serve not only as a model for developmental anomalies in cell fate and pattern formation but also for complex developmental traits showing variable expressivity, low penetrance, and sporadic occurrence in mice and humans.     

Congenital malformations and genetic diseases in Iranian infants

Summary Data of 13,037 live-born infants from a hospital in Tehran, Iran were analysed for congenital malformations and genetic diseases. The results showed that the rates of joint dislocation, eleft lip, cleft palate and finger anomalies are similar to those of the other populations. The rates of chromosomal, thorax and abdominal, external genital anomalies and other syndromes were higher compared with other populations, whereas the rates of multiple births and limb anomalies were lower.     

The effects of El Niño–La Niña on reproductive parameters of elephant seals feeding in the Bellingshausen Sea

Aim To assess the impacts of El Niño–La Niña events on the pup weaning mass and diet of female southern elephant seals (Mirounga leonina) feeding in the Bellingshausen Sea, Antarctica, and to understand the ecological processes that drive these impacts. Location Atlantic southern elephant seal weaning mass and diet were measured at King George Island (62º14′ S, 58º30′ W). Feeding areas for pregnant female seals from King George Island are located west of Alexander Island in the Bellingshausen Sea. Methods Data on weaning mass were collected between 1985 and 1994 during the breeding season (September–November). Moulting females were anaesthetized and cephalopod beaks were isolated and identified from stomach contents obtained from stomach lavages. Sea‐surface temperature anomaly (SSTA) data for the ‘El Niño 3.4’ geographical region (5º N–5º S, 120º W–170º W) were used to define El Niño–Southern Oscillation (ENSO) event years (grouped as El Niño, La Niña and Neutral) as well as the strength of each ENSO event year. Using data from the US National Center for Environmental Prediction, temperature, sea ice concentration and atmospheric pressure anomalies in the Bellingshausen Sea were calculated from March to August, corresponding to the feeding period of pregnant female seals. Results Positive temperature anomalies and negative pressure anomalies in the Bellingshausen Sea were observed during La Niña years and negative temperature anomalies and positive pressure anomalies during El Niño years. These data correlate with sea ice concentration anomalies, which are highly negative during La Niña years and highly positive during El Niño years. Warm temperature conditions in the Bellingshausen Sea during La Niña years are strongly related to both higher weaning mass in elephant seals and to an increase in squid beaks in the stomach contents of females. Main conclusions It is possible that higher elephant seal weaning masses in La Niña years correlate with warmer waters in the Bellingshausen Sea leading to the rapid growth of squid and their more frequent descents to depths frequented by elephant seals. This results in increased predation by pregnant females, leading to a greater mass among weaned pups. This hypothesis may guide future research about interactions between climate and the marine biosphere.     

Pacific sardine (<Emphasis Type="Italic">Sardinops melanostictus</Emphasis>) migrations to the shores of Sakhalin Island in the 20th–early 21st centuries

Historical data for the period 1929?2011 were used to generalize information on the seasonal feeding migrations of Pacific sardine to the shores of Sakhalin Island. In the 20th century, the cyclicity of sardine occurrence in the Tatar Strait and southwestern part of the Sea of Okhotsk appeared to have a similar character. Sardine distribution patterns are considered in connection with the oceanological characteristics on these areas. A close correlated relationship was revealed between the SST anomalies and northern boundary of distribution of this subtropical fish. Besides the water temperature, Pacific sardine northern migrations have been formed under the influence of many other factors (by origin and impact), including fluctuations in abundance, index of stock biomass, food supply, state of marine ecosystems, and climatic conditions.     

Detection of renal anomalies by abdominal palpation in newborn infants.

In a new technique of palpation for renal anomalies in the newborn one hand supports the infant while the fingers of the other hand support the loin and the thumb explores the abdomen. In a series of 11 000 otherwise normal newborn children superficial palpation detected 11 renal anomalies, and deep palpation led to the discovery of another 42 anomalies. One of two other series in which palpation was performed bimanually gave a similar incidence of renal anomalies (0-5%). Early discovery of an asymptomatic anomaly enables early treatment of the complications that are often found in patients with congenital renal anomalies detected in later life.     

Periodic segmental anomalies induced by heat shock in the chick embryo are associated with the cell cycle

This study provides evidence that cells destined to segment together into somites have a degree of cell division synchrony. We have measured the duration of the cell division cycle in somite and segmental plate cells of the chick embryo as 9.5 h using [3H]thymidine pulse- and-chase. Treatment of embryos with any of a variety of inhibitors known to affect the cell division cycle causes discrete periodic segmental anomalies: these anomalies appear about 6-7 somites after treatment and, in some cases, a second anomaly is observed 6 to 7 somites after the first. Since somites take 1.5 h to form, the 6- to 7- somite interval corresponds to about 9-10 h, which is the duration of the cell cycle as determined in these experiments. The anomalies are similar to those seen after heat shock of 2-day chick embryos. Heat shock and some of the other treatments induce the expression of heat-shock proteins (hsp); however, since neither the expression nor the distribution of these proteins relate to the presence or distribution of anomalies seen, we conclude that hsps are not responsible for the pattern of segmental anomalies observed. The production of periodic segmental anomalies appears to be linked to the cell cycle. A simple model is proposed, in which we suggest that the cell division cycle is involved directly in gating cells that will segment together.     

Hirschsprung disease in a large birth cohort

The incidence of Hirschsprung disease was studied in a series of almost 700,000 consecutive livebirths in British Columbia from 1964-1982, by means of the records of a health surveillance registry that uses multiple sources of ascertainment. The estimated liveborn incidence rate for Hirschsprung disease was 1 in 4,417 livebirths (156 cases out of 689,118 livebirths). Data pertaining to sex ratio, additional anomalies, recurrence, and mortality were also analyzed over the caseload period 1952 to 1983. A total of 29.8% of cases had some additional anomaly--the majority being nonregional anomalies in other systems or more distantly in the gastrointestinal tract. Cardiovascular and gastrointestinal anomalies not a direct consequence of Hirschsprung disease were the most frequent additional anomalies found, occurring in 10 and 12 of 178 cases, respectively. Sensorineural anomalies were also frequent, occurring in 12 of 178 cases. Clinical implications arising from the study regarding the neonatal assessment of infants with these anomalies are discussed.     

Dental anomalies in the Japanese mole <Emphasis Type="Italic">Mogera wogura</Emphasis> from northeast China and the Primorsky region of Russia

Dental anomalies in the Japanese mole, Mogera wogura Temminck, 1842, from northeast China and the Primorsky region of Russia were examined based on 241 specimens. The most frequent dental anomaly was oligodonty, i.e., missing P² (18 cases) or P₃ (one case). Supernumerary teeth were observed in three cases, two of which were characterized by abnormal shapes. Morphological abnormalities in teeth (six cases) and an asymmetrically curved rostrum (one case) were also observed. Dental anomalies were found at higher frequencies in populations near the northern range limit of the species. This was not caused by size effects. We suggest that the high incidence of dental anomalies was the result of genetic drift, which increases in marginal populations. Considering the nature of subterranean mammals, our results suggest that the high frequency of dental anomalies in a marginal population could have initiated the evolution of dental formulae if parapatric or peripatric speciation occurs in such populations.     

Global evaluation of a semiempirical model for yield anomalies and application to within‐season yield forecasting

Quantifying the influence of weather on yield variability is decisive for agricultural management under current and future climate anomalies. We extended an existing semiempirical modeling scheme that allows for such quantification. Yield anomalies, measured as interannual differences, were modeled for maize, soybeans, and wheat in the United States and 32 other main producer countries. We used two yield data sets, one derived from reported yields and the other from a global yield data set deduced from remote sensing. We assessed the capacity of the model to forecast yields within the growing season. In the United States, our model can explain at least two‐thirds (63%–81%) of observed yield anomalies. Its out‐of‐sample performance (34%–55%) suggests a robust yield projection capacity when applied to unknown weather. Out‐of‐sample performance is lower when using remote sensing‐derived yield data. The share of weather‐driven yield fluctuation varies spatially, and estimated coefficients agree with expectations. Globally, the explained variance in yield anomalies based on the remote sensing data set is similar to the United States (71%–84%). But the out‐of‐sample performance is lower (15%–42%). The performance discrepancy is likely due to shortcomings of the remote sensing yield data as it diminishes when using reported yield anomalies instead. Our model allows for robust forecasting of yields up to 2 months before harvest for several main producer countries. An additional experiment suggests moderate yield losses under mean warming, assuming no major changes in temperature extremes. We conclude that our model can detect weather influences on yield anomalies and project yields with unknown weather. It requires only monthly input data and has a low computational demand. Its within‐season yield forecasting capacity provides a basis for practical applications like local adaptation planning. Our study underlines high‐quality yield monitoring and statistics as critical prerequisites to guide adaptation under climate change.     

Cardiovascular anomalies produced by nimustine hydrochloride in the rat fetus

The cardiovascular teratogenicity of nimustine hydrochloride (ACNU) was studied in rat fetuses. This drug is a nitrosourea derivative anticancer agent and produces alkylation of DNA. Pregnant Donryu rats were treated with single doses of 10, 11 or 13 mg/kg of the teratogen at various stages during gestation. Examination of the hearts was performed by microdissection after sacrificing the animals on the 20th day of gestation. The highest frequency of cardiovascular anomalies was found in the groups treated on the 8th day of gestation, but there was no difference in the rates induced by the three dosages of ACNU administered. The most common cardiovascular anomalies observed were ventricular septal defect (76.8%) and double outlet right ventricle (10.3%). A considerable number of affected fetuses (37/263) showed complex cardiac anomalies with atrioventricular (AV) malalignment and other AV valve anomalies. These anomalies include: double inlet left ventricle, straddling AV valve, atresia or stenosis of the AV valve, and dysplastic AV valve. ACNU appears to be a useful teratogenic agent for inducing complexes of cardiac anomalies which include AV malalignment.     

Anomalies in the backbone structure in roach (<Emphasis Type="Italic">Rutilus rutilus</Emphasis>) (Cyprinidae,Cypriniformes) underyearlings following toxic impacts during early developmental stages

The roach eggs were developed for 54 h postfertilization in solutions of chlorophos at low concentrations (10^?6, 10^?5, 10^?4, 10^?3, and 10^?2 mg/l) and of N-methyl-M′-nitro-N-nitrozoguanidin (MNNG) (0.3 mg/l). The underyealings developed in these eggs differed from control ones by presence of higher number of backbone anomalies. The following axial skeleton anomalies were found in juvenile fish: fusions of vertebrae; underdevelopment of vertebrae; deformations of vertebrae; open-ended neural or hemal arcs; lack of vertebral arcs; nonunion of arc with body of vertebra; dislocation of branch base of the neural or hemal arcs to the neighboring vertebra; presence of extra branch of the arc. The positive correlation between number of anomalies in underyearlings and survival of experimental fish was revealed.     

Plattenanomalien beiEchinocorys sulcata (Goldfuss 1826) aus dem Dan (Alttertiär) von Dalbyover,Dänemark

In a collection of 2000 specimens of the echinoidEchinocorys sulcata from the Danian of Dalbyover, northern Jutland, Denmark, two percent of the coronae investigated show characteristic coronal plate anomalies which are largely missing in other echinoid species. These anomalies are formed by split coronal plates or mosaic-like plate arrangements instead of regularly grown plates. Plate anomalies occurring in ambulacral and interambulacral zones, classified into 14 different types, have been used for a statistical analysis. Data on the relative age of the echinoid animals with anormal coronal plates, and on the most abundant types of plate anomalies are given. Two specimens ofEchinocorys sulcata from the same locality show deviations from the regular pentameric pattern and comparable finds from other localities and of otherEchinocorys species were incorporated in the analysis. The anomalies described here are named forma aegrainconstans n.f. Literature data on echinoid coronal plate anomalies, which have been related to coronal deformations caused by evironmental parameters, are discussed.     

Thermal stress markers in <Emphasis Type="Italic">Colpophyllia</Emphasis><Emphasis Type="Italic">natans</Emphasis> provide an archive of site-specific bleaching events

Tropical coral reef monitoring relies heavily on in situ diver observations. However, in many reef regions resources are not available to regularly monitor reefs. This lack of historical baseline data makes it difficult to determine how different reefs respond to environmental stressors and what the implications are for management. To test whether coral cores could be used to identify bleaching events retrospectively, three sites in Tobago with pre-existing reef data including water quality and bleaching observations were identified. Colpophyllia natans cores were examined for growth anomalies which occurred during periods of thermal stress. If present, anomalies were compared to in situ, real-time bleaching observations and water quality data. Interestingly, sites with better water quality during the 2005 thermal anomaly were less prone to bleaching. We suggest that by reducing terrestrial run-off (e.g., sediment and nutrients), and therefore improving marine water quality, reef managers could enhance near-shore coral reef resilience during high-temperature events.     

Vegetation resistance and resilience to a decade‐long dry period in the temperate grasslands in China

The duration of climate anomalies has been increasing across the globe, leading to ecosystem function loss. Thus, we need to understand the responses of the ecosystem to long‐term climate anomalies. It remains unclear how ecosystem resistance and resilience respond to long‐term climate anomalies, for example, continuous dry years at a regional scale. Taking the opportunity of a 13‐year dry period in the temperate grasslands in northern China, we quantified the resistance and resilience of the grassland in response to this periodic dry period. We found vegetation resistance to the dry period increased with mean annual precipitation (MAP), while resilience increased at first until at MAP of 250 mm and then decreased slightly. No trade‐off between resistance and resilience was detected when MAP < 250 mm. Our results highlight that xeric ecosystems are most vulnerable to the long‐term dry period. Given expected increases in drought severity and duration in the coming decades, our findings may be helpful to identify vulnerable ecosystems in the world for the purpose of adaptation.     

From karyotyping to array-CGH in prenatal diagnosis

Conventional karyotyping detects chromosomal anomalies in up to 35% of pregnancies with fetal ultrasound anomalies, depending on the number and type of these anomalies. Extensive experience gained in the past decades has shown that prenatal karyotyping is a robust technique which can detect the majority of germline chromosomal anomalies. For most of these anomalies the phenotype is known. In postnatal diagnosis of patients with congenital anomalies and intellectual disability, array-CGH/SNP array has become the first-tier investigation. The higher abnormality detection yield and its amenability to automation renders array-CGH also suitable for prenatal diagnosis. As both findings of unclear significance and unexpected findings may be detected, studies on the outcome of array-CGH in prenatal diagnosis were initially performed retrospectively. Recently, prospective application of array-CGH in pregnancies with ultrasound anomalies, and to a lesser extent in pregnancies referred for other reasons, was studied. Array-CGH showed an increased diagnostic yield compared to karyotyping, varying from 1-5%, depending on the reason for referral. Knowledge of the spectrum of array-CGH anomalies detected in the prenatal setting will increase rapidly in the years to come, thus facilitating pre- and posttest counseling. Meanwhile, new techniques like non-invasive prenatal diagnosis are emerging and will claim their place. In this review, we summarize the outcome of studies on prenatal array-CGH, the clinical relevance of differences in detection rate and range as compared to standard karyotyping, and reflect on the future integration of new molecular techniques in the workflow of prenatal diagnosis.     

Anomalies of the early stages of development of <Emphasis Type="Italic">Erysiphe graminis tritici</Emphasis> under oxidative stress

Early stage interactions between the powdery mildew pathogen and a host plant are studied. Treatment of wheat leaves with various concentrations of hydrogen peroxide and 3-amino-1,2,4-triazole resulted in the formation of morphological anomalies of germ tubes and nonviable colonies on host plant leaves. The observed effect of oxidative stress on germination anomalies of powdery mildew is similar to previously reported interactions between the pathogen and mildew resistant plants. We conclude that abnormal infectious structure formation of wheat powdery mildew may be associated with increased presence of reactive oxygen species during plant defense responses.     

Frequency of congenital anomalies at the Instituto Materno Infantil,Bogota, Colombia

At the Instituto Materno Infantil (IMI) in Bogotá (Colombia), 5,686 births (5,597 live births and 89 stillbirths) were analyzed during two periods: from October, 1997, to April, 1998, and from July to November, 2000 (12 months). Congenital anomalies were detected in 4.4% of live newborn babies and in 7.8% of stillbirths. Major anomalies corresponded to 69% and mild anomalies to 31% (3% and 1.4% of all live births, respectively). The newborn babies with major anomalies, in comparison to the normal controls, had higher mortality at hospital discharge (p = 0.0001), lower average birth weight (p = 0.003), and family history of congenital anomalies (p = 0.0001). The only significant association for mild anomalies was with family history of congenital anomalies (p = 0.0001). The frequency of congenital anomalies was similar to that in other studies, although certain kinds of anomalies showed noticeable frequency differences. This may be a consequence of differences in record keeping or in detection methods.     

A histopathological report of some epidermal anomalies of Dover sole, Solea solea L., and other flatfish species in coastal waters off south-east England

The gross pathological and histological changes of typical examples of epidermal anomalies of Dover sole, Solea solea L., and other flatfish from the sewage dumping areas of the Thames Estuary and two 'control' areas are described. Five per cent of flatfish showed anomalies including trawl damage abrasions, fin-rot, ulcers, nodules and tumours, lymphocystis and skeletal anomalies. Many of the anomalies suggested a traumatic aetiology and were often chronic. There was no significant difference in disease incidence between the areas sampled, except more evidence of lymphocystis in one of the control areas.