We provide detailed breeding parameters for the population of monk parakeets, Myiopsitta monachus, in Barcelona, Spain, based on data collected for 651 nests over five breeding seasons. This invasive population has a high reproductive capacity compared to the native range: fledging success was double, the percentage of pairs attempting second broods three times higher, and 55% of one-year old birds bred compared to almost zero in South America.
Food is a main limiting factor for most populations. As a consequence, knowledge about the diet of invasive alien species determines the design of control measures. The Monk and Rose-ringed parakeets are two typical species of successful invasive parrots that are highly appreciated by people. Although some observations suggest that Monk parakeets rely on a higher percentage of anthropogenic food than Rose-ringed parakeets, no detailed quantitative data is available. The aim of this study was to compare the diet of the two parakeets using stable isotope analysis (SIA). We performed SIA of carbon and nitrogen in feathers collected in Barcelona, Spain. We also measured isotopic ratios for potential food sources. We reconstructed the diet of parakeets using Bayesian mixing models. The two species differed in the isotopic signatures of their feathers for both δ13C and δ15N. Diet reconstruction showed that Monk parakeets feed mainly on anthropogenic food (41.7%), herbaceous plants (26.9%) and leaves/seeds (22.2%), while Rose-ringed parakeets feed mainly on flowers/fruits (44.1%), anthropogenic food provided in the trap located at the museum (32.4%) and leaves/seeds (23.1%). The more detailed information we can obtain from the diet of these species is useful to develop more effective control measures for their populations. The Monk parakeet may be more susceptible to control through education local residents, given the greater use of anthropogenic food in this species compared to Rose-ringed parakeet. Our conclusions also indicate that SIA is a powerful tool in providing crucial information about the diet and informing measures to control invasive species.
Many species only show sexual dimorphism at the age of maturity, such that juveniles typically resemble females. Under these circumstances, estimating accurate age‐specific demographic parameters is challenging. Here, we propose a multievent model parameterization able to estimate age‐dependent survival using capture–recapture data with uncertainty in age and sex assignment of individuals. We illustrate this modeling approach with capture–recapture data from the ring‐necked parakeet Psittacula krameri. We analyzed capture, recapture, and resighting data (439 recaptures/resightings) of 156 ring‐necked parakeets tagged with neck collars in Barcelona city from 2003 to 2016 to estimate the juvenile and adult survival rate. Our models successfully estimated the survival probabilities of the different age classes considered. Survival probability was similar between adults (0.83, 95% CI = 0.77–0.87) and juveniles during their second (0.79, 95% CI = 0.58–0.87) and third winter (0.83, 95% CI = 0.65–0.88). The youngest juveniles (1st winter) showed a slightly lower survival (0.57, 95% CI = 0.37–0.79). Among adults, females showed a slightly higher survival than males (0.87, 95% CI = 0.78–0.93; and 0.80, 95% CI = 0.73–0.86, respectively). These high survival figures predict high population persistence in this species and urge management policies. The analysis also stresses the usefulness of multievent models to estimate juvenile survival when age cannot be fully ascertained.
Invasive species can have wide-ranging negative impacts, and an understanding of the process and success of invasions can be vital to determine management strategies, mitigate impacts and predict range expansions of such species. Monk parakeets (Myiopsitta monachus) and ring-necked parakeets (Psittacula krameri) are both widespread invasive species, but there has been little research into the genetic and social structure of these two species despite the potential links with invasion success. The aim of this study was to isolate novel microsatellite loci from the monk parakeet and characterise them in both monk and ring-necked parakeets in order to facilitate future investigations into their behaviour and population ecology. Sex-typing markers were also tested in both species. Of the 20 microsatellite loci assessed in 24 unrelated monk parakeets, 16 successfully amplified and were polymorphic displaying between 2 and 14 alleles (mean = 8.06). Expected heterozygosity ranged from 0.43 to 0.93 and observed heterozygosity ranged from 0.23 to 0.96. Nine of the 20 loci also successfully amplified and were polymorphic in the ring-necked parakeet, displaying between 2 and 10 alleles. Suitable markers to sex both species and a Z-linked microsatellite locus were identified. A multiplex marker set was validated for monk parakeets. These novel microsatellite loci will facilitate fine and broad-scale population genetic analyses of these two widespread invasive species.Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Stable isotope analyses (SIAs) have been widely used in recent years to infer the diet of many species. This isotopic approach requires using diet to tissue discrimination factors (DTDFs) for each prey type and predator tissue, i.e., to determine the difference between the isotopic composition of the predator tissues and the different prey that conform its diet. Information on DTDF values in Psittaciformes is scarce. The aim of this study was to assess DTDF values for the carbon and nitrogen isotopes of the monk parakeet (Myiopsitta monachus) and the ring–necked parakeet (Psittacula krameri), two invasive alien species of concern. We fed captive birds of the two parakeet species on a single–species diet based on sunflower seeds to establish the DTDFs for the blood and feathers. In the monk parakeet (N = 9) DTDFs were Δδ13C 2.14 ‰ ± 0.90 and Δδ15N 3.21 ‰ ± 0.75 for the blood, and Δδ13C 3.97 ‰ ± 0.90 and Δδ15N 3.67 ‰ ± 0.74 for the feathers. In the ring–necked parakeet (N = 9), the DTDFs were Δδ13C (‰) 2.58 ± 0.90 and Δδ15N (‰) 2.35 ± 0.78 for the blood, and Δδ13C 3.64 ‰ ± 0.98 and Δδ15N 4.10 ‰ ± 1.84 for the feathers. DTDF values for the ring–necked parakeet blood were significantly higher than those for the monk parakeet blood. No difference was found between the two species in the DTDF for feathers. Our findings provide the first values of DTDFs for blood and feathers in these parakeets, factors that are key to infer the diet of these species based on SIA.
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