One goal of conservation biology is to explain population declines. We present field survey data and experimental evidence that implicate introduced predators as a possible cause of decline in the California newt (Taricha torosa). In 1994 and 1995 we surveyed 10 streams in the Santa Monica Mountains of southern California for amphibians. These streams contained California newts when surveyed between 1981 and 1986. Of the 10 streams surveyed in 1994, three contained introduced mosquitofish (Gambusia affinis) and/or crayfish (Procambarus clarkii). These three streams contained no California newt eggs, larvae, or adults. The seven streams without introduced predators contained California newts. We conducted laboratory and field experiments to determine if California newt larvae and egg masses are susceptible to predation by mosquitofish and crayfish. Results from these experiments indicate that crayfish consume California newt egg masses and that both mosquitofish and crayfish consume larval newts. In 24‐hour field experiments, no newt larvae survived in crayfish enclosures, and only 13% of the larvae survived with mosquitofish. Newt larvae are known to have antipredator adaptations for native predators. Apparently, these adaptations are not adequate for coexistence with introduced crayfish or mosquitofish. Heavy rains in 1995 removed introduced crayfish from one stream. We found newt egg masses, larvae, and adults in that stream the following spring. This same stream showed no evidence of California newts when crayfish were present in matched‐date surveys in 1994. These experiments and surveys present evidence that predation by mosquitofish and crayfish may cause localized decline of newts in mountain streams of southern California. Understanding the effects of nonnative species is an important step in preventing detrimental introductions in the future.
Proximal avulsions of the rectus femoris can be treated nonoperatively with a high degree of predictability for return to full, unrestricted participation in professional American football.
The purpose of this study was to evaluate the role of BMPs on the formation of metastatic prostate cancer lesions to bone. Our results show that BMPs influence the development and progression of osteoblastic lesions and suggest that therapies that inhibit BMP activity may reduce the formation and progression of osteoblastic lesions.Introduction: Prostate adenocarcinoma is the leading cause of cancer in North American men. The formation of skeletal metastases affects∼70% of patients with advanced disease, and a majority of these patients have osteoblastic lesions. Although BMPs have been found to be expressed in multiple oncogenic cell lines, their role in the formation of metastatic osteoblastic lesions remains uncharacterized. We hypothesized that BMPs influence the development of metastatic osteoblastic lesions associated with prostate cancer. Materials and Methods: Western blot analysis and RT-PCR was used to determine BMP receptor expression on osteoblastic prostate cancer cell lines LAPC-4 and LAPC-9. Migration, invasion, and cellular proliferation assays were used to quantify the effects of BMP-2, -4, and -7 on LAPC-4 cells in vitro. LAPC-9 cells alone or transfected with a retrovirus overexpressing noggin were injected into the tibias of SCID mice, and the animals were followed for 8 weeks. Tumor size was determined by radiographs and direct measurement. Histology was performed at the time of death. Results: We determined that BMP receptor mRNA and protein was expressed on osteoblastic prostate cancer cell lines LAPC-4 and LAPC-9. In vitro studies showed that BMP-2 and -7 stimulated cellular migration and invasion of prostate cancer cells in a dose-dependent fashion, although BMP-4 had no effect. Noggin inhibited cellular migration and invasion of BMP-2-and -7-stimulated LAPC-4 cells. LAPC-9 cells implanted into immunodeficient mouse tibias formed an osteoblastic lesion with sclerotic bone at 8 weeks. Formation of osteoblastic lesions was inhibited by overexpression of noggin by prostate cancer cells transduced with a retrovirus containing the cDNA for noggin. Conclusions: BMPs are critical in the formation of the osteoblastic lesions associated with prostate cancer metastases, and future treatment strategies that inhibit local BMP activity may reduce the formation and progression of osteoblastic lesions.
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