oak woodlands
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2022 ◽  
Vol 504 ◽  
pp. 119811
Author(s):  
Teresa Mexia ◽  
Xavier Lecomte ◽  
Maria Conceição Caldeira ◽  
Miguel Nuno Bugalho

Forests ◽  
2021 ◽  
Vol 12 (12) ◽  
pp. 1739
Author(s):  
Carl Nordman ◽  
Don Faber-Langendoen ◽  
Joanne Baggs

Open woodlands dominated by shortleaf pine (Pinus echinata Mill.) and oak are historically an important component of the landscape across the southeastern United States. These ecosystems support numerous wildlife species, many of which have declined in recent years as the amount and condition of their habitat have declined. Land managers and private landowners need guidance on how to efficiently and accurately quantify the condition and wildlife habitat value of the pine stands that they manage. Here we provide a set of rapid assessment metrics, based on NatureServe’s ecological integrity assessment (EIA) method, to (a) identify exemplary tracts that provide the best habitat for key wildlife species, and (b) monitor restoration efforts to assess progress toward the improved quality of existing tracts. To ensure an ecologically appropriate scaling of metrics, we distinguished six types of shortleaf pine–oak woodland: A.—Interior Highlands shortleaf pine–oak (including A.1—shortleaf pine–oak forest and woodlands; A.2—shortleaf pine–bluestem woodlands); B—montane longleaf pine–shortleaf pine woodlands; C—southern Appalachian pine–oak woodlands; D—West Gulf coastal plain shortleaf pine–oak woodlands; and E—southeast coastal plain and Piedmont shortleaf pine–oak woodlands. We relied on a narrative conceptual model and peer review-based indicator selection to identify a core set of 15 stand-level metrics (two were optional). Individual assessment points (thresholds) and ratings (Excellent, Good, Fair, and Poor) were developed that were sensitive to the distinct attributes of each of the five shortleaf pine–oak and Appalachian pine–oak types. Values for the metrics can all be collected using rapid field methods, such as using basal area prisms and ocular (visual) estimates of cover. Protocols for the consistent application of these EIA methods are provided. A case study is presented from the Cherokee National Forest in Tennessee. These methods provide improved and rapid EIA metrics for all shortleaf pine–oak ecosystems in the southeastern US to help guide conservation-minded landowners in assessing the biodiversity and priority wildlife values of shortleaf pine–oak and southern Appalachian pine–oak ecosystems.


2021 ◽  
Vol 13 (24) ◽  
pp. 13581
Author(s):  
María Pilar González-Hernández ◽  
Juan Gabriel Álvarez-González

Wooded pastures serve as a traditional source of forage in Europe, where forest grazing is valued as an efficient tool for maintaining the diversity of semi-natural habitats. In a forest grazing setting with diverse diet composition, assessing the energy content of animal diets can be a difficult task because of its dependency on digestibility measures. In the present study, prediction equations of metabolizable energy (ME) were obtained performing stepwise regression with data (n = 297; 44 plant species) on nutritional attributes (Acid Detergent Fiber, lignin, silica, dry matter, crude protein, in vitro organic matter digestibility) from 20 representative stands of Atlantic dry heathlands and pedunculate oak woodlands. The results showed that the prediction accuracy of ME is reduced when the general model (R2 = 0.64) is applied, as opposed to the use of the specific prediction equations for each vegetation type (R2 = 0.61, 0.66, 0.71 for oak woodlands; R2 = 0.70 heather-gorse dominated heathlands, R2 = 0.41 continental heathlands). The general model tends to overestimate the ME concentrations in heaths with respect to the observed ME values obtained from IVOMD as a sole predictor, and this divergence could be corrected by applying the specific prediction equations obtained for each vegetation type. Although the use of prediction equations by season would improve accuracy in the case of a Winter scenario, using the general model as opposed to the prediction equations for Spring, Summer or Fall would represent a much smaller loss of accuracy.


2021 ◽  
Vol 40 (4) ◽  
pp. 392-400
Author(s):  
Diana Yuzyk ◽  
Angela Chaplyhina

Abstract The diet spectrum of the great tit (Parus major L., 1758) was studied in transformed forests of northeastern Ukraine. Four forest ecosystems were surveyed: four model sites in oak woodlands and in a pine–oak forest with different stages of recreational digression. Forty-seven taxa of invertebrates (n = 325) were detected in the ration of great tit chicks. Insecta (72.4%): Lepidoptera (seven families, 35.9%), Hymenoptera (two families, 21.0%), Diptera (seven families, 2.7%) and Coleoptera (four families, 1.8%) were among them. In terms of the qualitative composition of invertebrates (20 species, 42.6%) and the proportion of seized food objects (159 objects), phytophages prevailed. The food composition of great tit chicks was the most similar in territories MS1 and MS4. It contained six common taxa for these territories (Stugren–Radulescu Index = 0.7, Jaccard = 0.2, Sorensen = 0.3).


2021 ◽  
Vol 300 ◽  
pp. 113741
Author(s):  
Ondřej Košulič ◽  
Jiří Procházka ◽  
Ivan H. Tuf ◽  
Radek Michalko

CATENA ◽  
2021 ◽  
Vol 206 ◽  
pp. 105514
Author(s):  
Esther Bochet ◽  
María José Molina ◽  
Vicente Monleón ◽  
Tíscar Espigares ◽  
José Manuel Nicolau ◽  
...  

Plant Disease ◽  
2021 ◽  
Author(s):  
Sean A. Wright ◽  
Bradley Lalande ◽  
Nick Wilhemi ◽  
Jane E. Stewart

In 2019, a decline of Quercus emoryi (Emory oak) was observed on the Coronado National Forest located in southeastern Arizona. Symptoms associated with oak mortality included crown die-back and large cankers revealing charcoal-like stromal growth. Trunks and root collars showed girdling and many affected trees also displayed evidence of gold-spotted oak borer activity. Initial surveys in stands identified clusters of severe infections. Samples with black perithecia and stromal tissue were collected from symptomatic hosts. Morphological characterization of the fungus was completed on fresh perithecial tissue. Stromata were pulvinate and black showing embedded perithecial bumps, with ostioles visible from the surface of the stroma. Asci were short stipitate and cylindrical with visible oil drops, 6.6 to 9.4 (mean: 8.8) × 139.8 to 179.9 μm (mean: 166.4). Ascospores were smooth ovoid, brown to dark brown, with narrowed and round ends, 6.9 to 9.1 (mean: 7.7) × 13.8 to 25.9 μm (mean: 16.5). Colonies grown on ½ strength potato dextrose agar (½ PDA) (Korhonen 1980) at 25°C for 14 days were whitish-grey when viewed from the top and darkened embedded spheres were visible from the bottom. Single-spored cultures were isolated by dissecting the hymenium and placing in distilled water. The suspension was streaked onto ½ PDA plates and incubated for 12 hours, and pure cultures were grown on ½ PDA. DNA was isolated from a mycelial scrape and extracted using a 10% Chelex solution (Safaee 2017). The internal transcribed spacer region was amplified with the ITS1/ITS4 primers (White et al. 1990) and PCR products were sequenced at Eurofins Scientific (Lewisville, KY). Isolates (BSS1, BSS2, BSS3, BSS4) were compared to other Biscogniauxia mediterranea sequences in the NCBI database (MG098274, EF026134) and had 100% sequence identity. Pathogenicity assays were conducted using 8-year-old Emory oaks in a greenhouse. The oaks were drought stressed and watered at 50% pot capacity for two months prior to inoculation. Each tree received approximately 2400 ml of water every two weeks for the remainder of the experiment. Eight trees were wounded three times with a 5mm corer. A 5mm plug of mycelium of isolate BSS2 was used to inoculate wounds. Four trees were used as controls and inoculated with ½ PDA plugs. Wounded and inoculated areas were assessed after three months. All eight trees exhibited dark necrotic tissue in the vascular cambium and lesions ranged from 11.4 – 25.8 mm in length and were 3.9 – 13.3 mm wide. The controls exhibited no fungal sign, lesions, or necrotic tissues. The pathogen B. mediterranea was recovered from 13 of the 24 total inoculations and its identity was confirmed with ITS sequencing. Mortality and die-back caused by Biscogniauxia spp. are commonly associated with drought-stressed trees, with increasingly hot and dry conditions routinely noted as inciting factors (Desprez Loustau et al.). Emory oaks are among the dominant tree species in much of the Madrean oak woodlands of the southwestern US and Mexico and provide vital ecological and cultural services. As southwestern states continue to experience hotter and drier, conditions, it is likely Emory oak will become increasingly susceptible to die-back and mortality due to this Biscogniauxia species (Southern et al.).


2021 ◽  
Author(s):  
Nathan Lamb ◽  
Kayri Havens ◽  
Jalen Holloway ◽  
James F. Steffen ◽  
Jacob Zeldin ◽  
...  

Western Birds ◽  
2021 ◽  
Vol 52 (3) ◽  
pp. 222-239
Author(s):  
Daniel A. Airola ◽  
Lily A. Douglas ◽  
Layla Airola

Most research on the ecology of the Yellow-billed Magpie (Pica nuttalli) has been focused in oak woodlands and savannas in California’s Coast Ranges; urban and suburban populations, some of which are sizable, have received little attention. In 2020, we studied eight colonies in six parks around Sacramento and in 2021 expanded the survey to 43 sites, detecting 827 breeding magpies. Population estimates based on nest counts were generally higher than those from direct counts, and nest counts were more repeatable and efficient. Counts of recently fledged young in family groups yielded reproductive rates similar to those observed near the coast before arrival of West Nile virus in 2003, suggesting that the virus is not currently affecting nestlings’ survival. Sacramento magpies nested in the upper canopy of a wide variety of large trees, both native and non-native. They foraged preferentially in low herbaceous habitat—irrigated turf and unirrigated annual grassland that was mowed or grazed. The presence of rivers and streams influenced occupancy strongly. Colony size was strongly related to the amount of low herbaceous foraging habitat within 0.5 km of colony sites with nearby flowing water. Our results suggest that at least 4 ha of low herbaceous foraging habitat is needed to support a small nesting colony. Retention of herbaceous habitat near large trees and flowing water, plus mowing or grazing to keep herbaceous growth low, should benefit urban Yellow-billed Magpies.


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